Inactivating mutations of the mineralocorticoid receptor in Type I pseudohypoaldosteronism-Reference-Cited by-同舟云学术

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Inactivating mutations of the mineralocorticoid receptor in Type I pseudohypoaldosteronism

Published:2004-03 Issue:1-2 Volume:217 Page:119-125
ISSN:0303-7207
Container-title:Molecular and Cellular Endocrinology
language:en
Short-container-title:Molecular and Cellular Endocrinology

Author:

Sartorato P,Khaldi Y,Lapeyraque A.-L,Armanini D,Kuhnle U,Salomon R,Caprio M,Viengchareun S,Lombès M,Zennaro M.-C

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

Reference29 articles.

1. No apparent mineralocorticoid receptor defect in a series of sporadic cases of pseudohypoaldosteronism;Arai;J. Clin. Endocrinol. Metab.,1995

2. Functional polymorphisms in the mineralocorticoid receptor and amirolide-sensitive sodium channel genes in a patient with sporadic pseudohypoaldosteronism;Arai;Hum. Genet.,2003

3. Nuclear hormone receptors and gene expression;Aranda;Physiol. Rev.,2001

4. Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor;Arriza;Science,1987

5. A corticosteroid-induced gene expressing an “IsK-like” k+ channel activity in xenopus oocytes;Attali;Proc. Natl. Acad. Sci. U.S.A.,1995

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