Cargando…
Endoplasmic reticulum-translocation is essential for APOL1 cellular toxicity
Two variants at the APOL1 gene, encoding apolipoprotein L1, account for more than 70% of the increased risk for chronic kidney disease in individuals of African ancestry. While the initiating event for APOL1 risk variant cell injury remains to be clarified, we explored the possibility of blocking AP...
Autores principales: | Kruzel-Davila, Etty, Bavli-Kertselli, Ira, Ofir, Ayala, Cheatham, Amber M., Shemer, Revital, Zaknoun, Eid, Chornyy, Sergiy, Tabachnikov, Orly, Davis, Shamara E., Khatua, Atanu K., Skorecki, Karl, Popik, Waldemar |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762391/ https://www.ncbi.nlm.nih.gov/pubmed/35072009 http://dx.doi.org/10.1016/j.isci.2021.103717 |
Ejemplares similares
-
Blocking the 5′ splice site of exon 4 by a morpholino oligomer triggers APOL1 protein isoform switch
por: Cheatham, Amber M., et al.
Publicado: (2018) -
Nucleosomal dsDNA Stimulates APOL1 Expression in Human Cultured Podocytes by Activating the cGAS/IFI16-STING Signaling Pathway
por: Davis, Shamara E., et al.
Publicado: (2019) -
Effect of APOL1 disease risk variants on APOL1 gene product
por: Haque, Shabirul, et al.
Publicado: (2017) -
APOL1, Sickle Cell Trait, and Glutathione S-Transferase 1—More Complicated Than It Seems
por: Kruzel-Davila, Etty, et al.
Publicado: (2022) -
The double-edged sword of evolution
por: Kruzel-Davila, Etty, et al.
Publicado: (2017)