HAYASAKA Kiyoshi 早坂清

… Alternative Names

早坂清ハヤサカキヨシ

Less

Researcher Number	20142961
Other IDs
External Links
Affiliation (Current)	2025: 山形大学, 医学部, 名誉教授
Affiliation (based on the past Project Information) *help	2014 – 2020: 山形大学, 医学部, 名誉教授 2015: 山形大学, 医学部, 教授 2009 – 2013: Yamagata University, 医学部, 教授 2002 – 2007: 山形大学, 医学部, 教授 2005: Yamagata Univertisy, Pediatrics, Professor, 医学部発達生体崩御学講座小児医学化学分野, 教授 … More 2005: 山形大学, 医学部発達生体崩御学講座小児医科学分野, 教授 2004: 山形大学, 医学部発達生体防御学講座小児医科学分野, 教授 1994 – 2000: 山形大学, 医学部, 教授 1994 – 1995: 山形大, 医学部, 教授 1992: 秋田大学, 医学部, 講師 Less
Review Section/Research Field	Principal Investigator Pediatrics / Pediatrics Except Principal Investigator Pediatrics / Embryonic/Neonatal medicine / Experimental pathology / Neurology / General physiology / 広領域
Keywords	Principal Investigator Charcot-Marie-Tooth病 / 遺伝性ニューロパチー / PRX / Charcot-Marie-Tooth disease / sodium channel / MLPA / DHPLC / denaturing high performance liquid chromatography / ミエリン / HSP27 … More / MFN2 / distal hereditary motor neuropathy / Nav1.6 / Po / SCN8A / 軸索 / CMT / Po蛋白 / Connexin32 / P0蛋白 / Peripheral Myelin Protein 22 / Charcot-Marie-Tooth病1型 / CMT1A / hereditary neuropath / 抹消神経 / 遺伝子欠失 / 髄鞘 / MPLA / hereditary neuropathy / Hsp27 / Hsp22 / distal heredistary motor nuerophathy / 遺伝子ニューロパチー / Nav 1.6 / Charcot-Marie-Tooth / Hereditary neurophaties / EGR2SCN8A / Cx32 / PMP22 / 17p11.2遺伝子重複 / ナトリウムチャネル / MTMR2 / myelin associated glycoprotein / connexin 32 / peripheral myelin protein 22 / myelin / hereditary neuropathies / 膜電位依存性Naチャンネルαサブユニット / コネキシン32 / 膜電位依存性Naチャンネルαサブユニッ / ミエリン会合性糖蛋白 / コネキシン3 2 / PO蛋白 / Peripheral Myelin Protein22 / PeripheralMyelin Protein 22 / シャルコ-マリ-ツース病 / 遺伝子診断 / シャルコーマリーツース病 / エクソーム解析 / 次世代シークエンサー / 呼吸鎖複合体 / 連鎖解析 / respiratory complex IV / cytochrome c oxidase / COX6A1 / チトクロームオキシダーゼ / 混合型 / 軸索型 / 遺伝子重複 / MLPA法 / DHPLC法 / multiplex ligation-dependent probe analysis / PNP22 / P2蛋白 / P_2蛋白質 / P_0蛋白質 … More Except Principal Investigator 遺伝性ニューロパチー / 切断型遺伝子異常 / G-CSF受容体 / 先天性好中球減少症 / シュワン細胞 / 先天性中枢性低換気症候群 / 膵島 / 膵β細胞 / 生物時計 / 糖尿病 / 白血病化 / CSF3R / アポトーシス / Charcot-Marie-Tooth病 / PMP22蛋白 / PASII / PO蛋白 / 遺伝子診断 / SBDS / PHOX2B遺伝子 / 体内時計 / 分化転換 / 脱分化 / アラニン伸長変異 / PHOX2B / クリプトクロム(CRY) / インスリン / 視交叉上核 / インスリン分泌 / 概日リズム / 受容体切断型遺伝子異常 / Shwachman-Diamond症候群 / CSF3受容体 / ゲノム不安定性 / ミエリン / ミエリン形成 / 摂食同調振動体 / 組織リモデリング / HES1 / 膵管上皮細胞 / 膵β細胞新生 / tubular complex / 膵上皮内腫瘍性病変（PanIN） / 膵癌 / 繊維化 / 膵管細胞 / 膵上皮内腫瘍性病変 (PanIN) / CRY1亜鉛結合モチーフ配列 / 亜鉛結合変異mCRY1(C414A-CRY1) / 膵β細胞-膵管細胞分化転換 / KPNA2（インポーティンα1） / 膵癌前駆病変 / 膵上皮内腫瘍性病変(PanIN) / 膵島構造リモデリング / 細胞老化関連分泌形質(SASP) / 次世代シークエンサー / 次世代シーケンサ / 末期腎不全 / genetic FSGS / 日本人遺伝的背景 / クリニカルシーケンス / 巣状分節性糸球体硬化症 / ステロイド抵抗性ネフローゼ症候群 / エクソーム解析 / 遺伝性腎疾患 / 骨髄機能不全症候群 / G-CSF受容体切断型異常 / mutation screening / inherited neuropathy / molecular diagnosis / genetic diagnosis / reseguencing method / DNA chip / CMT / Charcot-Marie-Tooth disease / 遺伝子検査 / multiple PCR / resequencing array / マイクロアイレ / Charcol-Marie-Tooth病 / 新規原因遺伝子発見 / リーシークエンスアレイ / マイクロアレイ / Shwachman-Diamond syndrome / Truncation mutation / Granulocyte colony stimulating factor receptor / Severe congenital neutropenia / 先天佳節中球減少症 / phosphatase / PTEN / ankyrin / sodium channel / persistent sodium current / inactivation / voltage sensor / ion channel / 不完全長型タンパク / 電位依存性チャネル / バッチクランプ / 活動電位 / 脱髄 / アンキリン / Naチャネル / P2 protein / Dejerine-Sottas disease / connexin 32 / P0 protein / Schwann cell / Myelin / Peripheral Nerve / hereditary neuropathy / 圧迫麻痺性遺伝性ニューロパチー(HNPP) / 先天性低ミエリン形成性ニューロパチー(CHN) / 遺伝性圧脆弱性ニューロパチー(HNPP) / Connexin32 / P2蛋白 / Dejerine-Sottas病 / コネキシン32 / 末梢神経 / ｱﾎﾟﾘﾎﾟ蛋白E / AopE-Sendai / アポリポ蛋白E / 創始者効果 / ApoE-Sendai / リポ蛋白糸球体症 / HAX1 / G-CSF 受容体 / 切断型遺伝子変異 / MODY / 時計遺伝子 / SASP / サーカディアンリズム / ヘッジホッグ / 膵α細胞 / 給餌同調振動体（FEO) / 視交叉上核（SCN) / ヘッジホッグシグナル伝達経路 / 細胞老化 / mCRY1亜鉛結合部位 (Cys414残基) / ポリアラニン伸長変異 / 不等姉妹染色分体交換 / 給餌性概日リズム / 耐糖能異常 / リズム同調 / 制限給餌 / MODY(若年発症成人型糖尿病) / 膵ベータ細胞 / インスリン分泌不全 / 生天性好中球減少症 / GGF / 細胞接着因子 / 神経軸索 / オリゴデンドロサイト / Charcot‐Marie‐Tooth病 Less

Towards a treatment for congenital central hypoventilation syndrome based on the pathophysiology
- Principal Investigator
  
  Sasaki Ayako
- Project Period (FY)
  2017 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Yamagata University
Searching leukemia predisposition gene in bone marrow failure syndrome with functional analysis.
- Principal Investigator
  
  Mitsui Tetsuo
- Project Period (FY)
  2016 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Epidemiology and pathological elucidation of focal segmental glomerulosclerosis in Japan
- Principal Investigator
  
  Hashimoto Taeko
- Project Period (FY)
  2016 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Elucidation the roles of senescence-like phenotype in pancreatic beta-cells in diabetic mutant cryptochrome1 transgenic mice
- Principal Investigator
  
  Okano Satoshi
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Experimental pathology
- Research Institution
  Yamagata University
Pathogenesis of Charcot-Marie-Tooth diseasePrincipal Investigator
- Principal Investigator
  
  HAYASAKA Kiyoshi
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Epidemiology and pathology of lipoprotein glomerulopathy
- Principal Investigator
  
  hashimoto taeko
- Project Period (FY)
  2013 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Pathophysiology of congenital central hypoventilation syndrome
- Principal Investigator
  
  Sasaki Ayako
- Project Period (FY)
  2013 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Yamagata University
Elucidation of molecular mechanisms of unusual circadian locomotor behavior and non-obese early onset diabetes mellitus in mutant (Cys414-Ala) cryptochrome1 transgenic mice
- Principal Investigator
  
  OKANO Satoshi
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Experimental pathology
- Research Institution
  Yamagata University
Clinical and biological significance of granulocyte colony stimulating factor receptor gene abnormalities those found in severe congenital neutropenia.
- Principal Investigator
  
  Mitsui Tetsuo
- Project Period (FY)
  2012 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Analysis of diabetes mellitus in mutant cryptochrome1 transgenic mice
- Principal Investigator
  
  OKANO Satoshi
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Experimental pathology
- Research Institution
  Yamagata University
Molecular basis of Charcot-Marie-Tooth diseasePrincipal Investigator
- Principal Investigator
  
  HAYASAKA Kiyoshi
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Molecular basis of congenital central hypoventilation syndrome : PHOX2B mutation and its haplotypes
- Principal Investigator
  
  SASAKI Ayako
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Yamagata University
Clinical and biological significance of granulocyte colony stimulating factor receptor gene abnormalities those found in severe congenital neutropenia
- Principal Investigator
  
  MITSUI Tetsuo (MTSUI Tetsuo)
- Project Period (FY)
  2008 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Comprehensive genetic analysis by DNA Chip in inherited neuropathies
- Principal Investigator
  
  ARIMURA Kimiyoshi
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Neurology
- Research Institution
  Kagoshima University
Research and treatment of hereditary neuropathyPrincipal Investigator
- Principal Investigator
  
  HAYASAKA Kiyoshi
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Clinical and biological significance of granulocyte colony stimulating factor receptor gene abnormalities those found in severe congenital neutropenia
- Principal Investigator
  
  MITSUI Tetuo
- Project Period (FY)
  2005 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Mechanism of expression of voltage-gated sodium and calcium channels
- Principal Investigator
  
  OKAMURA Yasushi
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  General physiology
- Research Institution
  National Institute of Natural Sciences Okazaki Research Facilities
Molecular Basis of Hereditary NeuropathyPrincipal Investigator
- Principal Investigator
  
  HAYASAKA Kiyoshi
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Molecular Basis of Charcot-Marie-Tooth DiseasePrincipal Investigator
- Principal Investigator
  
  HAYASAKA Kiyoshi
- Project Period (FY)
  2002 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Molecular Pathology of Hereditary NeuropathyPrincipal Investigator
- Principal Investigator
  
  HAYASAKA Kiyoshi
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (B).
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
遺伝性ニューロバチーの遺伝子診断法の確立Principal Investigator
- Principal Investigator
  
  早坂清
- Project Period (FY)
  1997 – 1998
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
遺伝性ニューロパチーの病態分子生物学的研究
- Principal Investigator
  
  植村慶一
- Project Period (FY)
  1996
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Research Institution
  Keio University
Charcot-Marie-Tooth病の病態解明Principal Investigator
- Principal Investigator
  
  早坂清
- Project Period (FY)
  1996 – 1997
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
遺伝性ニューロパチーの病態分子生物学的研究
- Principal Investigator
  
  植村慶一
- Project Period (FY)
  1995
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Research Institution
  Keio University
遺伝性ニューロパチーの病態分子生物学的研究
- Principal Investigator
  
  UYEMURA Keiichi
- Project Period (FY)
  1994
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Research Institution
  Keio University
Charcot-Marie-Tooth病の病態解明Principal Investigator
- Principal Investigator
  
  早坂清
- Project Period (FY)
  1994
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Molecular and patho-physiological atudies on hereditary neuropathy.
- Principal Investigator
  
  UYEMURA Keiichi
- Project Period (FY)
  1994 – 1995
- Research Category
  
  Grant-in-Aid for Co-operative Research (A)
- Research Field
  
  広領域
- Research Institution
  Keio University
先天性末梢ミエリン低形成症の病態解明Principal Investigator
- Principal Investigator
  
  早坂清
- Project Period (FY)
  1992
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Institution
  Akita University

[Book] Annual Review 神経2004
- Author(s)
  早坂清
- Total Pages
  366
- Publisher
  中外医学社
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16591008
[Journal Article] 難病研究の進歩】呼吸器　先天性中枢性低換気症候群2020
- Author(s)
  佐々木綾子、早坂清
- Journal Title
  
  生体の科学
  
  Volume: 71 Pages: 454-455
- Data Source
  KAKENHI-PROJECT-17K10171
[Journal Article] Adult cases of late-onset congenital central hypoventilation syndrome and paired-like homeobox 2B-mutation carriers: an additional case report and pooled analysis2020
- Author(s)
  Hino Aoi、Terada Jiro、Kasai Hajime、Shojima Hikaru、Ohgino Keiko、Sasaki Ayako、Hayasaka Kiyoshi、Tatsumi Koichiro
- Journal Title
  
  Journal of Clinical Sleep Medicine
  
  Volume: 16 Issue: 11 Pages: 1891-1900
- DOI
  10.5664/jcsm.8732
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10171
[Journal Article] 呼吸生理学的に軽症と診断した先天性中枢性肺胞低換気症候群　非ポリアラニン伸長変異2020
- Author(s)
  山田恵、大森さゆ、山田洋輔、長谷川久弥、佐々木綾子、早坂清、佐藤清二
- Journal Title
  
  日本小児科学会誌
  
  Volume: 124 Pages: 1509-1513
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10171
[Journal Article] Novel PHOX2B mutation in congenital central hypoventilation syndrome.2019
- Author(s)
  Sasaki A, Kisikawa Y, Imaji R, Fukushima Y, Nakamura Y, Nishimura Y, Yamada M, Mino Y, Mitsui T, Hayasaka K.
- Journal Title
  
  Pediatr International
  
  Volume: 61 Issue: 4 Pages: 393-396
- DOI
  10.1111/ped.13812
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10171
[Journal Article] Genetic Diagnosis and Characteristics of CCHS in Japan.2019
- Author(s)
  Sasaki A, Hayasaka K.
- Journal Title
  
  Pediatric Pulmonology
  
  Volume: 54
- Data Source
  KAKENHI-PROJECT-17K10171
[Journal Article] In Vivo Expression of NUP93 and Its Alteration by NUP93 Mutations Causing Focal Segmental Glomerulosclerosis.2019
- Author(s)
  Hashimoto T, Harita Y, Takizawa K, Urae S, Ishizuka K, Miura K, Horita S, Ogino D, Tamiya G, Ishida H, Mitsui T, Hayasaka K, Hattori M.
- Journal Title
  
  Kidney Int Rep
  
  Volume: 4(9) Issue: 9 Pages: 1312-1322
- DOI
  10.1016/j.ekir.2019.05.1157
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07029, KAKENHI-PROJECT-18K07857, KAKENHI-PROJECT-18K07872, KAKENHI-PUBLICLY-19H05200, KAKENHI-PROJECT-16K10057
[Journal Article] A novel PHOX2B gene mutation in an extremely low birth weight infant with congenital central hypoventilation syndrome and variant Hirschsprung's disease2018
- Author(s)
  Miura Yuichiro、Watanabe Tatsuya、Uchida Toshihiko、Nawa Tatsuro、Endo Naobumi、Fukuzawa Taichi、Ohkubo Ryuji、Takeyama Junji、Sasaki Ayako、Hayasaka Kiyoshi
- Journal Title
  
  European Journal of Medical Genetics
  
  Volume: - Issue: 9 Pages: 103541-103541
- DOI
  10.1016/j.ejmg.2018.09.008
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10171
[Journal Article] 日本における先天性中枢性低換気症候群の発達予後2018
- Author(s)
  佐々木綾子, 三井哲夫, 早坂清
- Journal Title
  
  日本小児呼吸器学会雑誌
  
  Volume: 29 Pages: 146-152
- NAID
  40021801866
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10171
[Journal Article] 先天性中枢性低換気症候群 (CCHS) を合併したmacrocephaly capillary malformation (M-CM) 症候群の1例2018
- Author(s)
  兵頭勇紀, 竹内章人, 山田洋輔, 長谷川久弥, 佐々木綾子, 早坂清, 森本大作, 玉井圭, 森茂弘, 中村和恵, 中村信, 影山操
- Journal Title
  
  日本新生児成育医学会雑誌
  
  Volume: 30 Pages: 73-78
- NAID
  40021505684
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10171
[Journal Article] Unique food-entrained circadian rhythm in Cysteine414-Alanine mutant mCRY1 transgenic mice2016
- Author(s)
  Okano S, Yasui A, Hayasaka K, Nakajima O
- Journal Title
  
  Sleep and Biological Rhythms
  
  Volume: 印刷中 Issue: 3 Pages: 261-269
- DOI
  10.1007/s41105-016-0050-1
- NAID
  40020888020
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-15K08417
[Journal Article] 先天性中枢性低換気症候群の臨床と病態2015
- Author(s)
  早坂　清
- Journal Title
  
  日本小児呼吸器学会雑誌
  
  Volume: 26 Pages: 52-56
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461640
[Journal Article] 先天性中枢性低換気症候群の現況と展望2014
- Author(s)
  早坂清、佐々木綾子
- Journal Title
  
  日本臨床
  
  Volume: 72 Pages: 363-370
- NAID
  40019951635
- Data Source
  KAKENHI-PROJECT-25461640
[Journal Article] 先天性中枢性低換気症候群2014
- Author(s)
  早坂清、佐々木綾子、岸川由美子
- Journal Title
  
  周産期医学
  
  Volume: 44 Pages: 255-257
- Data Source
  KAKENHI-PROJECT-25461640
[Journal Article] Identification of Novel ALK Rearrangement A2M-ALK in a Neonate with Fetal Lung Interstitial Tumor2014
- Author(s)
  Onoda T, Kanno M, Sato H, Takahashi N, Izumino H, Ohta H, Emura T, Katoh H, Ohizumi H, Ohtake H, Asao H, Dehner LP, Hill AD, Hayasaka K, Mitsui T
- Journal Title
  
  Genes Chromosomes Cancer
  
  Volume: 53 Issue: 10 Pages: 865-874
- DOI
  10.1002/gcc.22199
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591539
[Journal Article] A case of congenital central hypoventilation syndrome with a novel mutation of the PHOX2B gene presenting as central sleep apnea2014
- Author(s)
  Amimoto Y, Okada K, Nakano H, Sasaki A, Hayasaka K, Odajima H
- Journal Title
  
  J Clin Sleep Med
  
  Volume: 10 Issue: 03 Pages: 327-329
- DOI
  10.5664/jcsm.3542
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25461640
[Journal Article] A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth disease.2014
- Author(s)
  Tamiya G, Makino S, Hayashi M, Abe A, Numakura C, Ueki M, Tanaka A, Ito C, Toshimori K, Ogawa N, Terashima T, Maegawa H, Yanagisawa D, Tooyama I, Tada M, Onodera O, Hayasaka K.
- Journal Title
  
  Am J Hum Genet.
  
  Volume: 95 Issue: 3 Pages: 294-300
- DOI
  10.1016/j.ajhg.2014.07.013
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24590400, KAKENHI-PROJECT-24592441, KAKENHI-PUBLICLY-25129701, KAKENHI-PROJECT-25293041, KAKENHI-PROJECT-25460403, KAKENHI-PROJECT-25461537, KAKENHI-PROJECT-25670087, KAKENHI-PROJECT-25860842, KAKENHI-PROJECT-25870074, KAKENHI-PROJECT-26870067
[Journal Article] The first Japanese case of Charcot-Marie-Tooth disease type 4H with a novel FGD4 c.837-1G>A mutation.2013
- Author(s)
  Arai H, Hayashi M, Hayasaka K, Kanda T, Tanabe Y.
- Journal Title
  
  Neuromuscul Disord.
  
  Volume: 23 Issue: 8 Pages: 652-655
- DOI
  10.1016/j.nmd.2013.04.010
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461537
[Journal Article] 高インスリン性低血糖症を呈したPHOX2B遺伝子異常による先天性中枢性低換気症候群の2例2013
- Author(s)
  武田良淳，後藤正博，井垣純子，高木優樹，立花奈緒，吉橋博史，沼倉周彦，早坂清，長谷川行洋
- Journal Title
  
  日本小児科学会雑誌
  
  Volume: 113 Pages: 1615-1619
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461640
[Journal Article] INF2 mutationsin Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis.2013
- Author(s)
  Toyota K, Ogino D, Hayashi M, Taki M, Saito K, Abe A, Hashimoto T, Umetsu K, Tsukaguchi H, Hayasaka K.
- Journal Title
  
  J Peripher Nerv Syst.
  
  Volume: 18(1) Issue: 1 Pages: 97-98
- DOI
  10.1111/jns5.12014
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22406027, KAKENHI-PROJECT-24659504, KAKENHI-PROJECT-25461537, KAKENHI-PROJECT-25860842
[Journal Article] Molecular analysis of the genes causing recessive demyelinating Charcot-Marie-Tooth disease in Japan.2013
- Author(s)
  Hayashi M, Abe A, Murakami T, Yamao S, Arai H, Hattori H, Iai M, Watanabe K, Oka N, Chida K, Kishikawa Y, Hayasaka K.
- Journal Title
  
  J Hum Genet.
  
  Volume: 58 Issue: 5 Pages: 273-278
- DOI
  10.1038/jhg.2013.15
- NAID
  10031177222
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461537, KAKENHI-PROJECT-25860842
[Journal Article] Characterization of age-associated alterations of islet function and structure in diabetic mutant cryptochrome1 transgenic mice2013
- Author(s)
  Okano S, Hayasaka K, Igarashi M, Togashi Y, Nakajima O
- Journal Title
  
  Journal of Diabetes Investigation
  
  Volume: 4 Issue: 5 Pages: 428-435
- DOI
  10.1111/jdi.12080
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24590473
[Journal Article] Successful treatment of acute myeloid leukaemia in a patient with ataxia telangiectasia.2013
- Author(s)
  Tadashi Onoda, Miyako Kanno, Toru Meguro, Hiroko Sato, Noriyuki Takahashi, Takako Kawakami, Tetsuo Mitsui, Kiyoshi Hayasakai
- Journal Title
  
  Europ J Haematol
  
  Volume: 91 Issue: 6 Pages: 557-560
- DOI
  10.1111/ejh.12186
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591539
[Journal Article] Treatment with lactose (galactose)-restricted and medium-chain triglyceride-supplemented formula for neonatal intrahepatic cholestasis caused by citrin deficiency2012
- Author(s)
  Hayasaka K, et al
- Journal Title
  
  J Inher Meta Dis
  
  Volume: 2 Pages: 37-44
- DOI
  10.1007/8904_2011_42
- ISBN
  9783642247576, 9783642247583
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591243
[Journal Article] Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome2012
- Author(s)
  Meguro T, Yoshida Y, Hayashi M, Toyota K, Otagiri T, Mochizuki N, Kishikawa Y, Sasaki A, Hayasaka K
- Journal Title
  
  J.Hum Genet
  
  Volume: 22(In Press)
- NAID
  10030663222
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591411
[Journal Article] Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome2012
- Author(s)
  Meguro T, Yoshida Y, Hayashi M, Toyota K, Otagiri T, Mochizuki N, Kishikawa Y, Sasaki A, Hayasaka K.
- Journal Title
  
  J Hum Genet
  
  Volume: 22(in press) Issue: 5 Pages: 335-337
- DOI
  10.1038/jhg.2012.27
- NAID
  10030663222
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591411
[Journal Article] Congenital dysplastic microcephaly and hypoplasia of the brainstem and cerebellum with diffuse intracranial calcification2012
- Author(s)
  Nakamura K, Hayasaka K, et al
- Journal Title
  
  J Child Neurol
  
  Volume: 27 Issue: 2 Pages: 218-221
- DOI
  10.1177/0883073811416239
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591243, KAKENHI-PROJECT-21591312, KAKENHI-PROJECT-24591500
[Journal Article] Slowly progressive sleep apnea in late-onset central hypoventilation syndrome2012
- Author(s)
  Fujiwaki T, Hasegawa H, Arai H, Hayasaka K, Ohta S.
- Journal Title
  
  Pediatr Int
  
  Volume: 254 Issue: 2 Pages: 290-292
- DOI
  10.1111/j.1442-200x.2011.03431.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591411
[Journal Article] Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan2011
- Author(s)
  Abe A, Hayasaka K, et al
- Journal Title
  
  J Hum Genet
  
  Volume: 56 Issue: 5 Pages: 364-368
- DOI
  10.1038/jhg.2011.20
- NAID
  10030659221
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591243, KAKENHI-PROJECT-21591311, KAKENHI-PROJECT-22790964
[Journal Article] 先天性中枢性低換気症候群におけるPHOX2B遺伝子異常について2011
- Author(s)
  早坂清, 荒井博子, 吉田悠紀, 小田切徹州, 佐々木綾子
- Journal Title
  
  日本小児科学会雑誌
  
  Volume: 115 Pages: 769-776
- NAID
  10029385399
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591411
[Journal Article] 当院においてRosen T20プロトコールで治療した若年骨肉腫12例2011
- Author(s)
  川上貴子, 簡野美弥子, 高橋憲幸, 目黒亨, 仙道大, 三井哲夫, 樋口智佳子, 土屋登嗣, 勝浦理彦, 清水行敏, 小山内俊久, 早坂清
- Journal Title
  
  小児がん
  
  Volume: 48 Pages: 276-283
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591243
[Journal Article] Compound heterozygous PMP22 deletion mutations causing severe Charcot-Marie-Tooth disease type 1.2010
- Author(s)
  Abe A, Hayasaka K, 他7人
- Journal Title
  
  J Hum Genet
  
  Volume: 55 Issue: 11 Pages: 771-773
- DOI
  10.1038/jhg.2010.106
- NAID
  10030737757
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591243, KAKENHI-PROJECT-21591311, KAKENHI-PROJECT-22790964
[Journal Article] Non-obese early onset diabetes mellitus in mutant cryptochromel transgenic mice2010
- Author(s)
  Okano S, Hayasaka K, Igarashi M, Iwai H, Togashi Y, Nakajiroa O
- Journal Title
  
  European journal of clinical investigation
  
  Volume: 40 Pages: 1011-1017
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590429
[Journal Article] Polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : rs17884724 : A>C is associated with seven-alanine expansion2010
- Author(s)
  Arai H, Hayasaka K, 他5名
- Journal Title
  
  J Hum Genet
  
  Volume: 55 Issue: 1 Pages: 4-7
- DOI
  10.1038/jhg.2009.109
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591243
[Journal Article] Polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : rs17884724:A>C is associated with 7-alanine expansion.2010
- Author(s)
  Arai H, Otagiri T, Sasaki A, Umetsu K, Hayasaka K
- Journal Title
  
  J Hum Genet 55
  
  Pages: 4-7
- NAID
  10030733021
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591411
[Journal Article] Frameshift mutations of the ARX gene in familial Ohtahara syndrome2010
- Author(s)
  Kato M, Hayasaka K, 他3名
- Journal Title
  
  Epilepsia
  
  Volume: 51 Issue: 9 Pages: 1679-84
- DOI
  10.1111/j.1528-1167.2010.02559.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591243, KAKENHI-PROJECT-21591312
[Journal Article] Non-obese early onset diabetes mellitus in mutant cryptochrome1 transgenic mice2010
- Author(s)
  Okano S, Hayasaka K, Igarashi M, Iwai H, Togashi Y, Nakajima O
- Journal Title
  
  Eur J Clin Invest
  
  Volume: 40 Pages: 1011-1017
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590429
[Journal Article] 変異型CRY1過剰発現マウスの給餌性概日リズム2010
- Author(s)
  岡野聡、早坂清、中島修
- Journal Title
  
  山形ニューロサイエンス研究会会誌 VOL.10(掲載確定)
- Data Source
  KAKENHI-PROJECT-21590429
[Journal Article] Non-obese early onset diabetes mellitus in mutant cryptochrome 1 transgenic mice2010
- Author(s)
  Okano S, Hayasaka K, 他4名
- Journal Title
  
  Eur J Clin Invest
  
  Volume: 40 Issue: 11 Pages: 1011-1017
- DOI
  10.1111/j.1365-2362.2010.02359.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591243
[Journal Article] Supernumerary impacted teeth in a patient with SOX2 anophthalmia syndrome2010
- Author(s)
  Numakura C, Hayasaka K, 他5名
- Journal Title
  
  Am J Med Genet
  
  Volume: 152A Issue: 9 Pages: 2355-2359
- DOI
  10.1002/ajmg.a.33556
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591243
[Journal Article] Phenotypic variability in a family with Townes-Brocks syndrome2010
- Author(s)
  Sudo Y, Hayasaka K, 他4名
- Journal Title
  
  J Hum Genet
  
  Volume: 55 Issue: 8 Pages: 550-551
- DOI
  10.1038/jhg.2010.64
- NAID
  10030736454
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591243, KAKENHI-PROJECT-22790964
[Journal Article] Polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : rs17884724 : A>C is associated with seven-alanine expansion2010
- Author(s)
  Arai H, Otagiri T, Sasaki A, Umetsu K, Hayasaka K.
- Journal Title
  
  J. Hum. Genet
  
  Volume: 55 Pages: 4-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591411
[Journal Article] The GARS gene is rarely mutated in Japanese patients with Charcot-Marie-Tooth neuropathy2009
- Author(s)
  Abe A, Hayasaka K
- Journal Title
  
  J.Hum.Genet. 54
  
  Pages: 310-312
- NAID
  10030730527
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591311
[Journal Article] A clinical phenotype of distal hereditary motor neuronopathy type II with a novel HSPB1 mutation2009
- Author(s)
  Ikeda Y, Abe A, MD, Ishida C, Takahashi K, Hayasaka K, Yamada M
- Journal Title
  
  J Neurol Sci 277
  
  Pages: 9-12
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591311
[Journal Article] Severe hemorrhagic colitis caused by dasatinib in Philadelphia chromosome-positive acute lymphoblastic leukemia2009
- Author(s)
  Shimokaze T, Mitsui T, Takeda H, Kawakami T, Arai T, Ito M, Iwaba A, Izumino H, Takahashi N, Kanno M, Sendo D, Hayasaka K.
- Journal Title
  
  Pediatr Hematol Oncol
  
  Volume: 26 Pages: 448-53
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591243
[Journal Article] The GARS gene is rarely mutated in Japanese patients with Charcot-Marie-Tooth neuropathy2009
- Author(s)
  Abe A, Hayasaka K
- Journal Title
  
  J. Hum. Genet
  
  Volume: 54 Issue: 5 Pages: 310-312
- DOI
  10.1038/jhg.2009.25
- NAID
  10030730527
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591311
[Journal Article] Neurofilament light chain polypeptide (NEFL) gene mutations in Charcot-Marie-Tooth disease : Nonsense mutation probably causes a recessive phenotype2009
- Author(s)
  Abe A, Numakura C, Nakayama T, Saito K, Koide H, Oka N, Ando K, Honma A, Kishikawa Y, Hayasaka K
- Journal Title
  
  J. Hum. Genet
  
  Volume: 54 Issue: 2 Pages: 94-97
- DOI
  10.1038/jhg.2008.13
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591311
[Journal Article] Neurofilament light chain polypeptide (NEFL) gene mutations in Charcot-Marie-Tooth disease Nonsense mutation probably causes a recessive phenotype2009
- Author(s)
  Abe A, Numakura C, Nakayama T, Saito K, Koide H, Oka N, Ando K, Honma A, Kishikawa Y, Hayasaka K
- Journal Title
  
  J.Hum.Genet 54
  
  Pages: 94-97
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591311
[Journal Article] A longer polyalanine expansion in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattem (Ohtahara syndrome)2007
- Author(s)
  Kato, M・Saitoh, S・Kamei, A・Shiraishi, H・Ueda, Y・Akasaka, M・Tohyama, J・Akasaka, N・Hayasaka, K
- Journal Title
  
  Am J Hum Genet 81
  
  Pages: 361-366
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591141
[Journal Article] A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome)2007
- Author(s)
  Kato M, Saitoh S, Kamei A, Shiraishi H, Ueda Y, Akasaka M, Tohyama J, Akasaka N, Hayasaka K
- Journal Title
  
  Am J Hum Genet 81
  
  Pages: 361-366
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591141
[Journal Article] Periaxin mutation in Japanese patients with Charcot-Marie-Tooth disease.2006
- Author(s)
  Otagiri T, Sugai K, Kijima K, Hayasaka K, et al.
- Journal Title
  
  J Hum Genet 51(7)
  
  Pages: 625-628
- NAID
  10017989690
- Data Source
  KAKENHI-PROJECT-18390262
[Journal Article] Periaxin mutation in Japanese patients with Charcot-Marie-Tooth disease.2006
- Author(s)
  Otagiri, T・Sugai, K・Kijima, K・Arai, H・Sawaishi, Y・Shimohata, M・Hayasaka, K
- Journal Title
  
  J Hum Genet 51
  
  Pages: 625-628
- NAID
  10017989690
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591141
[Journal Article] Genetic analysis of Shwachman-Diamond syndrome : phenotypic heterogeneity in patients carrying identical SBDS mutations2005
- Author(s)
  Kawakami T, Mitsui T, Kanai M, Shirahata E, Sendo D, Kanno M, Noro M, Endoh M, Hama A, Tono C, Ito E, Tsuchiya S, Igarashi Y, Abukawa D, Hayasaka K
- Journal Title
  
  Tohoku J Exp Med. 206
  
  Pages: 253-259
- NAID
  10016132588
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591069
[Journal Article] 本邦におけるCharcot-Marie-Tooth病の特徴
- Author(s)
  早坂清, 阿部暁子
- Journal Title
  
  Annual review 2009神経
  
  Pages: 218-225
- Data Source
  KAKENHI-PROJECT-20591243
[Presentation] Genetic Diagnosis and Characteristics of Congenital Central Hypoventilation Syndrome in Japan2019
- Author(s)
  Ayako Sasaki, Kiyoshi Hayasaka.
- Organizer
  CIPP ⅩⅧ
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10171
[Presentation] Nucleoporin遺伝子変異を有するステロイド抵抗性ネフローゼ症候群の臨床経過と分子病理像の解析2018
- Author(s)
  橋本多恵子、張田豊、三浦健一郎、石塚喜世伸、秋岡祐子、久野正貴、堀江弘、北村博司、　荻野大助、田宮元、山口裕、三井哲夫、早坂清、服部元史
- Organizer
  第53回日本小児腎臓病学会　学術集会　福島
- Data Source
  KAKENHI-PROJECT-16K10057
[Presentation] Clinicopathological characterization of steroid-resistant nephrotic syndrome caused by NUP107 mutations2018
- Author(s)
  Hashimoto T, Harita Y, Miura K, Ishizuka K, Akioka Y, Hisano M, Horie H, Matsumura C, Tamiya G, Ogino D, Mitsui T, Hayasaka K, Hattori M
- Organizer
  第16回日韓中小児腎セミナー　韓国、釜山
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10057
[Presentation] Pancreatic intraepithelial neoplasia-like cells in diabetic cysteine414-alanine-mCRY1 transgenic mice2017
- Author(s)
  岡野聡, 安井明, 菅野新一郎, 佐藤賢一, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  Tohoku Forum on Aging Science (IDAC, Tohoku University)
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08417
[Presentation] Features of pancreatic intraepithelial neoplasia and tubular complex in diabetic cysteine414-alanine-mCRY1 transgenic mice2017
- Author(s)
  岡野聡, 安井明, 菅野新一郎, 佐藤賢一, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  XV European Biological Rhythms Society Congress
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08417
[Presentation] mCRY1-C414A変異体過剰発現マウスの膵臓におけるtubular complexからの膵β細胞の新生とKPNA2の発現2017
- Author(s)
  岡野聡, 安井明, 菅野新一郎, 佐藤賢一, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  2017年度生命科学系学会合同年次大会
- Data Source
  KAKENHI-PROJECT-15K08417
[Presentation] 孤発性ステロイド抵抗性ネフローゼ症候群として発症したLAMB2変異例2017
- Author(s)
  橋本多恵子、張田豊、三浦健一郎、秋岡祐子、久野正貴、堀江弘荻野大助、田宮元、山口裕、三井哲夫、早坂清、服部元史
- Organizer
  第５２回小児腎臓病学会　学術集会
- Data Source
  KAKENHI-PROJECT-16K10057
[Presentation] Reduced expression of KPNA2 and dysfunction of β-cells in C414A-CRY1 transgenic mice2017
- Author(s)
  岡野聡, 安井明, 菅野新一郎, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  77th Scientific Sessions American Diabetes Association
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08417
[Presentation] 日本における先天性中枢性低換気症候群について：疫学および遺伝子型と臨床型の関係2016
- Author(s)
  早坂清,下風朋章，佐々木綾子，目黒亨，長谷川久弥，平工由香，吉川哲史
- Organizer
  第119回日本小児科学会学術集会
- Place of Presentation
  ロイトン　札幌　札幌
- Year and Date
  2016-05-13
- Data Source
  KAKENHI-PROJECT-25461640
[Presentation] システイン414-アラニン変異型CRY1過剰発現マウス膵島の導管様細胞2016
- Author(s)
  岡野聡, 安井明, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  第59回日本糖尿病学会年次学術集会
- Place of Presentation
  国立京都国際会館 (京都府京都市)
- Year and Date
  2016-05-19
- Data Source
  KAKENHI-PROJECT-15K08417
[Presentation] Anomalous ductal structure in the islet of diabetic cysteine414-alanine-mCRY1 transgenic mice2016
- Author(s)
  岡野聡, 安井明, 菅野新一郎, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  76th Scientific Sessions American Diabetes Association (ADA)
- Place of Presentation
  Ernest N. Morial Convention Center (ルイジアナ州ニューオーリンズ)
- Year and Date
  2016-06-10
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08417
[Presentation] Anomalous islet structure in diabetic cysteine414-alanine-mCRY1 transgenic mice2016
- Author(s)
  岡野聡, 安井明, 菅野新一郎, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  第89回日本生化学会大会
- Place of Presentation
  仙台国際センター (宮城県仙台市)
- Year and Date
  2016-09-25
- Data Source
  KAKENHI-PROJECT-15K08417
[Presentation] 先天性中枢性低換気症候群における神経学的予後について.2016
- Author(s)
  佐々木綾子，下風朋章，三井哲夫，早坂　清
- Organizer
  第61回日本新生児成育医学会・学術集会
- Place of Presentation
  大阪国際会議場　大阪
- Year and Date
  2016-12-01
- Data Source
  KAKENHI-PROJECT-25461640
[Presentation] C414A変異mCRY1トランスジェニックマウスの膵島の異常と導管構造2016
- Author(s)
  岡野聡, 安井明, 菅野新一郎, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜 (神奈川県横浜市)
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-15K08417
[Presentation] Food-entrainable circadian rhythm and pathophisiology in Cys414-Ala mCRY1 transgenic mice2015
- Author(s)
  岡野聡, 安井明, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  第15回ヨーロッパ時間生物学会(EBRS)・第4回世界時間生物学会連合大会(WCC)
- Place of Presentation
  マンチェスター大学 (イギリス)
- Year and Date
  2015-08-02
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08417
[Presentation] 劣性軸索型および混合型Charcot-Marie-Tooth病における新規病因遺伝子COX6A1の同定2015
- Author(s)
  早坂清，田宮元，牧野悟士，沼倉周彦，林真貴子，阿部暁子，植木優夫，田中敦，他田正義，小野寺理
- Organizer
  第57回日本先天代謝異常学会
- Place of Presentation
  大阪国際会議場（大阪府大阪市）
- Year and Date
  2015-11-14
- Data Source
  KAKENHI-PROJECT-25461537
[Presentation] Unusual ductal structure in the islet of diabetic cysteine414-alanine mutant mCRY1 transgenic mice2015
- Author(s)
  岡野聡, 安井明, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  キーストンシンポジア (糖尿病: 新しい分子メカニズムと治療戦略)
- Place of Presentation
  ウエスティン都ホテル京都 (京都府京都市)
- Year and Date
  2015-10-25
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08417
[Presentation] Senescence-like phenotype in pancreatic β-cells in diabetic mutant cryptochrome1 transgenic mice2015
- Author(s)
  岡野聡, 安井明, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  第75回米国糖尿病学会（ADA）
- Place of Presentation
  Boston Convention and Exhibition Center (アメリカ)
- Year and Date
  2015-06-04
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08417
[Presentation] 変異型CRY1過剰発現マウスと野生型マウスの恒明条件下での給餌性概日リズム2014
- Author(s)
  岡野聡、早坂清、中島修
- Organizer
  第21回日本時間生物学会学術大会
- Place of Presentation
  九州大学医学部百年講堂(福岡県)
- Year and Date
  2014-11-09
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] Regulation of Rgs4 in the islet of mutant cryptochrome1 transgenic mice2014
- Author(s)
  岡野聡, 安井明, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  Homeodynamics in Clocks, Sleep and Metabolism Tokyo Translational Therapeutics Meeting
- Place of Presentation
  東京大学伊藤謝恩ホール(東京都)
- Year and Date
  2014-09-24
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] 糖尿病を示す変異型CRY1過剰発現マウス膵島の遺伝子発現及びCRY1 結合タンパク質の解析2014
- Author(s)
  岡野聡, 安井明, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第57回日本糖尿病学会年次学術集会
- Place of Presentation
  リーガロイヤルホテル(大阪府)
- Year and Date
  2014-05-22
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] 糖尿病を示す変異型CRY1過剰発現マウス膵島の遺伝子発現及びCRY1結合蛋白質の解析2014
- Author(s)
  岡野聡, 安井明, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第57回日本糖尿病学会年次学術集会
- Place of Presentation
  リーガロイヤルホテル(大阪府)
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] 時計タンパク質CRY1の変異体過剰発現マウスの膵β細胞の老化様変化と脱分化2014
- Author(s)
  岡野聡, 安井明, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  第37回日本分子生物学会学術大会
- Place of Presentation
  パシフィコ横浜(神奈川県)
- Year and Date
  2014-11-26
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] 時計タンパク質CRY1 の変異体過剰発現マウスにおける膵β細胞の機能不全2014
- Author(s)
  岡野聡, 安井明, 早坂清, 五十嵐雅彦, 中島修
- Organizer
  第26回分子糖尿病学シンポジウム
- Place of Presentation
  高知市文化プラザかるぽーと(高知県)
- Year and Date
  2014-12-06
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] 変異型CRY1過剰発現マウスの糖尿病と若齢における膵島の遺伝子発現2013
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第36回日本分子生物学会年会
- Place of Presentation
  神戸国際展示場(兵庫県)
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] Unusual food-entrained circadian rhythm and diabetes mellitus in mutant CRY1 transgenic mice2013
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  XIII European Biological Rhythms Society Congress
- Place of Presentation
  ルートヴィヒ・マクシミリアン大学ミュンヘン(ドイツ)
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] 糖尿病を示す変異型 CRY1 過剰発現マウスの若齢における膵島の遺伝子発現2013
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第20回日本時間生物学会学術大会
- Place of Presentation
  近畿大学東大阪キャンパス(大阪府)
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] 髄鞘型Charcot-Marie-Tooth病の病態解明2012
- Author(s)
  林真貴子, 阿部暁子, 早坂清
- Organizer
  第115回日本小児科学会学術集会
- Place of Presentation
  福岡国際会議場(福岡市)
- Year and Date
  2012-04-21
- Data Source
  KAKENHI-PROJECT-21591311
[Presentation] 非肥満若齢発症の糖尿病を示す変異型CRY1過剰発現マウスの膵島の異常2011
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第54回日本糖尿病学会年次学術集会
- Place of Presentation
  札幌プリンスホテル国際館パミール
- Year and Date
  2011-05-20
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] Features of diabetes mellitus in mutant cryptochromel transgenic mice at young and mature stages(一般講演「慢性疾患生物学」)2011
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第34回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜
- Year and Date
  2011-12-14
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] Diabetes mellitus in mutant cryptochrome1 transgenic mice at young and mature stages2011
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  The 16th Japan-Korea Symposium on Diabetes Mellitus
- Place of Presentation
  ヒルトン東京ベイ(東京都)
- Year and Date
  2011-10-22
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] Features of diabetes mellitus in mutant cryptochrome1 transgenic mice at young and mature stages2011
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第34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)
- Year and Date
  2011-12-14
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] Features of diabetes mellitus in mutant cryptochromel transgenic mice at young and mature stages2011
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第34回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜(ポスター発表)
- Year and Date
  2011-12-14
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] 先天性中枢性低換気症候群におけるPHOX2B遺伝子異常について2011
- Author(s)
  早坂清
- Organizer
  第114回日本小児科学会総会
- Place of Presentation
  東京都港区グランドプリンスホテル新高輪国際館パミール
- Data Source
  KAKENHI-PROJECT-21591411
[Presentation] Diabetes mellitus in mutant cryptochromel transgenic mice at young and mature stages2011
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  The 16th Japan-Korea Symposium on Diabetes Mellitus
- Place of Presentation
  ヒルトン東京ベイ
- Year and Date
  2011-10-22
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] Unusual circadian rhythm and diabetes mellitus in mutant cryptochromel transgenic mice2011
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  Worldsleep2011
- Place of Presentation
  京都国際会議場
- Year and Date
  2011-10-17
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] 日本人におけるCharcot-Marie-Tooth病1A型重複について2011
- Author(s)
  阿部暁子, 早坂清, ほか
- Organizer
  第114回日本小児科学会学術集会
- Place of Presentation
  東京グランドプリンスホテル新高輪国際館パミール(東京都)
- Year and Date
  2011-08-13
- Data Source
  KAKENHI-PROJECT-21591311
[Presentation] Unusual circadian rhythm and diabetes mellitus in mutant cryptochrome1 transgenic mice2011
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  Worldsleep2011
- Place of Presentation
  京都国際会議場(京都府)
- Year and Date
  2011-10-17
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] 変異型CRY1過剰発現マウスの若齢における膵臓の異常2011
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  日本糖尿病学会第49回東北地方会
- Place of Presentation
  仙台国際センター
- Year and Date
  2011-11-05
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] 変異型CRY1過剰発現マウスの若齢における膵臓の異常2011
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  日本糖尿病学会第49回東北地方会
- Place of Presentation
  仙台国際センター(宮城県)
- Year and Date
  2011-11-05
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] 非肥満若齢発症の糖尿病を示す変異型CRY1過剰発現マウスの膵島の異常2011
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第54回日本糖尿病学会年次学術集会
- Place of Presentation
  札幌プリンスホテル国際館パミール(北海道)
- Year and Date
  2011-05-20
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] 変異型CRY1トランスジェニックマウスの示す非肥満・若年発症糖尿病2010
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 岩井晴恵, 富樫義之, 中島修
- Organizer
  第53回日本糖尿病学会年次学術集会
- Place of Presentation
  岡山市デジタルミュージアム(岡山県)
- Year and Date
  2010-05-27
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] linical and molecular diagnosis of Charcot-Marie-Tooth disease in Japan2010
- Author(s)
  Hayasaka K
- Organizer
  Peripheral nerve society Satellite meeting
- Place of Presentation
  Sydney
- Data Source
  KAKENHI-PROJECT-21591311
[Presentation] 変異型CRY1トランスジェニックマウスの示す非肥満・若年発症糖尿病2010
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 岩井晴恵, 富樫義之, 中島修
- Organizer
  第53回日本糖尿病学会年次学術集会(プレジデントポスター発表)
- Place of Presentation
  岡山コンベンションセンター(岡山県)
- Year and Date
  2010-05-28
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] Abnormal islet architecture in diabetic mutant cryptochrome1 transgenic mice2010
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第33回日本分子生物学会年会・第83回日本生化学会大会合同大会(BMB2010)
- Place of Presentation
  神戸国際展示場(兵庫県)
- Year and Date
  2010-12-10
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] 変異型CRY1トランスジェニックマウスの示す非肥満・若年発症糖尿病2010
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 岩井晴恵, 富樫義之, 中島修
- Organizer
  第53回日本糖尿病学会年次学術集会
- Place of Presentation
  岡山コンベンションセンター(岡山県)
- Year and Date
  2010-05-28
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] 変異型CRY過剰発現マウスの膵島の構成異常2010
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 岩井晴恵, 富樫義之, 中島修
- Organizer
  第48回日本糖尿病学会東北地方会
- Place of Presentation
  仙台国際センター(宮城県)
- Year and Date
  2010-11-06
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] Abnormal islet architecture in diabetic mutant cryptochromel transgenic mice2010
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第33回日本分子生物学会年会・第83回日本生化学会大会合同大会(BMB2010)
- Place of Presentation
  神戸国際展示場(兵庫県)
- Year and Date
  2010-12-10
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] 変異型CRY1過剰発現マウスの膵島の異常2010
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 岩井晴恵, 富樫義之, 中島修
- Organizer
  第17回日本時間生物学会学術大会
- Place of Presentation
  早稲田大学(東京都)
- Year and Date
  2010-11-21
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] Diabetes mellitus in mutant CRY1 transgenic mice2009
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 岩井晴恵, 中島修
- Organizer
  ワークショップ「癌・生活習慣病の発現と時計遺伝子」第32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)
- Year and Date
  2009-12-12
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] 変異型CRY1トランスジェニックマウスの示す糖尿病2009
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 岩井晴恵, 中島修
- Organizer
  第32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)
- Year and Date
  2009-12-10
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] Food-entrained circadian rhythm in mutant CRY1 transgenic mice2009
- Author(s)
  岡野聡、早坂清、中島修
- Organizer
  The 6th Congress of Asian Sleep Research Society(the 6th ASRS), the 34th Annual Meeting of Japanese Society of Sleep Research(the 34th JSSR) and the 16th Annual Meeting of Japanese Society for Chronobiology(the 16th JSC)
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2009-10-27
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] Unusual circadian behavior and diabetes mellitus in mutant CRY1 transgenic mice2009
- Author(s)
  岡野聡、早坂清、五十嵐雅彦、岩井晴恵、中島修
- Organizer
  The 36th Congress of the International Union of Physiological Sciences(IUPS2009)
- Place of Presentation
  京都国際会議場(京都府)
- Year and Date
  2009-08-01
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] Food-entrained circadian rhythm in mutant CRY1 transgenic mice The 6th Congress of Asian Sleep Research Society (the 6th ASRS)2009
- Author(s)
  岡野聡, 早坂清, 中島修
- Organizer
  the 34th Annual Meeting of Japanese Society of Sleep Research (the 34th JSSR) and the 16th Annual Meeting of Japanese Society for Chronobiology (the 16th JSC)
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2009-10-27
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] Unusual circadian behavior and diabetes mellitus in mutant CRY1 transgenic mice2009
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 岩井晴恵, 中島修
- Organizer
  The 36th Congress of the International Union of Physiological Sciences (IUPS2009)
- Place of Presentation
  京都国際会議場(京都府)
- Year and Date
  2009-08-01
- Data Source
  KAKENHI-PROJECT-21590429
[Presentation] INSS分類Stage1で腫瘍全摘後無治療経過観察中、Stage4で再発した神経芽腫4歳女児2008
- Author(s)
  三井哲夫, 川上貴子, 高橋憲幸, 金井雅代, 本間信夫, 仙道大, 簡野美弥子, 早坂清, 山際岩男, 江村隆起, 太田寛
- Organizer
  第24回日本小児がん学会
- Place of Presentation
  千葉市幕張メッセ国際会議場
- Year and Date
  2008-11-16
- Data Source
  KAKENHI-PROJECT-20591243
[Presentation] Charcot-Marie-Tooth病の遺伝子診断2007
- Author(s)
  阿部暁子、木島一己、早坂清
- Organizer
  第49回日本小児神経学会
- Place of Presentation
  大阪国際会議場
- Year and Date
  2007-07-05
- Data Source
  KAKENHI-PROJECT-18591141
[Presentation] Charoot-Marie-Tooth病の遺伝子診断2007
- Author(s)
  阿部暁子・木島一己・早坂清
- Organizer
  .第49回日本小児神経学会
- Place of Presentation
  大阪国際会議場
- Year and Date
  2007-07-05
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591141
[Presentation] ALK 2p23転座と新規融合遺伝子A2M-ALKを同定したFetal Lung Interstitial Tumor
- Author(s)
  小野田正志, 簡野美弥子, 佐藤裕子, 高橋憲幸, 五十野博子, 太田寛, 江村隆起, 大竹浩也, Hill Ashley D., 早坂清, 三井哲夫
- Organizer
  日本小児血液がん学会
- Place of Presentation
  岡山コンベンションセンター岡山
- Year and Date
  2014-11-28 – 2014-11-30
- Data Source
  KAKENHI-PROJECT-24591539
[Presentation] 先天性中枢性低換気症候群の臨床と分子病態
- Author(s)
  早坂清
- Organizer
  日本小児呼吸器学会
- Place of Presentation
  秋葉原コンベンションホール、東京
- Year and Date
  2014-10-24 – 2014-10-25
- Invited
- Data Source
  KAKENHI-PROJECT-25461640
[Presentation] 非肥満若齢発症の糖尿病を示す変異型CRY1過剰発現マウスの膵β細胞の増殖能の低下
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第50回日本糖尿病学会東北地方会
- Place of Presentation
  フォレスト仙台
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] 重症好中球減少症の経過中、5歳時急性脳症を契機に退行を認め神経発達障害が顕在化したHAX1を有する女児
- Author(s)
  目黒亨、中村和幸、佐藤裕子、簡野美弥子、高橋憲幸、小野田正志、川上貴子、三井哲夫、加藤光広、早坂清
- Organizer
  第55回日本小児血液・がん学会学術集会
- Place of Presentation
  福岡市、ヒルトン福岡シーホーク
- Data Source
  KAKENHI-PROJECT-24591539
[Presentation] 小児がん治療後の口腔内がん3例
- Author(s)
  三井哲夫, 川上貴子, 簡野美弥子, 高橋憲幸, 小野田正志, 目黒亨, 佐藤裕子, 早坂清
- Organizer
  日本小児血液がん学会
- Place of Presentation
  岡山コンベンションセンター岡山
- Year and Date
  2014-11-28 – 2014-11-30
- Data Source
  KAKENHI-PROJECT-24591539
[Presentation] 変異型CRY1過剰発現マウスの膵β細胞の若齢における異常
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第19回日本時間生物学会学術大会
- Place of Presentation
  北海道大学学術交流会館
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] 非肥満若齢発症の糖尿病を示す変異型CRY1過剰発現マウスの若齢における遺伝子発現
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  日本生化学会東北支部第78回例会・シンポジウム
- Place of Presentation
  山形大学医学部
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] 2013年山形県南部で発症した甲状腺がん18歳男児の1例
- Author(s)
  本間信夫、橋本敏夫、角田力彌、三井哲夫、早坂清
- Organizer
  第55回日本小児血液・がん学会学術集会
- Place of Presentation
  福岡市、ヒルトン福岡シーホーク
- Data Source
  KAKENHI-PROJECT-24591539
[Presentation] 非肥満若齢発症の糖尿病を示す変異型CRY1過剰発現マウスの若齢における膵β細胞遺伝子の発現低下
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第55回日本糖尿病学会年次学術集会
- Place of Presentation
  パシフィコ横浜
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] Features of pancreatic islets in mutant cryptochrome1 transgenic mice at young stage
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第35回日本分子生物学会年会
- Place of Presentation
  マリンメッセ福岡
- Data Source
  KAKENHI-PROJECT-24590473
[Presentation] Features of diabetes mellitus in mutant cryptochrome1 transgenic mice at young stage
- Author(s)
  岡野聡, 早坂清, 五十嵐雅彦, 富樫義之, 中島修
- Organizer
  第9回国際糖尿病連合西太平洋地区会議/第4回アジア糖尿病学会学術集会
- Place of Presentation
  国立京都国際会館
- Data Source
  KAKENHI-PROJECT-24590473
[]
[]

1. MITSUI Tetsuo (30270846)

# of Collaborated Projects: 5 results

# of Collaborated Products: 10 results
2. UYEMURA Keiichi (90049792)

# of Collaborated Projects: 4 results

# of Collaborated Products: 0 results
3. TAKEDA Yasuo (60245462)

# of Collaborated Projects: 4 results

# of Collaborated Products: 0 results
4. SASAKI Ayako (60333960)

# of Collaborated Projects: 4 results

# of Collaborated Products: 19 results
5. KAWAKAMI Takako (90312743)

# of Collaborated Projects: 3 results

# of Collaborated Products: 7 results
6. OKANO Satoshi (60300860)

# of Collaborated Projects: 3 results

# of Collaborated Products: 55 results
7. NAKAJIMA Osamu (80312841)

# of Collaborated Projects: 3 results

# of Collaborated Products: 54 results
8. YASUI Akira (60191110)

# of Collaborated Projects: 2 results

# of Collaborated Products: 17 results
9. NUMAKURA Chikahiko (00400549)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
10. hashimoto taeko (30507629)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
11. KIMURA Toshiyuki (90292432)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
12. 中尾純治 (80255570)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
13. 池田博行 (80261709)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
14. IGARASHI Masahiko

# of Collaborated Projects: 2 results

# of Collaborated Products: 26 results
15. ABE Akiko (10536949)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
16. TAKAHASHI Nobuya (20536958)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. TACHI Nobutada (80136944)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. OHNISHI Akio (50091278)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. KATO Mitsuhiro (10292434)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. OKAMURA Yasushi (80201987)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. KUKITA Fumio (40113427)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
22. IWASAKI Hirohide (30342752)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
23. EBIHARA Tatsuhiko (00344119)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
24. SHIIHARA Takashi (90372333)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
25. ARIMURA Kimiyoshi (20159510)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
26. TAKASHIMA Hiroshi (80372803)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
27. SOBUE Gen (20148315)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
28. NAKAGAWA Masanori (50198040)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
29. ODAGIRI Tesshu (30400550)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
30. SATOH KENNICHI (10282055)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
31. 三浦正幸 (50202338)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
32. 岡本仁 (40183769)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
33. 矢崎貴仁 (80200484)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
34. 白幡恵美 (60400553)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
35. 簡野美弥子 (40400551)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
36. KISHIKAWA Yumiko

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
37. KANNO SHINICHIROU

# of Collaborated Projects: 1 results

# of Collaborated Products: 7 results
38. MAKINO Satoshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
39. HARITA Yutaka

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
40. ISHIZUKA Kiyonobu

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
41. 塚口裕康

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
42. 遠山育夫

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
43. 服部元史

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

HAYASAKA Kiyoshi 早坂 清

早坂 清 ハヤサカ キヨシ

Research Projects

Research Products

Co-Researchers

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Pathogenesis of Charcot-Marie-Tooth diseasePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular basis of Charcot-Marie-Tooth diseasePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Research and treatment of hereditary neuropathyPrincipal Investigator

Principal Investigator

Project Period (FY)

HAYASAKA Kiyoshi 早坂清

早坂清ハヤサカキヨシ