Number of the records: 1
priony
SYS d011328 LBL 02132nz--a2200265n--4500 003 CZ-PrNML 005 20240206162307.5 008 850510-n-ancnnbaba----------||-ana-----d 035 $a (DNLM)D011328 040 $a ABA008 $b cze $f czmesh 072 $a D12. $x 776. $x 785 150 $a priony $2 czmesh 450 $w i $a Mink Encephalopathy Virus $i UF 450 $w i $a Prion $i UF 450 $w i $a prionové proteiny $i UF 450 $w i $a proteiny PrP $i UF 450 $w i $a virus encefalopatie norků $i UF 550 $w g $a proteiny $7 upol_us_auth*d011506 550 $w h $a prionová bílkovina $7 upol_us_auth*d000072002 680 $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. 688 $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 1975-92 750 -2
$a Prions $2 czmesh 980 $x M 982 $a 1
Number of the records: 1