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

ターナー症候群とその類縁疾患の表現型に対する染色体モザイクとX染色体不活化の影響の研究

Research Project

Project/Area Number 11670758
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionKYOTO UNIVERSITY

Principal Investigator

YORIFUJI Tonru  Kyoto University, Faculty of Medicine Assistant Prof., 医学研究科, 助手 (60220779)

Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 2000: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 1999: ¥1,600,000 (Direct Cost: ¥1,600,000)
KeywordsTurner Syndrome / Xchromosome / Ychromosome / 染色体モザイク / X染色体不活化
Research Abstract

(1) We have shown that in Turner syndrome patients with a 45, X/46, XX karyotype, X inactivation pattern in 46, XX cells are much more skewed compared with normal female subjects. This result suggests that there could be submicroscopic defects in normal looking 46, XX cells of these patients which could be part of the variety in clinical phenotypes of these patients.
(2) We sequenced the SRY gene of Turner syndrome patients with a 45, X/46, XY karyotype and showed that SRY mutation is a rare event in these patients. This suggests that 46, XY female and 45, X/46, XY Turner syndrome are made by different mechanisms.

Report

(3 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report
  • Research Products

    (19 results)

All Other

All Publications (19 results)

  • [Publications] 依藤亨 他: "大部分の細胞が正常核型(46,XX)であるにもかかわらず高度の低身長をきたした45.X/46,XXターナー症候群の一例"ホルモンと臨床. 48. 195-198 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Muroya K,Yorifuji T et al: "Deletion mapping and X inactivation analysis of a non-specific mental retardation gene at Xp21.3-Xp22.11"J.Med Genet. 36. 187-191 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Yorifuji,T et al: "Hyperinsulinism-hyperammonemia syndrome caused by mutant glutamate dehydrogenase accompanied by novel enzyme kinetics"Hum Genet. 104. 476-479 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tohru Yorifuji et al: "Living-related liver transplantation for neonatal-onset propionic acidemia"J Pediatr. 137. 572-574 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] J.Muroi,T.Yorifuji et al: "Molecular and clinical analysis of Japanese patients with 3-hydroxy-3-methylglutaryl CoA lyase (HL) deficiency"Hum Genet. 107. 320-326 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 依藤亨(分担): "「ターナー症候群の性腺機能」「新版ターナー症候群」"メディカルレビュー社(予定). (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Muroya, K., Kinoshita, E., Kamimaki, T., Matsuo, N., Yorifuji, T., Ogata, T.: "Deletion Mapping and X inactivation analysis of a non-specific mental retardation gene at Xp21.3-Xp22.11"J Med Genet. 36. 187-191 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Muroi, J., Uematsu, A., Yorifuji, T.: "Identification of a novel single base-pair polymorphism in the glutamate dehydrogenase (GLUD1) gene."J Hum Genet. 44. 268-269 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Yorifuji, T., Muroi, J., Uematsu, A., Hiramatsu, H., Momoi: "T.Hyperinsulinism-hyperammonemia syndrome caused by mutant glutamate dehydrogenase accompanied by novel enzyme kinetics."Hum Genet. 104. 476-479 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] J.Muroi, T.Yorifuji: "A.Cerebral infarction and pancreatitis ; possible complications of patients with 3-hydroxy-3-methylglutaryl CoA lyase deficiency"J Inher Metab Dis. 23. 636-637 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Tohru Yorifuji, Junko Muroi, Ayumi Uematsu, Tatsutoshi Nakahata, Hiroto Egawa, Koichi Tanaka: "Living-related liver transplantation for neonatal-onset propionic acidemia."J Pediatr. 137. 572-574 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Junko Muroi, Tohru Yorifuji, Ayumi Uematsu, Yosuke Shigematsu, Kazumichi Onigata, Hiroaki Maruyama, Tatsuro Nobutoki, Akiko Kitamura, Tatsutoshi Nakahata: "Molecular and clinical analysis of Japanese patients with 3-hydroxy-3-methylglutaryl CoA Lyase (HL) deficiency."Hum Genet. 107. 320-326 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Uematsu,A.,Yorifuji,T., et al.: "Relatively longer hand in patients with Ullrich-Turner syndrome."Am J Med Genet. 82. 245-256 (1999)

    • Related Report
      2000 Annual Research Report
  • [Publications] Muroya,K.,Yorifuji,T, et al.: "Deletion mapping and X inactivation analysis of a non-specific mental retardation geneat Xp21.3-Xp22.11."J Med Genet. 36. 187-191 (1999)

    • Related Report
      2000 Annual Research Report
  • [Publications] Tohru Yorifuji,Junko Muroi et al.: "Living-related liver transplantation for neonatal-onset propionic acidemia."J Pediatr. 137. 572-574 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Muroi,J.,Yorifuji,T., et al.: "Molecular and clinical analysis of Japanese patients with 3-hydroxy-3-methylglutaryl CoAlyase (HL) deficiency."Hum Genet. 107. 320-326 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] 依藤亨 他: "大部分の細胞が正常核型(46,XX)であるにもかかわらず高度の低身長をきたした45,X/46,XXターナー症候群の一例"ホルモンと臨床. 48. 195-198 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] 依藤亨(分担執筆): "新版 ターナー症候群(ターナー症候群の性腺機能)"メディカルレビュー社. (2001)

    • Related Report
      2000 Annual Research Report
  • [Publications] Yorifuji,T.,Muroi,J.,Uematsu,A,Hiramatsu,H.,Momoi,T.: "Hyperinsulinism-hyperammonemia syndrome caused by mutant glutamate dehydrogenase accompanied by novel enzyme kinetics"Hum Genet. 104. 476-479 (1999)

    • Related Report
      1999 Annual Research Report

URL: 

Published: 1999-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi