A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)
about
Genetic alterations in primary aldosteronismThe G-protein-coupled estrogen receptor GPER in health and diseaseEstrogen biology: new insights into GPER function and clinical opportunitiesDetecting multiple variants associated with disease based on sequencing data of case-parent trios.Identification and characterization of human archaemetzincin-1 and -2, two novel members of a family of metalloproteases widely distributed in Archaea.Minireview: G protein-coupled estrogen receptor-1, GPER-1: its mechanism of action and role in female reproductive cancer, renal and vascular physiologyDiagnosis and management of primary aldosteronism.Adrenocortical causes of hypertensionRecurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism.Primary Aldosteronism and ARMC5 Variants.cAMP/PKA signaling defects in tumors: genetics and tissue-specific pluripotential cell-derived lesions in human and mouse.Heritable forms of hypertension.Signaling, physiological functions and clinical relevance of the G protein-coupled estrogen receptor GPER.Non-genomic regulation of vascular cell function and growth by estrogen.Regulatory role of G protein-coupled estrogen receptor for vascular function and obesityCACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism.Role of KCNJ5 in familial and sporadic primary aldosteronism.Genetics of adrenocortical tumours.Rare diseases in clinical endocrinology: a taxonomic classification system.The protective role of G protein-coupled estrogen receptor 1 (GPER-1) on methotrexate-induced nephrotoxicity in human renal epithelium cells.High Frequency of Variants of Candidate Genes in Black Africans with Low Renin-Resistant Hypertension.[The role of aldosterone in hypertension].The syndromes of low-renin hypertension: "separating the wheat from the chaff".Examination of chromosome 7p22 candidate genes RBaK, PMS2 and GNA12 in familial hyperaldosteronism type II.CLCN2 chloride channel mutations in familial hyperaldosteronism type II.GPCRS IN CONTEXT: SEXUAL DIMORPHISM IN THE CARDIOVASCULAR SYSTEM.ARMC5 is not implicated in familial hyperaldosteronism type II (FH-II).Disordered zonal and cellular CYP11B2 enzyme expression in familial hyperaldosteronism type 3.Further study of chromosome 7p22 to identify the molecular basis of familial hyperaldosteronism type II.Retention of heterozygosity at chromosome 7p22 and 11q13 in aldosterone-producing tumours of patients with familial hyperaldosteronism not remediable by glucocorticoids.
P2860
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P2860
A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)
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2000 nî lūn-bûn
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2000 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
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2000 թվականի նոյեմբերին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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name
A novel genetic locus for low ...... II maps to chromosome 7 (7p22)
@ast
A novel genetic locus for low ...... II maps to chromosome 7 (7p22)
@en
A novel genetic locus for low ...... II maps to chromosome 7 (7p22)
@nl
type
label
A novel genetic locus for low ...... II maps to chromosome 7 (7p22)
@ast
A novel genetic locus for low ...... II maps to chromosome 7 (7p22)
@en
A novel genetic locus for low ...... II maps to chromosome 7 (7p22)
@nl
prefLabel
A novel genetic locus for low ...... II maps to chromosome 7 (7p22)
@ast
A novel genetic locus for low ...... II maps to chromosome 7 (7p22)
@en
A novel genetic locus for low ...... II maps to chromosome 7 (7p22)
@nl
P2093
P2860
P356
P1476
A novel genetic locus for low ...... II maps to chromosome 7 (7p22)
@en
P2093
A R Lafferty
C A Stratakis
M Stowasser
R D Gordon
S E Taymans
P2860
P356
10.1136/JMG.37.11.831
P407
P577
2000-11-01T00:00:00Z