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Nature Communications|August 3, 2021
Compounds targeting OSBPL7 increase ABCA1-dependent cholesterol efflux preserving kidney function in two models of kidney diseaseMatthew B Wright, Javier Varona Santos, Christian Kemmer, et al.
Human Molecular Genetics|January 31, 2021
APOL1 risk variants affect podocyte lipid homeostasis and energy production in focal segmental glomerulosclerosisMengyuan Ge, Judith Molina, G Michelle Ducasa, et al.
Kidney International|October 11, 2018
Hydroxypropyl-β-cyclodextrin protects from kidney disease in experimental Alport syndrome and focal segmental glomerulosclerosisAlla Mitrofanova, Judith Molina, Javier Varona Santos, et al.
Kidney International|June 1, 2025
The enzyme SMPDL3b in podocytes decouples proteinuria from chronic kidney disease progression in experimental Alport SyndromeAlla Mitrofanova, Antonio M Fontanella, Judith Molina, et al.
The Journal of Clinical Investigation|July 23, 2019
ATP-binding cassette A1 deficiency causes cardiolipin-driven mitochondrial dysfunction in podocytesG Michelle Ducasa, Alla Mitrofanova, Shamroop K Mallela, et al.
The Journal of Clinical Investigation|August 3, 2016
Local TNF causes NFATc1-dependent cholesterol-mediated podocyte injuryChristopher E Pedigo, Gloria Michelle Ducasa, Farah Leclercq, et al.
ACS Chemical Biology|November 20, 2018
DNA-Encoded Library-Derived DDR1 Inhibitor Prevents Fibrosis and Renal Function Loss in a Genetic Mouse Model of Alport SyndromeHans Richter, Alexander L Satz, Marc Bedoucha, et al.
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