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Biochemical Pharmacology|October 4, 2011
MG-2477, a new tubulin inhibitor, induces autophagy through inhibition of the Akt/mTOR pathway and delayed apoptosis in A549 cellsGiampietro Viola, Roberta Bortolozzi, Ernest Hamel, et al.Journal of Neuroscience Methods|September 5, 2021
A novel integrated approach to estimate the mitochondrial content of neuronal cells and brain tissuesSara Spadini, Gabriella Racchetti, Alice Adiletta, et al.Biochemical Pharmacology|March 22, 2012
Discovery of novel A3 adenosine receptor ligands based on chromone scaffoldAlexandra Gaspar, Joana Reis, Sonja Kachler, et al.Farmaco (Societa Chimica Italiana : 1989)|April 26, 2005
Synthesis, biological studies and molecular modeling investigation of 1,3-dimethyl-2,4-dioxo-6-methyl-8-(substituted) 1,2,3,4-tetrahydro [1,2,4]-triazolo [3,4-f]-purines as potential adenosine receptor antagonistsGiorgia Pastorin, Chiara Bolcato, Barbara Cacciari, et al.Magnetic Resonance in Medicine|October 10, 2013
Field camera measurements of gradient and shim impulse responses using frequency sweepsS Johanna Vannesjo, Benjamin E Dietrich, Matteo Pavan, et al.Magnetic Resonance in Medicine|November 1, 2016
Gradient and shim pre-emphasis by inversion of a linear time-invariant system modelS Johanna Vannesjo, Yolanda Duerst, Laetitia Vionnet, et al.Medicinal Chemistry Research : an International Journal for Rapid Communications on Design and Mechanisms of Action of Biologically Active Agents|July 14, 2026
From empirical screening to lipid trolling: the evolution of extrahelical allosteric modulators of A1 and A3 adenosine receptorsMatteo Pavan, Siva Hariprasad Kurma, Paola Oliva, et al.Italian Journal of Pediatrics|May 27, 2018
Impact of near infrared light in pediatric blood drawing Centre on rate of first attempt success and time of procedureEster Conversano, Giorgio Cozzi, Matteo Pavan, et al.Bioorganic & Medicinal Chemistry|April 19, 2021
Amphiphilic peptide-based MMP3 inhibitors for intra-articular treatment of knee OACristian Guarise, Davide Ceradini, Martina Tessari, et al.Journal of Medicinal Chemistry|December 13, 2005
1,2,4-Triazolo[1,5-a]quinoxaline as a versatile tool for the design of selective human A3 adenosine receptor antagonists: synthesis, biological evaluation, and molecular modeling studies of 2-(hetero)aryl- and 2-carboxy-substituted derivativesDaniela Catarzi, Vittoria Colotta, Flavia Varano, et al.Pageof 31