Swimming into prominence: the zebrafish as a valuable tool for studying human myopathies and muscular dystrophies.
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Model organisms in the fight against muscular dystrophy: lessons from drosophila and ZebrafishSpatio-Temporal Differences in Dystrophin Dynamics at mRNA and Protein Levels Revealed by a Novel FlipTrap LineRecent advances using zebrafish animal models for muscle disease drug discoveryMutations in INPP5K, Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive ImpairmentPOMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentationsComputational and experimental approaches to reveal the effects of single nucleotide polymorphisms with respect to disease diagnosticsPharmacologic management of Duchenne muscular dystrophy: target identification and preclinical trialsFish is Fish: the use of experimental model species to reveal causes of skeletal diversity in evolution and diseaseHigh throughput screening in duchenne muscular dystrophy: from drug discovery to functional genomicsZebrafish ambra1a and ambra1b knockdown impairs skeletal muscle development.Swimming-induced exercise promotes hypertrophy and vascularization of fast skeletal muscle fibres and activation of myogenic and angiogenic transcriptional programs in adult zebrafish.Zebrafish needle EMG: a new tool for high-throughput drug screensA novel early onset phenotype in a zebrafish model of merosin deficient congenital muscular dystrophyAnalysis of Zebrafish Larvae Skeletal Muscle Integrity with Evans Blue Dye.Transcriptional changes and developmental abnormalities in a zebrafish model of myotonic dystrophy type 1.Membrane-myofibril cross-talk in myofibrillogenesis and in muscular dystrophy pathogenesis: lessons from the zebrafish.Gene therapy in monogenic congenital myopathies.Tmem2 regulates cell-matrix interactions that are essential for muscle fiber attachmentGne depletion during zebrafish development impairs skeletal muscle structure and function.Ferulic Acid Promotes Hypertrophic Growth of Fast Skeletal Muscle in Zebrafish Model.Muscle dysfunction in a zebrafish model of Duchenne muscular dystrophy.[Potential of the zebrafish model to study congenital muscular dystrophies].Evaluation of anaesthetic protocols for laboratory adult zebrafish (Danio rerio).
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P2860
Swimming into prominence: the zebrafish as a valuable tool for studying human myopathies and muscular dystrophies.
description
2013 nî lūn-bûn
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2013 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Swimming into prominence: the ...... thies and muscular dystrophies
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Swimming into prominence: the ...... hies and muscular dystrophies.
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Swimming into prominence: the ...... hies and muscular dystrophies.
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Swimming into prominence: the ...... thies and muscular dystrophies
@nl
Swimming into prominence: the ...... hies and muscular dystrophies.
@ast
Swimming into prominence: the ...... hies and muscular dystrophies.
@en
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Swimming into prominence: the ...... thies and muscular dystrophies
@nl
Swimming into prominence: the ...... hies and muscular dystrophies.
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Swimming into prominence: the ...... hies and muscular dystrophies.
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P2860
P356
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Swimming into prominence: the ...... thies and muscular dystrophies
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P2093
Elizabeth M Gibbs
James J Dowling
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P304
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10.1111/FEBS.12412
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P577
2013-07-25T00:00:00Z