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Kay E Davies

Showing results (1-10 of 160) with videos related to

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Annual Review of Genomics and Human Genetics|March 3, 2020
The Long Journey from Diagnosis to TherapyKay E Davies
Human Molecular Genetics|October 5, 2021
Happy 30th Birthday, HMGKay E Davies
American Journal of Human Genetics|March 5, 2016
2015 William Allan AwardKay E Davies
Neural Regeneration Research|April 10, 2019
Regenerative biomarkers for Duchenne muscular dystrophySimon Guiraud, Kay E Davies
Methods in Molecular Biology (Clifton, N.J.)|January 4, 2011
Engineering exon-skipping vectors expressing U7 snRNA constructs for Duchenne muscular dystrophy gene therapyAurélie Goyenvalle, Kay E Davies
Skeletal Muscle|July 30, 2011
Challenges to oligonucleotides-based therapeutics for Duchenne muscular dystrophyAurélie Goyenvalle, Kay E Davies
Handbook of Clinical Neurology|September 24, 2008
Chapter 7 Spinal muscular atrophies and hereditary motor neuropathiesKevin Talbot, Kay E Davies
Neuromuscular Disorders : NMD|April 23, 2024
Long-term clinical follow-up of a family with Becker muscular dystrophy associated with a large deletion in the DMD geneKay E Davies, Julie Vogt
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 16, 2019
Micro-dystrophin Genes Bring Hope of an Effective Therapy for Duchenne Muscular DystrophyKay E Davies, Simon Guiraud
European Journal of Human Genetics : EJHG|February 10, 2021
Evaluating the potential of novel genetic approaches for the treatment of Duchenne muscular dystrophyVratko Himič, Kay E Davies
Pageof 16

Showing results (1-10 of 160) with videos related to

Sort By:
Pageof 16
Annual Review of Genomics and Human Genetics|March 3, 2020
The Long Journey from Diagnosis to TherapyKay E Davies
Human Molecular Genetics|October 5, 2021
Happy 30th Birthday, HMGKay E Davies
American Journal of Human Genetics|March 5, 2016
2015 William Allan AwardKay E Davies
Neural Regeneration Research|April 10, 2019
Regenerative biomarkers for Duchenne muscular dystrophySimon Guiraud, Kay E Davies
Methods in Molecular Biology (Clifton, N.J.)|January 4, 2011
Engineering exon-skipping vectors expressing U7 snRNA constructs for Duchenne muscular dystrophy gene therapyAurélie Goyenvalle, Kay E Davies
Skeletal Muscle|July 30, 2011
Challenges to oligonucleotides-based therapeutics for Duchenne muscular dystrophyAurélie Goyenvalle, Kay E Davies
Handbook of Clinical Neurology|September 24, 2008
Chapter 7 Spinal muscular atrophies and hereditary motor neuropathiesKevin Talbot, Kay E Davies
Neuromuscular Disorders : NMD|April 23, 2024
Long-term clinical follow-up of a family with Becker muscular dystrophy associated with a large deletion in the DMD geneKay E Davies, Julie Vogt
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 16, 2019
Micro-dystrophin Genes Bring Hope of an Effective Therapy for Duchenne Muscular DystrophyKay E Davies, Simon Guiraud
European Journal of Human Genetics : EJHG|February 10, 2021
Evaluating the potential of novel genetic approaches for the treatment of Duchenne muscular dystrophyVratko Himič, Kay E Davies
Pageof 16