Gudermann T - Search Results

1

Autosomal-dominant mode of inheritance of a melanocortin-4 receptor mutation in a patient with severe early-onset obesity is due to a dominant-negative effect caused by receptor dimerization.

Biebermann H, Krude H, Elsner A, Chubanov V, Gudermann T, Grüters A. Biebermann H, et al. Among authors: gudermann t. Diabetes. 2003 Dec;52(12):2984-8. doi: 10.2337/diabetes.52.12.2984. Diabetes. 2003. PMID: 14633860

2

Congenital hypothyroidism caused by mutations in the thyrotropin-receptor gene.

Biebermann H, Grüters A, Schöneberg T, Gudermann T. Biebermann H, et al. Among authors: gudermann t. N Engl J Med. 1997 May 8;336(19):1390-1. doi: 10.1056/NEJM199705083361914. N Engl J Med. 1997. PMID: 9139226 No abstract available.

3

Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism.

Biebermann H, Schöneberg T, Krude H, Schultz G, Gudermann T, Grüters A. Biebermann H, et al. Among authors: gudermann t. J Clin Endocrinol Metab. 1997 Oct;82(10):3471-80. doi: 10.1210/jcem.82.10.4286. J Clin Endocrinol Metab. 1997. PMID: 9329388

4

Severe congenital hyperthyroidism caused by a germ-line neo mutation in the extracellular portion of the thyrotropin receptor.

Grüters A, Schöneberg T, Biebermann H, Krude H, Krohn HP, Dralle H, Gudermann T. Grüters A, et al. Among authors: gudermann t. J Clin Endocrinol Metab. 1998 May;83(5):1431-6. doi: 10.1210/jcem.83.5.4776. J Clin Endocrinol Metab. 1998. PMID: 9589634

5

V2 vasopressin receptor dysfunction in nephrogenic diabetes insipidus caused by different molecular mechanisms.

Schöneberg T, Schulz A, Biebermann H, Grüters A, Grimm T, Hübschmann K, Filler G, Gudermann T, Schultz G. Schöneberg T, et al. Among authors: gudermann t. Hum Mutat. 1998;12(3):196-205. doi: 10.1002/(SICI)1098-1004(1998)12:3<196::AID-HUMU7>3.0.CO;2-F. Hum Mutat. 1998. PMID: 9711877

6

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, Schultz G, Gudermann T. Biebermann H, et al. Among authors: gudermann t. FASEB J. 1998 Nov;12(14):1461-71. doi: 10.1096/fasebj.12.14.1461. FASEB J. 1998. PMID: 9806755

7

Alterations of neonatal thyroid function.

Grüters A, Krude H, Biebermann H, Liesenkötter KP, Schöneberg T, Gudermann T. Grüters A, et al. Among authors: gudermann t. Acta Paediatr Suppl. 1999 Feb;88(428):17-22. doi: 10.1111/j.1651-2227.1999.tb14346.x. Acta Paediatr Suppl. 1999. PMID: 10102047 Review.

8

Constitutively activating TSH-receptor mutations as a molecular cause of non-autoimmune hyperthyroidism in childhood.

Biebermann H, Schöneberg T, Krude H, Gudermann T, Grüters A. Biebermann H, et al. Among authors: gudermann t. Langenbecks Arch Surg. 2000 Oct;385(6):390-2. doi: 10.1007/s004230000145. Langenbecks Arch Surg. 2000. PMID: 11127522

9

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, Grüters A. Biebermann H, et al. Among authors: gudermann t. J Clin Endocrinol Metab. 2001 Sep;86(9):4429-33. doi: 10.1210/jcem.86.9.7888. J Clin Endocrinol Metab. 2001. PMID: 11549687

10

TRPM5 is a voltage-modulated and Ca(2+)-activated monovalent selective cation channel.

Hofmann T, Chubanov V, Gudermann T, Montell C. Hofmann T, et al. Among authors: gudermann t. Curr Biol. 2003 Jul 1;13(13):1153-8. doi: 10.1016/s0960-9822(03)00431-7. Curr Biol. 2003. PMID: 12842017 Free article.

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