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Biomedical Research and Clinical Practice|September 11, 2020
Risk assessment for indeterminate pulmonary nodules using a novel, plasma-protein based biomarker assayNeil N Trivedi, Mehrdad Arjomandi, James K Brown, et al.
Human Molecular Genetics|March 18, 2010
Functional muscle analysis of the Tcap knockout mouseC D Markert, M P Meaney, K A Voelker, et al.
Human Molecular Genetics|November 10, 2011
Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotypeChristopher R Pierson, Ashley N Dulin-Smith, Ashley N Durban, 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.
Journal of the Neurological Sciences|December 14, 2002
Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscleC G Bönnemann, T G Thompson, P F M van der Ven, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 1, 2014
Sclerostin inhibition prevents spinal cord injury-induced cancellous bone lossLuke A Beggs, Fan Ye, Payal Ghosh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 22, 2022
Parents' decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq ProjectStacey Pereira, Amanda M Gutierrez, Jill Oliver Robinson, et al.
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