Modifiers of heart and muscle function: where genetics meets physiology.
about
Therapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug DiscoveryThe FVB Background Does Not Dramatically Alter the Dystrophic Phenotype of Mdx MiceDuchenne muscular dystrophy gene therapy in the canine model.Two novel MYH7 proline substitutions cause Laing Distal Myopathy-like phenotypes with variable expressivity and neck extensor contracture.Serotonin and Histamine Therapy Increases Tetanic Forces of Myoblasts, Reduces Muscle Injury, and Improves Grip Strength Performance of Dmd(mdx) Mice.Translating golden retriever muscular dystrophy microarray findings to novel biomarkers for cardiac/skeletal muscle function in Duchenne muscular dystrophy.Cardiac phenotype determines survival in Duchenne muscular dystrophy.Multidisciplinary study of a new ClC-1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathiesTGF-β1 affects cell-cell adhesion in the heart in an NCAM1-dependent mechanism.Contractile function recovery in severely injured gastrocnemius muscle of rats treated with either oleic or linoleic acid."Of Mice and Measures": A Project to Improve How We Advance Duchenne Muscular Dystrophy Therapies to the Clinic
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Modifiers of heart and muscle function: where genetics meets physiology.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
@zh-my
2013年学术文章
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2013年學術文章
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2013年學術文章
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2013年學術文章
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name
Modifiers of heart and muscle function: where genetics meets physiology.
@en
type
label
Modifiers of heart and muscle function: where genetics meets physiology.
@en
prefLabel
Modifiers of heart and muscle function: where genetics meets physiology.
@en
P2860
P1476
Modifiers of heart and muscle function: where genetics meets physiology.
@en
P2093
Elizabeth M McNally
Kayleigh A Swaggart
P2860
P304
P356
10.1113/EXPPHYSIOL.2013.075887
P577
2013-11-08T00:00:00Z