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Literature DB >> 2563037

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease.

F Owen, M Poulter, R Lofthouse, J Collinge, T J Crow, D Risby, H F Baker, R M Ridley, K Hsiao, S B Prusiner.

Abstract

Entities: Mutation Species

Mesh：

Substances：

Year: 1989 PMID： 2563037 DOI： 10.1016/s0140-6736(89)91713-3

Source DB: PubMed Journal: Lancet ISSN： 0140-6736 Impact factor: 79.321

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64 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

Review 2. Genetic PrP Prion Diseases.

Authors: Mee-Ohk Kim; Leonel T Takada; Katherine Wong; Sven A Forner; Michael D Geschwind
Journal: Cold Spring Harb Perspect Biol Date: 2018-05-01 Impact factor: 10.005

Review 3. Current status review: cerebral amyloid.

Authors: L W Duchen
Journal: Int J Exp Pathol Date: 1992-08 Impact factor: 1.925

4. Starting again with clinical research.

Authors: T J Crow
Journal: BMJ Date: 1991-03-02

5. High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes.

Authors: U Finckh; T Müller-Thomsen; U Mann; C Eggers; J Marksteiner; W Meins; G Binetti; A Alberici; C Hock; R M Nitsch; A Gal
Journal: Am J Hum Genet Date: 2000-01 Impact factor: 11.025

Review 6. Prions.

Authors: David W Colby; Stanley B Prusiner
Journal: Cold Spring Harb Perspect Biol Date: 2011-01-01 Impact factor: 10.005

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease.

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

Review 2. Genetic PrP Prion Diseases.

Review 3. Current status review: cerebral amyloid.

4. Starting again with clinical research.

5. High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes.

Review 6. Prions.

7. Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases.

Review 8. Molecular neurology of prion disease.

9. Human amyloid-beta synthesis and clearance rates as measured in cerebrospinal fluid in vivo.

10. Codon 129 changes in the prion protein gene in Caucasians.