Involvement of Lipid Rafts in Nephrin Phosphorylation and Organization of the Glomerular Slit Diaphragm

NPHS1 has recently been identified as the gene whose mutations cause congenital nephrotic syndrome of the Finnish type. The respective gene product nephrin is a transmembrane protein expressed in glomerular podocytes and primarily localized to the glomerular slit diaphragm. This interpodocyte juncti...

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Bibliografiske detaljer
Main Authors: Simons, Matias, Schwarz, Karin, Kriz, Wilhelm, Miettinen, Aaro, Reiser, Jochen, Mundel, Peter, Holthöfer, Harry
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Investigative Pathology 2001
Fag:
Regular Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1850447/
https://ncbi.nlm.nih.gov/pubmed/11549599
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