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The International Journal of Biochemistry & Cell Biology|July 6, 2010
TDP-43: a DNA and RNA binding protein with roles in neurodegenerative diseasesSadaf T Warraich, Shu Yang, Garth A Nicholson, et al.Neurobiology of Aging|December 27, 2011
Mutation analysis of VCP in familial and sporadic amyotrophic lateral sclerosisKelly L Williams, Jennifer A Solski, Garth A Nicholson, et al.Molecular Genetics & Genomic Medicine|March 25, 2018
Structural variations causing inherited peripheral neuropathies: A paradigm for understanding genomic organization, chromatin interactions, and gene dysregulationAnthony N Cutrupi, Megan H Brewer, Garth A Nicholson, et al.Biochimica Et Biophysica Acta|March 3, 2004
Activity of partially inhibited serine palmitoyltransferase is sufficient for normal sphingolipid metabolism and viability of HSN1 patient cellsVadim N Dedov, Irina V Dedova, Alfred H Merrill, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 3, 2013
Axonal excitability in X-linked dominant Charcot Marie Tooth diseaseChristina Liang, James Howells, Marina Kennerson, et al.Neurobiology of Aging|October 22, 2011
Mutation analysis of the optineurin gene in familial amyotrophic lateral sclerosisJennifer A Solski, Kelly L Williams, Shu Yang, et al.JAMA Neurology|November 11, 2014
Axonal ion channel dysfunction in c9orf72 familial amyotrophic lateral sclerosisNimeshan Geevasinga, Parvathi Menon, James Howells, et al.Neurogenetics|June 5, 2021
Revisiting the pathogenic mechanism of the GJB1 5' UTR c.-103C > T mutation causing CMTX1Bianca R Grosz, John Svaren, Gonzalo Perez-Siles, et al.Human Genetics|March 14, 2007
A novel locus for distal motor neuron degeneration maps to chromosome 7q34-q36Sumana Gopinath, Ian P Blair, Marina L Kennerson, et al.Journal of Human Genetics|September 13, 2022
Identity-by-descent analysis of CMTX3 links three families through a common founderLyndal Henden, Bianca R Grosz, Melina Ellis, et al.Pageof 10