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Annual Review of Genomics and Human Genetics
|
March 3, 2020
The Long Journey from Diagnosis to Therapy
Kay E Davies
Human Molecular Genetics
|
October 5, 2021
Happy 30th Birthday, HMG
Kay E Davies
American Journal of Human Genetics
|
March 5, 2016
2015 William Allan Award
Kay E Davies
Neural Regeneration Research
|
April 10, 2019
Regenerative biomarkers for Duchenne muscular dystrophy
Simon 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 therapy
Aurélie Goyenvalle, Kay E Davies
Skeletal Muscle
|
July 30, 2011
Challenges to oligonucleotides-based therapeutics for Duchenne muscular dystrophy
Aurélie Goyenvalle, Kay E Davies
Handbook of Clinical Neurology
|
September 24, 2008
Chapter 7 Spinal muscular atrophies and hereditary motor neuropathies
Kevin 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 gene
Kay 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 Dystrophy
Kay 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 dystrophy
Vratko Himič, Kay E Davies
Page
of 16
Search research articles
Search
Showing results (1-10 of 160) with videos related to
Sort By:
Page
of 16
Annual Review of Genomics and Human Genetics
|
March 3, 2020
The Long Journey from Diagnosis to Therapy
Kay E Davies
Human Molecular Genetics
|
October 5, 2021
Happy 30th Birthday, HMG
Kay E Davies
American Journal of Human Genetics
|
March 5, 2016
2015 William Allan Award
Kay E Davies
Neural Regeneration Research
|
April 10, 2019
Regenerative biomarkers for Duchenne muscular dystrophy
Simon 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 therapy
Aurélie Goyenvalle, Kay E Davies
Skeletal Muscle
|
July 30, 2011
Challenges to oligonucleotides-based therapeutics for Duchenne muscular dystrophy
Aurélie Goyenvalle, Kay E Davies
Handbook of Clinical Neurology
|
September 24, 2008
Chapter 7 Spinal muscular atrophies and hereditary motor neuropathies
Kevin 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 gene
Kay 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 Dystrophy
Kay 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 dystrophy
Vratko Himič, Kay E Davies
Page
of 16