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.
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