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Kevin L Seburn

Showing results (11-20 of 33) with videos related to

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Genetics|October 30, 2004
Mutation rate and predicted phenotypic target sizes in ethylnitrosourea-treated miceDorothy Concepcion, Kevin L Seburn, Gen Wen, et al.
Journal of Cell Science|April 24, 2008
A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelinationBruce L Patton, Bing Wang, Yukie S Tarumi, et al.
Neuron|September 20, 2006
An active dominant mutation of glycyl-tRNA synthetase causes neuropathy in a Charcot-Marie-Tooth 2D mouse modelKevin L Seburn, Leslie A Nangle, Gregory A Cox, et al.
Physiology & Behavior|November 26, 2008
Age, experience and genetic background influence treadmill walking in miceChristine M Wooley, Shuqin Xing, Robert W Burgess, et al.
Brain Research|March 7, 2006
Auditory brainstem responses in 10 inbred strains of miceXiaoming Zhou, Philip H-S Jen, Kevin L Seburn, et al.
Neurobiology of Disease|July 4, 2012
Motor terminal degeneration unaffected by activity changes in SOD1(G93A) mice; a possible role for glycolysisDario I Carrasco, Edyta K Bichler, Mark M Rich, et al.
Muscle & Nerve|May 10, 2005
Gait analysis detects early changes in transgenic SOD1(G93A) miceChristine M Wooley, Roger B Sher, Ajit Kale, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 7, 2006
Grey, a novel mutation in the murine Lyst gene, causes the beige phenotype by skipping of exon 25Fabian Runkel, Heinrich Büssow, Kevin L Seburn, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 18, 2016
Synaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot-Marie-Tooth Type 2dEmily L Spaulding, James N Sleigh, Kathryn H Morelli, et al.
Journal of Neural Engineering|June 7, 2016
Enhancing the versatility of wireless biopotential acquisition for myoelectric prosthetic controlRebecca A Bercich, Zhi Wang, Henry Mei, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Genetics|October 30, 2004
Mutation rate and predicted phenotypic target sizes in ethylnitrosourea-treated miceDorothy Concepcion, Kevin L Seburn, Gen Wen, et al.
Journal of Cell Science|April 24, 2008
A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelinationBruce L Patton, Bing Wang, Yukie S Tarumi, et al.
Neuron|September 20, 2006
An active dominant mutation of glycyl-tRNA synthetase causes neuropathy in a Charcot-Marie-Tooth 2D mouse modelKevin L Seburn, Leslie A Nangle, Gregory A Cox, et al.
Physiology & Behavior|November 26, 2008
Age, experience and genetic background influence treadmill walking in miceChristine M Wooley, Shuqin Xing, Robert W Burgess, et al.
Brain Research|March 7, 2006
Auditory brainstem responses in 10 inbred strains of miceXiaoming Zhou, Philip H-S Jen, Kevin L Seburn, et al.
Neurobiology of Disease|July 4, 2012
Motor terminal degeneration unaffected by activity changes in SOD1(G93A) mice; a possible role for glycolysisDario I Carrasco, Edyta K Bichler, Mark M Rich, et al.
Muscle & Nerve|May 10, 2005
Gait analysis detects early changes in transgenic SOD1(G93A) miceChristine M Wooley, Roger B Sher, Ajit Kale, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 7, 2006
Grey, a novel mutation in the murine Lyst gene, causes the beige phenotype by skipping of exon 25Fabian Runkel, Heinrich Büssow, Kevin L Seburn, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 18, 2016
Synaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot-Marie-Tooth Type 2dEmily L Spaulding, James N Sleigh, Kathryn H Morelli, et al.
Journal of Neural Engineering|June 7, 2016
Enhancing the versatility of wireless biopotential acquisition for myoelectric prosthetic controlRebecca A Bercich, Zhi Wang, Henry Mei, et al.
Pageof 4