Literature DB >> 7901326

The neurochemistry of prion diseases.

S J DeArmond1, S B Prusiner.   

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Year:  1993        PMID： 7901326     DOI： 10.1111/j.1471-4159.1993.tb09792.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN： 0022-3042            Impact factor:   5.372


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  5 in total

1.  Early appearance but lagged accumulation of detergent-insoluble prion protein in the brains of mice inoculated with a mouse-adapted Creutzfeldt-Jakob disease agent.

Authors:  R Nakaoke; S Sakaguchi; R Atarashi; N Nishida; K Arima; K Shigematsu; S Katamine
Journal:  Cell Mol Neurobiol       Date:  2000-12       Impact factor: 5.046

Review 2.  Etiology and pathogenesis of prion diseases.

Authors:  S J DeArmond; S B Prusiner
Journal:  Am J Pathol       Date:  1995-04       Impact factor: 4.307

3.  Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion-body myopathy.

Authors:  E Sarkozi; V Askanas; W K Engel
Journal:  Am J Pathol       Date:  1994-12       Impact factor: 4.307

4.  Activation effects of a prion protein fragment [PrP-(106-126)] on human leucocytes.

Authors:  L Diomede; S Sozzani; W Luini; M Algeri; L De Gioia; R Chiesa; P M Lievens; O Bugiani; G Forloni; F Tagliavini; M Salmona
Journal:  Biochem J       Date:  1996-12-01       Impact factor: 3.857

Review 5.  Prions and related neurological diseases.

Authors:  M Pocchiari
Journal:  Mol Aspects Med       Date:  1994
  5 in total

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