Use of the dog model for Duchenne muscular dystrophy in gene therapy trials.
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Man's best friend becomes biology's best in show: genome analyses in the domestic dogDystrophin deficiency in canine X-linked muscular dystrophy in Japan (CXMDJ) alters myosin heavy chain expression profiles in the diaphragm more markedly than in the tibialis cranialis muscle.Mammalian models of Duchenne Muscular Dystrophy: pathological characteristics and therapeutic applications.Duchenne muscular dystrophy gene therapy: Lost in translation?An Intronic SINE insertion in FAM161A that causes exon-skipping is associated with progressive retinal atrophy in Tibetan Spaniels and Tibetan TerriersMotor physical therapy affects muscle collagen type I and decreases gait speed in dystrophin-deficient dogs.Wild-type mouse models to screen antisense oligonucleotides for exon-skipping efficacy in Duchenne muscular dystrophy.Duchenne's muscular dystrophy: animal models used to investigate pathogenesis and develop therapeutic strategies.Understanding hereditary diseases using the dog and human as companion model systems.GRMD cardiac and skeletal muscle metabolism gene profiles are distinctCardiac Niche Influences the Direct Reprogramming of Canine Fibroblasts into Cardiomyocyte-Like Cells.Translating golden retriever muscular dystrophy microarray findings to novel biomarkers for cardiac/skeletal muscle function in Duchenne muscular dystrophy.Muscular dystrophy associated with alpha-dystroglycan deficiency in Sphynx and Devon Rex cats.Kinematics of gait in golden retriever muscular dystrophy.Gene therapy in large animal models of muscular dystrophy.Gene transfer into canine myoblasts.Dystrophin deficiency compromises force production of the extensor carpi ulnaris muscle in the canine model of Duchenne muscular dystrophy.A novel mutation in TTC8 is associated with progressive retinal atrophy in the golden retriever.Antisense oligonucleotide-induced exon skipping restores dystrophin expression in vitro in a canine model of DMD.Abnormal carbohydrate metabolism in a canine model for muscular dystrophy.Multiple Species Comparison of Cardiac Troponin T and Dystrophin: Unravelling the DNA behind Dilated Cardiomyopathy.
P2860
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P2860
Use of the dog model for Duchenne muscular dystrophy in gene therapy trials.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
Use of the dog model for Duchenne muscular dystrophy in gene therapy trials.
@en
Use of the dog model for Duchenne muscular dystrophy in gene therapy trials.
@nl
type
label
Use of the dog model for Duchenne muscular dystrophy in gene therapy trials.
@en
Use of the dog model for Duchenne muscular dystrophy in gene therapy trials.
@nl
prefLabel
Use of the dog model for Duchenne muscular dystrophy in gene therapy trials.
@en
Use of the dog model for Duchenne muscular dystrophy in gene therapy trials.
@nl
P2093
P1476
Use of the dog model for Duchenne muscular dystrophy in gene therapy trials
@en
P2093
P304
P356
10.1016/S0960-8966(97)00057-6
P577
1997-07-01T00:00:00Z