OGI Tomoo 荻朋男

Researcher Number	80508317
Other IDs	https://orcid.org/0000-0002-5492-9072
External Links
Affiliation (Current)	2025: 名古屋大学, 環境医学研究所, 教授
Affiliation (based on the past Project Information) *help	2015 – 2024: 名古屋大学, 環境医学研究所, 教授 2013 – 2014: 長崎大学, 原爆後障害医療研究所, 准教授 2013: 長崎大学, 7原爆後障害医療研究所, 准教授 2012: 長崎大学, 医歯薬学総合研究科, 准教授 2012: 長崎大学, 大学院・医歯薬学総合研究科, 准教授 … More 2011 – 2012: 長崎大学, 医歯(薬)学総合研究科, 准教授 2011: 長崎大学, 医歯(薬)学総合研究科, 助教 2008 – 2011: Nagasaki University, 大学院・医歯薬学総合研究科, 助教 Less
Review Section/Research Field	Principal Investigator Risk sciences of radiation/Chemicals / Medium-sized Section 63:Environmental analyses and evaluation and related fields / Risk sciences of radiation and chemicals / Pediatrics / Human genetics / Molecular biology / Dermatology Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Medium-sized Section 58:Society medicine, nursing, and related fields / Basic Section 63020:Radiation influence-related … More / Risk sciences of radiation and chemicals / Basic Section 52040:Radiological sciences-related / Basic Section 53050:Dermatology-related / Basic Section 48040:Medical biochemistry-related / Basic Section 43010:Molecular biology-related / Tumor biology / Pediatrics / Epidemiology and preventive medicine / Pathological medical chemistry / Human genetics Less
Keywords	Principal Investigator DNA修復 / ヌクレオチド除去修復 / DNA修復欠損性疾患 / ゲノムインスタビリティ / ゲノム不安定性疾患 / 修復 / 転写と共役したヌクレオチド除去修復 / マルチオミクス解析 / 損傷DNA修復・損傷応答機構 / 環境ストレス … More / ユビキチン化 / RNAポリメラーゼII / 紫外線高感受性症候群 / UVSSA / ヌクレオチド除去修復機構 / Cockyane syndrome / RNA polymerase II / UV sensitive syndrome / Ubiquitination / RNA polymerase Ⅱ / TC-NER / がん・老化関連疾患 / DNA修復・転写共役修復 / 環境ストレス・環境変異原 / 転写共役修復 (TC-NER) / 次世代オミクス解析 / DNA損傷応答 / 遺伝性小頭症 / 遺伝・先天異常学 / DNA損傷 / 発がん / 突然変異 / 放射線DNA損傷 … More Except Principal Investigator 放射線 / DNA修復 / ゲノム / RNAポリメラーゼ / 急性脳症 / MERS / 可逆性脳梁膨大部病変 / オリゴデンドロサイト / MYRF / 転写 / 感染症診断 / 重症感染症 / 次世代シークエンス / ゲノム不安定性 / プロテオーム解析 / コケイン症候群 / 甲状腺癌 / DNA損傷応答 / タンパク質間相互作用 / 画像認識 / 中心体 / 放射性ヨウ素 / オルガノイド / 遺伝性皮膚疾患 / 自己炎症 / 角化異常症 / 色素性乾皮症 (XP) / XPJ / ユビキチン化 / 転写と共役したDNA修復 / ゲノム刻印 / ウイルス変異株 / 薬剤耐性 / リアルタイムシークエンス / 病原微生物診断 / 呼吸器感染症 / ロングリード法 / リアルタイムシークエンス法 / HPRTクローン / HPRT変異クローン / ミエリン / ミクログリア / 可逆性脳梁膨大部病変を有する軽症脳炎・脳症 / DNA損傷 / 解析パイプライン / 病原微生物 / リキッドバイオプシー / ナノポアシークエンス / ショートリード / マルチオミクス解析 / 疾患ゲノム解析 / 遺伝性疾患 / DNA損傷応答システム / 修復 / 小頭症 / 蛋白質間相互作用 / インタラクトーム解析 / 遺伝子破壊 / 低酸素 / 分子内責任部位 / RNA polymerase II / 転写共役型ヌクレオチド除去修復 / 塩基除去修復 / 紫外線高感受性症候群 / ヌクレオチド除去修復 / 甲状腺がん / 細胞死 / アポトーシス / ゲノム編集 / 相同組換え / RAD51 / CBP / p300 / RAD52 / DNA相同組換え / 脱アセチル化 / アセチル化 / U2OS / DR-GFP / 中心体複製 / DNA損傷修復 / BRCA2 / BRCA / 乳癌 / 軟口蓋裂 / 脳動静脈奇形 / 遺伝子座マッピング / 骨髄異形成症 / SOLiD / emulsion PCR / 筋萎縮性側索硬化症 / 歌舞伎症候群 / エキソンキャプチャー法 / 次世代型シーケンサー / ゲノム医科学 Less

色素性乾皮症の新規責任遺伝子XPJによるDNA修復と転写制御機構の解明
- Principal Investigator
  
  中沢由華
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 48040:Medical biochemistry-related
- Research Institution
  Nagoya University
自己炎症性角化症の未知の炎症メカニズムの解析と治療法の確立
- Principal Investigator
  
  武市拓也
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 53050:Dermatology-related
- Research Institution
  Nagoya University
MYRF遺伝子による可逆性大脳白質障害と発熱時異常言動の病態解明
- Principal Investigator
  
  倉橋宏和
- Project Period (FY)
  2024 – 2027
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Aichi Medical University
放射線被ばくによるゲノム不安定性の解明
- Principal Investigator
  
  光武範吏
- Project Period (FY)
  2024 – 2025
- Research Category
  
  Grant-in-Aid for Challenging Research (Exploratory)
- Review Section
  
  Medium-sized Section 58:Society medicine, nursing, and related fields
- Research Institution
  Nagasaki University
人はなぜ老い・病(やまい)になるのか－環境ストレス病態相関の理解Principal Investigator
- Principal Investigator
  
  荻朋男
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Review Section
  
  Medium-sized Section 63:Environmental analyses and evaluation and related fields
- Research Institution
  Nagoya University
甲状腺癌オルガノイドを用いた放射性ヨウ素治療抵抗性機序の解明
- Principal Investigator
  
  光武範吏
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 52040:Radiological sciences-related
- Research Institution
  Nagasaki University
薬剤耐性・変異株解析可能なリアルタイム次世代シークエンスによる重症感染症迅速診断
- Principal Investigator
  
  伊藤嘉規
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Aichi Medical University
  Nihon University
細胞種によって放射線被ばく刻印は異なるのか？
- Principal Investigator
  
  光武範吏
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Challenging Research (Exploratory)
- Review Section
  
  Medium-sized Section 58:Society medicine, nursing, and related fields
- Research Institution
  Nagasaki University
Molecular mechanisms of transcription-coupled repair (TCR) and pathogenesis of TCR-deficient human genetic disorders
- Principal Investigator
  
  NAKAZAWA Yuka
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 43010:Molecular biology-related
- Research Institution
  Nagoya University
MYRF遺伝子を起点とした発熱時言動異常の病態解明
- Principal Investigator
  
  倉橋宏和
- Project Period (FY)
  2020 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Aichi Medical University
Identification of genomic radiation signature using long-read sequencing
- Principal Investigator
  
  MITSUTAKE Norisato
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Challenging Research (Exploratory)
- Review Section
  
  Medium-sized Section 58:Society medicine, nursing, and related fields
- Research Institution
  Nagasaki University
Molecular pathogenesis of human disorders associated with deficiencies in the DNA repair and environmental stress response systemsPrincipal Investigator
- Principal Investigator
  
  OGI Tomoo
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Review Section
  
  Medium-sized Section 63:Environmental analyses and evaluation and related fields
- Research Institution
  Nagoya University
Next-generation sequencing
- Principal Investigator
  
  ITO Yoshinori
- Project Period (FY)
  2019 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nihon University
  Nagoya University
Development of new technology to evaluate the transcription-coupling repair factors.
- Principal Investigator
  
  Hashimoto Satoru
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 63020:Radiation influence-related
- Research Institution
  Oita University
  Nagoya University
Interactome analysis after induction of DNA damage in human cells
- Principal Investigator
  
  Kurotani Kenichi
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 63020:Radiation influence-related
- Research Institution
  Nagoya University
Elucidation of the molecular pathogenesis of genetic disorders caused by defects in DNA damage response using deep proteomic analysis
- Principal Investigator
  
  Oka Yasuyoshi
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 63020:Radiation influence-related
- Research Institution
  Nagoya University
Molecular pathogenesis of human genetic disorders associated with deficiency in the DNA repair and damage response systemPrincipal Investigator
- Principal Investigator
  
  OGI Tomoo
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Risk sciences of radiation and chemicals
- Research Institution
  Nagoya University
DNA double strand break repair factors mutated in a new syndrome with microcephaly
- Principal Investigator
  
  NAKAZAWA Yuka
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Risk sciences of radiation and chemicals
- Research Institution
  Nagoya University
  Nagasaki University
Genetic diagnosis of microcephalyPrincipal Investigator
- Principal Investigator
  
  OGI Tomoo
- Project Period (FY)
  2016 – 2017
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Pediatrics
- Research Institution
  Nagoya University
Biochemical analysis of transcription coupled nucleotide excision repair factors
- Principal Investigator
  
  KARATA Kiyonobu
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Risk sciences of radiation and chemicals
- Research Institution
  Nagoya University
Molecular regions of BRCA proteins responsible for cancer suppression
- Principal Investigator
  
  Takenaka Katsuya
- Project Period (FY)
  2015 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Tumor biology
- Research Institution
  Kanagawa Cancer Center Research Institute
Molecular epidemiology studies on rare genetic disorders and pediatric cancer cohorts associated with genome instabilityPrincipal Investigator
- Principal Investigator
  
  OGI Tomoo
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Human genetics
- Research Institution
  Nagoya University
Mechanism of genomic DNA damage response mediated by acetylation of non-histone proteins
- Principal Investigator
  
  YASUDA Takeshi
- Project Period (FY)
  2014 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Risk sciences of radiation and chemicals
- Research Institution
  National Institutes for Quantum and Radiological Science and Technology
In vitro reconstitution of the initiation process of transcription-coupled nucleotide-excision repairPrincipal Investigator
- Principal Investigator
  
  OGI Tomoo
- Project Period (FY)
  2014 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Molecular biology
- Research Institution
  Nagoya University
  Nagasaki University
The molecular epidemiological study of DNA repair-related genes in post-Chernobyl radiation-induced thyroid cancers
- Principal Investigator
  
  MITSUTAKE Norisato
- Project Period (FY)
  2014 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Epidemiology and preventive medicine
- Research Institution
  Nagasaki University
Identification of novel disease-causing gene mutations in patients with UV-sensitive syndromes
- Principal Investigator
  
  SHIMADA Mayuko
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Nagasaki University
転写共役修復開始反応の分子機能解析（遺伝性光線過敏症の分子基盤）Principal Investigator
- Principal Investigator
  
  荻朋男
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for JSPS Fellows
- Research Field
  
  Risk sciences of radiation and chemicals
- Research Institution
  Nagoya University
  Nagasaki University
A rapid, comprehensive system for assaying DNA repair activity and cytotoxic effects of DNA-damaging reagentsPrincipal Investigator
- Principal Investigator
  
  OGI Tomoo
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Dermatology
- Research Institution
  Nagasaki University
Stalled RNA polymerase processing in transcription-coupled nucleotide-excision repairPrincipal Investigator
- Principal Investigator
  
  OGI Tomoo
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Young Scientists (A)
- Research Field
  
  Risk sciences of radiation/Chemicals
- Research Institution
  Nagasaki University
Function of novel BRCA2-associating proteins in centrosomal regulation and DNA repair
- Principal Investigator
  
  TAKENAKA Katsuya
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  Tokyo Medical and Dental University
Comprehensive analyses of the nucleotide excision repair (NER) molecular mechanismsPrincipal Investigator
- Principal Investigator
  
  OGI Tomoo
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Risk sciences of radiation/Chemicals
- Research Institution
  Nagasaki University
Mapping of the disease loci using SNP genotyping and identification of the gene by the sequence capture method
- Principal Investigator
  
  YOSHIURA Koichiro
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Human genetics
- Research Institution
  Nagasaki University
Functional analyses of DNA polymerases in nucleotide excision repairPrincipal Investigator
- Principal Investigator
  
  OGI Tomoo
- Project Period (FY)
  2008 – 2009
- Research Category
  
  Grant-in-Aid for Young Scientists (Start-up)
- Research Field
  
  Risk sciences of radiation/Chemicals
- Research Institution
  Nagasaki University

[Journal Article] Genetic background variation impacts microglial heterogeneity and disease progression in amyotrophic lateral sclerosis model mice.2024
- Author(s)
  Komine O., Ohnuma S., Hinohara K., Hara Y., Shimada M., Akashi T., Watanabe S., Sobue A., Kawade N., Ogi T., Yamanaka K..
- Journal Title
  
  iScience
  
  Volume: 27 Issue: 2 Pages: 108872-108872
- DOI
  10.1016/j.isci.2024.108872
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K13902, KAKENHI-PROJECT-23K14687, KAKENHI-PROJECT-23K06826, KAKENHI-PROJECT-20K16488, KAKENHI-PROJECT-21K20569, KAKENHI-PROJECT-22H00467, KAKENHI-PROJECT-23H00516
[Journal Article] Endogenous aldehyde-induced DNA-protein crosslinks are resolved by transcription-coupled repair2024
- Author(s)
  Oka Yasuyoshi、Nakazawa Yuka、Shimada Mayuko、Ogi Tomoo
- Journal Title
  
  Nature Cell Biology
  
  Volume: - Issue: 5 Pages: 784-796
- DOI
  10.1038/s41556-024-01401-2
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02399
[Journal Article] Lysosomal cholesterol overload in macrophages promotes liver fibrosis in a mouse model of NASH2023
- Author(s)
  Itoh Michiko、Tamura Atsushi、Kanai Sayaka、Tanaka Miyako、Kanamori Yohei、Shirakawa Ibuki、Ito Ayaka、Oka Yasuyoshi、Hidaka Isao、Takami Taro、Honda Yasushi、Maeda Mitsuyo、Saito Yasuyuki、Murata Yoji、Matozaki Takashi、Nakajima Atsushi、Kataoka Yosky、Ogi Tomoo、Ogawa Yoshihiro、Suganami Takayoshi
- Journal Title
  
  Journal of Experimental Medicine
  
  Volume: 220 Issue: 11
- DOI
  10.1084/jem.20220681
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K19524, KAKENHI-PROJECT-22K08504, KAKENHI-PROJECT-22K08667, KAKENHI-PROJECT-22K11700, KAKENHI-PROJECT-21K08526, KAKENHI-PROJECT-22K19458, KAKENHI-PROJECT-19KK0249, KAKENHI-PROJECT-20H00629, KAKENHI-PUBLICLY-22H04806, KAKENHI-PUBLICLY-23H04776, KAKENHI-PROJECT-21H04807
[Journal Article] A case of Cockayne syndrome with unusually mild clinical manifestations2023
- Author(s)
  Tsujimoto Mariko、Nakano Eiji、Nakazawa Yuka、Kanda Fumio、Ueda Takehiro、Ogi Tomoo、Nishigori Chikako
- Journal Title
  
  The Journal of Dermatology
  
  Volume: 50 Issue: 4 Pages: 541-545
- DOI
  10.1111/1346-8138.16679
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K19844, KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02399
[Journal Article] Patients with keratinization disorders due to ABCA12 variants showing pityriasis rubra pilaris phenotypes.2023
- Author(s)
  Takeichi T, Hamada T, Yamamoto M, Ito Y, Kawaguchi A, Kobashi H, Yoshikawa T, Koga H, Ishii N, Nakama T, Muro Y, Ogi T, Akiyama M.
- Journal Title
  
  J Dermatol.
  
  Volume: 51 Issue: 1 Pages: 101-105
- DOI
  10.1111/1346-8138.16967
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08648, KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02941
[Journal Article] Deep intronic founder mutations identified in the ERCC4/XPF gene are potential therapeutic targets for a high-frequency form of xeroderma pigmentosum2023
- Author(s)
  Senju Chikako、Nakazawa Yuka、Oso Taichi、Shimada Mayuko、Kato Kana、Matsuse Michiko、Tsujimoto Mariko、Masaki Taro、Miyazaki Yasushi、Fukushima Satoshi、Tateishi Satoshi、Utani Atsushi、Murota Hiroyuki、Tanaka Katsumi、Mitsutake Norisato、Moriwaki Shinichi、Nishigori Chikako、Ogi Tomoo
- Journal Title
  
  Proceedings of the National Academy of Sciences
  
  Volume: 120 Issue: 27
- DOI
  10.1073/pnas.2217423120
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K19674, KAKENHI-PROJECT-22K07668, KAKENHI-PROJECT-21K08351, KAKENHI-PROJECT-21K19844, KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02399
[Journal Article] Utility of nanopore sequencing for detecting pathogens in bronchoalveolar lavage fluid from pediatric patients with respiratory failure.2023
- Author(s)
  Yamaguchi M, Horiba K, Haruta K, Takeuchi S, Suzuki T, Torii Y, Kawabe S, Wada S, Ikeyama T, Ito Y, Ogi T, Kawada JI.
- Journal Title
  
  J Clin Virol Plus
  
  Volume: 3 Issue: 2 Pages: 100154-100154
- DOI
  10.1016/j.jcvp.2023.100154
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22K07818
[Journal Article] Mitochondria-associated membrane collapse impairs TBK1-mediated proteostatic stress response in ALS2023
- Author(s)
  Watanabe Seiji、Murata Yuri、Oka Yasuyoshi、Oiwa Kotaro、Horiuchi Mai、Iguchi Yohei、Komine Okiru、Sobue Akira、Katsuno Masahisa、Ogi Tomoo、Yamanaka Koji
- Journal Title
  
  Proceedings of the National Academy of Sciences
  
  Volume: 120 Issue: 47
- DOI
  10.1073/pnas.2315347120
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K14687, KAKENHI-PROJECT-19KK0214, KAKENHI-PROJECT-23K06826, KAKENHI-PROJECT-22K19506, KAKENHI-PROJECT-20K16488, KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-22H00467
[Journal Article] Two patients with Hailey-Hailey disease with novel pathogenic ATP2C1 variants suggesting possible genotype/phenotype correlations2023
- Author(s)
  Omi Michiya、Takeichi Takuya、Ito Yasutoshi、Yoshikawa Takenori、Mizutani Yuki、Nagai Miki、Seishima Mariko、Ogi Tomoo、Muro Yoshinao、Akiyama Masashi
- Journal Title
  
  The Journal of Dermatology
  
  Volume: - Issue: 6
- DOI
  10.1111/1346-8138.17081
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20H00629
[Journal Article] Live cell transcription-coupled nucleotide excision repair dynamics revisited2023
- Author(s)
  Llerena Schiffmacher Diana A、Kliza Katarzyna W、Theil Arjan F、Kremers Gert-Jan、Demmers Jeroen AA、Ogi Tomoo、Vermeulen Michiel、Vermeulen Wim、Pines Alex
- Journal Title
  
  DNA Repair
  
  Volume: 130 Pages: 103566-103566
- DOI
  10.1016/j.dnarep.2023.103566
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23H00516, KAKENHI-PROJECT-21H02399
[Journal Article] DDA1, a novel factor in transcription-coupled repair, modulates CRL4CSA dynamics at DNA damage-stalled RNA polymerase II2023
- Author(s)
  Schiffmacher Diana Llerena、(他16名)、Ogi Tomoo、Vermeulen Wim、Pines Alex
- Journal Title
  
  Research Squar
  
  Volume: -
- DOI
  10.21203/rs.3.rs-3385435/v1
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02399, KAKENHI-PROJECT-23H00516
[Journal Article] Inducing multiple nicks promotes interhomolog homologous recombination to correct heterozygous mutations in somatic cells2023
- Author(s)
  Tomita Akiko、Sasanuma Hiroyuki、Owa Tomoo、Nakazawa Yuka、Shimada Mayuko、Fukuoka Takahiro、Ogi Tomoo、Nakada Shinichiro
- Journal Title
  
  Nature Communications
  
  Volume: 14 Issue: 1 Pages: 5607-5607
- DOI
  10.1038/s41467-023-41048-5
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K18314, KAKENHI-PROJECT-23H00516, KAKENHI-PROJECT-21H02399
[Journal Article] Case of ichthyosis with confetti caused by KRT10 mutation, complicated with multiple malignant melanomas.2022
- Author(s)
  Ito Yasutoshi、Takeichi Takuya、Nakagawa Koichi、Tanahashi Kana、Muro Yoshinao、Ogi Tomoo、Akiyama Masashi
- Journal Title
  
  The Journal of Dermatology
  
  Volume: 49 Issue: 7
- DOI
  10.1111/1346-8138.16348
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02941
[Journal Article] Aicardi-Goutieres syndrome with SAMHD1 deficiency can be diagnosed by unscheduled DNA synthesis test2022
- Author(s)
  Senju C, Nakazawa Y, Shimada M, Iwata D, Matsuse M, Tanaka K, Miyazaki Y, Moriwaki S, Mitsutake N, Ogi T.
- Journal Title
  
  Frontiers in Pediatrics
  
  Volume: 10 Pages: 1048002-1048002
- DOI
  10.3389/fped.2022.1048002
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K19844, KAKENHI-PROJECT-22K19674, KAKENHI-PROJECT-20K21718, KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02399
[Journal Article] Global landscape of replicative DNA polymerase usage in the human genome2022
- Author(s)
  Koyanagi Eri、Kakimoto Yoko、Minamisawa Tamiko、Yoshifuji Fumiya、Natsume Toyoaki、Higashitani Atsushi、Ogi Tomoo、Carr Antony M.、Kanemaki Masato T.、Daigaku Yasukazu
- Journal Title
  
  Nature Communications
  
  Volume: 13 Issue: 1 Pages: 7221-7221
- DOI
  10.1038/s41467-022-34929-8
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K19203, KAKENHI-PROJECT-22H04925, KAKENHI-PROJECT-20H03233, KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02399
[Journal Article] Deep Phenotyping of Superficial Epidermolytic Ichthyosis due to a Recurrent Mutation in KRT22022
- Author(s)
  Suzuki Yuika、Takeichi Takuya、Tanahashi Kana、Muro Yoshinao、Suga Yasushi、Ogi Tomoo、Akiyama Masashi
- Journal Title
  
  International Journal of Molecular Sciences
  
  Volume: 23 Issue: 14 Pages: 7791-7791
- DOI
  10.3390/ijms23147791
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02941
[Journal Article] Epithelioid cell granuloma formation in CARD14-associated papulosquamous eruptions.2022
- Author(s)
  Takeichi T, Ikeda K, Muro Y, Ogi T, Morizane S, Akiyama M.
- Journal Title
  
  J Eur Acad Dermatol Venereol.
  
  Volume: 36 Issue: 5
- DOI
  10.1111/jdv.17890
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08648, KAKENHI-PROJECT-20H00629
[Journal Article] Expanding the phenotypic spectrum of ARCN1-related syndrome.2022
- Author(s)
  Ritter AL, et.al
- Journal Title
  
  Genet Med.
  
  Volume: S1098-3600 Issue: 6 Pages: 00651-7
- DOI
  10.1016/j.gim.2022.02.005
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PLANNED-20H05940, KAKENHI-PROJECT-20H00629
[Journal Article] Whole-exome analysis of 177 pediatric patients with undiagnosed diseases.2022
- Author(s)
  Narita K, Muramatsu H, Narumi S, Nkawa T, Okumura A, et al.
- Journal Title
  
  Sci Rep
  
  Volume: 12(1) Issue: 1 Pages: 14589-14589
- DOI
  10.1038/s41598-022-14161-6
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07810, KAKENHI-PROJECT-20H03646, KAKENHI-PROJECT-18K07890, KAKENHI-PROJECT-20H00629
[Journal Article] The iodide transporter Slc26a7 impacts thyroid function more strongly than Slc26a4 in mice.2022
- Author(s)
  Yamaguchi N, Suzuki A, Yoshida A, Tanaka T, Aoyama K, Oishi H, Hara Y, Ogi T, Amano I, Kameo S, Koibuchi N, Shibata Y, Ugawa S, Mizuno H, Saitoh S
- Journal Title
  
  Sci Rep.
  
  Volume: 12 Issue: 1 Pages: 11259-11259
- DOI
  10.1038/s41598-022-15151-4
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K11714, KAKENHI-PROJECT-20K16934, KAKENHI-PROJECT-20H03646, KAKENHI-PROJECT-20H00629
[Journal Article] Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome2022
- Author(s)
  Stephenson Sarah E.M.、(他70名)、Ogi Tomoo、(他33名)、Tan Tiong Yang
- Journal Title
  
  The American Journal of Human Genetics
  
  Volume: 109 Issue: 4 Pages: 601-617
- DOI
  10.1016/j.ajhg.2022.03.002
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H00629
[Journal Article] Ceramide profiling of stratum corneum in Sjogren-Larsson syndrome2022
- Author(s)
  Arai Ayami, Takeichi Takuya, Wakamoto Hiroyuki, Sassa Takayuki, Ito Yasutoshi, Murase Yuya, Ogi Tomoo, Akiyama Masashi, Kihara Akio
- Journal Title
  
  Journal of Dermatological Science
  
  Volume: 107 Issue: 3 Pages: 114-122
- DOI
  10.1016/j.jdermsci.2022.08.003
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22H04986, KAKENHI-PROJECT-23K24020, KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02941
[Journal Article] Performance of Nanopore and Illumina Metagenomic Sequencing for Pathogen Detection and Transcriptome Analysis in Infantile Central Nervous System Infections2022
- Author(s)
  Horiba, K. Torii, Y. Aizawa, Y. Yamaguchi, M. Haruta, K. Okumura, T. Suzuki, T. Kawano, Y. Kawada, J. I. Hara, S. Saitoh, A. Giske, C. G. Ogi, T. Ito, Y.
- Journal Title
  
  Open forum infectious diseases
  
  Volume: 9 Issue: 10 Pages: 504-504
- DOI
  10.1093/ofid/ofac504
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07748, KAKENHI-PROJECT-19K08298
[Journal Article] The sodium-glucose cotransporter-2 inhibitor Tofogliflozin prevents the progression of nonalcoholic steatohepatitis-associated liver tumors in a novel murine model.2021
- Author(s)
  Yoshioka N, Tanaka M, Ochi K, Watanabe A, Ono K, Sawada M, Ogi T, Itoh M, Ito A, Shiraki Y, Enomoto A, Ishigami M, Fujishiro M, Ogawa Y, Suganami T.
- Journal Title
  
  Biomed Pharmacother
  
  Volume: 140 Pages: 111738-111738
- DOI
  10.1016/j.biopha.2021.111738
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K07475, KAKENHI-PROJECT-19K11765, KAKENHI-PROJECT-18H03372, KAKENHI-ORGANIZER-17H06391, KAKENHI-PLANNED-18H05429, KAKENHI-PUBLICLY-20H04944, KAKENHI-PUBLICLY-20H05503, KAKENHI-PROJECT-19H01054, KAKENHI-PROJECT-20H03447, KAKENHI-PROJECT-20K06871, KAKENHI-PROJECT-21K08526, KAKENHI-PROJECT-19KK0249
[Journal Article] Next-Generation Sequencing to Detect Pathogens in Pediatric Febrile Neutropenia: A Single-Center Retrospective Study of 112 Cases2021
- Author(s)
  Horiba K, Torii Y, Okumura T, Takeuchi S, Suzuki T, Kawada J, Muramatsu H, Takahashi Y, Ogi T, Ito Y
- Journal Title
  
  Open Forum Infect Dis
  
  Volume: 8 Issue: 11 Pages: 223-223
- DOI
  10.1093/ofid/ofab223
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08298, KAKENHI-PROJECT-20K17464, KAKENHI-PROJECT-21K07748
[Journal Article] Protein instability associated with AARS1 and MARS1 mutations causes Trichothiodystrophy2021
- Author(s)
  Botta E, Theil AF, Raams A, Caligiuri G, Giachetti S, Bione S, Accadia M, Lombardi A, Smith DEC, Mendes MI, Swagemakers SMA, van der Spek PJ, Salomons GS, Hoeijmakers JHJ, Yesodharan D, Nampoothiri S, Ogi T, Lehmann AR, Orioli D, Vermeulen W.
- Journal Title
  
  Human Molecular Genetics
  
  Volume: 30 Issue: 18 Pages: 1711-1720
- DOI
  10.1093/hmg/ddab123
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02399
[Journal Article] Updated allele frequencies of SERPINB7 founder mutations in Asian patients with Nagashima-type palmoplantar keratosis/keratoderma.2021
- Author(s)
  Ito Y, Takeichi T, Ikeda K, Tanahashi K, Yoshikawa T, Murase Y, Muro Y, Kawakami Y, Nakamura Y, Matsuyama K, Muto J, Oiso N, Morizane S, Sugiura K, Suga Y, Seishima M, Kawada A, Ogi T, Akiyama M.
- Journal Title
  
  J Dermatol Sci
  
  Volume: 103 Issue: 2 Pages: 116-119
- DOI
  10.1016/j.jdermsci.2021.06.002
- NAID
  120007190665
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K08336, KAKENHI-PROJECT-20H00629
[Journal Article] Extensive multiple organ involvement in VEXAS syndrome2021
- Author(s)
  Takahashi Noriyuki、Takeichi Takuya、Nishida Tetsuya、Takahashi Yasuhiro、Sato Juichi、Yamamura Masahiro、Ogi Tomoo、Akiyama Masashi
- Journal Title
  
  Arthritis & Rheumatology
  
  Volume: - Issue: 10 Pages: 1896-1897
- DOI
  10.1002/art.41775
- NAID
  120007126470
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K10375, KAKENHI-PROJECT-18H03372
[Journal Article] Temporal dynamics of the plasma microbiome in recipients at early post-liver transplantation: a retrospective study.2021
- Author(s)
  Okumura T, Horiba K, Kamei H, Takeuchi S, Suzuki T, Torii Y, Kawada J, Takahashi Y, Ogura Y, Ogi T, Ito Y.
- Journal Title
  
  BMC Microbiol
  
  Volume: 21 Issue: 1 Pages: 104-104
- DOI
  10.1186/s12866-021-02154-w
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08298, KAKENHI-PROJECT-21K07748
[Journal Article] Transcription-Coupled DNA Repair: From Mechanism to Human Disorder2021
- Author(s)
  van den Heuvel Diana、van der Weegen Yana、Boer Daphne E.C.、Ogi Tomoo、Luijsterburg Martijn S.
- Journal Title
  
  Trends in Cell Biology
  
  Volume: 31 Issue: 5 Pages: 359-371
- DOI
  10.1016/j.tcb.2021.02.007
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02399
[Journal Article] Predominant cellular mitochondrial dysfunction in the TOP3A gene-caused Bloom syndrome-like disorder2021
- Author(s)
  Jiang Wenjun、Jia Nan、Guo Chaowan、Wen Juan、Wu Lingqian、Ogi Tomoo、Zhang Huiwen
- Journal Title
  
  Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
  
  Volume: 1867 Issue: 6 Pages: 166106-166106
- DOI
  10.1016/j.bbadis.2021.166106
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-20H00629
[Journal Article] Dealing with transcription-blocking DNA damage: Repair mechanisms, RNA polymerase II processing and human disorders2021
- Author(s)
  Jia Nan、Guo Chaowan、Nakazawa Yuka、van den Heuvel Diana、Luijsterburg Martijn S.、Ogi Tomoo
- Journal Title
  
  DNA Repair
  
  Volume: 106 Pages: 103192-103192
- DOI
  10.1016/j.dnarep.2021.103192
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-21K19844, KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02399
[Journal Article] ELOF1 is a transcription-coupled DNA repair factor that directs RNA polymerase II ubiquitylation2021
- Author(s)
  van der Weegen Yana、(著者19人)、Ogi Tomoo、Wolthuis Rob M. F.、Luijsterburg Martijn S.
- Journal Title
  
  Nature Cell Biology
  
  Volume: 23 Issue: 6 Pages: 595-607
- DOI
  10.1038/s41556-021-00688-9
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-21K19844, KAKENHI-PROJECT-20H00629, KAKENHI-PROJECT-21H02399
[Journal Article] Reduced stratum corneum acylceramides in autosomal recessive congenital ichthyosis with a NIPAL4 mutation.2020
- Author(s)
  Murase Y, Takeichi T, Kawamoto A, Tanahashi K, Okuno Y, Takama H, Shimizu E, Ishikawa J, Ogi T, Akiyama M.
- Journal Title
  
  Journal of Dermatological Science
  
  Volume: 97 Issue: 1 Pages: 50-56
- DOI
  10.1016/j.jdermsci.2019.12.001
- NAID
  120006849002
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-18H02832
[Journal Article] Digenic mutations in ALDH2 and ADH5 impair formaldehyde clearance and cause a multisystem disorder, AMeD syndrome2020
- Author(s)
  Oka Y, Hamada M, Nakazawa Y, ..., Tanaka M, Suganami T, Nakada S, Mitsutake N, Hara Y, Kato K, ..., Kaneko H, Matsumoto N, Matsuda F, Matsuo K, Takahashi Y, Mashimo T, Kojima S, Ogi T
- Journal Title
  
  Science Advances
  
  Volume: 6 Issue: 51 Pages: 7197-7197
- DOI
  10.1126/sciadv.abd7197
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K21718, KAKENHI-PROJECT-20KK0217, KAKENHI-PROJECT-18H03974, KAKENHI-PROJECT-18K08508, KAKENHI-PROJECT-18K19585, KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-20H03447, KAKENHI-PROJECT-20H00629
[Journal Article] Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants2020
- Author(s)
  Murase Chiaki、Takeichi Takuya、Nomura Toshifumi、Ogi Tomoo、Akiyama Masashi
- Journal Title
  
  Journal of Investigative Dermatology
  
  Volume: in press Issue: 6 Pages: 1596-1598
- DOI
  10.1016/j.jid.2020.09.035
- NAID
  120007175360
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K21591, KAKENHI-PROJECT-19H03679, KAKENHI-PROJECT-18H02832, KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-21H02941
[Journal Article] Topoisomerase I-driven repair of UV-induced damage in NER-deficient cells2020
- Author(s)
  Saha Liton Kumar、Wakasugi Mitsuo、Akter Salma、Prasad Rajendra、Wilson Samuel H.、Shimizu Naoto、Sasanuma Hiroyuki、Huang Shar-yin Naomi、Agama Keli、Pommier Yves、Matsunaga Tsukasa、Hirota Kouji、Iwai Shigenori、Nakazawa Yuka、Ogi Tomoo、Takeda Shunichi
- Journal Title
  
  Proceedings of the National Academy of Sciences
  
  Volume: 117 Issue: 25 Pages: 14412-14420
- DOI
  10.1073/pnas.1920165117
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K12319, KAKENHI-PROJECT-19KK0210, KAKENHI-PROJECT-16H06306, KAKENHI-PROJECT-19H04265, KAKENHI-PROJECT-19H04267, KAKENHI-PROJECT-20H04337, KAKENHI-PROJECT-18K19585, KAKENHI-PROJECT-19K22561, KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-20H00629
[Journal Article] Severe achondroplasia due to two de novo variants in the transmembrane domain of FGFR3 on the same allele: A case report.2020
- Author(s)
  Nagata T, Matsushita M, Mishima K, Kamiya Y, Kato K, Toyama M, Ogi T, Ishiguro N, Kitoh H.
- Journal Title
  
  Molecular Genetics & Genomic Medicine
  
  Volume: 8 Issue: 3 Pages: 1-1
- DOI
  10.1002/mgg3.1148
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-17H04312, KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-19K09573
[Journal Article] Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled Repair2020
- Author(s)
  Nakazawa Y, Hara Y, Oka Y, Komine O, van den Heuvel D, Guo C, Daigaku Y, Isono M, He Y, Shimada M, Kato K, Jia N, Hashimoto S, Kotani Y, Miyoshi Y, Tanaka M, Sobue A, Mitsutake N, Suganami T, Masuda A, Ohno K, Nakada S, Mashimo T, Yamanaka K, Luijsterburg MS, Ogi T
- Journal Title
  
  Cell
  
  Volume: 19 Issue: 6 Pages: 1228-1244
- DOI
  10.1016/j.cell.2020.02.010
- NAID
  120006871293
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K06058, KAKENHI-PROJECT-18K08508, KAKENHI-PROJECT-18K11639, KAKENHI-PROJECT-18K19585, KAKENHI-PROJECT-19K22802, KAKENHI-PROJECT-18KK0307, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-18H03974, KAKENHI-PROJECT-17H01877, KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-16H06151, KAKENHI-PROJECT-17K12821, KAKENHI-PROJECT-19K21221
[Journal Article] Expanding the phenotype of biallelic loss‐of‐function variants in the <scp> <i>NSUN2</i> </scp> gene: Description of four individuals with juvenile cataract, chronic nephritis, or brain anomaly as novel complications2020
- Author(s)
  Kato Kohji、Mizuno Seiji、Morton Jenny、Toyama Miho、Hara Yuichiro、Wasmer Evangeline、Lehmann Alan、Ogi Tomoo
- Journal Title
  
  American Journal of Medical Genetics Part A
  
  Volume: 185 Issue: 1 Pages: 282-285
- DOI
  10.1002/ajmg.a.61927
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-20K16897, KAKENHI-PROJECT-19K23823, KAKENHI-PROJECT-20H00629
[Journal Article] Biallelic VPS35L pathogenic variants cause 3C/Ritscher-Schinzel-like syndrome through dysfunction of retriever complex.2020
- Author(s)
  Kato K, Okuno Y, Vasilev FF, Otomo T, Oishi H, Muramatsu H, Kawano Y, Oka Y, Nakazawa Y, Ogi T, Takahashi Y, Saitoh S.
- Journal Title
  
  Journal of Medical genetics
  
  Volume: 57 Issue: 4 Pages: 245-253
- DOI
  10.1136/jmedgenet-2019-106213
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-17H01877, KAKENHI-PROJECT-17H05088, KAKENHI-PROJECT-17K10075, KAKENHI-PROJECT-20K21583, KAKENHI-PROJECT-19K23823, KAKENHI-PROJECT-20H05700, KAKENHI-PROJECT-18K19585, KAKENHI-PROJECT-20H00629
[Journal Article] A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease.2020
- Author(s)
  Takeichi T, Matsumoto T, Nomura T, Takeda M, Niwa H, Kono M, Shimizu H, Ogi T, Akiyama M.
- Journal Title
  
  Br J Dermatol.
  
  Volume: 182 Issue: 2 Pages: 491-493
- DOI
  10.1111/bjd.18445
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K16058, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-18H03372
[Journal Article] A Japanese Case of Galli-Galli Disease due to a Previously Unreported POGLUT1 Mutation2019
- Author(s)
  Kono M、Sawada M、Nakazawa Y、Ogi T、Muro Y、Akiyama M
- Journal Title
  
  Acta Dermato Venereologica
  
  Volume: 99 Issue: 4 Pages: 458-459
- DOI
  10.2340/00015555-3119
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-17H01877, KAKENHI-PROJECT-15H02654, KAKENHI-PROJECT-18H03372
[Journal Article] Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype.2019
- Author(s)
  Theil AF, Botta E, Raams A, Smith DEC, Mendes MI, Caligiuri G, Giachetti S, Bione S, Carriero R, Liberi G, Zardoni L, Swagemakers SMA, Salomons GS, Sarasin A, Lehmann A, van der Spek PJ, Ogi T, Hoeijmakers JHJ, Vermeulen W, Orioli D.
- Journal Title
  
  American Journal of Human Genetics
  
  Volume: 105 Issue: 2 Pages: 434-440
- DOI
  10.1016/j.ajhg.2019.06.017
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-18H03372
[Journal Article] Hailey-Hailey disease with oesophageal involvement due to a previously unreported ATP2C1 mutation2019
- Author(s)
  Kono M, Kodera M, Inasaka Y, Hasegawa I, Muro Y, Nakazawa Y, Ogi T, Akiyama M.
- Journal Title
  
  European Journal of Dermatology
  
  Volume: 印刷中
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18H03372
[Journal Article] Functional Comparison of XPF Missense Mutations Associated to Multiple DNA Repair Disorders2019
- Author(s)
  Marin M, Ramirez MJ, Carmona MA, Jia N, Ogi T, Bogliolo M, Surralles J.
- Journal Title
  
  Genes
  
  Volume: 10 Issue: 1 Pages: 60-60
- DOI
  10.3390/genes10010060
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K11639, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-17K17806, KAKENHI-PROJECT-15H02654
[Journal Article] Hailey-Hailey disease with oesophageal involvement due to a previously unreported ATP2C1 mutation.2019
- Author(s)
  Kono M, Kodera M, Inasaka Y, Hasegawa I, Muro Y, Nakazawa Y, Ogi T, Akiyama M.
- Journal Title
  
  European Journal of Dermatology
  
  Volume: 印刷中
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17H00783
[Journal Article] The JAK/STAT3 and NF-kappa B signaling pathways regulate cancer stem cell properties in anaplastic thyroid cancer cells2019
- Author(s)
  K. Shiraiwa, M. Mitsutake, Y. Nakazawa, T. Ogi, K. Suzuki, V. Saenko, K. Umezawa, S. Yamashita, K. Tsukamoto
- Journal Title
  
  Thyroid
  
  Volume: in press Issue: 5 Pages: 674-682
- DOI
  10.1089/thy.2018.0212
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K01967, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-17H01877, KAKENHI-PROJECT-15H02654, KAKENHI-PROJECT-19K07471, KAKENHI-PROJECT-19K09913, KAKENHI-PROJECT-18K19585, KAKENHI-PROJECT-19KK0267, KAKENHI-PROJECT-16H05832, KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-16K08912, KAKENHI-PROJECT-16K09804
[Journal Article] Hailey-Hailey disease with oesophageal involvement due to a previously unreported ATP2C1 mutation.2019
- Author(s)
  Kono M, Kodera M, Inasaka Y, Hasegawa I, Muro Y, Nakazawa Y, Ogi T, Akiyama M.
- Journal Title
  
  European Journal of Dermatology
  
  Volume: 印刷中
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17H01877
[Journal Article] Functional and clinical relevance of novel mutations in a large cohort of patients with Cockayne syndrome.2018
- Author(s)
  Calmels N, Botta E, Jia N, Fawcett H, Nardo T, Nakazawa Y, Lanzafame M, Moriwaki S, Sugita K, Kubota M, Obringer C, Spitz MA, Stefanini M, Laugel V, Orioli D, Ogi T, Lehmann A.
- Journal Title
  
  Journal of Medical Genetics
  
  Volume: 55 Issue: 5 Pages: 329-343
- DOI
  10.1136/jmedgenet-2017-104877
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H05333, KAKENHI-PROJECT-26291005, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-16H03053, KAKENHI-PROJECT-16K15526, KAKENHI-PROJECT-18K08283, KAKENHI-PROJECT-18K11639, KAKENHI-PROJECT-18K19585, KAKENHI-PROJECT-17H01877, KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-17K17806, KAKENHI-PROJECT-15H02654
[Journal Article] Novel function of HATs and HDACs in homologous recombination through acetylation of human RAD52 at double-strand break sites2018
- Author(s)
  Yasuda Takeshi、Kagawa Wataru、Tajima Katsushi
- Journal Title
  
  PLOS Genetics
  
  Volume: 14 Issue: 3 Pages: 1007277-1007277
- DOI
  10.1371/journal.pgen.1007277
- NAID
  120006459820
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10376, KAKENHI-PROJECT-15H05333, KAKENHI-PROJECT-26281026, KAKENHI-PUBLICLY-16H01316, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-15K14953, KAKENHI-PROJECT-17K16332, KAKENHI-PROJECT-18J13707, KAKENHI-PROJECT-16K10377, KAKENHI-PROJECT-17K19615, KAKENHI-PROJECT-15H04646, KAKENHI-PROJECT-17H01877
[Journal Article] Cerebellar ataxia-dominant phenotype in patients with ERCC4 mutations2018
- Author(s)
  Doi H、Koyano S、Miyatake S、Nakajima S、Nakazawa Y、Kunii M、Tomita-Katsumoto A、Oda K、Yamaguchi Y、Fukai R、Ikeda S、Kato R、Ogata K、Kubota S、Hayashi N、Takahashi K、Tada M、Tanaka K、Nakashima M、Tsurusaki Y et al.
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 63 Issue: 4 Pages: 417-423
- DOI
  10.1038/s10038-017-0408-5
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K19536, KAKENHI-PROJECT-17K16128, KAKENHI-PROJECT-15H05333, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-16H05357, KAKENHI-PROJECT-15K09344, KAKENHI-PROJECT-16K15526, KAKENHI-PROJECT-18K07503, KAKENHI-PROJECT-18K07504, KAKENHI-PROJECT-18K11639, KAKENHI-PROJECT-17H01539, KAKENHI-PROJECT-17H01877, KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-15H02654
[Journal Article] An XPA gene splicing mutation resulting in trace protein expression in an elderly xeroderma pigmentosum group A patient without neurological abnormalities.2017
- Author(s)
  Takahashi Y, Endo Y, Kusaka A, Nakamaura S, Nakazawa Y, Ogi T, Uryu M, Tsuji M, Furue M, Moriwaki S.
- Journal Title
  
  British Journal of Dermatology
  
  Volume: 印刷中 Issue: 1 Pages: 253-257
- DOI
  10.1111/bjd.15051
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654, KAKENHI-PROJECT-14F04093, KAKENHI-PROJECT-26461528, KAKENHI-PROJECT-15H05333, KAKENHI-PROJECT-26291005, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-15K09751, KAKENHI-PROJECT-16K15526, KAKENHI-PROJECT-17H01877
[Journal Article] PCNA ubiquitylation ensures timely completion of unperturbed DNA replication in fission yeast.2017
- Author(s)
  Daigaku Y, Etheridge TJ, Nakazawa Y, Nakayama M, Watson AT, Miyabe I, Ogi T, Osborne MA, Carr AM.
- Journal Title
  
  PLoS Genetics
  
  Volume: 13 Issue: 5 Pages: e1006789-e1006789
- DOI
  10.1371/journal.pgen.1006789
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H05333, KAKENHI-PROJECT-26291005, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-17H01877, KAKENHI-PROJECT-16H06151
[Journal Article] Analysis of clinical symptoms and ABCC6 mutations in 76 Japanese patients with pseudoxanthoma elasticum.2017
- Author(s)
  Iwanaga A, Okubo Y, Yozaki M, Koike Y, Kuwatsuka Y, Tomimura S, Yamamoto Y, Tamura H, Ikeda S, Maemura K, Tsuiki E, Kitaoka T, Endo Y, Mishima H, Yoshiura KI, Ogi T, Tanizaki H, Wataya-Kaneda M, Hattori T, Utani A.
- Journal Title
  
  Journal of Dermatology
  
  Volume: 印刷中 Issue: 6 Pages: 644-650
- DOI
  10.1111/1346-8138.13727
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654, KAKENHI-PROJECT-15H04793, KAKENHI-PROJECT-14F04093, KAKENHI-PROJECT-26291005, KAKENHI-PROJECT-26461528, KAKENHI-PROJECT-15K19693, KAKENHI-PROJECT-15K10839, KAKENHI-PROJECT-16K10155, KAKENHI-PROJECT-16K15526, KAKENHI-PROJECT-16KT0112, KAKENHI-PROJECT-17K09592, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-16H05159, KAKENHI-PROJECT-16K19727
[Journal Article] Transplantation of bioengineered rat lungs recellularized with endothelial and adipose-derived stromal cells2017
- Author(s)
  Doi Ryoichiro, Tsuchiya Tomoshi, Mitsutake Norisato, Nishimura Satoshi, Matsuu-Matsuyama Mutsumi, Nakazawa Yuka, Ogi Tomoo, Akita Sadanori, Yukawa Hiroshi, Baba Yoshinobu, Yamasaki Naoya, Matsumoto Keitaro, Miyazaki Takuro, Kamohara Ryotaro, Hatachi Go, Sengyoku Hideyori et al.
- Journal Title
  
  Scientific Reports
  
  Volume: 7 Issue: 1 Pages: 1-15
- DOI
  10.1038/s41598-017-09115-2
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K00554, KAKENHI-PROJECT-15H05333, KAKENHI-PLANNED-17H06354, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-15H04944, KAKENHI-PROJECT-17H01877
[Journal Article] Calcification in dermal fibroblasts from a patient with GGCX syndrome accompanied by upregulation of osteogenic molecules.2017
- Author(s)
  Okubo Y, Masuyama R, Iwanaga A, Koike Y, Kuwatsuka Y, Ogi T, Yamamoto Y, Endo Y, Tamura H, Utani A.
- Journal Title
  
  PLoS One.
  
  Volume: 12 Issue: 5 Pages: 99-99
- DOI
  10.1371/journal.pone.0177375
- NAID
  120007185935
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K19771, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-15H04793, KAKENHI-PROJECT-17H01967, KAKENHI-PROJECT-16K19727, KAKENHI-PROJECT-15H02654
[Journal Article] ALC1/CHD1L, a chromatin-remodeling enzyme, is required for efficient base excision repair.2017
- Author(s)
  Tsuda M, Cho K, Ooka M, Shimizu N, Watanabe R, Yasui A, Nakazawa Y, Ogi T, Harada H, Agama K, Nakamura J, Asada R, Fujiike H, Sakuma T, Yamamoto T, Murai J, Hiraoka M, Koike K, Pommier Y, Takeda S, Hirota K.
- Journal Title
  
  PLos One
  
  Volume: 12 Issue: 11 Pages: e0188320-e0188320
- DOI
  10.1371/journal.pone.0188320
- NAID
  120006800808
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H05333, KAKENHI-PUBLICLY-16H01314, KAKENHI-PROJECT-16H06306, KAKENHI-PROJECT-15H01737, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-16H02957, KAKENHI-PROJECT-16J02252, KAKENHI-PROJECT-16K12598, KAKENHI-PROJECT-16K18478, KAKENHI-PROJECT-17H01877
[Journal Article] Common TFIIH recruitment mechanism in global genome and transcription-coupled repair subpathways.2017
- Author(s)
  Okuda M, Nakazawa Y, Guo C, Ogi T, Nishimura Y.
- Journal Title
  
  Nucleic Acids Research
  
  Volume: 45 Issue: 22 Pages: 13043-13055
- DOI
  10.1093/nar/gkx970
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H05333, KAKENHI-PROJECT-26291005, KAKENHI-PROJECT-17H00783, KAKENHI-PROJECT-16K15526, KAKENHI-PROJECT-17H01877
[Journal Article] A ten-year follow up of a child with mild case of xeroderma pigmentosum complementation group D diagnosed by whole genome sequencing.2016
- Author(s)
  Ono R, Masaki T, Mayca Pozo F, Nakazawa Y, Swagemakers SM, Nakano E, Sakai W, Takeuchi S, Kanda F, Ogi T, van der Spek PJ, Sugasawa K, Nishigori C.
- Journal Title
  
  Photodermatol Photoimmunol Photomed.
  
  Volume: 未定 Issue: 4 Pages: 174-180
- DOI
  10.1111/phpp.12240
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19690, KAKENHI-PROJECT-26870356, KAKENHI-PROJECT-15H05333, KAKENHI-PROJECT-15H02654, KAKENHI-PROJECT-14F04093, KAKENHI-PROJECT-26291005, KAKENHI-PROJECT-26461528, KAKENHI-PROJECT-16K15526
[Journal Article] SETDB1, HP1 and SUV39 promote repositioning of 53BP1 to extend resection during homologous recombination in G2 cells2015
- Author(s)
  Meryem Alagoz, Yoko Katsuki, Hideaki Ogiwara, Tomoo Ogi, Atsushi Shibata, Andreas Kakarougkas, and Penny Jeggo
- Journal Title
  
  Nucleic Acids Research
  
  Volume: 43(16) Issue: 16 Pages: 7931-7944
- DOI
  10.1093/nar/gkv722
- NAID
  120006986903
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26670549, KAKENHI-PROJECT-26830122, KAKENHI-PROJECT-26291005, KAKENHI-PROJECT-26701005, KAKENHI-PROJECT-15H02654
[Journal Article] Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly-progressing radiosensitive-severe combined immunodeficiency2015
- Author(s)
  Tamura S, Higuchi K, Tamaki M, Inoue C, Awazawa R, Mitsuki N, Nakazawa Y, Mishima H, Takahashi K, Kondo O, Imai K, Morio T, Ohara O,et al
- Journal Title
  
  Clin Immunol
  
  Volume: 160 Issue: 2 Pages: 255-260
- DOI
  10.1016/j.clim.2015.07.004
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09640, KAKENHI-PROJECT-15K09747, KAKENHI-PROJECT-25430183, KAKENHI-PROJECT-26461567, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25293084, KAKENHI-PROJECT-26291005, KAKENHI-PROJECT-15H02654
[Journal Article] A rapid, comprehensive system for assaying DNA repair activity and cytotoxic effects of DNA-damaging reagents.2015
- Author(s)
  Nan Jia, Yuka Nakazawa, Chaowan Guo, Mayuko Shimada, Mieran Sethi, Yoshito Takahashi, Hiroshi Ueda, Yuji Nagayama, Tomoo Ogi
- Journal Title
  
  Nature Protocols
  
  Volume: 10 Issue: 1 Pages: 12-24
- DOI
  10.1038/nprot.2014.194
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-14F04093, KAKENHI-PROJECT-24591368, KAKENHI-PROJECT-24659533, KAKENHI-PROJECT-24681008, KAKENHI-PROJECT-24790321, KAKENHI-PROJECT-25870534, KAKENHI-PROJECT-26291005, KAKENHI-PROJECT-26461528, KAKENHI-PROJECT-15K09437
[Journal Article] XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency.2015
- Author(s)
  Guo C, Nakazawa Y, Woodbine L, Bjorkman A, Shimada M, Fawcett H, Jia N, Ohyama K, Li TS,Nagayama Y, Mitsutake N, Pan-Hammarström Q, Gennery AR, Lehmann AR, Jeggo PA, Ogi T.
- Journal Title
  
  J Allergy Clin Immunol.
  
  Volume: 136 (4) Issue: 4 Pages: 1007-1017
- DOI
  10.1016/j.jaci.2015.06.007
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09437, KAKENHI-PROJECT-26461528, KAKENHI-PROJECT-14F04093, KAKENHI-PROJECT-26291005, KAKENHI-PROJECT-15H02654, KAKENHI-PROJECT-15H05333
[Journal Article] Hypomorphic PCNA mutation underlies a human DNA repair disorder.2014
- Author(s)
  Baple EL, Chambers H, Cross HE, Fawcett H, Nakazawa Y, Chioza BA, Harlalka GV, Mansour S, Sreekantan-Nair A, Patton MA, Muggenthaler M, Rich P, Wagner K, Coblentz R, Stein CK, Last JI, Taylor AM, Jackson AP, Ogi T, Lehmann AR, Green CM, Crosby AH.
- Journal Title
  
  Journal of Clinical Investigation
  
  Volume: 124 Issue: 7 Pages: 3137-3146
- DOI
  10.1172/jci74593
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24659533, KAKENHI-PROJECT-24681008, KAKENHI-PROJECT-24790321, KAKENHI-PROJECT-26291005
[Journal Article] Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia.2013
- Author(s)
  Kashiyama, K, Nakazawa, Y, Pilz, DT, Guo, C, Sasaki, K, et al.
- Journal Title
  
  The American Journal of Human Genetics
  
  Volume: 92 Issue: 5 Pages: 807-819
- DOI
  10.1016/j.ajhg.2013.04.007
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-13J11173, KAKENHI-PROJECT-22710056, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24659533, KAKENHI-PROJECT-24790321, KAKENHI-PROJECT-25293084, KAKENHI-PROJECT-25550033, KAKENHI-PROJECT-25870534
[Journal Article] PRKDC mutations in a SCID patient with profound neurological abnormalities.2013
- Author(s)
  Woodbine L, Neal JA, Sasi NK, Shimada M, Deem K, Coleman H, Dobyns WB, Ogi T, §Meek K, §Davies EG, §Jeggo PA.
- Journal Title
  
  The Journal of Clinical Investigation
  
  Volume: 123 Issue: 7 Pages: 2969-2980
- DOI
  10.1172/jci67349
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24659533
[Journal Article] Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair2012
- Author(s)
  Nakazawa Y, Sasaki K, Mitsutake N, Yamashita S, Ogi T, et al
- Journal Title
  
  Nat Genet
  
  Volume: 44(5) Issue: 5 Pages: 586-92
- DOI
  10.1038/ng.2229
- NAID
  120006985586
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22390189, KAKENHI-PROJECT-22710056, KAKENHI-PROJECT-22791204, KAKENHI-PROJECT-23510065, KAKENHI-PROJECT-23590355, KAKENHI-PROJECT-24300328, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24590403, KAKENHI-PROJECT-24659533, KAKENHI-PROJECT-24681008, KAKENHI-PROJECT-24790321
[Journal Article] Identification of the first ATRIP-deficient patient and novel mutations in ATR define a clinical spectrum for ATR-ATRIP Seckel syndrome2012
- Author(s)
  *Ogi T , Walker S, Stiff T, Hobson E, Limsirichaikul S, Carpenter G, Prescott K, Suri M, Byrd P, Matsuse M, Mitsutake N, Nakazawa Y, Vasudevan P, Barrow M, Stewart G, Taylor M, O'Driscoll M, and Jeggo P
- Journal Title
  
  PLoS Genetics
  
  Volume: 8 Issue: 11 Pages: e1002945-e1002945
- DOI
  10.1371/journal.pgen.1002945
- NAID
  120006985789
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22710056, KAKENHI-PROJECT-22791204, KAKENHI-PROJECT-24659533, KAKENHI-PROJECT-24681008, KAKENHI-PROJECT-24790321
[Journal Article] Three DNA polymerases, recruited by different mechanisms, carry out NER repair synthesis in human cells2010
- Author(s)
  荻朋男(責任著者), S. Limsirichaikul, R. Overmeer, M. Volker, K. Takenaka, R. Cloney, Y. Nakazawa, A. Niimi, Y. Miki, N. Jaspers, L. Mullenders, S. Yamashita, M. Fousteri, A. Lehmann
- Journal Title
  
  Molecular Cell 37
  
  Pages: 714-27
- NAID
  120006984627
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20810021
[Journal Article] A semi-automated non-radioactive system for measuring recovery of RNA synthesis and unscheduled DNA synthesis using ethynyluracil derivatives2010
- Author(s)
  Nakazawa, Y., S. Yamashita, A. Lehmann, 荻朋男(責任著者)
- Journal Title
  
  DNA Repair 9
  
  Pages: 506-16
- NAID
  120006984626
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20810021
[Journal Article] Three DNA Polymerases, Recruited by Different Mechanisms, Carry Out NER Repair Synthesis in Human Cells2010
- Author(s)
  Ogi, et al.
- Journal Title
  
  Molecular Cell 37
  
  Pages: 714-727
- NAID
  120006984627
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20810021
[Journal Article] A rapid non-radioactive technique for measurement of repair synthesis in primary human fibroblasts by incorporation of ethynyl deoxyuridine (EdU)2009
- Author(s)
  Limsirichaikul, S., A. Niimi, H. Fawcett, A. Lehmann, S. Yamashita, 荻朋男(責任著者)
- Journal Title
  
  Nucleic Acids Research 37
  
  Pages: 1-10
- NAID
  120006982811
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20810021
[Patent] 造血不全、発育遅滞、高発がん性、精神機能障害のモデル動物2020
- Inventor(s)
  荻朋男、岡泰由
- Industrial Property Rights Holder
  荻朋男、岡泰由
- Industrial Property Rights Type
  特許
- Industrial Property Number
  2020-166756
- Filing Date
  2020
- Data Source
  KAKENHI-PROJECT-18H03372
[Patent] 造血不全、発育遅滞、高発がん性、精神機能障害のモデル動物2020
- Inventor(s)
  荻朋男、岡泰由
- Industrial Property Rights Holder
  東海国立大学機構
- Industrial Property Rights Type
  特許
- Industrial Property Number
  2020-166756
- Filing Date
  2020
- Data Source
  KAKENHI-PROJECT-20H00629
[Patent] 色素性乾皮症Ｆ群治療薬 (日本にのみ移行済み)2020
- Inventor(s)
  荻朋男、中沢由華、小泉誠、小路貴生
- Industrial Property Rights Holder
  東海国立大学機構、第一三共株式会社
- Industrial Property Rights Type
  特許
- Filing Date
  2020
- Overseas
- Data Source
  KAKENHI-PROJECT-20H00629
[Patent] 老化マウスモデル2019
- Inventor(s)
  荻朋男
- Industrial Property Rights Holder
  名古屋大学
- Industrial Property Rights Type
  特許
- Industrial Property Number
  2019-203237
- Filing Date
  2019
- Data Source
  KAKENHI-PROJECT-18H03372
[Patent] 老化マウスモデル2019
- Inventor(s)
  荻朋男
- Industrial Property Rights Holder
  名古屋大学
- Industrial Property Rights Type
  特許
- Industrial Property Number
  2019-203237
- Filing Date
  2019
- Data Source
  KAKENHI-PROJECT-17H00783
[Patent] 日焼けの原因遺伝子発明者:荻朋男他3名2011
- Inventor(s)
  荻朋男他3名
- Industrial Property Rights Holder
  長崎大学
- Industrial Property Number
  2011-071082
- Filing Date
  2011-03-28
- Data Source
  KAKENHI-PROJECT-22710056
[Patent] 損傷DNA修復物質のスクリーニング方法2010
- Inventor(s)
  荻朋男他3名
- Industrial Property Rights Holder
  長崎大学
- Industrial Property Number
  2009-172521
- Filing Date
  2010-01-28
- Overseas
- Data Source
  KAKENHI-PROJECT-22710056
[Patent] 損傷DNA修復物質のスクリーニング方法2010
- Inventor(s)
  荻朋男, 他2名
- Industrial Property Rights Holder
  長崎大学
- Filing Date
  2010-01-28
- Overseas
- Data Source
  KAKENHI-PROJECT-20810021
[Patent] 損傷DNA修復物質のスクリーニング方法2009
- Inventor(s)
  荻朋男, 他2名
- Industrial Property Rights Holder
  長崎大学
- Industrial Property Number
  2009-172521
- Filing Date
  2009-07-23
- Data Source
  KAKENHI-PROJECT-20810021
[Patent] 日本国特許2009
- Inventor(s)
  荻, ら
- Industrial Property Rights Holder
  長崎大学
- Industrial Property Number
  2009-172521
- Filing Date
  2009-07-23
- Data Source
  KAKENHI-PROJECT-20810021
[Patent] 損傷DNA修復物質のスクリーニング方法2009
- Inventor(s)
  荻朋男他3名
- Industrial Property Rights Holder
  長崎大学
- Industrial Property Number
  2009-172521
- Filing Date
  2009-07-23
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] DNA損傷に対する生体内防御機構の理解とその破綻による疾患の分子病態2023
- Author(s)
  荻朋男
- Organizer
  令和5年度国立大学附置研究所・センター会議第2部会シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] DNA修復機構の異常により発症する光線過敏を伴う遺伝性皮膚疾患の分子病態2023
- Author(s)
  荻朋男
- Organizer
  第74回日本皮膚科学会中部支部学術大会
- Invited
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] DNA損傷に対する生体内防御機構の理解とその破綻による疾患の分子病態2023
- Author(s)
  荻朋男
- Organizer
  令和5年度国立大学附置研究所・センター会議第2部会シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-23H00516
[Presentation] Deep intronic mutations identified in XP-F cases are potential therapeutic targets for xeroderma pigm entosum2023
- Author(s)
  Nakazawa Y, Senju C, Oso T, Kato K, Shimada M, Ogi T
- Organizer
  The EXPS Annual Symposium
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] Transcription-coupled repair of aldehyde-induced DNA damage2023
- Author(s)
  岡泰由, 荻朋男
- Organizer
  第96回日本生化学会大会シンポジウム「多面化したDNA修復研究」
- Invited
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] DNA修復機構の異常により発症する光線過敏を伴う遺伝性皮膚疾患の分子病態2023
- Author(s)
  荻朋男
- Organizer
  第74回日本皮膚科学会中部支部学術大会
- Invited
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] Transcription-coupled repair of aldehyde-induced DNA damage2023
- Author(s)
  岡泰由, 荻朋男
- Organizer
  第96回日本生化学会大会シンポジウム「多面化したDNA修復研究」
- Invited
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] Transcription-coupled repair of aldehyde-induced DNA damage2023
- Author(s)
  岡泰由, 荻朋男
- Organizer
  第96回日本生化学会大会シンポジウム「多面化したDNA修復研究」
- Invited
- Data Source
  KAKENHI-PROJECT-23H00516
[Presentation] Deep intronic mutations identified in XP-F cases are potential therapeutic targets for xeroderma pigm entosum2023
- Author(s)
  Nakazawa Y, Senju C, Oso T, Kato K, Shimada M, Ogi T
- Organizer
  The EXPS Annual Symposium
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] DNA修復機構の異常により発症する光線過敏を伴う遺伝性皮膚疾患の分子病態2023
- Author(s)
  荻朋男
- Organizer
  第74回日本皮膚科学会中部支部学術大会
- Invited
- Data Source
  KAKENHI-PROJECT-23H00516
[Presentation] DNA損傷に対する生体内防御機構の理解とその破綻による疾患の分子病態2023
- Author(s)
  荻朋男
- Organizer
  令和5年度国立大学附置研究所・センター会議第2部会シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] ゲノム安定維持機構の分子メカニズムとその破綻により発症する疾患の病態解明2022
- Author(s)
  荻朋男
- Organizer
  第83回応用物理学会秋季学術講演会シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] RNA polymerase II ubiquitination regulates transcription-coupled repair2022
- Author(s)
  Ogi T
- Organizer
  The 29th Federation of Asian and Oceanian Biochemists and Molecular Biologists Conference & the 2022 Chinese Society of Biochemistry and Molecular Biology Online Conference
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] RNA polymerase II ubiquitination regulates transcription-coupled repair2022
- Author(s)
  Ogi T
- Organizer
  The 29th Federation of Asian and Oceanian Biochemists and Molecular Biologists Conference & the 2022 Chinese Society of Biochemistry and Molecular Biology Online Conference
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] 転写共役修復とヒトの疾患2022
- Author(s)
  荻朋男
- Organizer
  日本遺伝学会第94回大会ワークショップ
- Invited
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] ナノポアシークエンサーによる小児中枢神経感染症の病原微生物検出および宿主遺伝子発現解析2022
- Author(s)
  堀場千尋、鳥居ゆか、山口慎、春田一憲、奥村俊彦、鈴木高子、河野好彦、川田潤一、原紳也、荻朋男、伊藤嘉規.
- Organizer
  NGS EXPO 2022
- Data Source
  KAKENHI-PROJECT-19K08298
[Presentation] Digenic inheritanceにより発症するゲノム不安定性疾患の分子病態 -内因性アルデヒドによるDNA損傷と転写障害-.2022
- Author(s)
  荻朋男.
- Organizer
  日本人類遺伝学会第67回大会シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] Ubiquitination of RNA polymerase II and transcription-coupled repair.2022
- Author(s)
  Ogi T.
- Organizer
  Webinar for the IBS Center for Genomic Integrity
- Invited
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] 転写共役修復とヒトの疾患2022
- Author(s)
  荻朋男
- Organizer
  日本遺伝学会第94回大会ワークショップ
- Invited
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] Digenic inheritanceにより発症するゲノム不安定性疾患の分子病態 -内因性アルデヒドによるDNA損傷と転写障害-2022
- Author(s)
  荻朋男
- Organizer
  日本人類遺伝学会第67回大会シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] Ubiquitination of RNA polymerase II and transcription-coupled repair2022
- Author(s)
  Ogi T
- Organizer
  Webinar for the IBS Center for Genomic Integrity
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] Ubiquitination of RNA polymerase II and transcription-coupled repair.2022
- Author(s)
  Ogi T.
- Organizer
  11th quinquennial conference on DNA repair
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] Digenic inheritanceにより発症するゲノム不安定性疾患の分子病態 -内因性アルデヒドによるDNA損傷と転写障害-.2022
- Author(s)
  荻朋男.
- Organizer
  日本人類遺伝学会第67回大会シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] ゲノム安定維持機構の分子メカニズムとその破綻により発症する疾患の病態解明2022
- Author(s)
  荻朋男
- Organizer
  第83回応用物理学会秋季学術講演会シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] 転写共役修復機構の分子メカニズムとその破綻による生体影響の解明2022
- Author(s)
  中沢由華, 岡泰由, 森永浩伸, 何予希, 荻朋男
- Organizer
  第45回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] Genetic Diagnosis of Cockayne Syndrome2022
- Author(s)
  Ogi T
- Organizer
  Amy and Friends
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] 転写共役修復機構の分子メカニズムとその破綻による生体影響の解明2022
- Author(s)
  中沢由華, 岡泰由, 森永浩伸, 何予希, 荻朋男
- Organizer
  第45回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] long read sequenceによる小児重症呼吸不全患者の網羅的ウイルス検索2022
- Author(s)
  山口慎、堀場千尋、福田悠人、春田一憲、武内俊、鈴木高子、鳥居ゆか、河邉慎司、伊藤嘉規、荻朋男、川田潤一
- Organizer
  第54回日本小児感染症学会
- Data Source
  KAKENHI-PROJECT-22K07818
[Presentation] Digenic inheritanceにより発症するゲノム不安定性疾患の分子病態 -内因性アルデヒドによるDNA損傷と転写障害-2022
- Author(s)
  荻朋男
- Organizer
  日本人類遺伝学会第67回大会シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] Ubiquitination of RNA polymerase II and transcription-coupled repair2022
- Author(s)
  Ogi T
- Organizer
  Webinar for the IBS Center for Genomic Integrity
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] Genetic Diagnosis of Cockayne Syndrome2022
- Author(s)
  Ogi T
- Organizer
  Amy and Friends
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] Ubiquitination of RNA polymerase II and transcription-coupled repair.2022
- Author(s)
  Ogi T
- Organizer
  11th quinquennial conference on DNA repair
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] Ubiquitination of RNA polymerase II and transcription-coupled repair.2022
- Author(s)
  Ogi T.
- Organizer
  Webinar for the IBS Center for Genomic Integrity
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] 出生時に呼吸障害を呈した新生児における次世代シークエンスを用いた網羅的病原微生物検索2021
- Author(s)
  奥村俊彦、堀場千尋、手塚宜行、佐藤義朗、杉山裕一朗、春田一憲、山口慎、鈴木高子、鳥居ゆか、川田潤一、荻朋男、早川昌弘、伊藤嘉規.
- Organizer
  第53回日本小児感染症学会
- Data Source
  KAKENHI-PROJECT-19K08298
[Presentation] プロテオーム解析を用いたDNA損傷応答機構の破綻により発症する遺伝性疾患の分子病態解明2021
- Author(s)
  岡泰由、荻朋男
- Organizer
  日本放射線影響学会
- Invited
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] RNA polymerase II のユビキチン化修飾と転写共役修復の制御.2021
- Author(s)
  荻朋男.
- Organizer
  第26回DNA複製・組換え・修復ワークショップ
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] RNA polymerase II のユビキチン化修飾と転写共役修復の制御.2021
- Author(s)
  中沢由華, 原雄一郎, 岡泰由, 小峯起, Diana van den Heuvel, 郭朝万, 大学保一, 磯野真由, 何予希, 嶋田繭子, 加藤香奈, 賈楠, 橋下悟, 田中都, 祖父江顕, 光武範吏, 菅波孝祥, 増田章男, 大野欽司, 中田慎一郎, 真下知士, 山中宏二, Martijn S. Luijsterburg, 荻朋男.
- Organizer
  第26回DNA複製・組換え・修復ワークショップ
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] 転写と共役したDNA修復機構にはRNAPIIのユビキチン化修飾が必須である.2020
- Author(s)
  中沢由華, 原雄一郎, 岡泰由, 小峯起, Diana van den Heuvel, 郭朝万, 大学保一, 磯野真由, 何予希, 嶋田繭子, 加藤香奈, 賈楠, 橋下悟, 田中都, 祖父江顕, 光武範吏, 菅波孝祥, 増田章男, 大野欽司, 中田慎一郎, 真下知士, 山中宏二, Martijn S. Luijsterburg, 荻朋男.
- Organizer
  第10回名古屋大学医学系研究科・生理学研究所合同シンポジウム
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] 次世代シークエンスデータ解析の効率を向上させる病原微生物予測パイプラインPATHDETの開発.2020
- Author(s)
  堀場千尋, 原雄一郎, 遠山美穂, 奥村俊彦, 鈴木高子, 鳥居ゆか, 川田潤一, 尾崎紀夫, 荻朋男, 伊藤嘉規.
- Organizer
  第52回日本小児感染症学会総会・学術集会
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] 次世代シークエンスデータ解析の効率を向上させる病原微生物予測パイプラインPATHDETの開発2020
- Author(s)
  堀場千尋、原雄一郎、遠山美穂、奥村俊彦、鈴木高子、鳥居ゆか、川田潤一、尾崎紀夫、荻朋男、伊藤嘉規.
- Organizer
  第52回日本小児感染症学会
- Data Source
  KAKENHI-PROJECT-19K08298
[Presentation] 「ゲノムの安定性維持機構の破綻による細胞影響から病態理解へ」ストレスの多さはゲノムから: 複製ストレス、転写ストレス、DNAダメージ.2020
- Author(s)
  荻朋男, 村井純子.
- Organizer
  第43回日本分子生物学会年会
- Invited
- Data Source
  KAKENHI-PROJECT-20H00629
[Presentation] マルチオミクス解析により同定した重症アイカルディ・ゴーティエ症候群の分子病態解析.2019
- Author(s)
  岡泰由, 荻朋男.
- Organizer
  第41回日本小児遺伝学会学術集会
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] マルチオミクス解析により同定した重症アイカルディ・ゴーティエ症候群の分子病態解析.2019
- Author(s)
  岡泰由, 荻朋男.
- Organizer
  第41回日本小児遺伝学会学術集会
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] マルチオミクス解析により同定した重症アイカルディ・ゴーティエ症候群の分子病態解析.2019
- Author(s)
  岡泰由, 荻朋男.
- Organizer
  第41回日本小児遺伝学会学術集会
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] DNA損傷依存的なRNAポリメラーゼのユビキチン化修飾の異常はDNA修復経路の欠損マウスで老化表現型を示す.2019
- Author(s)
  荻朋男.
- Organizer
  国立遺伝学研究所・研究集会「ゲノムの維持継承を支える分子基盤の包括的理解とその発展」
- Invited
- Data Source
  KAKENHI-PROJECT-18K11639
[Presentation] RNA polymerase IIのユビキチン化修飾による転写共役修復開始反応の分子機構とその破綻により発症する哺乳類の神経変性のメカニズム2019
- Author(s)
  荻朋男
- Organizer
  第42回日本分子生物学会年会
- Invited
- Data Source
  KAKENHI-PROJECT-18K11639
[Presentation] ゲノム不安定性疾患群を中心とした希少難治性疾患の次世代マルチオミクス解析と難病プラットフォーム連携による疾患原因変異の検索.2019
- Author(s)
  荻朋男.
- Organizer
  難病プラットフォーム公開シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] 希少未診断疾患におけるゲノム解析およびデータ評価パイプラインの構築.2019
- Author(s)
  中沢由華, 原雄一郎, 遠山美穂, 岡泰由, 荻朋男.
- Organizer
  第4回名大医薬系3部局交流シンポジウム
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] ChIP-seqを利用したDNA損傷およびヌクレオチド除去修復のモニタリング.2019
- Author(s)
  原雄一郎, 中沢由華, 岡泰由, 小峯起, Diana van den Heuvel, 郭朝万, 大学保一, 磯野真由, 何予希, 嶋田繭子, 加藤香奈, 賈楠, 橋下悟, 小谷祐子, 三好由夏, 田中都, 祖父江顕, 光武範吏, 菅波孝祥, 増田章男, 大野欽司, 中田慎一郎, 真下知士, 山中宏二, Martijn S. Luijsterburg, 荻朋男.
- Organizer
  第42回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] DNA損傷依存的なRNAポリメラーゼのユビキチン化修飾の異常はDNA修復経路の欠損マウスで老化表現型を示す.2019
- Author(s)
  荻朋男.
- Organizer
  国立遺伝学研究所・研究集会「ゲノムの維持継承を支える分子基盤の包括的理解とその発展」
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性疾患群を中心とした希少難治性疾患の次世代マルチオミクス解析と難病プラットフォーム連携による疾患原因変異の検索.2019
- Author(s)
  荻朋男.
- Organizer
  難病プラットフォーム公開シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-18K11639
[Presentation] Alterations in RNA polymerase IIo ubiquitination cause Cockayne syndrome-like premature aging phenotype in mice due to TC-NER defect.2019
- Author(s)
  Ogi T.
- Organizer
  International Symposium on XP and other Nucleotide Excision Repair Disorders
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] DNA損傷依存的なRNAポリメラーゼのユビキチン化修飾の異常はDNA修復経路の欠損マウスで老化表現型を示す.2019
- Author(s)
  荻朋男.
- Organizer
  国立遺伝学研究所・研究集会「ゲノムの維持継承を支える分子基盤の包括的理解とその発展」
- Invited
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] Alterations in RNA polymerase IIo ubiquitination cause Cockayne syndrome-like premature aging phenotype in mice due to TC-NER defect.2019
- Author(s)
  Ogi T.
- Organizer
  International Symposium on XP and other Nucleotide Excision Repair Disorders
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K11639
[Presentation] 転写共役ヌクレオチド除去修復機構に重要なRNAポリメラーゼユビキチン化部位の同定2019
- Author(s)
  中沢由華, 原雄一郎, 岡泰由, 小峯起, Diana van den Heuvel, 郭朝万, 大学保一, 磯野真由, 何予希, 嶋田繭子, 加藤香奈, 賈楠, 橋下悟, 小谷祐子, 三好由夏, 田中都, 祖父江顕, 光武範吏, 菅波孝祥, 増田章男, 大野欽司, 中田慎一郎, 真下知士, 山中宏二, Martijn S. Luijsterburg, 荻朋男
- Organizer
  第42回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] ChIP-seqを利用したDNA損傷およびヌクレオチド除去修復のモニタリング2019
- Author(s)
  原雄一郎, 中沢由華, 岡泰由, 小峯起, Diana van den Heuvel, 郭朝万, 大学保一, 磯野真由, 何予希, 嶋田繭子, 加藤香奈, 賈楠, 橋下悟, 小谷祐子, 三好由夏, 田中都, 祖父江顕, 光武範吏, 菅波孝祥, 増田章男, 大野欽司, 中田慎一郎, 真下知士, 山中宏二, Martijn S. Luijsterburg, 荻朋男.
- Organizer
  第42回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-18K11639
[Presentation] 希少未診断疾患におけるゲノム解析およびデータ評価パイプラインの構築2019
- Author(s)
  中沢由華, 原雄一郎, 遠山美穂, 岡泰由, 荻朋男.
- Organizer
  第4回名大医薬系3部局交流シンポジウム
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] ChIP-seqを利用したDNA損傷およびヌクレオチド除去修復のモニタリング.2019
- Author(s)
  原雄一郎, 中沢由華, 岡泰由, 小峯起, Diana van den Heuvel, 郭朝万, 大学保一, 磯野真由, 何予希, 嶋田繭子, 加藤香奈, 賈楠, 橋下悟, 小谷祐子, 三好由夏, 田中都, 祖父江顕, 光武範吏, 菅波孝祥, 増田章男, 大野欽司, 中田慎一郎, 真下知士, 山中宏二, Martijn S. Luijsterburg, 荻朋男.
- Organizer
  第42回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] Alterations in RNA polymerase IIo ubiquitination cause Cockayne syndrome-like premature aging phenotype in mice due to TC-NER defect.2019
- Author(s)
  Nakazawa Y, Ogi T.
- Organizer
  International Symposium on XP and other Nucleotide Excision Repair Disorders
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] 転写共役ヌクレオチド除去修復機構に重要なRNAポリメラーゼユビキチン化部位の同定.2019
- Author(s)
  中沢由華, 原雄一郎, 岡泰由, 小峯起, Diana van den Heuvel, 郭朝万, 大学保一, 磯野真由, 何予希, 嶋田繭子, 加藤香奈, 賈楠, 橋下悟, 小谷祐子, 三好由夏, 田中都, 祖父江顕, 光武範吏, 菅波孝祥, 増田章男, 大野欽司, 中田慎一郎, 真下知士, 山中宏二, Martijn S. Luijsterburg, 荻朋男.
- Organizer
  第42回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] Alterations in RNA polymerase IIo ubiquitination cause Cockayne syndrome-like premature aging phenotype in mice due to TC-NER defect.2019
- Author(s)
  Ogi T.
- Organizer
  International Symposium on XP and other Nucleotide Excision Repair Disorders
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] VPS35Lの両アレルにおける機能喪失型バリアントは 3C/Ritscher-Schinzel 症候群に類似の先天異常症候群の原因となる2019
- Author(s)
  加藤耕治, 岡泰由, 村松秀城, Vasilev F, 大友孝信, 大石久史, 河野好彦, 中沢由華, 荻朋男, 高橋義行, 齋藤伸治.
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] Alterations in RNA polymerase IIo ubiquitination cause Cockayne syndrome-like premature aging phenotype in mice due to TC-NER defect.2019
- Author(s)
  Nakazawa Y, Ogi T.
- Organizer
  International Symposium on XP and other Nucleotide Excision Repair Disorders
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K11639
[Presentation] ゲノム不安定性疾患群を中心とした希少難治性疾患の次世代マルチオミクス解析と難病プラットフォーム連携による疾患原因変異の検索.2019
- Author(s)
  荻朋男.
- Organizer
  難病プラットフォーム公開シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] Alterations in RNA polymerase IIo ubiquitination cause Cockayne syndrome-like premature aging phenotype in mice due to TC-NER defect.2019
- Author(s)
  Ogi T.
- Organizer
  International Symposium on XP and other Nucleotide Excision Repair Disorders
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] DNA損傷依存的なRNAポリメラーゼのユビキチン化修飾の異常はDNA修復経路の欠損マウスで老化表現型を示す.2019
- Author(s)
  荻朋男.
- Organizer
  国立遺伝学研究所・研究集会「ゲノムの維持継承を支える分子基盤の包括的理解とその発展」
- Invited
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] RNA polymerase IIのユビキチン化修飾による転写共役修復開始反応の分子機構とその破綻により発症する哺乳類の神経変性のメカニズム.2019
- Author(s)
  荻朋男
- Organizer
  第42回日本分子生物学会年会
- Invited
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] RNA polymerase IIのユビキチン化修飾による転写共役修復開始反応の分子機構とその破綻により発症する哺乳類の神経変性のメカニズム.2019
- Author(s)
  荻朋男
- Organizer
  第42回日本分子生物学会年会
- Invited
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] ChIP-seqを利用したDNA損傷およびヌクレオチド除去修復のモニタリング.2019
- Author(s)
  原雄一郎, 中沢由華, 岡泰由, 小峯起, Diana van den Heuvel, 郭朝万, 大学保一, 磯野真由, 何予希, 嶋田繭子, 加藤香奈, 賈楠, 橋下悟, 小谷祐子, 三好由夏, 田中都, 祖父江顕, 光武範吏, 菅波孝祥, 増田章男, 大野欽司, 中田慎一郎, 真下知士, 山中宏二, Martijn S. Luijsterburg, 荻朋男.
- Organizer
  第42回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] 転写共役ヌクレオチド除去修復機構に重要なRNAポリメラーゼユビキチン化部位の同定2019
- Author(s)
  中沢由華, 原雄一郎, 岡泰由, 小峯起, Diana van den Heuvel, 郭朝万, 大学保一, 磯野真由, 何予希, 嶋田繭子, 加藤香奈, 賈楠, 橋下悟, 小谷祐子, 三好由夏, 田中都, 祖父江顕, 光武範吏, 菅波孝祥, 増田章男, 大野欽司, 中田慎一郎, 真下知士, 山中宏二, Martijn S. Luijsterburg, 荻朋男.
- Organizer
  第42回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-18K11639
[Presentation] 希少未診断疾患におけるゲノム解析およびデータ評価パイプラインの構築.2019
- Author(s)
  中沢由華, 原雄一郎, 遠山美穂, 岡泰由, 荻朋男.
- Organizer
  第4回名大医薬系3部局交流シンポジウム
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] Biallelic VPS35L pathogenic variants cause 3C/Ritscher-Schinzel-like syndrome through dysfunction of retriever complex2019
- Author(s)
  Kato K, Oka Y, Muramatsu H, Vasilev F, Otomo T, Oishi H, Kawano Y, Nakazawa Y, Ogi T, Takahashi Y, Saitoh S.
- Organizer
  ASHG 2019 Annual Meeting
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] Alterations in RNA polymerase IIo ubiquitination cause Cockayne syndrome-like premature aging phenotype in mice due to TC-NER defect.2019
- Author(s)
  Nakazawa Y, Ogi T.
- Organizer
  International Symposium on XP and other Nucleotide Excision Repair Disorders
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] 転写共役ヌクレオチド除去修復機構に重要なRNAポリメラーゼユビキチン化部位の同定.2019
- Author(s)
  中沢由華, 原雄一郎, 岡泰由, 小峯起, Diana van den Heuvel, 郭朝万, 大学保一, 磯野真由, 何予希, 嶋田繭子, 加藤香奈, 賈楠, 橋下悟, 小谷祐子, 三好由夏, 田中都, 祖父江顕, 光武範吏, 菅波孝祥, 増田章男, 大野欽司, 中田慎一郎, 真下知士, 山中宏二, Martijn S. Luijsterburg, 荻朋男.
- Organizer
  第42回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] VPS35Lの両アレルにおける機能喪失型バリアントは 3C/Ritscher-Schinzel 症候群に類似の先天異常症候群の原因となる.2019
- Author(s)
  加藤耕治, 岡泰由, 村松秀城, Vasilev F, 大友孝信, 大石久史, 河野好彦, 中沢由華, 荻朋男, 高橋義行, 齋藤伸治.
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] Alterations in RNA polymerase IIo ubiquitination cause Cockayne syndrome-like premature aging phenotype in mice due to TC-NER defect.2019
- Author(s)
  Nakazawa Y, Ogi T.
- Organizer
  International Symposium on XP and other Nucleotide Excision Repair Disorders
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] Biallelic VPS35L pathogenic variants cause 3C/Ritscher-Schinzel-like syndrome through dysfunction of retriever complex.2019
- Author(s)
  Kato K, Oka Y, Muramatsu H, Vasilev F, Otomo T, Oishi H, Kawano Y, Nakazawa Y, Ogi T, Takahashi Y, Saitoh S.
- Organizer
  ASHG 2019 Annual Meeting
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] マルチオミクス解析により同定した重症アイカルディ・ゴーティエ症候群の分子病態解析.2019
- Author(s)
  岡泰由, 荻朋男.
- Organizer
  第41回日本小児遺伝学会学術集会
- Data Source
  KAKENHI-PROJECT-18K11639
[Presentation] ゲノム不安定性を示す遺伝性疾患の分子病態.2018
- Author(s)
  中沢由華, 荻朋男.
- Organizer
  第3回名大医薬系3部局交流シンポジウム～岐阜薬科大学・岐阜大学G-CHAIN・ラクオリア創薬合同シンポジウム～
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] Identification of pathogenic mutations in patients with rare diseases using multiomics approaches.2018
- Author(s)
  Oka Y, Ogi T.
- Organizer
  Japanese Proteomics Society 2018 Conference (JPrOS 2018), 9th Asia-Oceania Human Proteome Organization (AOHUPO), and 66th Annual Conference on Mass Spectrometry
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K11639
[Presentation] Very mild Japanese Cockayne syndrome (type-IV) cases with a N-terminal truncation mutation in the ERCC6 / CSB gene.2018
- Author(s)
  Ogi T.
- Organizer
  国際シンポジウム「早老症と関連疾患」
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] RNAポリメラーゼのユビキチン化修飾による転写共役ヌクレオチド除去修復の反応制御とコケイン症候群の病態.2018
- Author(s)
  荻朋男.
- Organizer
  第41回日本分子生物学会年会
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す遺伝性疾患の分子病態.2018
- Author(s)
  中沢由華, 荻朋男.
- Organizer
  第3回名大医薬系3部局交流シンポジウム～岐阜薬科大学・岐阜大学G-CHAIN・ラクオリア創薬合同シンポジウム～
- Data Source
  KAKENHI-PROJECT-18K11639
[Presentation] Identification of pathogenic mutations in patients with rare diseases using multiomics approaches.2018
- Author(s)
  Oka Y, Ogi T.
- Organizer
  Japanese Proteomics Society 2018 Conference (JPrOS 2018), 9th Asia-Oceania Human Proteome Organization (AOHUPO), and 66th Annual Conference on Mass Spectrometry
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] RNAポリメラーゼのユビキチン化修飾による転写共役ヌクレオチド除去修復の反応制御とコケイン症候群の病態.2018
- Author(s)
  郭朝万, 賈楠, 岡泰由, 中沢由華, 荻朋男.
- Organizer
  第41回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] RNAポリメラーゼのユビキチン化修飾による転写共役ヌクレオチド除去修復の反応制御とコケイン症候群の病態.2018
- Author(s)
  荻朋男.
- Organizer
  第41回日本分子生物学会年会
- Invited
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] Identification of pathogenic mutations in patients with rare diseases using multiomics approaches.2018
- Author(s)
  Oka Y, Ogi T.
- Organizer
  Japanese Proteomics Society 2018 Conference (JPrOS 2018), 9th Asia-Oceania Human Proteome Organization (AOHUPO), and 66th Annual Conference on Mass Spectrometry
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] コケイン症候群の疾患責任遺伝子変異を特定する解析方法について.2018
- Author(s)
  荻朋男, 中沢由華.
- Organizer
  コケイン症候群勉強会
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] RNAポリメラーゼのユビキチン化修飾による転写共役ヌクレオチド除去修復の反応制御とコケイン症候群の病態.2018
- Author(s)
  荻朋男.
- Organizer
  第41回日本分子生物学会年会
- Invited
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] RNAポリメラーゼのユビキチン化修飾による転写共役ヌクレオチド除去修復の反応制御とコケイン症候群の病態.2018
- Author(s)
  荻朋男.
- Organizer
  第41回日本分子生物学会年会
- Invited
- Data Source
  KAKENHI-PROJECT-18K11639
[Presentation] Identification of pathogenic mutations in patients with rare diseases using multiomics approaches.2018
- Author(s)
  Oka Y, Ogi T.
- Organizer
  Japanese Proteomics Society 2018 Conference (JPrOS 2018), 9th Asia-Oceania Human Proteome Organization (AOHUPO), and 66th Annual Conference on Mass Spectrometry
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す遺伝性疾患の分子病態.2018
- Author(s)
  中沢由華, 荻朋男.
- Organizer
  第3回名大医薬系3部局交流シンポジウム～岐阜薬科大学・岐阜大学G-CHAIN・ラクオリア創薬合同シンポジウム～
- Data Source
  KAKENHI-PROJECT-18H03372
[Presentation] Very mild Japanese Cockayne syndrome (type-IV) cases with a N-terminal truncation mutation in the ERCC6 / CSB gene.2018
- Author(s)
  Ogi T.
- Organizer
  国際シンポジウム「早老症と関連疾患」
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] Very mild Japanese Cockayne syndrome (type-IV) cases with a N-terminal truncation mutation in the ERCC6 / CSB gene.2018
- Author(s)
  Ogi T.
- Organizer
  国際シンポジウム「早老症と関連疾患」
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] Very mild Japanese Cockayne syndrome (type-IV) cases with a N-terminal truncation mutation in the ERCC6 / CSB gene.2018
- Author(s)
  Ogi T
- Organizer
  国際シンポジウム「早老症と関連疾患」
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] ゲノム不安定性を示す遺伝性疾患の分子病態.2018
- Author(s)
  中沢由華, 荻朋男.
- Organizer
  第3回名大医薬系3部局交流シンポジウム～岐阜薬科大学・岐阜大学G-CHAIN・ラクオリア創薬合同シンポジウム～
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] Human genetics disorders associated with DNA repair deficiency.2017
- Author(s)
  Ogi T.
- Organizer
  6th US-Japan DNA Repair Meeting
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] Very mild CS type-IV cases with mutations in the CSB gene.2017
- Author(s)
  Jia N, Guo C, Oka Y, Nakazawa Y, Shimada M, Miyazaki H, Ogi T.
- Organizer
  第24回DNA複製・組換え・修復ワークショップ
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] ゲノム不安定性を示す遺伝性疾患群の疾患責任遺伝子変異の探索.2017
- Author(s)
  中沢由華、千住千佳子、岡泰由、嶋田繭子、宮崎仁美、郭朝万、賈楠、荻朋男.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] Molecular pathogenesis underlying Cockayne syndrome and UV-sensitive syndrome.2017
- Author(s)
  Jia N, Guo C, Oka Y, Nakazawa Y, Shimada M, Miyazaki H, Ogi T.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] A Novel Gene Mutation Of Japanese Xeroderma Pigmentosum Complementation Group F Patients.2017
- Author(s)
  Senju C, Nakazawa Y, Ogi T.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] Molecular pathogenesis underlying Cockayne syndrome and UV-sensitive syndrome.2017
- Author(s)
  Jia N, Guo C, Oka Y, Nakazawa Y, Shimada M, Miyazaki H, Ogi T.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す遺伝性疾患群の疾患責任遺伝子変異の探索.2017
- Author(s)
  中沢由華、千住千佳子、岡泰由、嶋田繭子、宮崎仁美、郭朝万、賈楠、荻朋男.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] Very mild CS type-IV cases with mutations in the CSB gene.2017
- Author(s)
  Jia N, Guo C, Oka Y, Nakazawa Y, Shimada M, Miyazaki H, Ogi T.
- Organizer
  第24回DNA複製・組換え・修復ワークショップ
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] DNA修復機構欠損性疾患の病態解明研究.2017
- Author(s)
  中沢由華、賈楠、嶋田繭子、宮崎仁美、千住千佳子、郭朝万、岡泰由、荻朋男.
- Organizer
  第２回放射線災害・医科学研究拠点カンファランス
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] ゲノム不安定性を示す遺伝性疾患の次世代マルチオミクス解析.2017
- Author(s)
  荻　朋男
- Organizer
  第7回名古屋大学医学系研究科・生理学研究所合同シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] DNA修復・損傷応答機構の異常により発症する疾患の病態解明.2017
- Author(s)
  荻朋男
- Organizer
  奈良先端科学技術大学院大学ワークショップ
- Place of Presentation
  奈良先端科学技術大学院大学（奈良県生駒市）
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] Identification of pathogenic mutations in patients with rare diseases using multi-omics analysis.2017
- Author(s)
  Oka Y, Nakazawa Y, Ogi T.
- Organizer
  日本プロテオーム学会2017年大会
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] DNA修復機構の異常と疾患2017
- Author(s)
  荻朋男
- Organizer
  太陽紫外線防御研究委員会第27回シンポジウム
- Place of Presentation
  佐治敬三メモリアルホール（大阪府大阪市）
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す遺伝性疾患の次世代マルチオミクス解析.2017
- Author(s)
  荻朋男.
- Organizer
  第7回名古屋大学医学系研究科・生理学研究所合同シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] DNA損傷依存的なRNAポリメラーゼの修飾とヒト疾患.2017
- Author(s)
  荻　朋男
- Organizer
  国立遺伝学研究所・研究集会「染色体構築と安定化を担う分子機構」
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] Identification of pathogenic mutations in patients with rare diseases using multi-omics analysis.2017
- Author(s)
  Oka Y, Nakazawa Y, Ogi T.
- Organizer
  日本プロテオーム学会2017年大会
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ミニレクチャー「ゲノム不安定性疾患群を中心とした希少疾患の次世代マルチオミクス病態解析」2017
- Author(s)
  荻朋男.
- Organizer
  第12回東海小児遺伝カンファレンス
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] DNA修復機構の異常と疾患.2017
- Author(s)
  荻朋男
- Organizer
  太陽紫外線防御研究委員会第27回シンポジウム
- Place of Presentation
  佐治敬三メモリアルホール（大阪府大阪市）
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] Human genetics disorders associated with DNA repair deficiency.2017
- Author(s)
  Ogi T.
- Organizer
  6th US-Japan DNA Repair Meeting
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] Very mild CS type-IV cases with mutation in the CSB gene.2017
- Author(s)
  Ogi T.
- Organizer
  Cockayne Syndrome Meeting.
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] Very mild CS type-IV cases with mutations in the CSB gene.2017
- Author(s)
  Jia N, Guo C, Oka Y, Nakazawa Y, Shimada M, Miyazaki H, Ogi T.
- Organizer
  第24回DNA複製・組換え・修復ワークショップ
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] A Novel Gene Mutation Of Japanese Xeroderma Pigmentosum Complementation Group F Patients.2017
- Author(s)
  Senju C, Nakazawa Y, Ogi T.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] Human genetic disorders associated with TC-NER deficiency.2017
- Author(s)
  Ogi T.
- Organizer
  第２回神戸大学バイオシグナル総合研究センター国際シンポジウム
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] Human genetic disorders associated with TC-NER deficiency.2017
- Author(s)
  Ogi T.
- Organizer
  第２回神戸大学バイオシグナル総合研究センター国際シンポジウム
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] Human genetic disorders associated with TC-NER deficiency.2017
- Author(s)
  Ogi T.
- Organizer
  第２回神戸大学バイオシグナル総合研究センター国際シンポジウム
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] Molecular pathogenesis underlying Cockayne syndrome and UV-sensitive syndrome.2017
- Author(s)
  Jia N, Guo C, Oka Y, Nakazawa Y, Shimada M, Miyazaki H, Ogi T.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] DNA損傷依存的なRNAポリメラーゼの修飾とヒト疾患.2017
- Author(s)
  荻　朋男
- Organizer
  国立遺伝学研究所・研究集会「染色体構築と安定化を担う分子機構」
- Invited
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] Very mild CS type-IV cases with mutations in the CSB gene.2017
- Author(s)
  Jia N, Guo C, Oka Y, Nakazawa Y, Shimada M, Miyazaki H, Ogi T.
- Organizer
  第24回DNA複製・組換え・修復ワークショップ
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] DNA修復・損傷応答機構の異常により発症する疾患の病態解明.2017
- Author(s)
  荻朋男
- Organizer
  奈良先端科学技術大学院大学ワークショップ
- Place of Presentation
  奈良先端科学技術大学院大学（奈良県生駒市）
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] Identification of pathogenic mutations in patients with rare diseases using multi-omics analysis.2017
- Author(s)
  Oka Y, Nakazawa Y, Ogi T.
- Organizer
  日本プロテオーム学会2017年大会
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] マルチオミクス解析による希少遺伝性疾患発症責任因子の同定.2017
- Author(s)
  岡泰由、中沢由華、荻朋男.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] マルチオミクス解析による希少遺伝性疾患発症責任因子の同定.2017
- Author(s)
  岡泰由、中沢由華、荻朋男.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] Whole exome sequencing of 14 schizophrenia multiplex families in Japan.2017
- Author(s)
  Toyama M, Takasaki Y, Aleksic B, Ogi T, Ozaki N.
- Organizer
  Human Genome Meeting 2018
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2017
- Author(s)
  Ogi T
- Organizer
  International Symposium on Immune Diversity and Cancer Therapy Kobe 2017
- Place of Presentation
  神戸ポートピアホテル（兵庫県神戸市）
- Year and Date
  2017-01-26
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] DNA修復機構の異常と疾患.2017
- Author(s)
  荻朋男
- Organizer
  太陽紫外線防御研究委員会第27回シンポジウム
- Place of Presentation
  佐治敬三メモリアルホール（大阪府大阪市）
- Invited
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] Molecular pathogenesis underlying Cockayne syndrome and UV-sensitive syndrome.2017
- Author(s)
  Jia N, Guo C, Oka Y, Nakazawa Y, Shimada M, Miyazaki H, Ogi T.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] DNA修復・損傷応答機構の異常により発症する疾患の病態解明.2017
- Author(s)
  荻朋男
- Organizer
  奈良先端科学技術大学院大学ワークショップ
- Place of Presentation
  奈良先端科学技術大学院大学（奈良県生駒市）
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] Molecular pathogenesis underlying Cockayne syndrome and UV-sensitive syndrome.2017
- Author(s)
  Jia N, Guo C, Oka Y, Nakazawa Y, Shimada M, Miyazaki H, Ogi T.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] DNA損傷依存的なRNAポリメラーゼの修飾とヒト疾患.2017
- Author(s)
  荻朋男.
- Organizer
  国立遺伝学研究所・研究集会「染色体構築と安定化を担う分子機構」
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2017
- Author(s)
  Ogi T
- Organizer
  International Symposium on Immune Diversity and Cancer Therapy Kobe 2017
- Place of Presentation
  神戸ポートピアホテル（兵庫県神戸市）
- Year and Date
  2017-01-26
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] Human genetics disorders associated with DNA repair deficiency.2017
- Author(s)
  Ogi T.
- Organizer
  6th US-Japan DNA Repair Meeting
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2017
- Author(s)
  Ogi T
- Organizer
  International Symposium on Immune Diversity and Cancer Therapy Kobe 2017
- Place of Presentation
  神戸ポートピアホテル（兵庫県神戸市）
- Year and Date
  2017-01-26
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2017
- Author(s)
  Ogi T
- Organizer
  International Symposium on Immune Diversity and Cancer Therapy Kobe 2017
- Place of Presentation
  神戸ポートピアホテル（兵庫県神戸市）
- Year and Date
  2017-01-26
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] Identification of pathogenic mutations in patients with rare diseases using multi-omics analysis.2017
- Author(s)
  Oka Y, Nakazawa Y, Ogi T.
- Organizer
  日本プロテオーム学会2017年大会
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] ミニレクチャー「ゲノム不安定性疾患群を中心とした希少疾患の次世代マルチオミクス病態解析」2017
- Author(s)
  荻　朋男
- Organizer
  第12回東海小児遺伝カンファレンス
- Invited
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] Human genetic disorders associated with TC-NER deficiency.2017
- Author(s)
  Ogi T.
- Organizer
  第２回神戸大学バイオシグナル総合研究センター国際シンポジウム
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す遺伝性疾患群の疾患責任遺伝子変異の探索.2017
- Author(s)
  中沢由華、千住千佳子、岡泰由、嶋田繭子、宮崎仁美、郭朝万、賈楠、荻朋男.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] ゲノム不安定性を示す遺伝性疾患の次世代マルチオミクス解析.2017
- Author(s)
  荻　朋男
- Organizer
  第7回名古屋大学医学系研究科・生理学研究所合同シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] Identification of pathogenic mutations in patients with rare diseases using multi-omics analysis.2017
- Author(s)
  Oka Y, Nakazawa Y, Ogi T.
- Organizer
  日本プロテオーム学会2017年大会
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] DNA修復機構欠損性疾患の病態解明研究.2017
- Author(s)
  中沢由華、賈楠、嶋田繭子、宮崎仁美、千住千佳子、郭朝万、岡泰由、荻朋男
- Organizer
  第２回放射線災害・医科学研究拠点カンファランス
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] マルチオミクス解析による希少遺伝性疾患発症責任因子の同定.2017
- Author(s)
  岡泰由、中沢由華、荻朋男.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] Very mild CS type-IV cases with mutation in the CSB gene.2017
- Author(s)
  Ogi T.
- Organizer
  Cockayne Syndrome Meeting
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す遺伝性疾患群の疾患責任遺伝子変異の探索.2017
- Author(s)
  中沢由華、千住千佳子、岡泰由、嶋田繭子、宮崎仁美、郭朝万、賈楠、荻朋男.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] マルチオミクス解析による希少遺伝性疾患発症責任因子の同定.2017
- Author(s)
  岡泰由、中沢由華、荻朋男.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] DNA損傷依存的なRNAポリメラーゼの修飾とヒト疾患.2017
- Author(s)
  荻　朋男
- Organizer
  国立遺伝学研究所・研究集会「染色体構築と安定化を担う分子機構」
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] A Novel Gene Mutation Of Japanese Xeroderma Pigmentosum Complementation Group F Patients.2017
- Author(s)
  Senju C, Nakazawa Y, Ogi T.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2017
- Author(s)
  Ogi T.
- Organizer
  International Symposium on Immune Diversity and Cancer Therapy Kobe 2017
- Place of Presentation
  神戸ポートピアホテル（兵庫県神戸市）
- Year and Date
  2017-01-26
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] ゲノム不安定性を示す遺伝性疾患群の疾患責任遺伝子変異の探索.2017
- Author(s)
  中沢由華、千住千佳子、岡泰由、嶋田繭子、宮崎仁美、郭朝万、賈楠、荻朋男.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] Very mild CS type-IV cases with mutations in the CSB gene.2017
- Author(s)
  Jia N, Guo C, Oka Y, Nakazawa Y, Shimada M, Miyazaki H, Ogi T.
- Organizer
  第24回DNA複製・組換え・修復ワークショップ
- Data Source
  KAKENHI-PROJECT-17H01877
[Presentation] DNA修復・損傷応答機構の異常により発症する疾患の病態解明.2017
- Author(s)
  荻朋男
- Organizer
  奈良先端科学技術大学院大学ワークショップ
- Place of Presentation
  奈良先端科学技術大学院大学（奈良県生駒市）
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] DNA修復機構欠損性疾患の病態解明研究.2017
- Author(s)
  中沢由華、賈楠、嶋田繭子、宮崎仁美、千住千佳子、郭朝万、岡泰由、荻朋男.
- Organizer
  第２回放射線災害・医科学研究拠点カンファランス
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] DNA修復機構欠損性疾患の病態解明研究.2017
- Author(s)
  中沢由華、賈楠、嶋田繭子、宮崎仁美、千住千佳子、郭朝万、岡泰由、荻朋男.
- Organizer
  第２回放射線災害・医科学研究拠点カンファランス
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] DNA修復・損傷応答機構の異常により発症する疾患の病態解明.2017
- Author(s)
  荻朋男、中沢由華、唐田清伸、郭朝万、岡泰由、賈楠、嶋田繭子、宮﨑仁美、千住千佳子.
- Organizer
  奈良先端科学技術大学院大学ワークショップ
- Place of Presentation
  奈良先端科学技術大学院大学（奈良県生駒市）
- Invited
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] A Novel Gene Mutation Of Japanese Xeroderma Pigmentosum Complementation Group F Patients.2017
- Author(s)
  Senju C, Nakazawa Y, Ogi T.
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] Very mild CS type-IV cases with mutation in the CSB gene.2017
- Author(s)
  Ogi T.
- Organizer
  Cockayne Syndrome Meeting.
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] DNA修復機構の異常と疾患.2017
- Author(s)
  荻朋男
- Organizer
  太陽紫外線防御研究委員会第27回シンポジウム
- Place of Presentation
  佐治敬三メモリアルホール（大阪府大阪市）
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] Human genetics disorders associated with DNA repair deficiency.2017
- Author(s)
  Ogi T.
- Organizer
  6th US-Japan DNA Repair Meeting
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] DNA修復機構の異常と疾患.2017
- Author(s)
  荻　朋男
- Organizer
  太陽紫外線防御研究委員会第27回シンポジウム
- Place of Presentation
  佐治敬三メモリアルホール（大阪府大阪市）
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] Very mild CS type-IV cases with mutation in the CSB gene.2017
- Author(s)
  Ogi T.
- Organizer
  Cockayne Syndrome Meeting.
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H00783
[Presentation] ミニレクチャー「ゲノム不安定性疾患群を中心とした希少疾患の次世代マルチオミクス病態解析」2017
- Author(s)
  荻　朋男
- Organizer
  第12回東海小児遺伝カンファレンス
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] TC-NER因子UVSSAによるRNAポリメラーゼIIのユビキチン化に関する分子機能解析2016
- Author(s)
  郭朝万、中沢由華、嶋田繭子、唐田清伸、賈楠、岡泰由、宮崎仁美、千住千佳子、荻朋男
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Data Source
  KAKENHI-PROJECT-15K00541
[Presentation] DNA修復の異常により発症するゲノム不安定性疾患の分子病態解明研究2016
- Author(s)
  荻朋男
- Organizer
  東北大学学際科学フロンティア研究所第1回ワークショップ「多様な核酸サイエンス」
- Place of Presentation
  東北大学（宮城県仙台市）
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] ヒト WDR4 遺伝子の先天的な異常はゲノム不安定性に起因する発育異常を誘発する2016
- Author(s)
  荻朋男
- Organizer
  第75回日本癌学会学術総会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-10-06
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] Genetics disorders associated with defects in transcription coupled nucleotide excision repair.2016
- Author(s)
  Ogi T.
- Organizer
  10th Quinquennial Conference on Responses to DNA damage: from molecule to disease
- Place of Presentation
  Egmond aan Zee（オランダ）
- Year and Date
  2016-04-17
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2016
- Author(s)
  Ogi T
- Organizer
  上海交通大学医学院附属上海新華医院セミナー
- Place of Presentation
  Shanghai（中国）
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] コケイン症候群のゲノム診断2016
- Author(s)
  荻朋男
- Organizer
  日本コケイン症候群ネットワーク勉強会
- Place of Presentation
  東京ビジネスアットセンター東京駅（東京都千代田区）
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] ゲノム不安定性により先天性小頭症を示すヒト遺伝性疾患の症例解析と病態解明研究2016
- Author(s)
  荻朋男
- Organizer
  日本遺伝学会第88回大会
- Place of Presentation
  日本大学国際関係学部（静岡県三島市）
- Year and Date
  2016-09-07
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] コケイン症候群と紫外線高感受性症候群の分子病態解析.2016
- Author(s)
  賈楠、中沢由華、郭朝万、唐田清伸、岡泰由、嶋田繭子、宮﨑仁美、千住千佳子、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2016
- Author(s)
  Ogi T
- Organizer
  上海交通大学医学院附属上海新華医院セミナー
- Place of Presentation
  Shanghai（中国）
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す遺伝性疾患群の病態解析と新規疾患責任遺伝子変異探索.2016
- Author(s)
  中沢由華、岡泰由、郭朝万、賈楠、唐田清伸、嶋田繭子、宮﨑仁美、千住千佳子、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] DNA修復システムの異常とゲノムDNAの不安定化により発症する疾患の分子病態2016
- Author(s)
  荻朋男
- Organizer
  第42回北里医学学会総会
- Place of Presentation
  小田急ホテルセンチュリー相模大野（神奈川県相模原市）
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す遺伝性疾患群の病態解析と新規疾患責任遺伝子変異探索2016
- Author(s)
  中沢由華、岡泰由、郭朝万、賈楠、唐田清伸、嶋田繭子、宮崎仁美、千住千佳子、荻朋男
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Data Source
  KAKENHI-PROJECT-15K00541
[Presentation] DNA損傷応答と遺伝病疾患2016
- Author(s)
  荻朋男
- Organizer
  平成28年度若手放射線生物学研究会専門研究会
- Place of Presentation
  東京工業大学（東京都目黒区）
- Year and Date
  2016-09-03
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] DNA修復システムの異常とゲノムDNAの不安定化により発症する疾患の分子病態2016
- Author(s)
  荻朋男
- Organizer
  第42回北里医学学会総会
- Place of Presentation
  小田急ホテルセンチュリー相模大野（神奈川県相模原市）
- Invited
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] 新規のDNA 修復因子WDR4の欠損により発症する小頭症症例の分子病態2016
- Author(s)
  荻朋男
- Organizer
  国立遺伝学研究所・研究集会「生物ゲノム安定維持の分子機構」
- Place of Presentation
  国立遺伝学研究所（静岡県三島市）
- Year and Date
  2016-10-24
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2016
- Author(s)
  荻朋男
- Organizer
  京都大学放射線生物研究センター第32回国際シンポジウム” Growing Edge of Radiation Biology, from principles to applications”
- Place of Presentation
  ホテルコープイン京都（京都府京都市）
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] コケイン症候群と紫外線高感受性症候群の分子病態解析.2016
- Author(s)
  賈楠、中沢由華、郭朝万、唐田清伸、岡泰由、嶋田繭子、宮﨑仁美、千住千佳子、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] 次世代マルチオミクス解析を用いた希少性難治性遺伝性疾患原因因子の新規同定法の開発2016
- Author(s)
  荻朋男
- Organizer
  第29回バイオメディカル分析化学シンポジウムランチョンセミナー
- Place of Presentation
  京都大学（京都府京都市）
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] New DNA-repair gene mutations associated with Cokayne syndrome like progeroid disorders.2016
- Author(s)
  Ogi T.
- Organizer
  2016 Spring International Conference of the Korean Society for Gerontology The 15th Korea-Japan Gerontologist Joint Meeting,
- Place of Presentation
  Daegu（韓国）
- Year and Date
  2016-06-15
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2016
- Author(s)
  荻朋男
- Organizer
  京都大学放射線生物研究センター第32回国際シンポジウム” Growing Edge of Radiation Biology, from principles to applications”
- Place of Presentation
  ホテルコープイン京都（京都府京都市）
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] コケイン症候群と紫外線高感受性症候群の分子病態解析2016
- Author(s)
  賈楠、中沢由華、郭朝万、唐田清伸、岡泰由、嶋田繭子、宮崎仁美、千住千佳子、荻朋男
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Data Source
  KAKENHI-PROJECT-15K00541
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2016
- Author(s)
  荻朋男
- Organizer
  京都大学放射線生物研究センター第32回国際シンポジウム” Growing Edge of Radiation Biology, from principles to applications”
- Place of Presentation
  ホテルコープイン京都（京都府京都市）
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] Genetics disorders associated with defects in transcription coupled nucleotide excision repair.2016
- Author(s)
  Ogi T
- Organizer
  10th Quinquennial Conference on Responses to DNA damage: from molecule to disease
- Place of Presentation
  Egmond aan Zee（オランダ）
- Year and Date
  2016-04-17
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] トランスオミクス解析を用いた希少遺伝性疾患原因因子の新規同定法の開発.2016
- Author(s)
  岡泰由、郭　朝万、賈楠、唐田清伸、中沢由華、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] 新規のDNA 修復因子WDR4の欠損により発症する小頭症症例の分子病態2016
- Author(s)
  荻朋男
- Organizer
  国立遺伝学研究所・研究集会「生物ゲノム安定維持の分子機構」
- Place of Presentation
  国立遺伝学研究所（静岡県三島市）
- Year and Date
  2016-10-24
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] コケイン症候群のゲノム診断2016
- Author(s)
  荻朋男
- Organizer
  日本コケイン症候群ネットワーク勉強会
- Place of Presentation
  東京ビジネスアットセンター東京駅（東京都千代田区）
- Invited
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] 「紫外線から遺伝子を守る」紫外線DNA損傷を修復する分子メカニズムとその破綻により発症する疾患の病態解明」.2016
- Author(s)
  荻　朋男
- Organizer
  太陽紫外線防御研究委員会第26回シンポジウム
- Place of Presentation
  グランフロント大阪（大阪府大阪市）
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] DNA修復システムの異常により発症するヒト疾患の分子病態.2016
- Author(s)
  荻朋男
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Invited
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] DNA修復の異常により発症するゲノム不安定性疾患の分子病態解明研究2016
- Author(s)
  荻朋男
- Organizer
  東北大学学際科学フロンティア研究所第1回ワークショップ「多様な核酸サイエンス」
- Place of Presentation
  東北大学（宮城県仙台市）
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] ゲノム不安定性により先天性小頭症を示すヒト遺伝性疾患の症例解析と病態解明研究2016
- Author(s)
  荻朋男
- Organizer
  日本遺伝学会第88回大会
- Place of Presentation
  日本大学国際関係学部（静岡県三島市）
- Year and Date
  2016-09-07
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] TC-NER因子UVSSAによるRNAポリメラーゼIIのユビキチン化に関する分子機能解析.2016
- Author(s)
  郭朝万、中沢由華、嶋田繭子、唐田清伸、賈楠、岡泰由、宮﨑仁美、千住千佳子、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] DNA修復の異常により発症するゲノム不安定性疾患の分子病態解明研究2016
- Author(s)
  荻朋男
- Organizer
  東北大学学際科学フロンティア研究所第1回ワークショップ「多様な核酸サイエンス」
- Place of Presentation
  東北大学（宮城県仙台市）
- Invited
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] ヒト WDR4 遺伝子の先天的な異常はゲノム不安定性に起因する発育異常を誘発する2016
- Author(s)
  荻朋男
- Organizer
  第75回日本癌学会学術総会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-10-06
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] コケイン症候群と紫外線高感受性症候群の分子病態解析.2016
- Author(s)
  賈楠、中沢由華、郭朝万、唐田清伸、岡泰由、嶋田繭子、宮﨑仁美、千住千佳子、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] トランスオミクス解析を用いた希少遺伝性疾患原因因子の新規同定法の開発2016
- Author(s)
  岡泰由、郭朝万、賈楠、唐田清伸、中沢由華、荻朋男
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Data Source
  KAKENHI-PROJECT-15K00541
[Presentation] 次世代ゲノム解析と精密質量分析を基盤としたマルチオミクスデータの臨床診断へ応用2016
- Author(s)
  荻朋男
- Organizer
  サーモフィッシャーサイエンティフィック質量分析フォーラム2016
- Place of Presentation
  ザ・リッツ・カールトン大阪（大阪府大阪市）、東京コンファレンスセンター・品川（東京都港区）
- Year and Date
  2016-08-02
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] トランスオミクス解析を用いた希少遺伝性疾患原因因子の新規同定法の開発.2016
- Author(s)
  岡泰由、郭朝万、賈楠、唐田清伸、中沢由華、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ヒト WDR4 遺伝子の先天的な異常はゲノム不安定性に起因する発育異常を誘発する2016
- Author(s)
  荻朋男
- Organizer
  第75回日本癌学会学術総会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-10-06
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] コケイン症候群のゲノム診断2016
- Author(s)
  荻朋男
- Organizer
  日本コケイン症候群ネットワーク勉強会
- Place of Presentation
  東京ビジネスアットセンター東京駅（東京都千代田区）
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] DNA修復システムの異常により発症するヒト疾患の分子病態.2016
- Author(s)
  荻朋男
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] DNA修復の異常により発症するゲノム不安定性疾患の分子病態解明研究2016
- Author(s)
  荻朋男
- Organizer
  東北大学学際科学フロンティア研究所第1回ワークショップ「多様な核酸サイエンス」
- Place of Presentation
  東北大学（宮城県仙台市）
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] トランスオミクス解析を用いた希少遺伝性疾患原因因子の新規同定法の開発.2016
- Author(s)
  岡泰由、郭　朝万、賈楠、唐田清伸、中沢由華、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] 次世代ゲノム解析と精密質量分析を基盤としたマルチオミクスデータの臨床診断へ応用2016
- Author(s)
  荻朋男
- Organizer
  サーモフィッシャーサイエンティフィック質量分析フォーラム2016
- Place of Presentation
  ザ・リッツ・カールトン大阪（大阪府大阪市）、東京コンファレンスセンター・品川（東京都港区）
- Year and Date
  2016-08-02
- Invited
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] コケイン症候群と紫外線高感受性症候群の分子病態解析.2016
- Author(s)
  賈　楠、中沢由華、郭　朝万、唐田清伸、岡　泰由、嶋田繭子、宮﨑仁美、千住千佳子、荻　朋男
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県・横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] ゲノム不安定性により先天性小頭症を示すヒト遺伝性疾患の症例解析と病態解明研究2016
- Author(s)
  荻朋男
- Organizer
  日本遺伝学会第88回大会
- Place of Presentation
  日本大学国際関係学部（静岡県三島市）
- Year and Date
  2016-09-07
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2016
- Author(s)
  Ogi T.
- Organizer
  上海交通大学医学院附属上海新華医院セミナー
- Place of Presentation
  Shanghai（中国）
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] トランスオミクス解析を用いた希少遺伝性疾患原因因子の新規同定法の開発.2016
- Author(s)
  岡泰由、郭　朝万、賈楠、唐田清伸、中沢由華、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] ハイコンテントイメージングシステムを利用した難治性遺伝性疾患の臨床診断2016
- Author(s)
  荻朋男
- Organizer
  サーモフィッシャーサイエンティフィックバイオサイエンス事業本部2016HCAユーザーミーティング
- Place of Presentation
  サーモフィッシャーサイエンティフィック株式会社三田オフィス（東京都港区）、サーモフィッシャーサイエンティフィック株式会社大阪営業所（大阪府大阪市）
- Year and Date
  2016-05-26
- Invited
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] DNA修復システムの異常により発症するヒト疾患の分子病態.2016
- Author(s)
  荻朋男
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] 次世代マルチオミクス解析を用いた希少性難治性遺伝性疾患原因因子の新規同定法の開発2016
- Author(s)
  荻朋男
- Organizer
  第29回バイオメディカル分析化学シンポジウムランチョンセミナー
- Place of Presentation
  京都大学（京都府京都市）
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] コケイン症候群のゲノム診断2016
- Author(s)
  荻朋男
- Organizer
  日本コケイン症候群ネットワーク勉強会
- Place of Presentation
  東京ビジネスアットセンター東京駅（東京都千代田区）
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] New DNA-repair gene mutations associated with Cokayne syndrome like progeroid disorders.2016
- Author(s)
  Ogi T
- Organizer
  2016 Spring International Conference of the Korean Society for Gerontology The 15th Korea-Japan Gerontologist Joint Meeting,
- Place of Presentation
  Daegu（韓国）
- Year and Date
  2016-06-15
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] コケイン症候群と紫外線高感受性症候群の分子病態解析.2016
- Author(s)
  賈楠、中沢由華、郭朝万、唐田清伸、岡泰由、嶋田繭子、宮﨑仁美、千住千佳子、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ハイコンテントイメージングシステムを利用した難治性遺伝性疾患の臨床診断2016
- Author(s)
  荻朋男
- Organizer
  サーモフィッシャーサイエンティフィックバイオサイエンス事業本部2016HCAユーザーミーティング
- Place of Presentation
  サーモフィッシャーサイエンティフィック株式会社三田オフィス（東京都港区）、サーモフィッシャーサイエンティフィック株式会社大阪営業所（大阪府大阪市）
- Year and Date
  2016-05-26
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] TC-NER因子UVSSAによるRNAポリメラーゼIIのユビキチン化に関する分子機能解析.2016
- Author(s)
  郭朝万、中沢由華、嶋田繭子、唐田清伸、賈楠、岡泰由、宮﨑仁美、千住千佳子、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] DNA修復の異常により発症するゲノム不安定性疾患の分子病態解明研究2016
- Author(s)
  荻朋男
- Organizer
  東北大学学際科学フロンティア研究所第1回ワークショップ「多様な核酸サイエンス」
- Place of Presentation
  東北大学（宮城県仙台市）
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] TC-NER因子UVSSAによるRNAポリメラーゼIIのユビキチン化に関する分子機能解析.2016
- Author(s)
  郭朝万、中沢由華、嶋田繭子、唐田清伸、賈楠、岡泰由、宮﨑仁美、千住千佳子、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] 次世代ゲノム解析と精密質量分析を基盤としたマルチオミクスデータの臨床診断へ応用2016
- Author(s)
  荻朋男
- Organizer
  サーモフィッシャーサイエンティフィック質量分析フォーラム
- Place of Presentation
  ザ・リッツ・カールトン大阪（大阪府大阪市）, 東京コンファレンスセンター・品川（東京都港区）
- Year and Date
  2016-08-02
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性により先天性小頭症を示すヒト遺伝性疾患の症例解析と病態解明研究2016
- Author(s)
  荻朋男
- Organizer
  日本遺伝学会第88回大会
- Place of Presentation
  日本大学国際関係学部（静岡県三島市）
- Year and Date
  2016-09-07
- Invited
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] New DNA-repair gene mutations associated with Cokayne syndrome like progeroid disorders.2016
- Author(s)
  Ogi T
- Organizer
  2016 Spring International Conference of the Korean Society for Gerontology The 15th Korea-Japan Gerontologist Joint Meeting,
- Place of Presentation
  Daegu（韓国）
- Year and Date
  2016-06-15
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] DNA修復システムの異常により発症するヒト疾患の分子病態2016
- Author(s)
  荻朋男、岡泰由、郭朝万、賈楠、唐田清伸、中沢由華
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Data Source
  KAKENHI-PROJECT-15K00541
[Presentation] TC-NER因子UVSSAによるRNAポリメラーゼIIのユビキチン化に関する分子機能解析.2016
- Author(s)
  郭　朝万、中沢由華、嶋田繭子、唐田清伸、賈　楠、岡　泰由、宮﨑仁美、千住千佳子、荻　朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県・横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] DNA損傷応答と遺伝病疾患2016
- Author(s)
  荻朋男
- Organizer
  平成28年度若手放射線生物学研究会専門研究会
- Place of Presentation
  東京工業大学（東京都目黒区）
- Year and Date
  2016-09-03
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] 次世代マルチオミクス解析を用いた希少性難治性遺伝性疾患原因因子の新規同定法の開発2016
- Author(s)
  荻朋男
- Organizer
  第29回バイオメディカル分析化学シンポジウムランチョンセミナー
- Place of Presentation
  京都大学（京都府京都市）
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] Genetics disorders associated with defects in transcription coupled nucleotide excision repair.2016
- Author(s)
  Ogi T
- Organizer
  10th Quinquennial Conference on Responses to DNA damage: from molecule to disease
- Place of Presentation
  Egmond aan Zee（オランダ）
- Year and Date
  2016-04-17
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2016
- Author(s)
  Ogi T
- Organizer
  上海交通大学医学院附属上海新華医院セミナー
- Place of Presentation
  Shanghai（中国）
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] DNA修復システムの異常とゲノムDNAの不安定化により発症する疾患の分子病態2016
- Author(s)
  荻朋男
- Organizer
  第42回北里医学学会総会
- Place of Presentation
  小田急ホテルセンチュリー相模大野（神奈川県相模原市）
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] TC-NER因子UVSSAによるRNAポリメラーゼIIのユビキチン化に関する分子機能解析.2016
- Author(s)
  郭朝万、中沢由華、嶋田繭子、唐田清伸、賈楠、岡泰由、宮﨑仁美、千住千佳子、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] 次世代ゲノム解析と精密質量分析を基盤としたマルチオミクスデータの臨床診断へ応用2016
- Author(s)
  荻朋男
- Organizer
  サーモフィッシャーサイエンティフィック質量分析フォーラム2016
- Place of Presentation
  ザ・リッツ・カールトン大阪（大阪府大阪市）, 東京コンファレンスセンター・品川（東京都港区）
- Year and Date
  2016-08-02
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] ゲノム不安定性を示す遺伝性疾患群の病態解析と新規疾患責任遺伝子変異探索.2016
- Author(s)
  中沢由華、岡泰由、郭朝万、賈楠、唐田清伸、嶋田繭子、宮﨑仁美、千住千佳子、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] DNA損傷応答と遺伝病疾患2016
- Author(s)
  荻朋男
- Organizer
  平成28年度若手放射線生物学研究会専門研究会
- Place of Presentation
  東京工業大学（東京都目黒区）
- Year and Date
  2016-09-03
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] New DNA-repair gene mutations associated with Cokayne syndrome like progeroid disorders.2016
- Author(s)
  Ogi T
- Organizer
  2016 Spring International Conference of the Korean Society for Gerontology The 15th Korea-Japan Gerontologist Joint Meeting
- Place of Presentation
  Daegu（韓国）
- Year and Date
  2016-06-15
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] 次世代ゲノム解析と精密質量分析を基盤としたマルチオミクスデータの臨床診断へ応用2016
- Author(s)
  荻朋男
- Organizer
  サーモフィッシャーサイエンティフィック質量分析フォーラム2016
- Place of Presentation
  ザ・リッツ・カールトン大阪（大阪府大阪市）, 東京コンファレンスセンター・品川（東京都港区）
- Year and Date
  2016-08-02
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2016
- Author(s)
  荻朋男
- Organizer
  京都大学放射線生物研究センター第32回国際シンポジウム” Growing Edge of Radiation Biology, from principles to applications”
- Place of Presentation
  ホテルコープイン京都（京都府京都市）
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性により先天性小頭症を示すヒト遺伝性疾患の症例解析と病態解明研究2016
- Author(s)
  荻朋男
- Organizer
  日本遺伝学会第88回大会
- Place of Presentation
  日本大学国際関係学部（静岡県三島市）
- Year and Date
  2016-09-07
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] Genetics disorders associated with defects in transcription coupled nucleotide excision repair.2016
- Author(s)
  Ogi T
- Organizer
  10th Quinquennial Conference on Responses to DNA damage: from molecule to disease
- Place of Presentation
  Egmond aan Zee（オランダ）
- Year and Date
  2016-04-17
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] トランスオミクス解析を用いた希少遺伝性疾患原因因子の新規同定法の開発.2016
- Author(s)
  岡泰由、郭朝万、賈楠、唐田清伸、中沢由華、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] DNA損傷応答と遺伝病疾患2016
- Author(s)
  荻朋男
- Organizer
  平成28年度若手放射線生物学研究会専門研究会
- Place of Presentation
  東京工業大学（東京都目黒区）
- Year and Date
  2016-09-03
- Invited
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] DNA修復システムの異常とゲノムDNAの不安定化により発症する疾患の分子病態2016
- Author(s)
  荻朋男
- Organizer
  第42回北里医学学会総会
- Place of Presentation
  小田急ホテルセンチュリー相模大野（神奈川県相模原市）
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] 新規のDNA 修復因子WDR4の欠損により発症する小頭症症例の分子病態2016
- Author(s)
  荻朋男
- Organizer
  国立遺伝学研究所・研究集会「生物ゲノム安定維持の分子機構」
- Place of Presentation
  国立遺伝学研究所（静岡県三島市）
- Year and Date
  2016-10-24
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] Genetics disorders associated with defects in transcription coupled nucleotide excision repair.2016
- Author(s)
  Ogi T.
- Organizer
  10th Quinquennial Conference on Responses to DNA damage: from molecule to disease
- Place of Presentation
  Egmond aan Zee（オランダ）
- Year and Date
  2016-04-17
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] DNA修復システムの異常とゲノムDNAの不安定化により発症する疾患の分子病態2016
- Author(s)
  荻朋男
- Organizer
  第42回北里医学学会総会
- Place of Presentation
  小田急ホテルセンチュリー相模大野（神奈川県相模原市）
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] ゲノム不安定性を示す遺伝性疾患群の病態解析と新規疾患責任遺伝子変異探索.2016
- Author(s)
  中沢由華、岡　泰由、郭　朝万、賈　楠、唐田清伸、嶋田繭子、宮﨑仁美、千住千佳子、荻　朋男
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県・横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] ゲノム不安定性を示す遺伝性疾患群の病態解析と新規疾患責任遺伝子変異探索.2016
- Author(s)
  中沢由華、岡泰由、郭朝万、賈楠、唐田清伸、嶋田繭子、宮﨑仁美、千住千佳子、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] DNA修復システムの異常により発症するヒト疾患の分子病態.2016
- Author(s)
  荻朋男
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2016
- Author(s)
  荻朋男
- Organizer
  京都大学放射線生物研究センター第32回国際シンポジウム” Growing Edge of Radiation Biology, from principles to applications”
- Place of Presentation
  ホテルコープイン京都（京都府京都市）
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] ハイコンテントイメージングシステムを利用した難治性遺伝性疾患の臨床診断2016
- Author(s)
  荻朋男
- Organizer
  サーモフィッシャーサイエンティフィックバイオサイエンス事業本部2016HCAユーザーミーティング
- Place of Presentation
  サーモフィッシャーサイエンティフィック株式会社三田オフィス（東京都港区）、サーモフィッシャーサイエンティフィック株式会社大阪営業所（大阪府大阪市）
- Year and Date
  2016-05-26
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] 次世代マルチオミクス解析を用いた希少性難治性遺伝性疾患原因因子の新規同定法の開発2016
- Author(s)
  荻朋男
- Organizer
  第29回バイオメディカル分析化学シンポジウムランチョンセミナー
- Place of Presentation
  京都大学（京都府京都市）
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] コケイン症候群のゲノム診断2016
- Author(s)
  荻朋男
- Organizer
  日本コケイン症候群ネットワーク勉強会
- Place of Presentation
  東京ビジネスアットセンター東京駅（東京都千代田区）
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] 次世代マルチオミクス解析を用いた希少性難治性遺伝性疾患原因因子の新規同定法の開発2016
- Author(s)
  荻朋男
- Organizer
  第29回バイオメディカル分析化学シンポジウムランチョンセミナー
- Place of Presentation
  京都大学（京都府京都市）
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] 「紫外線から遺伝子を守る」紫外線DNA損傷を修復する分子メカニズムとその破綻により発症する疾患の病態解明2016
- Author(s)
  荻　朋男
- Organizer
  太陽紫外線防御研究委員会第26回シンポジウム
- Place of Presentation
  グランフロント大阪（大阪府大阪市）
- Year and Date
  2016-03-04
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] ハイコンテントイメージングシステムを利用した難治性遺伝性疾患の臨床診断2016
- Author(s)
  荻朋男
- Organizer
  サーモフィッシャーサイエンティフィックバイオサイエンス事業本部2016HCAユーザーミーティング
- Place of Presentation
  サーモフィッシャーサイエンティフィック株式会社三田オフィス（東京都港区）、サーモフィッシャーサイエンティフィック株式会社大阪営業所（大阪府大阪市）
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] ゲノム不安定性を示す遺伝性疾患群の病態解析と新規疾患責任遺伝子変異探索.2016
- Author(s)
  中沢由華、岡泰由、郭朝万、賈楠、唐田清伸、嶋田繭子、宮﨑仁美、千住千佳子、荻朋男.
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] Human genetic disorders associated with deficiencies in the DNA repair system.2016
- Author(s)
  Ogi T
- Organizer
  上海交通大学医学院附属上海新華医院セミナー
- Place of Presentation
  Shanghai（中国）
- Invited
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] DNA修復システムの異常により発症するヒト疾患の分子病態.2016
- Author(s)
  荻朋男
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2016-11-30
- Invited
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] ハイコンテントイメージングシステムを利用した難治性遺伝性疾患の臨床診断2016
- Author(s)
  荻朋男
- Organizer
  サーモフィッシャーサイエンティフィックバイオサイエンス事業本部2016HCAユーザーミーティング
- Place of Presentation
  サーモフィッシャーサイエンティフィック株式会社三田オフィス（東京都港区）、サーモフィッシャーサイエンティフィック株式会社大阪営業所（大阪府大阪市）
- Year and Date
  2016-05-26
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] New DNA-repair gene mutations associated with Cokayne syndrome like progeroid disorders.2016
- Author(s)
  Ogi T.
- Organizer
  2016 Spring International Conference of the Korean Society for Gerontology The 15th Korea-Japan Gerontologist Joint Meeting,
- Place of Presentation
  Daegu, （韓国）
- Year and Date
  2016-06-15
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] DNA損傷応答と遺伝病疾患2016
- Author(s)
  荻朋男
- Organizer
  平成28年度若手放射線生物学研究会専門研究会
- Place of Presentation
  東京工業大学（東京都目黒区）
- Year and Date
  2016-09-03
- Invited
- Data Source
  KAKENHI-PROJECT-16K15526
[Presentation] ゲノム不安定性を示す難治性遺伝性疾患群の症例収集とゲノム・分子機能解析による病態解明研究2015
- Author(s)
  中沢　由華、荻　朋男、郭　朝万、唐田　清伸、岡　泰由、賈　楠、嶋田　繭子、宮崎　仁美、千住　千佳子
- Organizer
  第23回DNA複製・組換え・修復ワークショップ
- Place of Presentation
  焼津グランドホテル（静岡県焼津市）
- Year and Date
  2015-10-20
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency2015
- Author(s)
  郭　朝万、中沢　由華、嶋田　繭子、賈　楠、唐田　清伸、岡　泰由、宮崎　仁美、千住　千佳子、荻　朋男
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Year and Date
  2015-12-02
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] XRCC4deficiencyinhumansubjectscausesamarkedneurologicalphenotypebut no overt immunodeficiency2015
- Author(s)
  郭　朝万、中沢　由華、嶋田　繭子、賈　楠、唐田　清伸、岡　泰由、宮崎　仁美、千住　千佳子、荻　朋男
- Organizer
  第23回DNA複製・組換え・修復ワークショップ
- Place of Presentation
  焼津グランドホテル（静岡県焼津市）
- Year and Date
  2015-10-20
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency2015
- Author(s)
  郭　朝万、中沢　由華、嶋田　繭子、賈　楠、唐田　清伸、岡　泰由、宮崎　仁美、千住　千佳子、荻　朋男
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Year and Date
  2015-12-02
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] XRCC4deficiencyinhumansubjectscausesamarkedneurologicalphenotypebut no overt immunodeficiency2015
- Author(s)
  郭　朝万、中沢　由華、嶋田　繭子、賈　楠、唐田　清伸、岡　泰由、宮崎　仁美、千住　千佳子、荻　朋男
- Organizer
  第23回DNA複製・組換え・修復ワークショップ
- Place of Presentation
  焼津グランドホテル（静岡県焼津市）
- Year and Date
  2015-10-20
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] 転写の異常により発症する疾患の診断法と分子病態2015
- Author(s)
  荻　朋男
- Organizer
  第67回日本皮膚科学会西部支部学術大会
- Place of Presentation
  長崎ブリックホール（長崎県長崎市）
- Year and Date
  2015-10-18
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] ゲノム不安定性を示す遺伝性疾患の症例収集と病態解析研究2015
- Author(s)
  荻朋男、中沢由華、唐田清伸、郭朝万、岡泰由、賈楠、嶋田繭子、宮崎仁美、千住千佳子
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（神戸市）
- Year and Date
  2015-12-03
- Data Source
  KAKENHI-PROJECT-15K00541
[Presentation] ゲノム不安定性を示す難治性遺伝性疾患群の症例収集とゲノム・分子機能解析による病態解明研究2015
- Author(s)
  中沢　由華、荻　朋男、唐田　清伸、郭　朝万、岡　泰由、賈　楠、嶋田　繭子、宮崎　仁美、千住　千佳子
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Year and Date
  2015-12-02
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] ゲノム不安定性を示す難治性遺伝性疾患群の症例収集とゲノム・分子機能解析による病態解明研究2015
- Author(s)
  中沢　由華、荻　朋男、郭　朝万、唐田　清伸、岡　泰由、賈　楠、嶋田　繭子、宮崎　仁美、千住　千佳子
- Organizer
  第23回DNA複製・組換え・修復ワークショップ
- Place of Presentation
  焼津グランドホテル（静岡県焼津市）
- Year and Date
  2015-10-20
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] XRCC4deficiencyinhumansubjectscausesamarkedneurologicalphenotypebut no overt immunodeficiency2015
- Author(s)
  郭　朝万、中沢　由華、嶋田　繭子、賈　楠、唐田　清伸、岡　泰由、宮崎　仁美、千住　千佳子、荻　朋男
- Organizer
  第23回DNA複製・組換え・修復ワークショップ
- Place of Presentation
  焼津グランドホテル（静岡県焼津市）
- Year and Date
  2015-10-20
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] ヒトXRCC4遺伝子機能の欠損は神経変性と強い放射線感受性を示すが正常な免疫機能を保持する2015
- Author(s)
  荻　朋男
- Organizer
  第74回日本癌学会学術総会
- Place of Presentation
  名古屋国際会議場（愛知県名古屋市）
- Year and Date
  2015-10-08
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ヒトRAD52のアセチル化を介した相同組換えにおけるアセチル化および脱アセチル化酵素の新機能の解明2015
- Author(s)
  安田武嗣、香川　亘、荻　朋男、齊藤健吾、加藤宝光、鈴木健祐、藤堂　直、滝澤和也、早乙女（中邑）愛、中沢由華、Matthew D. Genet、宇井彩子、花岡文雄、菅澤　薫、岡安隆一、Penny A. Jeggo、胡桃坂仁志、田嶋克史
- Organizer
  BMB2015
- Place of Presentation
  神戸ポートアイランド
- Year and Date
  2015-12-01
- Invited
- Data Source
  KAKENHI-PROJECT-26281026
[Presentation] 各種コケイン症候群の分子診断2015
- Author(s)
  賈　楠、中沢　由華、荻　朋男、唐田　清伸、郭　朝万、岡　泰由、嶋田　繭子、宮崎　仁美、千住　千佳子
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Year and Date
  2015-12-02
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] ゲノム不安定性疾患の症例収集と新規DNA修復遺伝子の同定2015
- Author(s)
  荻　朋男
- Organizer
  遺伝研研究集会
- Place of Presentation
  国立遺伝学研究所（静岡県三島市）
- Year and Date
  2015-10-01
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す難治性遺伝性疾患群の症例収集とゲノム・分子機能解析による病態解明研究2015
- Author(s)
  中沢　由華、荻　朋男、唐田　清伸、郭　朝万、岡　泰由、賈　楠、嶋田　繭子、宮崎　仁美、千住　千佳子
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Year and Date
  2015-12-02
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] 各種コケイン症候群の分子診断2015
- Author(s)
  賈　楠、中沢　由華、荻　朋男、唐田　清伸、郭　朝万、岡　泰由、嶋田　繭子、宮崎　仁美、千住　千佳子
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Year and Date
  2015-12-02
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] ゲノム不安定性を示す難治性遺伝性疾患群の症例収集とゲノム・分子機能解析による病態解明研究2015
- Author(s)
  中沢　由華、荻　朋男、唐田　清伸、郭　朝万、岡　泰由、賈　楠、嶋田　繭子、宮崎　仁美、千住　千佳子
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Year and Date
  2015-12-02
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] 各種コケイン症候群の分子診断2015
- Author(s)
  賈楠、中沢由華、荻朋男、唐田清伸、郭朝万、岡泰由、嶋田繭子、宮崎仁美、千住千佳子
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（神戸市）
- Year and Date
  2015-12-02
- Data Source
  KAKENHI-PROJECT-15K00541
[Presentation] ヒトXRCC4遺伝子機能の欠損は神経変性と強い放射線感受性を示すが正常な免疫機能を保持する2015
- Author(s)
  荻　朋男
- Organizer
  第74回日本癌学会学術総会
- Place of Presentation
  名古屋国際会議場（愛知県名古屋市）
- Year and Date
  2015-10-08
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] 各種コケイン症候群の分子診断.2015
- Author(s)
  賈楠、中沢由華、荻朋男、唐田清伸、郭朝万、岡泰由、嶋田繭子、宮崎仁美、千住千佳子.
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency2015
- Author(s)
  郭　朝万、中沢　由華、嶋田　繭子、賈　楠、唐田　清伸、岡　泰由、宮崎　仁美、千住　千佳子、荻　朋男
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Year and Date
  2015-12-02
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] Molecular cloning and characterisation of novel pathogenic genes for DNA repair deficient disorders.2015
- Author(s)
  Ogi T
- Organizer
  The Fourth Forum of International Translational Genetic Medicine in Beijing
- Place of Presentation
  Beijing（China）
- Year and Date
  2015-10-23
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency.2015
- Author(s)
  郭　朝万、中沢由華、嶋田繭子、賈　楠、唐田清伸、岡　泰由、宮崎仁美、千住千佳子、荻　朋男.
- Organizer
  第23回DNA複製・組換え・修復ワークショップ
- Place of Presentation
  焼津グランドホテル（静岡県焼津市）
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す遺伝性疾患の症例収集と病態解析研究.2015
- Author(s)
  荻朋男、中沢由華、唐田清伸、郭朝万、岡泰由、賈楠、嶋田繭子、宮﨑仁美、千住千佳子.
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す難治性遺伝性疾患群の症例収集とゲノム・分子機能解析による病態解明研究2015
- Author(s)
  中沢由華、荻朋男、唐田清伸、郭朝万、岡泰由、賈楠、嶋田繭子、宮崎仁美、千住千佳子
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（神戸市）
- Year and Date
  2015-12-02
- Data Source
  KAKENHI-PROJECT-15K00541
[Presentation] 転写の異常により発症する疾患の診断法と分子病態2015
- Author(s)
  荻　朋男
- Organizer
  第67回日本皮膚科学会西部支部学術大会
- Place of Presentation
  長崎ブリックホール（長崎県長崎市）
- Invited
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す難治性遺伝性疾患群の症例収集とゲノム・分子機能解析による病態解明研究2015
- Author(s)
  中沢　由華、荻　朋男、郭　朝万、唐田　清伸、岡　泰由、賈　楠、嶋田　繭子、宮崎　仁美、千住　千佳子
- Organizer
  第23回DNA複製・組換え・修復ワークショップ
- Place of Presentation
  焼津グランドホテル（静岡県焼津市）
- Year and Date
  2015-10-20
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] ゲノム不安定性を示す難治性遺伝性疾患群の症例収集とゲノム・分子機能解析による病態解明研究2015
- Author(s)
  中沢由華、荻朋男、郭朝万、唐田清伸、岡泰由、賈楠、嶋田繭子、宮崎仁美、千住千佳子
- Organizer
  第23回DNA複製・組換え・修復ワークショップ
- Place of Presentation
  焼津グランドホテル（静岡県焼津市）
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性疾患の症例収集と新規DNA修復遺伝子の同定2015
- Author(s)
  荻　朋男
- Organizer
  遺伝研研究集会
- Place of Presentation
  国立遺伝学研究所（静岡県三島市）
- Year and Date
  2015-10-01
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] ファンコニ貧血経路におけるユビキチン様タンパク質UBL5の役割.2015
- Author(s)
  岡　泰由、荻　朋男、ベッカージェンセン　シモン、メイランド　ニールズ
- Organizer
  第44回日本環境変異原学会大会
- Place of Presentation
  九州大学（福岡県福岡市）
- Year and Date
  2015-11-27
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] ゲノム不安定性を示す難治性遺伝性疾患群の症例収集とゲノム・分子機能解析による病態解明研究2015
- Author(s)
  中沢由華、荻朋男、唐田清伸、郭朝万、岡泰由、賈楠、嶋田繭子、宮崎仁美、千住千佳子
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] 各種コケイン症候群の分子診断2015
- Author(s)
  賈　楠、中沢　由華、荻　朋男、唐田　清伸、郭　朝万、岡　泰由、嶋田　繭子、宮崎　仁美、千住　千佳子
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Year and Date
  2015-12-02
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] XRCC4欠損性遺伝性疾患の病態解析.2015
- Author(s)
  中沢由華、荻朋男、郭朝万、嶋田繭子、賈楠.
- Organizer
  第44回日本環境変異原学会大会
- Place of Presentation
  九州大学（福岡県福岡市）
- Year and Date
  2015-11-27
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency.2015
- Author(s)
  郭朝万、中沢由華、嶋田繭子、賈楠、唐田清伸、岡泰由、宮崎仁美、千住千佳子、荻朋男.
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Data Source
  KAKENHI-PROJECT-15H02654
[Presentation] XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency2015
- Author(s)
  郭朝万、中沢由華、嶋田繭子、賈楠、唐田清伸、岡泰由、宮崎仁美、千住千佳子、荻朋男
- Organizer
  第38回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド（神戸市）
- Year and Date
  2015-12-02
- Data Source
  KAKENHI-PROJECT-15K00541
[Presentation] ゲノム不安定性疾患群の新規責任遺伝子の同定と分子機能解析2014
- Author(s)
  荻朋男
- Organizer
  第57回日本甲状腺学会学術集会
- Place of Presentation
  コングレコンベンションセンター（大阪府大阪市）
- Year and Date
  2014-11-14
- Invited
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] ゲノム不安定性疾患群の新規責任遺伝子の同定と分子機能解析2014
- Author(s)
  荻朋男
- Organizer
  第57回日本甲状腺学会学術集会
- Place of Presentation
  コングレコンベンションセンター（大阪府大阪市）
- Year and Date
  2014-11-14
- Invited
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] DNA修復機構の異常により発症する先天性疾患とゲノム不安定性/発がん2014
- Author(s)
  荻朋男
- Organizer
  第20回日本家族性腫瘍学会学術集会教育講演
- Place of Presentation
  コラッセ福島（福島県福島市）
- Year and Date
  2014-06-13
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] DNA修復機構の異常により発症する先天性疾患とゲノム不安定性/発がん2014
- Author(s)
  荻朋男
- Organizer
  第20回日本家族性腫瘍学会学術集会教育講演
- Place of Presentation
  コラッセ福島（福島県福島市）
- Year and Date
  2014-06-13
- Invited
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] DNA修復機構の異常により発症する先天性疾患とゲノム不安定性/発がん2014
- Author(s)
  荻朋男
- Organizer
  第20回日本家族性腫瘍学会学術集会教育講演
- Place of Presentation
  コラッセ福島（福島県福島市）
- Year and Date
  2014-06-13
- Invited
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] Transcription, DNA damage and Repair2014
- Author(s)
  荻朋男
- Organizer
  International Symposium on Xeroderma Pigmentosum and Related Diseases
- Place of Presentation
  神戸国際会議場（神戸市）
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] ゲノム不安定性疾患群の新規責任遺伝子の同定と分子機能解析2014
- Author(s)
  荻朋男
- Organizer
  第57回日本甲状腺学会学術集会
- Place of Presentation
  コングレコンベンションセンター（大阪府大阪市）
- Year and Date
  2014-11-14
- Invited
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] Function of BRCA2 and its associating proteins in centrosomal regulation2013
- Author(s)
  Teshirogi, Miki, and Takenaka
- Organizer
  第72回日本癌学会学術総会
- Place of Presentation
  パシフィコ横浜
- Data Source
  KAKENHI-PROJECT-23590355
[Presentation] 紫外線高感受性症候群～UVSSA遺伝子の発見と病態解析2013
- Author(s)
  荻朋男
- Organizer
  第22回DNA複製・組換え・修復ワークショップ
- Place of Presentation
  ホテルニュー水戸屋（仙台市）
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] DNA 修復欠損性遺伝性疾患の責任因子の検索と分子機構の解析2013
- Author(s)
  荻朋男
- Organizer
  日本環境変異原学会-変異機構研究会第26回夏の学校
- Place of Presentation
  アイプラザ一宮（一宮市）
- Invited
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] Transcription, DNA damage and Repair2013
- Author(s)
  荻朋男
- Organizer
  11th International Conference on Environmental Mutagens
- Place of Presentation
  Bourbon Convention & Spa Resort Cataratas do Iguassu（ブラジル）
- Invited
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] DNA repair deficient genetic disorders and their clinical diagnosis2013
- Author(s)
  荻朋男
- Organizer
  CS meeting Amy and freiends
- Place of Presentation
  St David's Park Hotel（イギリス）
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] 転写共役修復とRNAポリメラーゼの修飾分子基盤2013
- Author(s)
  荻朋男
- Organizer
  2013年度国立遺伝学研究所研究会「染色体DNAの安定維持の分子メカニズム」
- Place of Presentation
  国立遺伝学研究所（三島市）
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] Repair of UV-induced DNA damage2013
- Author(s)
  荻朋男
- Organizer
  Youth Scientific School "Problems of Basic and Applied Radiobiology"
- Place of Presentation
  Medical Radiological Research Center（ロシア）
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] 紫外線高感受性症候群～UVSSA遺伝子の発見と病態解析2013
- Author(s)
  荻朋男
- Organizer
  日本美容皮膚科学会・学術大会
- Place of Presentation
  神戸国際会議場（神戸市）
- Invited
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair2012
- Author(s)
  荻朋男
- Organizer
  3R meeting
- Place of Presentation
  兵庫
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] Molecular cloning and characterisation of KIAA1530/UVSSA, the responsible gene for UV sensitive syndrome complementation group-A2012
- Author(s)
  荻　朋男
- Organizer
  駿河台国際シンポジウム
- Place of Presentation
  東京
- Invited
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] 紫外線感受性症候群責任遺伝子UVSSAの同定と分子機能解析2012
- Author(s)
  荻朋男
- Organizer
  日本皮膚科学会
- Place of Presentation
  長崎(招待講演)
- Year and Date
  2012-04-08
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] Molecular cloning and characterisation of KIAA1530/UVSSA, the responsible gene for UV sensitive syndrome complementation group-A2012
- Author(s)
  荻　朋男
- Organizer
  BIO JAPAN
- Place of Presentation
  横浜
- Invited
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] 紫外線高感受性症候群責任因子UVSSAによる損傷停止RNAポリメラーゼのユビキチン化修飾メカニズムの解析2012
- Author(s)
  荻朋男
- Organizer
  日本遺伝学会第84回大会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] Molecular cloning and characterisation of KIAA1530/UVSSA, the responsible gene for UV sensitive syndrome complementation group-A2012
- Author(s)
  荻朋男
- Organizer
  BIO JAPAN
- Place of Presentation
  横浜(招待講演)
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair2012
- Author(s)
  荻　朋男
- Organizer
  3R meeting
- Place of Presentation
  兵庫
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] Molecular cloning and characterisation of KIAA1530/UVSSA, the responsible gene for UV sensitive syndrome complementation group-A2012
- Author(s)
  荻　朋男
- Organizer
  駿河台国際シンポジウム
- Place of Presentation
  東京
- Invited
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] UVSSA, a novel VHS-domain protein responsible for UV-sensitive syndrome, facilitates damage-dependent processing of RNA polymerase IIo in TC-NER2012
- Author(s)
  荻　朋男
- Organizer
  第34回日本分子生物学会年会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] Molecular cloning andcharacterisation of KIAA1530/UVSSA,the responsible gene for UV sensitive syndrome complementation group-A2012
- Author(s)
  荻朋男
- Organizer
  バイオジャパン(招待講演)
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] Molecular cloning and characterisation of KIAA1530/UVSSA, the responsible gene for UV sensitive syndrome complementation group-A2012
- Author(s)
  荻朋男
- Organizer
  駿河台国際シンポジウム
- Place of Presentation
  東京(招待講演)
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] 紫外線高感受性症候群責任因子UVSSAによる損傷停止RNAポリメラーゼのユビキチン化修飾メカニズムの解析2012
- Author(s)
  荻　朋男
- Organizer
  日本遺伝学会第84回大会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] Molecular cloning and characterisation of KIAA1530/UVSSA, the responsible gene for UV sensitive syndrome complementation group-A2012
- Author(s)
  荻　朋男
- Organizer
  BIO JAPAN
- Place of Presentation
  横浜
- Invited
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair2012
- Author(s)
  荻　朋男
- Organizer
  3R meeting
- Place of Presentation
  兵庫
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] 紫外線高感受性症候群責任因子UVSSAによる損傷停止RNAポリメラーゼのユビキチン化修飾メカニズムの解析2012
- Author(s)
  荻　朋男
- Organizer
  日本遺伝学会第84回大会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] 紫外線感受性症候群責任遺伝子UVSSAの同定と分子機能解析2012
- Author(s)
  荻朋男
- Organizer
  日本皮膚科学会(招待講演)
- Place of Presentation
  長崎
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] The role of three DNA polymerases and their accessory factors in the repair synthesis step of nucleotide excision repair.2011
- Author(s)
  荻　朋男
- Organizer
  Responses to DNA damage: from molecular mechanism to human disease
- Place of Presentation
  Egmond aan Zee (オランダ)
- Invited
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] Molecular cloning andcharacterisation of UVSSA, the responsiblegene for UV sensitive syndromecomplementation group-A (UVsS-A)2011
- Author(s)
  荻朋男
- Organizer
  Responses to DNA damage: frommolecular mechanism to human disease(招待講演)
- Place of Presentation
  Egmond aan Zee (オランダ)
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] ヌクレオチド除去修復機構でのDNAポリメラーゼの機能解析2010
- Author(s)
  荻朋男
- Organizer
  日本がん学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] Three DNApolymerasesrecruited by differentmechanisms carry out NER repairsynthesis in human cells2010
- Author(s)
  荻朋男
- Organizer
  日本がん学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] Three DNA Polymerases, Recruited by Different Mechanisms, Carry Out NER Repair Synthesis in Human Cells2010
- Author(s)
  Tomoo Ogi
- Organizer
  International Conference on Radiation and Cancer Biology at Nagasaki 2010
- Place of Presentation
  長崎
- Year and Date
  2010-02-18
- Data Source
  KAKENHI-PROJECT-20810021
[Presentation] ヌクレオチド除去修復過程での修復DNA合成分子メカニズムの解析2008
- Author(s)
  荻朋男
- Organizer
  日本分子生物学会
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-20810021
[Presentation] エキソーム解析を用いたDNA修復機構欠損性疾患の新規責任遺伝子の探索
- Author(s)
  嶋田繭子、中沢由華、郭朝万、賈楠、宮崎仁美、唐田清伸、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] 放射線感受性および各種発達異常を示す遺伝性疾患の新規責任遺伝子の同定と分子機能解析
- Author(s)
  中沢由華、郭朝万、嶋田繭子、宮崎仁美、唐田清伸、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] Molecular cloning and characterisation of new human DNA repair genes
- Author(s)
  Ogi T
- Organizer
  The 9th 3R Symposium
- Place of Presentation
  御殿場高原ホテル（静岡県御殿場市）
- Year and Date
  2014-11-17 – 2014-11-21
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] Molecular characterization and functional analysis of XRCC4, a novel pathological gene for radiation sensitivity and developmental abnormalities
- Author(s)
  Guo C, Nakazawa Y, Shimada M, Woodbine L, Jia N, Karata K, Miyazaki H, Lehmann A, Jeggo PA, Ogi T.
- Organizer
  The 9th 3R Symposium
- Place of Presentation
  御殿場高原ホテル（静岡県御殿場市）
- Year and Date
  2014-11-17 – 2014-11-21
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] 転写共役ヌクレオチド除去修復の開始反応の分子機構
- Author(s)
  荻朋男
- Organizer
  日本放射線影響学会第57回大会ワークショップ
- Place of Presentation
  鹿児島県民交流センター（鹿児島県鹿児島市）
- Year and Date
  2014-10-01 – 2014-10-03
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] Molecular characterization and functional analysis of XRCC4, a novel pathological gene for radiation sensitivity and developmental abnormalities
- Author(s)
  Guo C, Nakazawa Y, Shimada M, Woodbine L, Jia N, Karata K, Miyazaki H, Lehmann A, Jeggo PA, Ogi T.
- Organizer
  The 9th 3R Symposium
- Place of Presentation
  御殿場高原ホテル（静岡県御殿場市）
- Year and Date
  2014-11-17 – 2014-11-21
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] 放射線感受性および各種発達異常を示す遺伝性疾患の新規責任遺伝子の同定と分子機能解析
- Author(s)
  中沢由華、郭朝万、嶋田繭子、宮崎仁美、唐田清伸、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] Molecular and functional study on the initiation of transcription coupled nucleo tide excision repair
- Author(s)
  Guo C, Nakazawa Y, Shimada M, Jia N, Karata K, Miyazaki H, Ogi T.
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] Molecular and functional study on the initiation of transcription coupled nucleo tide excision repair
- Author(s)
  Guo C, Nakazawa Y, Shimada M, Jia N, Karata K, Miyazaki H, Ogi T.
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] ヒストンH3K9メチル化酵素類のDNA二重鎖切断修復反応への関与
- Author(s)
  荻朋男
- Organizer
  第87回日本生化学会大会シンポジウム
- Place of Presentation
  国立京都国際会館（京都府京都市）
- Year and Date
  2014-10-15 – 2014-10-18
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] 紫外線感受性症候群責任遺伝子UVSSAの同定と分子機能解析
- Author(s)
  荻　朋男
- Organizer
  日本皮膚科学会
- Place of Presentation
  長崎
- Invited
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] エキソーム解析を用いたDNA修復機構欠損性疾患の新規責任遺伝子の探索
- Author(s)
  嶋田繭子、中沢由華、郭朝万、賈楠、宮崎仁美、唐田清伸、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] Molecular cloning and characterisation of new human DNA repair genes
- Author(s)
  Ogi T
- Organizer
  The 9th 3R Symposium
- Place of Presentation
  御殿場高原ホテル（静岡県御殿場市）
- Year and Date
  2014-11-17 – 2014-11-21
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] 紫外線感受性症候群責任遺伝子UVSSAの同定と分子機能解析
- Author(s)
  荻　朋男
- Organizer
  日本皮膚科学会
- Place of Presentation
  長崎
- Invited
- Data Source
  KAKENHI-PROJECT-22710056
[Presentation] 転写と共役したヌクレオチド除去修復のin vitro反応系の構築
- Author(s)
  唐田清伸、郭朝万、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] コケイン症候群様の臨床症状を示す遺伝性疾患の責任遺伝子探索
- Author(s)
  宮崎仁美、中沢由華、郭朝万、嶋田繭子、賈楠、唐田清伸、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] Molecular and functional study on the initiation of transcription coupled nucleotide excision repair
- Author(s)
  郭朝万、中沢由華、嶋田繭子、賈楠、唐田清伸、宮崎仁美、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-14F04093
[Presentation] エキソーム解析を用いたDNA修復機構欠損性疾患の新規責任遺伝子の探索
- Author(s)
  嶋田繭子、中沢由華、郭朝万、賈楠、宮崎仁美、唐田清伸、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] ERCC1/XPF deficiency causes three NER- deficient disorders: a patient with various symptoms of xeroderma pigmentosum, Cockayne syndrome & Fanconi anemia.
- Author(s)
  Nakazawa Y, Kashiyama K, Pilz DT, Guo C, Shimada M, Sasaki K, Fawcett H, Wing JF, Lewin SO, Carr L, Li TS, Yoshiura K, Utani A, Hirano A, Greenblatt D, Nardo T, Stefanini M, McGibbon D, Sarkany R, Fassihi H, Mitsutake N, Lehmann AR, Ogi T.
- Organizer
  The 9th 3R Symposium
- Place of Presentation
  御殿場高原ホテル（静岡県御殿場市）
- Year and Date
  2014-11-17 – 2014-11-21
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] 転写共役ヌクレオチド除去修復の開始反応の分子機構
- Author(s)
  荻朋男
- Organizer
  日本放射線影響学会第57回大会ワークショップ
- Place of Presentation
  鹿児島県民交流センター（鹿児島県鹿児島市）
- Year and Date
  2014-10-01 – 2014-10-03
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] エキソーム解析を用いたDNA修復機構欠損性疾患の新規責任遺伝子の探索
- Author(s)
  嶋田繭子、中沢由華、郭朝万、賈楠、宮崎仁美、唐田清伸、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] コケイン症候群様の臨床症状を示す遺伝性疾患の責任遺伝子探索
- Author(s)
  宮崎仁美、中沢由華、郭朝万、嶋田繭子、賈楠、唐田清伸、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] コケイン症候群様の臨床症状を示す遺伝性疾患の責任遺伝子探索
- Author(s)
  宮崎仁美、中沢由華、郭朝万、嶋田繭子、賈楠、唐田清伸、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] ヒトRAD52タンパク質のアセチル化制御
- Author(s)
  安田武嗣、香川亘、斎藤健吾、荻朋男、花岡文雄、菅澤薫、胡桃坂仁志、田嶋克史
- Organizer
  第37回　日本分子生物学会年会
- Place of Presentation
  横浜
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-26281026
[Presentation] Molecular characterization and functional analysis of XRCC4, a novel pathological gene for radiation sensitivity and developmental abnormalities
- Author(s)
  Guo C, Nakazawa Y, Shimada M, Woodbine L, Jia N, Karata K, Miyazaki H, Lehmann A, Jeggo PA, Ogi T.
- Organizer
  The 9th 3R Symposium
- Place of Presentation
  御殿場高原ホテル（静岡県御殿場市）
- Year and Date
  2014-11-17 – 2014-11-21
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] Molecular and functional study on the initiation of transcription coupled nucleo tide excision repair
- Author(s)
  Guo C, Nakazawa Y, Shimada M, Jia N, Karata K, Miyazaki H, Ogi T.
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] ヒストンH3K9メチル化酵素類のDNA二重鎖切断修復反応への関与
- Author(s)
  荻朋男
- Organizer
  第87回日本生化学会大会シンポジウム
- Place of Presentation
  国立京都国際会館（京都府京都市）
- Year and Date
  2014-10-15 – 2014-10-18
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] 放射線感受性および各種発達異常を示す遺伝性疾患の新規責任遺伝子の同定と分子機能解析
- Author(s)
  中沢由華、郭朝万、嶋田繭子、宮崎仁美、唐田清伸、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] ERCC1/XPF deficiency causes three NER- deficient disorders: a patient with various symptoms of xeroderma pigmentosum, Cockayne syndrome & Fanconi anemia.
- Author(s)
  Nakazawa Y, Kashiyama K, Pilz DT, Guo C, Shimada M, Sasaki K, Fawcett H, Wing JF, Lewin SO, Carr L, Li TS, Yoshiura K, Utani A, Hirano A, Greenblatt D, Nardo T, Stefanini M, McGibbon D, Sarkany R, Fassihi H, Mitsutake N, Lehmann AR, Ogi T.
- Organizer
  The 9th 3R Symposium
- Place of Presentation
  御殿場高原ホテル（静岡県御殿場市）
- Year and Date
  2014-11-17 – 2014-11-21
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] ヒトDNA修復遺伝子の同定と機能解析
- Author(s)
  荻朋男
- Organizer
  The International Kick-Off Symposium for Atomic Bomb Disease Institute at Nagasaki University
- Place of Presentation
  長崎大学医学部　良順会館（長崎市）
- Invited
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] 転写共役ヌクレオチド除去修復の開始反応の分子機構
- Author(s)
  荻朋男
- Organizer
  日本放射線影響学会第57回大会ワークショップ
- Place of Presentation
  鹿児島県民交流センター（鹿児島県鹿児島市）
- Year and Date
  2014-10-01 – 2014-10-03
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] Molecular cloning and characterisation of new human DNA repair genes
- Author(s)
  Ogi T
- Organizer
  The 9th 3R Symposium
- Place of Presentation
  御殿場高原ホテル（静岡県御殿場市）
- Year and Date
  2014-11-17 – 2014-11-21
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] ヒストンH3K9メチル化酵素類のDNA二重鎖切断修復反応への関与
- Author(s)
  荻朋男
- Organizer
  第87回日本生化学会大会シンポジウム
- Place of Presentation
  国立京都国際会館（京都府京都市）
- Year and Date
  2014-10-15 – 2014-10-18
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] ERCC1/XPF deficiency causes three NER- deficient disorders: a patient with various symptoms of xeroderma pigmentosum, Cockayne syndrome & Fanconi anemia.
- Author(s)
  Nakazawa Y, Kashiyama K, Pilz DT, Guo C, Shimada M, Sasaki K, Fawcett H, Wing JF, Lewin SO, Carr L, Li TS, Yoshiura K, Utani A, Hirano A, Greenblatt D, Nardo T, Stefanini M, McGibbon D, Sarkany R, Fassihi H, Mitsutake N, Lehmann AR, Ogi T.
- Organizer
  The 9th 3R Symposium
- Place of Presentation
  御殿場高原ホテル（静岡県御殿場市）
- Year and Date
  2014-11-17 – 2014-11-21
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] 放射線感受性および各種発達異常を示す遺伝性疾患の新規責任遺伝子の同定と分子機能解析
- Author(s)
  中沢由華、郭朝万、嶋田繭子、宮崎仁美、唐田清伸、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-24681008
[Presentation] コケイン症候群様の臨床症状を示す遺伝性疾患の責任遺伝子探索
- Author(s)
  宮崎仁美、中沢由華、郭朝万、嶋田繭子、賈楠、唐田清伸、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-26461528
[Presentation] 転写と共役したヌクレオチド除去修復のin vitro反応系の構築
- Author(s)
  唐田清伸、郭朝万、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-26291005
[Presentation] Molecular and functional study on the initiation of transcription coupled nucleo tide excision repair
- Author(s)
  Guo C, Nakazawa Y, Shimada M, Jia N, Karata K, Miyazaki H, Ogi T.
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-24659533
[Presentation] 転写と共役したヌクレオチド除去修復のin vitro反応系の構築
- Author(s)
  唐田清伸、郭朝万、荻朋男
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜（神奈川県横浜市）
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-24681008

1. MITSUTAKE Norisato (50404215)

# of Collaborated Projects: 9 results

# of Collaborated Products: 6 results
2. Oka Yasuyoshi (60762383)

# of Collaborated Projects: 4 results

# of Collaborated Products: 24 results
3. 真下知士 (80397554)

# of Collaborated Projects: 4 results

# of Collaborated Products: 3 results
4. NAKAZAWA Yuka (00533902)

# of Collaborated Projects: 3 results

# of Collaborated Products: 23 results
5. TAKENAKA Katsuya (20378706)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
6. SHIMADA Mayuko (80623834)

# of Collaborated Projects: 2 results

# of Collaborated Products: 14 results
7. KARATA Kiyonobu (90345017)

# of Collaborated Projects: 2 results

# of Collaborated Products: 9 results
8. ITO Yoshinori (20373491)

# of Collaborated Projects: 2 results

# of Collaborated Products: 8 results
9. 倉橋宏和 (30621817)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
10. 岡田洋平 (30383714)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
11. 奥村彰久 (60303624)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
12. GUO CHAOWAN

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
13. YOSHIURA Koichiro (00304931)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. TSUJINO Akira (70423639)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. KINOSHITA Akira (60372778)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. MISHIMA Hiroyuki (10513319)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. ARIMA Kazuhiko (30423635)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. NIIKAWA Norio (00111170)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. OTA Toru (10223835)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. IDA Hiroaki (60363496)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. KANAZAWA Nobuo (90343227)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
22. YASUDA Takeshi (60332269)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
23. Kurotani Kenichi (10402778)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
24. Hashimoto Satoru (60352150)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
25. 増本博司 (80423151)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
26. 小原千寿香 (90415977)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
27. サエンコウラジミール (30343346)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
28. 花岡文雄 (50012670)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
29. 李桃生 (50379997)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
30. 川田潤一 (20532831)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
31. 寺林健 (40452429)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
32. 鈴木啓司 (00196809)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
33. 武市拓也 (30754931)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
34. 吉川剛典 (20908884)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
35. 林深 (50596244)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
36. 工藤崇 (20330300)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
37. 星野大輔 (30571434)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
38. 菅沼伸康 (40724927)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
39. ITO Michiko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
40. NOMURA Toshifumi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
41. IMAI Kohsuke

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
42. MASUYAMA Ritsuko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
43. NAKADA Shinichiro

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
44. NAGAYAMA Yuji

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
45. 菅波孝祥

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
46. 柴田淳史

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
47. 川出野絵

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
48. 山下俊一

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
49. 杉浦一充

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
50. 高橋徳幸

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
51. 大学保一

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
52. 若杉光生

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
53. 松永司

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
54. 松鵜睦美

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
55. 祖父江顕

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
56. 田嶋克史

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
57. 増田章男

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
58. 鶴崎美徳

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
59. 亀尾聡美

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
60. 斎藤芳郎

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
61. 木原章雄

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
62. 梅沢一夫

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
63. 中野英司

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

OGI Tomoo 荻 朋男

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人はなぜ老い・病(やまい)になるのか－環境ストレス病態相関の理解Principal Investigator

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Molecular pathogenesis of human disorders associated with deficiencies in the DNA repair and environmental stress response systemsPrincipal Investigator

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OGI Tomoo 荻朋男