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Gregory A Cox

Showing results (11-20 of 60) with videos related to

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Experimental Neurology|December 31, 2020
Spinal motor neuron loss occurs through a p53-and-p21-independent mechanism in the Smn<sup>2B/-</sup> mouse model of spinal muscular atrophyEmily J Reedich, Martin Kalski, Nicholas Armijo, et al.
The American Journal of Pathology|October 31, 2009
Dysferlin deficiency and the development of cardiomyopathy in a mouse model of limb-girdle muscular dystrophy 2BThomas H Chase, Gregory A Cox, Lisa Burzenski, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 24, 2009
Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degenerationFrancesca Maltecca, Raffaella Magnoni, Federica Cerri, et al.
The Journal of Investigative Dermatology|July 13, 2004
Adult-onset Alopecia areata is a complex polygenic trait in the C3H/HeJ mouse modelJohn P Sundberg, Kathleen A Silva, Renhua Li, 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.
Genomics|February 7, 2002
The muscular dystrophy with myositis (mdm) mouse mutation disrupts a skeletal muscle-specific domain of titinSean M Garvey, Chandrika Rajan, Allen P Lerner, et al.
Human Molecular Genetics|April 8, 2004
Transgenic rescue of neurogenic atrophy in the nmd mouse reveals a role for Ighmbp2 in dilated cardiomyopathyTerry P Maddatu, Sean M Garvey, David G Schroeder, et al.
Human Molecular Genetics|March 21, 2009
Biochemical and genetic evidence for a role of IGHMBP2 in the translational machineryMariàngels de Planell-Saguer, David G Schroeder, Maria Celina Rodicio, et al.
Plos Genetics|August 7, 2007
Complex seizure disorder caused by Brunol4 deficiency in miceYan Yang, Connie L Mahaffey, Nathalie Bérubé, et al.
Pageof 6

Showing results (11-20 of 60) with videos related to

Sort By:
Pageof 6
Experimental Neurology|December 31, 2020
Spinal motor neuron loss occurs through a p53-and-p21-independent mechanism in the Smn<sup>2B/-</sup> mouse model of spinal muscular atrophyEmily J Reedich, Martin Kalski, Nicholas Armijo, et al.
The American Journal of Pathology|October 31, 2009
Dysferlin deficiency and the development of cardiomyopathy in a mouse model of limb-girdle muscular dystrophy 2BThomas H Chase, Gregory A Cox, Lisa Burzenski, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 24, 2009
Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degenerationFrancesca Maltecca, Raffaella Magnoni, Federica Cerri, et al.
The Journal of Investigative Dermatology|July 13, 2004
Adult-onset Alopecia areata is a complex polygenic trait in the C3H/HeJ mouse modelJohn P Sundberg, Kathleen A Silva, Renhua Li, 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.
Genomics|February 7, 2002
The muscular dystrophy with myositis (mdm) mouse mutation disrupts a skeletal muscle-specific domain of titinSean M Garvey, Chandrika Rajan, Allen P Lerner, et al.
Human Molecular Genetics|April 8, 2004
Transgenic rescue of neurogenic atrophy in the nmd mouse reveals a role for Ighmbp2 in dilated cardiomyopathyTerry P Maddatu, Sean M Garvey, David G Schroeder, et al.
Human Molecular Genetics|March 21, 2009
Biochemical and genetic evidence for a role of IGHMBP2 in the translational machineryMariàngels de Planell-Saguer, David G Schroeder, Maria Celina Rodicio, et al.
Plos Genetics|August 7, 2007
Complex seizure disorder caused by Brunol4 deficiency in miceYan Yang, Connie L Mahaffey, Nathalie Bérubé, et al.
Pageof 6