In vivo MRI characterization of progressive cardiac dysfunction in the mdx mouse model of muscular dystrophy.
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Hierarchical accumulation of RyR post-translational modifications drives disease progression in dystrophic cardiomyopathyMyocardial reperfusion injury: looking beyond primary PCIMulti-parametric MRI at 14T for muscular dystrophy mice treated with AAV vector-mediated gene therapyCurrent understanding of molecular pathology and treatment of cardiomyopathy in duchenne muscular dystrophyNon-invasive MRI and spectroscopy of mdx mice reveal temporal changes in dystrophic muscle imaging and in energy deficitsPrevention of exercised induced cardiomyopathy following Pip-PMO treatment in dystrophic mdx mice.Beta-blockers, left and right ventricular function, and in-vivo calcium influx in muscular dystrophy cardiomyopathy.The role of 1.5 tesla MRI and anesthetic regimen concerning cardiac analysis in mice with cardiomyopathyCardiomyocyte Regeneration in the mdx Mouse Model of Nonischemic CardiomyopathyFocal but reversible diastolic sheet dysfunction reflects regional calcium mishandling in dystrophic mdx mouse hearts.Coronary adventitial cells are linked to perivascular cardiac fibrosis via TGFβ1 signaling in the mdx mouse model of Duchenne muscular dystrophy.Non-invasive MRI biomarkers for the early assessment of iron overload in a humanized mouse model of β-thalassemia.Right ventricular dysfunction in the R6/2 transgenic mouse model of Huntington's disease is unmasked by dobutamineWhat has the mdx mouse model of Duchenne muscular dystrophy contributed to our understanding of this disease?Drug Discovery of Therapies for Duchenne Muscular Dystrophy.Quantitative MRI biomarkers to characterize regional left ventricular perfusion and function in nonhuman primates during dobutamine-induced stress: A reproducibility and reliability study.High field magnetic resonance imaging of rodents in cardiovascular research.Murine cardiosphere-derived cells are impaired by age but not by cardiac dystrophic dysfunction.Heart structural remodeling in a mouse model of Duchenne cardiomyopathy revealed using optical polarization tractography [Invited].Implications for Cardiac Function Following Rescue of the Dystrophic Diaphragm in a Mouse Model of Duchenne Muscular Dystrophy.Proteomic profiling of cardiomyopathic tissue from the aged mdx model of Duchenne muscular dystrophy reveals a drastic decrease in laminin, nidogen and annexin.Suramin attenuates dystrophin-deficient cardiomyopathy in the mdx mouse model of duchenne muscular dystrophy.Left Atrial Volume and Pulmonary Artery Diameter Are Noninvasive Measures of Age-Related Diastolic Dysfunction in Mice.Resveratrol Ameliorates Mitophagy Disturbance and Improves Cardiac Pathophysiology of Dystrophin-deficient mdx MiceMicro-utrophin Improves Cardiac and Skeletal Muscle Function of Severely Affected D2/ Mice
P2860
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P2860
In vivo MRI characterization of progressive cardiac dysfunction in the mdx mouse model of muscular dystrophy.
description
2012 nî lūn-bûn
@nan
2012 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
In vivo MRI characterization o ...... e model of muscular dystrophy.
@ast
In vivo MRI characterization o ...... e model of muscular dystrophy.
@en
In vivo MRI characterization o ...... e model of muscular dystrophy.
@nl
type
label
In vivo MRI characterization o ...... e model of muscular dystrophy.
@ast
In vivo MRI characterization o ...... e model of muscular dystrophy.
@en
In vivo MRI characterization o ...... e model of muscular dystrophy.
@nl
prefLabel
In vivo MRI characterization o ...... e model of muscular dystrophy.
@ast
In vivo MRI characterization o ...... e model of muscular dystrophy.
@en
In vivo MRI characterization o ...... e model of muscular dystrophy.
@nl
P2860
P50
P1433
P1476
In vivo MRI characterization o ...... se model of muscular dystrophy
@en
P2093
Kay E Davies
Kieran Clarke
P2860
P304
P356
10.1371/JOURNAL.PONE.0028569
P407
P577
2012-01-03T00:00:00Z