Number of the records: 1  

myši inbredné mdx

  1. Record numberd018101
    Date06.06.2025
    TypeM - MESH
    Topical termmyši inbredné mdx
    Other termSlovak (Pseudonym) myši inbrídované mdx
    See also(Later heading) dystrofie svalové
    (Later heading) dystrofín
    (Skutočné meno) dystrofie svalové
    UDCB01.050.050.199.520.520.420.500B01.050.150.900.649.313.992.635.505.500.400.420.500B01.050.150.900.649.313.992.635.505.500.550.265
    NoteA strain of mice arising from a spontaneous MUTATION (mdx) in inbred C57BL mice. This mutation is X chromosome-linked and produces viable homozygous animals that lack the muscle protein DYSTROPHIN, have high serum levels of muscle ENZYMES, and possess histological lesions similar to human MUSCULAR DYSTROPHY. The histological features, linkage, and map position of mdx make these mice a worthy animal model of DUCHENNE MUSCULAR DYSTROPHY.
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Number of the records: 1  

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