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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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Bibliografske podrobnosti
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
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2013
Teme:
Online dostop: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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