NAKAZAWA Yuka 中沢由華

Researcher Number	00533902
Other IDs	https://orcid.org/0000-0002-3835-3093
Affiliation (Current)	2024: 名古屋大学, 環境医学研究所, 講師
Affiliation (based on the past Project Information) *help	2021 – 2024: 名古屋大学, 環境医学研究所, 講師 2017 – 2020: 名古屋大学, 環境医学研究所, 助教 2013 – 2017: 長崎大学, 原爆後障害医療研究所, 助教 2012: 長崎大学, 医歯(薬)学総合研究科, 助教 2010: Nagasaki University, 医歯薬学総合研究科, COE研究員 2009 – 2010: Nagasaki University, 医歯(薬)学総合研究科, COE研究員
Review Section/Research Field	Principal Investigator Risk sciences of radiation and chemicals / Basic Section 48040:Medical biochemistry-related / Medium-sized Section 63:Environmental analyses and evaluation and related fields / Basic Section 43010:Molecular biology-related / Pathological medical chemistry / Risk sciences of radiation/Chemicals Except Principal Investigator Medium-sized Section 58:Society medicine, nursing, and related fields / Medium-sized Section 55:Surgery of the organs maintaining homeostasis and related fields / General surgery / Endocrinology / Plastic surgery
Keywords	Principal Investigator DNA修復 / RNAポリメラーゼ / 修復 / ヌクレオチド除去修復 / ゲノム不安定性 / 転写 / 色素性乾皮症 (XP) / XPJ / VUS / ゲノム不安定性疾患 … More / ユビキチン化 / 転写と共役したDNA修復 / コケイン症候群 / 小頭症 / 遺伝性疾患 / NHEJ / DNA損傷修復 / 分子遺伝子診断学 / In Cell Analyzer / エチニルウリジン / エチニルデオキシウリジン / 紫外線 … More Except Principal Investigator DNA修復 / 乳癌 / 放射線 / チェルノブイリ / 甲状腺癌 / 相同組み換え修復 / 相同組換え修復 / 乳がん / MiSeq NGS / RNA-seq NGS / mtDNA deletions / RNA-seq / Large-scale deletion / mtDNA / 脂肪由来幹細胞 / 増殖性疾患 / 放射線障害 / 創傷治癒 / 幹細胞 / 難治創傷 / ケロイド 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
- 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
転写共役修復 (TCR)の分子メカニズム解明とTCR欠損ヒト遺伝性疾患の分子病態Principal Investigator
- Principal Investigator
  
  中沢由華
- 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
ゲノム不安定性疾患の新規疾患原因遺伝子変異同定法の確立と探索Principal Investigator
- Principal Investigator
  
  中沢由華
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Challenging Research (Exploratory)
- Review Section
  
  Medium-sized Section 63:Environmental analyses and evaluation and related fields
- Research Institution
  Nagoya University
チェルノブイリ放射線誘発甲状腺がんの遺伝子バンク設立と分子遺伝疫学国際共同研究
- Principal Investigator
  
  光武範吏
- Project Period (FY)
  2020 – 2023
- Research Category
  
  Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))
- Review Section
  
  Medium-sized Section 58:Society medicine, nursing, and related fields
- Research Institution
  Nagasaki University
Establishment of a bio-assay for DNA homologous recombination ability using breast cancer cells to catalog responsible genetic alterations
- Principal Investigator
  
  MITSUTAKE Norisato
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Challenging Research (Exploratory)
- Review Section
  
  Medium-sized Section 55:Surgery of the organs maintaining homeostasis and related fields
- Research Institution
  Nagasaki University
DNA double strand break repair factors mutated in a new syndrome with microcephalyPrincipal Investigator
- 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
Mitochondrial DNA deletions as a bioindicator of radiation exposure in papillary thyroid carcinoma
- Principal Investigator
  
  ROGOUNOVITCH Tatiana
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Endocrinology
- Research Institution
  Nagasaki University
Establishment of a system to measure DNA repair activity using circulating tumor cells: the key to predict sensitivity to PARP inhibitors
- Principal Investigator
  
  MITSUTAKE Norisato
- Project Period (FY)
  2016 – 2017
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  General surgery
- Research Institution
  Nagasaki University
Implication of nerve growth factor in secondary lymphedema and pathogenesis
- Principal Investigator
  
  AKITA Sadanori
- Project Period (FY)
  2015
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Plastic surgery
- Research Institution
  Nagasaki University
Analysis of a new genetic disorder caused by the deficiency in radiation-induced DNA double-strand break repairPrincipal Investigator
- Principal Investigator
  
  NAKAZAWA Yuka
- Project Period (FY)
  2015 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (A)
- Research Field
  
  Risk sciences of radiation and chemicals
- Research Institution
  Nagasaki University
Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi AnemiaPrincipal Investigator
- Principal Investigator
  
  NAKAZAWA Yuka
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  Nagasaki University
Screening for novel factors involved in nucleotide excision repairPrincipal Investigator
- Principal Investigator
  
  NAKAZAWA Yuka
- Project Period (FY)
  2009 – 2010
- Research Category
  
  Grant-in-Aid for Research Activity Start-up
- Research Field
  
  Risk sciences of radiation/Chemicals
- Research Institution
  Nagasaki University

All 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 2010 2009 Other

All Journal Article Presentation Patent

[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
[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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly- progressing radiosensitive-severe combined immunodeficiency.2015
- 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, Ogi T, Furukawa F, Inoue M, Yoshiura K, Kanazawa N.
- Journal Title
  
  Journal of Clinical Immunology
  
  Volume: 160 Pages: 255-260
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H05333
[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] 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] A semi-automated non-radioactive system for measuring recovery of RNA synthesis and unscheduled DNA synthesis using ethynyluracil derivatives2010
- Author(s)
  中沢由華
- Journal Title
  
  DNA Repair 9
- NAID
  120006984626
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21810022
[Journal Article] A semi-automated non-radioactive system for measuring recovery of RNA synthesis and unscheduled DNA synthesis using ethynyluracil derivatives.2010
- Author(s)
  中沢由華.,S.Yamashita, A.Lehmann, T.Ogi.
- Journal Title
  
  DNA Repair 9
  
  Pages: 506-516
- NAID
  120006984626
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21810022
[Patent]2010
- Inventor(s)
  中沢由華, 他2名
- Industrial Property Rights Holder
  長崎大学
- Industrial Property Number
  2009-172521
- Filing Date
  2010-01-28
- Overseas
- Data Source
  KAKENHI-PROJECT-21810022
[Patent] 損傷DNA修復物質のスクリーニング方法2009
- Inventor(s)
  中沢由華, 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-21810022
[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-21K19844
[Presentation] RPB1-K1268とUVSSA-K414位でのユビキチン化修飾は転写と共役したヌクレオチド除去修復機構に必要.2021
- Author(s)
  中沢由華.
- Organizer
  日本放射線影響学会第64回大会
- Data Source
  KAKENHI-PROJECT-21H02399
[Presentation] RPB1-K1268とUVSSA-K414位でのユビキチン化修飾は転写と共役したヌクレオチド除去修復機構に必要.2021
- Author(s)
  中沢由華
- Organizer
  日本放射線影響学会第64回大会
- Data Source
  KAKENHI-PROJECT-21K19844
[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] 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-18K19585
[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] 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-18K19585
[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] 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.
- Organizer
  International Symposium on XP and other Nucleotide Excision Repair Disorders
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H01877
[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] 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] 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] 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
- 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-18K19585
[Presentation] Alterations in RNA polymerase IIo ubiquitination cause Cockayne syndrome-like premature aging phenotype in mice due to TC-NER defect2018
- Author(s)
  Nakazawa Y
- Organizer
  International Symposium on XP and other Nucleotide Excision Repair Disorders
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19585
[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.
- 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-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)
  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] 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-15H05333
[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-15H05333
[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] 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] 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] 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] 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] 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] 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-15H05333
[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-15H05333
[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] 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-15H05333
[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-15H05333
[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-15H05333
[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
- Organizer
  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-16K15594
[Presentation] A Screening of Cockayne syndrome like patients identified a new class of disease associated with mutations in the XRCC4 gene.2016
- Author(s)
  中沢由華
- 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
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H05333
[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）
- Data Source
  KAKENHI-PROJECT-15H05333
[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）
- Data Source
  KAKENHI-PROJECT-15H05333
[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-15H05333
[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-15H05333
[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-15H05333
[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-15H05333
[Presentation] Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia2013
- Author(s)
  中沢由華
- Organizer
  11th International Conference on Environmental Mutagens
- Place of Presentation
  Bourbon Convention & Spa Resort Cataratas do Iguassu（ブラジル）
- Data Source
  KAKENHI-PROJECT-24790321
[Presentation] A rapid non-radioactive technique for measurement of nucleotide excision repair (NER) activity in primary human fibroblasts by incorporation of ethynyluracil derivatives2010
- Author(s)
  中沢由華
- Organizer
  The 7th 3R International Conference
- Place of Presentation
  富山
- Data Source
  KAKENHI-PROJECT-21810022
[Presentation] A semi-automated non-radioactive system for measuring recovery of RNA synthesis and unscheduled DNA synthesis using ethynyluracil derivatives2010
- Author(s)
  中沢由華
- Organizer
  International Conference on Radiation and Cancer Biology at Nagasaki 2010
- Place of Presentation
  長崎
- Data Source
  KAKENHI-PROJECT-21810022
[Presentation] A rapid non-radioactive technique for measurement of nucleotide excision repair (NER) activity in primary human fibroblasts by incorporation of ethynyluracil derivatives2010
- Author(s)
  中沢由華
- Organizer
  The 7th 3R(Replication, Recombination & Repair) symposium
- Place of Presentation
  富山
- Data Source
  KAKENHI-PROJECT-21810022
[Presentation] A rarid non-radioactive technique for measurement of repair synthesis in primary human fibroblasts by incorporation of ethynyl deoxyuridine(EdU)2009
- Author(s)
  中沢由華
- Organizer
  第32回日本分子生物学会年会
- Place of Presentation
  横浜
- Year and Date
  2009-12-09
- Data Source
  KAKENHI-PROJECT-21810022
[Presentation] EdUを用いたUDS測定法とXP診断への応用2009
- Author(s)
  中沢由華
- Organizer
  第32回日本分子生物学会年会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21810022
[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-24790321
[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-24790321
[Presentation] RNA polymerase processing in nucleotide-excision-repair-deficient genetic disorders
- Author(s)
  中沢　由華
- Organizer
  第35回日本分子生物学会年会
- Place of Presentation
  福岡市
- Data Source
  KAKENHI-PROJECT-24790321
[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-24790321
[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-24790321
[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-24790321
[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-24790321

1. MITSUTAKE Norisato (50404215)

# of Collaborated Projects: 3 results

# of Collaborated Products: 4 results
2. 荻朋男 (80508317)

# of Collaborated Projects: 3 results

# of Collaborated Products: 23 results
3. AKITA Sadanori (90315250)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. YOHIMOTO Hiroshi (90513309)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. MATSUSE Michiko (30533905)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. ROGOUNOVITCH Tatiana (30423643)

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. 岡泰由 (60762383)

# of Collaborated Projects: 1 results

# of Collaborated Products: 12 results
9. 伊東正博 (30184691)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. 酒匂あやか (60884187)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. JEGGO Penny

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. TANAKA Aya

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. NAGAYAMA Yuji

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
14. 李桃生

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
15. 安田武嗣

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
20. 松永司

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
21. GUO Chaowan

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
22. 松鵜睦美

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

NAKAZAWA Yuka 中沢 由華

Research Projects

Research Products

Co-Researchers

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

Principal Investigator

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転写共役修復 (TCR)の分子メカニズム解明とTCR欠損ヒト遺伝性疾患の分子病態Principal Investigator

Principal Investigator

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ゲノム不安定性疾患の新規疾患原因遺伝子変異同定法の確立と探索Principal Investigator

Principal Investigator

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チェルノブイリ放射線誘発甲状腺がんの遺伝子バンク設立と分子遺伝疫学国際共同研究

Principal Investigator

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Establishment of a bio-assay for DNA homologous recombination ability using breast cancer cells to catalog responsible genetic alterations

Principal Investigator

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DNA double strand break repair factors mutated in a new syndrome with microcephalyPrincipal Investigator

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Mitochondrial DNA deletions as a bioindicator of radiation exposure in papillary thyroid carcinoma

Principal Investigator

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Establishment of a system to measure DNA repair activity using circulating tumor cells: the key to predict sensitivity to PARP inhibitors

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Implication of nerve growth factor in secondary lymphedema and pathogenesis

Principal Investigator

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Analysis of a new genetic disorder caused by the deficiency in radiation-induced DNA double-strand break repairPrincipal Investigator

Principal Investigator

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Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi AnemiaPrincipal Investigator

Principal Investigator

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Screening for novel factors involved in nucleotide excision repairPrincipal Investigator

Principal Investigator

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[Journal Article] Aicardi-Goutieres syndrome with SAMHD1 deficiency can be diagnosed by unscheduled DNA synthesis test2022

Author(s)

Journal Title

DOI

NAKAZAWA Yuka 中沢由華