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ADAMTS13 proteín
SYS d000071120 LBL 00000cy--a2200181n--4500 005 20250606222052.2 008 170101|-|anznnbabn-----------|-a|a------ 040 $b slo $a BA006 $d BA006 $d BA006 065 $a D08.811.277.656.675.374.102.500.813 065 $a D09.400.430.500.500.813 065 $a D12.776.395.033.500.813 065 $a D12.776.860.300.085.813 066 $a 01 $c 03 150 $a ADAMTS13 proteín $x AD $x AE $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 450 $w v $a disintegrín a metaloproteináza s proteínom s trombospondínovými motívmi 13 $2 slo 450 $w v $a ADAMTS-13 proteín $2 slo 450 $w v $a ADAMTS13 proteáza $2 slo 450 $w v $a proteáza štiepiaca vWF $2 slo 450 $w v $a proteináza štiepiaca von Willebrandov faktor $2 slo 665 $a 2017 $2 eng 665 $a ADAM Proteins (2006-2016) $2 eng 680 9-
$i An ADAMTS protease that contains eight thrombospondin (TS) motifs. It cleaves VON WILLEBRAND FACTOR to control vWF-mediated THROMBOSIS. Mutations in the ADAMTS13 gene have been identified in familial cases of PURPURA, THROMBOTIC THROMBOCYTOPENIC and defects in ADAMTS13 activity are associated with MYOCARDIAL INFARCTION; BRAIN ISCHEMIA; PRE-ECLAMPSIA; and MALARIA. $2 eng 750 $a ADAMTS13 Protein $2 eng 980 $x M
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