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Albee Messing

Showing results (81-90 of 96) with videos related to

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Nature|July 26, 2002
Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophySteven A Moore, Fumiaki Saito, Jianguo Chen, et al.
Nature Neuroscience|November 16, 2004
Receptor tyrosine kinase ErbB4 modulates neuroblast migration and placement in the adult forebrainE S Anton, H T Ghashghaei, Janet L Weber, et al.
Journal of Neurophysiology|July 20, 2007
Seizures and reduced life span in mice lacking the potassium channel subunit Kv1.2, but hypoexcitability and enlarged Kv1 currents in auditory neuronsHelen M Brew, Joshua X Gittelman, Robert S Silverstein, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 24, 2006
Different intracellular pathomechanisms produce diverse Myelin Protein Zero neuropathies in transgenic miceLawrence Wrabetz, Maurizio D'Antonio, Maria Pennuto, et al.
Cell Reports|October 26, 2018
Mutations in GFAP Disrupt the Distribution and Function of Organelles in Human AstrocytesJeffrey R Jones, Linghai Kong, Michael G Hanna, et al.
The Journal of Biological Chemistry|October 23, 2010
Brain-specific Phgdh deletion reveals a pivotal role for L-serine biosynthesis in controlling the level of D-serine, an N-methyl-D-aspartate receptor co-agonist, in adult brainJung Hoon Yang, Akira Wada, Kazuyuki Yoshida, et al.
Science Translational Medicine|November 17, 2021
Antisense therapy in a rat model of Alexander disease reverses GFAP pathology, white matter deficits, and motor impairmentTracy L Hagemann, Berit Powers, Ni-Hsuan Lin, et al.
Human Mutation|March 4, 2020
Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoformGuy Helman, Asako Takanohashi, Tracy L Hagemann, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 29, 2005
Region-specific myelin pathology in mice lacking the golli products of the myelin basic protein geneErin C Jacobs, Thomas M Pribyl, Ji-Ming Feng, et al.
Neurobiology of Disease|March 29, 2011
Knockdown of MLC1 in primary astrocytes causes cell vacuolation: a MLC disease cell modelAnna Duarri, Miguel Lopez de Heredia, Xavier Capdevila-Nortes, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
Nature|July 26, 2002
Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophySteven A Moore, Fumiaki Saito, Jianguo Chen, et al.
Nature Neuroscience|November 16, 2004
Receptor tyrosine kinase ErbB4 modulates neuroblast migration and placement in the adult forebrainE S Anton, H T Ghashghaei, Janet L Weber, et al.
Journal of Neurophysiology|July 20, 2007
Seizures and reduced life span in mice lacking the potassium channel subunit Kv1.2, but hypoexcitability and enlarged Kv1 currents in auditory neuronsHelen M Brew, Joshua X Gittelman, Robert S Silverstein, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 24, 2006
Different intracellular pathomechanisms produce diverse Myelin Protein Zero neuropathies in transgenic miceLawrence Wrabetz, Maurizio D'Antonio, Maria Pennuto, et al.
Cell Reports|October 26, 2018
Mutations in GFAP Disrupt the Distribution and Function of Organelles in Human AstrocytesJeffrey R Jones, Linghai Kong, Michael G Hanna, et al.
The Journal of Biological Chemistry|October 23, 2010
Brain-specific Phgdh deletion reveals a pivotal role for L-serine biosynthesis in controlling the level of D-serine, an N-methyl-D-aspartate receptor co-agonist, in adult brainJung Hoon Yang, Akira Wada, Kazuyuki Yoshida, et al.
Science Translational Medicine|November 17, 2021
Antisense therapy in a rat model of Alexander disease reverses GFAP pathology, white matter deficits, and motor impairmentTracy L Hagemann, Berit Powers, Ni-Hsuan Lin, et al.
Human Mutation|March 4, 2020
Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoformGuy Helman, Asako Takanohashi, Tracy L Hagemann, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 29, 2005
Region-specific myelin pathology in mice lacking the golli products of the myelin basic protein geneErin C Jacobs, Thomas M Pribyl, Ji-Ming Feng, et al.
Neurobiology of Disease|March 29, 2011
Knockdown of MLC1 in primary astrocytes causes cell vacuolation: a MLC disease cell modelAnna Duarri, Miguel Lopez de Heredia, Xavier Capdevila-Nortes, et al.
Pageof 10