Muscular Dystrophy Research Today is a free monthly online journal that collates and summarizes the latest research about Muscular Dystrophy, including details on duchenne muscular dystrophy, symptoms, treatment.

Volume 3 (2007), Issue 3 (March)

1. Gene expression microarrays and respiratory muscles.
   Respir Physiol Neurobiol, 156(2): 103-15. [Abstract] [Full-text]
2. The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure.
   BMC Med Genet, 8: 8. [Abstract] [Full-text]
3. Characterization of lobulated fibers in limb girdle muscular dystrophy type 2A by gene expression profiling.
   Neurosci Res, 57(4): 513-21. [Abstract] [Full-text]
4. Psychiatric disorders appear equally in patients with myotonic dystrophy, facioscapulohumeral dystrophy, and hereditary motor and sensory neuropathy type I.
   Acta Neurol Scand, 115(4): 265-70. [Abstract] [Full-text]
5. Haploinsuffciency for Znf9 in Znf9+/- mice is associated with multiorgan abnormalities resembling myotonic dystrophy.
   J Mol Biol, 368(1): 8-17. [Abstract] [Full-text]
6. Morphological changes in the trigemino-rubral pathway in dystrophic (mdx) mice.
   Neurosci Lett, 416(2): 175-9. [Abstract] [Full-text]
7. Genetic disruption of calcineurin improves skeletal muscle pathology and cardiac disease in a mouse model of limb-girdle muscular dystrophy.
   J Biol Chem, 282(13): 10068-78. [Abstract] [Full-text]
8. Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2).
   BMC Evol Biol, 7: 39. [Abstract] [Full-text]
9. Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression.
   FASEB J, 21(4): 1210-26. [Abstract] [Full-text]
10. Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients.
    Genet Test, 11(1): 84-90. [Abstract] [Full-text]

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