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Nature Chemical Biology|May 26, 2021
Acute pharmacological degradation of Helios destabilizes regulatory T cellsEric S Wang, Alyssa L Verano, Radosław P Nowak, et al.
Journal of Medicinal Chemistry|January 15, 2020
Structure-Based Design of a Potent and Selective Covalent Inhibitor for SRC Kinase That Targets a P-Loop CysteineGuangyan Du, Suman Rao, Deepak Gurbani, et al.
Cancer Research|November 18, 2022
Transcriptional Antagonism by CDK8 Inhibition Improves Therapeutic Efficacy of MEK InhibitorsClare F Malone, Minjee Kim, Gabriela Alexe, et al.
The Journal of Infectious Diseases|November 16, 2014
Differences in HIV type 1 neutralization breadth in 2 geographically distinct cohorts in AfricaGama P Bandawe, Penny L Moore, Lise Werner, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 6, 2004
Desensitization of 5-HT1A receptors by 5-HT2A receptors in neuroendocrine neurons in vivoYahong Zhang, Thackery S Gray, Deborah N D'Souza, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 18, 2012
Dual blockade of lipid and cyclin-dependent kinases induces synthetic lethality in malignant gliomaChristine K Cheng, W Clay Gustafson, Elizabeth Charron, et al.
Nature Communications|May 9, 2022
Molecular basis for cooperative binding and synergy of ATP-site and allosteric EGFR inhibitorsTyler S Beyett, Ciric To, David E Heppner, et al.
Leukemia & Lymphoma|June 22, 2022
Daratumumab, cyclophosphamide, bortezomib, and dexamethasone for multiple myeloma: final results of the LYRA studyHabte Yimer, Jason Melear, Edward Faber, et al.
Nature Communications|August 28, 2014
Screening of DUB activity and specificity by MALDI-TOF mass spectrometryMaria Stella Ritorto, Richard Ewan, Ana B Perez-Oliva, et al.
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