Prion Proteins [prionová bílkovina]
- Terms
-
prionový protein
protein fatální familiární insomnie
-
Alternative Prion Protein
AltPrP
CD230 Antigen
Creutzfeldt-Jakob Disease Protein
Fatal Familial Insomnia Protein
Major Prion Protein
Prion Protein
PrP Proteins
Membrane glycosylphosphatidylinositol-anchored glycoproteins that may aggregate into rod-like structures. The prion protein (PRNP) gene is characterized by five TANDEM REPEAT SEQUENCES that encode a highly unstable protein region of five octapeptide repeats. Mutations in the repeat region and elsewhere in this gene are associated with CREUTZFELDT-JAKOB DISEASE; FATAL FAMILIAL INSOMNIA; GERSTMANN-STRAUSSLER DISEASE; Huntington disease-like 1, and KURU.
- DUI
- D000072002 MeSH Browser
- CUI
- M000616231
- Previous indexing
- Prions (2006-2016)
- History note
- 2017: for PRION PROTEINS use PRIONS 1991-2016
- Public note
- 2017; for PRION PROTEINS see PRIONS 1991-2016
Allowable subheadings
- AD
- administration & dosage
- AE
- adverse effects 1
- AG
- agonists
- AN
- analysis 3
- AI
- antagonists & inhibitors
- BI
- biosynthesis
- BL
- blood 1
- CF
- cerebrospinal fluid
- CS
- chemical synthesis
- CH
- chemistry 2
- CL
- classification
- DF
- deficiency
- DE
- drug effects
- EC
- economics
- GE
- genetics 5
- HI
- history
- IM
- immunology
- IP
- isolation & purification 1
- ME
- metabolism 3
- PK
- pharmacokinetics
- PD
- pharmacology
- PH
- physiology 1
- PO
- poisoning
- RE
- radiation effects
- ST
- standards
- SD
- supply & distribution
- TU
- therapeutic use
- TO
- toxicity
- UL
- ultrastructure
- UR
- urine
PRNP protein, human Chemical MeSH Browser
Prnp protein, leucyl(101), mouse Chemical MeSH Browser
Prnp protein, mouse Chemical MeSH Browser