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In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy

Science (American Association for the Advancement of Science), 2016-01, Vol.351 (6271), p.403-407

2016

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Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy

Disease models & mechanisms, 2015-03, Vol.8 (3), p.195-213

2015

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Four-limb wireless IMU sensor system for automatic gait detection in canines

Scientific reports, 2022-03, Vol.12 (1), p.4788-4788, Article 4788

2022

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Dystrophin contains multiple independent membrane-binding domains

Human molecular genetics, 2016-09, Vol.25 (17), p.3647-3653

2016

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Non-invasive evaluation of muscle disease in the canine model of Duchenne muscular dystrophy by electrical impedance myography

PloS one, 2017-03, Vol.12 (3), p.e0173557-e0173557

2017

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The passive mechanical properties of the extensor digitorum longus muscle are compromised in 2- to 20-mo-old mdx mice

Journal of applied physiology (1985), 2011-06, Vol.110 (6), p.1656-1663

2011

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Automatic characterization of stride parameters in canines with a single wearable inertial sensor

PloS one, 2018-06, Vol.13 (6), p.e0198893-e0198893

2018

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Extensor carpi ulnaris muscle shows unexpected slow-to-fast fiber-type switch in Duchenne muscular dystrophy dogs

Disease models & mechanisms, 2021-12, Vol.14 (12)

2021

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Dystrophin deficiency compromises force production of the extensor carpi ulnaris muscle in the canine model of Duchenne muscular dystrophy

PloS one, 2012-09, Vol.7 (9), p.e44438-e44438

2012

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Nanotherapy for Duchenne muscular dystrophy

Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology, 2018-03, Vol.10 (2), p.e1472-n/a

2018

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Evaluation of muscle function of the extensor digitorum longus muscle ex vivo and tibialis anterior muscle in situ in mice

Journal of visualized experiments, 2013-02 (72)

2013

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A Five-Repeat Micro-Dystrophin Gene Ameliorated Dystrophic Phenotype in the Severe DBA/2J-mdx Model of Duchenne Muscular Dystrophy

Molecular therapy. Methods & clinical development, 2017-09, Vol.6 (C), p.216-230

2017

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SERCA2a overexpression improves muscle function in a canine Duchenne muscular dystrophy model

Molecular therapy. Methods & clinical development, 2024-06, Vol.32 (2), p.101268, Article 101268

2024

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Alpha 7 integrin preserves the function of the extensor digitorum longus muscle in dystrophin-null mice

Journal of applied physiology (1985), 2013-11, Vol.115 (9), p.1388-1392

2013

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Quantitative phenotyping of Duchenne muscular dystrophy dogs by comprehensive gait analysis and overnight activity monitoring

PloS one, 2013-03, Vol.8 (3), p.e59875-e59875

2013

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Temperature effects on morphological integrity and Ca²⁺ signaling in freshly isolated murine feed artery endothelial cell tubes

American journal of physiology. Heart and circulatory physiology, 2011-09, Vol.301 (3), p.H773-H783

2011

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Micro-dystrophin AAV Vectors Made by Transient Transfection and Herpesvirus System Are Equally Potent in Treating mdx Mouse Muscle Disease

Molecular therapy. Methods & clinical development, 2020-09, Vol.18, p.664-678

2020

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Safe and bodywide muscle transduction in young adult Duchenne muscular dystrophy dogs with adeno-associated virus

Human molecular genetics, 2015-10, Vol.24 (20), p.5880-5890

2015

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Widespread severe myodegeneration in a compound heterozygote female dog with dystrophin deficiency

Veterinary medicine and science, 2021-05, Vol.7 (3), p.654-659

2021

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Dual AAV Gene Therapy for Duchenne Muscular Dystrophy with a 7-kb Mini-Dystrophin Gene in the Canine Model

Human gene therapy, 2018-03, Vol.29 (3), p.299-311

2018

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Cas9-specific immune responses compromise local and systemic AAV CRISPR therapy in multiple dystrophic canine models

Nature communications, 2021-11, Vol.12 (1), p.6769-12, Article 6769

2021

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AAV-8 is more efficient than AAV-9 in transducing neonatal dog heart

Human gene therapy. Part B. Methods, 2015-04, Vol.26 (2), p.54-61

2015

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AAV9 Edits Muscle Stem Cells in Normal and Dystrophic Adult Mice

Molecular therapy, 2019-09, Vol.27 (9), p.1568-1585

2019

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Microdystrophin Ameliorates Muscular Dystrophy in the Canine Model of Duchenne Muscular Dystrophy

Molecular therapy, 2013-04, Vol.21 (4), p.750-757

2013

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Dual AAV therapy ameliorates exercise-induced muscle injury and functional ischemia in murine models of Duchenne muscular dystrophy

Human molecular genetics, 2013-09, Vol.22 (18), p.3720-3729

2013

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In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy

Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy

Four-limb wireless IMU sensor system for automatic gait detection in canines

Dystrophin contains multiple independent membrane-binding domains

Non-invasive evaluation of muscle disease in the canine model of Duchenne muscular dystrophy by electrical impedance myography

The passive mechanical properties of the extensor digitorum longus muscle are compromised in 2- to 20-mo-old mdx mice

Automatic characterization of stride parameters in canines with a single wearable inertial sensor

Extensor carpi ulnaris muscle shows unexpected slow-to-fast fiber-type switch in Duchenne muscular dystrophy dogs

Dystrophin deficiency compromises force production of the extensor carpi ulnaris muscle in the canine model of Duchenne muscular dystrophy

Nanotherapy for Duchenne muscular dystrophy

Evaluation of muscle function of the extensor digitorum longus muscle ex vivo and tibialis anterior muscle in situ in mice

A Five-Repeat Micro-Dystrophin Gene Ameliorated Dystrophic Phenotype in the Severe DBA/2J-mdx Model of Duchenne Muscular Dystrophy

SERCA2a overexpression improves muscle function in a canine Duchenne muscular dystrophy model

Alpha 7 integrin preserves the function of the extensor digitorum longus muscle in dystrophin-null mice

Quantitative phenotyping of Duchenne muscular dystrophy dogs by comprehensive gait analysis and overnight activity monitoring

Temperature effects on morphological integrity and Ca²⁺ signaling in freshly isolated murine feed artery endothelial cell tubes

Micro-dystrophin AAV Vectors Made by Transient Transfection and Herpesvirus System Are Equally Potent in Treating mdx Mouse Muscle Disease

Safe and bodywide muscle transduction in young adult Duchenne muscular dystrophy dogs with adeno-associated virus

Widespread severe myodegeneration in a compound heterozygote female dog with dystrophin deficiency

Dual AAV Gene Therapy for Duchenne Muscular Dystrophy with a 7-kb Mini-Dystrophin Gene in the Canine Model

Cas9-specific immune responses compromise local and systemic AAV CRISPR therapy in multiple dystrophic canine models

AAV-8 is more efficient than AAV-9 in transducing neonatal dog heart

AAV9 Edits Muscle Stem Cells in Normal and Dystrophic Adult Mice

Microdystrophin Ameliorates Muscular Dystrophy in the Canine Model of Duchenne Muscular Dystrophy

Dual AAV therapy ameliorates exercise-induced muscle injury and functional ischemia in murine models of Duchenne muscular dystrophy

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