-
1
-
-
0346628520
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
|