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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 31, 2021
An Fc-free EGFR-specific 4-1BB-agonistic Trimerbody Displays Broad Antitumor Activity in Humanized Murine Cancer Models without ToxicityMarta Compte, Seandean L Harwood, Ainhoa Erce-Llamazares, et al.Plos One|July 8, 2016
Type 2 Diabetes Risk Allele Loci in the Qatari PopulationSarah L O'Beirne, Jacqueline Salit, Juan L Rodriguez-Flores, et al.Human Molecular Genetics|August 20, 2011
Fine-mapping of breast cancer susceptibility loci characterizes genetic risk in African AmericansFang Chen, Gary K Chen, Robert C Millikan, et al.Nature Biomedical Engineering|April 1, 2024
Mesenchymal stromal cells with chimaeric antigen receptors for enhanced immunosuppressionOlivia Sirpilla, R Leo Sakemura, Mehrdad Hefazi, et al.BMC Medicine|March 7, 2023
Water intake, hydration status and 2-year changes in cognitive performance: a prospective cohort studyStephanie K Nishi, Nancy Babio, Indira Paz-Graniel, et al.ACS Chemical Neuroscience|January 25, 2026
Discovery of VU6025733 (AG06827): A Highly Selective, Orally Bioavailable, and Structurally Distinct M4 Muscarinic Acetylcholine Receptor Positive Allosteric Modulator (PAM) with Robust In Vivo EfficacyAlison R Gregro, Charlotte Park, Madeline F Long, et al.Gigascience|January 13, 2021
Genome diversity in UkraineTaras K Oleksyk, Walter W Wolfsberger, Alexandra M Weber, et al.Journal of Medicinal Chemistry|April 13, 2022
Development of VU6019650: A Potent, Highly Selective, and Systemically Active Orthosteric Antagonist of the M5 Muscarinic Acetylcholine Receptor for the Treatment of Opioid Use DisorderAaron T Garrison, Douglas L Orsi, Rory A Capstick, et al.American Journal of Human Genetics|November 27, 2010
Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problemsMelissa B Ramocki, Magdalena Bartnik, Przemyslaw Szafranski, et al.Brain : a Journal of Neurology|December 16, 2014
Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2Alexander M Rossor, Emily C Oates, Hannah K Salter, et al.Pageof 252