Age-matched comparison reveals early electrocardiography and echocardiography changes in dystrophin-deficient dogs.
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Quantitative phenotyping of Duchenne muscular dystrophy dogs by comprehensive gait analysis and overnight activity monitoringAnimal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapyNight Activity Reduction is a Signature Physiological Biomarker for Duchenne Muscular Dystrophy Dogs.The golden retriever model of Duchenne muscular dystrophy.Systemic gene transfer reveals distinctive muscle transduction profile of tyrosine mutant AAV-1, -6, and -9 in neonatal dogs.Pharmacologic management of Duchenne muscular dystrophy: target identification and preclinical trialsCharacterization of 65 epitope-specific dystrophin monoclonal antibodies in canine and murine models of duchenne muscular dystrophy by immunostaining and western blot.AAV-8 is more efficient than AAV-9 in transducing neonatal dog heart.Duchenne muscular dystrophy gene therapy in the canine model.A simplified immune suppression scheme leads to persistent micro-dystrophin expression in Duchenne muscular dystrophy dogsHumoral immunity to AAV-6, 8, and 9 in normal and dystrophic dogsContemporary cardiac issues in Duchenne muscular dystrophy. Working Group of the National Heart, Lung, and Blood Institute in collaboration with Parent Project Muscular Dystrophy.Safe and bodywide muscle transduction in young adult Duchenne muscular dystrophy dogs with adeno-associated virus.Non-invasive evaluation of muscle disease in the canine model of Duchenne muscular dystrophy by electrical impedance myography.Microdystrophin ameliorates muscular dystrophy in the canine model of duchenne muscular dystrophyProgress in gene therapy of dystrophic heart disease.Long-term robust myocardial transduction of the dog heart from a peripheral vein by adeno-associated virus serotype-8.Canine models of Duchenne muscular dystrophy and their use in therapeutic strategies.Dual AAV gene therapy for Duchenne muscular dystrophy with a 7-kb mini-dystrophin gene in the canine model.A Five-Repeat Micro-Dystrophin Gene Ameliorated Dystrophic Phenotype in the Severe DBA/2J-mdx Model of Duchenne Muscular Dystrophy.Dystrophin deficiency compromises force production of the extensor carpi ulnaris muscle in the canine model of Duchenne muscular dystrophy.
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Age-matched comparison reveals early electrocardiography and echocardiography changes in dystrophin-deficient dogs.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh-hant
name
Age-matched comparison reveals ...... in dystrophin-deficient dogs.
@ast
Age-matched comparison reveals ...... in dystrophin-deficient dogs.
@en
type
label
Age-matched comparison reveals ...... in dystrophin-deficient dogs.
@ast
Age-matched comparison reveals ...... in dystrophin-deficient dogs.
@en
prefLabel
Age-matched comparison reveals ...... in dystrophin-deficient dogs.
@ast
Age-matched comparison reveals ...... in dystrophin-deficient dogs.
@en
P2093
P2860
P1476
Age-matched comparison reveals ...... in dystrophin-deficient dogs.
@en
P2093
Bruce F Smith
Deborah M Fine
Dietrich Volkmann
Jin-Hong Shin
Mark McIntosh
Stacey B Leach
Yongping Yue
P2860
P304
P356
10.1016/J.NMD.2011.03.010
P577
2011-05-13T00:00:00Z