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Literature DB >> 1979164

Deletion in prion protein gene in a Moroccan family.

J L Laplanche¹, J Chatelain, J M Launay, C Gazengel, M Vidaud.

Abstract

Entities: Species

Mesh：

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Year: 1990 PMID： 1979164 PMCID： PMC332684 DOI： 10.1093/nar/18.22.6745

Source DB: PubMed Journal: Nucleic Acids Res ISSN： 0305-1048 Impact factor: 16.971

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5 in total

1. Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome.

Authors: K Doh-ura; J Tateishi; H Sasaki; T Kitamoto; Y Sakaki
Journal: Biochem Biophys Res Commun Date: 1989-09-15 Impact factor: 3.575

2. Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysis.

Authors: J Collinge; A E Harding; F Owen; M Poulter; R Lofthouse; A M Boughey; T Shah; T J Crow
Journal: Lancet Date: 1989-07-01 Impact factor: 79.321

3. Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome.

Authors: K Hsiao; H F Baker; T J Crow; M Poulter; F Owen; J D Terwilliger; D Westaway; J Ott; S B Prusiner
Journal: Nature Date: 1989-03-23 Impact factor: 49.962

4. High incidence of Creutzfeldt-Jakob disease in North African immigrants to France.

Authors: F Cathala; P Brown; P LeCanuet; D C Gajdusek
Journal: Neurology Date: 1985-06 Impact factor: 9.910

5. Molecular cloning of a human prion protein cDNA.

Authors: H A Kretzschmar; L E Stowring; D Westaway; W H Stubblebine; S B Prusiner; S J Dearmond
Journal: DNA Date: 1986-08

5 in total

12 in total

1. Identification of heterogeneous PrP gene deletions in controls by detection of allele-specific heteroduplexes (DASH)

Authors: C L Vnencak-Jones; J A Phillips
Journal: Am J Hum Genet Date: 1992-04 Impact factor: 11.025

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

Review 3. Inherited prion diseases.

Authors: S B Prusiner
Journal: Proc Natl Acad Sci U S A Date: 1994-05-24 Impact factor: 11.205

10. PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.

Authors: Matthew T Bishop; Catherine Pennington; Craig A Heath; Robert G Will; Richard S G Knight
Journal: BMC Med Genet Date: 2009-12-26 Impact factor: 2.103

Deletion in prion protein gene in a Moroccan family.

1. Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome.

2. Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysis.

3. Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome.

4. High incidence of Creutzfeldt-Jakob disease in North African immigrants to France.

5. Molecular cloning of a human prion protein cDNA.

1. Identification of heterogeneous PrP gene deletions in controls by detection of allele-specific heteroduplexes (DASH)

Review 2. Etiology and pathogenesis of prion diseases.

Review 3. Inherited prion diseases.

4. A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformation.

5. Polymorphisms of the prion protein gene (PRNP) in a Korean population.

Review 6. Neurodegeneration in humans caused by prions.

7. Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells.

8. Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease.

9. Fibrils in brain of Rocky Mountain elk with chronic wasting disease contain scrapie amyloid.

10. PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.