Last Updated: 09/26/2026
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Found 16 publications
Thin Glomerular Basement Membrane Phenotypes With No Identified Pathogenic COL4A3/A4/A5 Variant.
Journal: Kidney international reports
Published: January 11, 2026
INF2 mutations cause kidney disease through a gain-of-function mechanism.
Journal: Science advances
Published: November 13, 2024
Missense Mutant Gain-of-Function Causes Inverted Formin 2 (INF2)-Related Focal Segmental Glomerulosclerosis (FSGS).
Journal: bioRxiv : the preprint server for biology
Published: June 25, 2024
CRISPR-enabled point-of-care genotyping for APOL1 genetic risk assessment.
Journal: EMBO molecular medicine
Published: February 22, 2024
A pragmatic approach to selective genetic testing in kidney transplant candidates.
Journal: Frontiers in transplantation
Published: November 21, 2023
ADAR regulates APOL1 via A-to-I RNA editing by inhibition of MDA5 activation in a paradoxical biological circuit.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: October 25, 2022
Apolipoprotein L1 (APOL1) cation current in HEK-293 cells and in human podocytes.
Journal: Pflugers Archiv : European journal of physiology
Published: August 17, 2022
DGAT2 Inhibition Potentiates Lipid Droplet Formation To Reduce Cytotoxicity in APOL1 Kidney Risk Variants.
Journal: Journal of the American Society of Nephrology : JASN
Published: May 31, 2021
Immunological Impact of a Gluten-Free Dairy-Free Diet in Children With Kidney Disease: A Feasibility Study.
Journal: Frontiers in immunology
Published: November 01, 2020
Small non-coding RNAs: from trash to treasure.
Journal: Jornal brasileiro de nefrologia
Published: April 12, 2019
APOL1-Associated Kidney Disease in Brazil.
Journal: Kidney international reports
Published: February 20, 2019
Last Updated: 09/26/2026