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Complement C3 activation in cyst fluid and urine from autosomal dominant polycystic kidney disease patients
Author(s) -
Mrug M.,
Zhou J.,
Mrug S.,
GuayWoodford L. M.,
Yoder B. K.,
Szalai A. J.
Publication year - 2014
Publication title -
journal of internal medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.625
H-Index - 160
eISSN - 1365-2796
pISSN - 0954-6820
DOI - 10.1111/joim.12307
Subject(s) - autosomal dominant polycystic kidney disease , pkd1 , polycystic kidney disease , alternative complement pathway , complement system , medicine , cyst , kidney , endocrinology , atypical hemolytic uremic syndrome , nephronophthisis , immunology , pathology , biology , gene , genetics , antibody , phenotype
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