Mammalian animal models for Duchenne muscular dystrophy.
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Dystrophin-deficient large animal models: translational research and exon skippingRNA-guided CRISPR-Cas technologies for genome-scale investigation of disease processesA comparative study of N-glycolylneuraminic acid (Neu5Gc) and cytotoxic T cell (CT) carbohydrate expression in normal and dystrophin-deficient dog and human skeletal muscleNovel long noncoding RNAs (lncRNAs) in myogenesis: a miR-31 overlapping lncRNA transcript controls myoblast differentiationAltered nuclear dynamics in MDX myofibers.An intronic LINE-1 element insertion in the dystrophin gene aborts dystrophin expression and results in Duchenne-like muscular dystrophy in the corgi breedPrimary Murine Myotubes as a Model for Investigating Muscular DystrophyGait characterization in golden retriever muscular dystrophy dogs using linear discriminant analysis.Effects of systemic multiexon skipping with peptide-conjugated morpholinos in the heart of a dog model of Duchenne muscular dystrophy.Collaborating to bring new therapies to the patient--the TREAT-NMD model.Functional muscle analysis of the Tcap knockout mouse.Architecture of healthy and dystrophic muscles detected by optical coherence tomography.Generation of muscular dystrophy model rats with a CRISPR/Cas system.Skeletal muscle homeostasis in duchenne muscular dystrophy: modulating autophagy as a promising therapeutic strategy.The different impact of a high fat diet on dystrophic mdx and control C57Bl/10 miceIncreased neointimal thickening in dystrophin-deficient mdx mice.Pharmacologic management of Duchenne muscular dystrophy: target identification and preclinical trialsA human-specific deletion in mouse Cmah increases disease severity in the mdx model of Duchenne muscular dystrophyVoluntary wheel running in dystrophin-deficient (mdx) mice: Relationships between exercise parameters and exacerbation of the dystrophic phenotypePredictive markers of clinical outcome in the GRMD dog model of Duchenne muscular dystrophyThe effects of glucocorticoid and voluntary exercise treatment on the development of thoracolumbar kyphosis in dystrophin-deficient mice.Effects of an immunosuppressive treatment in the GRMD dog model of Duchenne muscular dystrophy.A new web-based method for automated analysis of muscle histologyTemporal changes in magnetic resonance imaging in the mdx mouseRecovery of altered neuromuscular junction morphology and muscle function in mdx mice after injuryVBP15, a novel anti-inflammatory and membrane-stabilizer, improves muscular dystrophy without side effects.Skeletal muscle fibrosis in the mdx/utrn+/- mouse validates its suitability as a murine model of Duchenne muscular dystrophy.Changes in muscle T2 and tissue damage after downhill running in mdx mice.Dystropathology increases energy expenditure and protein turnover in the mdx mouse model of duchenne muscular dystrophyThe FVB Background Does Not Dramatically Alter the Dystrophic Phenotype of Mdx MiceEnhancing translation: guidelines for standard pre-clinical experiments in mdx miceAquapuncture Using Stem Cell Therapy to Treat Mdx Mice.FE65 and FE65L1 amyloid precursor protein-binding protein compound null mice display adult-onset cataract and muscle weaknessChronic Dosing with Membrane Sealant Poloxamer 188 NF Improves Respiratory Dysfunction in Dystrophic Mdx and Mdx/Utrophin-/- MiceDystrophin-compromised sarcoglycan-δ-knockout diaphragm requires full wild-type embryonic stem cell reconstitution for correction.Quantitative evaluation of the beneficial effects in the mdx mouse of epigallocatechin gallate, an antioxidant polyphenol from green tea.Musculoskeletal Geometry, Muscle Architecture and Functional Specialisations of the Mouse HindlimbPre- and postsynaptic changes in the neuromuscular junction in dystrophic mice.Structural and functional evaluation of branched myofibers lacking intermediate filamentsSevere burn increased skeletal muscle loss in mdx mutant mice.
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Mammalian animal models for Duchenne muscular dystrophy.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
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scientific article published on 12 February 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Mammalian animal models for Duchenne muscular dystrophy.
@en
Mammalian animal models for Duchenne muscular dystrophy.
@nl
type
label
Mammalian animal models for Duchenne muscular dystrophy.
@en
Mammalian animal models for Duchenne muscular dystrophy.
@nl
prefLabel
Mammalian animal models for Duchenne muscular dystrophy.
@en
Mammalian animal models for Duchenne muscular dystrophy.
@nl
P2093
P1476
Mammalian animal models for Duchenne muscular dystrophy.
@en
P2093
Judith Dubach-Powell
Markus A Ruegg
Raffaella Willmann
Stefanie Possekel
Thomas Meier
P304
P356
10.1016/J.NMD.2008.11.015
P577
2009-02-12T00:00:00Z