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Gregory A Cox

Showing results (1-10 of 60) with videos related to

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Cell|June 17, 2008
From ER to Eph receptors: new roles for VAP fragmentsSusan L Ackerman, Gregory A Cox
Methods in Molecular Biology (Clifton, N.J.)|May 7, 2016
Neuromuscular Disease Models and AnalysisRobert W Burgess, Gregory A Cox, Kevin L Seburn
Methods in Molecular Biology (Clifton, N.J.)|December 17, 2009
Neuromuscular disease models and analysisRobert W Burgess, Gregory A Cox, Kevin L Seburn
Biochimica Et Biophysica Acta|February 25, 2009
Understanding the muscular dystrophy caused by deletion of choline kinase beta in miceGengshu Wu, Roger B Sher, Gregory A Cox, et al.
Biochimica Et Biophysica Acta|December 23, 2009
Differential expression of choline kinase isoforms in skeletal muscle explains the phenotypic variability in the rostrocaudal muscular dystrophy mouseGengshu Wu, Roger B Sher, Gregory A Cox, et al.
Plos One|August 20, 2011
Rhabdomyosarcomas in aging A/J miceRoger B Sher, Gregory A Cox, Kevin D Mills, et al.
Brain Research|November 4, 2019
Overlapping spectrums: The clinicogenetic commonalities between Charcot-Marie-Tooth and other neurodegenerative diseasesPaige B Martin, Amy N Hicks, Sarah E Holbrook, et al.
American Journal of Physiology. Cell Physiology|August 30, 2008
Early mechanical dysfunction of the diaphragm in the muscular dystrophy with myositis (Ttnmdm) modelMichael A Lopez, Patricia S Pardo, Gregory A Cox, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 6, 2010
Anisotropic regulation of Ankrd2 gene expression in skeletal muscle by mechanical stretchJunaith S Mohamed, Michael A Lopez, Gregory A Cox, et al.
Human Molecular Genetics|March 24, 2012
Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6Mikhail Strokin, Kevin L Seburn, Gregory A Cox, et al.
Pageof 6

Showing results (1-10 of 60) with videos related to

Sort By:
Pageof 6
Cell|June 17, 2008
From ER to Eph receptors: new roles for VAP fragmentsSusan L Ackerman, Gregory A Cox
Methods in Molecular Biology (Clifton, N.J.)|May 7, 2016
Neuromuscular Disease Models and AnalysisRobert W Burgess, Gregory A Cox, Kevin L Seburn
Methods in Molecular Biology (Clifton, N.J.)|December 17, 2009
Neuromuscular disease models and analysisRobert W Burgess, Gregory A Cox, Kevin L Seburn
Biochimica Et Biophysica Acta|February 25, 2009
Understanding the muscular dystrophy caused by deletion of choline kinase beta in miceGengshu Wu, Roger B Sher, Gregory A Cox, et al.
Biochimica Et Biophysica Acta|December 23, 2009
Differential expression of choline kinase isoforms in skeletal muscle explains the phenotypic variability in the rostrocaudal muscular dystrophy mouseGengshu Wu, Roger B Sher, Gregory A Cox, et al.
Plos One|August 20, 2011
Rhabdomyosarcomas in aging A/J miceRoger B Sher, Gregory A Cox, Kevin D Mills, et al.
Brain Research|November 4, 2019
Overlapping spectrums: The clinicogenetic commonalities between Charcot-Marie-Tooth and other neurodegenerative diseasesPaige B Martin, Amy N Hicks, Sarah E Holbrook, et al.
American Journal of Physiology. Cell Physiology|August 30, 2008
Early mechanical dysfunction of the diaphragm in the muscular dystrophy with myositis (Ttnmdm) modelMichael A Lopez, Patricia S Pardo, Gregory A Cox, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 6, 2010
Anisotropic regulation of Ankrd2 gene expression in skeletal muscle by mechanical stretchJunaith S Mohamed, Michael A Lopez, Gregory A Cox, et al.
Human Molecular Genetics|March 24, 2012
Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6Mikhail Strokin, Kevin L Seburn, Gregory A Cox, et al.
Pageof 6