Results of a triple blind clinical study of myoblast transplantations without immunosuppressive treatment in young boys with Duchenne muscular dystrophy.
about
Muscle Satellite Cells: Exploring the Basic Biology to Rule ThemMyogenic Precursors from iPS Cells for Skeletal Muscle Cell Replacement TherapyAdvancements in stem cells treatment of skeletal muscle wastingStem cells for skeletal muscle regeneration: therapeutic potential and roadblocksRecent progress in satellite cell/myoblast engraftment -- relevance for therapyQuantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures.Systemic delivery of human microdystrophin to regenerating mouse dystrophic muscle by muscle progenitor cellsRepairing skeletal muscle: regenerative potential of skeletal muscle stem cells.Notch ligands regulate the muscle stem-like state ex vivo but are not sufficient for retaining regenerative capacity.The golden retriever model of Duchenne muscular dystrophy.A case for immunosuppression for myoblast transplantation in duchenne muscular dystrophy.Influence of immune responses in gene/stem cell therapies for muscular dystrophies.Contribution of human muscle-derived cells to skeletal muscle regeneration in dystrophic host mice.Skeletal muscle generated from induced pluripotent stem cells - induction and application.Stem cell transplantation for muscular dystrophy: the challenge of immune response.Hyperthermia differently affects connexin43 expression and gap junction permeability in skeletal myoblasts and HeLa cells.The emerging relationship between regenerative medicine and physical therapeutics.Stem cells in clinical practice: applications and warnings.Extraocular muscle satellite cells are high performance myo-engines retaining efficient regenerative capacity in dystrophin deficiency.The potential of stem cells in the treatment of skeletal muscle injury and diseaseSlowing down differentiation of engrafted human myoblasts into immunodeficient mice correlates with increased proliferation and migration.Inhibition of CD26/DPP-IV enhances donor muscle cell engraftment and stimulates sustained donor cell proliferationMMP1 gene expression enhances myoblast migration and engraftment following implanting into mdx/SCID miceTransient immunosuppressive treatment leads to long-term retention of allogeneic myoblasts in hybrid myofibersPartial laminin alpha2 chain restoration in alpha2 chain-deficient dy/dy mouse by primary muscle cell culture transplantationDevelopment of approaches to improve cell survival in myoblast transfer therapy.Dynamics of myoblast transplantation reveal a discrete minority of precursors with stem cell-like properties as the myogenic source.Identification of a novel population of muscle stem cells in mice: potential for muscle regeneration.Clonal isolation of muscle-derived cells capable of enhancing muscle regeneration and bone healing.Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapyEngraftment of ES-Derived Myogenic Progenitors in a Severe Mouse Model of Muscular Dystrophy.Long-term survival of transplanted stem cells in immunocompetent mice with muscular dystrophy.Hematopoietic cell transplantation provides an immune-tolerant platform for myoblast transplantation in dystrophic dogsCell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophyAntioxidant levels represent a major determinant in the regenerative capacity of muscle stem cells.Matrix metalloproteinase-1 promotes muscle cell migration and differentiation.Comparative Genomics of X-linked Muscular Dystrophies: The Golden Retriever ModelMyogenic endothelial cells purified from human skeletal muscle improve cardiac function after transplantation into infarcted myocardium.Aldehyde dehydrogenase activity promotes survival of human muscle precursor cells.CXCR4 enhances engraftment of muscle progenitor cells.
P2860
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P2860
Results of a triple blind clinical study of myoblast transplantations without immunosuppressive treatment in young boys with Duchenne muscular dystrophy.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh-hant
name
Results of a triple blind clin ...... h Duchenne muscular dystrophy.
@en
Results of a triple blind clin ...... h Duchenne muscular dystrophy.
@nl
type
label
Results of a triple blind clin ...... h Duchenne muscular dystrophy.
@en
Results of a triple blind clin ...... h Duchenne muscular dystrophy.
@nl
prefLabel
Results of a triple blind clin ...... h Duchenne muscular dystrophy.
@en
Results of a triple blind clin ...... h Duchenne muscular dystrophy.
@nl
P2093
P1433
P1476
Results of a triple blind clin ...... th Duchenne muscular dystrophy
@en
P2093
C L Richards
J P Bouchard
J P Tremblay
P304
P356
10.1177/096368979300200203
P577
1993-03-01T00:00:00Z