Progress toward Gene Therapy for Duchenne Muscular Dystrophy.

Progress toward Gene Therapy for Duchenne Muscular Dystrophy.

Item
http://www.wikidata.org/entity/Q39246797
Are mice good models for human neuromuscular disease? Comparing muscle excursions in walking between mice and humans.Inhibition of antigen presentation during AAV gene therapy using virus peptides.Utrophin up-regulation by artificial transcription factors induces muscle rescue and impacts the neuromuscular junction in mdx mice.Combined Therapies for Duchenne Muscular Dystrophy to Optimize Treatment Efficacy.Variable rescue of microtubule and physiological phenotypes in mdx muscle expressing different miniaturized dystrophins.At the Crossroads of Clinical and Preclinical Research for Muscular Dystrophy-Are We Closer to Effective Treatment for Patients?Systemic AAV Micro-dystrophin Gene Therapy for Duchenne Muscular DystrophyHuman Dystrophin Structural Changes upon Binding to Anionic Membrane LipidsGene and Cell Therapy for Muscular Dystrophies: Are We Getting There?
P2860

Progress toward Gene Therapy for Duchenne Muscular Dystrophy.

Item
http://www.wikidata.org/entity/Q39246797
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
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2017年學術文章
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2017年學術文章
@zh-hant
name
Progress toward Gene Therapy for Duchenne Muscular Dystrophy.
@en
Progress toward Gene Therapy for Duchenne Muscular Dystrophy.
@nl
type
label
Progress toward Gene Therapy for Duchenne Muscular Dystrophy.
@en
Progress toward Gene Therapy for Duchenne Muscular Dystrophy.
@nl
prefLabel
Progress toward Gene Therapy for Duchenne Muscular Dystrophy.
@en
Progress toward Gene Therapy for Duchenne Muscular Dystrophy.
@nl
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Progress toward Gene Therapy for Duchenne Muscular Dystrophy.
@en
P2093
P2860
P304
P31
P356
10.1016/J.YMTHE.2017.02.019
P433
P478
P577
P698
P921
P932