-
1
-
-
0021018019
-
The autonomously functioning thyroid adenoma
-
Hamburger J. 1983 The autonomously functioning thyroid adenoma. N Engl J Med. 309:1512-1513.
-
(1983)
N Engl J Med
, vol.309
, pp. 1512-1513
-
-
Hamburger, J.1
-
2
-
-
0025851976
-
High incidence of multinodular toxic goitre in the elderly population in a low iodine intake area vs. high incidence of Graves' disease in the young in a high iodine intake area: Comparative surveys of thyrotoxicosis epidemiology in East-Jutland Denmark and Iceland
-
Laurberg P, Pedersen KM, Vestergaard H, Sigurdsson G. 1991 High incidence of multinodular toxic goitre in the elderly population in a low iodine intake area vs. high incidence of Graves' disease in the young in a high iodine intake area: comparative surveys of thyrotoxicosis epidemiology in East-Jutland Denmark and Iceland. J Intern Med. 229:415-420.
-
(1991)
J Intern Med
, vol.229
, pp. 415-420
-
-
Laurberg, P.1
Pedersen, K.M.2
Vestergaard, H.3
Sigurdsson, G.4
-
3
-
-
0022402066
-
Pathogenesis of heterogenity in human multinodular goitre. A study on growth and function of thyroid tissue transplanted onto nude mice
-
Peter HJ, Gerber H, Studer H, Smeds S. 1985 Pathogenesis of heterogenity in human multinodular goitre. A study on growth and function of thyroid tissue transplanted onto nude mice. J Clin Invest. 76:1992.
-
(1985)
J Clin Invest
, vol.76
, pp. 1992
-
-
Peter, H.J.1
Gerber, H.2
Studer, H.3
Smeds, S.4
-
4
-
-
0026009016
-
Activating point mutations of the gsp oncogene in human thyroid adenomas
-
O'Sullivan C, Barton CM, Staddon SL, et al. 1991 Activating point mutations of the gsp oncogene in human thyroid adenomas. Mol Carcinog. 4:345-349.
-
(1991)
Mol Carcinog
, vol.4
, pp. 345-349
-
-
O'Sullivan, C.1
Barton, C.M.2
Staddon, S.L.3
-
6
-
-
0027369421
-
Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas
-
Parma J, Duprez L, Van Sande J, et al. 1993 Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas. Nature. 365:649-651.
-
(1993)
Nature
, vol.365
, pp. 649-651
-
-
Parma, J.1
Duprez, L.2
Van Sande, J.3
-
7
-
-
0026592357
-
Constitutive activation of the α1B-adrenergic receptor by all amino acid substitutions at a single site
-
Kjelsberg MA, Cotecchia S, Ostrowski J, et al. 1992 Constitutive activation of the α1B-adrenergic receptor by all amino acid substitutions at a single site. J Biol Chem. 267:1430-1433.
-
(1992)
J Biol Chem
, vol.267
, pp. 1430-1433
-
-
Kjelsberg, M.A.1
Cotecchia, S.2
Ostrowski, J.3
-
9
-
-
0030734932
-
Identification of a new TSH receptor germline mutation in a family with neonatal onset of autosomal dominant nonautoimmune hyperthyroidism
-
Führer D, Wonerow P, Willgerodt H, Scherbaum W, Paschke R. 1997 Identification of a new TSH receptor germline mutation in a family with neonatal onset of autosomal dominant nonautoimmune hyperthyroidism. J Clin Endocrinol Metab. 82: 4234-4238.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 4234-4238
-
-
Führer, D.1
Wonerow, P.2
Willgerodt, H.3
Scherbaum, W.4
Paschke, R.5
-
10
-
-
1842276431
-
A novel germline mutation in the thyrotropin receptor gene causing nonautoimmune congenital hyperthyroidism
-
Köhler B, Biebermann H, Krohn HP, et al. A novel germline mutation in the thyrotropin receptor gene causing nonautoimmune congenital hyperthyroidism [Abstract]. Proc of the Int Congr of Endocrinol. 1996; 641.
-
(1996)
Proc of the Int Congr of Endocrinol
, vol.641
-
-
Köhler, B.1
Biebermann, H.2
Krohn, H.P.3
-
11
-
-
0029360448
-
Somatic and germline mutations of the TSH receptor gene in thyroid disease
-
Van Sande J, Parma J, Tonacchera et al. 1995 Somatic and germline mutations of the TSH receptor gene in thyroid disease. J Clin Endocrinol Metab 80:2577-2585.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 2577-2585
-
-
Van Sande, J.1
Parma, J.2
Tonacchera3
-
12
-
-
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, 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
-
13
-
-
0024806929
-
Cloning, sequencing, and expression of the human thyrotropin (TSH) receptor: Evidence for binding of autoantibodies
-
12a. Libert F, Lefort A, Gerard C, et al. 1989 Cloning, sequencing, and expression of the human thyrotropin (TSH) receptor: evidence for binding of autoantibodies. Biochim Biophys Res Commun. 165:1250-1255.
-
(1989)
Biochim Biophys Res Commun
, vol.165
, pp. 1250-1255
-
-
Libert, F.1
Lefort, A.2
Gerard, C.3
-
15
-
-
0029012098
-
Interpretation of binding curves with high receptor concentrations: Practical aid for computer analysis
-
13a. Swillens S. 1995 Interpretation of binding curves with high receptor concentrations: practical aid for computer analysis. Mol Pharmacol. 47:1197-1203.
-
(1995)
Mol Pharmacol
, vol.47
, pp. 1197-1203
-
-
Swillens, S.1
-
16
-
-
0019061918
-
LIGAND: A versatile computerized approach for characterization of ligand-binding systems
-
Munson PJ, Rodbard D. 1980 LIGAND: a versatile computerized approach for characterization of ligand-binding systems. Anal Biochem. 107:220-239.
-
(1980)
Anal Biochem
, vol.107
, pp. 220-239
-
-
Munson, P.J.1
Rodbard, D.2
-
18
-
-
0028891649
-
Brief report: Congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene
-
Kopp P, Van Sande J, Parma J, et al. 1995 Brief report: Congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene. N Engl J Med. 332:150-154.
-
(1995)
N Engl J Med
, vol.332
, pp. 150-154
-
-
Kopp, P.1
Van Sande, J.2
Parma, J.3
-
19
-
-
0028588698
-
Identification and functional characterization of two new somatic mutations causing constitutive activation of the TSH receptor in hyperfunctioning autonomous adenomas of the thyroid
-
Paschke R, Tonacchera M, Van Sande J, et al. 1994 Identification and functional characterization of two new somatic mutations causing constitutive activation of the TSH receptor in hyperfunctioning autonomous adenomas of the thyroid. J Clin Endocrinol Metab. 79:1785-1789.
-
(1994)
J Clin Endocrinol Metab
, vol.79
, pp. 1785-1789
-
-
Paschke, R.1
Tonacchera, M.2
Van Sande, J.3
-
20
-
-
0028040908
-
Novel mutations of the thyrotropin receptor gene in thyroid hyperfunctioning adenomas
-
17a. Porcellini A, Ciullo I, Laviola L, Amabile G, Fenzi G, Avvedimento VE. 1994 Novel mutations of the thyrotropin receptor gene in thyroid hyperfunctioning adenomas. J Clin Endocrinol Metab. 79:657-661.
-
(1994)
J Clin Endocrinol Metab
, vol.79
, pp. 657-661
-
-
Porcellini, A.1
Ciullo, I.2
Laviola, L.3
Amabile, G.4
Fenzi, G.5
Avvedimento, V.E.6
-
21
-
-
0024576732
-
The clonal origin of thyroid nodules and adenomas
-
Thomas GA, Williams D, Williams ED. 1989 The clonal origin of thyroid nodules and adenomas. Am J Pathol. 134:141-147.
-
(1989)
Am J Pathol
, vol.134
, pp. 141-147
-
-
Thomas, G.A.1
Williams, D.2
Williams, E.D.3
-
23
-
-
0023871831
-
Thyroid autonomy: Sensitive detection in vivo and estimation of its functional relevance using quantified high-resolution scintigraphy
-
Copenh
-
Bahre M, Hilgers R, Lindemann C, Emrich D. 1988 Thyroid autonomy: sensitive detection in vivo and estimation of its functional relevance using quantified high-resolution scintigraphy. Acta Endocrinol (Copenh). 117:145-153.
-
(1988)
Acta Endocrinol
, vol.117
, pp. 145-153
-
-
Bahre, M.1
Hilgers, R.2
Lindemann, C.3
Emrich, D.4
-
24
-
-
8544221172
-
Diversity and prevalence of somatic mutations in the thyrotropin receptor and a Gsx gene as a cause of toxic-thyroid adenomas
-
Parma J, Duprez L, Van Sande J, et al. 1997 Diversity and prevalence of somatic mutations in the thyrotropin receptor and a Gsx gene as a cause of toxic-thyroid adenomas. J Clin Endocrinol Metab. 82:2695-2701.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 2695-2701
-
-
Parma, J.1
Duprez, L.2
Van Sande, J.3
-
25
-
-
0030710212
-
Somatic mutations in the thyrotropin receptor gene and not in the Gsα protein gene in 31 toxic thyroid nodules
-
21a. Führer D, Holzapfel HP, Wonerow P, Scherbaum WA, Paschke R. 1997 Somatic mutations in the thyrotropin receptor gene and not in the Gsα protein gene in 31 toxic thyroid nodules. J Clin Endocrinol Metab. 82:3885-3891.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3885-3891
-
-
Führer, D.1
Holzapfel, H.P.2
Wonerow, P.3
Scherbaum, W.A.4
Paschke, R.5
-
26
-
-
0020426661
-
Simple goiter and its variants: Euthyroid and hyperthyroid multinodular goiters
-
Studer H, Ramelli F. 1982 Simple goiter and its variants: euthyroid and hyperthyroid multinodular goiters. Endocr Rev. 3:40-61.
-
(1982)
Endocr Rev
, vol.3
, pp. 40-61
-
-
Studer, H.1
Ramelli, F.2
-
29
-
-
0025163524
-
Too many rodent carcinogens: Mitogenesis increases mutagenesis
-
Ames BN, Gold LS. 1990 Too many rodent carcinogens: mitogenesis increases mutagenesis. Science. 249:970-971.
-
(1990)
Science
, vol.249
, pp. 970-971
-
-
Ames, B.N.1
Gold, L.S.2
-
30
-
-
0029030316
-
Large goitre as a maladaption to iodine deficiency
-
Oxf
-
Dumont JE, Ermans AM, Maenhaut C, et al. 1995 Large goitre as a maladaption to iodine deficiency. Clin Endocrinol (Oxf). 43:1-10.
-
(1995)
Clin Endocrinol
, vol.43
, pp. 1-10
-
-
Dumont, J.E.1
Ermans, A.M.2
Maenhaut, C.3
-
31
-
-
0025924121
-
2-generating system modulates protein iodination and the activity of the pentose phosphate pathway in dog thyroid
-
2-generating system modulates protein iodination and the activity of the pentose phosphate pathway in dog thyroid. Endocrinology. 128:779-785.
-
(1991)
Endocrinology
, vol.128
, pp. 779-785
-
-
Corvilain, B.1
Van Sande, J.2
Laurent, E.3
Dumont, J.E.4
-
32
-
-
0027495785
-
Aberrant deoxyribonucleic acid methylation in human thyroid tumors
-
Matsuo K, Tang SH, Zeki K, et al. 1993 Aberrant deoxyribonucleic acid methylation in human thyroid tumors. J Clin Endocrinol Metab. 77:991-995.
-
(1993)
J Clin Endocrinol Metab
, vol.77
, pp. 991-995
-
-
Matsuo, K.1
Tang, S.H.2
Zeki, K.3
-
33
-
-
0025145277
-
S-Methylcytosine as an endogenous mutagen in the human LDL receptor and p53 genes
-
Rideout WM, Coetzee GA, Olumi AF, Jones PA. 1990 S-Methylcytosine as an endogenous mutagen in the human LDL receptor and p53 genes. Science. 249:1288-1290.
-
(1990)
Science
, vol.249
, pp. 1288-1290
-
-
Rideout, W.M.1
Coetzee, G.A.2
Olumi, A.F.3
Jones, P.A.4
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