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Gregory A Cox

Showing results (41-50 of 60) with videos related to

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Human Molecular Genetics|July 16, 2004
Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiencyMengfatt Ho, Cristina M Post, Leah R Donahue, et al.
Molecular Cell|June 5, 2012
A direct HDAC4-MAP kinase crosstalk activates muscle atrophy programMoon-Chang Choi, Todd J Cohen, Tomasa Barrientos, et al.
Molecular and Cellular Neurosciences|August 23, 2005
Ocular abnormalities in Large(myd) and Large(vls) mice, spontaneous models for muscle, eye, and brain diseasesYongsuk Lee, Shuhei Kameya, Gregory A Cox, et al.
Plos One|September 15, 2022
Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron diseaseGuillermo M Alexander, Terry D Heiman-Patterson, Frank Bearoff, et al.
Plos One|March 13, 2015
Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron diseaseTerry D Heiman-Patterson, Elizabeth P Blankenhorn, Roger B Sher, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 14, 2008
The mitochondrial protease AFG3L2 is essential for axonal developmentFrancesca Maltecca, Asadollah Aghaie, David G Schroeder, et al.
The Journal of Biological Chemistry|December 24, 2005
A rostrocaudal muscular dystrophy caused by a defect in choline kinase beta, the first enzyme in phosphatidylcholine biosynthesisRoger B Sher, Chieko Aoyama, Kimberly A Huebsch, et al.
Human Molecular Genetics|July 14, 2011
Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagySatomi Mitsuhashi, Hideyuki Hatakeyama, Minako Karahashi, et al.
Molecular Cell|April 28, 2021
Convergence of mammalian RQC and C-end rule proteolytic pathways via alanine tailingAnna Thrun, Aitor Garzia, Yu Kigoshi-Tansho, et al.
Plos One|January 10, 2013
Retrotransposon insertion in the T-cell acute lymphocytic leukemia 1 (Tal1) gene is associated with severe renal disease and patchy alopecia in Hairpatches (Hpt) miceVishnu Hosur, Melissa L Cox, Lisa M Burzenski, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|July 16, 2004
Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiencyMengfatt Ho, Cristina M Post, Leah R Donahue, et al.
Molecular Cell|June 5, 2012
A direct HDAC4-MAP kinase crosstalk activates muscle atrophy programMoon-Chang Choi, Todd J Cohen, Tomasa Barrientos, et al.
Molecular and Cellular Neurosciences|August 23, 2005
Ocular abnormalities in Large(myd) and Large(vls) mice, spontaneous models for muscle, eye, and brain diseasesYongsuk Lee, Shuhei Kameya, Gregory A Cox, et al.
Plos One|September 15, 2022
Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron diseaseGuillermo M Alexander, Terry D Heiman-Patterson, Frank Bearoff, et al.
Plos One|March 13, 2015
Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron diseaseTerry D Heiman-Patterson, Elizabeth P Blankenhorn, Roger B Sher, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 14, 2008
The mitochondrial protease AFG3L2 is essential for axonal developmentFrancesca Maltecca, Asadollah Aghaie, David G Schroeder, et al.
The Journal of Biological Chemistry|December 24, 2005
A rostrocaudal muscular dystrophy caused by a defect in choline kinase beta, the first enzyme in phosphatidylcholine biosynthesisRoger B Sher, Chieko Aoyama, Kimberly A Huebsch, et al.
Human Molecular Genetics|July 14, 2011
Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagySatomi Mitsuhashi, Hideyuki Hatakeyama, Minako Karahashi, et al.
Molecular Cell|April 28, 2021
Convergence of mammalian RQC and C-end rule proteolytic pathways via alanine tailingAnna Thrun, Aitor Garzia, Yu Kigoshi-Tansho, et al.
Plos One|January 10, 2013
Retrotransposon insertion in the T-cell acute lymphocytic leukemia 1 (Tal1) gene is associated with severe renal disease and patchy alopecia in Hairpatches (Hpt) miceVishnu Hosur, Melissa L Cox, Lisa M Burzenski, et al.
Pageof 6