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ACS Medicinal Chemistry Letters|July 24, 2018
Targeting Tumor Associated Carbonic Anhydrases IX and XII: Highly Isozyme Selective Coumarin and Psoralen InhibitorsClaudia Melis, Simona Distinto, Giulia Bianco, et al.The Journal of Antimicrobial Chemotherapy|January 27, 2018
Pathway involving the N155H mutation in HIV-1 integrase leads to dolutegravir resistanceIsabelle Malet, Francesca A Ambrosio, Frédéric Subra, et al.Antiviral Therapy|October 26, 2011
Identification and structural characterization of novel genetic elements in the HIV-1 V3 loop regulating coreceptor usageValentina Svicher, Claudia Alteri, Anna Artese, et al.Oncotarget|February 25, 2016
SI113, a SGK1 inhibitor, potentiates the effects of radiotherapy, modulates the response to oxidative stress and induces cytotoxic autophagy in human glioblastoma multiforme cellsCristina Talarico, Vincenzo Dattilo, Lucia D'Antona, et al.Plos One|November 14, 2013
Fhit delocalizes annexin a4 from plasma membrane to cytosol and sensitizes lung cancer cells to paclitaxelEugenio Gaudio, Francesco Paduano, Riccardo Spizzo, et al.Journal of Medicinal Chemistry|November 25, 2014
N-Methyl-N-((1-methyl-5-(3-(1-(2-methylbenzyl)piperidin-4-yl)propoxy)-1H-indol-2-yl)methyl)prop-2-yn-1-amine, a new cholinesterase and monoamine oxidase dual inhibitorOscar M Bautista-Aguilera, Abdelouahid Samadi, Mourad Chioua, et al.European Journal of Medicinal Chemistry|August 26, 2019
Targeting multiple G-quadruplex-forming DNA sequences: Design, biophysical and biological evaluations of indolo-naphthyridine scaffold derivativesRaffaella Catalano, Federica Moraca, Jussara Amato, et al.Bioorganic Chemistry|December 2, 2022
Design, synthesis, biological activity evaluation and structure-activity relationships of new steroidal aromatase inhibitors. The case of C-ring and 7β substituted steroidsFernanda M F Roleira, Saul C Costa, Ana R Gomes, et al.Bioorganic & Medicinal Chemistry|June 29, 2010
Synthesis, semipreparative HPLC separation, biological evaluation, and 3D-QSAR of hydrazothiazole derivatives as human monoamine oxidase B inhibitorsFranco Chimenti, Daniela Secci, Adriana Bolasco, et al.Blood|August 19, 2024
An unbiased lncRNA dropout CRISPR-Cas9 screen reveals RP11-350G8.5 as a novel therapeutic target for multiple myelomaKatia Grillone, Serena Ascrizzi, Paolo Cremaschi, et al.Pageof 29