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Microtubule binding distinguishes dystrophin from utrophin

Proceedings of the National Academy of Sciences - PNAS, 2014-04, Vol.111 (15), p.5723-5728

2014

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Microutrophin expression in dystrophic mice displays myofiber type differences in therapeutic effects

PLoS genetics, 2020-11, Vol.16 (11), p.e1009179-e1009179

2020

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Fnip1 regulates skeletal muscle fiber type specification, fatigue resistance, and susceptibility to muscular dystrophy

Proceedings of the National Academy of Sciences - PNAS, 2015-01, Vol.112 (2), p.424-429

2015

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Prevention of muscle aging by myofiber-associated satellite cell transplantation

Science translational medicine, 2010-11, Vol.2 (57), p.57ra83

2010

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Successful Regional Delivery and Long-term Expression of a Dystrophin Gene in Canine Muscular Dystrophy: A Preclinical Model for Human Therapies

Molecular therapy, 2012-08, Vol.20 (8), p.1501-1507

2012

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Muscle structure influences utrophin expression in mdx mice

PLoS genetics, 2014-06, Vol.10 (6), p.e1004431-e1004431

2014

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The polyproline site in hinge 2 influences the functional capacity of truncated dystrophins

PLoS genetics, 2010-05, Vol.6 (5), p.e1000958-e1000958

2010

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Dramatic elevation in urinary amino terminal titin fragment excretion quantified by immunoassay in duchenne muscular dystrophy patients and in dystrophin deficient rodents

Neuromuscular disorders : NMD, 2017-07, Vol.27 (7), p.635-645

2017

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Truncated dystrophins can influence neuromuscular synapse structure

Molecular and cellular neuroscience, 2009-04, Vol.40 (4), p.433-441

2009

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Loss of niche-satellite cell interactions in syndecan-3 null mice alters muscle progenitor cell homeostasis improving muscle regeneration

Skeletal muscle, 2016-10, Vol.6 (1), p.34-34, Article 34

2016

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Molecular and cellular adaptations to chronic myotendinous strain injury in mdx mice expressing a truncated dystrophin

Human molecular genetics, 2008-12, Vol.17 (24), p.3975-3986

2008

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Chapter 9 The Value of Mammalian Models for Duchenne Muscular Dystrophy in Developing Therapeutic Strategies

Current Topics in Developmental Biology, 2008, Vol.84, p.431-453

2008

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

Current topics in developmental biology, 2008, Vol.84, p.431-453

2008

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Glycinergic and GABAergic Synaptic Activity Differentially Regulate Motoneuron Survival and Skeletal Muscle Innervation

The Journal of neuroscience, 2005-02, Vol.25 (5), p.1249-1259

2005

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Myofiber branching rather than myofiber hyperplasia contributes to muscle hypertrophy in mdx mice

Skeletal muscle, 2014-05, Vol.4 (1), p.10-10, Article 10

2014

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Expression of the dystrophin isoform Dp116 preserves functional muscle mass and extends lifespan without preventing dystrophy in severely dystrophic mice

Human molecular genetics, 2011-12, Vol.20 (24), p.4978-4990

2011

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Sequencing protocols to genotype mdx, mdx(4cv), and mdx(5cv) mice

Muscle & nerve, 2010-08, Vol.42 (2), p.268-270

2010

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Neuromuscular synapses mediate motor axon branching and motoneuron survival during the embryonic period of programmed cell death

Developmental biology, 2003-05, Vol.257 (1), p.71-84

2003

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

Human molecular genetics, 2007-09, Vol.16 (17), p.2105-2113

2007

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rAAV6-Microdystrophin Rescues Aberrant Golgi Complex Organization in mdx Skeletal Muscles

Traffic (Copenhagen, Denmark), 2007-10, Vol.8 (10), p.1424-1439

2007

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Preclinical Studies for Gene Therapy of Duchenne Muscular Dystrophy

Journal of child neurology, 2010-09, Vol.25 (9), p.1149-1157

2010

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Sequencing protocols to genotype mdx, mdx4cv, and mdx5cv mice

Muscle & nerve, 2010-08, Vol.42 (2), p.268-270

2010

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Animal Models of Muscular Dystrophy

Animal Models of Molecular Pathology, 2012, Vol.105, p.83-111

2012

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Elucidating the molecular mechanisms that underlie the target control of motoneuron death

The International journal of developmental biology, 2002, Vol.46 (4), p.551

2002

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Relevance of motoneuron specification and programmed cell death in embryos to therapy of ALS

Birth defects research. Part C. Embryo today, 2005-12, Vol.75 (4), p.294-304

2005

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Microtubule binding distinguishes dystrophin from utrophin

Microutrophin expression in dystrophic mice displays myofiber type differences in therapeutic effects

Fnip1 regulates skeletal muscle fiber type specification, fatigue resistance, and susceptibility to muscular dystrophy

Prevention of muscle aging by myofiber-associated satellite cell transplantation

Successful Regional Delivery and Long-term Expression of a Dystrophin Gene in Canine Muscular Dystrophy: A Preclinical Model for Human Therapies

Muscle structure influences utrophin expression in mdx mice

The polyproline site in hinge 2 influences the functional capacity of truncated dystrophins

Dramatic elevation in urinary amino terminal titin fragment excretion quantified by immunoassay in duchenne muscular dystrophy patients and in dystrophin deficient rodents

Truncated dystrophins can influence neuromuscular synapse structure

Loss of niche-satellite cell interactions in syndecan-3 null mice alters muscle progenitor cell homeostasis improving muscle regeneration

Molecular and cellular adaptations to chronic myotendinous strain injury in mdx mice expressing a truncated dystrophin

Chapter 9 The Value of Mammalian Models for Duchenne Muscular Dystrophy in Developing Therapeutic Strategies

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

Glycinergic and GABAergic Synaptic Activity Differentially Regulate Motoneuron Survival and Skeletal Muscle Innervation

Myofiber branching rather than myofiber hyperplasia contributes to muscle hypertrophy in mdx mice

Expression of the dystrophin isoform Dp116 preserves functional muscle mass and extends lifespan without preventing dystrophy in severely dystrophic mice

Sequencing protocols to genotype mdx, mdx(4cv), and mdx(5cv) mice

Neuromuscular synapses mediate motor axon branching and motoneuron survival during the embryonic period of programmed cell death

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

rAAV6-Microdystrophin Rescues Aberrant Golgi Complex Organization in mdx Skeletal Muscles

Preclinical Studies for Gene Therapy of Duchenne Muscular Dystrophy

Sequencing protocols to genotype mdx, mdx4cv, and mdx5cv mice

Animal Models of Muscular Dystrophy

Elucidating the molecular mechanisms that underlie the target control of motoneuron death

Relevance of motoneuron specification and programmed cell death in embryos to therapy of ALS

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