Rosenthal W - Search Results

1

Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus.

Rosenthal W, Seibold A, Antaramian A, Lonergan M, Arthus MF, Hendy GN, Birnbaumer M, Bichet DG. Rosenthal W, et al. Nature. 1992 Sep 17;359(6392):233-5. doi: 10.1038/359233a0. Nature. 1992. PMID: 1356229

2

Structure and chromosomal localization of the human antidiuretic hormone receptor gene.

Seibold A, Brabet P, Rosenthal W, Birnbaumer M. Seibold A, et al. Among authors: rosenthal w. Am J Hum Genet. 1992 Nov;51(5):1078-83. Am J Hum Genet. 1992. PMID: 1415251 Free PMC article.

3

Molecular cloning of the receptor for human antidiuretic hormone.

Birnbaumer M, Seibold A, Gilbert S, Ishido M, Barberis C, Antaramian A, Brabet P, Rosenthal W. Birnbaumer M, et al. Among authors: rosenthal w. Nature. 1992 May 28;357(6376):333-5. doi: 10.1038/357333a0. Nature. 1992. PMID: 1534149

4

Mutations in the vasopressin V2 receptor gene in families with nephrogenic diabetes insipidus and functional expression of the Q-2 mutant.

Rosenthal W, Seibold A, Antaramian A, Gilbert S, Birnbaumer M, Bichet DG, Arthus MF, Lonergan M. Rosenthal W, et al. Cell Mol Biol (Noisy-le-grand). 1994 May;40(3):429-36. Cell Mol Biol (Noisy-le-grand). 1994. PMID: 7920187

5

An extracellular congenital nephrogenic diabetes insipidus mutation of the vasopressin receptor reduces cell surface expression, affinity for ligand, and coupling to the Gs/adenylyl cyclase system.

Birnbaumer M, Gilbert S, Rosenthal W. Birnbaumer M, et al. Among authors: rosenthal w. Mol Endocrinol. 1994 Jul;8(7):886-94. doi: 10.1210/mend.8.7.7984150. Mol Endocrinol. 1994. PMID: 7984150

6

The vasopressin type 2 receptor gene. Chromosomal localization and its role in nephrogenic diabetes insipidus.

Seibold A, Rosenthal W, Bichet DG, Birnbaumer M. Seibold A, et al. Among authors: rosenthal w. Regul Pept. 1993 Apr 29;45(1-2):67-71. doi: 10.1016/0167-0115(93)90184-a. Regul Pept. 1993. PMID: 8511369 Review. No abstract available.

7

Nephrogenic diabetes insipidus. A V2 vasopressin receptor unable to stimulate adenylyl cyclase.

Rosenthal W, Antaramian A, Gilbert S, Birnbaumer M. Rosenthal W, et al. J Biol Chem. 1993 Jun 25;268(18):13030-3. J Biol Chem. 1993. PMID: 8514744 Free article.

8

Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus.

Marr N, Bichet DG, Lonergan M, Arthus MF, Jeck N, Seyberth HW, Rosenthal W, van Os CH, Oksche A, Deen PM. Marr N, et al. Among authors: rosenthal w. Hum Mol Genet. 2002 Apr 1;11(7):779-89. doi: 10.1093/hmg/11.7.779. Hum Mol Genet. 2002. PMID: 11929850

9

Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidus.

Marr N, Bichet DG, Hoefs S, Savelkoul PJ, Konings IB, De Mattia F, Graat MP, Arthus MF, Lonergan M, Fujiwara TM, Knoers NV, Landau D, Balfe WJ, Oksche A, Rosenthal W, Müller D, Van Os CH, Deen PM. Marr N, et al. Among authors: rosenthal w. J Am Soc Nephrol. 2002 Sep;13(9):2267-77. doi: 10.1097/01.asn.0000027355.41663.14. J Am Soc Nephrol. 2002. PMID: 12191971

10

Two novel mutations in the aquaporin-2 and the vasopressin V2 receptor genes in patients with congenital nephrogenic diabetes insipidus.

Oksche A, Möller A, Dickson J, Rosendahl W, Rascher W, Bichet DG, Rosenthal W. Oksche A, et al. Among authors: rosenthal w. Hum Genet. 1996 Nov;98(5):587-9. doi: 10.1007/s004390050264. Hum Genet. 1996. PMID: 8882880

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