Showing results (41-50 of 79) with videos related to
Sort By:
Pageof 8
Cells|September 9, 2022
The Proteome Signatures of Fibroblasts from Patients with Severe, Intermediate and Mild Spinal Muscular Atrophy Show Limited OverlapSharon J Brown, Rachel A Kline, Silvia A Synowsky, et al.Cell Reports|April 25, 2019
Regional Molecular Mapping of Primate Synapses during Normal Healthy AgingLaura C Graham, Michael J Naldrett, Steven G Kohama, et al.Cells|November 27, 2024
Distinct Molecular Profiles Underpin Mild-To-Moderate Equine Asthma Cytological ProfilesAnna E Karagianni, Eric A Richard, Marie-Pierre Toquet, et al.Acta Neuropathologica Communications|October 30, 2022
Synaptic proteomics reveal distinct molecular signatures of cognitive change and C9ORF72 repeat expansion in the human ALS cortexZsofia I Laszlo, Nicole Hindley, Anna Sanchez Avila, et al.Human Molecular Genetics|August 14, 2010
SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophyThomas M Wishart, Jack P-W Huang, Lyndsay M Murray, et al.Human Molecular Genetics|July 31, 2009
Molecular correlates of axonal and synaptic pathology in mouse models of Batten diseaseCatherine Kielar, Thomas M Wishart, Alice Palmer, et al.Journal of Anatomy|June 24, 2020
Comparative anatomy of the mammalian neuromuscular junctionInes Boehm, Abrar Alhindi, Ana S Leite, et al.Human Molecular Genetics|August 16, 2011
Reversible molecular pathology of skeletal muscle in spinal muscular atrophyChantal A Mutsaers, Thomas M Wishart, Douglas J Lamont, et al.Human Molecular Genetics|April 12, 2011
ApoE isoform-specific regulation of regeneration in the peripheral nervous systemLaura H Comley, Heidi R Fuller, Thomas M Wishart, et al.Neurobiology of Disease|June 10, 2019
Altered mitochondrial bioenergetics are responsible for the delay in Wallerian degeneration observed in neonatal miceRachel A Kline, Kosala N Dissanayake, Maica Llavero Hurtado, et al.Pageof 8