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Volumn 134, Issue 5, 1996, Pages 560-562

No correlation of growth hormone receptor gene mutation P561T with body height

Author keywords

[No Author keywords available]

Indexed keywords

GROWTH HORMONE RECEPTOR;

EID: 0029890609     PISSN: 08044643     EISSN: None     Source Type: Journal    
DOI: 10.1530/eje.0.1340560     Document Type: Article
Times cited : (32)

References (10)
  • 1
    • 0346628520 scopus 로고
    • Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron type dwarfism
    • Godowski J, Leung W, Meacham R, Galgari J, Hellmiss R, Keret R, et al. Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron type dwarfism. Proc Natl Acad Sci USA. 1989; 86:8083-7
    • (1989) Proc Natl Acad Sci USA , vol.86 , pp. 8083-8087
    • Godowski, J.1    Leung, W.2    Meacham, R.3    Galgari, J.4    Hellmiss, R.5    Keret, R.6
  • 3
    • 0027931590 scopus 로고
    • Receptor mutations and haplotypes in growth hormone receptor deficiency: A global survey and identification of the Ecuadorean E180 splice mutation in a Oriental Jewish patient
    • Berg M. Peoples R, Perez-Jurado L, Guevara-Aguirre J, Rosenbloom L, Laron Z, et al. Receptor mutations and haplotypes in growth hormone receptor deficiency: a global survey and identification of the Ecuadorean E180 splice mutation in a Oriental Jewish patient. Acta Paediatri Suppl 1994;399: 112-4
    • (1994) Acta Paediatri Suppl , vol.399 , pp. 112-114
    • Berg, M.1    Peoples, R.2    Perez-Jurado, L.3    Guevara-Aguirre, J.4    Rosenbloom, L.5    Laron, Z.6
  • 4
    • 0027469409 scopus 로고
    • Amino acid substitutions in the intracellular part of the growth hormone receptor in a patient with the Laron syndrome
    • Kou K, Lajara R, Rotwein P. Amino acid substitutions in the intracellular part of the growth hormone receptor in a patient with the Laron syndrome. J Clin Endocrinol Metab 1993;76:54-9
    • (1993) J Clin Endocrinol Metab , vol.76 , pp. 54-59
    • Kou, K.1    Lajara, R.2    Rotwein, P.3
  • 5
    • 0028141525 scopus 로고
    • Regulation of the growth hormone (GH) receptor and GH-binding protein mRNA
    • Kaji H, Ohashi S, Abe H, Chihara K, Regulation of the growth hormone (GH) receptor and GH-binding protein mRNA. Proc Soc Exp Biol Med 1994;206:257-62
    • (1994) Proc Soc Exp Biol Med , vol.206 , pp. 257-262
    • Kaji, H.1    Ohashi, S.2    Abe, H.3    Chihara, K.4
  • 6
    • 0025787596 scopus 로고
    • Defective membrane expression of human growth hormone (GH) receptor causes Laron-type GH insensitivity syndrome
    • Duquesnoy P, Amselem S, Gossens M. Defective membrane expression of human growth hormone (GH) receptor causes Laron-type GH insensitivity syndrome. Proc Natl Acad Sci USA 1991;88:10272-6
    • (1991) Proc Natl Acad Sci USA , vol.88 , pp. 10272-10276
    • Duquesnoy, P.1    Amselem, S.2    Gossens, M.3
  • 7
    • 0027462456 scopus 로고
    • Lack of hormone binding in Cos-7 cells expressing a mutated growth hormone receptor found in Laron dwarfism
    • Edery M, Rozakis-Adocock M, Goujon L, Finidori J, Levi-Meyrueis C, Paly J, et al. Lack of hormone binding in Cos-7 cells expressing a mutated growth hormone receptor found in Laron dwarfism. J Clin Invest 1993;91:838-44
    • (1993) J Clin Invest , vol.91 , pp. 838-844
    • Edery, M.1    Rozakis-Adocock, M.2    Goujon, L.3    Finidori, J.4    Levi-Meyrueis, C.5    Paly, J.6
  • 8
    • 0025765004 scopus 로고
    • A systematic mutational analysis of hormone-binding determinants in the human growth hormone receptor
    • Bass H, Mulkerrin G, Wells A. A systematic mutational analysis of hormone-binding determinants in the human growth hormone receptor. Proc Natl Acad Sci USA 1991;88:4498-502
    • (1991) Proc Natl Acad Sci USA , vol.88 , pp. 4498-4502
    • Bass, H.1    Mulkerrin, G.2    Wells, A.3
  • 9
    • 0028294901 scopus 로고
    • A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH binding activity by abolishing receptor homodimerization
    • Duquesnoy P, Sobricer L, Duriez B, et al. A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH binding activity by abolishing receptor homodimerization. EMBO J, 1994;13:1386-95
    • (1994) EMBO J , vol.13 , pp. 1386-1395
    • Duquesnoy, P.1    Sobricer, L.2    Duriez, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.