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1999 Fiscal Year Final Research Report Summary

Difference in height associated with gene polymorphism in genes relating chondrocyte differentiation

Research Project

Project/Area Number 10670706
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionChiba University

Principal Investigator

YASUDA Toshiyuki  Chiba Univ. Peptog Med Lecture, 医学部, 講師 (00211615)

Co-Investigator(Kenkyū-buntansha) MINAMITANI Kanshi  Chiba Univ. Peptog Med Clinical fellow, 医学部・付属病院, 医員
MINAGAWA Masanori  Chiba Univ. Peptog Med Clinical fellow, 医学部・付属病院, 医員
Project Period (FY) 1998 – 1999
KeywordsHeight / growth / differentiation / vitamin D / receptor / PTH / PTHrP receptor / proportive
Research Abstract

Height growth is under a strong genetic control. 60% of height growth is achieved by endochondral bone formation of long bones. The process consists of proliferation, differentiation, apoptosis of chosndrocyte to give rise to final calcification.
1) There is a polymorphism in the first intiation codon of vitamin D receptor gene (AT/CG). The ACG genotype encodes vitamin D receptor protein of shorter form by three amino acids. In young adult females, ATG/ACG heetrozygotes showed significantly taller height(2-5.6 cm,p<0.05).
2) We have identified a novel AAAG repeat polymorphism in the human PTH/PTHrP receptor gene ranging in repeat number from 3 to 8. The increase in repeat number resulted in reduced promoter activity examined in two human osteosarcoma cell lines. This polymorphism is also associated with a difference in height.
3) Since there is none normal value for upper lower segment ratio in Japanese. We have decided to produce the normal value by measuring both height and lower segment length in more than 800 children. The normal values thus obtained should be useful in the future study.

  • Research Products

    (15 results)

All Other

All Publications (15 results)

  • [Publications] Watanabe T,Yasuda T et al.: "Familial hypoparathyroidism : Identification of a novel gain of function mutation in transmembrane domain 5 of the calcium-sensing receptor"J Clin Endocrinol Metab. 83(7). 2497-2502 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Minamitani K,Yasuda T, et al.: "Difference in height associated with a translation start site polymorphism in the vitamin D receptor gene"Pediatric Research. 42(10). 628-632 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Watanabe T,Yasuda T et al.: "Familial autosomal dominant hypoparathyroidism with sensorineural deafness without renal dysplasia"European Journal of Endocrinology. 139(12). 631-634 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishikawa M,Yasuda T et al.: "Serum levels of 20-kilodalton human growth hormone are parallel with 22-kilodalton human growth hormone in normal and short children"J Clin Endocrnol Metab. 84(1). 98-101 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yasuda T et al.: "Outcome of a baby born from a mother having undetectable thyroid hormone concentrations"J Clin Endocrinol Metab. 84(8). 2630-2632 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Nishi Y,Yasuda T et al.: "Determination of bone markers in Pycnodysostosis : Effects of Cathepsin K deficiency on bone matrix degradation"J Bone Miner Res. 14(10). 1902-1908 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 安田敏行: "小児の*断指針内頚部腫瘤と甲状腺腫・小児内分泌疾患の診断基準を分担"医学書院. 23/550 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 安田敏行: "医学のあゆみ2月号 PTH/PTHrP受容体活性型変異とJans*病を分担"医歯薬出版. 4/ (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Watanabe T, Yasuda T et al.: "Familial hypoparathyrodism : Identification of a novel gain of function mutation in transmembrane domain 5 of the calcium-sensing receptor."J Clin Endocrinol Metab. 83(7). 2497-2502 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Minamitani K, Yasuda T. et al.: "Difference in height associated with a translation start site polymorphism in the vitamin D receptor gene."Pediatric Research. 42(10). 628-632 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Watanabe T, Yasuda T et al.: "Familial autosomal dominant hypoparathyroidism with sensorineural deafiness without renal dysplasia."Euro J of Endocr. 139(12). 631-634 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ishikawa M, Yasuda T et al.: "Serum levels of 20-kilodalton human growth hormone are parallel with 22-kilodalton human growth hormone in normal and short children."J Clin Endocrinol Metab. 84(1). 98-101 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yasuda T et al.: "Outcome of a baby born from a mother having undetectable thyroid hormone concentrations."J Clin Endocrinol Metab. 84(8). 2630-2632 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Nishi Y, Yasuda T et al.: "Determination of bone markers in Pycnodysostosis : Effects of Cathepsin K deficiency on bone matrix degradation."J Bone Miner Res. 14(10). 1902-1908 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Saeki N, Yasuda T. et al.: "Long-term outcome of endocrine function in patients with neurohypophyseal germinomas."Endocrine J. 47(1). 83-89 (2000)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2001-10-23  

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