Showing results (31-40 of 46) with videos related to
Sort By:
Pageof 5
International Journal of Molecular Sciences|October 29, 2025
Mechanisms of Mitochondrial Impairment by SARS-CoV-2 Proteins: A Nexus of Pathogenesis with Significant Biochemical and Clinical ImplicationsMarco Refrigeri, Alessandra Tola, Rosangela Mogavero, et al.European Journal of Pharmacology|May 15, 2007
Mitochondria, ciglitazone and liver: a neglected interaction in biochemical pharmacologyRoberto Scatena, Patrizia Bottoni, Giuseppe E Martorana, et al.Biochemical and Biophysical Research Communications|June 9, 2004
Mitochondrial respiratory chain dysfunction, a non-receptor-mediated effect of synthetic PPAR-ligands: biochemical and pharmacological implicationsRoberto Scatena, Patrizia Bottoni, Giuseppe Ettore Martorana, et al.Bioorganic & Medicinal Chemistry Letters|September 17, 2005
Exploring the connection unit in the HDAC inhibitor pharmacophore model: novel uracil-based hydroxamatesAntonello Mai, Silvio Massa, Dante Rotili, et al.Chemmedchem|August 8, 2006
Aroyl-pyrrolyl hydroxyamides: influence of pyrrole C4-phenylacetyl substitution on histone deacetylase inhibitionAntonello Mai, Silvio Massa, Sergio Valente, et al.Journal of Medicinal Chemistry|February 20, 2004
3-(4-Aroyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamides as a new class of synthetic histone deacetylase inhibitors. 2. Effect of pyrrole-C2 and/or -C4 substitutions on biological activityAntonello Mai, Silvio Massa, Ilaria Cerbara, et al.The Journal of Membrane Biology|September 30, 2008
Oxidative effects of gemfibrozil on anion influx and metabolism in normal and Beta-thalassemic erythrocytes: physiological implicationsEster Tellone, Silvana Ficarra, Bruno Giardina, et al.Journal of Medicinal Chemistry|March 5, 2004
3-(4-Aroyl-1-methyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides as a new class of synthetic histone deacetylase inhibitors. 3. Discovery of novel lead compounds through structure-based drug design and docking studiesRino Ragno, Antonello Mai, Silvio Massa, et al.Journal of Medicinal Chemistry|April 19, 2002
Binding mode analysis of 3-(4-benzoyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamide: a new synthetic histone deacetylase inhibitor inducing histone hyperacetylation, growth inhibition, and terminal cell differentiationAntonello Mai, Silvio Massa, Rino Ragno, et al.Biological Chemistry|June 12, 2010
Resveratrol treatment induces redox stress in red blood cells: a possible role of caspase 3 in metabolism and anion transportAntonio Galtieri, Ester Tellone, Silvana Ficarra, et al.Pageof 5