IKEGAWA SHIRO 池川志郎

… Alternative Names

池川志郎イケガワシロウ

IKEGAWA Shiro 池川志郎

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Researcher Number	30272496
Affiliation (Current)	2025: 国立研究開発法人理化学研究所, 生命医科学研究センター, 客員主管研究員
Affiliation (based on the past Project Information) *help	2023 – 2024: 国立研究開発法人理化学研究所, 生命医科学研究センター, 客員主管研究員 2022: 国立研究開発法人理化学研究所, 生命医科学研究センター, チームリーダー 2018 – 2020: 国立研究開発法人理化学研究所, 生命医科学研究センター, チームリーダー 2018: 理化学研究所, 骨関節疾患研究チーム, 主任研究員 2015: 理化学研究所, 骨関節疾患研究チーム, 主任研究員 … More 2012: 理化学研究所, 骨関節疾患研究チーム, 主任研究員 2008 – 2011: The Institute of Physical and Chemical Research, 骨関節疾患研究チーム, チームリーダー 2010: 独立行政法人理化学研究所, 骨間接疾患研究チーム, チームリーダー 2008: 独立行政法人理化学研究所, 骨関節疾患研究チーム, チームリーダ 2005 – 2007: 独立行政法人理化学研究所, 変形性関節症関連遺伝子研究チーム, チームリーダー 2004: RIKEN, SNP Research Center, Laboratory Head, 遺伝子多型研究センター, チームリーダー 2002 – 2004: 理化学研究所, 遺伝子多型研究センター, チームリーダー(研究職) 2003: Riken, SNP Research Center, Chief, 理化学研究所・遺伝子多型センター, チームリーダー(研究職) 2003: RIKEN, Laboratory for Bone and Joint Diseases, Laboratory Head, 変形性関節症関連遺伝子研究チーム, チームリーダー 2002: 理化学研究所, 変形性関節症関連遺伝子研究チーム, チームリーダー 2001: 東京大学, 医学部・附属病院, 研究員 2000: SNP Research Center, RIKEN, Laboratory for Bone and Joint Diseases, Laboratory Head, 変形性関節症関連遺伝子研究チーム, チームリーダー(研究職) 1997 – 1999: 東京大学, 医科学研究所, 助手 Less
Review Section/Research Field	Principal Investigator Orthopaedic surgery / Orthopaedic surgery / Basic Section 56020:Orthopedics-related Except Principal Investigator Orthopaedic surgery / Biological pharmacy / Orthopaedic surgery / Human genetics
Keywords	Principal Investigator 骨系統疾患 / 遺伝子 / ゲノム / pseudoachondroplasia / 疾患遺伝子 / 遺伝子解析 / 遺伝子診断 / 分子病態 / 相関解析 / 腰椎椎間板ヘルニア … More / 椎間板ヘルニア / ゲノム解析 / CILP / MED / mutation / gene / skeletal dysplasia / SNP / 脊椎脊髄病学 / 疾患感受性遺伝子 / 椎間板変性症 / 骨・関節疾患 / コホート / 遺伝的関連 / 思春期特発性側湾症 / 遺伝相関 / 後縦靱帯骨化症 / 骨関節疾患 / 運動器疾患 / 遺伝的相関 / 骨関節 / 運動器 / GWAS / 大規模ゲノム解析 / 異骨性骨硬化症 / 大理石骨病 / 多因子遺伝病 / 単一遺伝子病 / メカニカルストレス / 骨硬化症 / 原因遺伝子 / メカニカルストレス病 / association study / susceptibility gene / herniation / Lumbar disc disease / 遺伝子多型 / COL2A1 / COMP / bone and joint disease / genetic diagnosis / pseudochondroplasia / COL2A1遺伝子 / COMP遺伝子 / 遺伝子変異 / cartilage / bone / cloning / genome / disease gene / diagnosis / Skeletal dysplasia / Shwachman症候群 / chondrodysplasia / genetic analysis / ポジショナル、クローニング / 分子遺伝学 / 偽性軟骨無形成症 / アジア / アスポリン / COLIIA1 / 相関解析分子病態 … More Except Principal Investigator 骨系統疾患 / cystatin 10 / 変形性関節症 / プロテオグリカン / デルマタン硫酸 / コンドロイチン硫酸 / 小児運動器学 / 遺伝子診断 / 軟骨 / ゲノム / 老化 / グリコサミノグリカン / 遺伝性骨・皮膚疾患 / ゴルジ体 / ゴルジン / 皮膚弛緩症 / 脊椎肋骨異骨症 / 結合組織疾患 / LFNG / 免疫不全症 / 骨異形成性老人性皮膚症 / 脊椎骨端骨幹端異形成症 / エーラス・ダンロス症候群 / GORAB / Golgin / 糖尿病 / てんかん / 骨・皮膚疾患 / ヘパラン硫酸 / アルツハイマー病 / 癌 / RAGE / skeletal dysplasia / surgery / gene / genetics / genome / 致死性骨格形成異常症 / 毛髪軟骨低形成症 / 脊椎肋骨異形成症 / DTDST / 多発性骨端異形成症 / 蝸牛様骨盤異形成症 / 糖鎖科学 / 糖ヌクレオチド輸送体 / II型コラーゲン / Perthes病 / 原因遺伝子 / 外科 / 遺伝子 / 遺伝学 / osteoarthritis / fracture / calcification / chondrocyte / bone turnover / bone growth / knockout mouse / 遺伝子組み換え / マウス / 異所性骨化 / 異所性石灰化 / 遺伝子改変マウス / cystain10 / 骨折 / 石灰化 / 軟骨細胞 / 骨代謝 / 骨成長 / 遺伝子操作マウス / camphorquinone / aglycan / Type II collagen / free radical / Bone marrow interstitial stem cell / scaffold / Chondrocyte Transplantation / Photo-polymerizing Gelatin / tvpe II コラーゲン / type IIコラーゲン / Type II コラーゲン / カンファキノン / アグリカン / Type IIコラーゲン / ラディカル / 間質系幹細胞 / 担体 / 関節軟骨再生 / 可視光重合性ゼラチン / bone / polymorphism / OPLL / cytatin 10 / ttw / nucleotide pyrophosphatase(NPPS) / 遺伝子解析 / SNP / ポリモルフィズム / ヌクレオチドピロフォスファターゼ(NPPS) / ヌクレオチドピロフォスファターゼ(NppS) / 後縦靭帯骨化症(OPLL) / cystatin10 / ttwマウス / 骨 / ヌクレオチドピロフォスファターゼ / 骨髄 / 脂肪細胞 / 骨芽細胞 / 骨粗鬆症 / PPARγ / POSITIONAL CLONING / ATRIAL SPEPTAL DEFECT / FAMILIAL CATARACT / Paroxysmal kinetogenic choreoathetosis / ENGELMANN DISEASE / MESOMELIC DYSPLASIA / DISEASE LOCUS / LINKAGE ANALYSIS / 肢中部短縮型小人症 / ポジショナルクローニング / 心房中隔欠損症 / 家族性白内症 / 発作性運動誘発性コレオアテトーシス / Engelmann病 / 中間肢短縮小人症 / 疾患遺伝子座 / 連鎖解析 / ニュージーランド / ドイツ / 遺伝病 / 骨形成 / ダンロス症候群/糖転移酵素/硫酸基転移酵素 / 皮膚/遺伝病/脊椎骨端異形成症/ エーラス / コンドロイチン硫酸/デルマタン硫酸/骨 Less

運動器疾患のMulti disease GWAS 解析Principal Investigator
- Principal Investigator
  
  池川志郎
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 56020:Orthopedics-related
- Research Institution
  Institute of Physical and Chemical Research
Identification of the genes for mechanical stress diseasesPrincipal Investigator
- Principal Investigator
  
  Ikegawa Shiro
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 56020:Orthopedics-related
- Research Institution
  Institute of Physical and Chemical Research
Mechanism of biosynthesis of glycosaminoglycan by Golgin, and its hereditary bone and skin disorders
- Principal Investigator
  
  Mizumoto Shuji
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Biological pharmacy
- Research Institution
  Meijo University
Roles of chondroitin sulfate interacting with RAGE involved in tumor and Alzheimer's disease
- Principal Investigator
  
  Shiji Mizumoto
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Biological pharmacy
- Research Institution
  Meijo University
骨系統疾患の疾患遺伝子と分子病態の解明
- Principal Investigator
  
  DAI JIN (DAI Jin)
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  The Institute of Physical and Chemical Research
Pathogenic mechanisms of the bone diseases caused by defect in chondroitin sulfate biosynthesis
- Principal Investigator
  
  MIZUMOTO Shuji
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Biological pharmacy
- Research Institution
  Hokkaido University
Identification of susceptibility gene for lumbar disc disease and clarification of its molecular pathogenesisPrincipal Investigator
- Principal Investigator
  
  IKEGAWA Shiro
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  The Institute of Physical and Chemical Research
Identification of the causative genes and investigation of the molecular pathogenesis for skeletal dysplasias
- Principal Investigator
  
  FURUICHI Tatsuya
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  The Institute of Physical and Chemical Research
Identification of susceptibility gene for lumbar disc herniation and clarification of its molecular pathogenesisPrincipal Investigator
- Principal Investigator
  
  IKEGAWA Shiro
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  The Institute of Physical and Chemical Research
Identification of the genes for skeletal dysplasia and onstruction of its diagnostic system
- Principal Investigator
  
  MIYAMOTO Yoshinari
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  The Institute of Physical and Chemical Research
Molecular pathogenesis of lumbar disc degenerationPrincipal Investigator
- Principal Investigator
  
  IKEGAWA Shiro
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  RIKEN
Regeneration of Articular Cartilage Tissue from Cultured Chondrocytes using a Photo-polymerizing Gelatin as a Cell Carrier
- Principal Investigator
  
  MABUCHI Kunihiko
- Project Period (FY)
  2002 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  The University of Tokyo
Study of the function of cystatin 10, a novel chondrocyte-specific gene.
- Principal Investigator
  
  TAKESHITA Katsushi, 阿久根徹, 佐藤和強
- Project Period (FY)
  2002 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  The University of Tokyo
Analysis of disease genes for skeletal dysplasiasPrincipal Investigator
- Principal Investigator
  
  IKEGAWA Shiro
- Project Period (FY)
  2002 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  RIKEN
Regulation of bona and cartilage metabolism by nucleotide pyrophosphatase (NPPS) -skeletal analysis of ttw mice and its contribution to the human npps gene SNPs -
- Principal Investigator
  
  TAKESHITA Katsushi
- Project Period (FY)
  2001 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  The University of Tokyo
Genetic analysis and diagnosis of skeletal dysplasiasPrincipal Investigator
- Principal Investigator
  
  IKEGAWA Shiro
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (B).
- Research Field
  
  Orthopaedic surgery
- Research Institution
  SNP Research Center, RIKEN
  The University of Tokyo
Genetic analysis of skeletal dysplasiasPrincipal Investigator
- Principal Investigator
  
  IKEGAWA Shiro
- Project Period (FY)
  1997 – 1998
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  The University of Tokyo
LINKAGE ANALYSIS OF UNKNOWN GENETIC DISEASES
- Principal Investigator
  
  NIIKAWA Norio
- Project Period (FY)
  1996 – 1998
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Human genetics
- Research Institution
  NAGASAKI UNIVERSITY

[Book] 後縦靭帯骨化症のモデルマウス～ttw(tiptoe walking)～(21)2011
- Author(s)
  池川志郎
- Publisher
  CLINICAL CALCIUM
- Data Source
  KAKENHI-PROJECT-20390408
[Book] 第20回日本整形外科学会骨系統疾患研究会記録集(蝸牛様骨盤異形成症の責任遺伝子SLC35D1の同定)2009
- Author(s)
  古市達哉、池川志郎
- Data Source
  KAKENHI-PROJECT-20390408
[Book] 最新医学(63)(骨系統疾患と遺伝子異常-蝸牛様骨盤異形成症の原因遺伝子SLC35D1の発見-)2008
- Author(s)
  池川志郎、古市達哉、西村玄
- Data Source
  KAKENHI-PROJECT-20390408
[Book] 実験医学(26)(糖ヌクレオチド輸送体SLC35D1は骨格形成に必須である)2008
- Author(s)
  池川志郎、古市達哉
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Impaired glycine neurotransmission causes adolescent idiopathic scoliosis.2023
- Author(s)
  Wang X, Yue M, Cheung JPY, Cheung PWH, Fan Y, Wu M, Wang X, Zhao S, Khanshour AM, Rios JJ, Chen Z, Wang X, Tu W, Chan D, Yuan Q, Qin D, Qiu G, Wu Z, Zhang J, Ikegawa S, Wu N, Wise CA, Hu Y, Luk KDK, Song YQ, Gao B.
- Journal Title
  
  J Clin Invest
  
  Volume: 134 Issue: 2
- DOI
  10.1172/jci168783
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K24466
[Journal Article] Improved genetic prediction of the risk of knee osteoarthritis using the risk factor-based polygenic score2023
- Author(s)
  Morita Yugo、Kamatani Yoichiro、Ito Hiromu、Ikegawa Shiro、Kawaguchi Takahisa、Kawaguchi Shuji、Takahashi Meiko、Terao Chikashi、Ito Shuji、Nishitani Kohei、Nakamura Shinichiro、Kuriyama Shinichi、Tabara Yasuharu、Matsuda Fumihiko、Matsuda Shuichi、on behalf of the Nagahama study group
- Journal Title
  
  Arthritis Research & Therapy
  
  Volume: 25 Issue: 1 Pages: 103-103
- DOI
  10.1186/s13075-023-03082-y
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21H04850, KAKENHI-PROJECT-23K24466
[Journal Article] Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization study.2023
- Author(s)
  Otomo N, Khanshour AM, Koido M, et al., Ikegawa S, Watanabe K, Terao C.
- Journal Title
  
  Front Endocrinol (Lausanne)
  
  Volume: 14 Pages: 1089414-1089414
- DOI
  10.3389/fendo.2023.1089414
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K24466, KAKENHI-PROJECT-23K27724
[Journal Article] Genetic insights into ossification of the posterior longitudinal ligament of the spine2023
- Author(s)
  Koike Yoshinao、Inose Hiroyuki, et al.
- Journal Title
  
  eLife
  
  Volume: 12 Pages: 86514-86514
- DOI
  10.7554/elife.86514
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K09394, KAKENHI-PROJECT-21H03057, KAKENHI-PROJECT-23K24466
[Journal Article] A novel CCDC91 isoform associated with ossification of the posterior longitudinal ligament of the spine works as a non-coding RNA to regulate osteogenic genes2023
- Author(s)
  Nakajima Masahiro、Koido Masaru、Guo Long、Terao Chikashi、Ikegawa Shiro
- Journal Title
  
  The American Journal of Human Genetics
  
  Volume: 110 Issue: 4 Pages: 638-647
- DOI
  10.1016/j.ajhg.2023.03.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20H03811, KAKENHI-PROJECT-20K15773, KAKENHI-PROJECT-20H00462, KAKENHI-PROJECT-23K24466
[Journal Article] Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.2023
- Author(s)
  Yu H, Khanshour AM, Ushiki A, Otomo N, Koike Y, Einarsdottir E, Fan Y, Antunes L, Kidane YH, Cornelia R, Sheng RR, Zhang Y, Pei J, Grishin NV, Evers BM, Cheung JPY, Herring JA, Terao C, Song YQ, Gurnett CA, Gerdhem P, Ikegawa S, Rios JJ, Ahituv N, Wise CA.
- Journal Title
  
  Elife
  
  Volume: 12
- DOI
  10.7554/elife.89762
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K24466
[Journal Article] Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling2021
- Author(s)
  Guo Long、(他19名)、Ikegawa Shiro
- Journal Title
  
  Nature Communications
  
  Volume: 12 Issue: 1 Pages: 2046-2046
- DOI
  10.1038/s41467-021-22340-8
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932, KAKENHI-PROJECT-20H00551, KAKENHI-PROJECT-21H03098, KAKENHI-PROJECT-21K19554
[Journal Article] Expanding the phenotypic spectrum of TNFRSF11A-associated dysosteosclerosis: a case with intracranial extramedullary hematopoiesis2021
- Author(s)
  Xue Jing-Yi、Simsek-Kiper Pelin O.、Utine Gulen Eda、Yan Li、Wang Zheng、Taskiran Ekim Z.、Karaosmanoglu Beren、Imren Gozde、Gocmen Rahsan、Nishimura Gen、Matsumoto Naomichi、Miyake Noriko、Ikegawa Shiro、Guo Long
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 66 Issue: 6 Pages: 607-611
- DOI
  10.1038/s10038-020-00891-w
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932, KAKENHI-PROJECT-19H03621
[Journal Article] Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases2020
- Author(s)
  Ishigaki K, Akiyama M, Kanai M, Takahashi A, Kawakami E, Sugishita H, Sakaue S, Matoba N, Low SK, Okada Y, Yamaji T, et al
- Journal Title
  
  Nature Genetics
  
  Volume: 52 Issue: 7 Pages: 669-679
- DOI
  10.1038/s41588-020-0640-3
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K10655, KAKENHI-PROJECT-20K07709, KAKENHI-PROJECT-20K08288, KAKENHI-PROJECT-16H02468, KAKENHI-PROJECT-18H02894, KAKENHI-PLANNED-17H06419, KAKENHI-PROJECT-18H05285, KAKENHI-PROJECT-16H02676, KAKENHI-PROJECT-18H04053, KAKENHI-PROJECT-20H00543, KAKENHI-PROJECT-18H02688, KAKENHI-PROJECT-18H02931, KAKENHI-PROJECT-18H02932, KAKENHI-PROJECT-19H03559, KAKENHI-PROJECT-19H03881, KAKENHI-PROJECT-19K22525, KAKENHI-PROJECT-19K17962, KAKENHI-PROJECT-16H06277, KAKENHI-PROJECT-20H03695, KAKENHI-PROJECT-20H03943, KAKENHI-PROJECT-18H02940
[Journal Article] The third case of TNFRSF11A-associated dysosteosclerosis with a mutation producing elongating proteins2020
- Author(s)
  Xue Jing-Yi、Wang Zheng、Smithson Sarah F.、Burren Christine P.、Matsumoto Naomichi、Nishimura Gen、Ikegawa Shiro、Guo Long
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 66 Issue: 4 Pages: 371-377
- DOI
  10.1038/s10038-020-00831-8
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932
[Journal Article] Genetic disorders associated with the RANKL/OPG/RANK pathway2020
- Author(s)
  Xue Jing-Yi、Ikegawa Shiro、Guo Long
- Journal Title
  
  Journal of Bone and Mineral Metabolism
  
  Volume: 39 Issue: 1 Pages: 45-53
- DOI
  10.1007/s00774-020-01148-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18H02932
[Journal Article] 整形外科領域のゲノム医療－現状と今後の課題－2020
- Author(s)
  池川志郎
- Journal Title
  
  日本整形外科学会雑誌－別刷ー
  
  Volume: 94 Pages: 27-31
- Data Source
  KAKENHI-PROJECT-18H02932
[Journal Article] Crim1C140S mutant mice reveal the importance of cysteine 140 in the internal region 1 of CRIM1 for its physiological functions.2019
- Author(s)
  Furuichi T, Tsukamoto M, Saito M, Sato Y, Oiji N, Yagami K, Fukumura R, Gondo Y, Guo L, Ikegawa S, Yamamori Y, Tomii K.
- Journal Title
  
  Mamm Genome
  
  Volume: 30 Issue: 11-12 Pages: 329-338
- DOI
  10.1007/s00335-019-09822-3
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18H02932
[Journal Article] Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation2019
- Author(s)
  Guo L, Bertola DR, Takanohashi A, Saito A, Segawa Y, Yokota T, Ishibashi S, Nishida Y, Yamamoto GL, Franco JFdS, Honjo RS, Kim CA, Musso CM, Timmons M, Pizzino A, Taft RJ, (以下21名省略）, Ikegawa S.
- Journal Title
  
  The American Journal of Human Genetics
  
  Volume: 104 Issue: 5 Pages: 925-935
- DOI
  10.1016/j.ajhg.2019.03.004
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932, KAKENHI-PROJECT-17K16710, KAKENHI-PROJECT-17H01539, KAKENHI-PROJECT-19H03621
[Journal Article] Dysosteosclerosis is also caused by TNFRSF11A mutation.2018
- Author(s)
  Guo L, Elcioglu NH, Karalar OK, Topkar MO, Wang Z, Sakamoto Y, Matsumoto N, Miyake N, Nishimura G, Ikegawa S#.
- Journal Title
  
  J Hum Genet.
  
  Volume: 63(6) Issue: 6 Pages: 769-774
- DOI
  10.1038/s10038-018-0447-6
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H01539, KAKENHI-PROJECT-16H05357, KAKENHI-PROJECT-18H02932, KAKENHI-PROJECT-17K16710
[Journal Article] Identification of novel LFNG mutations in spondylocostal dysostosis.2018
- Author(s)
  Otomo N, Mizumoto S, Lu HF, Takeda K, Campos-Xavier B, Mittaz-Crettol L, Guo L, Takikawa K, Nakamura M, Yamada S, Matsumoto M, Watanabe K, Ikegawa S.
- Journal Title
  
  Journal of human genetics
  
  Volume: - Issue: 3 Pages: 261-264
- DOI
  10.1038/s10038-018-0548-2
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10986, KAKENHI-PROJECT-16K08251, KAKENHI-PROJECT-17K16709
[Journal Article] Chondroitin sulfate N-acetylgalactosaminyltransferase-1 (CSGalNAcT-1) deficiency results in a mild skeletal dysplasia and joint laxity.2017
- Author(s)
  Julia Vodopiutz, Shuji Mizumoto, Ekkehard Lausch, Antonio Rossi, Sheila Unger, Nikolaus Janocha, Rainer Seidl, Susanne Greber-Platzer, Shuhei Yamada, Thomas Muller, Bernd Jilma, Rudolf Ganger, Andrea Superti-Furga, Shiro Ikegawa, Kazuyuki Sugahara, Andreas R. Janecke.
- Journal Title
  
  Human Mutation
  
  Volume: 38 Issue: 1 Pages: 34-38
- DOI
  10.1002/humu.23070
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K07951, KAKENHI-PROJECT-16K08251
[Journal Article] Identification of biallelic EXTL3 mutations in a novel type of spondylo-epi-metaphyseal dysplasia2017
- Author(s)
  *Long Guo, *Nursel H Elcioglu, *Shuji Mizumoto, Zheng Wang, Bilge Noyan, Hatice M Albayrak, Shuhei Yamada, Naomichi Matsumoto, Noriko Miyake, Gen Nishimura, Shiro Ikegawa (equal contribution)
- Journal Title
  
  Journal of Human Genetics
  
  Volume: － Issue: 8 Pages: 797-801
- DOI
  10.1038/jhg.2017.38
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K08251, KAKENHI-PROJECT-17K16710, KAKENHI-PROJECT-17H01539, KAKENHI-PROJECT-16H05357, KAKENHI-PROJECT-15K07951
[Journal Article] Human genetic disorders caused by defective genes encoding biosynthetic enzymes for sulfated glycosaminoglycans2013
- Author(s)
  Shuji Mizumoto, Shiro Ikegawa, andKazuyuki Sugahara
- Journal Title
  
  Journal of Biological Chemistry
  
  Volume: 288 Issue: 16 Pages: 10953-10961
- DOI
  10.1074/jbc.r112.437038
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23790066, KAKENHI-PROJECT-25860037
[Journal Article] Mutations in B3GALT6 which Encodes a Glycosaminoglycan Linker Region Enzyme Cause a Spectrum of Skeletal and Connective Tissue Disorders2013
- Author(s)
  Masahiro Nakajima, Shuji Mizumoto et al.
- Journal Title
  
  American Journal of Human Genetics
  
  Volume: in press Issue: 6 Pages: 927-934
- DOI
  10.1016/j.ajhg.2013.04.003
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23790066, KAKENHI-PROJECT-24592230, KAKENHI-PROJECT-25293235, KAKENHI-PROJECT-25860037, KAKENHI-PROJECT-25860915
[Journal Article] Clinical and radiographic features of the autosomal recessive form of brachyolmia caused by PAPSS2 mutations2013
- Author(s)
  Aritoshi Iida*, Pelin Ozlem Simsek-Kiper*, Shuji Mizumoto*, Touma Hoshino, Nursel Elcioglu, Eva Horemuzova, Stefan Geiberger, Gozde Yesil, Hulya Kayserili, Gulen Eda Unite, Koray Boduroglu, Shigehiko Watanabe, Hirofumi Ohashi, Yasemin Alanay, Kazuyuki Sugahara, Gen Nishimura, Shiro Ikegawa (*equal contribution)
- Journal Title
  
  Human Mutation
  
  Volume: 34 Issue: 10 Pages: 1381-1386
- DOI
  10.1002/humu.22377
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25860037
[Journal Article] 一塩基多型を用いた大規模症例・対照相関解析による腰椎椎間板ヘルニアの原因遺伝子解析2011
- Author(s)
  池川志郎
- Journal Title
  
  Journal of Spine Research
  
  Volume: 2(9)
- Data Source
  KAKENHI-PROJECT-21249080
[Journal Article] TGF-βファミリーと骨・関節疾患2010
- Author(s)
  池川志郎
- Journal Title
  
  実験医学
  
  Volume: 29 Pages: 883-887
- Data Source
  KAKENHI-PROJECT-21249080
[Journal Article] TRPV4-pathy, a novel channelopathy affecting diverse systems.2010
- Author(s)
  Dai J, Ikegawa S
- Journal Title
  
  J Hum Genet. 55
  
  Pages: 400-402
- NAID
  10030735608
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210.2010
- Author(s)
  Smits P, Ikegawa S
- Journal Title
  
  New Engl J Med. 362
  
  Pages: 206-216
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Spondylo-epiphyseal dysplasia, Maroteaux type (pseudo-Morquio syndrome type 2), and parastremmatic dysplasia are caused by TRPV4 mutations.2010
- Author(s)
  Nishimura G, Ikegawa S
- Journal Title
  
  Am J Med Genet. 152A
  
  Pages: 1443-1449
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Association of the tag SNPs in the human SKT Gene (KIAA1217) with lumbar disc herniation2009
- Author(s)
  Karasugi T, Semba K, Hirose Y, Kelempisioti A, Nakajima M, Miyake A, Furuichi T, Kawaguchi Y, Mikami Y, Chiba K, Kamata M, Ozaki K, Takahashi A, Makela P, Karppinen J, Kimura T, Kubo T, Toyama Y, Yamamura KI, Mannikko M, Mizuta H, Ikegawa S
- Journal Title
  
  J Bone Miner Res (Epub ahead of print)
  
  Pages: 0-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19209049
[Journal Article] Association of the tag SNPs in the human SKT Gene(KIAA1217) with lumbar disc herniation2009
- Author(s)
  Karasugi T. Semba K, Hirose Y, Kelempisioti A, Nakajima M, Miyake A, Furuichi T, Kawaguchi Y, Mikami Y, Chiba K, Kamata M, Ozaki K, Takahashi A, Makela P, Karppinen J, Kimura T, Kubo T, Toyama Y, Yamamura K, Mannikko M, Mizuta H, Ikegawa S
- Journal Title
  
  J Bone Miner Res
  
  Volume: 24(9) Pages: 1537-1543
- Data Source
  KAKENHI-PROJECT-21249080
[Journal Article] Association of the Asporin D14 allele with lumbar disc degeneration in Asians.2008
- Author(s)
  Song Y-Q, Cheung KMC, Ho DWH, Poon SCS, Chiba K, Kawaguchi Y, Hirose Y, Alini M, Grad S, Yee AFY, Leong J CY, Luk KDK, Yip S-P, Karppinen J, Cheah KSE, Sham P, Ikegawa S, Chan D.
- Journal Title
  
  Am J Hum Genet (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19209049
[Journal Article] 骨系統疾患と遺伝子異常-蝸牛様骨盤異形成症の原因遺伝子SLC35D1の発見-2008
- Author(s)
  池川志郎
- Journal Title
  
  最新医学 63
  
  Pages: 2211-2217
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] 糖ヌクレオチド輸送体SLC35D1は骨格形成に必須である2008
- Author(s)
  池川志郎
- Journal Title
  
  実験医学 26
  
  Pages: 913-916
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Association of the asporin D14 allele with lumbar-disc degeneration in Asians2008
- Author(s)
  Song YQ, Cheung KM, Ho DW, Poon SC, Chiba K, Kawaguchi Y, Hirose Y, Alini M, Grad S, Yee AF, Leong JC, Luk KD, Yip SP, Karppinen J, Cheah KS, Sham P, Ikegawa S, Chan D
- Journal Title
  
  Am J Hum Genet 82(3)
  
  Pages: 744-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19209049
[Journal Article] A functional polymorphism in THBS2 that affects alternative splicing and MMP binding is associated with lumbar-disc herniation2008
- Author(s)
  Hirose Y, Chiba K, Karasugi T, Nakajima M, Kawaguchi Y, Mikami Y, Furuichi T, Mio F, Miyake A, Miyamoto T, Ozaki K, Takahashi A, Mizuta H, Kubo T, Kimura T, Tanaka T, Toyama Y, Ikegawa S
- Journal Title
  
  Am J Hum Genet 82(5)
  
  Pages: 1122-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19209049
[Journal Article] A recurrent mutation in type II collagen gene causes Legg-Calve-Perthes disease in a Japanese family.2007
- Author(s)
  Miyamoto Y, Matsuda T, Kitoh H, Haga N, Ohashi H, Nishimura G, Ikegawa S.
- Journal Title
  
  Hum Genet 121
  
  Pages: 625-629
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18390423
[Journal Article] Nucleotide-sugar transporter SLC35D1 is critical to chondroitin sulfate synthesis incartilage and skeletal development in mouse and human.2007
- Author(s)
  Hiraoka S, Funuichi T, Nishimura G, Shibata S, Yanagishita M, Rimoin DL, Superti-Furga A, Nikkels PG, Ogawa M, Katsuyama K, Toyoda H, Kinoshita-Toyoda A, Ishida N, Isono K, Sanai Y, Cohn DH, Koseki H, Ikegawa S.
- Journal Title
  
  Nature Med 13
  
  Pages: 1363-1367
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18390423
[Journal Article] A functional polymorphism in COL11A1,which encodes the alpha 1 chain of type XI collagen,is associated with susceptibility to lumbar dischemiation.2007
- Author(s)
  Mio F, Chiba K, Hirose Y, Kawaguchi Y, Mikami Y, Oya T, Mori M, Kamata M, Matsumoto M, Ozaki K, Tanaka T, Takahashi A, Kubo T. Kimura T, Toyama Y, Ikegawa S.
- Journal Title
  
  Am J Hum Genet 81
  
  Pages: 1271-1277
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19209049
[Journal Article] A functional polymorphism in COL11A1, which encodes the alpha 1 chain of type XI collagen, is associated with susceptibility to lumbar disc herniation2007
- Author(s)
  Mio F, Chiba K, Hirose Y, Kawaguchi Y, Mikami Y, Oya T, Mori M, Kamata M, Matsumoto M, Ozaki K, Tanaka T, Takahashi A, Kubo T, Kimura T, Toyama Y, Ikegawa S
- Journal Title
  
  Am J Hum Genet 81(6)
  
  Pages: 1271-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19209049
[Journal Article] Transcriptional regulation of the cartilage intermediate layer protein (CILP) gene.2006
- Author(s)
  Mori M, Nakajima M, Mikami Y, Seki S, Takigawa M, Kubo T, Ikegawa s.
- Journal Title
  
  Biochemical and Biophysical Research Communications 341・1
  
  Pages: 121-127
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] Genetic analysis of skeletal dysplasia : recent advances and perspectives in the post-genome-sequence era.2006
- Author(s)
  Ikegawa S
- Journal Title
  
  J Hum Genet 51(7)
  
  Pages: 581-6
- NAID
  10017989428
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18390423
[Journal Article] Association study of COL9A2 with lumbar disc disease in the Japanese population.2006
- Author(s)
  Seki S, Kawaguchi Y, Mori M, Mio F, Chiba K, Mikami Y, Tsunoda T, Kubo T, Toyama Y, Kimura T, Ikegawa S.
- Journal Title
  
  Journal of Human Genetics 51・12
  
  Pages: 1063-1067
- NAID
  10018641536
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] Association study of COL9A2 with lumbar disc disease in the Japanese population.2006
- Author(s)
  Seki S, Kawaguchi Y, Mori M, Mio F, Chiba K, Mikami Y, Tsunoda T, Kubo T, Toyama Y, Kimura T, Ikegawa S.
- Journal Title
  
  J Hum Genet 51.12
  
  Pages: 1063-1067
- NAID
  10018641536
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] Transcriptional regulation of the cartilage intermediate layer protein (CILP) gene.2006
- Author(s)
  Mori M, Nakajima M, Mikami Y, Seki S, Takigawa M, Kubo T, Ikegawa S.
- Journal Title
  
  Biochem Biophys Res Commun 341.1
  
  Pages: 121-127
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] A compound heterozygote harboring novel and recurrent DTDST mutations with intermediate phenotype between atelosteogenesis type II and diastrophic dysplasia.2006
- Author(s)
  Maeda K, Miyamoto Y, Sawai H, Kamiski LP, Nakashima E, Nishimura G, Ikegawa S.
- Journal Title
  
  American Journal of Medical Genetics A140・11
  
  Pages: 1143-1147
- Data Source
  KAKENHI-PROJECT-18390423
[Journal Article] A large-scale genetic association study of ossification of the posterior longitudinal ligament of the spine.2006
- Author(s)
  Horikoshi T, Maeda K, Kawaguchi Y, Chiba K, Mori K, Koshizuka Y, Hirabayashi S, Sugimori K, Matsumoto M, Inoue H, Kimura T, Matsusue Y, Inoue I, Baba H, Nakamura K, Ikegawa S.
- Journal Title
  
  Hum Genet 119・6
  
  Pages: 611-616
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] Genetic analysis of skeletal dysplasia : recent advances and perspectives in the post-genome-sequence era.2006
- Author(s)
  Ikegawa S.
- Journal Title
  
  Journal of Human Genetics 51・7
  
  Pages: 581-586
- NAID
  10017989428
- Data Source
  KAKENHI-PROJECT-18390423
[Journal Article] Identification of novel RMRP mutations and specific founder haplotypes in Japanese patients with cartilage-hair hypoplasia.2006
- Author(s)
  Hirose Y, Nakashima E, Ohashi H, Mochizuki H, Bando Y, Ogata T, Adachi M, Toba E, Nishimura G, Ikegawa S.
- Journal Title
  
  Journal of Human Genetics 51・8
  
  Pages: 706-710
- NAID
  10019286019
- Data Source
  KAKENHI-PROJECT-18390423
[Journal Article] Comprehensive screening of multiple epiphyseal dysplasia mutations in Japanese population.2006
- Author(s)
  Itoh T, Shirahama S, Nakashima E, Maeda K, Haga N, Kitoh H, Kosaki R, Ohashi H, Nishimura G, Ikegawa S.
- Journal Title
  
  American Journal of Medical Genetics A140・12
  
  Pages: 1280-1284
- Data Source
  KAKENHI-PROJECT-18390423
[Journal Article] Association study of COL9A2 with lumbar disc disease in the Japanese population.2006
- Author(s)
  Seki S, Kawaguchi Y, Mori M, Mio F, Chiba K, Mikami Y, Tsunoda T, Kubo T, Toyama Y, Kimura T, Ikegawa S
- Journal Title
  
  J Hum Genet 51 (12)
  
  Pages: 1063-1067
- NAID
  10018641536
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] Transcriptional regulation of the cartilage intermediate layer protein (CILP) gene.2006
- Author(s)
  Mori M, Nakajima M, Mikami Y, Seki S, Takigawa M, Kubo T, Ikegawa S
- Journal Title
  
  Biochem Biophys Res Commun 341 (1)
  
  Pages: 121-127
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] A large-scale genetic association study of ossification of the posterior longitudinal ligament of the spine.2006
- Author(s)
  Horikoshi T, Maeda K, Kawaguchi Y, Chiba K, Mori K, Koshizuka Y, Hirabayashi S, Sugimori K, Matsumoto M, Kawaguchi H, Takahashi M, Inoue H, Kimura T, Matsusue Y, Inoue I, Baba H, Nakamura K, Ikegawa S
- Journal Title
  
  Hum Genet 119 (6)
  
  Pages: 611-616
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] A large-scale genetic association study of ossification of the posterior longitudinal ligament of the spine.2006
- Author(s)
  Horikoshi T, Maeda K, Kawaguchi Y, Chiba K, Mori K, Koshizuka Y, Hirabayashi S, Sugimori K, Matsumoto M, Kawaguchi H, Takahashi M, Inoue H, Kimura T, Matsusue Y, Inoue I, Baba H, Nakamura K, Ikegawa S.
- Journal Title
  
  Hum Genet 119.6
  
  Pages: 611-616
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] MATN and LAPTM are parts of larger transcription units produced by intergenic splicing : intergenic splicing may be a common phenomenon.2005
- Author(s)
  Maeda K, Horikoshi T, Nakashima E, Miyamoto Y, Mabuchi A, Ikegawa S.
- Journal Title
  
  DNA Res 12.5
  
  Pages: 365-37
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease2005
- Author(s)
  Seki S, Kawaguchi Y, Chiba K, Mikami Y, Kizawa H, Oya T, Mio F, Mori M, Miyamoto Y, Masuda I, Tsunoda T, Kamata M, Kubo T, Toyama Y, Kimura T, Nakamura Y, Ikegawa S.
- Journal Title
  
  Nature Genet 37.6
  
  Pages: 607-612
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] MATN and LAPTM are parts of larger transcription units produced by intergenic splicing : intergenic splicing may be a common phenomenon.2005
- Author(s)
  Maeda K, Horikoshi T, Nakashima E, Miyamoto Y, Mabuchi A, Ikegawa S
- Journal Title
  
  DNA Res 12 (5)
  
  Pages: 365-372
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] 椎間板ヘルニアの原因遺伝子CILP2005
- Author(s)
  池川志郎
- Journal Title
  
  医学のあゆみ 214・9
  
  Pages: 755-756
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease.2005
- Author(s)
  Seki S, Kawaguchi Y, Chiba K, Mikami Y, Kizawa H, Oya T, Mio E, Mori M, Miyamoto Y, Masuda I, Tsunoda T, Kamata M, Kubo T, Toyama Y, Kimura T, Nakamura Y, Ikegawa S
- Journal Title
  
  Nature Genet 37 (6)
  
  Pages: 607-612
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209050
[Journal Article] The combination of SOX5,SOX6 and SOX9 (the SOX trio) provides signals sufficient for induction of permanent cartilage2004
- Author(s)
  T.Ikeda, S.Kamekura, A.Mabuchi, I.Kou, S.Seki, T.Takato, K.Nakamura, H.Kawaguchi, S.Ikegawa.U.Chung
- Journal Title
  
  Arthritis Rheum. Vol.50 No.11
  
  Pages: 3561-3573
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14207055
[Journal Article] The combination of SOX5,SOX6 and SOX9 (the SOX trio) provides signals sufficient for induction of permanent cartilage2004
- Author(s)
  T.Ikeda, S.Kamekura, A.Mabuchi, I.Kou, S.Seki, T.Takato, K.Nakamura, H.Kawaguchi, S.Ikegawa, U.Chung
- Journal Title
  
  Arthritis Rheum. Vol.50 No.11
  
  Pages: 3561-3573
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14207055
[Journal Article] SOX9-dependent and SOX9-independent transcriptional regulation of human cartilage link protein2004
- Author(s)
  I.Kou, S.Ikegawa
- Journal Title
  
  Journal of Biological Chemistry Vol.279 No.4
  
  Pages: 50942-50948
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14207055
[Journal Article] The combination of SOX5, SOX6 and SOX9 (the SOX trio) provides signals sufficient for induction of permanent cartilage2004
- Author(s)
  T.Ikeda, S.Kamekura, A.Mabuchi, I.Kou, S.Seki, T.Takato, K.Nakamura, H.Kawaguchi, S.Ikegawa, U.Chung
- Journal Title
  
  Arthritis Rheum Vol.50 No.11
  
  Pages: 3561-3573
- Data Source
  KAKENHI-PROJECT-14207055
[Journal Article] RMRP Mutations in Japanese Patients with Cartilage-Hair Hypoplasia.2003
- Author(s)
  Ikegawa S., et al.
- Journal Title
  
  American Journal of Medical Genetics 123A(3)
  
  Pages: 253-256
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14207055
[Journal Article] Cystatin 10,a novel chondrocyte-specific protein, may promote the last steps of the chondrocyte differentiation pathway.2003
- Author(s)
  Nakamura K, Ikegawa S., et al.
- Journal Title
  
  Journal Biological Chemistry 278(48)
  
  Pages: 48259-48266
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14207055
[Journal Article] Cystatin 10, a novel chondrocyte-specific protein, may promote the last steps of the chondrocyte differentiation pathway.2003
- Author(s)
  Nakamura K, Ikegawa S., et al.
- Journal Title
  
  Journal Biological Chemistry 278(48)
  
  Pages: 48259-48266
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14207055
[Journal Article] Identification and characterization of the human long form of Sox5 (L-SOX5) gene.2002
- Author(s)
  Ikeda I., Ikegawa S., et al.
- Journal Title
  
  Gene 298(1)
  
  Pages: 59-68
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14207055
[Journal Article] Identification and characterization of the human long form of Sox5 (L-SOX5) gene.2002
- Author(s)
  Ikeda T., Ikegawa S., et al.
- Journal Title
  
  Gene 298(1)
  
  Pages: 59-68
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14207055
[Journal Article] Association analysis of single nucleotide polymorphisms in cartilage-specific collagen genes with knee and hip osteoarthritis in the Japanese population.2002
- Author(s)
  Ikeda T., Ikegawa S., et al.
- Journal Title
  
  J.Bone Miner Res. 17(7)
  
  Pages: 1290-1296
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14207055
[Patent] 椎間板変性関連疾患感受性遺伝子およびその用途2008
- Inventor(s)
  池川志郎
- Industrial Property Rights Holder
  理化学研究所
- Filing Date
  2008-09-30
- Overseas
- Data Source
  KAKENHI-PROJECT-19209049
[Patent] 椎間板変性関連疾患感受性遺伝子およびその用途(トロンボスポンディン2遺伝子、マトリックスメタロプロテアーゼ2遺伝子、及びマトリックスメタロプロテアーゼ9遺伝子による椎間板変性症、及び椎間板ヘルニアの疾患感受性の診断と治療)2008
- Inventor(s)
  池川志郎
- Industrial Property Rights Holder
  理化学研究所
- Filing Date
  2008-09-30
- Data Source
  KAKENHI-PROJECT-19209049
[Patent] 椎間板変性関連疾患感受性遺伝子およびその用途(トロンボスポンディン2遺伝子、マトリックスメタロプロテアーゼ2遺伝子、及びマトリックスメタロプロテアーゼ9遺伝子による椎間板変性症、及び椎間板ヘルニアの疾患感受性の診断と治療)2007
- Inventor(s)
  池川志郎
- Industrial Property Rights Holder
  独立行政法人理化学研究所
- Industrial Property Number
  2007-257345
- Filing Date
  2007-10-01
- Data Source
  KAKENHI-PROJECT-19209049
[Patent] 椎間板変性関連疾患感受性遺伝子およびその用途2005
- Inventor(s)
  池川志郎
- Industrial Property Rights Holder
  理化学研究所
- Industrial Property Number
  2005-292359
- Filing Date
  2005-10-05
- Data Source
  KAKENHI-PROJECT-17209050
[Patent] 椎間板変性症関連疾患感受性遺伝子およびその用途2005
- Inventor(s)
  池川志郎
- Industrial Property Rights Holder
  独立行政法人理化学研究所
- Industrial Property Number
  2005-292359
- Filing Date
  2005-10-05
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209050
[Presentation] 運動器疾患のゲノム解析2023
- Author(s)
  池川志郎
- Organizer
  第４１回日本骨代謝学会
- Invited
- Data Source
  KAKENHI-PROJECT-23K24466
[Presentation] 側彎症の現状と今後の発展2022
- Author(s)
  池川志郎
- Organizer
  第95回日本整形外科学会学術総会
- Invited
- Data Source
  KAKENHI-PROJECT-23K24466
[Presentation] Genomic Study of Bone and Joint Diseases2022
- Author(s)
  池川志郎
- Organizer
  Foreign Expert Seminar, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, School of Basic Medicine, Peking Union Medical College
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K24466
[Presentation] 基礎からの運動器ゲノム学2022
- Author(s)
  池川志郎
- Organizer
  JOSKAS2022
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K24466
[Presentation] Genomic Study of Rare Diseases of Skeleton2020
- Author(s)
  池川志郎
- Organizer
  India -Japan Webinar on "Rare Genetic Disorders" by Embassy of India
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] 後縦靭帯骨化症のゲノム研究：過去・現在・未来2020
- Author(s)
  池川志郎
- Organizer
  第35回日本整形外科学会基礎学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] ゲノム医療と整形外科：パーソナルゲノム時代に取り残されないために2020
- Author(s)
  池川志郎
- Organizer
  ちば整形外科エキスパートカンファレンス 2020
- Invited
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] Differential diagnosis of skeletal dysplasias and genetic skeletal disorders2020
- Author(s)
  池川志郎
- Organizer
  Virtual APAC MPS Summit 2020 Webinar 2020
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] Identification of novel disease genes and re-classification of dysosteosclerosis2020
- Author(s)
  池川志郎
- Organizer
  The 65th Annual Meeting of the Japan Society of Human Genetics (English Symposium)
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] 病気と遺伝：これからの医学・医療を理解するための基礎知識2020
- Author(s)
  池川志郎
- Organizer
  愛媛大特別講義
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] 整形外科のゲノム医療：現在、過去、未来2020
- Author(s)
  池川志郎
- Organizer
  第135回中部日本整形外科災害外科学会・学術集会(教育研修講演)
- Invited
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] 運動器疾患におけるゲノム研究2019
- Author(s)
  池川志郎
- Organizer
  第62回日本手外科学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] 病気と遺伝：これからの医学・医療を理解するための基礎知識2019
- Author(s)
  池川志郎
- Organizer
  広島大学歯学部特別講義
- Invited
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] ゲノム医療について2019
- Author(s)
  池川志郎
- Organizer
  第46回難病患者・障害者と家族の全道集会
- Invited
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] ヒトゲノム解析の基礎知識：パーソナルゲノム時代に取り残されないために2019
- Author(s)
  池川志郎
- Organizer
  北里大学薬学研究科大学院特別講義
- Invited
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] Genetic study of skeletal dysplasia2019
- Author(s)
  池川志郎
- Organizer
  APSS-APPOS 2019
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] Identification of Novel Disease Genes and Re-classification of Dysosteosclerosis2019
- Author(s)
  池川志郎
- Organizer
  14th ISDS meeting, Oslo, Norway
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] 病気と遺伝：これからの医学・医療を理解するための基礎知識2019
- Author(s)
  池川志郎
- Organizer
  愛媛大特別講義
- Invited
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] Genomic study of skeletal dysplasia in the personal genome sequence era2019
- Author(s)
  池川志郎
- Organizer
  4th National Pediatric Genetics Congress
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] Genomic study of Diseases in the Genome Sequencing Era2019
- Author(s)
  池川志郎
- Organizer
  北京協和医学院病院骨科セミナー
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] ゲノム医療と整形外科2019
- Author(s)
  池川志郎
- Organizer
  ロコモ対策運動器疾患／骨・関節フォーラム
- Invited
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] 骨系統疾患のゲノム解析2019
- Author(s)
  池川志郎
- Organizer
  New Insights of Molecular Genetics on Growth Disorders
- Invited
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] Genomic study of Diseases in the Genome Sequencing Era2019
- Author(s)
  池川志郎
- Organizer
  中国医学科学院基礎研究所セミナー
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] 骨関節疾患のゲノム解析の現状と課題2019
- Author(s)
  池川志郎
- Organizer
  第46回日本股関節学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] A novel type of spondylo-epi-metaphyseal dysplasia with immuno-deficiency caused by mutation in EXTL3 encoding a glycosyltransferase responsible for biosynthesis of heparan sulfate2018
- Author(s)
  Shuji Mizumoto, Long Guo, Nursel H Elcioglu, Zheng Wang, Bilge Noyan, Hatice M Albayrak, Naomichi Matsumoto, Noriko Miyake, Gen Nishimura, Shuhei Yamada, and Shiro Ikegawa
- Organizer
  The 11th International Symposium on Glycosyltransferases, Qingdao, China, 6/19
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K08251
[Presentation] Structural studies on heparan sulfate produced by the lymphoblastoid cell lines prepared from a patient with a mutation in EXTL3 and embryonic cells from Extl3-deficient mice2018
- Author(s)
  Shuhei Yamada, Shuji Mizumoto, Hirofumi Ohashi, Etsuko Sakasai, Nursel H Elcioglu, Noriko Miyake, Naomichi Matsumoto, Daisuke Ibi, Akira Sugawara, and Shiro Ikegawa
- Organizer
  Gordon Research Conference on Proteoglycans 2018, Andover, Poster, USA, 7/8-13
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K08251
[Presentation] 免疫異常を伴う脊椎骨端骨幹端異形成症はヘパラン硫酸の生合成を担うEXTL3の変異により引き起こされる2018
- Author(s)
  水本秀二, Long Guo, Nursel H Elcioglu, Zheng Wang, Bilge Noyan, Hatice M Albayrak,松本直通, 三宅紀子, 西村玄, 山田修平, 池川志郎
- Organizer
  第37回日本糖質学会年会、仙台、8/30
- Data Source
  KAKENHI-PROJECT-16K08251
[Presentation] ヘパラン硫酸の生合成を担うEXTL3の変異は免疫不全を伴う脊椎骨端骨幹端異形成症を引き起こす2018
- Author(s)
  水本秀二, Long Guo, Nursel H Elcioglu, Zheng Wang, Bilge Noyan, Hatice M Albayrak, 松本直通, 三宅紀子, 西村玄, 山田修平, 池川志郎
- Organizer
  糖鎖科学中部拠点　第15回若手の力フォーラム、静岡、9/6
- Data Source
  KAKENHI-PROJECT-16K08251
[Presentation] ヘパラン硫酸生合成酵素であるEXTL3の変異は免疫異常を伴う新たなタイプの脊椎骨端骨幹端異形成症を引き起こす2018
- Author(s)
  Long Guo, Nursel H Elcioglu, Shuji Mizumoto, Zheng Wang, Bilge Noyan, Hatice M Albayrak, Shuhei Yamada, Naomichi Matsumoto, Noriko Miyake, Gen Nishimura1, Shiro Ikegawa
- Organizer
  日本生化学会中部支部第82回例会・シンポジウム、岐阜、5/19
- Data Source
  KAKENHI-PROJECT-16K08251
[Presentation] Genomic Study of Skeletal Dysplasia2018
- Author(s)
  池川志郎
- Organizer
  二国間交流事業
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] 病気と遺伝：これからの医学・医療を理解するための基礎知識2018
- Author(s)
  池川志郎
- Organizer
  愛媛大特別講義
- Invited
- Data Source
  KAKENHI-PROJECT-18H02932
[Presentation] デルマタン硫酸の生合成不全によるエーラス・ダンロス症候群の糖鎖生物学的研究2016
- Author(s)
  水本秀二, 古庄知己, 本田智子,中島正宏, Thomas Muller, 三宅紀子, 籏持淳, 松本直通, Andreas R Janecke, 池川志郎, 菅原一幸, ○山田修平
- Organizer
  第35回日本糖質学会年会
- Place of Presentation
  高知市文化プラザ（高知）
- Year and Date
  2016-09-03
- Data Source
  KAKENHI-PROJECT-16K08251
[Presentation] PAPS合成酵素2の変異は常染色体劣性型短脊柱症を引き起こす2014
- Author(s)
  水本秀二, 飯田有俊, Pelin Ozlem Simsek-Kiper, 星野冬馬, Nursel Elcioglu, Eva Horemuzova, Stefan Geiberger, Gozde Yesil, Hulya Kayserili, Gulen Eda Utine, Koray Boduroglu, 渡邉成彦, 大橋博文, Yasemin Alanay, 西村玄, 池川志郎, 菅原一幸
- Organizer
  第33回日本糖質学会年会
- Place of Presentation
  名古屋大学（名古屋）
- Year and Date
  2014-08-11
- Data Source
  KAKENHI-PROJECT-25860037
[Presentation] Spondyloepimetaphyseal dysplasia and Ehlers-Danlos syndrome caused by mutations of glycosaminoglycan biosynthetic enzymes, GalT-II and DS-epimerase2014
- Author(s)
  Shuji Mizumoto, Masahiro Nakajima, Thomas Muller Noriko Miyake, Ryo Kogawa, Yoshie Komatsu, Naomichi Matsumoto, Andreas R Janecke, Shiro Ikegawa, Kazuyuki Sugahara
- Organizer
  Joint Meeting of the Society for Glycobiology and the Japanese Society of Carbohydrate Research
- Place of Presentation
  Hilton Hotel (Hawaii, USA)
- Year and Date
  2014-11-19
- Data Source
  KAKENHI-PROJECT-25860037
[Presentation] ゲノム科学による疾患研究2012
- Author(s)
  池川志郎
- Organizer
  早稲田大学講義先端生命医科学特論イノベーティブディスカバリー
- Place of Presentation
  早稲田大学生命医科学センター(東京都)(招待講演)
- Year and Date
  2012-01-13
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] ゲノム科学による疾患研究2012
- Author(s)
  池川志郎
- Organizer
  早稲田大学講義先端生命医科学特論イノベーティブディスカバリー
- Place of Presentation
  早稲田大学生命医科学センター(東京都)
- Year and Date
  2012-01-13
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] Next steps for genetic study of skeletal diseases-problems and solutions from 10 years' experience2012
- Author(s)
  Ikegawa S
- Organizer
  Symposium on Developmental Genomics and Genetics Disorders
- Place of Presentation
  Hong Kong, China
- Year and Date
  2012-01-17
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] Next steps for genetic study of skeletal diseases-problems and solutions from 10 years' experience2012
- Author(s)
  Ikegawa Shiro
- Organizer
  Symposium on Developmental Genomics and Genetics Disorders
- Place of Presentation
  Hong Kong, China(招待講演)
- Year and Date
  2012-01-17
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] ゲノムから医療へ、創薬へ:相関解析により同定された骨・関節の生活習慣病の原因遺伝子(疾患感受性遺伝子)に関する知見・知財の臨床応用に向けての課題の克服2011
- Author(s)
  池川志郎
- Organizer
  次世代医療システム産業化フォーラム
- Place of Presentation
  シティプラザ大阪(大阪府)(招待講演)
- Year and Date
  2011-07-08
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] ゲノムから医療へ、創薬ヘ:相関解析により同定された骨・関節の生活習慣病の原因遺伝子(疾患感受性遺伝子)に関する知見・知財の臨床応用に向けての課題の克服2011
- Author(s)
  池川志郎
- Organizer
  次世代医療システム産業化フォーラム招待講演
- Place of Presentation
  シティプラザ大阪(大阪府)
- Year and Date
  2011-07-08
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] Genomic analysis of osteoarthritis-From patient to gene, from genome to molecular pathogenesis2011
- Author(s)
  Shiro Ikegawa
- Organizer
  1st Symposium of the Asia Pacific League of Associations for Rheumatology
- Place of Presentation
  Taipei, Taiwan(招待講演)
- Year and Date
  2011-04-16
- Data Source
  KAKENHI-PROJECT-23390370
[Presentation] Genomic analysis of osteoarthritis-From patient to gene, from genome to molecular pathogenesis2011
- Author(s)
  Ikegawa Shiro
- Organizer
  1st Symposium of the Asia Pacific League of Associations for Rheumatology
- Place of Presentation
  Taipei, Taiwan(招待講演)
- Year and Date
  2011-04-16
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] Genomic analysis of osteoarthritis-From patient to gene, from genome to molecular pathogenesis2011
- Author(s)
  Ikegawa S
- Organizer
  1st Symposium of the Asia Pacific League of Associations for Rheumatology
- Place of Presentation
  Taipei, Taiwan
- Year and Date
  2011-04-16
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] 疾患遺伝子研究の現状と未来:骨・関節疾患を例に2011
- Author(s)
  池川志郎
- Organizer
  徳島大学「次世代シーケンサーを用いた最先端研究」講演会
- Place of Presentation
  徳島大学医学部(徳島県)
- Year and Date
  2011-08-26
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] 疾患遺伝子研究の現状と未来:骨・関節疾患を例に2011
- Author(s)
  池川志郎
- Organizer
  徳島大学「次世代シーケンサーを用いた最先端研究」講演会
- Place of Presentation
  徳島大学医学部(徳島県)(招待講演)
- Year and Date
  2011-08-26
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] 遺伝学を用いた骨・関節疾患へのアプローチ2010
- Author(s)
  池川志郎
- Organizer
  第5回Skeletal Research Meeting
- Place of Presentation
  京都
- Year and Date
  2010-06-12
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] From genome to skeletal diseases-recent advances in the association study of osteoarthritis and lumbar disc herniation2010
- Author(s)
  Ikegawa S
- Organizer
  1st OARSI China Forum
- Place of Presentation
  Nanjing, China
- Year and Date
  2010-10-05
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] Genetic study of lumbar disc diseases2010
- Author(s)
  Ikegawa S
- Organizer
  The 3rd Jishuitan Orthopedics Forum
- Place of Presentation
  Beijing, China
- Year and Date
  2010-04-24
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] ヒト遺伝学を出発点とする運動器疾患研究2010
- Author(s)
  池川志郎
- Organizer
  第11回運動器科学研究会
- Place of Presentation
  長野県・軽井沢
- Year and Date
  2010-09-10
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] Genomic Analysis of Bone and Joint Diseases-Integrated Approach of Human & Mouse Genetics Toward Disease Genes & Molecular Pathogenesis of the Diseases2010
- Author(s)
  Ikegawa S
- Organizer
  The Fourth Margaret River Region Forum
- Place of Presentation
  Duns borough, Australia
- Year and Date
  2010-04-29
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] From genome to skeletal diseases- recent advances in the association study of osteoarthritis and lumbar disc herniation and its association with ECM biology2010
- Author(s)
  Ikegawa S
- Organizer
  Gordon Conference (Proteoglican)
- Place of Presentation
  New Hampshire, USA
- Year and Date
  2010-07-14
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] From genome to skeletal diseases- recent advances in the association study of osteoarthritis and lumbar disc herniation2010
- Author(s)
  Ikegawa S
- Organizer
  1st OARSI China Forum
- Place of Presentation
  Nanjing, China
- Year and Date
  2010-10-05
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] Genomic study of Bone and Joint Diseases using human and mouse genetics2010
- Author(s)
  Ikegawa S
- Organizer
  10th Annual meeting of the EAUHG(East Asian Union of Human Genetics Societies)
- Place of Presentation
  Jinan, China
- Year and Date
  2010-10-08
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] From genome to skeletal diseases-recent advances in the association study of osteoarthritis and lumbar disc herniation and its association with ECM biology2010
- Author(s)
  Ikegawa S
- Organizer
  Gordon Conference (Proteoglycan)
- Place of Presentation
  New Hampshire, USA(Invited speech)
- Year and Date
  2010-07-14
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] ゲノムから疾患へ-ヒト遺伝学(Human Genetics)を出発点とする疾患遺伝子と分子病態の解明2010
- Author(s)
  池川志郎
- Organizer
  京都大学再生医科学研究所第1回生命医科学セミナー
- Place of Presentation
  京都
- Year and Date
  2010-09-07
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] From genome to skeletal diseases-recent advances in the association study of osteoarthritis and lumbar disc herniation and its association with ECM biology.2010
- Author(s)
  池川志郎
- Organizer
  Gordon Conference (Proteoglycan).
- Place of Presentation
  NH USA
- Year and Date
  2010-07-14
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] From genome to skeletal diseases-recent advances in the association study of osteoarthritis and lumbar disc herniation and its association with ECM biology2010
- Author(s)
  Ikegawa S
- Organizer
  Gordon Conference(Proteoglican)
- Place of Presentation
  New Hampshire, USA
- Year and Date
  2010-07-14
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] ヒト遺伝学を出発点とする運動器疾患研究2010
- Author(s)
  池川志郎
- Organizer
  第11回運動器科学研究会
- Place of Presentation
  軽井沢,長野
- Year and Date
  2010-09-01
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] ゲノムから疾患へ-ヒト遺伝学(Human Genetics)を出発点とする疾患遺伝子と分子病態の解明2010
- Author(s)
  池川志郎
- Organizer
  京都大学再生医科学研究所第1回生命医科学セミナー
- Place of Presentation
  京都
- Year and Date
  2010-09-07
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] Genomic study of Bone and Joint Diseases using human and mouse genetics2010
- Author(s)
  Ikegawa S
- Organizer
  10th Annual meeting of the EAUHG (East Asian Union of Human Genetics Societies)
- Place of Presentation
  Jinan, China
- Year and Date
  2010-10-08
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] 大規模関連解析による変形性関節症感受性遺伝子の同定2009
- Author(s)
  古市達哉、池川志郎
- Organizer
  第82回日本生化学会シンポジウム : 「運動器」形成・再生のための分子基盤.
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] 骨関節疾患のゲノム解析-融合遺伝学アプローチによる疾患遺伝子の解明2009
- Author(s)
  池川志郎
- Organizer
  第14回Bone Research Joint Meeting
- Place of Presentation
  大阪
- Year and Date
  2009-05-26
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] From Mouse to Human, from Monogenic to Polygenic Disease2009
- Author(s)
  池川志郎
- Organizer
  Gordon Research Conference Catrilage Biology & Pathology 2009
- Place of Presentation
  Les Diablerets, Switzerland
- Year and Date
  2009-06-08
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] 糖ヌクレオチド輸送体SLC35D1は軟骨組織におけるコンドロイチン硫酸合成に必須であり、その機能欠損は重度な骨格形成不全を引き起こす2009
- Author(s)
  古市達哉、池川志郎
- Organizer
  第1回新潟プロテオグリカン研究会
- Place of Presentation
  新潟
- Year and Date
  2009-03-06
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] 骨・関節疾患のゲノム解析2009
- Author(s)
  池川志郎
- Organizer
  日本人類遺伝学会第54回大会
- Place of Presentation
  東京
- Year and Date
  2009-09-24
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] Integrated Approach toward Bone and Joint Diseases using Human and Mouse Genetics2009
- Author(s)
  Ikegawa S
- Organizer
  Yokosuka Science Festa 2009 (Joint Conference of 8th Pan-Pacific Connective Tissue Societies Symposium (PPCTSS), 41st Annual Meeting of the Japanese Society of Connective Tissue Research (JSCTR), and 56th Annual Meeting of the Japan Matrix Club (JMC) Concurrent Meeting: Yokosuka International Conference on Cancer Microenvironment (YICCM)).
- Place of Presentation
  Yokosuka, Japan
- Year and Date
  2009-06-04
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] 骨関節疾患のゲノム解析-融合遺伝学アプローチによる疾患遺伝子の解明2009
- Author(s)
  池川志郎
- Organizer
  第14回 Bone Research Joint Meeting
- Place of Presentation
  大阪
- Year and Date
  2009-05-26
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] Integrated Approach toward Bone & Joint Diseases using Human and Mouse Genetics2009
- Author(s)
  池川志郎
- Organizer
  Yokosuka Science Festa 2009(Joint Conference of 8th Pan-Pacific Connective Tissue Societies Symposium(PPCTSS), 41st Annual Meeting of the Japanese Society of Connective Tissue Research(JSCTR), and 56th Annual Meeting of the Japan Matrix Club(JMC)Concurrent Meeting : Yokosuka International Conference on Cancer Microenvironments(YICCM))
- Place of Presentation
  Yokosuka(神奈川県)
- Year and Date
  2009-06-04
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] 骨・関節疾患のゲノム解析2009
- Author(s)
  池川志郎
- Organizer
  日本人類遺伝学会第54回大会
- Place of Presentation
  東京、グランドプリンスホテル高輪
- Year and Date
  2009-09-24
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] マウスとヒトの融合遺伝アプローチによる新規のトランスポーター病の同定とその分子病態の解明2009
- Author(s)
  池川志郎、古市達哉
- Organizer
  日本薬学会129年会シンポジウム : 遺伝子改変マウスから見いだされたトランスポーター・チャンネルの新規機能
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] From Mouse to Human, from Monogenic to Polygenic Disease2009
- Author(s)
  Ikegawa S
- Organizer
  Gordon Research Conference Catrilage Biology & Pathology
- Place of Presentation
  Les Diablerets, Switzerland
- Year and Date
  2009-06-08
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] Common polymorphisms and risk for degenerative joiny diseases in human populations2009
- Author(s)
  Ikegawa S
- Organizer
  9th Biennial Meeting of International Skeletal Dysplasia Society
- Place of Presentation
  Boston, USA
- Year and Date
  2009-07-19
- Data Source
  KAKENHI-PROJECT-21249080
[Presentation] Genetic analysis of bone and joint diseases; From human, from mouse2008
- Author(s)
  池川志郎
- Organizer
  5th Bone Biology Forum
- Place of Presentation
  静岡
- Year and Date
  2008-08-22
- Data Source
  KAKENHI-PROJECT-19209049
[Presentation] Of Human, of Mouse : Integrated approach of human and mouse genetics toward bone and joint diseases2008
- Author(s)
  池川志郎
- Organizer
  Invited Lecture
- Place of Presentation
  南京大学
- Year and Date
  2008-01-19
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18390423
[Presentation] From Human, from Mouse: Integrated approach of human and mouse genetics toward the gene for bone and joint diseases2008
- Author(s)
  池川志郎
- Organizer
  The 17th International Rheumatology Symposium
- Place of Presentation
  札幌
- Year and Date
  2008-04-22
- Data Source
  KAKENHI-PROJECT-19209049
[Presentation] Of Human, of Mouse : Integrated approach of human and mouse genetics toward bone and joint diseases2008
- Author(s)
  Shiro Ikegawa
- Organizer
  Invited Lecture
- Place of Presentation
  Nanjing University
- Year and Date
  2008-01-19
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18390423
[Presentation] From genome to bone and joint diseases2008
- Author(s)
  池川志郎
- Organizer
  第13回アジア太平洋リウマチ学会
- Place of Presentation
  横浜
- Year and Date
  2008-10-08
- Data Source
  KAKENHI-PROJECT-19209049
[Presentation] 骨・関節疾患のゲノム解析.疾患感受性遺伝子の同定から医療へ2007
- Author(s)
  池川志郎
- Organizer
  日本人類遺伝学会第52回大会
- Place of Presentation
  東京
- Year and Date
  2007-09-14
- Data Source
  KAKENHI-PROJECT-19209049
[Presentation] From Genome to Disease, Gene to Medicine: Identification of susceptibility genes for common bone and joint diseases and clarification of molecular pathogenesis2007
- Author(s)
  池川志郎
- Organizer
  THE INDIAN SOCIETY OF DEVELOPMENTAL BIOLOGISTS (ISDB)
- Place of Presentation
  Agra,India
- Year and Date
  2007-10-18
- Data Source
  KAKENHI-PROJECT-19209049
[Presentation] GDF5 and OA-of Human and of Mouse2007
- Author(s)
  Ikegawa S
- Organizer
  8th Meeting of the International Skeletal Dysplasia Society
- Place of Presentation
  Gymnase de l' Athanor Place de l'Amitie entre les Peuples,Albi,France
- Year and Date
  2007-07-19
- Data Source
  KAKENHI-PROJECT-18390423
[Presentation] Unraveling the genetic basis of common bone and joint diseases2007
- Author(s)
  池川志郎
- Organizer
  The 8th Regional Osteoporosis Conference
- Place of Presentation
  HongKong
- Year and Date
  2007-05-20
- Data Source
  KAKENHI-PROJECT-19209049
[Presentation] From Genome to Disease,Gene to Medicine:Identification of susceptibility genes for common bone and joint diseases and clarification of molecular pathogenesis.2007
- Author(s)
  Ikegawa S.
- Organizer
  The Indian Society of Developmental Biologists(ISDB)
- Place of Presentation
  Conference Room,Hotel Holiday Inn,Agra India.
- Year and Date
  2007-10-18
- Data Source
  KAKENHI-PROJECT-19209049
[Presentation] Phenotypic extension of SBDS mutations2007
- Author(s)
  Ikegawa S
- Organizer
  8th Meeting of the International Skeletal Dysplasia Society
- Place of Presentation
  Gymnase de l' Athanor Place de l'Amitie entre les Peuples,Albi,France
- Year and Date
  2007-07-19
- Data Source
  KAKENHI-PROJECT-18390423
[Presentation] グリコサミノグリカンの生合成に関わる酵素の新規変異による脊椎骨端骨幹端異形成症とエーラス・ダンロス症候群の糖鎖生物学的研究
- Author(s)
  ○水本秀二, 中島正宏, Thomas Muller, 三宅紀子, Indrajit Suresh, 古川諒, 小松由枝, 松本直通, Andreas R Janecke, 池川志郎, 菅原一幸
- Organizer
  第32回日本糖質学会年会
- Place of Presentation
  大阪国際交流センター（大阪）
- Data Source
  KAKENHI-PROJECT-25860037
[Presentation] コンドロイチン硫酸/デルマタン硫酸の生合成に関わる酵素の変異による骨・皮膚疾患の糖鎖生物学的研究
- Author(s)
  ○水本秀二, 中島正宏, Thomas Muller, 三宅紀子, Indrajit Suresh, 古川諒, 小松由枝, 松本直通, Andreas R Janecke, 池川志郎, 菅原一幸
- Organizer
  日本生化学会北海道支部支部例会第50回記念大会
- Place of Presentation
  北海道大学医学部(札幌)
- Data Source
  KAKENHI-PROJECT-25860037
[Presentation] PAPS合成酵素2の変異によって引き起こされる常染色体劣性型短脊柱症
- Author(s)
  ○水本秀二, 飯田有俊, Pelin Ozlem Simsek-Kiper, 星野冬馬, Nursel Elcioglu, Eva Horemuzova, Stefan Geiberger, Gozde Yesil, Hulya Kayserili, Gulen Eda Utine, Koray Boduroglu, 渡邉成彦, 大橋博文, Yasemin Alanay, 西村玄, 池川志郎, 菅原一幸
- Organizer
  日本薬学会第134回年会
- Place of Presentation
  熊本大学工学部(熊本)
- Data Source
  KAKENHI-PROJECT-25860037

1. MIZUMOTO Shuji (40443973)

# of Collaborated Projects: 3 results

# of Collaborated Products: 16 results
2. NAKAMURA Kozo (60126133)

# of Collaborated Projects: 3 results

# of Collaborated Products: 5 results
3. FURUICHI Tatsuya (30392103)

# of Collaborated Projects: 3 results

# of Collaborated Products: 9 results
4. INABA Ikuyo (60415081)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
5. SUGAHARA Kazuyuki (60154449)

# of Collaborated Projects: 3 results

# of Collaborated Products: 10 results
6. YAMADA Shuhei (70240017)

# of Collaborated Projects: 3 results

# of Collaborated Products: 8 results
7. MATSUMOTO Naomichi (80325638)

# of Collaborated Projects: 3 results

# of Collaborated Products: 11 results
8. MIYAKE Noriko (40523494)

# of Collaborated Projects: 3 results

# of Collaborated Products: 10 results
9. KOSHO Tomoki (90276311)

# of Collaborated Projects: 3 results

# of Collaborated Products: 1 results
10. TAKESHITA Katsushi (30262009)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
11. KAWAGUCHI Hiroshi (40282660)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
12. Janecke Andreas

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
13. NIIKAWA Norio (00111170)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. SHIDA Takafumi (20184533)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. MATSUO Masafumi (10157266)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. SONTA Shinichi (00100165)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. FUKUSHIMA Yoshimitsu (70273084)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. HIRAOKA Hisatada (10262007)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. MABUCHI Kunihiko (50192349)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
20. NAKAYAMA Yasuhide (50250262)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. MATSUDA Takehisa (60142189)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
22. HOSHIKAWA Atsuto (50383021)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
23. HOSHI Kazuto (30344451)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
24. KATO Shigeaki (60204468)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
25. MIYAMOTO Yoshinari (10345217)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
26. YOSHIZAWA TAKAHIRO (40713392)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
27. DAI JIN (00593675)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
28. 松本正 (70190535)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
29. 鈴木隆文 (50302659)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
30. 阿久根徹 (60282662)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
31. 佐藤和強 (50302691)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
32. 尾崎浩一 (50373288)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
33. 寺尾知可史 (60610459)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
34. 郭竜 (50784055)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
35. 王錚 (90794313)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
36. STEFAN Mundlos

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
37. LIHADH Al-gazali

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
38. KATRIN Hoffmann

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
39. ANDREAS Janecke

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
40. Nürnberg Peter

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
41. Kennerknecht Ingo

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
42. Vodopiutz Julia

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
43. Kornak Uwe

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
44. KURIYAMA Nagato

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
45. YAMAJI Taiki

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
46. INOSE Hiroyuki

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
47. NAKAJIMA Masahiro

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
48. WATANABE Kota

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
49. 田原康玄

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
50. 松田文彦

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
51. 武田和樹

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

IKEGAWA SHIRO 池川 志郎

池川 志郎 イケガワ シロウ

IKEGAWA Shiro 池川 志郎

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運動器疾患のMulti disease GWAS 解析Principal Investigator

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Identification of the genes for mechanical stress diseasesPrincipal Investigator

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Identification of susceptibility gene for lumbar disc disease and clarification of its molecular pathogenesisPrincipal Investigator

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Identification of susceptibility gene for lumbar disc herniation and clarification of its molecular pathogenesisPrincipal Investigator

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Molecular pathogenesis of lumbar disc degenerationPrincipal Investigator

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Analysis of disease genes for skeletal dysplasiasPrincipal Investigator

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IKEGAWA SHIRO 池川志郎

池川志郎イケガワシロウ

IKEGAWA Shiro 池川志郎

[Book] 第20回日本整形外科学会骨系統疾患研究会記録集(蝸牛様骨盤異形成症の責任遺伝子SLC35D1の同定)2009