Number of the records: 1
prióny
SYS d011328 LBL 00000cz--a2200000n--4500 005 20250606214811.6 008 920510|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 $d BA006 065 $a D12.776.785 066 $a 01 $c 03 150 $a prióny $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 EC $x GE $x HI $x IM $x IP $x ME $x PD $x PH $x PK $x PO $x PY $x RE $x SD $x ST $x TO $x TU $x UL $x UR $2 slo 450 $w v $a Mink Encephalopathy Virus $2 eng 450 $w v $a Prion $2 eng 450 $w v $a prión $2 slo 450 $w v $a vírus encefalopatie noriek $2 slo 550 $7 sllk_us_auth*d012608 $Y Scrapie $w b $a scrapie 665 $a 86; MINK ENCEPHALOPATHY VIRUS was heading 1991-92, was see under VERTEBRATE VIRUSES, UNCLASSIFIED (now VIRUSES, UNCLASSIFIED) 1975-90; TRANSMISSIBLE ENCEPHALOPATHY VIRUS OF MINK was see MINK ENCEPHALOPATHY VIRUS 1975-92 $2 eng 665 $a PrPSc Proteins (1966-1985) $2 eng 665 $a Viral Proteins (1966-1985) $2 eng 680 9-
$i Small proteinaceous infectious particles which resist inactivation by procedures that modify NUCLEIC ACIDS and contain an abnormal isoform of a cellular protein which is a major and necessary component. The abnormal (scrapie) isoform is PrPSc (PRPSC PROTEINS) and the cellular isoform PrPC (PRPC PROTEINS). The primary amino acid sequence of the two isoforms is identical. Human diseases caused by prions include CREUTZFELDT-JAKOB SYNDROME; GERSTMANN-STRAUSSLER SYNDROME; and INSOMNIA, FATAL FAMILIAL. $2 eng 750 -2
$a Prions $2 eng 980 $x M
Number of the records: 1