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Plos One|January 12, 2016
Functions of Ceramide Synthase Paralogs YPR114w and YJR116w of Saccharomyces cerevisiaeShamroop K Mallela, Reinaldo Almeida, Christer S Ejsing, et al.
Plos Genetics|July 28, 2016
Chemogenetic E-MAP in Saccharomyces cerevisiae for Identification of Membrane Transporters Operating Lipid Flip FlopHector M Vazquez, Christine Vionnet, Carole Roubaty, et al.
Eukaryotic Cell|October 4, 2015
Saccharomyces cerevisiae Is Dependent on Vesicular Traffic between the Golgi Apparatus and the Vacuole When Inositolphosphorylceramide Synthase Aur1 Is InactivatedNatalia S Voynova, Carole Roubaty, Hector M Vazquez, et al.
FEMS Yeast Research|May 29, 2014
Characterization of yeast mutants lacking alkaline ceramidases YPC1 and YDC1Natalia S Voynova, Shamroop K Mallela, Hector M Vazquez, et al.
Elife|May 2, 2023
Empagliflozin reduces podocyte lipotoxicity in experimental Alport syndromeMengyuan Ge, Judith Molina, Jin-Ju Kim, 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.
Ebiomedicine|December 19, 2020
Discoidin domain receptor 1 activation links extracellular matrix to podocyte lipotoxicity in Alport syndromeJin-Ju Kim, Judith M David, Sydney S Wilbon, 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.
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