Patologías del receptor V2 de la vasopresina: diabetes insípida nefrógena congénita y síndrome de antidiuresis inapropiada nefrógena-Reference-Cited by-同舟云学术

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Patologías del receptor V2 de la vasopresina: diabetes insípida nefrógena congénita y síndrome de antidiuresis inapropiada nefrógena

Published:2024-09 Issue:3 Volume:59 Page:1-9
ISSN:1245-1789
Container-title:EMC - Pediatría
language:es
Short-container-title:EMC - Pediatría

Author:

Morin D.

Publisher

Elsevier BV

Reference58 articles.

1. Structural bases of vasopressin/oxytocin receptor function;Barberis;J Neuroendocrinol,1998

2. Hemodynamic and coagulation responses to 1-desamino[8-D-arginine] vasopressin in patients with congenital nephrogenic diabetes insipidus;Bichet;N Engl J Med,1988

3. Generation and phenotype of mice harboring a nonsense mutation in the V2 vasopressin receptor gene;Yun;J Clin Invest,2000

4. Vasopressin increases water permeability of kidney collecting duct by inducing translocation of aquaporin water channels to plasma membrane;Nielsen;Proc Natl Acad Sci USA,1995

5. Defective store-operated calcium entry causes partiel nephrogenic diabtetes insipidus;Mamenko;J Am Soc Nephrol,2015

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