Search research articles
Contact Us
Filters
Showing results (1-10 of 60) with videos related to
Page
of 6
Sort By:
Cell
|
June 17, 2008
From ER to Eph receptors: new roles for VAP fragments
Susan L Ackerman, Gregory A Cox
Methods in Molecular Biology (Clifton, N.J.)
|
May 7, 2016
Neuromuscular Disease Models and Analysis
Robert W Burgess, Gregory A Cox, Kevin L Seburn
Methods in Molecular Biology (Clifton, N.J.)
|
December 17, 2009
Neuromuscular disease models and analysis
Robert 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 mice
Gengshu 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 mouse
Gengshu Wu, Roger B Sher, Gregory A Cox, et al.
Plos One
|
August 20, 2011
Rhabdomyosarcomas in aging A/J mice
Roger 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 diseases
Paige 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) model
Michael 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 stretch
Junaith 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 Pla2g6
Mikhail Strokin, Kevin L Seburn, Gregory A Cox, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 60) with videos related to
Sort By:
Page
of 6
Cell
|
June 17, 2008
From ER to Eph receptors: new roles for VAP fragments
Susan L Ackerman, Gregory A Cox
Methods in Molecular Biology (Clifton, N.J.)
|
May 7, 2016
Neuromuscular Disease Models and Analysis
Robert W Burgess, Gregory A Cox, Kevin L Seburn
Methods in Molecular Biology (Clifton, N.J.)
|
December 17, 2009
Neuromuscular disease models and analysis
Robert 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 mice
Gengshu 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 mouse
Gengshu Wu, Roger B Sher, Gregory A Cox, et al.
Plos One
|
August 20, 2011
Rhabdomyosarcomas in aging A/J mice
Roger 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 diseases
Paige 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) model
Michael 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 stretch
Junaith 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 Pla2g6
Mikhail Strokin, Kevin L Seburn, Gregory A Cox, et al.
Page
of 6