Associated Papers
Apolipoprotein L1 (APOL1): Consideration of Molecular Evolution, Interaction with APOL3, and Impact of Splice Isoforms Advances Understanding of Cellular and Molecular Mechanisms of Cell Injury.
Khalaila R et al.
Cells, 2025
Platform-dependent effects of genetic variants on plasma APOL1.
Wang QS et al.
Biorxiv : the Preprint Server for Biology, 2025
The APOL1 p.N264K variant is co-inherited with the G2 kidney disease risk variant through a proximity recombination event.
Simeone CA et al.
G3 (bethesda, Md.), 2025
Protein-truncating variant in APOL3 increases chronic kidney disease risk in epistasis with APOL1 risk alleles.
Zhang DY et al.
Jci Insight, 2024
Apolipoprotein L1 (APOL1) renal risk variant-mediated podocyte cytotoxicity depends on African haplotype and surface expression.
Gupta N et al.
Scientific Reports, 2024
Genetic Inhibition of APOL1 Pore-Forming Function Prevents APOL1-Mediated Kidney Disease.
Hung AM et al.
Journal of the American Society of Nephrology : Jasn, 2023
Inhibition of endoplasmic reticulum stress signaling rescues cytotoxicity of human apolipoprotein-L1 risk variants in Drosophila.
Gerstner L et al.
Kidney International, 2022
Recessive, gain-of-function toxicity in an APOL1 BAC transgenic mouse model mirrors human APOL1 kidney disease.
McCarthy GM et al.
Disease Models & Mechanisms, 2021
Structures of the ApoL1 and ApoL2 N-terminal domains reveal a non-classical four-helix bundle motif.
Ultsch M et al.
Communications Biology, 2021
Integrated Genomic, Functional, and Prognostic Characterization of Atypical Chronic Myeloid Leukemia.
Fontana D et al.
Hemasphere, 2020
33196013 (PubMed )
Supplement: hs9-4-e497-s008.xlsx › Sheet1
New Mutation of Coenzyme Q10 Monooxygenase 6 Causing Podocyte Injury in a Focal Segmental Glomerulosclerosis Patient.
Song CC et al.
Chinese Medical Journal, 2018
Apolipoprotein L1 Variant Associated with Increased Susceptibility to Trypanosome Infection.
Cuypers B et al.
Mbio, 2016
Sequencing rare and common APOL1 coding variants to determine kidney disease risk.
Limou S et al.
Kidney International, 2015
BH3 domain-independent apolipoprotein L1 toxicity rescued by BCL2 prosurvival proteins.
Heneghan JF et al.
American Journal of Physiology. Cell Physiology, 2015
Human apolipoprotein L1 (ApoL1) in cancer and chronic kidney disease.
Hu CA et al.
Febs Letters, 2012
Advances in our understanding of the pathogenesis of HIV-1 associated nephropathy in children.
Ray PE et al.
Future Virology, 2011
ApoL1, a BH3-only lipid-binding protein, induces autophagic cell death.
Zhaorigetu S et al.
Autophagy, 2008
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