Curcumin alleviates the effects of heat stress on broiler pectoral muscle via decorin (DCN) -mediated TGF-β Signaling pathway. [PDF]
Bai D, Hu Y, Liu Y, Xue M, Liu X.
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Oculopharyngeal muscular dystrophy (OPMD) associated alanine expansion impairs the function of the nuclear polyadenosine RNA binding protein PABPN1 as revealed by proximity labeling and comparative proteomics. [PDF]
Mezzell AT, Zhang Y, Perez AM, Vest KE.
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Glutamine Promotes Myogenesis in Myoblasts Through Glutaminolysis-Mediated Histone H3 Acetylation That Enhances Myogenin Transcription. [PDF]
Takatoya M +9 more
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TBC1D1 functions as a negative regulator of satellite cells for muscle regeneration. [PDF]
Yang X +8 more
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Myoblast transplantation was the first quasi-gene therapy to be suggested for Duchenne muscular dystrophy. Animal experiments established the principles that the missing gene could be targeted to muscle by grafting of genetically normal myoblasts that were able to repair the disease-damaged muscle fibres.
Daniel Skuk, Jacques P. Tremblay
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Myoblast differentiation in vitro: Morphological differentiation of mononucleated myoblasts
Developmental Biology, 1976Abstract Phospholipase C from Clostridium perfringens has been shown previously to inhibit the fusion of cultured chick myoblasts without affecting recognition or cell cycle parameters. In this paper we report that the mononucleated myoblasts, in phospholipase C, synthesize thick and thin filaments and organize them into myofibrils, and that T ...
J A, Trotter, M, Nameroff
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Myoblasts, Satellite Cells, and Myoblast Transfer
1990The prospects for introducing “foreign” nuclei through the cell fusion process have been considered since it first became clear that skeletal muscle fibers form by fusion of many mononucleated myoblasts rather than the proliferation of skeletal muscle nuclei within fibers (Stockdale and Holtzer, 1961).
F E, Stockdale +3 more
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Rapid death of injected myoblasts in myoblast transfer therapy
Muscle & Nerve, 1996Myoblast transplantation has been proposed as a potential therapy for Duchenne muscular dystrophy (DMD). A Y-chromosome-specific probe was used to track the fate of donor male myoblasts injected into dystrophic muscles of female mdx mice (which are an animal model for DMD).
Y, Fan +3 more
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AbstractSomatic muscle formation is an unusual process as it requires the cells involved, the myoblasts, to relinquish their individual state and fuse with one another to form a syncitial muscle fiber. The potential use of myoblast fusion therapies to rebuild damaged muscles has generated continuing interest in elucidating the molecular basis of the ...
Heather A, Dworak, Helen, Sink
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