Early onset of lipofuscin accumulation in dystrophin-deficient skeletal muscles of DMD patients and mdx mice.
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The Dietary Supplement Protandim® Decreases Plasma Osteopontin and Improves Markers of Oxidative Stress in Muscular Dystrophy Mdx MiceLong-term blinded placebo-controlled study of SNT-MC17/idebenone in the dystrophin deficient mdx mouse: cardiac protection and improved exercise performanceIdentification of Atypical Peri-Nuclear Multivesicular Bodies in Oxidative and Glycolytic Skeletal Muscle of Aged and Pompe's Disease Mouse Models.Are human and mouse satellite cells really the same?Sialylation and muscle performance: sialic acid is a marker of muscle ageing.Lipid peroxidation inhibition blunts nuclear factor-kappaB activation, reduces skeletal muscle degeneration, and enhances muscle function in mdx mice.Quantification of ceroid and lipofuscin in skeletal muscle.Modulation of p38 mitogen-activated protein kinase cascade and metalloproteinase activity in diaphragm muscle in response to free radical scavenger administration in dystrophin-deficient Mdx mice.A novel mechanism of autophagic cell death in dystrophic muscle regulated by P2RX7 receptor large-pore formation and HSP90.Quantitative evaluation of the beneficial effects in the mdx mouse of epigallocatechin gallate, an antioxidant polyphenol from green tea.The value of muscle biopsies in Pompe disease: identifying lipofuscin inclusions in juvenile- and adult-onset patientsContribution of oxidative stress to pathology in diaphragm and limb muscles with Duchenne muscular dystrophy.Oxidative stress and pathology in muscular dystrophies: focus on protein thiol oxidation and dysferlinopathies.Oxidative stress in muscular dystrophy: from generic evidence to specific sources and targets.Sarcolemmal damage in dystrophin deficiency is modulated by synergistic interactions between mechanical and oxidative/nitrosative stressesOxidative damage in muscular dystrophy correlates with the severity of the pathology: role of glutathione metabolism.The high correlation between counts and area fractions of lipofuscin granules, a biomarker of oxidative stress in muscular dystrophies.Protein thiol oxidation does not change in skeletal muscles of aging female mice.Ultra-structural time-course study in the C. elegans model for Duchenne muscular dystrophy highlights a crucial role for sarcomere-anchoring structures and sarcolemma integrity in the earliest steps of the muscle degeneration process.Fascial preadipocytes: another missing piece of the puzzle to understand fibromyalgia?
P2860
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P2860
Early onset of lipofuscin accumulation in dystrophin-deficient skeletal muscles of DMD patients and mdx mice.
description
2004 nî lūn-bûn
@nan
2004 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Early onset of lipofuscin accu ...... of DMD patients and mdx mice.
@ast
Early onset of lipofuscin accu ...... of DMD patients and mdx mice.
@en
type
label
Early onset of lipofuscin accu ...... of DMD patients and mdx mice.
@ast
Early onset of lipofuscin accu ...... of DMD patients and mdx mice.
@en
prefLabel
Early onset of lipofuscin accu ...... of DMD patients and mdx mice.
@ast
Early onset of lipofuscin accu ...... of DMD patients and mdx mice.
@en
P2093
P1476
Early onset of lipofuscin accu ...... of DMD patients and mdx mice.
@en
P2093
Akiko Akagi
Ikuya Nonaka
Masayuki Shono
Peter J Stoward
Tatsuo Kashiyama
Tetsuya Matsuzaki
Yoshiko Nakae
P304
P356
10.1023/B:HIJO.0000045947.83628.A7
P577
2004-06-01T00:00:00Z