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Journal Abstract Search

133 related items for PubMed ID: 17539938

  • 1.
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  • 2. Lack of association between PRNP 1368 polymorphism and Alzheimer's disease or vascular dementia.
    Jeong BH, Lee KH, Lee YJ, Kim YJ, Choi EK, Kim YH, Cho YS, Carp RI, Kim YS.
    BMC Med Genet; 2009 Apr 08; 10():32. PubMed ID: 19351416
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  • 4. Absence of association between codon 129 and 219 polymorphisms of the prion protein gene and vascular dementia.
    Jeong BH, Na HR, Bae JC, Lee KH, Lee YJ, Kim NH, Song JH, Carp RI, Kim YS.
    Dement Geriatr Cogn Disord; 2007 Apr 08; 24(2):86-90. PubMed ID: 17570906
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  • 5. Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population.
    Jeong BH, Lee KH, Kim NH, Jin JK, Kim JI, Carp RI, Kim YS.
    Neurogenetics; 2005 Dec 08; 6(4):229-32. PubMed ID: 16217673
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  • 6. Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease.
    Poleggi A, Bizzarro A, Acciarri A, Antuono P, Bagnoli S, Cellini E, Forno GD, Giannattasio C, Lauria A, Matera MG, Nacmias B, Puopolo M, Seripa D, Sorbi S, Wekstein DR, Pocchiari M, Masullo C.
    Eur J Neurol; 2008 Feb 08; 15(2):173-8. PubMed ID: 18217885
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  • 7. 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 08; 15(8):846-50. PubMed ID: 18549395
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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 08; 12(5):389-94. PubMed ID: 14970845
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  • 9. Polymorphisms of the prion protein gene (PRNP) in a Korean population.
    Jeong BH, Nam JH, Lee YJ, Lee KH, Jang MK, Carp RI, Lee HD, Ju YR, Ahn Jo S, Park KY, Kim YS.
    J Hum Genet; 2004 May 08; 49(6):319-324. PubMed ID: 15148589
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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 May 08; 6(7):e22090. PubMed ID: 21799773
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  • 11. Codon 129 polymorphism of prion protein gene in is not a risk factor for Alzheimer's disease.
    Smid J, Landemberger MC, Bahia VS, Martins VR, Nitrini R.
    Arq Neuropsiquiatr; 2013 Jul 08; 71(7):423-7. PubMed ID: 23857619
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  • 12. Epidemiological genetics and meta-analysis of a polymorphism at codon 129 of the PRNP gene in Alzheimer's disease in Brazil.
    Pimentel LF, Gomes da Cunha JE, Morelato RL, de Paula F, de Oliveira JR.
    Neurol Res; 2014 Sep 08; 36(9):775-8. PubMed ID: 24620982
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  • 13. 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 Sep 08; 50(6):311-314. PubMed ID: 15933804
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  • 14. 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
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  • 19. 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 26; 43(10):e53. PubMed ID: 17047093
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  • 20. Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis.
    Del Bo R, Scarlato M, Ghezzi S, Martinelli-Boneschi F, Fenoglio C, Galimberti G, Galbiati S, Virgilio R, Galimberti D, Ferrarese C, Scarpini E, Bresolin N, Comi GP.
    Neurobiol Aging; 2006 May 26; 27(5):770.e1-770.e5. PubMed ID: 16099550
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