Pharmacological chaperone for the structured domain of human prion protein-Reference-Cited by-同舟云学术

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Pharmacological chaperone for the structured domain of human prion protein

Published:2010-09-27 Issue:41 Volume:107 Page:17610-17615
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proc Natl Acad Sci USA

Author:

Nicoll Andrew J.,Trevitt Clare R.,Tattum M. Howard,Risse Emmanuel,Quarterman Emma,Ibarra Amaurys Avila,Wright Connor,Jackson Graham S.,Sessions Richard B.,Farrow Mark,Waltho Jonathan P.,Clarke Anthony R.,Collinge John

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference59 articles.

1. Therapeutic approaches to protein-misfolding diseases

2. Getting into the fold

3. Targeted rescue of a destabilized mutant of p53 by an in silico screened drug

4. Hot spots in prion protein for pathogenic conversion

5. Rational targeting for prion therapeutics

Cited by 71 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. Therapeutic targeting of cellular prion protein: toward the development of dual mechanism anti-prion compounds;Neural Regeneration Research;2024-06-03

2. Sigma Receptor Ligands Are Potent Antiprion Compounds that Act Independently of Sigma Receptor Binding;ACS Chemical Neuroscience;2024-05-14

3. New implications for prion diseases therapy and prophylaxis;Frontiers in Molecular Neuroscience;2024-03-04

4. Prions;Molecular Medical Microbiology;2024

5. Sigma receptor ligands are potent anti-prion compounds that act independently of sigma receptor binding;2023-11-29

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