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Volumn 15, Issue 7, 2001, Pages 471-474

Systematic screening of type B human natriuretic peptide receptor gene polymorphisms and association with essential hypertension

Author keywords

Essential hypertension; Gene; NPRB; Polymorphism; SSCP

Indexed keywords

BRAIN NATRIURETIC PEPTIDE; BRAIN NATRIURETIC PEPTIDE RECEPTOR; DNA FRAGMENT; MARKER; NUCLEOTIDE; RECEPTOR; UNCLASSIFIED DRUG;

EID: 0034939708     PISSN: 09509240     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.jhh.1001199     Document Type: Article
Times cited : (11)

References (14)
  • 1
    • 0025860062 scopus 로고
    • Selective activation of the B natriuretic peptide receptor by C-type natriuretic peptide (CNP)
    • (1991) Science , vol.252 , pp. 120-123
    • Koller, K.J.1
  • 4
    • 0025123680 scopus 로고
    • Chromosomal distribution of three members of the human natriuretic peptide receptor/guanylyl cyclase gene family
    • (1990) Genomics , vol.8 , pp. 304-312
    • Lowe, D.G.1
  • 5
    • 0024432129 scopus 로고
    • Differential activation by atrial and brain natriuretic peptides of two different receptor guanylate cyclases
    • (1989) Nature , vol.341 , pp. 68-72
    • Chang, M.1
  • 9
    • 0033582961 scopus 로고    scopus 로고
    • Structure of the type B human natriuretic peptide receptor gene and association of a novel microsatellite polymorphism with essential hypertension
    • (1999) Cir Res , vol.84 , pp. 605-610
    • Rehemdula, D.1
  • 10
    • 0022273874 scopus 로고
    • Atrial natriuretic factor: Structure and functional properties
    • (1985) Kidney Int , vol.27 , pp. 607-615
    • Maack, T.1
  • 12
    • 0028301971 scopus 로고
    • Atrial natriuretic peptide and C-type natriuretic peptide in spontaneously hypertensive rats and their vasorelaxing action in vitro
    • (1994) Hypertension , vol.23 , pp. 903-907
    • Wei, C.-M.1
  • 13
    • 0030604558 scopus 로고    scopus 로고
    • Nonsense mutation of prostacyclin synthase gene in a family
    • (1997) Lancet , vol.349 , pp. 1887-1888
    • Nakayama, T.1
  • 14
    • 0032971571 scopus 로고    scopus 로고
    • Genomic organization of KCNQ1 K+ channel gene and identification of C-terminal mutation in the long-QT syndrome
    • (1999) Cir Res , vol.19 , pp. 290-297
    • Neyroud, N.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.