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Transmissible spongiform encephalopathies.

author

Colin L. Masters

1947 -

published in: The Lancet

date of publication: 2004-01-01

language: English

Cites articles 116

Date

Title

Authors

2003-06-01

Copper coordination in the full-length, recombinant prion protein

Giuseppe Legname, Stanley B. Prusiner
2003-08-01

Trafficking of prion proteins through a caveolae-mediated endosomal pathway

Stanley B. Prusiner, Stephen J DeArmond, Dennis R. Burton
2003-03-26

Mutant PrP is delayed in its exit from the endoplasmic reticulum, but neither wild-type nor mutant PrP undergoes retrotranslocation prior to proteasomal degradation

David A Harris
2003-07-01

A prion protein epitope selective for the pathologically misfolded conformation

James Ironside, Harry C Ledebur, Avi Chakrabartty, Mark W Head, Neil Cashman, Katherine I. O'Rourke, Robert G. Will
2003-05-01

Novel prion protein insert mutation associated with prolonged neurodegenerative illness.

Andrew F. Hill
2003-11-01

Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease.

Markus Glatzel, Eugenio Abela, Adriano Aguzzi
2003-04-10

Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics

Elizabeth M. C. Fisher, Michael Stumpf, John Collinge
2003-05-20

Specific inhibition of pathological prion protein accumulation by small interfering RNAs
2003-08

Evaluation of quinacrine treatment for prion diseases
2003-03-01

Monoclonal antibodies inhibit prion replication and delay the development of prion disease

Anthony R. White, Mourad Tayebi, John Collinge
2002-04-04

Naturally secreted oligomers of amyloid beta protein potently inhibit hippocampal long-term potentiation in vivo

Michael J Rowan, Dennis J. Selkoe
2002-03-01

Molecular features of the copper binding sites in the octarepeat domain of the prion protein

Alice Vrielink, Marilyn M Olmstead
2002-11-25

Copper binding to the octarepeats of the prion protein. Affinity, specificity, folding, and cooperativity: insights from circular dichroism
2002-03-01

Conversion of raft associated prion protein to the protease-resistant state requires insertion of PrP-res (PrP(Sc)) into contiguous membranes

Byron Caughey, Bruce Chesebro
2002-10-17

Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol

Susan Lindquist
2002-10-17

Conversion of PrP to a self-perpetuating PrPSc-like conformation in the cytosol

Susan Lindquist
2002-11-01

Creutzfeldt-Jakob disease in Australia 1970-1999.
2002-03-01

14-3-3 Protein isoforms and atypical patterns of the 14-3-3 assay in the diagnosis of Creutzfeldt-Jakob disease
2002-01-01

Tau protein and 14-3-3 protein in the differential diagnosis of Creutzfeldt-Jakob disease
2002-09-01

Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy

Aleksey Shatunov, Herbert Budka, Pierluigi Gambetti
2002-06-01

First hundred cases of variant Creutzfeldt-Jakob disease: retrospective case note review of early psychiatric and neurological features

Richard S. G. Knight, Robert G. Will
2002-11-01

Transmission of prion diseases by blood transfusion
2002-03-01

Chronic subclinical prion disease induced by low-dose inoculum

Adriano Aguzzi
2002-12-01

BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein

Andrew F. Hill, Melanie Desbruslais, Emmanuel A. Asante, John Collinge
2002-12-01

Subclinical scrapie infection in a resistant species: persistence, replication, and adaptation of infectivity during four passages

Byron Caughey, Kimberly Meade-White, Bruce Chesebro
2002-07-13

Incidence of Creutzfeldt-Jakob disease in Switzerland

Johannes Streffer, Markus Glatzel, Adriano Aguzzi, Azra Ghani
2002-08-01

Sporadic Creutzfeldt-Jakob disease and surgery: a case-control study using community controls
2002-07-01

Creutzfeldt-Jakob disease cluster in an Australian rural city

Andrew F. Hill, Catriona A. McLean, John Kaldor
2002-11-01

Implications of BSE infection screening data for the scale of the British BSE epidemic and current European infection levels.

Christl Ann Donnelly, Azra Ghani, Neil Ferguson, Roy M. Anderson
2002-10-21

Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic mice

Giuseppe Legname, Stanley B. Prusiner, Laura Solforosi, Dennis R. Burton
2002-03-01

Prions in skeletal muscle.

Giuseppe Legname, Stanley B. Prusiner, Stephen J DeArmond, Glenn C. Telling
2002-06-01

Drug therapy in human and experimental transmissible spongiform encephalopathy

Article - wd:Q34289917

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