• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

MIYASHITA Toshiyuki  宮下 俊之

ORCIDConnect your ORCID iD *help
… Alternative Names

宮下 俊之  ミヤシタ トシユキ

Less
Researcher Number 60174182
External Links
Affiliation (based on the past Project Information) *help 2022: 北里大学, 医学部, 教授
2007 – 2020: Kitasato University, School of Medicine, Dept. of Molecular Genetics, Professor
2006 – 2007: 国立成育医療センター研究所, 成育遺伝研究部, 遺伝子構造研究室長
2005 – 2006: National Research Institute for Child Health and Development, Dept.of Genetics, Division Head, 成育遺伝研究部, 室長
2004: 国立成育医療センター研究所, 成育遺伝研究部, 室長 … More
2004: National Research Institute for Child Health and Development, Department of Genetics, Head of laboratory for gene analysis, 成育遺伝研究部, 疾患遺伝子構造室長
2003: 国立成育医療センター研究所, 成育遺伝研究部・疾患遺伝子構造研究室長
2003: 国立成育医療センター研究所, 成育遺伝研究部・遺伝子構造研究室, 室長
2002: National Research Institute for Child Health and Development, Dept. of Genetics, Division Head, 研究所・成育遺伝研究部疾患遺伝子構造研究室, 室長
2002: 国立成育医療センター研究所, 成育遺伝研究部・疾患遺伝子構造研究室, 室長
2001: 国立小児病院, (小児医療研究センター)・先天異常研究部・遺伝染色体研究室, 室長
1996 – 2000: 国立小児病院, 小児医療研究センター・先天異常研究部・遺伝染色体研究室, 室長
1998: 国立小児病院, 小児医療研究センター・先天異常研究部・遺伝染色体研究室部長, 室長
1997 – 1998: 国立小児病院, 遺伝染色体研究室, 室長
1995 – 1996: 国立小児病院, 先天異常研究部・遺伝染色体研究室, 室長
1986: 東京大学, 医学部, 助手
1986: 東大, 医学部, 助手 Less
Review Section/Research Field
Principal Investigator
Pediatrics / Pediatrics / Tumor biology
Except Principal Investigator
Pediatrics / Basic Section 52050:Embryonic medicine and pediatrics-related / Embryonic/Neonatal medicine / Pediatrics / Molecular biology / Human genetics
Keywords
Principal Investigator
アポトーシス / グルココルチコイド / apoptosis / glucocorticoid / カスペース / PTCH1 / 母斑基底細胞癌症候群 / 遺伝学 / p53 / NF-κB … More / Bim / 細胞死 / Bax / caspase / Bcl-2 / プロテアーゼ / ミトコンドリア / CRISPR/Cas9 / 髄芽腫 / iPS細胞 / CRISPR/Cas9システム / カスパーゼ / 白血病 / 癌 / 再生医学 / 遺伝子 / CRISPR/Cas9 システム / Gorlin症候群 / Polymorphism / Cerebral Development / Holoprosencephaly / Genetics / 遺伝子多型 / 脳・神経 / 全前脳症 / leukemia / transcription factor / microarray / RNA干渉 / マイクロアレイ / 転写因子 / isoform / caspage / DNAdamage / 選択的スプライシング / CNA損傷 / Fas / アイソフォーム / DNA損傷 / Green Fluorescent protein / Bc1-2 / 共焦点レーザー顕微鏡 / 緑色蛍光蛋白質 / mitochondria / proteolysis / 限定分解 / ラジオイムノアッセイ / リソゾーム酵素 / マンノースリン酸レセプター / I-cell病 / モザイク / LOH / 遺伝子編集 / 歯原性腫瘍 / 癌抑制遺伝子 / 相同組換え / RCAN1 / bcl-2 / c-myc / bax / プロモーター / 転写制御 … More
Except Principal Investigator
基底細胞癌 / ヘッジホッグ / Gorlin症候群 / DRPLA / PTCH1 / 皮膚線維芽細胞 / 髄芽腫 / 基底細胞母斑症候群 / トリプレットリピート / 神経変性疾患 / 遺伝病 / 歯状核赤核淡蒼球ルイ体萎縮症 / アポトーシス / 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 / ゲノム / 遺伝学 / 再生医学 / 脳神経疾患 / シグナル伝達 / 高発癌性疾患 / ゴーリン症候群 / ヘッジホッグシグナル / iPS細胞 / 乳児白血病 / 肝芽細胞 / 肝臓 / サイトカイン / 造血因子 / 胎児造血 / 造血微小環境 / 自然治癒 / 一過性白血病 / 胎児性白血病 / ダウン症候群 / fibroblast / hereditary dominant disease / two-dimensional electrophoresis / 二次元電気泳動法 / 高速液体クロマトグラフィー / 軟骨形成不全症 / 線維芽細胞 / 優性遺伝病 / 二次元電気泳動 / 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 / 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 / dentatorubral-pallidoluysian atrophy / DNA repair / DNA synthesis / neurodegenerative disorder / genetic disease / repetitive sequence / Triplet repeat / 歯状核赤核蒼球ルイ体萎縮症 / DNA修復 / DNA合成 / 反復配列 / プロモーター / ハンチントン舞踏病 / ポリグルタミン / トリプレットリピート伸長病 Less
  • Research Projects

    (19 results)
  • Research Products

    (181 results)
  • Co-Researchers

    (22 People)
  •  Identification of hedgehog signal inhibitors in tumors

    • 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
  •  Investigation of molecular pathogenesis of nevoid basal cell carcinoma syndrome using disease-specific and gene-edited iPSCsPrincipal Investigator

    • Principal Investigator
      Miyashita Toshiyuki
    • Project Period (FY)
      2017 – 2019
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kitasato University
  •  Hedgehog signaling in human diseases

    • 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
  •  The role of hematopoietic microenvironment in the pathogenesis and spontaneous remission of fetal leukemia

    • Principal Investigator
      Miyauchi Jun
    • Project Period (FY)
      2015 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Embryonic/Neonatal medicine
    • Research Institution
      Tokyo Dental College
  •  Basic studies toward CRISPR/Cas9-mediated cell therapyPrincipal Investigator

    • Principal Investigator
      Miyashita Toshiyuki
    • Project Period (FY)
      2014 – 2016
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kitasato University
  •  Dysregulation of hedgehog signaling and tumorigenesisPrincipal Investigator

    • Principal Investigator
      MIYASHITA Toshiyuki
    • Project Period (FY)
      2011 – 2013
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Tumor biology
    • Research Institution
      Kitasato University
  •  Investigation of Molecular Mechanisms of Apoptosis using gene knock-out leukemic cell linesPrincipal Investigator

    • Principal Investigator
      MIYASHITA Toshiyuki
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kitasato University
  •  Biology of 14-3 3 proteins regulating neuronal cell death

    • 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 HoloprosencephalyPrincipal Investigator

    • 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
  •  Analysis of Glucocorticoid Target GenesPrincipal Investigator

    • Principal Investigator
      MIYASHITA Toshiyuki
    • Project Period (FY)
      2003 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      National Research Institute for Child Health and Development
  •  Molecular mechanisms of tumorigenesis in nevoid basal cell carcinoma syndrome

    • 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
  •  Subcellular localization of the proteins implicated in DNA damage-induced cell deathPrincipal Investigator

    • Principal Investigator
      MIYASHITA Toshiyuki
    • Project Period (FY)
      2001 – 2002
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      National Research Institute for Child Health and Development
  •  Analysis of genes that are implicated in glucocorticoid-induced apoptosisPrincipal Investigator

    • Principal Investigator
      MIYASHITA Toshiyuki
    • Project Period (FY)
      1999 – 2000
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      National Children's Medical Research Center
  •  遺伝性神経変性疾患におけるトリプレットリピート伸張

    • Principal Investigator
      YAMADA Masao
    • Project Period (FY)
      1997 – 1998
    • Research Category
      Grant-in-Aid for international Scientific Research
    • Research Field
      Human genetics
    • Research Institution
      National Research Institute for Child Health and Development
  •  Molecular mechanism of glucocorticoid-induced apoptosisPrincipal Investigator

    • Principal Investigator
      MIYASHITA Toshiyuki
    • Project Period (FY)
      1997 – 1998
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      National Children's Hospital
  •  アポトーシスを制御する遺伝子間の転写調節Principal Investigator

    • Principal Investigator
      宮下 俊之
    • Project Period (FY)
      1996
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      National Research Institute for Child Health and Development
  •  Dynamic mutations in genome, like triplet repeat expansion

    • Principal Investigator
      YAMADA Masao
    • Project Period (FY)
      1995 – 1996
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Molecular biology
    • Research Institution
      National Children's Medical Research Center
  •  I-cell病におけるリソゾーム酵素レセプターの研究Principal Investigator

    • Principal Investigator
      宮下 俊之
    • Project Period (FY)
      1986 – 1988
    • Research Category
      Grant-in-Aid for General Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      The University of Tokyo
  •  Development of a screening system for the pathogenesis of hereditary dominant diseases

    • Principal Investigator
      SUZUKI Yoshiyuki
    • Project Period (FY)
      1986 – 1988
    • Research Category
      Grant-in-Aid for Developmental Scientific Research
    • Research Field
      Pediatrics
    • Research Institution
      The Tokyo Metropolitan Institute of Medical Science
      National Center of Neurology and Psychiatry
      The University of Tokyo

All 2022 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2005 2004 2003 Other

All Journal Article Presentation Book

  • [Book] 最新遺伝性腫瘍・家族性腫瘍研究と遺伝カウンセリング2016

    • Author(s)
      宮下俊之、藤井克則
    • Total Pages
      336
    • Publisher
      メディカルドゥ
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Book] Methods in Molecular Biology 12782015

    • Author(s)
      Miyashita, T.
    • Total Pages
      620
    • Publisher
      Humana Press
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Book] Human SOS Biological Science2012

    • Author(s)
      Fujii, K., Suzuki, N., Uchikawa, H., Sugita, K., and Miyashita, T
    • Total Pages
      121
    • Publisher
      Transworld Research Network
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Book] 希少疾患/難病 の診断・治療と製品開発2012

    • Author(s)
      藤井 克則、宮下 俊之
    • Total Pages
      1270
    • Publisher
      技術情報協会
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Book] メディカル・サイエンス・インターナショナル(症例でわかる新臨床遺伝学 水谷修紀 監訳)2008

    • Author(s)
      宮下俊之(分担翻訳)
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Book] 症例でわかる新臨床遺伝学(分担翻訳)2008

    • Author(s)
      Andrew Read宮下 俊之
    • Total Pages
      431
    • Publisher
      メディカル・サイエンス・インターナショナル
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Book] Protein-Protein Interactions Methods and Applications Methods in Molecular Biology Volume #:2612004

    • Author(s)
      Toshiyuki Miyashita
    • Total Pages
      12
    • Publisher
      Humana Press
    • Data Source
      KAKENHI-PROJECT-15390331
  • [Book] Confocal Microscopy for Intracellular Co-Localization of Proteins. In Fu H. (ed.), "Methods in Molecular Biology Vol. 26 : Protein-Protein Interactions : Methods and Applications"2004

    • Author(s)
      Miyashita T
    • Total Pages
      12
    • Publisher
      Humana Press
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15390331
  • [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] A familial case of overgrowth syndrome caused by a 9q22.3 microdeletion in a mother and daughter2020

    • Author(s)
      Yamada Hikari、Shimura Masaru、Takahashi Hidekuni、Nara Shonosuke、Morishima Yasuyuki、Go Soken、Miyashita Toshiyuki、Numabe Hironao、Kawashima Hisashi
    • Journal Title

      European Journal of Medical Genetics

      Volume: 印刷中 Issue: 5 Pages: 103872-103872

    • DOI

      10.1016/j.ejmg.2020.103872

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [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] 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、Toyoda Masashi、Umezawa Akihiro
    • Journal Title

      Aging

      Volume: 印刷中

    • DOI

      10.1101/858555

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [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] Dysregulated DNA methylation of GLA gene was associated with dysfunction of autophagy2019

    • Author(s)
      Hiroko Yanagisawa, Mohammad Arif Hossaina, Takashi Miyajima, KazuakiNagao, Toshiyuki Miyashita, Yoshikatsu Eto
    • Journal Title

      Molecular Genetics and Metabolism

      Volume: 126 Issue: 4 Pages: 460-465

    • DOI

      10.1016/j.ymgme.2019.03.003

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18K07205, KAKENHI-PROJECT-17K10061
  • [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. and Shimojo N.
    • Journal Title

      Journal of Human Genetics

      Volume: 印刷中

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [Journal Article] Gorlin症候群の遺伝子診断2019

    • Author(s)
      宮下俊之、高山吉永
    • Journal Title

      医学のあゆみ

      Volume: 268 Pages: 123-126

    • Data Source
      KAKENHI-PROJECT-16K09960
  • [Journal Article] MicroRNAs profiling in fibroblasts derived from patients with Gorlin syndrome2019

    • Author(s)
      Shiohama Tadashi、Fujii Katsunori、Miyashita Toshiyuki、Takatani Tomozumi、Ikehara Hajime、Uchikawa Hideki、Motojima Toshino、Uchida Tomoko、Shimojo Naoki
    • Journal Title

      Journal of Human Genetics

      Volume: 64 Issue: 8 Pages: 757-765

    • DOI

      10.1038/s10038-019-0607-3

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [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] Gorlin症候群の遺伝子診断2019

    • Author(s)
      宮下俊之、高山吉永
    • Journal Title

      医学のあゆみ

      Volume: 268 Pages: 123-126

    • Data Source
      KAKENHI-PROJECT-17K10061
  • [Journal Article] Recommendations for the Description of Sequence Variants Part 32018

    • Author(s)
      宮下 俊之
    • Journal Title

      JOURNAL OF FAMILIAL TUMORS

      Volume: 18 Issue: 1 Pages: 12-14

    • DOI

      10.18976/jsft.18.1_12

    • NAID

      130007499068

    • ISSN
      1346-1052, 2189-6674
    • Language
      Japanese
    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [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] Brain morphology in children with nevoid basal cell carcinoma syndrome.2017

    • Author(s)
      Shiohama, T., Fuji, K., Miyashita, T., Mizuochi, H., Uchikawa, H., Shimojo, N.
    • Journal Title

      American Journal of Medical Genetics A

      Volume: 173 Issue: 4 Pages: 946-952

    • DOI

      10.1002/ajmg.a.38115

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PROJECT-26461530, KAKENHI-PROJECT-15K20911, KAKENHI-PROJECT-16K09960, KAKENHI-PROJECT-17K10061
  • [Journal Article] The serine 106 residue within the N-terminal transactivation domain is crucial for Oct4 function in mice2017

    • Author(s)
      Mitani A, Fukuda A, Miyashita T, Umezawa A, Akutsu H
    • Journal Title

      zygote

      Volume: 25 Issue: 2 Pages: 197-204

    • DOI

      10.1017/s0967199417000053

    • Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K15716, KAKENHI-PROJECT-17K10061, KAKENHI-PROJECT-17H01588, KAKENHI-PROJECT-15K09729
  • [Journal Article] L-leucine and SPNS1 coordinately ameliorate dysfunction of autophagy in mouse and human Niemann-Pick type C disease.2017

    • Author(s)
      Yanagisawa H, Ishii T, Endo K, Kawakami E, Nagao K, Miyashita T, Akiyama K, Watabe K, Komatsu M, Yamamoto D, Eto Y.
    • Journal Title

      Sci Rep

      Volume: 7 Issue: 1 Pages: 15994-15994

    • DOI

      10.1038/s41598-017-15305-9

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K06763, KAKENHI-PROJECT-17K10061, KAKENHI-PROJECT-17K10067, KAKENHI-PROJECT-17K19371, KAKENHI-PUBLICLY-17H05935, KAKENHI-PLANNED-25111006, KAKENHI-PROJECT-16H06371, KAKENHI-PROJECT-15K09729
  • [Journal Article] Gorlin syndrome with an ovarian leiomyoma associated with a PTCH1 second hit.2016

    • Author(s)
      Akizawa Y, Miyashita T, Sasaki R, Nagata R, Aoki R, Ishitani K, Nagashima Y, Matsui H, Saito K
    • Journal Title

      Am J Med Genet (Part A)

      Volume: 170 Pages: 1029-1034

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Journal Article] Brain morphology in children with nevoid basal cell carcinoma syndrome.2016

    • Author(s)
      Shiohama T, Fuji K, Miyashita T, Mizuochi H, Uchikawa H, Shimojo N
    • Journal Title

      Am J Med Genet (Part A)

      Volume: 173 Pages: 946-952

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Journal Article] Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene.2016

    • Author(s)
      Kato C, Fujii K, Arai Y, Hatsuse H, Nagao K, Takayama Y, Kameyama K, Fujii K, Miyashita T
    • Journal Title

      Fam Cancer

      Volume: 16 Pages: 131-138

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Journal Article] Gorlin syndrome with an ovarian leiomyoma associated with a PTCH1 second hit2016

    • Author(s)
      Akizawa, Y., Miyashita, T., Sasaki, R., Nagata, R., Aoki, R., Ishitani, K., Nagashima, Y., Matsui, H., Saito, K
    • Journal Title

      Am J Med A

      Volume: 170 Issue: 4 Pages: 1029-1034

    • DOI

      10.1002/ajmg.a.37517

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K09729, KAKENHI-PROJECT-26461530, KAKENHI-PROJECT-26460456
  • [Journal Article] A rare case of a symptomatic tumor found in the groin area: An atypical location unexposed to the known causes2015

    • Author(s)
      Toyonaga, E., Hata, H., Nakayama, C., Homma, E., Miyashita, T., Shimizu, H
    • Journal Title

      Case Rep. Oncol

      Volume: 8 Issue: 3 Pages: 536-539

    • DOI

      10.1159/000442148

    • NAID

      120006363266

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K09729, KAKENHI-PROJECT-26461530
  • [Journal Article] Transient abnormal myelopoiesis of extremely immature infant followed by blast cell resurgence two months later: a case study2015

    • Author(s)
      Nomura Y, Miyauchi J, Ota E, Yanai F, Miyashita T, Terui K, Ito E, Hirose S
    • Journal Title

      Jap J Pediatr Hematol/Oncol

      Volume: 52 Pages: 36-39

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Journal Article] Mirror syndrome associated with fetal transient abnormal myelopoiesis in Down syndrome2015

    • Author(s)
      Kobayashi, Y., Miyoshi, T., Matsuyama, T., Miyauchi, J., Miyashita, T., Ishibashi-Ueda, H. and Yoshimatsu, J.
    • Journal Title

      Pathology International

      Volume: 印刷中 Issue: 8 Pages: 443-445

    • DOI

      10.1111/pin.12291

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-26461530, KAKENHI-PROJECT-15K09729, KAKENHI-PROJECT-26461601, KAKENHI-PROJECT-15K19666
  • [Journal Article] PTCH1, PTCH2, SUFU2015

    • Author(s)
      宮下俊之
    • Journal Title

      日本臨牀

      Volume: 73 Pages: 375-379

    • Data Source
      KAKENHI-PROJECT-26461530
  • [Journal Article] Confocal microscopy for intracellular co-localization of proteins2015

    • Author(s)
      Miyashita, T
    • Journal Title

      Methods in Molecular Biology

      Volume: 1278 Pages: 515-526

    • DOI

      10.1007/978-1-4939-2425-7_34

    • ISBN
      9781493924240, 9781493924257
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Journal Article] Chromatin condensation of Xist genomic loci during oogenesis in mice2015

    • Author(s)
      Fukuda, A., Mitani, A., Miyashita, T., Umezawa, A., Akutsu, H
    • Journal Title

      Development

      Volume: 142 Pages: 4049-4055

    • DOI

      10.1242/dev.127308

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K09729, KAKENHI-PROJECT-26461530, KAKENHI-PROJECT-26861350, KAKENHI-PROJECT-25670710, KAKENHI-PROJECT-26293364
  • [Journal Article] PTCH1, PTCH2, SUFU2015

    • Author(s)
      宮下俊之
    • Journal Title

      日本臨牀

      Volume: 増刊号 Pages: 375-379

    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Journal Article] Transient abnormal myelopoiesis of extremely immature infant followed by blast cell resurgence two months later: a case study.2015

    • Author(s)
      Nomura, Y., Miyauchi, J., Ota, E., Yanai, F., Miyashita, T., Terui, K., Ito, E. and Hirose, S.
    • Journal Title

      Jpn. J. Pediatr. Hematol. Oncol.

      Volume: 52 Pages: 36-39

    • Data Source
      KAKENHI-PROJECT-26461530
  • [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 interferon-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., Kita, K., Sugita, K., Imazeki, F., Miyashita, T., Kaneda, A., and Yokosuka, O
    • Journal Title

      Int. J. Oncol

      Volume: 44 Issue: 5 Pages: 1685-1690

    • DOI

      10.3892/ijo.2014.2317

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269, KAKENHI-PROJECT-24510065
  • [Journal Article] Downregulation of microRNA-431 by human interferon-β inhibits viability of medulloblastoma and glioblastoma cells via upregulation of SOCS6.2014

    • Author(s)
      Tanaka.T., Arai, M., Jiang, X., Sugaya, S., Kanda, T., Fujii, K., Kita, K., Sugita, K., Imazeki, F., Miyashita, T., Kaneda, A., and Yokosuka, O.
    • Journal Title

      Int. J. Oncol.

      Volume: 44 Pages: 1685-1690

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] Molecular pathogenesis of keratocystic odontogenic tumors developing in nevoid basal cell carcinoma syndrome2013

    • Author(s)
      Suzuki, M., Nagao, K., Hatsuse, H., Sasaki, R., Saito, K., Fujii, K., and Miyashita, T
    • Journal Title

      Oral Surg. Oral Med. Oral Pathol. Oral Radiol

      Volume: 116 Pages: 348-353

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome2013

    • Author(s)
      Fujii. K., Ohashi, H. ,Suzuki, M., Hatsuse, H., Shiohama, T., Uchikawa, H., and Miyashita, T
    • Journal Title

      Fam. Cancer

      Volume: 12 Pages: 611-614

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [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] Falx cerebri calcification and microphthalmia in Gorlin syndrome2013

    • Author(s)
      Fujita Y., Fujita T., Fujii, K., and Miyashita, T
    • Journal Title

      Neurol. Clin. Neurosci

      Volume: 1 Pages: 88-89

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] Falx cerebri calcification and microphthalmia in Gorlin syndrome.2013

    • Author(s)
      Fujita Y., Fujita T., Fujii, K., and Miyashita, T.
    • Journal Title

      Neurol. Clin. Neurosci.

      Volume: 1 Pages: 88-89

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [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 Issue: 3 Pages: 348-353

    • DOI

      10.1016/j.oooo.2013.06.017

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] Role of FK506 binding protein 5 (FKBP5) in osteoclast differentiation.2013

    • Author(s)
      Kimura, M., Nagai, T., Matsushita. R., Hashimoto. A., Miyashita. T., and Hirohata. S.
    • Journal Title

      Mod. Rheumatol.

      Volume: 23 Pages: 1133-1139

    • DOI

      10.1007/s10165-012-0809-4

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269, KAKENHI-PROJECT-23591447
  • [Journal Article] Selective haploinsufficiency of longer isoforms of PTCH1 protein can cause nevoid basal cell carcinoma syndrome2012

    • Author(s)
      Suzuki, M., Hatsuse, H., Nagao, K., Takayama, Y., Kameyama, K., Kabasawa, Y., Omura, K., Yoshida, M., Fujii, K., and Miyashita, T
    • Journal Title

      J. Hum. Genet

      Volume: 57 Pages: 422-426

    • NAID

      10030965596

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] Selective haploinsufficiency of longer isoforms of PTCH1 protein can cause nevoid basal cell carcinoma syndrome2012

    • Author(s)
      Suzuki, M., Hatsuse, H., Nagao, K., Takayama, Y., Kameyama, K., Kabasawa, Y., Omura, K., Yoshida, M., Fujii, K., and Miyashita, T.
    • Journal Title

      J. Hum. Genet.

      Volume: 57 Issue: 7 Pages: 422-426

    • DOI

      10.1038/jhg.2012.45

    • NAID

      10030965596

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] Splicing aberration in nevoid basal cell nevus syndrome2012

    • Author(s)
      Ishitsuka, Y., Furuta, J., Miyashita, T., and Otsuka, F
    • Journal Title

      Acta Derm. Venereol

      Volume: 92 Pages: 619-620

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] Heterozygous Tandem Duplication Within the PTCH1 Gene Results in Nevoid Basal Cell Carcinoma Syndrome2012

    • Author(s)
      Kosaki, R., Nagao, K., Kameyama, K., Suzuki, M., Fujii, K., and Miyashita T
    • Journal Title

      Am. J. Med. Genet A

      Volume: 158A Pages: 1724-1728

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] Heterozygous Tandem Duplication Within the PTCH1 Gene Results in Nevoid Basal Cell Carcinoma Syndrome2012

    • Author(s)
      Kosaki, R., Nagao, K., Kameyama, K., Suzuki, M., Fujii, K., and Miyashita T.
    • Journal Title

      Am. J. Med. Genet. A

      Volume: 158A Issue: 7 Pages: 1724-1728

    • DOI

      10.1002/ajmg.a.35412

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] Splicing aberration in nevoid basal cell nevus syndrome2012

    • Author(s)
      Ishitsuka, Y., Furuta, J., Miyashita, T.
    • Journal Title

      Acta Derm. Venereol.

      Volume: 92 Issue: 6 Pages: 619-620

    • DOI

      10.2340/00015555-1332

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation2012

    • Author(s)
      Kijima C., Miyashita T., Suzuki M., Oka H., and Fujii K
    • Journal Title

      Fam. Cancer

      Volume: 11 Pages: 565-570

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [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] 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., and Miyashita, T
    • Journal Title

      Am. J. Med. Genet A

      Volume: 158A Pages: 351-357

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [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., and Miyashita, T.
    • Journal Title

      American Journal of Medical Genetics A

      Volume: 158A Pages: 351-357

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] RCAN1 is an important mediator of glucocorticoid-induced apoptosis in human leukemic cells2012

    • Author(s)
      Nagao, K., Iwai Y., and Miyashita T.
    • Journal Title

      PLOS ONE

      Volume: 7 Issue: 11 Pages: e49926-e49926

    • DOI

      10.1371/journal.pone.0049926

    • Peer Reviewed
    • Data Source
      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
    • Journal Title

      家族性腫瘍

      Volume: 11 Pages: 14-18

    • NAID

      130007529694

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [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. and Miyashita, T.
    • Journal Title

      Clinical Genetics

      Volume: 79 Issue: 2 Pages: 196-198

    • DOI

      10.1111/j.1399-0004.2010.01527.x

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] Entire PTCH1 deletion is a common event in point mutation-negative cases with nevoid basal cell carcinoma syndrome in Japan.2011

    • Author(s)
      Miyashita, T.
    • Journal Title

      Clin.Genet.

      Volume: 79 Pages: 196-198

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] Entire PTCH1 deletion is a common event in point mutation-negative cases with nevoid basal cell carcinoma syndrome in Japan.2011

    • Author(s)
      Nagao K., Fujii K., Saito K., Sugita K., Endo M., Motojima T., Hatsuse H., Miyashita T.
    • Journal Title

      Clin.Genet. 79

      Pages: 196-198

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [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、齋藤加代子、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

    • Data Source
      KAKENHI-PROJECT-23501269
  • [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. and Miyashita, T
    • Journal Title

      Clin. Genet

      Volume: 79 Pages: 196-198

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Journal Article] Blasts in transient leukemia in neonates with Down syndrome differentiate into basophil/mast-cell and megakaryocyte lineages in vitro in association with down-regulation of truncated form of GATA1.2010

    • Author(s)
      Miyauchi J., Ito Y., Tsukamoto K., Takahashi H., Ishikura K., Sugita K., Miyashita T.
    • Journal Title

      Brit.J.Haematol. 148

      Pages: 898-909

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] Multiple keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome having distinct PTCH1 mutations : a case report.2010

    • Author(s)
      Miyashita, T.
    • Journal Title

      Oral Surg.Oral Med.Oral Pathol.Oral Radiol.Endod.

      Volume: 110

    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] ヘッジホッグと形態形成-Gorlin症候群とPTCH遺伝子変異-2010

    • 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-20591261
  • [Journal Article] グルココルチコイド受容体2010

    • Author(s)
      宮下俊之
    • Journal Title

      日本薬理学会誌 135

      Pages: 117-118

    • NAID

      10026334909

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] Blasts in transient leukemia in neonates with Down syndrome differentiate into basophil/mast-cell and megakaryocyte lineages in vitro in association with down-regulation of truncated form of GATAl.2010

    • Author(s)
      Miyashita, T.
    • Journal Title

      Brit.J.Haematol. 148

      Pages: 898-909

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] Multiple keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome having distinct PTCH1 mutations : a case report.2010

    • Author(s)
      Sasaki R., Miyashita T., Matsumoto N., Fujii K., Saito K., Ando T.
    • Journal Title

      Oral Surg.Oral Med.Oral Pathol.Oral Radiol.Endod. 110

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [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-20591261
  • [Journal Article] EYA4, Deleted in a case with middle interhemispheric variant of holoprosencephaly, interacts with SIX3 both physically and functionally.2009

    • Author(s)
      Abe Y., Oka A., Mizuguchi M., Igarashi T., Ishikawa S., Aburatani H., Yokoyama S., Asahara H., Nagao K., Yamada M., Miyashita T.
    • Journal Title

      Hum.Mutat. 30

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] Nevoid basal cell carcinoma syndrome with cleft lip and palate associated with the novel PTCH gene mutations.2009

    • Author(s)
      Sasaki R., Saito K., Watanabe Y., Miyashita T., Fujii K., Agawa K., Takayama Y., Ando T., Akizuki, T.
    • Journal Title

      J.Hum.Genet. 54

      Pages: 398-402

    • NAID

      10030731005

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] Nevoid basal cell carcinoma syndrome with cleft lip and palate associated with the novel PTCH gene mutations.2009

    • Author(s)
      Miyashita, T.
    • Journal Title

      J.Hum.Genet. 54

      Pages: 398-402

    • NAID

      10030731005

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [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,他
    • Journal Title

      脳と発達 41

      Pages: 259-263

    • NAID

      10024846313

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [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,他
    • Journal Title

      脳と発達 41

      Pages: 253-257

    • NAID

      10024846296

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] EYA4, deleted in a case with middle interhemispheric variant of holoprosencephaly, interacts with SIX3 both physically and functionally.2009

    • Author(s)
      Miyashita, T.
    • Journal Title

      Hum.Mutat. 30

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] ステロイドの抗腫瘍作用マイクロアレイを用いた作用機序の解析2008

    • Author(s)
      宮下俊之,押田忠弘
    • Journal Title

      日本臨床 66

      Pages: 89-93

    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] Patchedl haploinsufficiency increases adult bone mass and modulates Gli3 repressor activity.2008

    • Author(s)
      Ohba S, Miyashita T
    • Journal Title

      Dev. Cell 14

      Pages: 689-699

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] Anti-tumor activities of steroids - lessons from microarray analysis2008

    • Author(s)
      Miyashita, T., et. al.
    • Journal Title

      Nippon Rinsho 66

      Pages: 89-93

    • NAID

      40015772102

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18591177
  • [Journal Article] Patched1 haploinsufficiency increases adult bone mass and modulates Gli3 repressor activity.2008

    • Author(s)
      Ohba S., Kawaguchi H., Kugimiya F., Ogasawara T., Kawamura N., Saito T., Ikeda T., Fujii K., Miyajima T., Kuramochi A., Miyashita T., Oda H., Nakamura K., Takato T., Chung, U.I.
    • Journal Title

      Dev.Cell 14

      Pages: 689-699

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] ステロイドの抗腫瘍作用-マイクロアレイを用いた作用機序の解析-2008

    • Author(s)
      宮下 俊之
    • Journal Title

      日本臨床 66

      Pages: 89-93

    • Data Source
      KAKENHI-PROJECT-20591261
  • [Journal Article] ステロイドの抗腫瘍作用-マイクロアレイを用いた作用機序の解析-2008

    • Author(s)
      宮下 俊之
    • Journal Title

      日本臨床 66

      Pages: 89-93

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18591177
  • [Journal Article] Spectrum of mutations in the tumor-suppressor gene, PATCHED-1,in patients with nevoid basal cell carcinoma syndrome2007

    • Author(s)
      Miyashita, T.
    • Journal Title

      Neuro-oncol 9

      Pages: 183-183

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18591177
  • [Journal Article] Patched-1遺伝子と母斑基底細胞癌症候群.2007

    • Author(s)
      宮下 俊之
    • Journal Title

      家族性腫瘍 34

      Pages: 97-101

    • NAID

      130007534760

    • Data Source
      KAKENHI-PROJECT-18591177
  • [Journal Article] Patched-1 and Nevoid Basal Cell Carcinoma Syndrome2007

    • Author(s)
      Miyashita, T., et. al.
    • Journal Title

      Journal of Familial Tumor 7

      Pages: 97-101

    • NAID

      130007534760

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18591177
  • [Journal Article] Spectrum of mutations in the tumor-suppressor gene, PATCHED-1, in patients with nevoid basal cell carcinoma syndrome2007

    • Author(s)
      Miyashita, T., et. al.
    • Journal Title

      Neuro-oncol 9

      Pages: 183-183

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18591177
  • [Journal Article] Pached-1遺伝子と母斑基底細胞癌症候群2007

    • Author(s)
      宮下 俊之
    • Journal Title

      家族性腫瘍 7

      Pages: 97-101

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18591177
  • [Journal Article] Spectrum of mutations in the tumor-suppressor gene,PATCHED-1,in patients with nevoid basal cell carcinoma syndrome.2007

    • Author(s)
      Miyashita, T.
    • Journal Title

      Neuro-oncol. 9

      Pages: 183-183

    • Data Source
      KAKENHI-PROJECT-18591177
  • [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] Confocal Microscopy for Intracellular Co-Localization of Proteins.2004

    • Author(s)
      Miyashita T.
    • Journal Title

      Methods in Molecular Biology : Protein-Protein Interactions : Methods and Applications(Fu H.(ed.))(Humana Press, Totowa, USA) Vol.261

      Pages: 399-410

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15390331
  • [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
  • [Presentation] ヘッジホッグシグナル伝達の亢進と疾患2020

    • Author(s)
      宮下 俊之
    • Organizer
      お茶の水がん学アカデミア第161 回集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [Presentation] ヘッジホッグ異常症のiPS細胞とゲノム編集2019

    • Author(s)
      宮下 俊之
    • Organizer
      第61回日本小児神経学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [Presentation] PTCH1遺伝子の全欠失を伴うGorlin症候群(9q22.3微細欠失)の親子例2019

    • Author(s)
      志村優、山田ひかり、長谷川里奈、高橋英城、奈良昇乃助、森島靖行、呉宗憲、宮下俊之、沼部博直、河島尚志
    • Organizer
      第122回日本小児科学会学術集会
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [Presentation] Generation of iPSC cells as a model for NBCCS by using CRISPR/Cas9 system2018

    • Author(s)
      長尾 和右、加藤 千勢、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77回日本癌学会学術総会
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [Presentation] ゲノム編集を行った母斑基底細胞癌症候群由来iPS細胞の細胞生物学的特性の解析2018

    • Author(s)
      宮下 俊之、長尾 和右、藤井克則
    • Organizer
      第24回日本家族性腫瘍学会学術集会
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [Presentation] マウスのインプリンティング型X染色体不活化においてRNF12はREX1の抑制によって父由来non-coding RNA Tsix を抑制する2018

    • Author(s)
      中村 茜里、福田 篤、阿久津 英憲、宮下 俊之
    • Organizer
      第41回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [Presentation] 母斑基底細胞癌症候群患者由来細胞を用いた腫瘍の作製2018

    • Author(s)
      長尾 和右、加藤 千勢、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41回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [Presentation] 母斑基底細胞がん症候群(NBCCS)の責任遺伝子に見られる遺伝子変異解析2018

    • Author(s)
      高山 吉永、初瀬 洋美、長尾 和右、亀山 孝三、藤井克則、宮下 俊之
    • Organizer
      第50回 日本臨床分子形態学会総会・学術集会
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [Presentation] 次世代シークエンサーを用いたGorlin症候群患者に発症した各種腫瘍の遺伝子解析2018

    • Author(s)
      兼友裕大、高山吉永、初瀬洋美、藤谷和子、長尾 和右、亀山 孝三、宮下 俊之
    • Organizer
      第41回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-16K09960
  • [Presentation] 次世代シークエンサーを用いたGorlin症候群患者に発症した各種腫瘍の遺伝子解析2018

    • Author(s)
      兼友裕大、高山吉永、初瀬洋美、藤谷和子、長尾 和右、亀山 孝三、宮下 俊之
    • Organizer
      第41回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [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-15K09729
  • [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回小児神経学会総会
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [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回小児神経学会総会
    • Data Source
      KAKENHI-PROJECT-17K10061
  • [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-17K10061
  • [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] 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-17K10061
  • [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-15K09729
  • [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-17K10061
  • [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] 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-15K09729
  • [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] 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-17K10061
  • [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] 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-15K09729
  • [Presentation] 角化嚢胞性歯原性腫瘍を合併したB前駆細胞型急性リンパ性白血病の一例2016

    • Author(s)
      渡邊敦、杣津晋平、大城浩子、赤羽弘資、合井久美子、犬飼岳史、藤井克則、宮下俊之、杉田完爾
    • Organizer
      第58回日本小児血液・がん学会学術集会
    • Place of Presentation
      品川プリンスホテル(東京都港区)
    • Year and Date
      2016-12-15
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Presentation] Entire PTCH1 deletions detected in 9 families with nevoid basal cell carcinoma syndrome2016

    • Author(s)
      高山吉永、長尾一右、藤井克則、宮下俊之
    • Organizer
      第75回日本癌学会学術総会
    • Place of Presentation
      パシフィコ横浜(横浜市)
    • Year and Date
      2016-10-06
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Presentation] Entire PTCH1 deletions detected in 9 families with nevoid basal cell carcinoma syndrome2016

    • Author(s)
      高山吉永、長尾一右、藤井克則、宮下俊之
    • Organizer
      第75回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2016-10-06
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Presentation] Gorlin症候群における脳形態解析-ヘッジホッグシグナルのヒト脳への影響-2016

    • Author(s)
      塩浜直、藤井克則、宮下俊之、内川英紀、水落弘美、池原甫、福原知之、下条直樹
    • Organizer
      第58回日本小児神経学会学術集会
    • Place of Presentation
      京王プラザホテル(東京都新宿区)
    • Year and Date
      2016-06-03
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Presentation] 多発する手掌の小陥凹を契機に発見されたGorlin症候群の1例2016

    • Author(s)
      大橋洋之、武内聡美、北澤智子、村上富美子、宮下俊之
    • Organizer
      第870回日本皮膚科学会東京地方会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Presentation] Gorlin症候群患者由来iPS細胞を用いた髄芽腫の作製2016

    • Author(s)
      池本 優、豊田 雅士、那須 道世、初瀬 洋美、長尾 和右、高山 吉永、亀山 孝三、梅澤 明弘、宮下 俊之
    • Organizer
      第39回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜(横浜市)
    • Year and Date
      2016-11-30
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Presentation] 母斑基底細胞癌症候群におけるスプライシング変異の検討2016

    • Author(s)
      宮下俊之、藤井克則
    • Organizer
      第22回日本家族性腫瘍学会学術集会
    • Place of Presentation
      ひめぎんホール(愛媛県松山市)
    • Year and Date
      2016-06-03
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Presentation] 角化嚢胞性歯原性腫瘍を合併したB前駆細胞型急性リンパ性白血病の一例2016

    • Author(s)
      渡邊敦、杣津晋平、大城浩子、赤羽弘資、合井久美子、犬飼岳史、藤井克則、宮下俊之、杉田完爾
    • Organizer
      第58回日本小児血液・がん学会学術集会
    • Place of Presentation
      東京
    • Year and Date
      2016-12-15
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Presentation] Gorlin症候群における脳形態解析-ヘッジホッグシグナルのヒト脳への影響-2016

    • Author(s)
      塩浜直、藤井克則、宮下俊之、内川英紀、水落弘美、池原甫、福原知之、下条直樹
    • Organizer
      第58回日本小児神経学会学術集会
    • Place of Presentation
      東京
    • Year and Date
      2016-06-03
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Presentation] マウス初期杯におけるOct4の機能解析2015

    • Author(s)
      三谷温、宮下俊之、阿久津英憲
    • Organizer
      第28回北里大学バイオサイエンスフォーラム
    • Place of Presentation
      相模原市
    • Year and Date
      2015-08-06
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Presentation] CRISPR/Cas9システムを用いた広域欠損ゲノムを有する細胞株の作製2015

    • Author(s)
      加藤千勢、高山吉永、亀山孝三、初瀬洋美、長尾和右、宮下俊之
    • Organizer
      第28回北里大学バイオサイエンスフォーラム
    • Place of Presentation
      相模原市
    • Year and Date
      2015-08-06
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Presentation] Establishment of the cell lines with a large genomic deletion by CRISPR/Cas9 system2015

    • Author(s)
      長尾和右、高山吉永、宮下俊之
    • Organizer
      第74回日本癌学会学術総会
    • Place of Presentation
      名古屋市
    • Year and Date
      2015-10-08
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Presentation] Establishment of the cell lines with a large genomic deletion by CRISPR/Cas9 system.2015

    • Author(s)
      長尾和右、高山吉永、宮下俊之
    • 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
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Presentation] CRISPR/Cas9システムを用いた2点同時切断による目的ゲノム領域除去細胞株の作製2015

    • Author(s)
      加藤千勢、長尾和右、初瀬洋美、高山吉永、亀山孝三、宮下俊之
    • Organizer
      第38回日本分子生物学会年会
    • Place of Presentation
      神戸市
    • Year and Date
      2015-12-01
    • Data Source
      KAKENHI-PROJECT-15K09729
  • [Presentation] CRISPR/Cas9システムを用いた2点同時切断による目的ゲノム領域除去細胞株の作製2015

    • Author(s)
      加藤千勢、長尾和右、初瀬洋美、高山吉永、亀山孝三、宮下俊之
    • Organizer
      第38回日本分子生物学会年会
    • Place of Presentation
      神戸国際会議場(兵庫県神戸市)
    • Year and Date
      2015-12-01
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Presentation] Functional analysis of a sonic hedgehog signaling pathway inhibitor SUFU2013

    • Author(s)
      長尾和右、宮下俊之
    • Organizer
      第72回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] PTCH2とSUFU遺伝子に配偶子変異をもつ母斑基底細胞癌症候群の検討2012

    • Author(s)
      鈴木麻衣子、長尾和右、高山吉永、岡秀宏、藤井克則、宮下俊之
    • Organizer
      第71回日本癌学会学術総会
    • Place of Presentation
      札幌
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] 母斑基底細胞癌症候群で見出されたスプライシング変異と異常mRNA の分解2012

    • Author(s)
      志村将人、鈴木麻衣子、初瀬洋美、長尾和右、高山吉永、亀山孝三、藤井克則、宮下俊之
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] Suppressor of fused (SUFU)遺伝子の配偶子変異は高い髄芽腫の発症リスクをもたらす2012

    • Author(s)
      鈴木麻衣子、宮下俊之、木島千尋、岡秀宏、藤井清孝
    • Organizer
      第16回日本家族性腫瘍学会学術集会
    • Place of Presentation
      大阪
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] PTCH2とSUFU 遺伝子に配偶子変異をもつ母斑基底細胞癌症候群の検討2012

    • Author(s)
      鈴木麻衣子、長尾和右、高山吉永、岡秀宏、藤井克則、宮下俊之
    • Organizer
      第71回日本癌学会学術総会
    • Place of Presentation
      札幌
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] Gorlin症候群の遺伝子解析2012

    • Author(s)
      宮下俊之
    • Organizer
      厚生労働科学研究費補助金 難治性疾患克服研究事業(招待講演)
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] 母斑基底細胞癌症候群で見出されたスプライシング変異と異常mRNAの分解2012

    • Author(s)
      志村将人、鈴木麻衣子、初瀬洋美、長尾和右、高山吉永、亀山孝三、藤井克則、宮下俊之
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡
    • Data Source
      KAKENHI-PROJECT-23501269
  • [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
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] 母斑基底細胞癌症候群に発症した歯原性腫瘍の遺伝子解析2011

    • Author(s)
      宮下俊之、桐生麻衣子、佐々木亮、齋藤加代子、藤井克則
    • Organizer
      家族性腫瘍学会
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-23501269
  • [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
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] 母斑基底細胞癌症候群の分子遺伝学2011

    • Author(s)
      宮下俊之
    • Organizer
      第56回日本人類遺伝学会(招待講演)
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] 母斑基底細胞癌症候群に発症した角化嚢胞性歯原性腫瘍の発症機序の解析2011

    • Author(s)
      鈴木麻衣子、長尾和右、高山吉永、亀山孝三、藤井克則、宮下俊之
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] 母斑基底細胞癌症候群の分子遺伝学2011

    • Author(s)
      宮下俊之
    • Organizer
      第56回日本人類遺伝学会・第11回東アジア人類遺伝学会共同大会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] 母斑基底細胞癌症候群に発症した歯原性腫瘍の遺伝子解析2011

    • Author(s)
      宮下俊之、桐生麻衣子、佐々木亮、齋藤加代子、藤井克則
    • Organizer
      遺伝医学合同学術集会
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation]2010

    • Author(s)
      宮下俊之,遠藤真美子,齋藤加代子,杉田克生,藤井克則
    • Organizer
      第16回日本家族性腫瘍学会学術集会
    • Place of Presentation
      新潟
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] ヒトPatched1(PTCH1)レセプターに対して作製したマウスモノクロナル抗体の評価2010

    • Author(s)
      高山吉永,志村将人,桐生麻衣子,長尾和右,亀山孝三,宮下俊之
    • Organizer
      第33回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] 母斑基底細胞癌症候群症例の16%がPTCH1遺伝子の全欠失によって発症する2010

    • Author(s)
      宮下俊之
    • Organizer
      第33回日本分子生物学会年会
    • Place of Presentation
      神戸国際会議場(兵庫県)
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] ヘッジホッグシグナル伝達経路に抑制的に働く抗PTCH1マウスモノクロナル抗体の作製2010

    • Author(s)
      高山吉永,長尾和右,桐生麻衣子,宮下俊之
    • Organizer
      第69回日本癌学会学術総会
    • Place of Presentation
      大阪
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] 日本人母斑基底細胞癌症候群の16%はPTCH1遺伝子の片アレル欠損で発症する2010

    • Author(s)
      宮下俊之,長尾和右,遠藤真美子,本島敏乃,齋藤加代子,杉田克生,藤井克則
    • Organizer
      第16回日本家族性腫瘍学会学術集会
    • Place of Presentation
      新潟
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] 母斑基底細胞癌症候群症例の16%がPTCH1遺伝子の全欠失によって発症する2010

    • Author(s)
      長尾和右,高山吉永,亀山孝三,宮下俊之
    • Organizer
      第33回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] 母斑基底細胞癌症候群の約16%がPTCH1遺伝子全欠損で発症する2010

    • Author(s)
      長尾和右,桐生麻衣子,高山吉永,宮下俊之
    • Organizer
      第69回日本癌学会学術総会
    • Place of Presentation
      大阪
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] 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2010

    • Author(s)
      宮下俊之
    • Organizer
      第16回日本家族性腫瘍学会学術集会
    • Place of Presentation
      朱鷺メッセ(新潟県)
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] ヘッジホッグシグナル伝達経路に抑制的に働く抗PTCH1マウスモノクロナル抗体の作製2010

    • Author(s)
      宮下俊之
    • Organizer
      第69回日本癌学会学術総会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] FKBP5ノックアウト白血病細胞株を用いたグルココルチコイドによるアポトーシス誘導機序の解析2009

    • Author(s)
      長尾和右、宮下俊之
    • Organizer
      第32回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] FKBP5ノックアウト細胞株を用いたアポトーシス誘導機序の解析2009

    • Author(s)
      長尾和右、山田正夫、宮下俊之
    • Organizer
      第68回日本癌学会総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] 多発性顎嚢胞を契機に診断したPTCH遺伝子異常を伴った基底細胞母斑症候群2009

    • Author(s)
      佐々木亮、齋藤加代子、宮下俊之、渡辺頼勝、藤井克則、阿川かおり、高山吉永、秋月種高、安藤智博
    • Organizer
      第15回日本家族性腫瘍学会学術集会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] 6番染色体長腕に欠損を認めた全前脳胞症亜型における原因遺伝子についての検討2009

    • Author(s)
      阿部裕一、島田隆史、古山晶子、星野英紀、久保田雅也、宮下俊之、岡明
    • Organizer
      第51回日本小児神経学会総会
    • Place of Presentation
      米子
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] PTCH1遺伝子領域を含むゲノム欠損による母斑基底細胞癌症候群3例の解析2008

    • Author(s)
      宮下俊之、藤井克則
    • Organizer
      第14回日本家族性腫瘍学会学術集会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] Nevoid basal cell careinoma syndrome with cleft lip and palate associated with mutation of the PTCH gene : report of two cases2008

    • Author(s)
      Sasaki R, Miyashita T
    • Organizer
      XIX Congress of the European Association for Cranio-MaXillo-Facial Surgery
    • Place of Presentation
      Bologna, Italy
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] 全前脳症原因候補遺伝子としてのEYA4に関する検討2008

    • Author(s)
      阿部裕一, 宮下 俊之
    • Organizer
      第31回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] 全前脳症原因候補遺伝子としてのEYA4に関する検討2008

    • Author(s)
      阿部裕一、石川俊平、油谷浩幸、横山成俊、浅原弘嗣、山田正夫、岡明、五十嵐隆、宮下俊之
    • Organizer
      第31回日本分子生物学会年会・第80回日本生化学会大会合同大会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-20591261
  • [Presentation] Rapid identification of deletion breakpoints using high resolution oligonucleotide microarrays2007

    • Author(s)
      Miyashita, T., et. al.
    • Organizer
      Annual Meeting, the Molecular Biology Society of Japan
    • Place of Presentation
      Yokohama
    • Year and Date
      2007-12-13
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18591177
  • [Presentation] 高密度オリゴヌクレオチドマイクロアレイを用いた遺伝子欠損の解析と切断点の迅速決定2007

    • Author(s)
      宮下 俊之
    • Organizer
      第30回日本分子生物学会年会
    • Place of Presentation
      横浜市
    • Year and Date
      2007-12-13
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18591177
  • [Presentation] Gorlin症候群におけるPTCH2変異の同定

    • Author(s)
      藤井克則、大橋博文、内川英紀、塩浜直、宮下俊之
    • Organizer
      第25回千葉県小児神経懇話会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] Oxidative stress-induced JNK1 phosphorylation inhibits hedgehog signaling and osteoblast differentiation

    • Author(s)
      Fujii, K., Shiohama, T., Mizuochi, H., Uchikawa, H., Takatani, T., Kohno, Y. and Miyashita, T
    • Organizer
      Hedgehog 2014
    • Place of Presentation
      Ann Arbor, USA
    • Year and Date
      2014-08-04 – 2014-08-08
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Presentation] CRISPR/Cas9システムを用いた広域欠損ゲノムを有する細胞株の作製

    • Author(s)
      長尾和右 加藤千勢 初瀬洋美 高山吉永 亀山孝三 宮下俊之
    • 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-26461530
  • [Presentation] PTCH1遺伝子以外の遺伝子変異によって発症する母斑基底細胞癌症候群 ―多遺伝子1症候群?―

    • Author(s)
      宮下俊之、鈴木麻衣子、長尾和右、初瀬弘美、藤井克則
    • Organizer
      第17回日本家族性腫瘍学会学術集会
    • Place of Presentation
      別府
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] 母斑基底細胞癌症候群に発症した腫瘍の遺伝子解析

    • Author(s)
      宮下俊之 藤井克則
    • Organizer
      第20回日本家族性腫瘍学会学術集会
    • Place of Presentation
      コラッセふくしま(福島県福島市)
    • Year and Date
      2014-06-13 – 2014-06-14
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Presentation] CRISPR/Cas9システムを用いたソニックヘッジホッグシグナル伝達系構成遺伝子ノックアウト細胞株の作製

    • Author(s)
      長尾和右 高山吉永 宮下俊之
    • Organizer
      第73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
      2014-09-25 – 2014-09-27
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Presentation] CRISPR/Cas9システムを用いたヘッジホッグシグナル伝達系構成遺伝子ノックアウト細胞株の作製

    • Author(s)
      長尾和右、遠藤葉月、加藤千勢、初瀬洋美、高山吉永、亀山孝三、宮下俊之
    • Organizer
      第36回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] 卵巣腫瘍においてPTCH1遺伝子の セカンドヒットを同定したGorlin症候群の1例

    • Author(s)
      秋澤叔香 宮下俊之 佐々木亮 浦野真理 佐藤裕子 青木亮子 石谷健 山内あけみ 松井英雄 齋藤加代子
    • Organizer
      日本人類遺伝学会第59回大会
    • Place of Presentation
      タワーホール船堀(東京都江戸川区)
    • Year and Date
      2014-11-19 – 2014-11-22
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Presentation] グルココルチコイド誘導性アポトーシスの解析

    • Author(s)
      岩井祐二郎、高山吉永、亀山孝三、初瀬洋美、長尾和右、宮下俊之
    • Organizer
      第26回北里大学バイオサイエンスフォーラム
    • Place of Presentation
      相模原
    • Data Source
      KAKENHI-PROJECT-23501269
  • [Presentation] CRISPR/Cas9システムを用いたSNPジェノタイプ転換の試み

    • Author(s)
      高山吉永 初瀬洋美 中島早耶 鈴木香織 加藤千勢 長尾和右 亀山孝三 宮下俊之
    • 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-26461530
  • [Presentation] CRISPR/Cas9システムによる欠失導入効率の検討

    • Author(s)
      加藤千勢 高山吉永 亀山孝三 初瀬洋美 長尾和右 宮下俊之
    • Organizer
      第27回北里大学バイオサイエンスフォーラム
    • Place of Presentation
      北里大学(神奈川県相模原市)
    • Year and Date
      2014-08-21 – 2014-08-22
    • Data Source
      KAKENHI-PROJECT-26461530
  • [Presentation] Hedgehog signaling is synergistically enhanced by nutritional deprivation and ligands stimulation in human fibroblasts of Gorlin syndrome

    • Author(s)
      Mizuochi, H., Fujii, K., Shiohama, T., Uchikawa, H., Miyashita, T. and Shimojo, N
    • Organizer
      Hedgehog 2014
    • Place of Presentation
      Ann Arbor, USA
    • Year and Date
      2014-08-04 – 2014-08-08
    • Data Source
      KAKENHI-PROJECT-26461530
  • 1.  FUJII Katsunori (70344992)
    # of Collaborated Projects: 5 results
    # of Collaborated Products: 17 results
  • 2.  YAMADA Masao (40124218)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 3.  KAMEYAMA Kohzoh (40214556)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 16 results
  • 4.  NAGAO Kazuaki (60392487)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 30 results
  • 5.  SAKAKIHARA Yoich (10143463)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 6.  SUZUKI Yoshiyuki (90010389)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 7.  OKUYAMA Torayuki (40177192)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 8.  Miyauchi Jun (20146707)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 1 results
  • 9.  TAKAYAMA Yoshinaga (90245407)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 10 results
  • 10.  TADOKORO Keiko (00236564)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 11.  OSHIMA Akihiro (20203763)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 12.  SAKURABA Hitoshi (60114493)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 13.  床枝 康伸 (10172157)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 14.  大村 清 (70047348)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 15.  川口 裕之 (00313130)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 16.  梅澤 明弘 (70213486)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 17.  塩浜 直 (10737034)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 18.  POTTER Nich
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 19.  BURKE James
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 20.  POTTER Nicho
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 21.  AKUTSU Hidenori
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 22.  渡部 和彦
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

URL: 

Are you sure that you want to link your ORCID iD to your KAKEN Researcher profile?
* This action can be performed only by the researcher himself/herself who is listed on the KAKEN Researcher’s page. Are you sure that this KAKEN Researcher’s page is your page?

この研究者とORCID iDの連携を行いますか?
※ この処理は、研究者本人だけが実行できます。

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi