N-terminal Domain of Prion Protein Directs Its Oligomeric Association-Reference-Cited by-同舟云学术

N-terminal Domain of Prion Protein Directs Its Oligomeric Association

Published:2014-09 Issue:37 Volume:289 Page:25497-25508
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Trevitt Clare R.,Hosszu Laszlo L.P.,Batchelor Mark,Panico Silvia,Terry Cassandra,Nicoll Andrew J.,Risse Emmanuel,Taylor William A.,Sandberg Malin K.,Al-Doujaily Huda,Linehan Jacqueline M.,Saibil Helen R.,Scott David J.,Collinge John,Waltho Jonathan P.,Clarke Anthony R.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference81 articles.

1. Prion diseases of humans and animals: their causes and molecular basis;Collinge;Annu. Rev. Neurosci,2001

2. Prions;Prusiner;Proc. Natl. Acad. Sci. U.S.A,1998

3. A protease-resistant protein is a structural omponent of the scrapie prion;McKinley;Cell,1983

4. Identification of prion amyloid filaments in scrapie-infected brain;DeArmond;Cell,1985

5. The ultrastructural diversity of scrapie-associated fibrils isolated from experimental scrapie and Creutzfeld-Jakob disease;Liberski;J. Comp. Pathol,1991

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Prion protein conversion at two distinct cellular sites precedes fibrillisation;Nature Communications;2023-12-15

2. Loss of Residues 119–136, Including the First β-strand of Human Prion Protein, Generates an Aggregation-competent Partially “Open” Form;Journal of Molecular Biology;2023-08

3. Direct Observation of Competing Prion Protein Fibril Populations with Distinct Structures and Kinetics;ACS Nano;2023-02-20

4. Anchorless risk or released benefit? An updated view on the ADAM10-mediated shedding of the prion protein;Cell and Tissue Research;2022-01-27

5. Can Chemical Exchange Saturation Transfer (CEST MRI) be used as biomarker of disease progression in Prion Disease?;2021-12-17