(Q37383091)

20 August 2017

1 reference

title

The value of mammalian models for duchenne muscular dystrophy in developing therapeutic strategies (English)

1 reference

Duchenne muscular dystrophy

20 August 2017

main subject

1 reference

Glen B Banks

1

1 reference

20 August 2017

Jeffrey S Chamberlain

series ordinal

2

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20 August 2017

publication date

1 January 2008

1 reference

Current Topics in Developmental Biology

20 August 2017

published in

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20 August 2017

volume

84

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20 August 2017

page(s)

431-453

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How calcium influx through calcium leak channels is responsible for the elevated levels of calcium-dependent proteolysis in dystrophic myotubes

20 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathology

1 reference

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7 January 2021

A cluster of basic repeats in the dystrophin rod domain binds F-actin through an electrostatic interaction

1 reference

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7 January 2021

The postsynaptic submembrane machinery at the neuromuscular junction: requirement for rapsyn and the utrophin/dystrophin-associated complex.

1 reference

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7 January 2021

Functional capacity of dystrophins carrying deletions in the N-terminal actin-binding domain

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Dynamics of myoblast transplantation reveal a discrete minority of precursors with stem cell-like properties as the myogenic source

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Histopathological changes in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Multipotential mesoangioblast stem cell therapy in the mdx/utrn-/- mouse model for Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Function and genetics of dystrophin and dystrophin-related proteins in muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Lateral Force Transmission Across Costameres in Skeletal Muscle

1 reference

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7 January 2021

Ca2+-independent phospholipase A2 enhances store-operated Ca2+ entry in dystrophic skeletal muscle fibers

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Intrinsic changes and extrinsic influences of myogenic stem cell function during aging

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Studies of sarcolemmal integrity in myopathic muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Stem cell treatment of dystrophic dogs

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Rapid recovery following contraction-induced injury to in situ skeletal muscles in mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

X chromosome-linked muscular dystrophy (mdx) in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

A second promoter provides an alternative target for therapeutic up-regulation of utrophin in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Adult dystrophic (mdx) endplates exhibit reduced quantal size and enhanced quantal variation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Imbalance between pSmad3 and Notch induces CDK inhibitors in old muscle stem cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter study

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Dystrophin-deficient mdx mice display a reduced life span and are susceptible to spontaneous rhabdomyosarcoma.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Dystrophin gene transcribed from different promoters in neuronal and glial cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Tissue Doppler assessment of diastolic and systolic alterations of radial and longitudinal left ventricular motions in Golden Retrievers during the preclinical phase of cardiomyopathy associated with muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Tissue Doppler imaging detects early asymptomatic myocardial abnormalities in a dog model of Duchenne?s cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Eccentric contraction injury in dystrophic canine muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Stem cell function, self-renewal, and behavioral heterogeneity of cells from the adult muscle satellite cell niche.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Notch-mediated restoration of regenerative potential to aged muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Rejuvenation of aged progenitor cells by exposure to a young systemic environment

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

A novel dystrophin isoform is required for normal retinal electrophysiology

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

The frequency of revertants in mdx mouse genetic models for Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Functional skeletal muscle regeneration from differentiating embryonic stem cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Pathophysiology of duchenne muscular dystrophy: current hypotheses

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Postsynaptic abnormalities at the neuromuscular junctions of utrophin-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Pericytes of human skeletal muscle are myogenic precursors distinct from satellite cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Tibialis anterior muscles in mdx mice are highly susceptible to contraction-induced injury

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Body-wide gene therapy of Duchenne muscular dystrophy in the mdx mouse model.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Bone marrow stromal cells generate muscle cells and repair muscle degeneration.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

1 reference

7 January 2021

Costameres: the Achilles' heel of Herculean muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Dystrophin, its interactions with other proteins, and implications for muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Diaphragm muscle strip preparation for evaluation of gene therapies in mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Muscle regeneration by bone marrow-derived myogenic progenitors

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Morpholino oligomer-mediated exon skipping averts the onset of dystrophic pathology in the mdx mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

The role of Ca2+ in muscle cell damage

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Rescue of dystrophic muscle through U7 snRNA-mediated exon skipping

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Systemic delivery of genes to striated muscles using adeno-associated viral vectors.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

rAAV6-microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Role of dystrophin and utrophin for assembly and function of the dystrophin glycoprotein complex in non-muscle tissue

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

PGC-1alpha regulates the neuromuscular junction program and ameliorates Duchenne muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Differential expression of dystrophin isoforms in strains of mdx mice with different mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Utrophin deficiency worsens cardiac contractile dysfunction present in dystrophin-deficient mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Sildenafil and cardiomyocyte-specific cGMP signaling prevent cardiomyopathic changes associated with dystrophin deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Pharmacological strategies for muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Naturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Asymmetric self-renewal and commitment of satellite stem cells in muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Sub-domains of the dystrophin rod domain display contrasting lipid-binding and stability properties

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Skeletal muscle satellite cells and adult myogenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Dp140: a novel 140 kDa CNS transcript from the dystrophin locus

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

An autosomal transcript in skeletal muscle with homology to dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Role of contraction-induced injury in the mechanisms of muscle damage in muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Structure and function of the neuromuscular junction in young adultmdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Visualization of dystrophic muscle fibers in mdx mouse by vital staining with Evans blue: evidence of apoptosis in dystrophin-deficient muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Increased susceptibility of EDL muscles from mdx mice to damage induced by contractions with stretch

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Direct isolation of satellite cells for skeletal muscle regeneration.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Long-term persistence and migration of myogenic cells injected into pre-irradiated muscles of mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Genetic treatments in muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Deletions in the 5' region of dystrophin and resulting phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Dystrophin and mutations: one gene, several proteins, multiple phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Interactions between neutrophils and macrophages promote macrophage killing of rat muscle cells in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Muscle lesions associated with dystrophin deficiency in neonatal golden retriever puppies

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Proximal Dystrophin Gene Deletions and Protein Alterations in Becker Muscular Dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Microutrophin delivery through rAAV6 increases lifespan and improves muscle function in dystrophic dystrophin/utrophin-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Creatine kinase, cell membrane and Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Hematopoietic cell transplantation provides an immune-tolerant platform for myoblast transplantation in dystrophic dogs

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Disciplining the stem cell into myogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Dystrophin protects the sarcolemma from stresses developed during muscle contraction

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patient

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Dystrophin and utrophin influence fiber type composition and post-synaptic membrane structure.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Muscle cells from mdx mice have an increased susceptibility to oxidative stress

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Alteration in calcium handling at the subcellular level in mdx myotubes.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

A translational approach for limb vascular delivery of the micro-dystrophin gene without high volume or high pressure for treatment of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Utrophin binds laterally along actin filaments and can couple costameric actin with sarcolemma when overexpressed in dystrophin-deficient muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Dystrophin and utrophin bind actin through distinct modes of contact

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Structural cooperativity in spectrin type repeats motifs of dystrophin

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Cell Therapy of -Sarcoglycan Null Dystrophic Mice Through Intra-Arterial Delivery of Mesoangioblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Sampaolesi et al. reply

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Alternative dystrophin gene transcripts in golden retriever muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Molecular analysis of a spontaneous dystrophin 'knockout' dog.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Extension of murine life span by overexpression of catalase targeted to mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Analyses of the differentiation potential of satellite cells from myoD-/-, mdx, and PMP22 C22 mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Skeletal muscle satellite cells: changes in proliferation potential as a function of age

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Canine X-linked muscular dystrophy in Japan (CXMDJ)

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

The molecular basis of muscular dystrophy in the mdx mouse: a point mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Structural determinants of the reliability of synaptic transmission at the vertebrate neuromuscular junction

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Overexpression of a calpastatin transgene in mdx muscle reduces dystrophic pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Mechanosensitive channel properties and membrane mechanics in mouse dystrophic myotubes

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Amino-terminal deletion of 53% of dystrophin results in an intermediate Duchenne-Becker muscular dystrophy phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

The role of free radicals in the pathophysiology of muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Expression of full-length utrophin prevents muscular dystrophy in mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Canine X-linked muscular dystrophy: Selective involvement of muscles in neonatal dogs

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Canine X-linked muscular dystrophy. An animal model of Duchenne muscular dystrophy: clinical studies.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Canine X-linked muscular dystrophy as an animal model of Duchenne muscular dystrophy: a review

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Prevention of the dystrophic phenotype in dystrophin/utrophin-deficient muscle following adenovirus-mediated transfer of a utrophin minigene

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Adeno-associated virus serotype 8 efficiently delivers genes to muscle and heart

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Sustained AAV-mediated dystrophin expression in a canine model of Duchenne muscular dystrophy with a brief course of immunosuppression

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Expression of Dp260 in muscle tethers the actin cytoskeleton to the dystrophin-glycoprotein complex and partially prevents dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Accelerated age-related decline in replicative life-span of Duchenne muscular dystrophy myoblasts: implications for cell and gene therapy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

A nitric oxide synthase transgene ameliorates muscular dystrophy in mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

A- and B-utrophin have different expression patterns and are differentially up-regulated in mdx muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

PTC124 targets genetic disorders caused by nonsense mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

N-Acetylcysteine ameliorates skeletal muscle pathophysiology in mdx mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Effects of stretch-activated channel blockers on [Ca2+]i and muscle damage in the mdx mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

C-terminal-truncated microdystrophin recruits dystrobrevin and syntrophin to the dystrophin-associated glycoprotein complex and reduces muscular dystrophy in symptomatic utrophin/dystrophin double-knockout mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

Dystrophin and a dystrophin-related protein in intrafusal muscle fibers, and neuromuscular and myotendinous junctions

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900609-1

7 January 2021

10.1016/S0070-2153(08)00609-1

Identifiers

DOI

1 reference

20 August 2017

1 reference