-
1
-
-
0000437998
-
Characterization of two LGR genes homologous to gonadotropin and thyrotropin receptors with extracellular leucine-rich repeats and a G-protein-coupled, seven-transmembrane region
-
Hsu SH, Liang S-G & Hsueh AJW. Characterization of two LGR genes homologous to gonadotropin and thyrotropin receptors with extracellular leucine-rich repeats and a G-protein-coupled, seven-transmembrane region. Molecular Endocrinology 1998 12 1830-1845.
-
(1998)
Molecular Endocrinology
, vol.12
, pp. 1830-1845
-
-
Hsu, S.H.1
Liang, S.-G.2
Hsueh, A.J.W.3
-
2
-
-
0030912536
-
A model of the lutropin/ choriogonadotropin receptor: Insights into the structural and functional effects of constitutively activating mutations
-
Lin Z, Shenker A & Pearlstein R. A model of the lutropin/ choriogonadotropin receptor: insights into the structural and functional effects of constitutively activating mutations. Protein Engineering 1997 10 501-510.
-
(1997)
Protein Engineering
, vol.10
, pp. 501-510
-
-
Lin, Z.1
Shenker, A.2
Pearlstein, R.3
-
3
-
-
0027372340
-
A constitutive activating mutation of the luteinizing hormone receptor in familial male precocious puberty
-
Shenker A, Laue L, Kosugi S, Meredino JJ, Minegishi T & Cutler GB. A constitutive activating mutation of the luteinizing hormone receptor in familial male precocious puberty. Nature 1993 365 652-654.
-
(1993)
Nature
, vol.365
, pp. 652-654
-
-
Shenker, A.1
Laue, L.2
Kosugi, S.3
Meredino, J.J.4
Minegishi, T.5
Cutler, G.B.6
-
4
-
-
0027369421
-
Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas
-
Parma J, Duprez L, Van Sande J, Cochaux P, Gervy C, Mockel J et al. Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas. Nature 1993 365 649-651.
-
(1993)
Nature
, vol.365
, pp. 649-651
-
-
Parma, J.1
Duprez, L.2
Van Sande, J.3
Cochaux, P.4
Gervy, C.5
Mockel, J.6
-
5
-
-
85037953458
-
-
http://www.unvi-leipzig~innerre/TSH
-
-
-
-
6
-
-
0032542355
-
Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin
-
Rodien P, Bremont C, Raffin Sanson M-L, Parma J, Van Sande J, Costagliola S et al. Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin. New England Journal of Medicine 1998 339 1823-1826.
-
(1998)
New England Journal of Medicine
, vol.339
, pp. 1823-1826
-
-
Rodien, P.1
Bremont, C.2
Raffin Sanson, M.-L.3
Parma, J.4
Van Sande, J.5
Costagliola, S.6
-
7
-
-
0033312613
-
A germline mutation of the thyrotropin receptor gene associated with thyrotoxicosis and mitral valve prolapse in a Chinese family
-
Khoo DH, Parma J, Rajasoorya C, Ho SC & Vassart G. A germline mutation of the thyrotropin receptor gene associated with thyrotoxicosis and mitral valve prolapse in a Chinese family. Journal of Clinical Endocrinology and Metabolism 1999 84 1459-1462.
-
(1999)
Journal of Clinical Endocrinology and Metabolism
, vol.84
, pp. 1459-1462
-
-
Khoo, D.H.1
Parma, J.2
Rajasoorya, C.3
Ho, S.C.4
Vassart, G.5
-
8
-
-
0033025188
-
A Val 677 activating mutation of the thyrotropin receptor in a Hurthle cell thyroid carcinoma associated with thyrotoxicosis
-
Russo D, Wong MG, Costante G, Chiefari E, Tresler PA, Arturi F, Filetti S et al. A Val 677 activating mutation of the thyrotropin receptor in a Hurthle cell thyroid carcinoma associated with thyrotoxicosis. Thyroid 1999 9 13-17.
-
(1999)
Thyroid
, vol.9
, pp. 13-17
-
-
Russo, D.1
Wong, M.G.2
Costante, G.3
Chiefari, E.4
Tresler, P.A.5
Arturi, F.6
Filetti, S.7
-
9
-
-
0032968013
-
Screening of thyrotropin receptor mutations by fine needle aspiration biopsy in autonomous functioning thyroid nodules in multinodular goiters
-
Tassi V, Di Cerbo A, Porcellini A, Papini E, Cisternino C, Crescenzi A et al. Screening of thyrotropin receptor mutations by fine needle aspiration biopsy in autonomous functioning thyroid nodules in multinodular goiters. Thyroid 1999 9 353-357.
-
(1999)
Thyroid
, vol.9
, pp. 353-357
-
-
Tassi, V.1
Di Cerbo, A.2
Porcellini, A.3
Papini, E.4
Cisternino, C.5
Crescenzi, A.6
-
10
-
-
0029913238
-
Can activating mutation of the follicle-stimulating hormone receptor autonomously sustain spermatogenesis in a hypophysectomized man?
-
Gromoll J, Simoni M, Nordhoff V & Nieschlag E. Can activating mutation of the follicle-stimulating hormone receptor autonomously sustain spermatogenesis in a hypophysectomized man? Journal of Clinical Endocrinology and Metabolism 1996 81 1367-1370.
-
(1996)
Journal of Clinical Endocrinology and Metabolism
, vol.81
, pp. 1367-1370
-
-
Gromoll, J.1
Simoni, M.2
Nordhoff, V.3
Nieschlag, E.4
-
11
-
-
0031916977
-
The luteinizing hormone receptor
-
Dufau ML. The luteinizing hormone receptor. Annual Review of Physiology 1998 60 461-496.
-
(1998)
Annual Review of Physiology
, vol.60
, pp. 461-496
-
-
Dufau, M.L.1
-
12
-
-
0032796619
-
A novel luteinizing hormone receptor mutation in a patient with familial male-limited precocious puberty: Effect of the size of a critical amino acid on receptor activity
-
Wu SM, Leschek EW, Brain C & Chan WY. A novel luteinizing hormone receptor mutation in a patient with familial male-limited precocious puberty: effect of the size of a critical amino acid on receptor activity. Molecular Genetics and Metabolism 1999 66 68-73.
-
(1999)
Molecular Genetics and Metabolism
, vol.66
, pp. 68-73
-
-
Wu, S.M.1
Leschek, E.W.2
Brain, C.3
Chan, W.Y.4
-
13
-
-
0031754903
-
Certain activating mutations within helix 6 of the human luteinizing hormone receptor may be explained by alterations that allow transmembrane regions to activate Gs
-
Abell AN, McCormick DJ & Segaloff DL. Certain activating mutations within helix 6 of the human luteinizing hormone receptor may be explained by alterations that allow transmembrane regions to activate Gs. Molecular Endocrinology 1998 12 1857-1869.
-
(1998)
Molecular Endocrinology
, vol.12
, pp. 1857-1869
-
-
Abell, A.N.1
McCormick, D.J.2
Segaloff, D.L.3
-
14
-
-
0029657910
-
The role of Asp 578 in maintaining the inactive conformation of the human lutrotropin/ choriogonadotropin receptor
-
Kosugi S, Mori T & Shenker A. The role of Asp 578 in maintaining the inactive conformation of the human lutrotropin/ choriogonadotropin receptor. Journal of Biological Chemistry 1996 271 31813-31817.
-
(1996)
Journal of Biological Chemistry
, vol.271
, pp. 31813-31817
-
-
Kosugi, S.1
Mori, T.2
Shenker, A.3
-
15
-
-
85047680596
-
Phe 576 plays an important role in the secondary structure and intracellular signaling of the human luteinizing/chorionic gonadotropin receptor
-
Yano K, Kohn LD, Saji M, Okuno A & Cutler GB Jr. Phe 576 plays an important role in the secondary structure and intracellular signaling of the human luteinizing/chorionic gonadotropin receptor. Journal of Clinical Endocrinology and Metabolism 1997 82 2586-2591.
-
(1997)
Journal of Clinical Endocrinology and Metabolism
, vol.82
, pp. 2586-2591
-
-
Yano, K.1
Kohn, L.D.2
Saji, M.3
Okuno, A.4
Cutler G.B., Jr.5
-
16
-
-
2642703472
-
Deletions in the third intracellular loop of the thyrotropin receptor. A new mechanism for constitutive activation
-
Worerow P, Schoneberg T, Schultz G, Gudermann T & Paschke P. Deletions in the third intracellular loop of the thyrotropin receptor. A new mechanism for constitutive activation. Journal of Biological Chemistry 1998 273 7900-7905.
-
(1998)
Journal of Biological Chemistry
, vol.273
, pp. 7900-7905
-
-
Worerow, P.1
Schoneberg, T.2
Schultz, G.3
Gudermann, T.4
Paschke, P.5
-
17
-
-
0031728024
-
A unique constitutive activating mutation in the third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty
-
Latronico AC, Abell AN, Arnhold IJ, Liu X, Lins TS, Billerbeck AE et al. A unique constitutive activating mutation in the third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty. Journal of Clinical Endocrinology and Metabolism 1998 83 2435-2340.
-
(1998)
Journal of Clinical Endocrinology and Metabolism
, vol.83
, pp. 2435-12340
-
-
Latronico, A.C.1
Abell, A.N.2
Arnhold, I.J.3
Liu, X.4
Lins, T.S.5
Billerbeck, A.E.6
-
18
-
-
0031407694
-
Genetic alterations in N-bis (2-hyroxypropyl) nitrosamine-induced rat transplantable thyroid carcinoma cell line: Analysis of the TSH-R, #Gs (alpha), ras and p53 genes
-
Kitahori Y, Naitoh H, Konishi N, Ohnishi T & Hiasa Y. Genetic alterations in N-bis (2-hyroxypropyl) nitrosamine-induced rat transplantable thyroid carcinoma cell line: analysis of the TSH-R, #Gs (alpha), ras and p53 genes. Carcinogenesis 1997 18 265-269.
-
(1997)
Carcinogenesis
, vol.18
, pp. 265-269
-
-
Kitahori, Y.1
Naitoh, H.2
Konishi, N.3
Ohnishi, T.4
Hiasa, Y.5
-
19
-
-
0032991946
-
A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty
-
Kremer H, Martens JWM, van Reen M, Verhoeff-Post M, Wit JW, Otten BJ et al. A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty. Journal of Clinical Endocrinology and Metabolism 1999 84 1136-1140.
-
(1999)
Journal of Clinical Endocrinology and Metabolism
, vol.84
, pp. 1136-1140
-
-
Kremer, H.1
Martens, J.W.M.2
Van Reen, M.3
Verhoeff-Post, M.4
Wit, J.W.5
Otten, B.J.6
|