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Literature DB >> 1347972

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

C L Vnencak-Jones, J A Phillips.

Abstract

Entities: Gene

Mesh：

Substances：

Year: 1992 PMID： 1347972 PMCID： PMC1682631

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

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4 in total

1. Deletion in prion protein gene in a Moroccan family.

Authors: J L Laplanche; J Chatelain; J M Launay; C Gazengel; M Vidaud
Journal: Nucleic Acids Res Date: 1990-11-25 Impact factor: 16.971

2. Genomic structure of the human prion protein gene.

Authors: C Puckett; P Concannon; C Casey; L Hood
Journal: Am J Hum Genet Date: 1991-08 Impact factor: 11.025

3. 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

4. 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

4 in total

8 in total

1. Research on familial Creutzfeldt-Jakob disease (FCJD) resulting in presymptomatic testing: implications for the Human Genome Project.

Authors: Janet E Ulm; Cindy L Vnencak-Jones; Patrick Bosque
Journal: J Genet Couns Date: 1993-03 Impact factor: 2.537

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

Review 4. A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene).

Authors: R B Petersen; L G Goldfarb; M Tabaton; P Brown; L Monari; P Cortelli; P Montagna; L Autilio-Gambetti; D C Gajdusek; E Lugaresi
Journal: Mol Neurobiol Date: 1994 Apr-Jun Impact factor: 5.590

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

1. Deletion in prion protein gene in a Moroccan family.

2. Genomic structure of the human prion protein gene.

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

4. Molecular cloning of a human prion protein cDNA.

1. Research on familial Creutzfeldt-Jakob disease (FCJD) resulting in presymptomatic testing: implications for the Human Genome Project.

Review 2. Etiology and pathogenesis of prion diseases.

Review 3. Inherited prion diseases.

Review 4. A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene).

Review 5. Neurodegeneration in humans caused by prions.

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

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

Review 8. Prions and related neurological diseases.