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The European Journal of Neuroscience|February 5, 2010
Maintenance of the relative proportion of oligodendrocytes to axons even in the absence of BAX and BAKKumi Kawai, Takayuki Itoh, Aki Itoh, et al.Human Molecular Genetics|June 4, 2014
PMD patient mutations reveal a long-distance intronic interaction that regulates PLP1/DM20 alternative splicingJennifer R Taube, Karen Sperle, Linda Banser, et al.Human Mutation|November 16, 2005
Splice-site contribution in alternative splicing of PLP1 and DM20: molecular studies in oligodendrocytesGrace M Hobson, Zhong Huang, Karen Sperle, et al.Journal of the Neurological Sciences|September 1, 2010
Deficits in stepping response time are associated with impairments in balance and mobility in people with Huntington diseaseAllon Goldberg, Stacey L Schepens, Shawna M E Feely, et al.Brain : a Journal of Neurology|January 9, 2004
Phenotypic clustering in MPZ mutationsMichael E Shy, Agnes Jáni, Karen Krajewski, et al.Journal of the Neurological Sciences|November 5, 2011
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): a misdiagnosed disease entityChristina Sundal, Jennifer Lash, Jan Aasly, et al.Journal of Neuroscience Research|March 6, 2007
Plexiform-like neurofibromas develop in the mouse by intraneural xenograft of an NF1 tumor-derived Schwann cell lineGeorge Q Perrin, Lauren Fishbein, Susanne A Thomson, et al.Journal of Child Neurology|January 20, 2009
Variable expression of a novel PLP1 mutation in members of a family with Pelizaeus-Merzbacher diseaseAviva Fattal-Valevski, Miriam S DiMaio, Fuki M Hisama, et al.Neurogenetics|July 13, 2004
Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutationsIngrid K Svenson, Mark T Kloos, P Craig Gaskell, et al.Brain : a Journal of Neurology|April 17, 2010
A mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau depositionJames Y Garbern, Manuela Neumann, John Q Trojanowski, et al.Pageof 3