Acetylcholinesterase triggers the aggregation of PrP 106–126-Reference-Cited by-同舟云学术

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Acetylcholinesterase triggers the aggregation of PrP 106–126

Published:2006-07 Issue:1 Volume:346 Page:89-94
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Pera M.,Román S.,Ratia M.,Camps P.,Muñoz-Torrero D.,Colombo L.,Manzoni C.,Salmona M.,Badia A.,Clos M.V.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference34 articles.

1. Gerstmann–Straussler–Scheinker disease: immunohistological and experimental studies;Tateishi;Ann. Neurol.,1988

2. Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins;Pan;Proc. Natl. Acad. Sci. USA,1993

3. Molecular biology of prion diseases;Prusiner;Science,1991

4. Coexistence of Alzheimer-type neuropathology in Creutzfeldt–Jakob disease;Hainfellner;Acta Neuropathol.,1998

5. Prion protein (PrP(c)) promotes beta-amyloid plaque formation;Schwarze-Eicker;Neurobiol. Aging,2005

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2. Cytoskeleton Elements Contribute to Prion Peptide-Induced Endothelial Barrier Breakdown in a Blood–Brain Barrier In Vitro System;International Journal of Molecular Sciences;2022-10-12

3. Therapeutic strategies for identifying small molecules against prion diseases;Cell and Tissue Research;2022-01-06

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