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Disease Models & Mechanisms|March 11, 2020
Deterioration of muscle force and contractile characteristics are early pathological events in spinal and bulbar muscular atrophy miceAnna L Gray, Leonette Annan, James R T Dick, et al.
Brain Pathology (Zurich, Switzerland)|February 12, 2021
Automated and unbiased discrimination of ALS from control tissue at single cell resolutionCathleen Hagemann, Giulia E Tyzack, Doaa M Taha, et al.
The Journal of Cell Biology|May 25, 2005
A mutation in dynein rescues axonal transport defects and extends the life span of ALS miceDairin Kieran, Majid Hafezparast, Stephanie Bohnert, et al.
Journal of Molecular Neuroscience : MN|November 18, 2015
The Role of the Protein Quality Control System in SBMAPaola Rusmini, Valeria Crippa, Riccardo Cristofani, et al.
Science (New York, N.Y.)|November 29, 2014
Tetanus toxin entry. Nidogens are therapeutic targets for the prevention of tetanusKinga Bercsenyi, Nathalie Schmieg, J Barney Bryson, et al.
Human Molecular Genetics|February 15, 2011
Absence of disturbed axonal transport in spinal and bulbar muscular atrophyBilal Malik, Niranjanan Nirmalananthan, Lynsey G Bilsland, et al.
Plos One|September 12, 2013
Molecular chaperone mediated late-stage neuroprotection in the SOD1(G93A) mouse model of amyotrophic lateral sclerosisSergey S Novoselov, Wendy J Mustill, Anna L Gray, et al.
Cells, Tissues, Organs|November 9, 2016
Creating Interactions between Tissue-Engineered Skeletal Muscle and the Peripheral Nervous SystemAlec S T Smith, Samantha L Passey, Neil R W Martin, et al.
Annals of Clinical and Translational Neurology|March 8, 2021
The altered expression of neurofilament in mouse models and patients with spinal muscular atrophyCharlotte Spicer, Ching-Hua Lu, Francesco Catapano, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 19, 2014
Loss of Prox1 in striated muscle causes slow to fast skeletal muscle fiber conversion and dilated cardiomyopathyLouisa K Petchey, Catherine A Risebro, Joaquim M Vieira, et al.
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