New possibilities for prenatal diagnosis of muscular dystrophies: forced myogenesis with an adenoviral MyoD-vector
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
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2. Application of in vitro myo-differentiation of non-nuscle cells to enhance gene expression and facilitate analysis of muscle proteins;Roest;Neuromusc Disord,1996
3. Muscle differentiation during repair of myocardial necrosis in rats via gene transfer with MyoD;Murry;J Clin Invest,1996
4. Use of epitope libraries to identify exonspecific monoclonal antibodies for characterization of altered dystrophin in muscular dystrophy;Thi Man;Am J Hum Genet,1993
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1. MyoD-induced reprogramming of human fibroblasts and urinary stem cells in vitro: protocols and their applications;Frontiers in Physiology;2023-05-17
2. Lack of Myostatin Reduces MyoD Induced Myogenic Potential of Primary Muscle Fibroblasts;Journal of Cellular Biochemistry;2014-06
3. Transcription Factor Rational Design Improves Directed Differentiation of Human Mesenchymal Stem Cells Into Skeletal Myocytes;Molecular Therapy;2011-07
4. Dystrophinopathy carrier determination and detection of protein deficiencies in muscular dystrophy using lentiviral MyoD-forced myogenesis;Neuromuscular Disorders;2007-04
5. Adenoviral mediated MyoD gene transfer into fibroblasts: Myogenic disease diagnosis;Brain and Development;2006-08
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