Showing results (1001-1010 of 1,288) with videos related to

Sort By:
Pageof 129
Age (Dordrecht, Netherlands)|July 13, 2013
Rudimentary signs of immunosenescence in Cytomegalovirus-seropositive healthy young adultsJames E Turner, John P Campbell, Kate M Edwards, et al.
Cancer|June 23, 2021
Reassessing the measurement and presence of therapeutic misconception in a phase 1 settingEli R Abernethy, Gavin P Campbell, Rachel S Hianik, et al.
Science (New York, N.Y.)|December 16, 1998
Identification of alpha-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virusW Cao, M D Henry, P Borrow, et al.
Glycobiology|March 10, 2020
HNK-1 sulfotransferase modulates α-dystroglycan glycosylation by 3-O-sulfation of glucuronic acid on matriglycanM Osman Sheikh, David Venzke, Mary E Anderson, et al.
Ophthalmology|January 17, 2019
Evolution in the Risk of Cataract Surgical Complications among Patients Exposed to Tamsulosin: A Population-Based StudyRobert J Campbell, Sherif R El-Defrawy, Sudeep S Gill, et al.
Nature Communications|October 10, 2025
LARGE1 processively polymerizes length-controlled matriglycan on prodystroglycanSoumya Joseph, Nicholas J Schnicker, Nicholas Spellmon, et al.
Clinical Science (London, England : 1979)|June 4, 2013
Longitudinal characterization of a model of chronic allergic lung inflammation in mice using imaging, functional and immunological methodsKumar Changani, Catherine Pereira, Simon Young, et al.
Neuromuscular Disorders : NMD|February 5, 2014
A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutationsStephanie E Wallace, Jessie H Conta, Thomas L Winder, et al.
Molecular Genetics and Metabolism|July 17, 2013
Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophyAmy C Yang, Bobby G Ng, Steven A Moore, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1994
Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiencyN B Romero, F M Tomé, F Leturcq, et al.
Pageof 129