Literature DB >> 8197105

Inherited prion diseases.

S B Prusiner1.   

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Year:  1994        PMID： 8197105      PMCID： PMC43836          DOI： 10.1073/pnas.91.11.4611

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN： 0027-8424            Impact factor:   11.205


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  50 in total

1.  New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred.

Authors:  L G Goldfarb; M Haltia; P Brown; A Nieto; J Kovanen; W R McCombie; S Trapp; D C Gajdusek
Journal:  Lancet       Date:  1991-02-16       Impact factor: 79.321

Review 2.  Mutations and polymorphisms in the prion protein gene.

Authors:  M S Palmer; J Collinge
Journal:  Hum Mutat       Date:  1993       Impact factor: 4.878

3.  Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.

Authors:  L Monari; S G Chen; P Brown; P Parchi; R B Petersen; J Mikol; F Gray; P Cortelli; P Montagna; B Ghetti
Journal:  Proc Natl Acad Sci U S A       Date:  1994-03-29       Impact factor: 11.205

4.  Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins.

Authors:  K M Pan; M Baldwin; J Nguyen; M Gasset; A Serban; D Groth; I Mehlhorn; Z Huang; R J Fletterick; F E Cohen
Journal:  Proc Natl Acad Sci U S A       Date:  1993-12-01       Impact factor: 11.205

5.  Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter.

Authors:  M C Speer; D Goldgaber; L G Goldfarb; A D Roses; M A Pericak-Vance
Journal:  Genomics       Date:  1991-02       Impact factor: 5.736

6.  Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).

Authors:  R Gabizon; H Rosenmann; Z Meiner; I Kahana; E Kahana; Y Shugart; J Ott; S B Prusiner
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

Review 7.  Genetic and infectious prion diseases.

Authors:  S B Prusiner
Journal:  Arch Neurol       Date:  1993-11

8.  [18F]FDG PET in fatal familial insomnia: the functional effects of thalamic lesions.

Authors:  D Perani; P Cortelli; G Lucignani; P Montagna; P Tinuper; R Gallassi; P Gambetti; G L Lenzi; E Lugaresi; F Fazio
Journal:  Neurology       Date:  1993-12       Impact factor: 9.910

9.  Spontaneous neurodegeneration in transgenic mice with mutant prion protein.

Authors:  K K Hsiao; M Scott; D Foster; D F Groth; S J DeArmond; S B Prusiner
Journal:  Science       Date:  1990-12-14       Impact factor: 47.728

10.  Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins.

Authors:  D Westaway; S J DeArmond; J Cayetano-Canlas; D Groth; D Foster; S L Yang; M Torchia; G A Carlson; S B Prusiner
Journal:  Cell       Date:  1994-01-14       Impact factor: 41.582
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  10 in total

1.  Immobilized prion protein undergoes spontaneous rearrangement to a conformation having features in common with the infectious form.

Authors:  E Leclerc; D Peretz; H Ball; H Sakurai; G Legname; A Serban; S B Prusiner; D R Burton; R A Williamson
Journal:  EMBO J       Date:  2001-04-02       Impact factor: 11.598

2.  Affinity-tagged miniprion derivatives spontaneously adopt protease-resistant conformations.

Authors:  S Supattapone; H O Nguyen; T Muramoto; F E Cohen; S J DeArmond; S B Prusiner; M Scott
Journal:  J Virol       Date:  2000-12       Impact factor: 5.103

3.  Sphingosine kinase-dependent migration of immature dendritic cells in response to neurotoxic prion protein fragment.

Authors:  Nicole C Kaneider; Arthur Kaser; Stefan Dunzendorfer; Herbert Tilg; Christian J Wiedermann
Journal:  J Virol       Date:  2003-05       Impact factor: 5.103

4.  Requirements for mutant and wild-type prion protein misfolding in vitro.

Authors:  Geoffrey P Noble; Daniel J Walsh; Michael B Miller; Walker S Jackson; Surachai Supattapone
Journal:  Biochemistry       Date:  2015-01-22       Impact factor: 3.162

5.  Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity.

Authors:  D Riesner; K Kellings; K Post; H Wille; H Serban; D Groth; M A Baldwin; S B Prusiner
Journal:  J Virol       Date:  1996-03       Impact factor: 5.103

6.  Vertical transmission of bovine spongiform encephalopathy prions evaluated in a transgenic mouse model.

Authors:  J Castilla; A Brun; F Díaz-San Segundo; F J Salguero; A Gutiérrez-Adán; B Pintado; M A Ramírez; L del Riego; J M Torres
Journal:  J Virol       Date:  2005-07       Impact factor: 5.103

7.  Atomic structures suggest determinants of transmission barriers in mammalian prion disease.

Authors:  Marcin I Apostol; Jed J W Wiltzius; Michael R Sawaya; Duilio Cascio; David Eisenberg
Journal:  Biochemistry       Date:  2011-03-11       Impact factor: 3.162

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

Review 9.  Transgenic and knockout mice in the study of neurodegenerative diseases.

Authors:  A Aguzzi; S Brandner; S Marino; J P Steinbach
Journal:  J Mol Med (Berl)       Date:  1996-03       Impact factor: 4.599

10.  Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues.

Authors:  A Jiménez-Huete; P M Lievens; R Vidal; P Piccardo; B Ghetti; F Tagliavini; B Frangione; F Prelli
Journal:  Am J Pathol       Date:  1998-11       Impact factor: 4.307
  10 in total

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