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370 related items for PubMed ID: 17047093

  • 1. Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study.
    Vollmert C, Windl O, Xiang W, Rosenberger A, Zerr I, Wichmann HE, Bickeböller H, Illig T, KORA group, Kretzschmar HA.
    J Med Genet; 2006 Oct; 43(10):e53. PubMed ID: 17047093
    [Abstract] [Full Text] [Related]

  • 2. Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease.
    Croes EA, Alizadeh BZ, Bertoli-Avella AM, Rademaker T, Vergeer-Drop J, Dermaut B, Houwing-Duistermaat JJ, Wientjens DP, Hofman A, Van Broeckhoven C, van Duijn CM.
    Eur J Hum Genet; 2004 May; 12(5):389-94. PubMed ID: 14970845
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  • 5. A polymorphism in the regulatory region of PRNP is associated with increased risk of sporadic Creutzfeldt-Jakob disease.
    Sanchez-Juan P, Bishop MT, Croes EA, Knight RS, Will RG, van Duijn CM, Manson JC.
    BMC Med Genet; 2011 May 22; 12():73. PubMed ID: 21600043
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  • 8. Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
    Mead S, Uphill J, Beck J, Poulter M, Campbell T, Lowe J, Adamson G, Hummerich H, Klopp N, Rückert IM, Wichmann HE, Azazi D, Plagnol V, Pako WH, Whitfield J, Alpers MP, Whittaker J, Balding DJ, Zerr I, Kretzschmar H, Collinge J.
    Hum Mol Genet; 2012 Apr 15; 21(8):1897-906. PubMed ID: 22210626
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  • 9. Regulatory sequences of the PRNP gene influence susceptibility to sporadic Creutzfeldt-Jakob disease.
    Bratosiewicz-Wasik J, Liberski PP, Golanska E, Jansen GH, Wasik TJ.
    Neurosci Lett; 2007 Jan 16; 411(3):163-7. PubMed ID: 17134829
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  • 10. Genetic cross-interaction between APOE and PRNP in sporadic Alzheimer's and Creutzfeldt-Jakob diseases.
    Calero O, Bullido MJ, Clarimón J, Frank-García A, Martínez-Martín P, Lleó A, Rey MJ, Rábano A, Blesa R, Gómez-Isla T, Valdivieso F, de Pedro-Cuesta J, Ferrer I, Calero M.
    PLoS One; 2011 Jan 16; 6(7):e22090. PubMed ID: 21799773
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  • 11. Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
    Mead S, Poulter M, Uphill J, Beck J, Whitfield J, Webb TE, Campbell T, Adamson G, Deriziotis P, Tabrizi SJ, Hummerich H, Verzilli C, Alpers MP, Whittaker JC, Collinge J.
    Lancet Neurol; 2009 Jan 16; 8(1):57-66. PubMed ID: 19081515
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  • 12. Absence of Strong Genetic Linkage Disequilibrium between Single Nucleotide Polymorphisms (SNPs) in the Prion Protein Gene (PRNP) and the Prion-Like Protein Gene (PRND) in the Horse, a Prion-Resistant Species.
    Won SY, Kim YC, Do K, Jeong BH.
    Genes (Basel); 2020 May 07; 11(5):. PubMed ID: 32392732
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  • 13. Polymorphism at 3' UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt-Jakob disease.
    Jeong BH, Kim NH, Choi EK, Lee C, Song YH, Kim JI, Carp RI, Kim YS.
    Eur J Hum Genet; 2005 Sep 07; 13(9):1094-7. PubMed ID: 15986038
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  • 14. The First Report of Polymorphisms and Genetic Features of the prion-like Protein Gene (PRND) in a Prion Disease-Resistant Animal, Dog.
    Won SY, Kim YC, Kim K, Kim AD, Jeong BH.
    Int J Mol Sci; 2019 Mar 20; 20(6):. PubMed ID: 30897750
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  • 15. The First Meta-Analysis of the M129V Single-Nucleotide Polymorphism (SNP) of the Prion Protein Gene (PRNP) with Sporadic Creutzfeldt-Jakob Disease.
    Kim YC, Jeong BH.
    Cells; 2021 Nov 11; 10(11):. PubMed ID: 34831353
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  • 16. Polymorphisms at codons 56 and 174 of the prion-like protein gene (PRND) are not associated with sporadic Creutzfeldt-Jakob disease.
    Jeong BH, Kim NH, Kim JI, Carp RI, Kim YS.
    J Hum Genet; 2005 Nov 11; 50(6):311-314. PubMed ID: 15933804
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  • 17. No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease.
    Sánchez-Juan P, Bishop MT, Green A, Giannattasio C, Arias-Vasquez A, Poleggi A, Knight RS, van Duijn CM.
    BMC Med Genet; 2007 Dec 11; 8():77. PubMed ID: 18072964
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  • 19. Polymorphic microsatellite sites in the PRNP region point to excess of homozygotes in Creutzfeldt-Jakob disease patients.
    Geldermann H, Bartenschlager H, Preuss S, Melchinger-Wild E, Herzog K, Zerr I.
    Gene; 2006 Nov 01; 382():66-70. PubMed ID: 16889908
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  • 20. Increased frequency of positive family history of dementia in sporadic CJD.
    Krasnianski A, von Ahsen N, Heinemann U, Meissner B, Schulz-Schaeffer WJ, Kretzschmar HA, Armstrong VW, Zerr I.
    Neurobiol Aging; 2009 Apr 01; 30(4):615-21. PubMed ID: 17822808
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