Showing results (11-20 of 48) with videos related to
Sort By:
Pageof 5
Journal of Clinical Lipidology|September 12, 2018
Paradoxical fall in proteinuria during pregnancy in an LCAT-deficient patient-A case reportElinor V Hanna, Sara Simonelli, Sarah Chamney, et al.Journal of Proteomics|December 12, 2018
A proteomic approach to identify novel disease biomarkers in LCAT deficiencySara Simonelli, Alice Ossoli, Cristina Banfi, et al.Antioxidants (Basel, Switzerland)|October 27, 2022
Body Mass Index Modulates the Impact of Short-Term Exposure to Air Particulate Matter on High-Density Lipoprotein FunctionAlice Ossoli, Chiara Favero, Luisella Vigna, et al.European Heart Journal|September 16, 2021
Matrix metalloproteinase-2 on activated platelets triggers endothelial PAR-1 initiating atherosclerosisStefania Momi, Emanuela Falcinelli, Eleonora Petito, et al.Annals of Medicine|April 28, 2025
PPAR-mediated reduction of lipid accumulation in hepatocytes involves the autophagy-lysosome-mitochondrion axisFederica Cetti, Alice Ossoli, Carola Garavaglia, et al.Journal of Lipid Research|May 22, 2022
Plasma FA composition in familial LCAT deficiency indicates SOAT2-derived cholesteryl ester formation in humansChiara Pavanello, Alice Ossoli, Arianna Strazzella, et al.Biofactors (Oxford, England)|May 17, 2022
HDL-mediated reduction of cholesterol content inhibits the proliferation of prostate cancer cells induced by LDL: Role of ABCA1 and proteasome inhibitionAlice Ossoli, Eleonora Giorgio, Federica Cetti, et al.Journal of Clinical Lipidology|August 24, 2022
Plasma HDL pattern, cholesterol efflux and cholesterol loading capacity of serum in carriers of a novel missense variant (Gly176Trp) of endothelial lipaseLivia Pisciotta, Alice Ossoli, Annalisa Ronca, et al.Antioxidants (Basel, Switzerland)|August 26, 2023
Abnormal Lipoproteins Trigger Oxidative Stress-Mediated Apoptosis of Renal Cells in LCAT DeficiencyMonica Gomaraschi, Marta Turri, Arianna Strazzella, et al.Atherosclerosis Plus|July 24, 2025
Lipidome of high-density lipoprotein is strongly perturbed in hyperalphalipoproteinemia resulting from a rare mutation in endothelial lipaseLivia Pisciotta, Marie Lhomme, Chiara Pavanello, et al.Pageof 5