Showing results (11-20 of 41) with videos related to
Sort By:
Pageof 5
Annals of Clinical and Translational Neurology|August 14, 2020
Widespread tissue hypoxia dysregulates cell and metabolic pathways in SMAElena Hernandez-Gerez, Sergio Dall'Angelo, Jon M Collinson, et al.Neuroscience Letters|April 16, 2013
Increasing SMN levels using the histone deacetylase inhibitor SAHA ameliorates defects in skeletal muscle microvasculature in a mouse model of severe spinal muscular atrophyEilidh Somers, Markus Riessland, Julia Schreml, et al.Journal of Anatomy|February 24, 2018
Developmental and degenerative cardiac defects in the Taiwanese mouse model of severe spinal muscular atrophyGillian K Maxwell, Eva Szunyogova, Hannah K Shorrock, et al.Neuropathology and Applied Neurobiology|October 25, 2024
A reassessment of spinal cord pathology in severe infantile spinal muscular atrophy: Reassessment of spinal cord pathologyHazel Allardyce, Benjamin D Lawrence, Thomas O Crawford, et al.Human Molecular Genetics|November 4, 2009
Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophyLyndsay M Murray, Sheena Lee, Dirk Bäumer, et al.Neuroreport|July 14, 2005
Nonmuscle myosins IIA and IIB are present in adult motor nerve terminalsLaura J Vega-Riveroll, Steven R Wylie, Paul T Loughna, et al.Research Square|December 11, 2025
Microvascular pathology in the spinal cord of severe spinal muscular atrophy patientsHazel Allardyce, Heather Lanz, Benjamin D Lawrence, et al.Plos One|May 11, 2016
Histopathological Defects in Intestine in Severe Spinal Muscular Atrophy Mice Are Improved by Systemic Antisense Oligonucleotide TreatmentPalittiya Sintusek, Francesco Catapano, Napat Angkathunkayul, et al.Scientific Reports|October 5, 2016
Survival Motor Neuron (SMN) protein is required for normal mouse liver developmentEva Szunyogova, Haiyan Zhou, Gillian K Maxwell, et al.Journal of Neuroscience Research|March 30, 2004
Axotomy-dependent and -independent synapse elimination in organ cultures of Wld(s) mutant mouse skeletal muscleSimon H Parson, Richard R Ribchester, Neil Davie, et al.Pageof 5