-
6
-
-
0030724982
-
New pathophysiological mechanisms for hyperthyroidism
-
(1997)
Horm Res
, vol.48
, pp. 47-50
-
-
Vassart, G.1
-
8
-
-
0031033312
-
Molecular cloning, genomic organization, and developmental regulation of a novel receptor from Drosophila melanogaster structurally related to members of the thyroid-stimulating hormone, follicle-stimulating hormone, luteinizing hormone/choriogonadotropin receptor family from mammals
-
(1997)
J Biol Chem
, vol.272
, pp. 1002-1010
-
-
Hauser, F.1
Nothacker, H.P.2
Grimmelikhuijzen, C.J.3
-
10
-
-
0029081150
-
Effects of second intracellular loop mutations on signal transduction and internalization of the gonadotropin-releasing hormone receptor
-
(1995)
J Biol Chem
, vol.270
, pp. 22820-22826
-
-
Arora, K.K.1
Sakai, A.2
Catt, K.J.3
-
11
-
-
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
-
(1998)
Mol Endocrinol
, vol.12
, pp. 1830-1845
-
-
Hsu, S.Y.1
Liang, S.G.2
Hsueh, A.J.3
-
18
-
-
0033179830
-
Many G-protein-coupled receptors are encoded by retrogenes
-
(1999)
Trends Genet
, vol.15
, pp. 304-305
-
-
Brosius, J.1
-
22
-
-
0027959963
-
High agonist-independent activity is a distinguishing feature of the dopamine D1B receptor subtype
-
(1994)
J Biol Chem
, vol.269
, pp. 27925-27931
-
-
Tiberi, M.1
Caron, M.G.2
-
24
-
-
0030220018
-
Heterogeneity of activating mutations of the human luteinizing hormone receptor in male-limited precocious puberty
-
(1996)
Biochem Mol Med
, vol.58
, pp. 192-198
-
-
Laue, L.1
Wu, S.M.2
Kudo, M.3
Hsueh, A.J.W.4
Cutler G.B., Jr.5
Jelly, D.H.6
Diamond, F.B.7
Chan, W.Y.8
-
27
-
-
0028281397
-
Hereditary and acquired defects in signaling through the hormone-receptor-G protein complex
-
(1994)
Am J Physiol
, vol.266
-
-
Raymond, J.R.1
-
28
-
-
0027494368
-
G-protein-coupled receptors. Turned on to ill effect
-
(1993)
Nature
, vol.365
, pp. 603-604
-
-
Lefkowitz, R.J.1
-
31
-
-
0027413475
-
Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function
-
(1993)
Cell
, vol.72
, pp. 827-834
-
-
Robbins, L.S.1
Nadeau, J.H.2
Johnson, K.R.3
Kelly, M.A.4
Roselli-Rehfuss, L.5
Baack, E.6
Mountjoy, K.G.7
Cone, R.D.8
-
33
-
-
0028037143
-
Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation
-
(1994)
Nat Genet
, vol.8
, pp. 303-307
-
-
Pollak, M.R.1
Brown, E.M.2
Estep, H.L.3
McLaine, P.N.4
Kifor, O.5
Park, J.6
Hebert, S.C.7
Seidman, C.E.8
Seidman, J.G.9
-
34
-
-
0027787680
-
Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
-
(1993)
Cell
, vol.75
, pp. 1297-1303
-
-
Pollak, M.R.1
Brown, E.M.2
Chou, Y.H.3
Hebert, S.C.4
Marx, S.J.5
Steinmann, B.6
Levi, T.7
Seidman, C.E.8
Seidman, J.G.9
-
35
-
-
0029150958
-
A novel mutation of the luteinizing hormone receptor gene causing male gonadotropin-independent precocious puberty
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 2490-2494
-
-
Latronico, A.C.1
Anasti, J.2
Arnhold, I.J.3
Mendonca, B.B.4
Domenice, S.5
Albano, M.C.6
Zachman, K.7
Wajchenberg, B.L.8
Tsigos, C.9
-
36
-
-
0027369421
-
Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas
-
(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
Dumont, J.7
Vassart, G.8
-
37
-
-
0032509302
-
Genome sequence of the nematode C. elegans: A platform for investigating biology
-
(1998)
Science
, vol.282
, pp. 2012-2018
-
-
-
42
-
-
0026042543
-
Expression of human luteinizing hormone (LH) receptor: Interaction with LH and chorionic gonadotropin from human but not equine, rat, and ovine species
-
(1991)
Mol Endocrinol
, vol.5
, pp. 759-768
-
-
Jia, X.C.1
Oikawa, M.2
Bo, M.3
Tanaka, T.4
Ny, T.5
Boime, I.6
Hsueh, A.J.7
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