Abstract
Mutations in the NPHS1 gene cause congenital nephrotic syndrome of the Finnish type. The gene product nephrin is a structural component of the glomerular slit diaphragm formed by neighboring podocytes. Nephrin has also been suggested to be involved in signaling processes that are important for podocyte survival and differentiation. A new study by Doné et al. reports that the absence of nephrin leads to the lack of slit diaphragms but does not affect podocyte apoptosis and gene expression patterns.
Cite
CITATION STYLE
Simons, M., & Huber, T. B. (2008). It’s not all about nephrin. Kidney International. Nature Publishing Group. https://doi.org/10.1038/sj.ki.5002798
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