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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Autors principals: Simons, Matias, Schwarz, Karin, Kriz, Wilhelm, Miettinen, Aaro, Reiser, Jochen, Mundel, Peter, Holthöfer, Harry
Format: Artigo
Idioma:Inglês
Publicat: American Society for Investigative Pathology 2001
Matèries:
Regular Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1850447/
https://ncbi.nlm.nih.gov/pubmed/11549599
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