Literature DB >> 8154865

Human prion diseases.

S B Prusiner1, K K Hsiao.   

Abstract

The prion diseases, sometimes referred to as the "transmissible spongiform encephalopathies," include kuru, Creutzfeldt-Jakob disease, and Gerstmann-Sträussler-Scheinker disease of humans as well as scrapie and bovine spongiform encephalopathy of animals. For many years, the prion diseases were thought to be caused by viruses despite intriguing evidence to the contrary. The unique characteristic common to all of these disorders, whether sporadic, dominantly inherited, or acquired by infection, is that they involve the aberrant metabolism of the prion protein (PrP). In many cases, the cellular prion protein is converted into the scrapie isoform by a posttranslational process that involves a conformational change. Often, the human prion diseases are transmissible to experimental animals and all of the inherited prion diseases segregate with PrP gene mutations.

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Year:  1994        PMID: 8154865     DOI: 10.1002/ana.410350404

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  37 in total

1.  Consequences of manganese replacement of copper for prion protein function and proteinase resistance.

Authors:  D R Brown; F Hafiz; L L Glasssmith; B S Wong; I M Jones; C Clive; S J Haswell
Journal:  EMBO J       Date:  2000-03-15       Impact factor: 11.598

2.  [Decontamination and sterilization of surgical instruments in suspected Creutzfeldt-Jakob disease. Are we converting to the recommendations by the Robert Koch Institute?].

Authors:  A Tropitzsch; H P Zenner
Journal:  HNO       Date:  2004-10       Impact factor: 1.284

Review 3.  Motor neuron disease: etiology, pathogenesis and treatment--a review.

Authors:  D J Donohoe; B Brady
Journal:  Ir J Med Sci       Date:  1996 Jul-Sep       Impact factor: 1.568

Review 4.  More than Just a Phase: Prions at the Crossroads of Epigenetic Inheritance and Evolutionary Change.

Authors:  Anupam K Chakravarty; Daniel F Jarosz
Journal:  J Mol Biol       Date:  2018-07-19       Impact factor: 5.469

5.  Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform.

Authors:  S Lehmann; D A Harris
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-28       Impact factor: 11.205

6.  A prospective study of CSF markers in 250 patients with possible Creutzfeldt-Jakob disease.

Authors:  B Van Everbroeck; S Quoilin; J Boons; J J Martin; P Cras
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-09       Impact factor: 10.154

7.  A 2cM genome-wide scan of European Holstein cattle affected by classical BSE.

Authors:  Brenda M Murdoch; Michael L Clawson; William W Laegreid; Paul Stothard; Matthew Settles; Stephanie McKay; Aparna Prasad; Zhiquan Wang; Stephen S Moore; John L Williams
Journal:  BMC Genet       Date:  2010-03-29       Impact factor: 2.797

8.  PRNP haplotype associated with classical BSE incidence in European Holstein cattle.

Authors:  Brenda M Murdoch; Michael L Clawson; Samuel Yue; Urmila Basu; Stephanie McKay; Matthew Settles; Rossana Capoferri; William W Laegreid; John L Williams; Stephen S Moore
Journal:  PLoS One       Date:  2010-09-16       Impact factor: 3.240

Review 9.  Endocytosis of glycosylphosphatidylinositol-anchored proteins.

Authors:  Shaheen E Lakhan; Shefali Sabharanjak; Ananya De
Journal:  J Biomed Sci       Date:  2009-10-15       Impact factor: 8.410

10.  Mutations at codons 178, 200-129, and 232 contributed to the inherited prion diseases in Korean patients.

Authors:  Bo-Yeong Choi; Su Yeon Kim; So-Young Seo; Seong Soo A An; Sangyun Kim; Sang-Eun Park; Seung-Han Lee; Yun-Ju Choi; Sang-Jin Kim; Chi-Kyeong Kim; Jun-Sun Park; Young-Ran Ju
Journal:  BMC Infect Dis       Date:  2009-08-22       Impact factor: 3.090

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