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Items: 1 to 20 of 154

1.

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.

2.

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.

3.

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. doi: 10.1186/1471-2350-10-146.

4.

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 Sep-Oct;6(4):413-6. doi: 10.4161/pri.21773.

5.

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.

6.

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. doi: 10.1016/S1474-4422(08)70265-5.

7.

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.

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. doi: 10.1093/hmg/ddr607.

9.

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. Review.

10.

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. doi: 10.1007/s11033-011-1136-0.

PMID:
21739144
11.

Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.

Sanchez-Juan P, Bishop MT, Aulchenko YS, Brandel JP, Rivadeneira F, Struchalin M, Lambert JC, Amouyel P, Combarros O, Sainz J, Carracedo A, Uitterlinden AG, Hofman A, Zerr I, Kretzschmar HA, Laplanche JL, Knight RS, Will RG, van Duijn CM.

Neurobiol Aging. 2012 Jul;33(7):1487.e21-8. doi: 10.1016/j.neurobiolaging.2011.10.011.

PMID:
22137330
12.

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. doi: 10.1186/1471-2350-12-73.

13.

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.

PMID:
12034503
14.

Lack of association between 14-3-3 beta gene (YWHAB) polymorphisms and sporadic Creutzfeldt-Jakob disease (CJD).

Jeong BH, Jin HT, Choi EK, Carp RI, Kim YS.

Mol Biol Rep. 2012 Dec;39(12):10647-53. doi: 10.1007/s11033-012-1954-8.

PMID:
23053962
15.

The first report of RPSA polymorphisms, also called 37/67 kDa LRP/LR gene, in sporadic Creutzfeldt-Jakob disease (CJD).

Yun J, Jin HT, Lee YJ, Choi EK, Carp RI, Jeong BH, Kim YS.

BMC Med Genet. 2011 Aug 13;12:108. doi: 10.1186/1471-2350-12-108.

16.

Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study.

Balendra R, Uphill J, Collinson C, Druyeh R, Adamson G, Hummerich H, Zerr I, Gambetti P, Collinge J, Mead S.

BMC Med Genet. 2016 Apr 7;17:28. doi: 10.1186/s12881-016-0278-2.

17.

Raised CSF phospho-tau concentrations in variant Creutzfeldt-Jakob disease: diagnostic and pathological implications.

Goodall CA, Head MW, Everington D, Ironside JW, Knight RS, Green AJ.

J Neurol Neurosurg Psychiatry. 2006 Jan;77(1):89-91.

18.

The epidemiological, clinical, and laboratory features of sporadic Creutzfeldt-Jakob disease patients in China: surveillance data from 2006 to 2010.

Gao C, Shi Q, Tian C, Chen C, Han J, Zhou W, Zhang BY, Jiang HY, Zhang J, Dong XP.

PLoS One. 2011;6(8):e24231. doi: 10.1371/journal.pone.0024231.

19.

RARB and STMN2 polymorphisms are not associated with sporadic Creutzfeldt-Jakob disease (CJD) in the Korean population.

Jeong BH, Kim HJ, Lee KH, Carp RI, Kim YS.

Mol Biol Rep. 2014;41(4):2389-95. doi: 10.1007/s11033-014-3093-x.

PMID:
24414001
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;30(4):615-21.

PMID:
17822808
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