Showing results (731-740 of 823) with videos related to
Sort By:
Pageof 83
The Journal of Biological Chemistry|August 25, 2011
Caenorhabditis elegans UCP4 protein controls complex II-mediated oxidative phosphorylation through succinate transportMatthew Pfeiffer, Ernst-Bernhard Kayzer, Xianmei Yang, et al.European Journal of Human Genetics : EJHG|January 28, 2016
Prominent scapulae mimicking an inherited myopathy expands the phenotype of CHD7-related diseaseGina L O'Grady, Alan Ma, Deborah Sival, et al.Human Molecular Genetics|August 27, 2015
Muscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibresMichaela Yuen, Sandra T Cooper, Steve B Marston, et al.International Journal of Radiation Oncology, Biology, Physics|June 23, 2009
Radiation Therapy Oncology Group translational research program stem cell symposium: incorporating stem cell hypotheses into clinical trialsWendy A Woodward, Robert G Bristow, Michael F Clarke, et al.Proceedings of the National Academy of Sciences of the United States of America|December 10, 2009
Target identification using drug affinity responsive target stability (DARTS)Brett Lomenick, Rui Hao, Nao Jonai, et al.The New England Journal of Medicine|January 21, 2016
CDX2 as a Prognostic Biomarker in Stage II and Stage III Colon CancerPiero Dalerba, Debashis Sahoo, Soonmyung Paik, et al.Blood|January 10, 2002
Differential gene expression profiling of adult murine hematopoietic stem cellsIn-Kyung Park, Yaqin He, Fangming Lin, et al.Human Mutation|June 29, 2010
Recessive mutations in RYR1 are a common cause of congenital fiber type disproportionNigel F Clarke, Leigh B Waddell, Sandra T Cooper, et al.Journal of Neuropathology and Experimental Neurology|March 18, 2011
Dysferlin, annexin A1, and mitsugumin 53 are upregulated in muscular dystrophy and localize to longitudinal tubules of the T-system with stretchLeigh B Waddell, Frances A Lemckert, Xi F Zheng, et al.Annals of Neurology|May 10, 2016
Diagnosis and etiology of congenital muscular dystrophy: We are halfway thereGina L O'Grady, Monkol Lek, Shireen R Lamande, et al.Pageof 83