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Gregory A Cox

Showing results (51-60 of 60) with videos related to

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Human Molecular Genetics|December 3, 2005
Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome traffickingShinji Hadano, Susanna C Benn, Shigeru Kakuta, et al.
Biorxiv : the Preprint Server for Biology|September 4, 2024
Poly-alanine-tailing is a modifier of neurodegeneration caused by Listerin mutationHao-Chih Hung, Carlos Costas-Insua, Sarah E Holbrook, et al.
Annals of Clinical and Translational Neurology|May 28, 2016
Absence of UCHL 1 function leads to selective motor neuropathyBarış Genç, Javier H Jara, Megan C Schultz, et al.
Medicine and Science in Sports and Exercise|January 1, 2013
Alterations in osteopontin modify muscle size in females in both humans and miceEric P Hoffman, Heather Gordish-Dressman, Virginia D McLane, et al.
Human Molecular Genetics|November 15, 2015
Effect of genetic background on the dystrophic phenotype in mdx miceWilliam D Coley, Laurent Bogdanik, Maria Candida Vila, et al.
American Journal of Human Genetics|June 14, 2011
A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesisSatomi Mitsuhashi, Aya Ohkuma, Beril Talim, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 12, 2026
SORT LNPs encapsulating Cas9 mRNA achieve efficient editing in skeletal muscle in a dystrophic mouse modelSukanya Iyer, Katelyn Daman, Yehui Sun, et al.
Nature Communications|October 2, 2020
Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular diseasePaige B Martin, Yu Kigoshi-Tansho, Roger B Sher, et al.
Nature Communications|September 16, 2020
NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular diseasePaige B Martin, Yu Kigoshi-Tansho, Roger B Sher, et al.
Genome Research|April 29, 2015
Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disordersHeather Fairfield, Anuj Srivastava, Guruprasad Ananda, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Human Molecular Genetics|December 3, 2005
Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome traffickingShinji Hadano, Susanna C Benn, Shigeru Kakuta, et al.
Biorxiv : the Preprint Server for Biology|September 4, 2024
Poly-alanine-tailing is a modifier of neurodegeneration caused by Listerin mutationHao-Chih Hung, Carlos Costas-Insua, Sarah E Holbrook, et al.
Annals of Clinical and Translational Neurology|May 28, 2016
Absence of UCHL 1 function leads to selective motor neuropathyBarış Genç, Javier H Jara, Megan C Schultz, et al.
Medicine and Science in Sports and Exercise|January 1, 2013
Alterations in osteopontin modify muscle size in females in both humans and miceEric P Hoffman, Heather Gordish-Dressman, Virginia D McLane, et al.
Human Molecular Genetics|November 15, 2015
Effect of genetic background on the dystrophic phenotype in mdx miceWilliam D Coley, Laurent Bogdanik, Maria Candida Vila, et al.
American Journal of Human Genetics|June 14, 2011
A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesisSatomi Mitsuhashi, Aya Ohkuma, Beril Talim, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 12, 2026
SORT LNPs encapsulating Cas9 mRNA achieve efficient editing in skeletal muscle in a dystrophic mouse modelSukanya Iyer, Katelyn Daman, Yehui Sun, et al.
Nature Communications|October 2, 2020
Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular diseasePaige B Martin, Yu Kigoshi-Tansho, Roger B Sher, et al.
Nature Communications|September 16, 2020
NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular diseasePaige B Martin, Yu Kigoshi-Tansho, Roger B Sher, et al.
Genome Research|April 29, 2015
Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disordersHeather Fairfield, Anuj Srivastava, Guruprasad Ananda, et al.
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