KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome.

KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome.

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http://www.wikidata.org/entity/Q33698924
Intracellular Molecular Differences in Aldosterone- Compared to Cortisol-Secreting Adrenal Cortical AdenomasOverview of the genetic determinants of primary aldosteronism.Comprehensive re-sequencing of adrenal aldosterone producing lesions reveal three somatic mutations near the KCNJ5 potassium channel selectivity filter.Primary Aldosteronism and ARMC5 Variants.A novel point mutation in the KCNJ5 gene causing primary hyperaldosteronism and early-onset autosomal dominant hypertension.cAMP/PKA signaling defects in tumors: genetics and tissue-specific pluripotential cell-derived lesions in human and mouse.Integrated analysis of genome-wide methylation and gene expression shows epigenetic regulation of CYP11B2 in aldosteronomas.Recent genetic discoveries implicating ion channels in human cardiovascular diseasesRole of KCNJ5 in familial and sporadic primary aldosteronism.5th International ACC Symposium: The New Genetics of Benign Adrenocortical Neoplasia: Hyperplasias, Adenomas, and Their Implications for Progression into Cancer.Of channels and pumps: different ways to boost the aldosterone?CTNNB1 Mutation in Aldosterone Producing Adenoma.Genistein induces oestrogen receptor-α gene expression in osteoblasts through the activation of mitogen-activated protein kinases/NF-κB/activator protein-1 and promotes cell mineralisation.Functional characterization of two novel germline mutations of the KCNJ5 gene in hypertensive patients without primary aldosteronism but with ACTH-dependent aldosterone hypersecretion.Prevalence of Somatic Mutations in Thai Patients With Aldosterone-Producing Adrenal Adenomas
P2860

KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome.

Item
http://www.wikidata.org/entity/Q33698924
description
2012 nî lūn-bûn
@nan
2012 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
KCNJ5 mutations in the Nationa ...... etic cause of Conn's syndrome.
@ast
KCNJ5 mutations in the Nationa ...... etic cause of Conn's syndrome.
@en
type
label
KCNJ5 mutations in the Nationa ...... etic cause of Conn's syndrome.
@ast
KCNJ5 mutations in the Nationa ...... etic cause of Conn's syndrome.
@en
prefLabel
KCNJ5 mutations in the Nationa ...... etic cause of Conn's syndrome.
@ast
KCNJ5 mutations in the Nationa ...... etic cause of Conn's syndrome.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921
P932
P356
P1433
P1476
KCNJ5 mutations in the Nationa ...... etic cause of Conn's syndrome.
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921
P932