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Cardiovascular Research|September 8, 2020
Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conductionZeina R Al Sayed, Robin Canac, Bastien Cimarosti, et al.Journal of Autoimmunity|October 22, 2017
An intermediate level of CD161 expression defines a novel activated, inflammatory, and pathogenic subset of CD8+ T cells involved in multiple sclerosisBryan Nicol, Marion Salou, Isabel Vogel, et al.American Journal of Respiratory and Critical Care Medicine|April 29, 2022
Monocyte Signature Associated with Herpes Simplex Virus Reactivation and Neurological Recovery after Brain InjuryTanguy Chaumette, Raphael Cinotti, Alice Mollé, et al.Cell Reports|November 25, 2020
Induction of Human Trophoblast Stem Cells from Somatic Cells and Pluripotent Stem CellsGaël Castel, Dimitri Meistermann, Betty Bretin, et al.Nature|June 7, 2013
MBNL proteins repress ES-cell-specific alternative splicing and reprogrammingHong Han, Manuel Irimia, P Joel Ross, et al.Journal of Medicinal Chemistry|October 13, 2017
Design of Leucine-Rich Repeat Kinase 2 (LRRK2) Inhibitors Using a Crystallographic Surrogate Derived from Checkpoint Kinase 1 (CHK1)Douglas S Williamson, Garrick P Smith, Pamela Acheson-Dossang, et al.Acta Crystallographica. Section D, Biological Crystallography|February 18, 2014
Identification of the first small-molecule ligand of the neuronal receptor sortilin and structure determination of the receptor-ligand complexJacob Lauwring Andersen, Tenna Juul Schrøder, Søren Christensen, et al.Advanced Materials (Deerfield Beach, Fla.)|December 17, 2023
Subcutaneous Administration of a Zwitterionic Chitosan-Based Hydrogel for Controlled Spatiotemporal Release of Monoclonal AntibodiesThomas Gréa, Guillaume Jacquot, Arthur Durand, et al.Bioorganic & Medicinal Chemistry Letters|December 21, 2013
The identification of AF38469: an orally bioavailable inhibitor of the VPS10P family sorting receptor SortilinTenna Juul Schrøder, Søren Christensen, Samsa Lindberg, et al.European Heart Journal|May 23, 2019
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeNadjet Belbachir, Vincent Portero, Zeina R Al Sayed, et al.Pageof 25