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Neuromuscular Disorders : NMD|December 1, 1996
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophiesJ S Beckmann, I Richard, O Broux, et al.
Gastro Hep Advances|November 14, 2025
Whole Exome Sequencing in Children With Autoimmune Hepatitis Identified Mutations in Genes Involved in the mTORC1 Signaling PathwayLéa-Philippine Gaigne, Caroline Besnard, Orianne Debeaupuis, et al.
Journal of Medicinal Chemistry|May 28, 2025
The Discovery of C7-Substituted Norbornyl Bisamides as RXFP1 Small Molecule AgonistsShun Su, Michael C Myers, Donna M Bilder, et al.
Cancers|July 24, 2021
Management of Patients with Pancreatic Ductal Adenocarcinoma in the Real-Life Setting: Lessons from the French National Hospital DatabaseChristelle de la Fouchardière, Mustapha Adham, Anne-Marie Marion-Audibert, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 28, 2004
PKC412 inhibits the zinc finger 198-fibroblast growth factor receptor 1 fusion tyrosine kinase and is active in treatment of stem cell myeloproliferative disorderJing Chen, Daniel J Deangelo, Jeffery L Kutok, et al.
Journal of Veterinary Internal Medicine|December 11, 2024
Clinical findings, treatment, and outcomes in cats with naturally occurring hypoadrenocorticism: 41 casesEmma Roberts, Ian K Ramsey, Ruth Gostelow, et al.
Neurology|May 14, 2020
Liver transplantation as a rescue therapy for severe neurologic forms of Wilson diseaseAurélia Poujois, Rodolphe Sobesky, Wassilios G Meissner, et al.
Medchemcomm|August 16, 2018
Triazolopyrimidines identified as reversible myeloperoxidase inhibitorsFranck Duclos, Lynn M Abell, David G Harden, et al.
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