Literature DB >> 1504620

Prion diseases.

J Collinge1, M S Palmer.   

Abstract

There have been remarkably rapid advances in the understanding of prion diseases over the past year. The controversial notion that the transmissible agent may be an abnormal isoform of a host-encoded protein, the prion protein, is now gaining wide acceptance. The conundrum of how a disease can both be inherited as an autosomal dominant condition and also be experimentally transmissible by inoculation is beginning to make sense.

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Year:  1992        PMID: 1504620     DOI: 10.1016/s0959-437x(05)80156-x

Source DB:  PubMed          Journal:  Curr Opin Genet Dev        ISSN: 0959-437X            Impact factor:   5.578


  8 in total

1.  Manganese upregulates cellular prion protein and contributes to altered stabilization and proteolysis: relevance to role of metals in pathogenesis of prion disease.

Authors:  Christopher J Choi; Vellareddy Anantharam; Dustin P Martin; Eric M Nicholson; Jürgen A Richt; Arthi Kanthasamy; Anumantha G Kanthasamy
Journal:  Toxicol Sci       Date:  2010-02-22       Impact factor: 4.849

2.  Familial Pick's disease and dementia in frontal lobe degeneration of non-Alzheimer type are not variants of prion disease.

Authors:  J Collinge; M S Palmer; K C Sidle; S P Mahal; T Campbell; J Brown; J Hardy; A E Brun; L Gustafson; E Bakker
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-06       Impact factor: 10.154

3.  Structural analysis of prion proteins by means of drift cell and traveling wave ion mobility mass spectrometry.

Authors:  Gillian R Hilton; Konstantinos Thalassinos; Megan Grabenauer; Narinder Sanghera; Susan E Slade; Thomas Wyttenbach; Philip J Robinson; Teresa J T Pinheiro; Michael T Bowers; James H Scrivens
Journal:  J Am Soc Mass Spectrom       Date:  2010-01-28       Impact factor: 3.109

4.  Normal cellular prion protein protects against manganese-induced oxidative stress and apoptotic cell death.

Authors:  Christopher J Choi; Vellareddy Anantharam; Nathan J Saetveit; Robert S Houk; Arthi Kanthasamy; Anumantha G Kanthasamy
Journal:  Toxicol Sci       Date:  2007-05-04       Impact factor: 4.849

5.  Inherited prion disease (PrP lysine 200) in Britain: two case reports.

Authors:  J Collinge; M S Palmer; T Campbell; K C Sidle; D Carroll; A Harding
Journal:  BMJ       Date:  1993-01-30

6.  Transmissible spongiform encephalopathies with P102L mutation of PRNP manifesting different phenotypes: clinical, neuroimaging, and electrophysiological studies in Chinese kindred in Taiwan.

Authors:  Nai-Fang Chi; Yi-Chung Lee; Yi-Chun Lu; Hsiu-Mei Wu; Bing-Wen Soong
Journal:  J Neurol       Date:  2009-08-21       Impact factor: 4.849

7.  Allelic discrimination of genetic human prion diseases by real-time PCR genotyping.

Authors:  Olga Calero; Rafael Hortigüela; Carmen Albo; Jesés de Pedro-Cuesta; Miguel Calero
Journal:  Prion       Date:  2009-07-23       Impact factor: 3.931

8.  Spontaneous generation of infectious prion disease in transgenic mice.

Authors:  Juan-María Torres; Joaquín Castilla; Belén Pintado; Alfonso Gutiérrez-Adan; Olivier Andréoletti; Patricia Aguilar-Calvo; Ana-Isabel Arroba; Beatriz Parra-Arrondo; Isidro Ferrer; Jorge Manzanares; Juan-Carlos Espinosa
Journal:  Emerg Infect Dis       Date:  2013-12       Impact factor: 6.883

  8 in total

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