Identification and structural analysis of C-terminally truncated collapsin response mediator protein-2 in a murine model of prion diseases
<p>Abstract</p> <p>Background</p> <p>Prion diseases are fatal neurodegenerative disorders that accompany an accumulation of the disease-associated form(s) of prion protein (PrP<sup>Sc</sup>) in the central nervous system. The neuropathological changes in the...
Main Authors: | Nishijima Masahiro, Tobiume Minoru, Hara Hideyuki, Yamakawa Yoshio, Shinkai-Ouchi Fumiko, Hanada Kentaro, Hagiwara Ken'ichi |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2010-10-01
|
Series: | Proteome Science |
Online Access: | http://www.proteomesci.com/content/8/1/53 |
Similar Items
-
Tracking and clarifying differential traits of classical- and atypical L-type bovine spongiform encephalopathy prions after transmission from cattle to cynomolgus monkeys.
by: Ken'ichi Hagiwara, et al.
Published: (2019-01-01) -
Collapsin Response Mediator Proteins: Their Biological Functions and Pathophysiology in Neuronal Development and Regeneration
by: Fumio Nakamura, et al.
Published: (2020-06-01) -
N-Terminal Regions of Prion Protein: Functions and Roles in Prion Diseases
by: Hideyuki Hara, et al.
Published: (2020-08-01) -
Thiol-reactive reagents inhibits intracellular trafficking of human papillomavirus type 16 pseudovirions by binding to cysteine residues of major capsid protein L1
by: Hagiwara Ken'ichi, et al.
Published: (2007-10-01) -
Accumulation of L-type Bovine Prions in Peripheral Nerve Tissues
by: Yoshifumi Iwamaru, et al.
Published: (2010-07-01)