Literature DB >> 12383773

Mouse models of prion disease transmission.

Thierry Baron1.   

Abstract

The experimental transmissions of spongiform encephalopathies, neurodegenerative diseases found in humans and some animal species, allowed the important discovery of a host-encoded prion protein closely associated, if not identical, to the transmissible agent. Transmissions in mice addressed several questions regarding the understanding of the 'species barrier' that limits, or even prevents, the transmission between different species, and regarding the resistance to these diseases. The genetic control of the disease by the host could be studied in mouse models and showed the important role of the host prion gene, but several other genetic factors involved in these diseases remain to be discovered. Finally, the analysis of the features of these diseases in mice has been crucial to characterize the infectious agents and their biological properties, although the precise mechanisms underlying their apparent diversity largely remain to be elucidated.

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Year:  2002        PMID: 12383773     DOI: 10.1016/s1471-4914(02)02416-4

Source DB:  PubMed          Journal:  Trends Mol Med        ISSN: 1471-4914            Impact factor:   11.951


  9 in total

1.  Genetic variability of the coding region for the prion protein gene (PRNP) in gayal (Bos frontalis).

Authors:  Dongmei Xi; Qing Liu; Jianhong Guo; Hongman Yu; Yuai Yang; Yiduo He; Huaming Mao; Xiao Gou; Weidong Deng
Journal:  Mol Biol Rep       Date:  2011-06-03       Impact factor: 2.316

2.  Pathogenesis of chronic wasting disease in cervidized transgenic mice.

Authors:  Davis M Seelig; Gary L Mason; Glenn C Telling; Edward A Hoover
Journal:  Am J Pathol       Date:  2010-04-15       Impact factor: 4.307

3.  Gastrointestinal dissemination and transmission of Staphylococcus aureus following bacteremia.

Authors:  Elisabeth Kernbauer; Katie Maurer; Victor J Torres; Bo Shopsin; Ken Cadwell
Journal:  Infect Immun       Date:  2014-11-10       Impact factor: 3.441

4.  Genomic and post-genomic analyses of human prion diseases.

Authors:  Maurizio Pocchiari; Anna Poleggi; Serena Principe; Silvia Graziano; Franco Cardone
Journal:  Genome Med       Date:  2009-06-22       Impact factor: 11.117

5.  Mapping of multiple quantitative trait loci affecting bovine spongiform encephalopathy.

Authors:  Chi Zhang; Dirk-Jan De Koning; Jules Hernández-Sánchez; Chris S Haley; John L Williams; Pamela Wiener
Journal:  Genetics       Date:  2004-08       Impact factor: 4.562

6.  A non-Q/N-rich prion domain of a foreign prion, [Het-s], can propagate as a prion in yeast.

Authors:  Vibha Taneja; Marie-Lise Maddelein; Nicolas Talarek; Sven J Saupe; Susan W Liebman
Journal:  Mol Cell       Date:  2007-07-06       Impact factor: 17.970

7.  A bovine cell line that can be infected by natural sheep scrapie prions.

Authors:  Anja M Oelschlegel; Markus Geissen; Matthias Lenk; Roland Riebe; Marlies Angermann; Herman Schatzl; Hermann Schaetzl; Martin H Groschup
Journal:  PLoS One       Date:  2015-01-07       Impact factor: 3.240

8.  No major change in vCJD agent strain after secondary transmission via blood transfusion.

Authors:  Matthew T Bishop; Diane L Ritchie; Robert G Will; James W Ironside; Mark W Head; Val Thomson; Moira Bruce; Jean C Manson
Journal:  PLoS One       Date:  2008-08-06       Impact factor: 3.240

9.  A comparative study of modified confirmatory techniques and additional immuno-based methods for non-conclusive autolytic bovine spongiform encephalopathy cases.

Authors:  Rocío Sarasa; Dietmar Becher; Juan J Badiola; Marta Monzón
Journal:  BMC Vet Res       Date:  2013-10-18       Impact factor: 2.741

  9 in total

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