ISOJIMA Tsuyoshi 磯島豪

Researcher Number	00568230
Other IDs
Affiliation (Current)	2025: (財)冲中記念成人病研究所, その他部局等, 研究員
Affiliation (based on the past Project Information) *help	2022 – 2023: (財)冲中記念成人病研究所, その他部局等, 研究員 2016 – 2021: 帝京大学, 医学部, 講師 2010 – 2015: 東京大学, 医学部附属病院, 助教
Review Section/Research Field	Principal Investigator Pediatrics / Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Pediatrics / Basic Section 52050:Embryonic medicine and pediatrics-related
Keywords	Principal Investigator 骨代謝 / ゲノムワイド解析 / 遺伝子 / 先天性奇形症候群 / 成長 / 皮質骨 / 皮質骨　成長 / 成長障害 / 軟骨分化 / カルシウム・リン代謝 / 小児内分泌学 … More Except Principal Investigator … More オルガノイド / 小児腎臓病 / ネフローゼ症候群 / 自己抗体 / 特発性ネフローゼ症候群 / 小児 / エンドタイプ / ペプチド療法 / ペプチド / 治療 / 気管支喘息 / ビタミンD受容体 / ゲノム / 遺伝子多型 / 疾患感受性遺伝子 / くる病 / ビタミンD欠乏症 Less

骨細胞におけるSOCS3抑制シグナルを中心とした皮質骨と骨髄の相互関係の解明Principal Investigator
- Principal Investigator
  
  磯島豪
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Okinaka Memorial Institute for Medical Research
  Teikyo University
The role of autoantibody as pathogenesis of ideopatic nephrotic syndrome in children
- Principal Investigator
  
  Takahashi Kazuhiro
- Project Period (FY)
  2018 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Teikyo University
FAM111Aの骨成長、ミネラル代謝における役割の解明Principal Investigator
- Principal Investigator
  
  磯島豪
- Project Period (FY)
  2015 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Teikyo University
  The University of Tokyo
Development of a peptide as a novel therapy for brochial asthma
- Principal Investigator
  
  YASUDO HIROKI
- Project Period (FY)
  2014 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The University of Tokyo
Exploring for the causative gene of Kenny-Caffey syndrome type 2Principal Investigator
- Principal Investigator
  
  ISOJIMA Tsuyoshi
- Project Period (FY)
  2012 – 2013
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  The University of Tokyo
Association of vitamin D-related gene polymorphism with vitamin D deficiency.
- Principal Investigator
  
  KITANAKA Sachiko
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The University of Tokyo
Exploring for the causative gene of Kenny-Caffey syndrome type2Principal Investigator
- Principal Investigator
  
  ISOJIMA Tsuyoshi
- Project Period (FY)
  2010 – 2011
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  The University of Tokyo

All 2023 2022 2021 2020 2019 2018 2017 2014 2013 2012 2011 Other

All Journal Article Presentation Other

[Journal Article] Proposed reference intervals of serum insulin-like growth factor-1 (IGF-1) levels in older Japanese populations2023
- Author(s)
  Isojima Tsuyoshi、Shimatsu Akira
- Journal Title
  
  Endocr J
  
  Volume: 70 Issue: 10 Pages: 1023-1027
- DOI
  10.1507/endocrj.EJ23-0274
- ISSN
  0918-8959, 1348-4540
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K07827
[Journal Article] Growth in girls with Turner syndrome2023
- Author(s)
  Isojima Tsuyoshi、Yokoya Susumu
- Journal Title
  
  Frontiers in Endocrinology
  
  Volume: 13 Pages: 1068128-1068128
- DOI
  10.3389/fendo.2022.1068128
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07827
[Journal Article] <scp>G‐CSF</scp> Receptor Deletion Amplifies Cortical Bone Dysfunction in Mice With <scp>STAT3</scp> Hyperactivation in Osteocytes2022
- Author(s)
  Isojima Tsuyoshi、Walker Emma C、Poulton Ingrid J、McGregor Narelle E、Wicks Ian P、Gooi Jonathan H、Martin T John、Sims Natalie A
- Journal Title
  
  Journal of Bone and Mineral Research
  
  Volume: 37 Issue: 10 Pages: 1876-1890
- DOI
  10.1002/jbmr.4654
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07827
[Journal Article] Demographic characteristics of children with growth hormone deficiency from 1996 to 2015 in Japan: 20 years of data from the foundation for growth science in Japan2022
- Author(s)
  Isojima Tsuyoshi、Hasegawa Tomonobu、Yokoya Susumu、Tanaka Toshiaki
- Journal Title
  
  Endocr J
  
  Volume: 69 Issue: 8 Pages: 927-939
- DOI
  10.1507/endocrj.EJ21-0520
- ISSN
  0918-8959, 1348-4540
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K07827
[Journal Article] Cortical bone development, maintenance and porosity: genetic alterations in humans and mice influencing chondrocytes, osteoclasts, osteoblasts and osteocytes2021
- Author(s)
  Isojima Tsuyoshi、Sims Natalie A.
- Journal Title
  
  Cellular and Molecular Life Sciences
  
  Volume: 78 Issue: 15 Pages: 5755-5773
- DOI
  10.1007/s00018-021-03884-w
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07827
[Journal Article] <i> <scp>Dmp1Cre</scp> ‐ </i> directed knockdown of parathyroid hormone?related protein (PTHrP) in murine decidua is associated with a life‐long increase in bone mass, width, and strength in male progeny2021
- Author(s)
  Ansari Niloufar、Isojima Tsuyoshi、Crimeen‐Irwin Blessing、Poulton Ingrid J.、McGregor Narelle E.、Ho Patricia W. M.、Forwood Mark R.、Kovacs Christopher S.、Dimitriadis Evdokia、Gooi Jonathan H.、Martin T. John、Sims Natalie A.
- Journal Title
  
  Journal of Bone and Mineral Research
  
  Volume: 36 Issue: 10 Pages: 1999-2016
- DOI
  10.1002/jbmr.4388
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07827
[Journal Article] Trace element levels in mature breast milk of recent lactating Japanese women2020
- Author(s)
  Motoyama Kahoko、Isojima Tsuyoshi、Sato Yasuhiro、Aihara Ayaka、Asakura Hitomi、Hiraike Haruko、Hino Yuko、Mimaki Masakazu、Nomura Kyoko、Kodama Hiroko
- Journal Title
  
  Pediatrics International
  
  Volume: - Issue: 8 Pages: 14543-14543
- DOI
  10.1111/ped.14543
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16H05262, KAKENHI-PROJECT-18K07887
[Journal Article] Pregnancy outcome of Japanese patients with glucokinase?maturity‐onset diabetes of the young2019
- Author(s)
  Hosokawa Yuki、Higuchi Shinji、Kawakita Rie、Hata Ikue、Urakami Tatsuhiko、Isojima Tsuyoshi、Takasawa Kei、Matsubara Yohei、Mizuno Haruo、Maruo Yoshihiro、Matsui Katsuyuki、Aizu Katsuya、Jinno Kazuhiko、Araki Shunsuke、Fujisawa Yasuko、Osugi Koji、Tono Chikako、Takeshima Yasuhiro、Yorifuji Tohru
- Journal Title
  
  Journal of Diabetes Investigation
  
  Volume: N/A Issue: 6 Pages: 1586-1589
- DOI
  10.1111/jdi.13046
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07887, KAKENHI-PROJECT-18K07895, KAKENHI-PROJECT-18K07818
[Journal Article] A familial case of nail patella syndrome with a heterozygous in-frame indel mutation in the LIM domain of LMX1B2018
- Author(s)
  Mukai Miho、Fujita Harumi、Umegaki-Arao Noriko、Sasaki Takashi、Yasuda-Sekiguchi Fumiyo、Isojima Tsuyoshi、Kitanaka Sachiko、Amagai Masayuki、Kubo Akiharu
- Journal Title
  
  Journal of Dermatological Science
  
  Volume: 90 Issue: 1 Pages: 90-93
- DOI
  10.1016/j.jdermsci.2017.12.010
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07887, KAKENHI-PROJECT-16K09985, KAKENHI-PROJECT-15K09782
[Journal Article] Sexual precocity in a girl with early-onset Graves’ disease2018
- Author(s)
  Ogawa Eishin、Isojima Tsuyoshi、Sato Yasuhiro、Motoyama Kahoko、Kodama Hiroko
- Journal Title
  
  Clinical Pediatric Endocrinology
  
  Volume: 27 Issue: 3 Pages: 165-169
- DOI
  10.1297/cpe.27.165
- NAID
  130007427942
- ISSN
  0918-5739, 1347-7358
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K07887
[Journal Article] Impact of the Great East Japan Earthquake on Body Mass Index, Weight, and Height of Infants and Toddlers: An Infant Survey2018
- Author(s)
  Hiroshi YOKOMICHI, Hiroko MATSUBARA, Mami ISHIKURO, Masahiro KIKUYA, Tsuyoshi ISOJIMA, Susumu YOKOYA, Toshiaki TANAKA, Noriko KATO, Shoichi CHIDA, Atsushi ONO, Mitsuaki HOSOYA, Soichiro TANAKA, Shinichi KURIYAMA, Shigeo KURE, Zentaro YAMAGATA
- Journal Title
  
  Journal of Epidemiology
  
  Volume: 28 Issue: 5 Pages: 237-244
- DOI
  10.2188/jea.JE20170006
- NAID
  130006732097
- ISSN
  0917-5040, 1349-9092
- Year and Date
  2018-05-05
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K08730, KAKENHI-PROJECT-18K07887, KAKENHI-PROJECT-18K17376
[Journal Article] LMX1B Mutation with Residual Transcriptional Activity as a Cause of Isolated Glomerulopathy2014
- Author(s)
  Isojima T, Kitanaka S et al
- Journal Title
  
  Nephrol Dial Transplant
  
  Volume: 29 Pages: 81-8
- Data Source
  KAKENHI-PROJECT-23591489
[Journal Article] A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type22014
- Author(s)
  Isojima T, Doi K, Mitsui J, Oda Y, Tokuhiro E, Yasoda A, Yorifuji T, Horikawa R, Yoshimura J, Ishiura H, Morishita S, Tsuji S, Kitanaka S
- Journal Title
  
  J Bone Miner Res
  
  Volume: 29 Pages: 992-8
- Data Source
  KAKENHI-PROJECT-24791042
[Journal Article] LMX1B Mutation with Residual Transcriptional Activity as a Cause of Isolated Glomerulopathy.2014
- Author(s)
  Isojima T, Harita Y, Furuyama M, Sugawara N, Ishizuka K, Horita S, Kajiho Y, Miura K, Igarashi T, Hattori M, Kitanaka S
- Journal Title
  
  Nephrol Dial Transplant
  
  Volume: 29 Issue: 1 Pages: 81-8
- DOI
  10.1093/ndt/gft359
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591489, KAKENHI-PROJECT-24390259, KAKENHI-PROJECT-24591569, KAKENHI-PROJECT-25461617, KAKENHI-PROJECT-26670494
[Journal Article] A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 22013
- Author(s)
  Isojima T, Kitanaka S et al
- Journal Title
  
  J Bone Miner Res
- Data Source
  KAKENHI-PROJECT-23591489
[Journal Article] Association of vitamin D-related gene polymorphisms with manifestation of vitamin D deficiency in children.2013
- Author(s)
  Kitanaka S, Isojima T, Takaki M, Numakura C, Hayasaka K, Igarashi T
- Journal Title
  
  Endocr J
  
  Volume: 59 Pages: 1007-1014
- NAID
  10031146710
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591489
[Journal Article] A recurrent de novo FAM111A mutation causes Kenny–Caffey syndrome type 2.2013
- Author(s)
  Isojima T, Doi K, Mitsui J, Oda Y, Tokuhiro E, Yasoda A, Yorifuji T, Horikawa R, Yoshimura J, Ishiura H, Morishita S, Tsuji S, and Kitanaka S.
- Journal Title
  
  J Bone Mineral Res
  
  Volume: 29 Issue: 4 Pages: 992-998
- DOI
  10.1002/jbmr.2091
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-ORGANIZER-22129001, KAKENHI-PLANNED-22129008, KAKENHI-PROJECT-23591489, KAKENHI-PROJECT-24791042, KAKENHI-PROJECT-25860700, KAKENHI-PROJECT-26670494, KAKENHI-PROJECT-221S0002
[Journal Article] Growth hormone deficiency: A possible complication of glucose transporter 1 deficiency?2012
- Author(s)
  Nakagama Y, Isojima T, Kitanaka S et al.
- Journal Title
  
  Acta Peadiatrica
  
  Volume: Epub
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591489
[Journal Article] Growth hormone deficiency : A possible complication of glucose transporter 1 deficiency?2012
- Author(s)
  Nakagama Y, Isojima T, Kitanaka S, et al
- Journal Title
  
  Acta Peadiatrica
  
  Volume: 101
- Data Source
  KAKENHI-PROJECT-23591489
[Journal Article] Growth hormone deficiency: A possible complication of glucose transporter 1 deficiency?2012
- Author(s)
  Nakagama Y, Isojima T, Mizuno Y, Takahashi N, Kitanaka S, Igarashi T
- Journal Title
  
  Acta Peadiatrica
  
  Volume: 101 Issue: 6
- DOI
  10.1111/j.1651-2227.2012.02606.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591489
[Journal Article] Association of vitamin D-related gene polymorphisms with manifestation of vitamin D deficiency in children2012
- Author(s)
  Kitanaka S, Isojima T, Takaki M, Numakura C, Hayasaka K, Igarashi T
- Journal Title
  
  Endocr J
  
  Volume: 59 Pages: 1007-1014
- NAID
  10031146710
- Data Source
  KAKENHI-PROJECT-23591489
[Journal Article] Painful thyroiditis and subsequent atrophic hypothyroidism after cord blood transfusion2011
- Author(s)
  Makita N, Isojima T, Kitanaka S, et al
- Journal Title
  
  Thyroid
  
  Volume: 10 Pages: 1157-8
- Data Source
  KAKENHI-PROJECT-23591489
[Journal Article] Painful thyroiditis and subsequent atrophic hypothyroidism after cord blood transfusion.2011
- Author(s)
  Makita N, Isojima T, Kitanaka S et al.
- Journal Title
  
  Thyroid
  
  Volume: 10 Pages: 1157-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 日本人新生児生理的体重減少曲線の作成2023
- Author(s)
  磯島豪、加藤則子、森崎菜穗、盛一享徳、横山徹爾
- Organizer
  第126回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-21K07827
[Presentation] 成長障害に対する診断アプローチ2023
- Author(s)
  磯島豪
- Organizer
  第33回臨床内分泌代謝Update
- Invited
- Data Source
  KAKENHI-PROJECT-21K07827
[Presentation] 日本人高齢者における血中インスリン様成長因子-1(IGF-1)の基準値の再設定2023
- Author(s)
  磯島豪、島津章
- Organizer
  第33回臨床内分泌代謝Update
- Data Source
  KAKENHI-PROJECT-21K07827
[Presentation] Growth and bone health in childhood cancer survivor2023
- Author(s)
  Tsuyoshi Isojima
- Organizer
  18th congress of Asian Society for pediatric research
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07827
[Presentation] 皮質骨の発生、維持機構2022
- Author(s)
  磯島　豪
- Organizer
  第24回日本骨粗鬆症学会
- Invited
- Data Source
  KAKENHI-PROJECT-21K07827
[Presentation] 日本人新生児生理的体重減少曲線の作成2022
- Author(s)
  磯島　豪、加藤　則子、森崎　菜穂、盛一　享徳、横山　徹爾
- Organizer
  第55回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-21K07827
[Presentation] The role of SOCS3 suppression signaling in osteocytes for cortical maturation2022
- Author(s)
  Tsuyoshi Isojima
- Organizer
  第40回日本骨代謝学会
- Data Source
  KAKENHI-PROJECT-21K07827
[Presentation] 実は面白い新生児の骨代謝2022
- Author(s)
  磯島　豪
- Organizer
  第55回日本小児内分泌学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-21K07827
[Presentation] Dmp1Creによる脱落膜のPTHrPノックダウンは、生涯にわたり雄子マウスの骨量、骨幅、骨強度に影響する2021
- Author(s)
  磯島豪, Niloufar Ansari, Blessing Crimeen-Irwin, Ingrid J Poulton, Narelle E McGregor, Patricia W. M. Ho, Mark R Forwood, Christpher S Kovacs, Evdokia Dimitriadis, Jonathan H Gooi, T John Martin, Natalie A Sims
- Organizer
  第54回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-21K07827
[Presentation] 皮質骨構造の維持には、骨細胞のSOCS3依存性抑制シグナルと骨髄の相互作用が必要である2021
- Author(s)
  磯島豪, Emma C Walker, Blessing Crimeen-Irwin, Ingrid J Poulton, Narelle E McGregor, Jonathan H Gooi, T John Martin, Natalie A Sims
- Organizer
  第54回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-21K07827
[Presentation] 授乳婦の栄養状態調査と母乳成分の分析,乳児の発育に関する研究2020
- Author(s)
  佐藤恭弘、元山華穂子、磯島豪、三牧正和、児玉浩子、野村恭子
- Organizer
  第123回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07887
[Presentation] 低身長患者での亜鉛欠乏のバイオマーカーの検討および血清亜鉛値と亜鉛摂取量の検討2019
- Author(s)
  望月大史、佐藤恭弘、元山華穂子、泉陽一、磯島豪、三牧正和、児玉浩子
- Organizer
  第122回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07887
[Presentation] 骨成長におけるFAM111Aを中心とした分子メカニズムの解明2017
- Author(s)
  磯島　豪、田中　裕之、斉藤　琢、北中　幸子
- Organizer
  第51回小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-15K09612
[Presentation] Kenny-Caffey症候群2型の原因遺伝子であるFAM111Aの生体内での発現と軟骨分化への影響2017
- Author(s)
  田中　裕之、田村　麻由子、高橋　千恵、磯島　豪、齋藤　琢、岡　明、北中　幸子
- Organizer
  第51回小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-15K09612
[Presentation] Hereditary 1,25-dihydroxyvitamin D-resistant rickets with homozygous VDR mutation - an extremely rare case of maternal uniparental disomy of chromosome 12 detected by genome-wide SNP array2013
- Author(s)
  Mayuko Tamura, Tsuyoshi Isojima, Sachiko Kitanaka et al
- Organizer
  Joint Meeting of Pediatric Endocrinology
- Place of Presentation
  Milano
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 優性遺伝形式を示したビタミンD依存性くる病2型(HVDRR)の分子メカニズムの解明2013
- Author(s)
  磯島豪、北中幸子、他
- Organizer
  第31回小児代謝性骨疾患研究会
- Place of Presentation
  東京
- Year and Date
  2013-12-07
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 非典型的遺伝型式を示したビタミンD依存性くる病2型―極めて稀な12番染色体片親性ダイソミーの可能性2013
- Author(s)
  北中幸子、磯島豪、他
- Organizer
  第86回日本内分泌学会学術集会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 次世代シークエンサーを用いたKenny-Caffey症候群(KCS)2型の原因遺伝子の同定2013
- Author(s)
  磯島豪, 土井晃一郎, 三井純, 小田洋一郎, 徳弘悦郎, 八十田明宏, 依藤亨, 堀川玲子, 吉村淳, 石浦浩之, 森下真一, 辻省次, 北中幸子
- Organizer
  第58回日本人類遺伝学会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-24791042
[Presentation] 先天性心疾患を合併する骨形成不全症に対するパミドロネート治療の経験2013
- Author(s)
  田村麻由子磯島豪、北中幸子、他
- Organizer
  第47回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] Hereditary vitamin D-resistant rickets inherited as a dominant trait caused by a novel vitamin D receptor mutation with dominant negative effect2013
- Author(s)
  Tsuyoshi Isojima, Sachiko Kitanaka et al
- Organizer
  Joint Meeting of Pediatric Endocrinology
- Place of Presentation
  Milano
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 特発性若年性骨粗鬆症の1例2013
- Author(s)
  藤澤佑介、磯島豪、北中幸子、他
- Organizer
  第47回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 次世代シークエンサーを用いたKenny-Caffey 症候群(KCS)2型の原因遺伝子の同定2013
- Author(s)
  磯島豪, 土井晃一郎, 三井純, 小田洋一郎, 徳弘悦郎, 八十田明宏, 依藤亨, 堀川玲子, 吉村淳, 石浦浩之, 森下真一, 辻省次, 北中幸子
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791042
[Presentation] 次世代シークエンサーを用いたKenny-Caffey症候群(KCS)2型の原因遺伝子の同定2013
- Author(s)
  磯島豪、北中幸子、他
- Organizer
  第58回日本人類遺伝学会学術集会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 次世代シークエンサーを用いたKenny-Caffey 症候群(KCS)2型の原因遺伝子の同定2013
- Author(s)
  磯島豪, 土井晃一郎, 三井純, 小田洋一郎, 徳弘悦郎, 八十田明宏, 依藤亨, 堀川玲子, 吉村淳, 石浦浩之, 森下真一, 辻省次, 北中幸子
- Organizer
  第58回日本人類遺伝学会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-24791042
[Presentation] 次世代シークエンサーを用いたKenny-Caffey症候群(KCS)2型の原因遺伝子の同定2013
- Author(s)
  磯島豪、北中幸子、他
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] SNPアレイ解析が病因の解明に有用であった12番染色体片親性ダイソミーによるビタミンD依存性くる病2型2013
- Author(s)
  北中幸子、田村麻由子、磯島豪、他
- Organizer
  第58回日本人類遺伝学会学術集会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 次世代シークエンサーを用いたKenny-Caffey症候群(KCS)2型の原因遺伝子の同定2013
- Author(s)
  磯島豪, 土井晃一郎, 三井純, 小田洋一郎, 徳弘悦郎, 八十田明宏, 依藤亨, 堀川玲子, 吉村淳, 石浦浩之, 森下真一, 辻省次, 北中幸子
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791042
[Presentation] 社会的性の決定に6か月を要した左心低形成症候群を合併した46,XY性分化疾患の1例2013
- Author(s)
  田中裕之,磯島豪、北中幸子、他
- Organizer
  第116回日本小児科学会学術集会
- Place of Presentation
  広島
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 12番染色体片親性ダイソミーによって発症したビタミンD依存性くる病2型―SNPアレイ解析の有用性2013
- Author(s)
  田村麻由子、磯島豪、北中幸子、他
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] ヘテロ接合体変異による優性阻害効果により発症したと考えられたビタミンD依存性くる病2型の1家系2012
- Author(s)
  磯島豪、高木美奈子、吉村和子、廣瀬伸一、北中幸子、五十嵐隆
- Organizer
  日本内分泌学会学術集会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 日本人小児の血中ビタミンＤ濃度に関する研究―第二報2012
- Author(s)
  高橋千恵、磯島豪、小田洋一郎、伊藤純子、北中幸子
- Organizer
  小児内分泌学会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] FGF23遺伝子変異による常染色体優性低リン血症性くる病の本邦初報告家系　－血中FGF23値と無症状例について－2012
- Author(s)
  高木美奈子、磯島豪、堀倫子、福本誠二、皆川真規、北中幸子
- Organizer
  小児内分泌学会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] FGF23遺伝子変異による常染色体優性低リン血症性くる病の本邦初報告家系-血中FGF23値と無症状例について-2012
- Author(s)
  高木美奈子、磯島豪、北中幸子、他
- Organizer
  第46回小児内分泌学会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] FGF23遺伝子変異を同定した常染色体優性遺伝低リン血症性くる病の本邦初家系2012
- Author(s)
  北中幸子、磯島豪、他
- Organizer
  第30回日本骨代謝学会
- Place of Presentation
  東京(口演)
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 極低出生体重児における新生児期のカルシウム・リン代謝と身長予後についての検討2012
- Author(s)
  磯島豪、高橋千恵、五石圭司、土田晋也、高橋尚人、北中幸子、九島令子、渡辺とよ子
- Organizer
  小児内分泌学会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 日本人小児の血中ビタミンD濃度に関する研究―第二報2012
- Author(s)
  高橋千恵、磯島豪、北中幸子、他
- Organizer
  第46回小児内分泌学会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] アトピー性皮膚炎に合併した恥骨・坐骨骨髄炎の1例2012
- Author(s)
  野木森宣嗣、磯島豪、北中幸子、他
- Organizer
  第590回日本小児科学会東京都地方会講話会
- Place of Presentation
  東京
- Year and Date
  2012-03-10
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] LMX1B mutation with residual transcriptional activity as a cause of Nail-Patella-like renal disease2012
- Author(s)
  Isojima T, Kitanaka S, et al
- Organizer
  ASPR 2012
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] FGF23遺伝子変異を同定した常染色体優性遺伝低リン血症性くる病の本邦初家系2012
- Author(s)
  北中幸子、高木美奈子、磯島豪、堀倫子、福本誠二、皆川真規
- Organizer
  日本骨代謝学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] LMX1B mutation with residual transcriptional activity as a cause of Nail-Patella-like renal disease.2012
- Author(s)
  Isojima T, Harita Y, Kitanaka S, Igarashi T
- Organizer
  Congress of Asian Society for Pediatric Research
- Place of Presentation
  Seoul
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] ヘテロ接合体変異による優性阻害効果により発症したと考えられたビタミンD依存性くる病2型の1家系2012
- Author(s)
  磯島豪、北中幸子、他
- Organizer
  第85回日本内分泌学会学術集会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] LMX1B mutation with residual transcriptional activity as a cause of Nail-Patella-like renal disease2012
- Author(s)
  Isojima T, Kitanaka S, et al
- Organizer
  Congress of Asian Society for Pediatric Research
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 組織学的にnail-patella症候群腎症を呈し,外表所見のないnail-patella-like renal diseaseに認められたLMX1B機能低下型新規変異2012
- Author(s)
  磯島豪、北中幸子、他
- Organizer
  第47回日本小児腎臓病学会学術集会
- Year and Date
  2012-06-29
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 極低出生体重児における新生児期のカルシウム・リン代謝と身長予後についての検討2012
- Author(s)
  磯島豪、北中幸子、他
- Organizer
  第46回小児内分泌学会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] FGF23関連遺伝性低リン血症性くる病の病因の検討2011
- Author(s)
  齋藤祐、磯島豪、北中幸子、五十嵐隆
- Organizer
  第114回日本小児科学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 乳児期に糖尿病性ケトアシドーシスで発症した自己免疫性1型糖尿病の同胞例2011
- Author(s)
  藤野修平、磯島豪、北中幸子、他
- Organizer
  第45回小児内分泌学会
- Place of Presentation
  埼玉
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] ビタミンD欠乏症の発症に関連する遺伝子の解析2011
- Author(s)
  北中幸子、磯島豪、他
- Organizer
  第　114回日本小児科学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 乳糜胸水を伴ったGorham-Stout Syndromeの1例2011
- Author(s)
  吉田賢弘、磯島豪、北中幸子、他
- Organizer
  第29回小児代謝性骨疾患研究会
- Place of Presentation
  東京
- Year and Date
  2011-12-03
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 新規複合型ヘテロ接合性変異を認めた先天性無痛無汗症の1例2011
- Author(s)
  磯島豪,北中幸子,他
- Organizer
  第114回日本小児科学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] ビタミンD欠乏症と関連する遺伝子多型の解析2011
- Author(s)
  北中幸子、磯島豪、五十嵐隆
- Organizer
  第84回日本内分泌学会学術集会
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] Thyrotoxicosis After Unrelated Stem Cell Transplantationi n a Patient with Acute Myelogenous Leukemia2011
- Author(s)
  Hiwatari M, Isojima T, Kitanaka S, et al
- Organizer
  ASPR 2011
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] ビタミンD依存性くる病2型に認められ転写活性化能を解析したビタミンD受容体の新規複合ヘテロ接合体変異2011
- Author(s)
  磯島豪、北中幸子、他
- Organizer
  第45回小児内分泌学会
- Place of Presentation
  埼玉
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 極低出生体重児における高ALP血症と身長予後について2011
- Author(s)
  磯島豪,北中幸子,他
- Organizer
  第回新生児未熟児学会シンポジウム
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] ビタミンD欠乏症と関連する遺伝子多型の解析2011
- Author(s)
  北中幸子、磯島豪、他
- Organizer
  第８４回日本内分泌学会学術集会
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] ビタミンD欠乏症の発症に関連する遺伝子の解析2011
- Author(s)
  北中幸子、高木美奈子、磯島豪、五十嵐隆
- Organizer
  第114回日本小児科学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 日本人小児の血中ビタミンD濃度に関する研究―第一報2011
- Author(s)
  北中幸子、磯島豪、他
- Organizer
  第45回小児内分泌学会
- Place of Presentation
  埼玉
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 非典型的遺伝型式を示したビタミンD依存性くる病2型―極めて稀な12番染色体片親性ダイソミーの可能性
- Author(s)
  北中幸子、吉田秀樹、磯島豪
- Organizer
  第86回日本内分泌学会学術集会
- Place of Presentation
  仙台（仙台国際センター）
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] Hereditary 1,25-dihydroxyvitamin D-resistant rickets with homozygous VDR mutation - an extremely rare case of maternal uniparental disomy of chromosome 12 detected by genome-wide SNP array
- Author(s)
  Mayuko Tamura, Tsuyoshi Isojima, Hideki Yoshida, Minae Kawashima, Keiko Yamamoto, Taichi Kitaoka; Noriyuki Namba; Keiichi Ozono; Katsushi Tokunaga; Sachiko Kitanaka
- Organizer
  Joint Meeting of Pediatric Endocrinology
- Place of Presentation
  Milano Italy
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 12番染色体片親性ダイソミーによって発症したビタミンD依存性くる病2型―SNPアレイ解析の有用性
- Author(s)
  田村　麻由子、磯島　豪、吉田　秀樹、川嶋　実苗、山本　景子、北岡　太一、難波　範行、大薗　恵一、徳永　勝士、北中　幸子
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京（浅草ビューホテル）
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 次世代シークエンサーを用いたKenny-Caffey症候群(KCS)2型の原因遺伝子の同定
- Author(s)
  磯島豪、土井晃一郎、三井純、小田洋一郎、徳弘悦郎、八十田明宏、依藤亨、堀川玲子、吉村淳、石浦浩之、森下真一、辻省次、北中幸子
- Organizer
  第58回日本人類遺伝学会学術集会
- Place of Presentation
  仙台（江陽ホテル）
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] Hereditary vitamin D-resistant rickets inherited as a dominant trait caused by a novel vitamin D receptor mutation with dominant negative effect.
- Author(s)
  Tsuyoshi Isojima, Kazuko Yoshimura, Michiyasu Ishizawa, Shinichi Hirose, Makoto Makishima, Sachiko Kitanaka
- Organizer
  Joint Meeting of Pediatric Endocrinology
- Place of Presentation
  Milano Italy
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 次世代シークエンサーを用いたKenny-Caffey症候群(KCS)2型の原因遺伝子の同定
- Author(s)
  磯島豪、北中幸子、他
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京（浅草ビューホテル）
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 社会的性の決定に6か月を要した左心低形成症候群を合併した46,XY性分化疾患の1例
- Author(s)
  田中裕之, 磯島豪, 木村有希, 清水信隆, 井川靖彦, 北中幸子
- Organizer
  第116回日本小児科学会学術集会
- Place of Presentation
  広島（広島国際会議場）
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] 先天性心疾患を合併する骨形成不全症に対するパミドロネート治療の経験
- Author(s)
  田村　麻由子　磯島　豪　犬塚　亮、清水　信隆、北中　幸子
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京（浅草ビューホテル）
- Data Source
  KAKENHI-PROJECT-23591489
[Presentation] SNPアレイ解析が病因の解明に有用であった12番染色体片親性ダイソミーによるビタミンD依存性くる病2型
- Author(s)
  北中　幸子、田村　麻由子、磯島　豪、川嶋　実苗、吉田　秀樹、山本　景子、北岡　太一、難波　範行、大薗　恵一、徳永　勝士
- Organizer
  第58回日本人類遺伝学会学術集会
- Place of Presentation
  仙台（江陽ホテル）
- Data Source
  KAKENHI-PROJECT-23591489
[]
[]

1. KITANAKA Sachiko (30431638)

# of Collaborated Projects: 4 results

# of Collaborated Products: 64 results
2. 三牧正和 (40392419)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
3. YASUDO HIROKI (70422285)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. Takahashi Kazuhiro (60297447)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 加藤元博 (40708690)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 高里実 (40788676)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. MORISHITA Shinichi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
8. HIRAIKE Osamu

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
9. 辻省次

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
10. 野村恭子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
11. 平池春子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

ISOJIMA Tsuyoshi 磯島 豪

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骨細胞におけるSOCS3抑制シグナルを中心とした皮質骨と骨髄の相互関係の解明Principal Investigator

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The role of autoantibody as pathogenesis of ideopatic nephrotic syndrome in children

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FAM111Aの骨成長、ミネラル代謝における役割の解明Principal Investigator

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Development of a peptide as a novel therapy for brochial asthma

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Exploring for the causative gene of Kenny-Caffey syndrome type 2Principal Investigator

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Association of vitamin D-related gene polymorphism with vitamin D deficiency.

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Exploring for the causative gene of Kenny-Caffey syndrome type2Principal Investigator

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[Journal Article] Proposed reference intervals of serum insulin-like growth factor-1 (IGF-1) levels in older Japanese populations2023

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[Journal Article] Growth in girls with Turner syndrome2023

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[Journal Article] <scp>G‐CSF</scp> Receptor Deletion Amplifies Cortical Bone Dysfunction in Mice With <scp>STAT3</scp> Hyperactivation in Osteocytes2022

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[Journal Article] Demographic characteristics of children with growth hormone deficiency from 1996 to 2015 in Japan: 20 years of data from the foundation for growth science in Japan2022

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[Journal Article] Cortical bone development, maintenance and porosity: genetic alterations in humans and mice influencing chondrocytes, osteoclasts, osteoblasts and osteocytes2021

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[Journal Article] <i> <scp>Dmp1Cre</scp> ‐ </i> directed knockdown of parathyroid hormone?related protein (PTHrP) in murine decidua is associated with a life‐long increase in bone mass, width, and strength in male progeny2021

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ISOJIMA Tsuyoshi 磯島豪