Bichet DG - 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. Among authors: bichet dg. Nature. 1992 Sep 17;359(6392):233-5. doi: 10.1038/359233a0. Nature. 1992. PMID: 1356229

2

Diabetes insipidus.

Hendy GN, Bichet DG. Hendy GN, et al. Among authors: bichet dg. Baillieres Clin Endocrinol Metab. 1995 Jul;9(3):509-24. doi: 10.1016/s0950-351x(95)80570-2. Baillieres Clin Endocrinol Metab. 1995. PMID: 7575330 Review.

3

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. Among authors: bichet dg. Cell Mol Biol (Noisy-le-grand). 1994 May;40(3):429-36. Cell Mol Biol (Noisy-le-grand). 1994. PMID: 7920187

4

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: bichet dg. 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.

5

Report of 33 novel AVPR2 mutations and analysis of 117 families with X-linked nephrogenic diabetes insipidus.

Arthus MF, Lonergan M, Crumley MJ, Naumova AK, Morin D, DE Marco LA, Kaplan BS, Robertson GL, Sasaki S, Morgan K, Bichet DG, Fujiwara TM. Arthus MF, et al. Among authors: bichet dg. J Am Soc Nephrol. 2000 Jun;11(6):1044-1054. doi: 10.1681/ASN.V1161044. J Am Soc Nephrol. 2000. PMID: 10820168

6

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: bichet dg. Hum Mol Genet. 2002 Apr 1;11(7):779-89. doi: 10.1093/hmg/11.7.779. Hum Mol Genet. 2002. PMID: 11929850

7

Two novel aquaporin-2 mutations responsible for congenital nephrogenic diabetes insipidus in Chinese families.

Lin SH, Bichet DG, Sasaki S, Kuwahara M, Arthus MF, Lonergan M, Lin YF. Lin SH, et al. Among authors: bichet dg. J Clin Endocrinol Metab. 2002 Jun;87(6):2694-700. doi: 10.1210/jcem.87.6.8617. J Clin Endocrinol Metab. 2002. PMID: 12050236

8

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: bichet dg. 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

9

X-linked nephrogenic diabetes insipidus: from the ship Hopewell to RFLP studies.

Bichet DG, Hendy GN, Lonergan M, Arthus MF, Ligier S, Pausova Z, Kluge R, Zingg H, Saenger P, Oppenheimer E, et al. Bichet DG, et al. Am J Hum Genet. 1992 Nov;51(5):1089-1102. Am J Hum Genet. 1992. PMID: 1357965 Free PMC article.

10

Platelet vasopressin receptors in patients with congenital nephrogenic diabetes insipidus.

Bichet DG, Arthus MF, Lonergan M. Bichet DG, et al. Kidney Int. 1991 Apr;39(4):693-9. doi: 10.1038/ki.1991.83. Kidney Int. 1991. PMID: 1828844 Free article.

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