Literature DB >> 9873804

Prion diseases.

A Aguzzi1, C Weissmann.   

Abstract

Although the nature of the infectious agent causing prion diseases is still debated, several of its molecular characteristics have been clarified in remarkable detail. The transmissibility of bovine spongiform encephalopathy to humans dramatically highlights the need for research focused at interference with prion replication and spread, and at prevention of brain damage. Precondition to achieving these goals is a thorough understanding of prion biology, and in particular of its protein chemistry.

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Year:  1998        PMID： 9873804     DOI： 10.1046/j.1365-2516.1998.440619.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN： 1351-8216            Impact factor:   4.287


  13 in total

1.  Pregnancy status and fetal prion genetics determine PrPSc accumulation in placentomes of scrapie-infected sheep.

Authors:  Wenbin Tuo; Katherine I O'Rourke; Dongyue Zhuang; William P Cheevers; Terry R Spraker; Donald P Knowles
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-16       Impact factor: 11.205

Review 2.  The Role of Functional Prion-Like Proteins in the Persistence of Memory.

Authors:  Kausik Si; Eric R Kandel
Journal:  Cold Spring Harb Perspect Biol       Date:  2016-04-01       Impact factor: 10.005

3.  The 37 kDa/67 kDa laminin receptor is required for PrP(Sc) propagation in scrapie-infected neuronal cells.

Authors:  Christoph Leucht; Steve Simoneau; Clémence Rey; Karen Vana; Roman Rieger; Corinne Ida Lasmézas; Stefan Weiss
Journal:  EMBO Rep       Date:  2003-03       Impact factor: 8.807

4.  Anti-LRP/LR antibody W3 hampers peripheral PrPSc propagation in scrapie infected mice.

Authors:  Chantal Zuber; Gerda Mitteregger; Claudia Pace; Inga Zerr; Hans A Kretzschmar; Stefan Weiss
Journal:  Prion       Date:  2007-07-07       Impact factor: 3.931

5.  Toxic effects of intracerebral PrP antibody administration during the course of BSE infection in mice.

Authors:  Maxime Lefebvre-Roque; Elisabeth Kremmer; Sabine Gilch; Wen-Quan Zou; Cécile Féraudet; Chantal Mourton Gilles; Nicole Salès; Jacques Grassi; Pierluigi Gambetti; Thierry Baron; Hermann Schätzl; Corinne Ida Lasmézas
Journal:  Prion       Date:  2007-07-15       Impact factor: 3.931

6.  Yeast prions form infectious amyloid inclusion bodies in bacteria.

Authors:  Alba Espargaró; Anna Villar-Piqué; Raimon Sabaté; Salvador Ventura
Journal:  Microb Cell Fact       Date:  2012-06-25       Impact factor: 5.328

7.  Prion infection impairs lysosomal degradation capacity by interfering with rab7 membrane attachment in neuronal cells.

Authors:  Su Yeon Shim; Srinivasarao Karri; Sampson Law; Hermann M Schatzl; Sabine Gilch
Journal:  Sci Rep       Date:  2016-02-11       Impact factor: 4.379

8.  Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological Correlation.

Authors:  Laura Eisenmenger; Marie-Claire Porter; Christopher J Carswell; Andrew Thompson; Simon Mead; Peter Rudge; John Collinge; Sebastian Brandner; Hans R Jäger; Harpreet Hyare
Journal:  JAMA Neurol       Date:  2016-01       Impact factor: 18.302

9.  Multiparameter MR imaging in the 6-OPRI variant of inherited prion disease.

Authors:  E De Vita; G R Ridgway; R I Scahill; D Caine; P Rudge; T A Yousry; S Mead; J Collinge; H R Jäger; J S Thornton; H Hyare
Journal:  AJNR Am J Neuroradiol       Date:  2013-03-28       Impact factor: 3.825

10.  Semisynthetic prion protein (PrP) variants carrying glycan mimics at position 181 and 197 do not form fibrils.

Authors:  Can Araman; Robert E Thompson; Siyao Wang; Stefanie Hackl; Richard J Payne; Christian F W Becker
Journal:  Chem Sci       Date:  2017-07-24       Impact factor: 9.825
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