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Journal of Materials Chemistry. B|April 8, 2020
Cationic poly(ester amide) dendrimers: alluring materials for biomedical applicationsAlexandre Lancelot, Rebeca González-Pastor, Rafael Clavería-Gimeno, et al.Molecular & Cellular Oncology|September 19, 2019
Designing and repurposing drugs to target intrinsically disordered proteins for cancer treatment: using NUPR1 as a paradigmPatricia Santofimia-Castaño, Bruno Rizzuti, Yi Xia, et al.Journal of Molecular Biology|May 22, 2026
Citrullination at the nuclear localization signal of the inhibitor of growth 4 (ING4) interferes with its binding to importin α3María Gabriela Álvarez-Rodríguez, Sonia Vega, Felipe Hornos, et al.Macromolecular Bioscience|June 6, 2015
Shell Cross-Linked Polymeric Micelles as Camptothecin Nanocarriers for Anti-HCV TherapyIsabel Jiménez-Pardo, Rebeca González-Pastor, Alexandre Lancelot, et al.Biochimica Et Biophysica Acta. Proteins and Proteomics|November 13, 2022
The armadillo-repeat domain of Plakophilin 1 binds to human enzyme PADI4José L Neira, Bruno Rizzuti, Salome Araujo-Abad, et al.RSC Medicinal Chemistry|October 7, 2024
Inhibition of SARS-CoV-2 3CLpro by chemically modified tyrosinase from <i>Agaricus bisporus</i>David Aguilera-Rodriguez, David Ortega-Alarcon, Angela Vazquez-Calvo, et al.Biomacromolecules|June 11, 2019
Dendrimers as Competitors of Protein-Protein Interactions of the Intrinsically Disordered Nuclear Chromatin Protein NUPR1José L Neira, Juan Correa, Bruno Rizzuti, et al.International Journal of Biological Macromolecules|August 4, 2020
Structural stability of SARS-CoV-2 3CLpro and identification of quercetin as an inhibitor by experimental screeningOlga Abian, David Ortega-Alarcon, Ana Jimenez-Alesanco, et al.Protein Science : a Publication of the Protein Society|September 29, 2022
Repositioning small molecule drugs as allosteric inhibitors of the BFT-3 toxin from enterotoxigenic Bacteroides fragilisAna Jimenez-Alesanco, Ulrich Eckhard, Marta Asencio Del Rio, et al.European Journal of Medicinal Chemistry|April 1, 2019
Stereoselective synthesis and biological evaluation as inhibitors of hepatitis C virus RNA polymerase of GSK3082 analogues with structural diversity at the 5-positionJosé A Gálvez, Rafael Clavería-Gimeno, Juan J Galano-Frutos, et al.Pageof 9