Last Updated: 09/26/2026
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Found 131 publications
New ideas about mechanism in APOL1 kidney disease.
Journal: Kidney international
Published: May 16, 2026
Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective Variant.
Journal: JAMA network open
Published: March 11, 2026
Tension at the Barrier: Intraglomerular Pressure and the Podocyte Response.
Journal: Seminars in nephrology
Published: February 22, 2026
Purine Metabolism Regulates the Severity of APOL1 Nephropathy.
Journal: Journal of the American Society of Nephrology : JASN
Published: November 25, 2025
Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis.
Journal: Kidney international
Published: July 09, 2025
Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis.
Journal: Kidney international
Published: July 09, 2025
Testican-2 Interaction with the Extracellular Matrix and Podocyte Protection.
Journal: Journal of the American Society of Nephrology : JASN
Published: April 05, 2025
APOL1-associated kidney disease: modulators of the genotype-phenotype relationship.
Journal: Current opinion in nephrology and hypertension
Published: March 06, 2025
INF2 mutations cause kidney disease through a gain-of-function mechanism.
Journal: Science advances
Published: November 13, 2024
APOL1 Bi- and Monoallelic Variants and Chronic Kidney Disease in West Africans.
Journal: The New England journal of medicine
Published: October 28, 2024
The APOL1 p.N264K variant is co-inherited with the G2 kidney disease risk variant through a proximity recombination event.
Journal: G3 (Bethesda, Md.)
Published: September 25, 2024
In Search of the Mechanism of APOL1 Kidney Disease.
Journal: Journal of the American Society of Nephrology : JASN
Published: September 09, 2024
Last Updated: 09/26/2026