Creutzfeldt-Jakob disease with the V203I mutation and M129V polymorphism of the prion protein gene (PRNP) and a 17 kDa prion protein fragment
β Scribed by B-H. Jeong; Y-C. Jeon; Y-J. Lee; H-J. Cho; S-J. Park; D-I. Chung; J. Kim; S. H. Kim; H-T. Kim; E-K. Choi; K-C. Choi; R. I. Carp; Y-S. Kim
- Book ID
- 110852713
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 636 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0305-1846
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Inherited prion diseases are characterized by mutations in the PRNP gene encoding the prion protein (PrP). As the other sporadic or infectious prion disease forms, they are almost all characterized by the accumulation in the brain of an abnormal misfolded form of the patient's PrP. Brain extracts ca
## Abstract The prion protein, PrP^C^, is known mostly for its involvement in neurodegenerative spongiform encephalopathies. However, a role for this molecule in cancer is becoming increasingly recognized partly because it promotes cell proliferation and inhibits apoptosis. Moreover, the codon 129