APOL1: The Balance Imposed by Infection, Selection, and Kidney Disease
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference103 articles.
1. Racial differences in the progression from chronic renal insufficiency to end-stage renal disease in the United States;Hsu;J. Am. Soc. Nephrol.,2003
2. Sequencing rare and common APOL1 coding variants to determine kidney disease risk;Limou;Kidney Int.,2015
3. Differential effects of MYH9 and APOL1 risk variants on FRMD3 association with diabetic ESRD in African Americans;Freedman;PLoS Genet.,2011
4. APOL1 nephropathy: a population genetics and evolutionary medicine detective story;Kruzel-Davila;Semin. Nephrol.,2017
5. Patterns of kidney function decline associated with APOL1 genotypes: results from AASK;Tin;Clin. J. Am. Soc. Nephrol.,2016
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1. Interferon-γ induces combined pyroptotic angiopathy and APOL1 expression in human kidney disease;Cell Reports;2024-06
2. IFI16 Is Indispensable for Promoting HIF-1α-Mediated APOL1 Expression in Human Podocytes under Hypoxic Conditions;International Journal of Molecular Sciences;2024-03-15
3. Phenome-wide analysis reveals epistatic associations between APOL1 variants and chronic kidney disease and multiple other disorders;eBioMedicine;2024-03
4. APOL1 variants G1, G2 and N264K affect APOL1 plasma protein concentration: a UK Biobank study;2024-02-29
5. A human-specific insertion promotes cell proliferation and migration by enhancing TBC1D8B expression;Science China Life Sciences;2023-12-15
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