An inducible mouse model of podocin-mutation-related nephrotic syndrome

Mutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early disease onset and rapid progression to end-stage renal disease. Knock-in mice carrying a R140Q mutation, the mouse analogue of human R138Q, show devel...

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Detaylı Bibliyografya
Yayımlandı:PLoS One
Asıl Yazarlar: Tabatabaeifar, Mansoureh, Wlodkowski, Tanja, Simic, Ivana, Denc, Helga, Mollet, Geraldine, Weber, Stefanie, Moyers, John Julius, Brühl, Barbara, Randles, Michael Joseph, Lennon, Rachel, Antignac, Corinne, Schaefer, Franz
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2017
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5648285/
https://ncbi.nlm.nih.gov/pubmed/29049388
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0186574
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