Defective myoblasts identified in Duchenne muscular dystrophy.
about
Short telomeres and stem cell exhaustion model Duchenne muscular dystrophy in mdx/mTR miceAnalyses of the differentiation potential of satellite cells from myoD-/-, mdx, and PMP22 C22 mice.Oxidative Stress-Mediated Skeletal Muscle Degeneration: Molecules, Mechanisms, and TherapiesA muscle stem cell for every muscle: variability of satellite cell biology among different muscle groupsThe quasi-parallel lives of satellite cells and atrophying muscleOveractive bone morphogenetic protein signaling in heterotopic ossification and Duchenne muscular dystrophyEarly pathogenesis of Duchenne muscular dystrophy modelled in patient-derived human induced pluripotent stem cells.Absence of alpha 7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophyTelomere shortening and metabolic compromise underlie dystrophic cardiomyopathyActivation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ).MicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptomsPorcine skeletal muscle-derived multipotent PW1pos/Pax7neg interstitial cells: isolation, characterization, and long-term culture.Skeletal muscle generated from induced pluripotent stem cells - induction and application.Notch signaling deficiency underlies age-dependent depletion of satellite cells in muscular dystrophy.Neuronal nitric oxide synthase-rescue of dystrophin/utrophin double knockout mice does not require nNOS localization to the cell membraneTargeted cell fusion facilitates stable heterokaryon generation in vitro and in vivo.Rapid depletion of muscle progenitor cells in dystrophic mdx/utrophin-/- mice.Are human and mouse satellite cells really the same?Asynchronous remodeling is a driver of failed regeneration in Duchenne muscular dystrophy.Blocking the myostatin signal with a dominant negative receptor improves the success of human myoblast transplantation in dystrophic mice.Muscle side population cells from dystrophic or injured muscle adopt a fibro-adipogenic fateCellular senescence and tissue aging in vivo.Engraftment potential of dermal fibroblasts following in vivo myogenic conversion in immunocompetent dystrophic skeletal muscleA Wnt-TGFβ2 axis induces a fibrogenic program in muscle stem cells from dystrophic mice.Dystrophin analysis in clonal myoblasts derived from a Duchenne muscular dystrophy carrierMuscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasia.Activation of non-myogenic mesenchymal stem cells during the disease progression in dystrophic dystrophin/utrophin knockout mice.The skeletal muscle satellite cell: still young and fascinating at 50The muscular dystrophies: from genes to therapies.Muscle Regeneration with Intermuscular Adipose Tissue (IMAT) Accumulation Is Modulated by Mechanical Constraints.Skeletal muscle satellite cells: background and methods for isolation and analysis in a primary culture system.RMZ: a new cell line from a human alveolar rhabdomyosarcoma. In vitro expression of embryonic myosin.Myotubularin-deficient myoblasts display increased apoptosis, delayed proliferation, and poor cell engraftment.Transient immunosuppressive treatment leads to long-term retention of allogeneic myoblasts in hybrid myofibersSerotonin and Histamine Therapy Increases Tetanic Forces of Myoblasts, Reduces Muscle Injury, and Improves Grip Strength Performance of Dmd(mdx) Mice.Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy.Fibroadipogenic progenitors mediate the ability of HDAC inhibitors to promote regeneration in dystrophic muscles of young, but not old Mdx miceImproved regenerative myogenesis and muscular dystrophy in mice lacking Mkp5.Long-term survival of transplanted stem cells in immunocompetent mice with muscular dystrophy.Injection of vessel-derived stem cells prevents dilated cardiomyopathy and promotes angiogenesis and endogenous cardiac stem cell proliferation in mdx/utrn-/- but not aged mdx mouse models for duchenne muscular dystrophy.
P2860
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P2860
Defective myoblasts identified in Duchenne muscular dystrophy.
description
1983 nî lūn-bûn
@nan
1983 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1983 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1983年の論文
@ja
1983年論文
@yue
1983年論文
@zh-hant
1983年論文
@zh-hk
1983年論文
@zh-mo
1983年論文
@zh-tw
1983年论文
@wuu
name
Defective myoblasts identified in Duchenne muscular dystrophy.
@ast
Defective myoblasts identified in Duchenne muscular dystrophy.
@en
Defective myoblasts identified in Duchenne muscular dystrophy.
@nl
type
label
Defective myoblasts identified in Duchenne muscular dystrophy.
@ast
Defective myoblasts identified in Duchenne muscular dystrophy.
@en
Defective myoblasts identified in Duchenne muscular dystrophy.
@nl
prefLabel
Defective myoblasts identified in Duchenne muscular dystrophy.
@ast
Defective myoblasts identified in Duchenne muscular dystrophy.
@en
Defective myoblasts identified in Duchenne muscular dystrophy.
@nl
P2093
P2860
P356
P1476
Defective myoblasts identified in Duchenne muscular dystrophy.
@en
P2093
P2860
P304
P356
10.1073/PNAS.80.15.4856
P407
P577
1983-08-01T00:00:00Z