Electrocardiographic findings in mdx mice: a cardiac phenotype of Duchenne muscular dystrophy.
about
NOS1AP modulates intracellular Ca(2+) in cardiac myocytes and is up-regulated in dystrophic cardiomyopathyHierarchical accumulation of RyR post-translational modifications drives disease progression in dystrophic cardiomyopathyDeficiency in Cardiac Dystrophin Affects the Abundance of the $\alpha$ -/ $\beta$ -Dystroglycan ComplexProteomic profiling of the dystrophin-deficient mdx phenocopy of dystrophinopathy-associated cardiomyopathyCurrent understanding of molecular pathology and treatment of cardiomyopathy in duchenne muscular dystrophyProteomic analysis reveals new cardiac-specific dystrophin-associated proteinsDevelopment of electrocardiogram intervals during growth of FVB/N neonate mice.Proteomic Profiling of the Dystrophin-Deficient MDX Heart Reveals Drastically Altered Levels of Key Metabolic and Contractile Proteins.Adeno-associated virus serotype-9 microdystrophin gene therapy ameliorates electrocardiographic abnormalities in mdx mice.Lengthening-contractions in isolated myocardium impact force development and worsen cardiac contractile function in the mdx mouse model of muscular dystrophy.Lack of tryptophan hydroxylase-1 in mice results in gait abnormalities.Cerebellar ataxia, seizures, premature death, and cardiac abnormalities in mice with targeted disruption of the Cacna2d2 gene.Neurocardiovascular regulation in mice: experimental approaches and novel findings.Decreased mtDNA, oxidative stress, cardiomyopathy, and death from transgenic cardiac targeted human mutant polymerase gamma.Angiotensin-dependent autonomic dysregulation precedes dilated cardiomyopathy in a mouse model of muscular dystrophy.AAV micro-dystrophin gene therapy alleviates stress-induced cardiac death but not myocardial fibrosis in >21-m-old mdx mice, an end-stage model of Duchenne muscular dystrophy cardiomyopathy.Cardiac phenotype of Duchenne Muscular Dystrophy: insights from cellular studiesAutonomic dysfunction in muscular dystrophy: a theoretical framework for muscle reflex involvement.Evaluation of the therapeutic utility of phosphodiesterase 5A inhibition in the mdx mouse model of duchenne muscular dystrophy.Cardiac and respiratory dysfunction in Duchenne muscular dystrophy and the role of second messengers.Diastolic dysfunction precedes hypoxia-induced mortality in dystrophic mice.Developmental Changes in the ECG of a Hamster Model of Muscular Dystrophy and Heart Failure.Improvement of cardiac fibrosis in dystrophic mice by rAAV9-mediated microdystrophin transduction.Transient receptor potential channel 6 regulates abnormal cardiac S-nitrosylation in Duchenne muscular dystrophy.HIV viral protein R causes atrial cardiomyocyte mitosis, mesenchymal tumor, dysrhythmia, and heart failure.
P2860
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P2860
Electrocardiographic findings in mdx mice: a cardiac phenotype of Duchenne muscular dystrophy.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Electrocardiographic findings ...... f Duchenne muscular dystrophy.
@en
Electrocardiographic findings ...... f Duchenne muscular dystrophy.
@nl
type
label
Electrocardiographic findings ...... f Duchenne muscular dystrophy.
@en
Electrocardiographic findings ...... f Duchenne muscular dystrophy.
@nl
prefLabel
Electrocardiographic findings ...... f Duchenne muscular dystrophy.
@en
Electrocardiographic findings ...... f Duchenne muscular dystrophy.
@nl
P2093
P2860
P356
P1433
P1476
Electrocardiographic findings ...... f Duchenne muscular dystrophy.
@en
P2093
Ivo Amende
James P Morgan
Jose M Otero
Matthew F Sullivan
Orlando Lopez
Thomas G Hampton
Victor Chu
P2860
P304
P356
10.1002/MUS.10223
P577
2002-10-01T00:00:00Z