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Genetics
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October 30, 2004
Mutation rate and predicted phenotypic target sizes in ethylnitrosourea-treated mice
Dorothy 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 amyelination
Bruce 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 model
Kevin L Seburn, Leslie A Nangle, Gregory A Cox, et al.
Physiology & Behavior
|
November 26, 2008
Age, experience and genetic background influence treadmill walking in mice
Christine M Wooley, Shuqin Xing, Robert W Burgess, et al.
Brain Research
|
March 7, 2006
Auditory brainstem responses in 10 inbred strains of mice
Xiaoming 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 glycolysis
Dario I Carrasco, Edyta K Bichler, Mark M Rich, et al.
Muscle & Nerve
|
May 10, 2005
Gait analysis detects early changes in transgenic SOD1(G93A) mice
Christine 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 25
Fabian 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 2d
Emily 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 control
Rebecca A Bercich, Zhi Wang, Henry Mei, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
Genetics
|
October 30, 2004
Mutation rate and predicted phenotypic target sizes in ethylnitrosourea-treated mice
Dorothy 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 amyelination
Bruce 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 model
Kevin L Seburn, Leslie A Nangle, Gregory A Cox, et al.
Physiology & Behavior
|
November 26, 2008
Age, experience and genetic background influence treadmill walking in mice
Christine M Wooley, Shuqin Xing, Robert W Burgess, et al.
Brain Research
|
March 7, 2006
Auditory brainstem responses in 10 inbred strains of mice
Xiaoming 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 glycolysis
Dario I Carrasco, Edyta K Bichler, Mark M Rich, et al.
Muscle & Nerve
|
May 10, 2005
Gait analysis detects early changes in transgenic SOD1(G93A) mice
Christine 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 25
Fabian 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 2d
Emily 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 control
Rebecca A Bercich, Zhi Wang, Henry Mei, et al.
Page
of 4