Literature DB >> 2247227

Inherited human prion diseases.

K Hsiao1, S B Prusiner.   

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Year:  1990        PMID: 2247227     DOI: 10.1212/wnl.40.12.1820

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


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  32 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.  How now mad cow?

Authors:  P J Harrison; G W Roberts
Journal:  BMJ       Date:  1992-04-11

3.  Diffuse deposition of immunohistochemically labeled prion protein in the granular layer of the cerebellum in a patient with Creutzfeldt-Jakob disease.

Authors:  H A Kretzschmar; T Kitamoto; J Doerr-Schott; P Mehraein; J Tateishi
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

4.  Alzheimer's disease and the beta amyloid gene.

Authors:  P J Harrison
Journal:  BMJ       Date:  1991-06-22

5.  Binding of bovine T194A PrP(C) by PrP(Sc)-specific antibodies: potential implications for immunotherapy of familial prion diseases.

Authors:  Claudia A Madampage; Pekka Määttänen; Kristen Marciniuk; Robert Brownlie; Olga Andrievskaia; Andrew Potter; Neil R Cashman; Jeremy S Lee; Scott Napper
Journal:  Prion       Date:  2013-05-31       Impact factor: 3.931

Review 6.  The spongiform encephalopathies.

Authors:  R G Will
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-09       Impact factor: 10.154

7.  Prion protein expression and superoxide dismutase activity.

Authors:  D R Brown; A Besinger
Journal:  Biochem J       Date:  1998-09-01       Impact factor: 3.857

Review 8.  Cofactor molecules: Essential partners for infectious prions.

Authors:  Surachai Supattapone
Journal:  Prog Mol Biol Transl Sci       Date:  2020-08-24       Impact factor: 3.622

9.  Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.

Authors:  J Chapman; P Brown; L G Goldfarb; A Arlazoroff; D C Gajdusek; A D Korczyn
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-10       Impact factor: 10.154

10.  Human prion proteins with pathogenic mutations share common conformational changes resulting in enhanced binding to glycosaminoglycans.

Authors:  Shaoman Yin; Nancy Pham; Shuiliang Yu; Chaoyang Li; Poki Wong; Binggong Chang; Shin-Chung Kang; Emiliano Biasini; Po Tien; David A Harris; Man-Sun Sy
Journal:  Proc Natl Acad Sci U S A       Date:  2007-04-24       Impact factor: 11.205

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