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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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Detalhes bibliográficos
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3658879/
https://ncbi.nlm.nih.gov/pubmed/23648087
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2369-14-102
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