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Oncotarget
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December 13, 2017
Inhibitors of the PI3K/mTOR pathway prevent STAT5 phosphorylation in <i>JAK2V617F</i> mutated cells through PP2A/CIP2A axis
Niccolò Bartalucci, Laura Calabresi, Manjola Balliu, et al.
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids
|
December 15, 2022
Genetically determined deficiency of ANGPTL3 does not alter HDL ability to preserve endothelial homeostasis
Alice Ossoli, Ilenia Minicocci, Marta Turri, et al.
Atherosclerosis
|
August 21, 2015
Cholesterol trafficking-related serum lipoprotein functions in children with cholesteryl ester storage disease
Francesca Zimetti, Elda Favari, Paola Cagliero, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
September 27, 2020
Activation of Naturally Occurring Lecithin:Cholesterol Acyltransferase Mutants by a Novel Activator Compound
Chiara Pavanello, Alice Ossoli, Marta Turri, et al.
Journal of Clinical Lipidology
|
June 5, 2012
Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia
Paola Conca, Silvana Pileggi, Sara Simonelli, et al.
Cell Metabolism
|
August 3, 2010
Intestinal specific LXR activation stimulates reverse cholesterol transport and protects from atherosclerosis
Giuseppe Lo Sasso, Stefania Murzilli, Lorena Salvatore, et al.
Journal of Clinical Medicine
|
July 26, 2020
Low Plasma Lecithin: Cholesterol Acyltransferase (LCAT) Concentration Predicts Chronic Kidney Disease
Andrea Baragetti, Alice Ossoli, Arianna Strazzella, et al.
Atherosclerosis Plus
|
January 16, 2023
Two novel variants in the lecithin:cholesterol acyltransferase gene resulted in classic LCAT deficiency
Margareta Fistrek Prlic, Marijana Coric, Laura Calabresi, et al.
Atherosclerosis
|
August 24, 2005
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes
Livia Pisciotta, Laura Calabresi, Graziana Lupattelli, et al.
Journal of Clinical Lipidology
|
February 18, 2014
Nutraceutical approach to moderate cardiometabolic risk: results of a randomized, double-blind and crossover study with Armolipid Plus
Massimiliano Ruscica, Monica Gomaraschi, Giuliana Mombelli, et al.
Page
of 17
Search research articles
Search
Showing results (91-100 of 169) with videos related to
Sort By:
Page
of 17
Oncotarget
|
December 13, 2017
Inhibitors of the PI3K/mTOR pathway prevent STAT5 phosphorylation in <i>JAK2V617F</i> mutated cells through PP2A/CIP2A axis
Niccolò Bartalucci, Laura Calabresi, Manjola Balliu, et al.
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids
|
December 15, 2022
Genetically determined deficiency of ANGPTL3 does not alter HDL ability to preserve endothelial homeostasis
Alice Ossoli, Ilenia Minicocci, Marta Turri, et al.
Atherosclerosis
|
August 21, 2015
Cholesterol trafficking-related serum lipoprotein functions in children with cholesteryl ester storage disease
Francesca Zimetti, Elda Favari, Paola Cagliero, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
September 27, 2020
Activation of Naturally Occurring Lecithin:Cholesterol Acyltransferase Mutants by a Novel Activator Compound
Chiara Pavanello, Alice Ossoli, Marta Turri, et al.
Journal of Clinical Lipidology
|
June 5, 2012
Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia
Paola Conca, Silvana Pileggi, Sara Simonelli, et al.
Cell Metabolism
|
August 3, 2010
Intestinal specific LXR activation stimulates reverse cholesterol transport and protects from atherosclerosis
Giuseppe Lo Sasso, Stefania Murzilli, Lorena Salvatore, et al.
Journal of Clinical Medicine
|
July 26, 2020
Low Plasma Lecithin: Cholesterol Acyltransferase (LCAT) Concentration Predicts Chronic Kidney Disease
Andrea Baragetti, Alice Ossoli, Arianna Strazzella, et al.
Atherosclerosis Plus
|
January 16, 2023
Two novel variants in the lecithin:cholesterol acyltransferase gene resulted in classic LCAT deficiency
Margareta Fistrek Prlic, Marijana Coric, Laura Calabresi, et al.
Atherosclerosis
|
August 24, 2005
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes
Livia Pisciotta, Laura Calabresi, Graziana Lupattelli, et al.
Journal of Clinical Lipidology
|
February 18, 2014
Nutraceutical approach to moderate cardiometabolic risk: results of a randomized, double-blind and crossover study with Armolipid Plus
Massimiliano Ruscica, Monica Gomaraschi, Giuliana Mombelli, et al.
Page
of 17