Invited review: myoblast transfer: a possible therapy for inherited myopathies?
about
Laminin regulates PDGFRβ(+) cell stemness and muscle development.Direct cell surface modification with DNA for the capture of primary cells and the investigation of myotube formation on defined patterns.Myoblast transplantation for inherited myopathies: a clinical approach.Use of repeating dispensers to increase the efficiency of the intramuscular myogenic cell injection procedure.The man behind the syndrome: Guillaume Duchenne.The role of stem cells in skeletal and cardiac muscle repair.Muscle stem cells.Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation.Non-viral gene delivery in skeletal muscle: a protein factory.An absolute requirement for Pax7-positive satellite cells in acute injury-induced skeletal muscle regeneration.Recent advances in understanding muscular dystrophyThe development of mitochondrial medicine.MMP1 gene expression enhances myoblast migration and engraftment following implanting into mdx/SCID miceDevelopment of approaches to improve cell survival in myoblast transfer therapy.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 therapyHeterokaryon myotubes with normal mouse and Duchenne nuclei exhibit sarcolemmal dystrophin staining and efficient intracellular free calcium control.Expression of human factor IX in mice after injection of genetically modified myoblastsMatrix metalloproteinase-1 promotes muscle cell migration and differentiation.Progress in therapy for Duchenne muscular dystrophy.Invited review: Stem cells and muscle diseases: advances in cell therapy strategies.Steroid RU 486 inducible myogenesis by 10T1/2 fibroblastic mouse cells.Mass and functional capacity of regenerating muscle is enhanced by myoblast transfer.Successful histocompatible myoblast transplantation in dystrophin-deficient mdx mouse despite the production of antibodies against dystrophin.Functional improvement of damaged adult mouse muscle by implantation of primary myoblasts.High efficiency of muscle regeneration after human myoblast clone transplantation in SCID mice.Matching host muscle and donor myoblasts for myosin heavy chain improves myoblast transfer therapy.Chemotaxis of skeletal muscle satellite cells.Cell transplantation for treatment of acute myocardial infarction: unique capacity for repair by skeletal muscle satellite cells.First study of intra-arterial delivery of myogenic mononuclear cells to skeletal muscles in primates.
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Invited review: myoblast transfer: a possible therapy for inherited myopathies?
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on March 1991
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
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name
Invited review: myoblast transfer: a possible therapy for inherited myopathies?
@en
Invited review: myoblast transfer: a possible therapy for inherited myopathies?
@nl
type
label
Invited review: myoblast transfer: a possible therapy for inherited myopathies?
@en
Invited review: myoblast transfer: a possible therapy for inherited myopathies?
@nl
prefLabel
Invited review: myoblast transfer: a possible therapy for inherited myopathies?
@en
Invited review: myoblast transfer: a possible therapy for inherited myopathies?
@nl
P356
P1433
P1476
Invited review: myoblast transfer: a possible therapy for inherited myopathies?
@en
P2093
Partridge TA
P304
P356
10.1002/MUS.880140302
P577
1991-03-01T00:00:00Z