Apolipoprotein L1 (APOL1) risk variant toxicity depends on the haplotype background
Author:
Funder
U.S. Department of Defense
Doris Duke Charitable Foundation
National Institutes of Health
Nephcure Foundation
Publisher
Elsevier BV
Subject
Nephrology
Reference18 articles.
1. Association of trypanolytic ApoL1 variants with kidney disease in African Americans;Genovese;Science,2010
2. Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene;Tzur;Hum Genet,2010
3. Apolipoprotein L1 and kidney disease in African Americans;Friedman;Trends Endocrinol Metab,2016
4. APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy;Kopp;J Am Soc Nephrol,2011
5. ApoL1 overexpression drives variant-independent cytotoxicity;O’Toole;J Am Soc Nephrol,2018
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1. Defining Risk in APOL1-Associated Kidney Disease: The Story is Evolving!;American Journal of Kidney Diseases;2024-09
2. Variant upon variant: kidney-disease risk associated with APOL1 G2 genetic variants is abrogated by the APOL1 p.N264K variant;Kidney International;2024-09
3. APOL1 High-Risk Genotype is Not Associated With New or Worsening of Proteinuria or Kidney Function Decline Following COVID-19 Vaccination;Kidney International Reports;2024-09
4. Diagnostic Yield of APOL1 p.N264K Variant Screening in Daily Practice;Kidney International Reports;2024-06
5. Single-Cell Transcriptional Signatures of Glomerular Disease in Transgenic Mice with APOL1 Variants;Journal of the American Society of Nephrology;2024-05-06
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