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Neuromuscular Disorders : NMD|March 6, 2007
A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complexHeather MacLeod, Peter Pytel, Robert Wollmann, et al.
The Journal of Biological Chemistry|December 24, 2010
Endocytic recycling proteins EHD1 and EHD2 interact with fer-1-like-5 (Fer1L5) and mediate myoblast fusionAvery D Posey, Peter Pytel, Konstantina Gardikiotes, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 17, 2009
Myoferlin is required for insulin-like growth factor response and muscle growthAlexis R Demonbreun, Avery D Posey, Konstantina Heretis, et al.
The American Journal of Surgical Pathology|March 3, 2023
Endometrial Carcinomas With Subclonal Loss of Mismatch Repair Proteins: A Clinicopathologic and Genomic StudyRachelle P Mendoza, Peng Wang, Jefree J Schulte, et al.
Journal of Cell Science|June 24, 2010
Myoferlin regulation by NFAT in muscle injury, regeneration and repairAlexis R Demonbreun, Karen A Lapidos, Konstantina Heretis, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 13, 2004
Interferon-gamma induced medulloblastoma in the developing cerebellumWensheng Lin, April Kemper, Ken D McCarthy, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 27, 2014
Commensal bacteria protect against food allergen sensitizationAndrew T Stefka, Taylor Feehley, Prabhanshu Tripathi, et al.
Science Translational Medicine|July 6, 2018
BCL3 expression promotes resistance to alkylating chemotherapy in gliomasLongtao Wu, Giovanna M Bernal, Kirk E Cahill, et al.
Muscle & Nerve|May 26, 2021
Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutationsRicardo A Maselli, David T Wei, Trent S Hodgson, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculationLisa M Dellefave, Peter Pytel, Stephanie Mewborn, et al.
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