Lack of mRNA and dystrophin expression in DMD patients three months after myoblast transfer

This publication has 12 references indexed in Scilit:

• Very small dystrophin molecule in a family with a mild form of Becker dystrophy
  Neuromuscular Disorders, 1993
• Myoblast transfer in duchenne muscular dystrophy
  Annals of Neurology, 1993
• Human myoblast transplantation: Preliminary results of 4 cases
  Muscle & Nerve, 1992
• Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantation
  Nature, 1992
• Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients.
  Journal of Medical Genetics, 1992
• Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNA
  The Lancet, 1990
• Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
  Human Genetics, 1990
• Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblasts
  Nature, 1989
• Isolation of human myoblasts with the fluorescence-activated cell sorter
  Experimental Cell Research, 1988
• Monoclonal antibody analysis of mononuclear cells in myopathies. I: Quantitation of subsets according to diagnosis and sites of accumulation and demonstration and counts of muscle fibers invaded by T cells
  Annals of Neurology, 1984