180 related articles for article (PubMed ID: 22895088)
1. Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob disease.
Bratosiewicz-Wąsik J; Smoleń-Dzirba J; Rozemuller AJ; Jansen C; Spliet W; Jansen GH; Wąsik TJ; Liberski PP
Prion; 2012; 6(4):413-6. PubMed ID: 22895088
[TBL] [Abstract][Full Text] [Related]
2. 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; 50(1):68-73. PubMed ID: 22505365
[TBL] [Abstract][Full Text] [Related]
3. 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; ; Kretzschmar HA
J Med Genet; 2006 Oct; 43(10):e53. PubMed ID: 17047093
[TBL] [Abstract][Full Text] [Related]
4. 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; 12():73. PubMed ID: 21600043
[TBL] [Abstract][Full Text] [Related]
5. 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; 10():146. PubMed ID: 20035629
[TBL] [Abstract][Full Text] [Related]
6. 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; 411(3):163-7. PubMed ID: 17134829
[TBL] [Abstract][Full Text] [Related]
7. Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.
Mead S; Mahal SP; Beck J; Campbell T; Farrall M; Fisher E; Collinge J
Am J Hum Genet; 2001 Dec; 69(6):1225-35. PubMed ID: 11704923
[TBL] [Abstract][Full Text] [Related]
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; 12(5):389-94. PubMed ID: 14970845
[TBL] [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; 6(7):e22090. PubMed ID: 21799773
[TBL] [Abstract][Full Text] [Related]
10. 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(8):846-50. PubMed ID: 18549395
[TBL] [Abstract][Full Text] [Related]
11. 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; 6(4):229-32. PubMed ID: 16217673
[TBL] [Abstract][Full Text] [Related]
12. 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; 8():77. PubMed ID: 18072964
[TBL] [Abstract][Full Text] [Related]
13. A polymorphism in the YWHAH gene encoding 14-3-3 eta that is not associated with sporadic Creutzfeldt-Jakob disease (CJD).
Yun J; Jeong BH; Kim HJ; Park YJ; Lee YJ; Choi EK; Carp RI; Kim YS
Mol Biol Rep; 2012 Apr; 39(4):3619-25. PubMed ID: 21739144
[TBL] [Abstract][Full Text] [Related]
14. 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; 288(1-2):139-46. PubMed ID: 12034503
[TBL] [Abstract][Full Text] [Related]
15. 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; 21(8):1897-906. PubMed ID: 22210626
[TBL] [Abstract][Full Text] [Related]
16. 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; 10():32. PubMed ID: 19351416
[TBL] [Abstract][Full Text] [Related]
17. 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; 98(3):259-64. PubMed ID: 8707291
[TBL] [Abstract][Full Text] [Related]
18. 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; 94(4):375-9. PubMed ID: 7927332
[TBL] [Abstract][Full Text] [Related]
19. The First Meta-Analysis of the M129V Single-Nucleotide Polymorphism (SNP) of the Prion Protein Gene (
Kim YC; Jeong BH
Cells; 2021 Nov; 10(11):. PubMed ID: 34831353
[TBL] [Abstract][Full Text] [Related]
20. 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; 8(1):57-66. PubMed ID: 19081515
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
