Characterization of a short isoform of the kidney protein podocin in human kidney

BACKGROUND: Steroid resistant nephrotic syndrome is a severe hereditary disease often caused by mutations in the NPHS2 gene. This gene encodes the lipid binding protein podocin which localizes to the slit diaphragm of podocytes and is essential for the maintenance of an intact glomerular filtration...

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Detalles Bibliográficos
Autores principales: Völker, Linus A, Schurek, Eva-Maria, Rinschen, Markus M, Tax, Judit, Schutte, Barbara A, Lamkemeyer, Tobias, Ungrue, Denise, Schermer, Bernhard, Benzing, Thomas, Höhne, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658879/
https://www.ncbi.nlm.nih.gov/pubmed/23648087
http://dx.doi.org/10.1186/1471-2369-14-102

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658879/
https://www.ncbi.nlm.nih.gov/pubmed/23648087
http://dx.doi.org/10.1186/1471-2369-14-102

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