메뉴 건너뛰기




Volumn 19, Issue 2, 2008, Pages 190-191

Podocyte-specific gene mutations are coming of age

Author keywords

[No Author keywords available]

Indexed keywords

EDITORIAL; FOUNDER EFFECT; GENE; GENE MUTATION; GLOMERULUS FILTRATION; HUMAN; NEPHROTIC SYNDROME; NPHS1 GENE; NPHS2 GENE; PODOCYTE; PRIORITY JOURNAL; PROTEINURIA;

EID: 39049163567     PISSN: 10466673     EISSN: 15333450     Source Type: Journal    
DOI: 10.1681/ASN.2007121341     Document Type: Editorial
Times cited : (4)

References (7)
  • 1
    • 33645403170 scopus 로고    scopus 로고
    • Hereditary proteinuria syndromes and mechanisms of proteinuria
    • Tryggvason K, Patrakka J, Wartiovaara J: Hereditary proteinuria syndromes and mechanisms of proteinuria. N Engl J Med 354: 1387-1401, 2006
    • (2006) N Engl J Med , vol.354 , pp. 1387-1401
    • Tryggvason, K.1    Patrakka, J.2    Wartiovaara, J.3
  • 3
    • 34250339727 scopus 로고    scopus 로고
    • Contribution of the endothelium to the glomerular permselectivity barrier in health and disease
    • Ballermann BJ: Contribution of the endothelium to the glomerular permselectivity barrier in health and disease. Nephron Physiol 106: 19-25, 2007
    • (2007) Nephron Physiol , vol.106 , pp. 19-25
    • Ballermann, B.J.1
  • 6
    • 34447136072 scopus 로고    scopus 로고
    • Podocin organizes ion channel-lipid supercomplexes: Implications for mechanosensation at the slit diaphragm
    • Huber TB, Schermer B, Benzing T: Podocin organizes ion channel-lipid supercomplexes: Implications for mechanosensation at the slit diaphragm. Nephron Exp Nephrol 106: e27-e31, 2007
    • (2007) Nephron Exp Nephrol , vol.106
    • Huber, T.B.1    Schermer, B.2    Benzing, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.