PubMed (OMIM) for id: 4306

Year	Number of Results
1958	1
1959	1
1962	1
1978	1
1985	1
1987	1
1989	1
1990	1
1991	2
1995	3
1997	1
1998	3
2000	3
2001	3
2002	1
2003	4
2004	2
2005	1
2006	4
2007	1
2008	1
2009	1
2024	0

1

Aldosterone activates endothelial exocytosis.

Jeong Y, Chaupin DF, Matsushita K, Yamakuchi M, Cameron SJ, Morrell CN, Lowenstein CJ. Jeong Y, et al. Proc Natl Acad Sci U S A. 2009 Mar 10;106(10):3782-7. doi: 10.1073/pnas.0804037106. Epub 2009 Feb 17. Proc Natl Acad Sci U S A. 2009. PMID: 19223584 Free PMC article.

2

Modification of mineralocorticoid receptor function by Rac1 GTPase: implication in proteinuric kidney disease.

Shibata S, Nagase M, Yoshida S, Kawarazaki W, Kurihara H, Tanaka H, Miyoshi J, Takai Y, Fujita T. Shibata S, et al. Nat Med. 2008 Dec;14(12):1370-6. doi: 10.1038/nm.1879. Epub 2008 Nov 23. Nat Med. 2008. PMID: 19029984

3

Mineralocorticoid receptor mutations are the principal cause of renal type 1 pseudohypoaldosteronism.

Pujo L, Fagart J, Gary F, Papadimitriou DT, Claës A, Jeunemaître X, Zennaro MC. Pujo L, et al. Hum Mutat. 2007 Jan;28(1):33-40. doi: 10.1002/humu.20371. Hum Mutat. 2007. PMID: 16972228

4

Elucidating the underlying molecular pathogenesis of NR3C2 mutants causing autosomal dominant pseudohypoaldosteronism type 1.

Riepe FG, Finkeldei J, de Sanctis L, Einaudi S, Testa A, Karges B, Peter M, Viemann M, Grötzinger J, Sippell WG, Fejes-Toth G, Krone N. Riepe FG, et al. J Clin Endocrinol Metab. 2006 Nov;91(11):4552-61. doi: 10.1210/jc.2006-1161. Epub 2006 Sep 5. J Clin Endocrinol Metab. 2006. PMID: 16954160

5

Recurrence of the R947X mutation in unrelated families with autosomal dominant pseudohypoaldosteronism type 1: evidence for a mutational hot spot in the mineralocorticoid receptor gene.

Fernandes-Rosa FL, de Castro M, Latronico AC, Sippell WG, Riepe FG, Antonini SR. Fernandes-Rosa FL, et al. J Clin Endocrinol Metab. 2006 Sep;91(9):3671-5. doi: 10.1210/jc.2006-0605. Epub 2006 Jun 6. J Clin Endocrinol Metab. 2006. PMID: 16757525

6

Autosomal dominant pseudohypoaldosteronism type 1: mechanisms, evidence for neonatal lethality, and phenotypic expression in adults.

Geller DS, Zhang J, Zennaro MC, Vallo-Boado A, Rodriguez-Soriano J, Furu L, Haws R, Metzger D, Botelho B, Karaviti L, Haqq AM, Corey H, Janssens S, Corvol P, Lifton RP. Geller DS, et al. J Am Soc Nephrol. 2006 May;17(5):1429-36. doi: 10.1681/ASN.2005111188. Epub 2006 Apr 12. J Am Soc Nephrol. 2006. PMID: 16611713

7

Loss of the limbic mineralocorticoid receptor impairs behavioral plasticity.

Berger S, Wolfer DP, Selbach O, Alter H, Erdmann G, Reichardt HM, Chepkova AN, Welzl H, Haas HL, Lipp HP, Schütz G. Berger S, et al. Proc Natl Acad Sci U S A. 2006 Jan 3;103(1):195-200. doi: 10.1073/pnas.0503878102. Epub 2005 Dec 20. Proc Natl Acad Sci U S A. 2006. PMID: 16368758 Free PMC article.

8

Autosomal-dominant pseudohypoaldosteronism type 1 in a Turkish family is associated with a novel nonsense mutation in the human mineralocorticoid receptor gene.

Riepe FG, Krone N, Morlot M, Peter M, Sippell WG, Partsch CJ. Riepe FG, et al. J Clin Endocrinol Metab. 2004 May;89(5):2150-2. doi: 10.1210/jc.2003-031555. J Clin Endocrinol Metab. 2004. PMID: 15126534

9

A novel nonsense mutation of the mineralocorticoid receptor gene in a Swedish family with pseudohypoaldosteronism type I (PHA1).

Nyström AM, Bondeson ML, Skanke N, Mårtensson J, Strömberg B, Gustafsson J, Annerén G. Nyström AM, et al. J Clin Endocrinol Metab. 2004 Jan;89(1):227-31. doi: 10.1210/jc.2003-030762. J Clin Endocrinol Metab. 2004. PMID: 14715854

10

A salt-losing syndrome in infancy. Pseudo-hypoadrenocorticalism.

RAINE DN, ROY J. RAINE DN, et al. Arch Dis Child. 1962 Oct;37(195):548-56. doi: 10.1136/adc.37.195.548. Arch Dis Child. 1962. PMID: 13990509 Free PMC article. No abstract available.

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