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myši inbredné mdx
SYS d018101 LBL 00000nz--a2200000o--4500 005 20250606213439.2 008 930603|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a B01.050.050.199.520.520.420.500 065 $a B01.050.150.900.649.313.992.635.505.500.400.420.500 065 $a B01.050.150.900.649.313.992.635.505.500.550.265 066 $a 01 $c 03 150 $a myši inbredné mdx $x AB $x AH $x BL $x CF $x CL $x EM $x GD $x GE $x IM $x IN $x ME $x MI $x PH $x PS $x PX $x SU $x UR $x VI $2 slo 450 $w v $a myši inbrídované mdx $2 slo 550 $7 sllk_us_auth*d009136 $Y Muscular Dystrophies $w b $a dystrofie svalové 550 $7 sllk_us_auth*d016189 $Y Dystrophin $w b $a dystrofín 550 $7 sllk_us_auth*d009136 $Y Muscular Dystrophies $w p $a dystrofie svalové 665 $a 94 $2 eng 665 $a Mice, Inbred C57BL (1984-1993) $2 eng 665 $a Mice, Mutant Strains (1984-1993) $2 eng 680 9-
$i A 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. $2 eng 680 $a NIM with no qualifiers when experimental animal $2 eng 750 -2
$a Mice, Inbred mdx $2 eng 980 $x M
Počet záznamov: 1