Number of the records: 1
prióny
SYS d011328 LBL 00000cx--j2200000---45-- 005 20240119201156.8 100 $a 19920510asloy0103----ba0 152 $b mesh 250 $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 $8 slo 300 1-
$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 $8 eng 300 1-
$a PrPSc Proteins (1966-1985) $8 eng 300 1-
$a Viral Proteins (1966-1985) $8 eng 330 1-
$a 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. $8 eng 450 $a Mink Encephalopathy Virus $5 e $8 eng 450 $a Prion $5 e $8 eng 450 $a prión $5 e $8 slo 450 $a vírus encefalopatie noriek $5 e $8 slo 550 $3 sllk_un_auth*d012608 $Y Scrapie $5 B $a scrapie 686 $a D12.776.785 750 $a Prions $8 eng 801 -0
$a US $b DNLM $c 19920510 801 -2
$a SK $b BA006 $c 20010713 801 -2
$a SK $b BA006 $c 20180328 801 -2
$a SK $b BA006 $c 20211208 980 $x M
Number of the records: 1