Throwing off the keratin chains: a potential therapy for hereditary podocytopathy
Author:
Funder
National Research Development and Innovation Office
Publisher
Elsevier BV
Reference9 articles.
1. A small molecule chaperone rescues keratin-8 mediated trafficking of misfolded podocin to correct genetic Nephrotic Syndrome;Kuzmuk;Kidney Int,2024
2. Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations;Roselli;Traffic,2004
3. Endoplasmic reticulum-retained podocin mutants are massively degraded by the proteasome;Serrano-Perez;J Biol Chem,2018
4. Molecular basis of the functional podocin- nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains;Huber;Hum Mol Genet,2003
5. Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome;Hinkes;J Am Soc Nephrol,2008
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