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dystrofín
SYS d016189 LBL 00000nz--a2200000o--4500 005 20260512091147.9 008 920617|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a D12.776.210.500.250 065 $a D12.776.220.250 065 $a D12.776.543.250 066 $a 01 $c 03 150 $a dystrofín $x AD $x AE $x AG $x AI $x AN $x BI $x BL $x CF $x CH $x CL $x CS $x DE $x DF $x EC $x GE $x HI $x IM $x IP $x ME $x PD $x PH $x PK $x PO $x RE $x SD $x ST $x TO $x TU $x UL $x UR $2 slo 550 $7 sllk_us_auth*d018101 $Y Mice, Inbred mdx $w p $a myši inbredné mdx 550 $7 sllk_us_auth*d020388 $Y Muscular Dystrophy, Duchenne $w p $a Duchenneova svalová dystrofia 550 $7 sllk_us_auth*d020388 $Y Muscular Dystrophy, Duchenne $w b $a Duchenneova svalová dystrofia 665 $a 91 $2 eng 665 $a Muscle Proteins (1988-1990) $2 eng 680 $a a muscle protein: see MeSH definition for relation to musc dystrophy; /biosyn /drug eff /physiol /ultrastruct permitted $2 eng 680 9-
$i A muscle protein localized in surface membranes which is the product of the Duchenne/Becker muscular dystrophy gene. Individuals with Duchenne muscular dystrophy usually lack dystrophin completely while those with Becker muscular dystrophy have dystrophin of an altered size. It shares features with other cytoskeletal proteins such as SPECTRIN and alpha-actinin but the precise function of dystrophin is not clear. One possible role might be to preserve the integrity and alignment of the plasma membrane to the myofibrils during muscle contraction and relaxation. MW 400 kDa. $2 eng 750 -2
$a Dystrophin $2 eng 980 $x M
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