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NR3C2 gene

Known as: NUCLEAR RECEPTOR SUBFAMILY 3, GROUP C, MEMBER 2, MR, MLR 
This gene is involved in transcriptional regulation and signal transduction.
National Institutes of Health

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Related topics

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Aldosterone ReceptorsBiologic DevelopmentCell Differentiation processCell Proliferation

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NR3C2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Interstitial 4q Deletion Syndrome Including NR3C2 Causing Pseudohypoaldosteronism
Interstitial and terminal deletions of chromosome 4q have been described for many years and have variable phenotypes depending on… 
2019
2019
Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation
TATSUHIKO TANAKA, EISHIN OKI, TAKAYASU MORI, KAZUSHI TSURUGA, EISEI SOHARA, SHINICHI UCHIDA and HIROSHI TANAKA, Department of… 
2017
2017
Clinical Manifestation and Molecular Analysis of Three Korean Patients with the Renal Form of Pseudohypoaldosteronism Type 1.
Pseudohypoaldosteronism (PHA) type 1 is a rare, heterogeneous disease characterized by hyponatremia and hyperkalemia due to… 
2015
2015
Compound identification in GC / MS – based metabolomics by blind source separation
Metabolomics GC–MS samples involve high complexity data that must be effectively resolved to produce chemically meaningful… 
2014
2014
Reactions of 5-methylcytosine cation radicals in DNA and model systems: Thermal deprotonation from the 5-methyl group vs. excited state deprotonation from sugar
Abstract Purpose: To study the formation and subsequent reactions of the 5-methyl-2′-deoxycytidine cation radical (5-Me-2′-dC… 
Review
2012
Review
2012
Syndromes of impaired ion handling in the distal nephron: pseudohypoaldosteronism and familial hyperkalemic hypertension
The distal nephron, which is the site of the micro-regulation of water absorption and ion handling in the kidneys, is under the… 
2011
2011
A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene
Pseudohypoaldosteronism type 1 (PHA1) is a rare form of mineralocorticoid resistance characterized in newborns by salt wasting… 
2011
2011
Relationship of aldosterone synthase gene (C-344T) and mineralocorticoid receptor (S810L) polymorphisms with gestational hypertension
The extent of genetic influence in the aetiology of gestational hypertension has not been completely determined. The aim of this… 
1985
1985
Allorestricted cytotoxic T cells. Large numbers of allo-H-2Kb- restricted antihapten and antiviral cytotoxic T cell populations clonally develop in vitro from murine splenic precursor T cells
Cytotoxic T lymphocyte (CTL) responses of splenic T cells from C57BL/6 B6) mice and mutant H-2Kbm1 (bm1) mice to haptenic… 
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