Towards an understanding of kidney diseases associated with WT1 mutations

Mutations in Wilms' tumor 1 (WT1) cause a wide spectrum of renal manifestations, eventually leading to end-stage kidney failure. Insufficient understanding of WT1's molecular functions in kidney development has hampered efficient therapeutic applications for WT1-associated diseases. Recent...

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Detalles Bibliográficos
Autores principales: Dong, Lihua, Pietsch, Stefan, Englert, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Mini Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687464/
https://www.ncbi.nlm.nih.gov/pubmed/26154924
http://dx.doi.org/10.1038/ki.2015.198

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687464/
https://www.ncbi.nlm.nih.gov/pubmed/26154924
http://dx.doi.org/10.1038/ki.2015.198

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