z-logo
open-access-imgOpen Access
Expression of nephrin in acquired human glomerular disease
Author(s) -
Wooseong Huh,
Dae Joong Kim,
MiKyung Kim,
Yoon Goo Kim,
Hayoung Oh,
Vesa Ruotsalainen,
Karl Tryggvason
Publication year - 2002
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/17.3.478
Subject(s) - nephrin , immunoelectron microscopy , glomerular basement membrane , membranoproliferative glomerulonephritis , congenital nephrotic syndrome , podocyte , medicine , slit diaphragm , pathology , glomerulonephritis , nephrotic syndrome , renal biopsy , membranous nephropathy , minimal change disease , proteinuria , kidney , biopsy , focal segmental glomerulosclerosis , immunohistochemistry
Nephrin is a recently identified protein, which is synthesized in the podocytes and localized in the slit diaphragm area. Nephrin is a cell adhesion molecule of the immunoglobulin superfamily, and presumably is a part of the zipper-like structure of the slit membrane. As the mutation of the gene coding nephrin induces congenital nephrotic syndrome of Finnish type, which is a prototype of nephrotic syndrome, it has been suggested that nephrin also plays a role in acquired proteinuric kidney disease.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom