Muscling in on microarrays
© BioMed Central Ltd 2002
Published: 7 November 2002
Duchenne muscular dystrophy (DMD) is a degenerative disease of the skeletal muscle fibres and is caused by mutations in the dystrophin gene. In the Early Edition of the Proceedings of the National Academy of Sciences, Haslett et al. report microarray analysis of muscle from DMD patient biopsies to gain insights into the molecular pathways affected in dystrophic skeletal muscle. Twelve quadriceps biopsies from DMD patients were compared with unaffected controls and the hybridization data were analysed using two different statistical methods (t test analysis and geometric fold-change analysis). Over one hundred genes were identified, many of which fit with the histopathology of the disease. For example, several components of the proliferating connective tissue were found to be overexpressed in DMD muscle.
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