-
1
-
-
79251644004
-
Principles and determinants of G-protein coupling by the rhodopsin-like thyrotropin receptor
-
Kleinau G, Jaeschke H, Worth CL, Mueller S, Gonzalez J, et al. (2010) Principles and determinants of G-protein coupling by the rhodopsin-like thyrotropin receptor. PLoS One 18: e9745.
-
(2010)
PLoS One
, vol.18
-
-
Kleinau, G.1
Jaeschke, H.2
Worth, C.L.3
Mueller, S.4
Gonzalez, J.5
-
2
-
-
33750488472
-
Structural determinants for G-protein activation and specificity in the third intracellular loop of the thyroid-stimulating hormone receptor
-
Claus M, Neumann S, Kleinau G, Krause G, Paschke R (2006) Structural determinants for G-protein activation and specificity in the third intracellular loop of the thyroid-stimulating hormone receptor. J Mol Med 84: 943-954.
-
(2006)
J Mol Med
, vol.84
, pp. 943-954
-
-
Claus, M.1
Neumann, S.2
Kleinau, G.3
Krause, G.4
Paschke, R.5
-
3
-
-
0030030847
-
The human thyrotropin receptor: A heptahelical receptor capable of stimulating members of all four G protein families
-
Laugwitz KL, Allgeier A, Offermanns S, Spicher K, Van Sande J, et al. (1996) The human thyrotropin receptor: a heptahelical receptor capable of stimulating members of all four G protein families. Proc Natl Acad Sci 93: 116-120.
-
(1996)
Proc Natl Acad Sci
, vol.93
, pp. 116-120
-
-
Laugwitz, K.L.1
Allgeier, A.2
Offermanns, S.3
Spicher, K.4
Van Sande, J.5
-
4
-
-
0028240982
-
Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism
-
Duprez L, Parma J, Van Sande J, Allgeier A, Leclère, et al. (1994) Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism. Nat Genet 7: 396-401.
-
(1994)
Nat Genet
, vol.7
, pp. 396-401
-
-
Duprez, L.1
Parma, J.2
Van Sande, J.3
Allgeier, A.4
Leclère5
-
5
-
-
0034852079
-
A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism
-
Alberti L, Proverbio MC, Costagliola S, Weber G, Beck-Peccoz P, et al. (2001) A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism. Eur J Endocrinol 145: 249-254.
-
(2001)
Eur J Endocrinol
, vol.145
, pp. 249-254
-
-
Alberti, L.1
Proverbio, M.C.2
Costagliola, S.3
Weber, G.4
Beck-Peccoz, P.5
-
6
-
-
0030805829
-
Constitutive activation of the TSH receptor by spontaneous mutations affecting the N-terminal extracellular domain
-
Duprez L, Parma J, Costagliola S, Hermans J, Van Sande J, et al. (1997) Constitutive activation of the TSH receptor by spontaneous mutations affecting the N-terminal extracellular domain. FEBS Lett 409: 469-474.
-
(1997)
FEBS Lett
, vol.409
, pp. 469-474
-
-
Duprez, L.1
Parma, J.2
Costagliola, S.3
Hermans, J.4
Van Sande, J.5
-
7
-
-
0032542355
-
Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin
-
Rodien P, Brémont C, Sanson ML, Parma J, Van Sande J, et al. (1998) Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin. N Engl J Med 339: 1823-1826.
-
(1998)
N Engl J Med
, vol.339
, pp. 1823-1826
-
-
Rodien, P.1
Brémont, C.2
Sanson, M.L.3
Parma, J.4
Van Sande, J.5
-
8
-
-
0034853605
-
The first activating TSH receptor mutation in transmembrane domain 1 identified in a family with nonautoimmune hyperthyroidism
-
Biebermann H, Schöneberg T, Hess C, Germak J, Gudermann T, et al. (2001) The first activating TSH receptor mutation in transmembrane domain 1 identified in a family with nonautoimmune hyperthyroidism. J Clin Endocrinol Metab 86: 4429-4433.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 4429-4433
-
-
Biebermann, H.1
Schöneberg, T.2
Hess, C.3
Germak, J.4
Gudermann, T.5
-
9
-
-
0036002619
-
An activating mutation of the thyrotropin receptor gene in hereditary non-autoimmune hyperthyroidism
-
Lee YS, Poh L, Loke KY (2002) An activating mutation of the thyrotropin receptor gene in hereditary non-autoimmune hyperthyroidism. J Pediatr Endocrinol Metab 15: 211-215.
-
(2002)
J Pediatr Endocrinol Metab
, vol.15
, pp. 211-215
-
-
Lee, Y.S.1
Poh, L.2
Loke, K.Y.3
-
10
-
-
0029044073
-
Somatic mutations causing constitutive activity of the thyrotropin receptor are the major cause of hyperfunctioning thyroid adenomas: Identification of additional mutations activating both the cyclic adenosine 3′, 5′-monophosphate and inositol phosphate-Ca2+ cascades
-
Parma J, Van Sande J, Swillens S, Tonacchera M, Dumont J, et al. (1995) Somatic mutations causing constitutive activity of the thyrotropin receptor are the major cause of hyperfunctioning thyroid adenomas: identification of additional mutations activating both the cyclic adenosine 3′, 5′-monophosphate and inositol phosphate-Ca2+ cascades. Mol Endocrinol 9: 725-733.
-
(1995)
Mol Endocrinol
, vol.9
, pp. 725-733
-
-
Parma, J.1
Van Sande, J.2
Swillens, S.3
Tonacchera, M.4
Dumont, J.5
-
11
-
-
9044240477
-
Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia
-
Tonacchera M, Van Sande J, Cetani F, Swillens S, Schvartz C, et al. (1996) Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia. J Clin Endocrinol Metab 81: 547-554.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 547-554
-
-
Tonacchera, M.1
Van Sande, J.2
Cetani, F.3
Swillens, S.4
Schvartz, C.5
-
12
-
-
0031470487
-
Constitutively active germline mutation of the thyrotropin receptor gene as a cause of congenital hyperthyroidism
-
Schwab KO, Gerlich M, Broecker M, Söhlemann P, Derwahl M, et al. (1997) Constitutively active germline mutation of the thyrotropin receptor gene as a cause of congenital hyperthyroidism. J Pediatr 131: 899-904.
-
(1997)
J Pediatr
, vol.131
, pp. 899-904
-
-
Schwab, K.O.1
Gerlich, M.2
Broecker, M.3
Söhlemann, P.4
Derwahl, M.5
-
13
-
-
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 (1999) A germline mutation of the thyrotropin receptor gene associated with thyrotoxicosis and mitral valve prolapse in a Chinese family. J Clin Endocrinol Metab 84: 1459-1462.
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 1459-1462
-
-
Khoo, D.H.1
Parma, J.2
Rajasoorya, C.3
Ho, S.C.4
Vassart, G.5
-
14
-
-
9044240477
-
Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia
-
Tonacchera M, Van Sande J, Cetani F, Swillens S, Schvartz C, et al. (1996) Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia. J Clin Endocrinol Metab 81: 547-554.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 547-554
-
-
Tonacchera, M.1
Van Sande, J.2
Cetani, F.3
Swillens, S.4
Schvartz, C.5
-
15
-
-
0027250914
-
Substitutions of different regions of the third cytoplasmic loop of the thyrotropin (TSH) receptor have selective effects on constitutive, TSH-, and TSH receptor autoantibodystimulated phosphoinositide and 3′, 5′-cyclic adenosine monophosphate signal generation
-
Kosugi S, Okajima F, Ban T, Hidaka A, Shenker A, et al. (1993) Substitutions of different regions of the third cytoplasmic loop of the thyrotropin (TSH) receptor have selective effects on constitutive, TSH-, and TSH receptor autoantibodystimulated phosphoinositide and 3′, 5′-cyclic adenosine monophosphate signal generation. Mol Endocrinol 7: 1009-1020.
-
(1993)
Mol Endocrinol
, vol.7
, pp. 1009-1020
-
-
Kosugi, S.1
Okajima, F.2
Ban, T.3
Hidaka, A.4
Shenker, A.5
-
16
-
-
0026464910
-
Mutation of alanine 623 in the third cytoplasmic loop of the rat thyrotropin (TSH) receptor results in a loss in the phosphoinositide but not cAMP signal induced by TSH and receptor autoantibodies
-
Kosugi S, Okajima F, Ban T, Hidaka A, Shenker A, et al. (1992) Mutation of alanine 623 in the third cytoplasmic loop of the rat thyrotropin (TSH) receptor results in a loss in the phosphoinositide but not cAMP signal induced by TSH and receptor autoantibodies. J Biol Chem 267: 24153-24156.
-
(1992)
J Biol Chem
, vol.267
, pp. 24153-24156
-
-
Kosugi, S.1
Okajima, F.2
Ban, T.3
Hidaka, A.4
Shenker, A.5
-
17
-
-
43449125582
-
A novel TSHR gene mutation (Ile691Phe) in a Chinese family causing autosomal dominant nonautoimmune hyperthyroidism
-
Liu Z, Sun Y, Dong Q, He M, Cheng CH, et al. (2008) A novel TSHR gene mutation (Ile691Phe) in a Chinese family causing autosomal dominant nonautoimmune hyperthyroidism. J Hum Genet 53: 475-478.
-
(2008)
J Hum Genet
, vol.53
, pp. 475-478
-
-
Liu, Z.1
Sun, Y.2
Dong, Q.3
He, M.4
Cheng, C.H.5
-
18
-
-
0036083401
-
Thyroidstimulating hormone and thyroid-stimulating hormone receptor structurefunction relationships
-
Szkudlinski MW, Fremont V, Ronin C, Weintraub BD (2002) Thyroidstimulating hormone and thyroid-stimulating hormone receptor structurefunction relationships. Physiol Rev 82: 473-502.
-
(2002)
Physiol Rev
, vol.82
, pp. 473-502
-
-
Szkudlinski, M.W.1
Fremont, V.2
Ronin, C.3
Weintraub, B.D.4
-
19
-
-
0033790195
-
Functional characterization of five constitutively activating thyrotrophin receptor mutations
-
Wonerow P, Chey S, Führer D, Holzapfel HP, Paschke R (2000) Functional characterization of five constitutively activating thyrotrophin receptor mutations. Clin Endocrinol 53: 461-468.
-
(2000)
Clin Endocrinol
, vol.53
, pp. 461-468
-
-
Wonerow, P.1
Chey, S.2
Führer, D.3
Holzapfel, H.P.4
Paschke, R.5
-
21
-
-
0031790855
-
A conserved tyrosine residue (Y601) in transmembrane domain 5 of the human thyrotropin receptor serves as a molecular switch to determine G-protein coupling
-
Biebermann H, Schöneberg T, Schulz A, Krause G, Grüters A (1998) A conserved tyrosine residue (Y601) in transmembrane domain 5 of the human thyrotropin receptor serves as a molecular switch to determine G-protein coupling. FASEB J 12: 1461-1471.
-
(1998)
FASEB J
, vol.12
, pp. 1461-1471
-
-
Biebermann, H.1
Schöneberg, T.2
Schulz, A.3
Krause, G.4
Grüters, A.5
-
22
-
-
0036312956
-
Expression of G(alpha)(s) proteins and TSH receptor signalling in hyperfunctioning thyroid nodules with TSH receptor mutations
-
Holzapfel HP, Bergner B, Wonerow P, Paschke R (2002) Expression of G(alpha)(s) proteins and TSH receptor signalling in hyperfunctioning thyroid nodules with TSH receptor mutations. Eur J Endocrinol 147: 109-116.
-
(2002)
Eur J Endocrinol
, vol.147
, pp. 109-116
-
-
Holzapfel, H.P.1
Bergner, B.2
Wonerow, P.3
Paschke, R.4
-
23
-
-
0141447331
-
Proper targeting and activity of a nonfunctioning thyroid-stimulating hormone receptor (TSHR) combining an inactivating and activating TSHR mutation in one receptor
-
Agretti P, De Marco G, Collecchi P, Chiovato L, Vitti P, et al. (2003) Proper targeting and activity of a nonfunctioning thyroid-stimulating hormone receptor (TSHR) combining an inactivating and activating TSHR mutation in one receptor. Eur J Biochem 270: 3839-3847.
-
(2003)
Eur J Biochem
, vol.270
, pp. 3839-3847
-
-
Agretti, P.1
De Marco, G.2
Collecchi, P.3
Chiovato, L.4
Vitti, P.5
-
24
-
-
4344662529
-
Minireview: Structural and functional evolution of the thyrotropin receptor
-
Farid NR, Szkudlinski MW (2004) Minireview: structural and functional evolution of the thyrotropin receptor. Endocrinology 145: 4048-4057.
-
(2004)
Endocrinology
, vol.145
, pp. 4048-4057
-
-
Farid, N.R.1
Szkudlinski, M.W.2
-
25
-
-
0025608144
-
Functional analysis of the cytoplasmic domains of the human thyrotropin receptor by site-directed mutagenesis
-
Chazenbalk GD, Nagayama Y, Russo D, Wadsworth HL, Rapoport B (1990) Functional analysis of the cytoplasmic domains of the human thyrotropin receptor by site-directed mutagenesis. J Biol Chem 265: 20970-20975.
-
(1990)
J Biol Chem
, vol.265
, pp. 20970-20975
-
-
Chazenbalk, G.D.1
Nagayama, Y.2
Russo, D.3
Wadsworth, H.L.4
Rapoport, B.5
-
26
-
-
0028287809
-
The amino-terminal half of the cytoplasmic tail of the thyrotropin receptor is essential for full activities of receptor function
-
Kosugi S, Mori T (1994) The amino-terminal half of the cytoplasmic tail of the thyrotropin receptor is essential for full activities of receptor function. Biochem Biophys Res Commun 200: 401-407.
-
(1994)
Biochem Biophys Res Commun
, vol.200
, pp. 401-407
-
-
Kosugi, S.1
Mori, T.2
-
27
-
-
0034892924
-
Tolerance of point substitution of methionine for isoleucine in hen egg white lysozyme
-
Ohmura T, Ueda T, Hashimoto Y, Imoto T (2001) Tolerance of point substitution of methionine for isoleucine in hen egg white lysozyme. Protein Eng 14: 421-425.
-
(2001)
Protein Eng
, vol.14
, pp. 421-425
-
-
Ohmura, T.1
Ueda, T.2
Hashimoto, Y.3
Imoto, T.4
|