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Journal Abstract Search

211 related items for PubMed ID: 21600043

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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 22; 43(10):e53. PubMed ID: 17047093
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  • 4. PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.
    Bishop MT, Pennington C, Heath CA, Will RG, Knight RS.
    BMC Med Genet; 2009 Dec 26; 10():146. PubMed ID: 20035629
    [Abstract] [Full Text] [Related]

  • 5. 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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  • 6. Association of the PRNP regulatory region polymorphisms with the occurrence of sporadic Creutzfeldt-Jakob disease.
    Bratosiewicz-Wąsik J, Smoleń-Dzirba J, Watała C, Rozemuller AJ, Jansen C, Spliet W, Jansen GH, Wąsik TJ, Liberski PP.
    Folia Neuropathol; 2012 Jan 16; 50(1):68-73. PubMed ID: 22505365
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  • 8. 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 16; 12(5):389-94. PubMed ID: 14970845
    [Abstract] [Full Text] [Related]

  • 9. 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 May 16; 6(7):e22090. PubMed ID: 21799773
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. 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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  • 12. PRNP 1368 polymorphism is not associated with sporadic Creutzfeldt-Jakob disease in the Korean population.
    Jeong BH, Lee KH, Lee YJ, Kim YH, Cho YS, Carp RI, Kim YS.
    Eur J Neurol; 2008 Aug 15; 15(8):846-50. PubMed ID: 18549395
    [Abstract] [Full Text] [Related]

  • 13. 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 15; 8(1):57-66. PubMed ID: 19081515
    [Abstract] [Full Text] [Related]

  • 14. Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.
    Baiardi S, Rossi M, Mammana A, Appleby BS, Barria MA, Calì I, Gambetti P, Gelpi E, Giese A, Ghetti B, Herms J, Ladogana A, Mikol J, Pal S, Ritchie DL, Ruf V, Windl O, Capellari S, Parchi P.
    Acta Neuropathol; 2021 Oct 15; 142(4):707-728. PubMed ID: 34324063
    [Abstract] [Full Text] [Related]

  • 15. Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease.
    Salvatore M, Genuardi M, Petraroli R, Masullo C, D'Alessandro M, Pocchiari M.
    Hum Genet; 1994 Oct 15; 94(4):375-9. PubMed ID: 7927332
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  • 16. Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures.
    Cassard H, Huor A, Espinosa JC, Douet JY, Lugan S, Aron N, Vilette D, Delisle MB, Marín-Moreno A, Peran P, Beringue V, Torres JM, Ironside JW, Andreoletti O.
    mBio; 2020 Jun 16; 11(3):. PubMed ID: 32546613
    [Abstract] [Full Text] [Related]

  • 17. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
    Schmitz M, Lüllmann K, Zafar S, Ebert E, Wohlhage M, Oikonomou P, Schlomm M, Mitrova E, Beekes M, Zerr I.
    Neurobiol Aging; 2014 May 16; 35(5):1177-88. PubMed ID: 24360565
    [Abstract] [Full Text] [Related]

  • 18. Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.
    Windl O, Dempster M, Estibeiro JP, Lathe R, de Silva R, Esmonde T, Will R, Springbett A, Campbell TA, Sidle KC, Palmer MS, Collinge J.
    Hum Genet; 1996 Sep 16; 98(3):259-64. PubMed ID: 8707291
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  • 19. PRNP contains both intronic and upstream regulatory regions that may influence susceptibility to Creutzfeldt-Jakob Disease.
    McCormack JE, Baybutt HN, Everington D, Will RG, Ironside JW, Manson JC.
    Gene; 2002 Apr 17; 288(1-2):139-46. PubMed ID: 12034503
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  • 20. Neuropathologically directed profiling of PRNP somatic and germline variants in sporadic human prion disease.
    McDonough GA, Cheng Y, Morillo KS, Doan RN, Zhou Z, Kenny CJ, Foutz A, Kim C, Cohen ML, Appleby BS, Walsh CA, Safar JG, Huang AY, Miller MB.
    Acta Neuropathol; 2024 Jul 24; 148(1):10. PubMed ID: 39048735
    [Abstract] [Full Text] [Related]

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