Fujii Katsunori 藤井克則

… Alternative Names

FUJII KATSUNORI 藤井克則

FUJII Katsurnori 藤井克則

FUJII Katsunori 藤井克則

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Researcher Number	70344992
Affiliation (Current)	2025: 地方独立行政法人長野県立病院機構長野県立こども病院(生命科学研究センター), 生命科学研究センター, 主任研究員(副センター長) 2025: 国際医療福祉大学, 国際医療福祉大学成田病院, 教授 2025: 千葉大学, 医学部附属病院, 特任教授
Affiliation (based on the past Project Information) *help	2023: 千葉大学, 医学部附属病院, 特任教授 2022: 千葉大学, 大学院医学研究院, 特任教授 2016 – 2020: 千葉大学, 大学院医学研究院, 講師 2012 – 2016: 千葉大学, 医学(系)研究科(研究院), 講師 2010 – 2011: 千葉大学, 大学院・医学研究院, 講師 … More 2009: Chiba University, 大学院・医学研究院, 助教 2007: Chiba University, Graduate School of Medicine, Assistant Professor 2006: Chiba University, Graduate School of Medicine, Assistant Professor, 大学院医学研究院, 助手 2003 – 2006: 千葉大学, 医学部附属病院, 助手 Less
Review Section/Research Field	Principal Investigator Pediatrics / Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Pediatrics / 膠原病・アレルギー・感染症内科学 / Science education
Keywords	Principal Investigator Gorlin症候群 / ヘッジホッグ / 基底細胞母斑症候群 / 基底細胞癌 / PTCH1 / 皮膚線維芽細胞 / 髄芽腫 / シグナル伝達 / ゴーリン症候群 / 遺伝学 … More / ゲノム / 骨密度 / 骨代謝 / iPS / 天然化合物ライブラリー / 疾患iPS細胞 / 阻害薬 / 創薬スクリーニング / GLI1 / Gorlin 症候群 / ヘッジホッグシグナリング / 再生医学 / 脳神経疾患 / 高発癌性疾患 / ヘッジホッグシグナル / iPS細胞 / Pediatric Neurology / molecular regulations / Neuronal cell death / apoptosis / 14-3-3 proteins / 小児神経疾患 / 分子調節 / 神経細胞死 / アポトーシス / 14-3-3タンパク / Hedgehog Signalling / PTCH gene / Gorlin syndrome / Nevoid basal cell carcinoma syndrome / NBCCS / PTCH / PTCH遺伝子 / 母斑性基底細胞癌症候群 / GLI / SMO / 高発癌性遺伝 / 癌形成 / 形態形成 / 放射線 / 癌 / 遺伝子 … More Except Principal Investigator 脳・神経 / 遺伝子多型 / CD14 / 発生・分化 / ゴーリン症候群 / 損害回避 / 扁桃体 / セロトニン / パーソナリティー / Gorlin症候群 / ヘッジホッグシグナル / Polymorphism / Cerebral Development / Holoprosencephaly / Genetics / 全前脳症 / 遺伝学 / tumor necrosis factor alpha / bronchiolitis / genetic polymorphism / Respiratory syncytial virus / TLR4 / TNFα / 細気管支炎 / RSウイルス / 国際情報交換（英国） / 生体影響 / 放射線生体影響 / 科学教育 / 持続発展教育 / 教材開発 / 教員養成 / 学習プログラム / リスク教育 / 放射線教育 Less

Molecular mechanism of bone metabolism in Gorlin syndromePrincipal Investigator
- Principal Investigator
  
  藤井克則
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Chiba University
Identification of hedgehog signal inhibitors in tumorsPrincipal Investigator
- Principal Investigator
  
  FUJII KATSUNORI
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Chiba University
The role of hedgehog signaling in personality formation
- Principal Investigator
  
  Uchikawa Hideki
- Project Period (FY)
  2017 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Chiba University
Hedgehog signaling in human diseasesPrincipal Investigator
- Principal Investigator
  
  FUJII KATSUNORI
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Chiba University
Learning program development for ESD based on radiation education and training for science teachers
- Principal Investigator
  
  SUGITA KATSUO
- Project Period (FY)
  2013 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Science education
- Research Institution
  Chiba University
Hedgehog signaling in murine and humanPrincipal Investigator
- Principal Investigator
  
  FUJII Katsunori
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Chiba University
Morphogenesis and Carcinogenesis regulated by PTCH1 genePrincipal Investigator
- Principal Investigator
  
  FUJII Katsurnori
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Chiba University
Biology of 14-3 3 proteins regulating neuronal cell deathPrincipal Investigator
- Principal Investigator
  
  FUJII Katsunori
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Chiba University
Molecular Genetics of Holoprosencephaly
- Principal Investigator
  
  MIYASHITA Toshiyuki
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Kitasato University
  National Research Institute for Child Health and Development
Study on molecular genetics of respiratory syncytial virus bronchiolitis
- Principal Investigator
  
  KOHNO Yoichi
- Project Period (FY)
  2004 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  膠原病・アレルギー・感染症内科学
- Research Institution
  Chiba University
Molecular mechanisms of tumorigenesis in nevoid basal cell carcinoma syndromePrincipal Investigator
- Principal Investigator
  
  FUJII Katsunori
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Chiba University

[Book] 「基底細胞母斑症候群」小児科臨床ピクシス17年代別子どもの皮膚疾患2010
- Author(s)
  藤井克則
- Total Pages
  180
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] PTCH1 null induced pluripotent stem cells exclusively differentiate into immature ectodermal cells with large areas of medulloblastoma like tissue2022
- Author(s)
  Kazuaki Nagao, Chise Kato, Yu Ikemoto, Toshino Motojima, Katsunori Fujii, Akihiro Umezawa, Toshiyuki Miyashita
- Journal Title
  
  Discovery Oncology
  
  Volume: 13 Issue: 1 Pages: 36-36
- DOI
  10.1007/s12672-022-00498-x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08252
[Journal Article] Specific temperament in patients with nevoid basal cell carcinoma syndrome2021
- Author(s)
  Uchikawa Hideki、Fujii Katsunori、Shiohama Tadashi、Nakazato Michiko、Shimizu Eiji、Miyashita Toshiyuki、Shimojo Naoki
- Journal Title
  
  Pediatrics International
  
  Volume: 63 Issue: 2 Pages: 177-182
- DOI
  10.1111/ped.14419
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10048
[Journal Article] Gorlin syndrome-induced pluripotent stem cells form medulloblastoma with loss of heterozygosity in PTCH12020
- Author(s)
  Ikemoto Yu、Miyashita Toshiyuki、Nasu Michiyo、Hatsuse Hiromi、Kajiwara Kazuhiro、Fujii Katsunori、Motojima Toshino、Kokido Ibuki、Toyoda Masashi、Umezawa Akihiro
- Journal Title
  
  Aging
  
  Volume: 12 Issue: 10 Pages: 9935-9947
- DOI
  10.18632/aging.103258
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08252
[Journal Article] MicroRNAs profiling in fibroblasts derived from patients with Gorlinsyndrome2019
- Author(s)
  Shiohama T., Fujii K., Miyashita T., Takatani T., Ikehara H., Uchikawa H., Motojima T., Uchida T, Shimojo N
- Journal Title
  
  Journal of Human Genetics
  
  Volume: -
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09960
[Journal Article] A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features2019
- Author(s)
  Murata Y, Kurosaka H, Ohata Y, Aikawa T, Takahata S, Fujii K, Miyashita T, Morita C, Inubushi T, Kubota T, Sakai N, Ozono K, Kogo M, Yamashiro T.
- Journal Title
  
  Human Genome Variation
  
  Volume: 6 Issue: 1 Pages: 16-16
- DOI
  10.1038/s41439-019-0047-9
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09960, KAKENHI-PROJECT-16K15836, KAKENHI-PROJECT-16K11682, KAKENHI-PROJECT-17K10061, KAKENHI-PROJECT-18K19645, KAKENHI-PROJECT-18K17255
[Journal Article] Somatic mosaicism containing double mutations in PTCH1 revealed by generation of induced pluripotent stem cells from nevoid basal cell carcinoma syndrome.2017
- Author(s)
  Ikemoto, Y., Takayama, Y., Fujii, K., Masuda, M., Kato, C., Hatsuse, H., Fujitani, K., Nagao, K., Kameyama, K., Ikehara, H., Toyoda, M., Umezawa, A. and Miyashita, T.
- Journal Title
  
  Journal of Medical Genetics
  
  Volume: － Issue: 8 Pages: 579-584
- DOI
  10.1136/jmedgenet-2016-104490
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26461530, KAKENHI-PROJECT-15K19041, KAKENHI-PROJECT-15K09729, KAKENHI-PROJECT-16K09960, KAKENHI-PROJECT-17K10061
[Journal Article] Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene.2017
- Author(s)
  Kato, C., Fujii, K., Arai, Y., Hatsuse, H., Nagao, K., Takayama, Y., Kameyama, K., Fujii, K., and Miyashita, T.
- Journal Title
  
  Familial Cancer
  
  Volume: 16 Issue: 1 Pages: 131-138
- DOI
  10.1007/s10689-016-9924-2
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26461530, KAKENHI-PROJECT-16K09960
[Journal Article] 放射線生体リスクにおける学習プログラム開発2016
- Author(s)
  前田彩香、高橋あかり、杉田克生、野村純、加藤徹也、高橋博代、藤井克則、喜多和子、小林芳枝、吉本一紀
- Journal Title
  
  千葉大学教育学部研究紀要
  
  Volume: 64 Pages: 365-374
- NAID
  120007088860
- Data Source
  KAKENHI-PROJECT-25282033
[Journal Article] Hedgehog signaling is synergistically enhanced by nutritional deprivation and ligand stimulation in human fibroblasts of Gorlin syndrome2015
- Author(s)
  Mizuochi H, Fujii K, Shiohama T, Uchikawa H, Shimojo N
- Journal Title
  
  Biochem Biophys Res Commun
  
  Volume: 457 Issue: 3 Pages: 318-323
- DOI
  10.1016/j.bbrc.2014.12.108
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-24591502
[Journal Article] ゴーリン症候群2014
- Author(s)
  藤井克則、宮下俊之
- Journal Title
  
  日本臨牀　新領域別症候群シリーズNo. 28　神経症候群
  
  Volume: 28 Pages: 581-4
- Data Source
  KAKENHI-PROJECT-24591502
[Journal Article] Gorlin syndrome (nevoid basal cell carcinoma syndrome): update and literature review2014
- Author(s)
  Fujii K, Miyashita T
- Journal Title
  
  Pediatric International
  
  Volume: 56 Issue: 5 Pages: 667-674
- DOI
  10.1111/ped.12461
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-24591502, KAKENHI-PROJECT-26461530
[Journal Article] Downregulation of microRNA-431 by human IFN-β inhibits viability of medulloblastoma and glioblastoma cells via upregulation of SOCS62014
- Author(s)
  Tanaka T, Arai M, Jiang X, Sugaya S, Kanda T, Fujii K, K Kita, Sugita K, Imazeki F, T Miyashita, A Kaneda, Yokosuka O.
- Journal Title
  
  Int J Oncol.
  
  Volume: 44 Pages: 1685-1690
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25282033
[Journal Article] Oxidative stress-induced JNK1 phosphorylation inhibits hedgehog signalling and osteoblast differentiation2014
- Author(s)
  Shiohama T, Fujii K, Uchikawa H, Takatani T, Mizuochi H, Kohno Y
- Journal Title
  
  Cell Biology International Reports
  
  Volume: 9999 Pages: 1-10
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-24591502
[Journal Article] Gorlin症候群2014
- Author(s)
  藤井克則、宮下俊之
- Journal Title
  
  日本臨床　新領域別症候群シリーズNo. 29 神経症候群
  
  Volume: 29 Pages: 744-7
- Data Source
  KAKENHI-PROJECT-24591502
[Journal Article] 14-3-3 proteins, particularly of the epsilon isoform, are detectable in cerebrospinal fluids of cerebellar diseases in children.2013
- Author(s)
  Fujii K, Uchikawa H, Tanabe Y, Omata T, Nonaka I, Kohno Y.
- Journal Title
  
  Brain and Development
  
  Volume: 35 Issue: 6 Pages: 555-560
- DOI
  10.1016/j.braindev.2012.09.007
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591502
[Journal Article] PTCH1遺伝子のスプライシング変異を認めた母斑基底細胞癌症候群の1例2013
- Author(s)
  古賀陽子，藤井克則，西條英人，平松信旭，森良之，高戸毅
- Journal Title
  
  日本歯科口腔外科学会雑誌
  
  Volume: 59 Pages: 367-371
- NAID
  40019694759
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25282033
[Journal Article] Reversible white matter lesions during ketogenic diet therapy in glucose transporter 1 deficiency syndrome.2013
- Author(s)
  Shiohama T, Fujii K, Takahashi S, Nakamura F, Kohno Y.
- Journal Title
  
  Brain and Development
  
  Volume: 49 Issue: 6 Pages: 493-496
- DOI
  10.1016/j.pediatrneurol.2013.06.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591502
[Journal Article] Sudden onset odontoid fracture caused by cervical instability in hypotonic cerebral palsy.2013
- Author(s)
  Shiohama T, Fujii K, Kitazawa K, Takahashi A, Maemoto T, Honda A.
- Journal Title
  
  Brain and Development
  
  Volume: 35 Issue: 10 Pages: 925-928
- DOI
  10.1016/j.braindev.2012.11.012
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591502
[Journal Article] Artery tortuosity syndrome exhibiting early-onset emphysema with novel compound heterozygous SLC2A10 mutations.2013
- Author(s)
  Takahashi Y, Fujii K, Yoshida A, Morisaki H, Kohno Y, Morisaki T.
- Journal Title
  
  American Journal of Medical Genetics
  
  Volume: 161A Issue: 4 Pages: 856-859
- DOI
  10.1002/ajmg.a.35776
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591502
[Journal Article] Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome.2013
- Author(s)
  Fujii. K., Ohashi, H. ,Suzuki, M., Hatsuse, H., Shiohama, T., Uchikawa, H., and Miyashita, T.
- Journal Title
  
  Fam. Cancer
  
  Volume: 12 Issue: 4 Pages: 611-614
- DOI
  10.1007/s10689-013-9623-1
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23501269, KAKENHI-PROJECT-24591502
[Journal Article] Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome.2013
- Author(s)
  Fujii K, Ohashi H, Suzuki M, Hatsuse H, Shiohama T, Uchikawa H, Miyashita T.
- Journal Title
  
  Familial Cancer
  
  Volume: 1 Pages: 1-1
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591502
[Journal Article] 14-3-3 Proteins, particularly of the epsilon isoform, are detectable in cerebrospinal fluids of cerebellar diseases in children.2013
- Author(s)
  Fujii K, Uchikawa H, Tanabe Y, Omata T, Nonaka I, Kohno Y.
- Journal Title
  
  Brain and Development
  
  Volume: 1 Pages: 1-1
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591502
[Journal Article] Molecular pathogenesis of keratocystic odontogenic tumors developing in nevoid basal cell carcinoma syndrome.2013
- Author(s)
  Suzuki M, Nagao K, Hatsuse H, Sasaki R, Saito K, Fujii K, Miyashita T.
- Journal Title
  
  Oral Surg Oral Med Oral Pathol Oral Radiol
  
  Volume: 116 Pages: 348-53
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25282033
[Journal Article] Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome.2013
- Author(s)
  Fujii K, Ohashi H, Hatsuse H, Uchikawa H, Miyashita T.
- Journal Title
  
  Fam Cancer
  
  Volume: 12 Pages: 611-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25282033
[Journal Article] ヘッジホッグシグナルと脳腫瘍2012
- Author(s)
  塩浜直, 内川英紀, 水落弘美, 宮下俊之, 藤井克則
- Journal Title
  
  脳神経外科速報
  
  Volume: 第22巻第1号 Pages: 66-73
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Selective haploinsufficiency of longer isoforms of PTCH1 protein can cause nevoid basal cell carcinoma syndrome.2012
- Author(s)
  Suzuki M, Hatsuse H, Nagao K, Takayama Y, Kameyama K, Kabasawa Y, Omura K, Yoshida M, Fujii K, Miyashita T.
- Journal Title
  
  Jounal of human genetics
  
  Volume: 57 Pages: 422-6
- Data Source
  KAKENHI-PROJECT-24591502
[Journal Article] Multiple cavitations in posterior reversible leukoencephalopathy syndrome associated with hemolytic-uremic syndrome2012
- Author(s)
  Fujii K, Matsuo K, Takatani T, Uchikawa H, Kohno H
- Journal Title
  
  Brain Dev
  
  Volume: 34 Pages: 318-21
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Inhibition of cell viability by human IFN-b is mediated by microRNA-4312012
- Author(s)
  Tanaka T, Sugaya S, Kita K, Arai M, Kanda T, Fujii K, Imazeki F, Sugita K, Yokosuka O, Suzuki N
- Journal Title
  
  Int J Oncol
  
  Volume: 40 Pages: 1470-6
- DOI
  10.3892/ijo.2012.1345
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313, KAKENHI-PROJECT-24701002
[Journal Article] Heterozygous tandem duplication within the PTCH1 gene results in nevoid basal cell carcinoma syndrome.2012
- Author(s)
  Kosaki R, Nagao K, Kameyama K, Suzuki M, Fujii K, Miyashita T.
- Journal Title
  
  American Journal of Medical Genetics A
  
  Volume: 158A Pages: 1724-8
- Data Source
  KAKENHI-PROJECT-24591502
[Journal Article] Nationwide survey of nevoid basal cell carcinoma syndrome in Japan revealing the low frequency of basal cell carcinoma2012
- Author(s)
  Endo M, Fujii K, Sugita K, Saito K, Kohno Y, Miyashita T
- Journal Title
  
  American Journal of Medical Genetics
  
  Volume: 158A Pages: 351-358
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Nationwide survey of nevoid basal cell carcinoma syndrome in Japan revealing low frequency of basal cell carcinoma2012
- Author(s)
  Endo M, Fujii K, Sugita K, Saito K, Kohno Y, Miyashita T
- Journal Title
  
  Am J Med Genet A
  
  Volume: 158A Issue: 2 Pages: 351-7
- DOI
  10.1002/ajmg.a.34421
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313, KAKENHI-PROJECT-23501269
[Journal Article] 見逃してはいけない家族性腫瘍:本邦における母斑基底細胞癌症候群の遺伝子変異と臨床的特徴2011
- Author(s)
  宮下俊之、桐生麻衣子、斎藤加代子、杉田克生、遠藤真美子、藤井克則
- Journal Title
  
  家族性腫瘍
  
  Volume: 11 Pages: 14-18
- NAID
  130007529694
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] 逃してはいけない家族性腫瘍:本邦における母斑基底細胞癌症候群の遺伝子変異と臨床的特徴2011
- Author(s)
  宮下俊之, 桐生麻衣子, 斎藤加代子, 杉田克生, 遠藤真美子, 藤井克則
- Journal Title
  
  家族性腫瘍
  
  Volume: 第11巻第1号 Pages: 14-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Entire PTCH1 deletion is a common event in point mutation-negative cases with nevoid basal cell carcinoma syndrome in Japan2011
- Author(s)
  Nagao K, Fujii K, Saito K, Sugita K, Endo M, Motojima T, Hatsuse H, Miyashita T
- Journal Title
  
  Clin Genet
  
  Volume: 79 Pages: 196-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Entire PTCH1 deletion is a common event in point mutation-negative cases with nevoid basal cell carcinoma syndrome in Japan2011
- Author(s)
  Nagao K, Fujii K, Saito K, et al.
- Journal Title
  
  Clinical Genetics
  
  Volume: 79 Pages: 196-198
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Multiple keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome having distinct PTCH mutations2010
- Author(s)
  Sasaki R, Miyashita T, Saito K, Fujii K, Ando T, Akizaki T.
- Journal Title
  
  Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endocrinology
  
  Volume: 110
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] 顎骨内嚢胞、手掌小陥凹、粗野顔貌を呈した11歳女児例2010
- Author(s)
  藤井克則
- Journal Title
  
  イメージからせまる小児神経疾患
  
  Volume: 50 Pages: 35-36
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Zebrafish gene knockdowns imply roles for human YWHAG in infantile spasms and cardiomegaly2010
- Author(s)
  Komoike Y, Fujii K, Nishimura A, Hiraki Y, Hayashidani M, Shimojima K, et al.
- Journal Title
  
  Genesis
  
  Volume: 48 Pages: 233-243
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] 基底細胞母斑症候群」小児科臨床ピクシス17「年代別子どもの皮膚疾患2010
- Author(s)
  藤井克則
- Journal Title
  
  中山書店五十嵐隆総編集、専門編集馬場直子
  
  Pages: 34-35
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Zebrafish gene knockdowns imply roles for human YWHAG in infantile spasms and cardiomegaly2010
- Author(s)
  Komoike Y, Fujii K, Nishimura A, Hiraki Y, Hayashidani M, Shimojima K, Nishizawa T, Higashi K, Yasukawa K, Saitsu H, Miyake N, Mizuguchi T, Matsumoto N, Osawa M, Kohno Y, Higashinakagawa T, Yamamoto T
- Journal Title
  
  Genesis
  
  Volume: 48 Pages: 233-43
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Multiple keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome having distinct PTCH1 mutations2010
- Author(s)
  Sasaki R, Miyashita T, Saito K, Fujii K, Ando T, Akizuki T
- Journal Title
  
  Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology (Oral Surg Oral Med Oral Pathol Oral Radiol Endod)
  
  Volume: 110
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Nevoid basal cell carcinoma syndrome with cleft lip and palate associated with the novel PTCH gene mutations2009
- Author(s)
  Sasaki R, Saito K, Watanabe Y, Takayama Y, Fujii K, Agawa K, Miyashita T, Ando T, Akizuki T
- Journal Title
  
  J Hum Genet
  
  Volume: 54 Pages: 398-402
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Nevoid basal cell carcinoma syndrome with cleft lip and palate associated with the novel PTCH gene mutations2009
- Author(s)
  Sasaki R, Saito K, Watanabe Y, Takayama Y, Fujii K, et al
- Journal Title
  
  Journal of Human Genetics 54
  
  Pages: 398-402
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Gorlin症候群における臨床的検討-主要症状を中心とした多様な症候スペクトラム-2009
- Author(s)
  田辺良, 藤井克則, 宮下俊之, 杉田克生, 内川英紀, 遠藤真美子, 新井ひでえ, 河野陽一
- Journal Title
  
  脳と発達
  
  Volume: 41 Pages: 253-257
- NAID
  10024846296
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Acute disseminated encephalomyelitis associated with 2009 H1N1 influenza vaccine2009
- Author(s)
  Fujii K, Suyama M, Chiba K, Okunushi T, Oikawa J, Kohno Y
- Journal Title
  
  Pediatr Int
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Homozygous Female Becker muscular dystrophy2009
- Author(s)
  Fujii K, Minami N, Hayashi Y, Nishino I, Nonaka I, Tanabe Y, Takanashi J, Kohno Y
- Journal Title
  
  Am J Med Genet
  
  Volume: 149A Pages: 1052-5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] 顎骨嚢胞および大脳鎌の石灰化を契機に診断されたGorlin症候群の1例2009
- Author(s)
  藤井克則, 内川英紀, 杉田克生, 河野陽一
- Journal Title
  
  児疾患アトラス目で見る小児科150小児科別冊
  
  Volume: 46 Pages: 288-9
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] ヘッジホッグと形態形成-Gorlin症候群とPTCH遺伝子変異-2009
- Author(s)
  藤井克則, 宮下俊之
- Journal Title
  
  日本小児皮膚科学会雑誌
  
  Volume: 28 Pages: 65-71
- NAID
  10026418020
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] ヘッジホッグと形態形成-発生生物学から臨床医学への応用-2009
- Author(s)
  藤井克則, 宮下俊之
- Journal Title
  
  脳と発達
  
  Volume: 41 Pages: 247-252
- NAID
  10024846234
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Kernicteroid Syndrome of Preterm Infants2009
- Author(s)
  Okumura A, Kidokoro H, Shoji H, Nakazawa T, Mimaki M, Fujii K, Oba H, Shimizu T
- Journal Title
  
  Pediatrics
  
  Volume: 123(6)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] ヘッジホッグと形態形成-発生生物学から臨床医学への応用-2009
- Author(s)
  藤井克則、宮下俊之
- Journal Title
  
  脳と発達 41
  
  Pages: 247-252
- NAID
  10024846234
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] ヘッジホッグと形態形成-Gorlin症候群とPTCH遺伝子変異2009
- Author(s)
  藤井克則、宮下俊之
- Journal Title
  
  日本小児皮膚科学会雑誌 28
  
  Pages: 65-71
- NAID
  10026418020
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Gorlin症候群における分子遺伝学的検討-PTCH1遺伝子変異とその多様な変異スペクトラム-2009
- Author(s)
  遠藤真美子、藤井克則、宮下俊之, ら
- Journal Title
  
  脳と発達 41
  
  Pages: 259-263
- NAID
  10024846313
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] A splenial lesion with transiently reduced diffusion in clinically mild encephalitis is not always reversible2009
- Author(s)
  Hashimoto Y, Takanashi J, Kaiho K, Fujii K, Okubo T, Ota S, Kohno Y
- Journal Title
  
  A case report
  
  Volume: 31 Pages: 710-2
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Gorlin症候群における分子遺伝学的検討-PTCH1遺伝子変異とその多様な変異スペクトラム-2009
- Author(s)
  遠藤真美子, 藤井克則, 宮下俊之, 杉田克生, 内川英紀, 田辺良, 新井ひでえ, 河野陽一
- Journal Title
  
  脳と発達
  
  Volume: 41 Pages: 259-263
- NAID
  10024846313
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] High-density oligonucleotide array with sub-kilobase resolution reveals breakpoint information of submicroscopic deletions in nevoid basal cell carcinoma syndrome2007
- Author(s)
  Fujii, K.
- Journal Title
  
  Hum.Genet 122
  
  Pages: 459-466
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591177
[Journal Article] High-density oligonucleotide array with sub-kilobase resolution reveals breakpoint information of submicroscopic deletions in nevoid basal cell carcinoma syndrome2007
- Author(s)
  Fujii, K., et. al.
- Journal Title
  
  Hum. Genet 122
  
  Pages: 459-466
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591177
[Journal Article] High-density oligonucleotide array with sub-kilobase resolution reveals breakpoint information of submicroscopic deletions in nevoid basal cell carcinoma syndrome.2007
- Author(s)
  Fujii, K.
- Journal Title
  
  Hum.Genet. 122
  
  Pages: 459-466
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591177
[Journal Article] 14-3-3 protein detection in the cerebrospinal fluid of patients with influenza-associated encephalopathy2006
- Author(s)
  Fujii K, Tanabe Y, Uchikawa H, Kobayashi K, Kubota H, Takanashi J, Kohno Y
- Journal Title
  
  Journal of Child Neurology 21・7
  
  Pages: 562-5
- Data Source
  KAKENHI-PROJECT-18591143
[Journal Article] Identification and characterization of multiple isoforms of a marine and human tumor suppressor, patched, having distinct first exons.2005
- Author(s)
  Nagao K, Toyoda M, Takeuchi-Inoue K, Fujii K, Yamada M, Miyashita T.
- Journal Title
  
  Genomics 85
  
  Pages: 462-471
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591085
[Journal Article] Identification and characterization of multiple isoforms of a murine human tumor suppressor, patched, having distinct first exons.2005
- Author(s)
  Nagao K, Toyoda M, Takeuchi-Inoue K, Fujii K, Yamada M, Miyashita T.
- Journal Title
  
  Genomics 85
  
  Pages: 462-471
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591085
[Journal Article] Identification and characterization of multiple isoforms of a murine and human tumor suppressor, patched, having distinct first exons.2005
- Author(s)
  Nagao K, Toyoda M, Takeuchi-Inoue K, Fujii K, Yamada M, Miyashita T.
- Journal Title
  
  Genomics 85
  
  Pages: 462-471
- Data Source
  KAKENHI-PROJECT-15591085
[Journal Article] Identification of a novel polymorphism involving a CGG repeat in the PTCH gene and a genome-wide screening of CGG-containing genes.2004
- Author(s)
  Nagao K, Fujii K, Yamada M, Miyashita T.
- Journal Title
  
  Journal of Human Genetics 49
  
  Pages: 97-101
- NAID
  10012114886
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591085
[Journal Article] Mutations in the human homologue of Drosophila patched in Japanese nevoid basal cell carcinoma syndrome patients.2003
- Author(s)
  Fujii K, Kohno Y, Sugita K, Nakamura M, Moroi Y, Urabe K, Furue M, Yamada M, Miyashita T.
- Journal Title
  
  Human Mutation 25
  
  Pages: 451-452
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591085
[Journal Article] Gorlin syndrome with ulcerative colitis in a Japanese girl.2003
- Author(s)
  Fujii K, Miyashita T, Omata T, Kobayashi K, Takanashi J, Kouchi K, Yamada M, Kohno Y.
- Journal Title
  
  American Journal of Medical Genetics 121
  
  Pages: 65-68
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591085
[Journal Article] Heterozygous tandem duplication within the PTCH1 gene results in nevoid basal cell carcinoma syndrome
- Author(s)
  Kosaki R, Nagao K, Kameyama K, Suzuki M, Fujii K, Miyashita T
- Journal Title
  
  Am J Med Genet
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Prevention of Pancreatic Cancer
- Author(s)
  Jiang X, Sugaya S, Ren Q, Sato T, Tanaka T, Fujii K, Kita K, Suzuki N
- Journal Title
  
  Intech
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Journal Article] Reversible cerebral vasoconstriction syndrome associated with brain parenchymal hemorrhage
- Author(s)
  Kazato Y, Fujii K, Oba H, Hino M, Ochiai H, Uchikawa H, Kohno Y
- Journal Title
  
  Brain and Dev
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] Gorlin症候群モデルマウスにおける扁桃体の解析2021
- Author(s)
  内川英紀、塩浜直、佐原佑治、松田真悟、清水栄司、新田展大、青木伊知男、藤井克則
- Organizer
  第63回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-17K10048
[Presentation] Specific personality and amygdala volume in Gorlin syndrome.2019
- Author(s)
  Hideki Uchikawa, Katsunori Fujii, Tadashi Shiohama, Naoki Shimojo.
- Organizer
  13th EPNS Congress
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10048
[Presentation] Gorlin症候群における扁桃体と中脳の検討2018
- Author(s)
  内川英紀、藤井克則、塩浜直、下条直樹
- Organizer
  第60回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-17K10048
[Presentation] Temperament and Character in Patients with Gorlin syndrome.2017
- Author(s)
  Uchikawa H, Fujii K, Shiohama T, Shimojo N.
- Organizer
  14th Asian and Oceanian Congress of Child Neurology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10048
[Presentation] Gorlin症候群責任遺伝子PTCH1のディープシークエンス解析2017
- Author(s)
  増田木理、兼友裕大、高山吉永、初瀬洋美、藤谷和子、長尾和右、亀山孝三、藤井克則、宮下俊之
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-16K09960
[Presentation] MicroRNA analysis in dermal fibroblasts derived from Gorlin syndrome patients2017
- Author(s)
  Shiohama, T. Fujii, K. Takatani, T. Miyashita, T. Ikehara, H. Fujita, M. Fukuhara, T. Shimojo, N.
- Organizer
  第59回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-16K09960
[Presentation] 母斑基底細胞癌症候群患者由来のiPS細胞に見いだされたPTCH1遺伝子の体細胞モザイク変異2017
- Author(s)
  高山吉永、長尾和右、宮下俊之、藤井克則
- Organizer
  第76回日本癌学会学術総会
- Data Source
  KAKENHI-PROJECT-16K09960
[Presentation] 疾患特異的iPS細胞の解析を契機に発見された母斑基底細胞癌症候群のモザイク症例2017
- Author(s)
  宮下俊之、高山吉永、藤井克則、梅澤明弘
- Organizer
  第23回日本家族性腫瘍学会学術集会
- Data Source
  KAKENHI-PROJECT-16K09960
[Presentation] CRISPR/Cas9システムを用いたNBCCS疾患モデルiPS細胞の作製2017
- Author(s)
  荒井佑斗、加藤千勢、長尾和右、初瀬洋美、高山吉永、亀山孝三、梅澤明弘、藤井克則、宮下俊之
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-16K09960
[Presentation] Alu配列を介したPTCH遺伝子全欠失のGorlin症候群親子例2011
- Author(s)
  本島敏乃, 藤井克則, 宮下俊之, 引間昭夫, 遠藤真美子, 河野陽一
- Organizer
  第53回日本小児神経学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] Alu配列を介したPTCH遺伝子全欠失のGorlin症候群親子例2011
- Author(s)
  本島敏乃、藤井克則、宮下俊之、引間昭夫、遠藤真美子、河野陽一
- Organizer
  第53回日本小児神経学会
- Place of Presentation
  横浜
- Year and Date
  2011-05-27
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] Identification of PTCH1 mutations in Japanese Gorlin syndrome patient2011
- Author(s)
  Uchikawa H, Fujii K, Miyashita T, Endo M, Mizuochi H, Kohno Y
- Organizer
  5^<th> Europediatrics
- Place of Presentation
  Vienna (Austria)
- Year and Date
  2011-06-25
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] 本邦におけるGorlin症候群157例の臨床的検討2011
- Author(s)
  遠藤真美子, 藤井克則, 水落弘美, 須山麻衣子, 内川英紀, 宮下俊之, 斎藤加代子, 杉田克生, 河野陽一
- Organizer
  第53回日本小児神経学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] 母斑基底細胞癌症候群に発症する角化嚢胞性歯原性腫瘍の腫瘍化機序の解析2011
- Author(s)
  鈴木麻衣子、長尾和右、高山吉永、藤井克則、宮下俊之
- Organizer
  第70回日本癌学会学術総会
- Place of Presentation
  名古屋
- Year and Date
  2011-10-04
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] 日本における母斑性基底細胞癌症候群における基底細胞癌発症率2011
- Author(s)
  藤井克則, 宮下俊之
- Organizer
  第70回日本癌学会学術総会
- Year and Date
  2011-10-04
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] Nationwide survey of Gorlin syndrome in Japan2011
- Author(s)
  Fujii K, Endo M, Mizuochi H, Uchikawa H, Sugita K, Kohno Y, Saito K, Miyashita T
- Organizer
  2011 5th Europediatrics
- Place of Presentation
  Vienna, Austria
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] Bone mass density in patients with Gorlin syndrome is partially regulated by hedgehog signaling2011
- Author(s)
  Mizuochi H, Fujii K, Miyashita T, Suyama M, Endo M, Uchikawa H, Kohno Y
- Organizer
  2011 5th Europediatrics
- Place of Presentation
  Vienna, Austria
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] 日本における母斑性基底細胞癌症候群における基底細胞癌発症率2011
- Author(s)
  藤井克則、宮下俊之
- Organizer
  第70回日本癌学会学術総会
- Place of Presentation
  名古屋
- Year and Date
  2011-10-04
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] 母斑基底細胞癌症候群に発症する角化嚢胞性歯原性腫瘍の腫瘍化機序の解析2011
- Author(s)
  鈴木麻衣子, 長尾和右, 高山吉永, 藤井克則, 宮下俊之
- Organizer
  第70回日本癌学会学術総会
- Year and Date
  2011-10-04
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] Nasal gliomaを合併したGorlin症候群の1男児例2011
- Author(s)
  内川英紀, 藤井克則, 大場洋, 宮下俊之, 遠藤真美子, 須山麻衣子, 水落弘美, 河野陽一
- Organizer
  第53回日本小児神経学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] 本邦におけるGorlin症候群157例の臨床的検討2011
- Author(s)
  遠藤真美子、藤井克則、水落弘美、須山麻衣子、内川英紀、宮下俊之、斎藤加代子、杉田克生、河野陽一
- Organizer
  第53回日本小児神経学会
- Place of Presentation
  横浜
- Year and Date
  2011-05-27
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] Nasal gliomaを合併したGorlin症候群の1男児例2011
- Author(s)
  内川英紀、藤井克則、大場洋、宮下俊之、遠藤真美子、須山麻衣子、水落弘美、河野陽一
- Organizer
  第53回日本小児神経学会
- Place of Presentation
  横浜
- Year and Date
  2011-05-27
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] Gorlin症候群と骨形成の検討-動物モデルと骨密度との関連-2011
- Author(s)
  水落弘美, 藤井克則, 宮下俊之, 須山麻衣子, 遠藤真美子, 内川英紀, 河野陽一
- Organizer
  第53回日本小児神経学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] Gorlin症候群と骨形成の検討-動物モデルと骨密度との関連-2011
- Author(s)
  水落弘美、藤井克則、宮下俊之、須山麻衣子、遠藤真美子、内川英紀、河野陽一
- Organizer
  第53回日本小児神経学会
- Place of Presentation
  横浜
- Year and Date
  2011-05-27
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] Nationwide survey of Gorlin syndrome in Japan2011
- Author(s)
  Fujii K, Endo M, Mizuochi H, Uchikawa H, Sugita K, Kohno Y, Saito K, Miyashita T
- Organizer
  5^<th> Europediatrics
- Place of Presentation
  Vienna (Austria)
- Year and Date
  2011-06-25
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] Bone mass density in patients with Gorlin syndrome is partially regulated by hedgehog signaling2011
- Author(s)
  Mizuochi H, Fujii K, Miyashita T, Suyama M, Endo M, Uchikawa H, Kohno Y
- Organizer
  5^<th> Europediatrics
- Place of Presentation
  Vienna (Austria)
- Year and Date
  2011-06-25
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] Identification of PTCH1 mutations in Japanese Gorlin syndrome patients2011
- Author(s)
  Uchikawa H, Fujii K, Miyashita T, Endo M, Mizuochi H, Kohno Y
- Organizer
  2011 5th Europediatrics
- Place of Presentation
  Vienna, Austria
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] ヘッジホッグと形態形成-Gorlin症候群とPTCH遺伝子変異2009
- Author(s)
  藤井克則
- Organizer
  第33回日本児皮膚科学会
- Place of Presentation
  幕張メッセ国際会議場
- Year and Date
  2009-07-04
- Data Source
  KAKENHI-PROJECT-21591313
[Presentation] 14-3-3 protein detection in cerebellar diseases in children2008
- Author(s)
  藤井克則
- Organizer
  Cordon Research Conference
- Place of Presentation
  Ventula, California, U.S.A
- Year and Date
  2008-02-25
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591143
[Presentation] 14-3-3 protein detection in cerebellar diseases in children2008
- Author(s)
  藤井克則
- Organizer
  Gordon Research Conference
- Place of Presentation
  Ventula,California,U.S.A
- Year and Date
  2008-02-25
- Data Source
  KAKENHI-PROJECT-18591143
[Presentation] Detection of 14-3-3 proteins in cerebellar diseases in children2008
- Author(s)
  Katsunori Fujii
- Organizer
  Gordon Research Conference on Biology of 14-3-3 proteins
- Place of Presentation
  Ventura, CA, U .S. A
- Year and Date
  2008-02-25
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591143
[Presentation] Hedgehog signaling is synergistically enhanced by nutritional deprivation and ligands stimulation in human fibroblasts of Gorlin syndrome
- Author(s)
  Hiromi Mizuochi, Katsunori Fujii, Tadashi Shiohama, Hideki Uchikawa, Toshiyuki Miyashita, Naoki Shimojo
- Organizer
  2015 Hedgehog meeting
- Place of Presentation
  Ann Arbour, Michigan, USA
- Year and Date
  2014-08-04 – 2014-08-08
- Data Source
  KAKENHI-PROJECT-24591502
[Presentation] Oxidative stress-induced JNK1 phosphorylation inhibits hedgehog signaling and osteoblast differentiation
- Author(s)
  Katsunori Fujii, Tadashi Shiohama, Hiromi Mizuochi, Hideki Uchikawa, Tomozumi Takatani, Toshiyuki Miyashita, Yoichi Kohno
- Organizer
  2015 Hedgehog meeting
- Place of Presentation
  Ann Arbour, Michigan, USA
- Year and Date
  2014-08-04 – 2014-08-08
- Data Source
  KAKENHI-PROJECT-24591502
[Presentation] Hedgehog signaling is enhanced by nutritional deprivation in human fibroblasts of Gorlin syndrome
- Author(s)
  Hiromi Mizuochi, Katsunori Fujii, Tadashi Shiohama, Hideki Uchikawa, Naoki Shimojo
- Organizer
  日本小児神経学会学術総会
- Place of Presentation
  Tahoe City, California, USA
- Year and Date
  2014-05-29 – 2014-05-31
- Data Source
  KAKENHI-PROJECT-24591502
[Presentation] コケイン症候群の自験例からの考察した診療管理体制の今後の課題
- Author(s)
  本島敏乃、小俣　卓、杉田克生　藤井克則
- Organizer
  日本小児神経学会
- Place of Presentation
  大分オアシスタワーホテル
- Data Source
  KAKENHI-PROJECT-25282033

1. MIYASHITA Toshiyuki (60174182)

# of Collaborated Projects: 5 results

# of Collaborated Products: 18 results
2. KATO Tetsuya (00224519)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
3. 塩浜直 (10737034)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
4. SUGITA KATSUO (40211304)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
5. KOHNO Yoichi (60161882)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. SHIMOJO Naoki (40221303)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. TOMITA Minako (60344991)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. ISHIWADA Naruhiko (30344980)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. Uchikawa Hideki (80618059)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
10. 島田義也 (10201550)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. 山下修一 (10272296)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. 柿沼志津子 (20392219)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. 野村純 (30252886)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
14. 飯塚正明 (40396669)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. 喜多和子 (80302545)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
16. 梅澤明弘 (70213486)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
17. 長尾和右 (60392487)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
18. KAMEYAMA Kohzoh

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
19. 高山吉永

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

Fujii Katsunori 藤井 克則

FUJII KATSUNORI 藤井 克則

FUJII Katsurnori 藤井 克則

FUJII Katsunori 藤井 克則

Research Projects

Research Products

Co-Researchers

Molecular mechanism of bone metabolism in Gorlin syndromePrincipal Investigator

Principal Investigator

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Identification of hedgehog signal inhibitors in tumorsPrincipal Investigator

Principal Investigator

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Review Section

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The role of hedgehog signaling in personality formation

Principal Investigator

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Hedgehog signaling in human diseasesPrincipal Investigator

Principal Investigator

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Learning program development for ESD based on radiation education and training for science teachers

Principal Investigator

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Hedgehog signaling in murine and humanPrincipal Investigator

Principal Investigator

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Research Institution

Morphogenesis and Carcinogenesis regulated by PTCH1 genePrincipal Investigator

Principal Investigator

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Biology of 14-3 3 proteins regulating neuronal cell deathPrincipal Investigator

Principal Investigator

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Molecular Genetics of Holoprosencephaly

Principal Investigator

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Study on molecular genetics of respiratory syncytial virus bronchiolitis

Principal Investigator

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Molecular mechanisms of tumorigenesis in nevoid basal cell carcinoma syndromePrincipal Investigator

Principal Investigator

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Research Institution

[Book] 「基底細胞母斑症候群」小児科臨床ピクシス17年代別子どもの皮膚疾患2010

Author(s)

Total Pages

Publisher

Data Source

[Journal Article] PTCH1 null induced pluripotent stem cells exclusively differentiate into immature ectodermal cells with large areas of medulloblastoma like tissue2022

Author(s)

Fujii Katsunori 藤井克則

FUJII KATSUNORI 藤井克則

FUJII Katsurnori 藤井克則

FUJII Katsunori 藤井克則