메뉴 건너뛰기




Volumn 63, Issue 4, 2014, Pages 668-669

Primary aldosteronism: A channelopathy?

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE (CALCIUM); ALDOSTERONE SYNTHASE; ANGIOTENSIN II; G PROTEIN COUPLED INWARDLY RECTIFYING POTASSIUM CHANNEL; GENOMIC DNA;

EID: 84897101518     PISSN: 0194911X     EISSN: 15244563     Source Type: Journal    
DOI: 10.1161/HYPERTENSIONAHA.113.02335     Document Type: Note
Times cited : (5)

References (10)
  • 2
    • 79951506090 scopus 로고    scopus 로고
    • K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension
    • Choi M, Scholl UI, Yue P, et al. K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension. Science. 2011;331:768-772.
    • (2011) Science. , vol.331 , pp. 768-772
    • Choi, M.1    Scholl, U.I.2    Yue, P.3
  • 3
    • 84879950195 scopus 로고    scopus 로고
    • Genetics of mineralocorticoid excess: An update for clinicians
    • Zennaro MC, Rickard AJ, Boulkroun S. Genetics of mineralocorticoid excess: an update for clinicians. Eur J Endocrinol. 2013;169:R15-R25.
    • (2013) Eur J Endocrinol. , vol.169
    • Zennaro, M.C.1    Rickard, A.J.2    Boulkroun, S.3
  • 5
    • 84865427053 scopus 로고    scopus 로고
    • The potassium channel Kir3.4 participates in angiotensin II-stimulated aldosterone production by a human adrenocortical cell line
    • Oki K, Plonczynski MW, Lam ML, Gomez-Sanchez EP, Gomez-Sanchez CE. The potassium channel, Kir3.4 participates in angiotensin II-stimulated aldosterone production by a human adrenocortical cell line. Endocrinology. 2012;153:4328-4335.
    • (2012) Endocrinology. , vol.153 , pp. 4328-4335
    • Oki, K.1    Plonczynski, M.W.2    Lam, M.L.3    Gomez-Sanchez, E.P.4    Gomez-Sanchez, C.E.5
  • 7
    • 84897054016 scopus 로고    scopus 로고
    • Role for germline mutations and a rare coding single nucleotide polymorphism within the KCNJ5 potassium channel in a large cohort of sporadic cases of primary aldosteronism
    • Murthy M, Xu S, Massimo G, Wolley M, Gordon RD, Stowasser M, O'Shaughnessy K M. Role for germline mutations and a rare coding single nucleotide polymorphism within the KCNJ5 potassium channel in a large cohort of sporadic cases of primary aldosteronism. Hypertension. 2014;63:783-789.
    • (2014) Hypertension. , vol.63 , pp. 783-789
    • Murthy, M.1    Xu, S.2    Massimo, G.3    Wolley, M.4    Gordon, R.D.5    Stowasser, M.6    O'Shaughnessy, K.M.7
  • 9
    • 84858705991 scopus 로고    scopus 로고
    • Visinin-like 1 is upregulated in aldosterone-producing adenomas with KCNJ5 mutations and protects from calcium-induced apoptosis
    • Williams TA, Monticone S, Crudo V, Warth R, Veglio F, Mulatero P. Visinin-like 1 is upregulated in aldosterone-producing adenomas with KCNJ5 mutations and protects from calcium-induced apoptosis. Hypertension. 2012;59:833-839.
    • (2012) Hypertension. , vol.59 , pp. 833-839
    • Williams, T.A.1    Monticone, S.2    Crudo, V.3    Warth, R.4    Veglio, F.5    Mulatero, P.6
  • 10
    • 84883452469 scopus 로고    scopus 로고
    • Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension
    • Azizan EA, Poulsen H, Tuluc P, et al. Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension. Nat Genet. 2013;45:1055-1060.
    • (2013) Nat Genet. , vol.45 , pp. 1055-1060
    • Azizan, E.A.1    Poulsen, H.2    Tuluc, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.