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Results: 1 to 20 of 147

1.

The hOGG1 Ser326Cys polymorphism and Huntington's disease.

Coppedè F, Migheli F, Ceravolo R, Bregant E, Rocchi A, Petrozzi L, Unti E, Lonigro R, Siciliano G, Migliore L.

Toxicology. 2010 Dec 5;278(2):199-203. doi: 10.1016/j.tox.2009.10.019. Epub 2009 Oct 24.

PMID:
19857538
[PubMed - indexed for MEDLINE]
2.

Association of the hOGG1 Ser326Cys polymorphism with sporadic amyotrophic lateral sclerosis.

Coppedè F, Mancuso M, Lo Gerfo A, Carlesi C, Piazza S, Rocchi A, Petrozzi L, Nesti C, Micheli D, Bacci A, Migliore L, Murri L, Siciliano G.

Neurosci Lett. 2007 Jun 13;420(2):163-8. Epub 2007 May 5.

PMID:
17531381
[PubMed - indexed for MEDLINE]
3.

The hOGG1 Ser326Cys polymorphism is not associated with sporadic Parkinson's disease.

Coppedè F, Ceravolo R, Migheli F, Fanucchi F, Frosini D, Siciliano G, Bonuccelli U, Migliore L.

Neurosci Lett. 2010 Apr 12;473(3):248-51. doi: 10.1016/j.neulet.2010.02.059. Epub 2010 Mar 1.

PMID:
20193742
[PubMed - indexed for MEDLINE]
4.

A Ser326Cys polymorphism in the DNA repair gene hOGG1 is not associated with sporadic Alzheimer's disease.

Coppedè F, Mancuso M, Lo Gerfo A, Manca ML, Petrozzi L, Migliore L, Siciliano G, Murri L.

Neurosci Lett. 2007 Mar 13;414(3):282-5. Epub 2006 Dec 29.

PMID:
17240059
[PubMed - indexed for MEDLINE]
5.

Expansion of a (CAG)n repeat region in a sporadic case of HD.

Bozza A, Malagù S, Calzolari E, Novelletto A, Pavoni M, del Senno L.

Acta Neurol Scand. 1995 Aug;92(2):132-4.

PMID:
7484060
[PubMed - indexed for MEDLINE]
6.

8-Oxoguanine incision activity is impaired in lung tissues of NSCLC patients with the polymorphism of OGG1 and XRCC1 genes.

Janik J, Swoboda M, Janowska B, Cieśla JM, Gackowski D, Kowalewski J, Olinski R, Tudek B, Speina E.

Mutat Res. 2011 May 10;709-710:21-31. doi: 10.1016/j.mrfmmm.2011.02.009. Epub 2011 Mar 3.

PMID:
21376741
[PubMed - indexed for MEDLINE]
7.

Genetic polymorphisms adjacent to the CAG repeat influence clinical features at onset in Huntington's disease.

Vuillaume I, Vermersch P, Destée A, Petit H, Sablonnière B.

J Neurol Neurosurg Psychiatry. 1998 Jun;64(6):758-62.

PMID:
9647305
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Stoichiometry of base excision repair proteins correlates with increased somatic CAG instability in striatum over cerebellum in Huntington's disease transgenic mice.

Goula AV, Berquist BR, Wilson DM 3rd, Wheeler VC, Trottier Y, Merienne K.

PLoS Genet. 2009 Dec;5(12):e1000749. doi: 10.1371/journal.pgen.1000749. Epub 2009 Dec 4.

PMID:
19997493
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Methyltetrahydrofolate reductase polymorphism influences onset of Huntington's disease.

Brune N, Andrich J, Gencik M, Saft C, Müller T, Valentin S, Przuntek H, Epplen JT.

J Neural Transm Suppl. 2004;(68):105-10.

PMID:
15354395
[PubMed - indexed for MEDLINE]
10.

The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease.

Klempíř J, Zidovská J, Stochl J, Ing VK, Uhrová T, Roth J.

Mov Disord. 2011 Jan;26(1):125-9. doi: 10.1002/mds.23436. Epub 2010 Nov 10.

PMID:
21322024
[PubMed - indexed for MEDLINE]
11.

The impact of single-nucleotide polymorphisms (SNPs) in OGG1 and XPC on the age at onset of Huntington disease.

Berger F, Vaslin L, Belin L, Asselain B, Forlani S, Humbert S, Durr A, Hall J.

Mutat Res. 2013 Aug 15;755(2):115-9. doi: 10.1016/j.mrgentox.2013.04.020. Epub 2013 Jul 2.

PMID:
23830927
[PubMed - indexed for MEDLINE]
12.

Linkage disequilibrium between the expanded (CAG)n repeat and an allele of the adjacent (CCG)n repeat in Huntington's disease patients of Greek origin.

Yapijakis C, Vassilopoulos D, Tzagournisakis M, Maris T, Fesdjian C, Papageorgiou C, Plaitakis A.

Eur J Hum Genet. 1995;3(4):228-34.

PMID:
8528671
[PubMed - indexed for MEDLINE]
13.

Polymorphism of HD and UCHL-1 genes in Huntington's disease.

Xu EH, Tang Y, Li D, Jia JP.

J Clin Neurosci. 2009 Nov;16(11):1473-7. doi: 10.1016/j.jocn.2009.03.027. Epub 2009 Aug 14.

PMID:
19683447
[PubMed - indexed for MEDLINE]
14.

Inherited CAG.CTG allele length is a major modifier of somatic mutation length variability in Huntington disease.

Veitch NJ, Ennis M, McAbney JP; US-Venezuela Collaborative Research Project, Shelbourne PF, Monckton DG.

DNA Repair (Amst). 2007 Jun 1;6(6):789-96. Epub 2007 Feb 12.

PMID:
17293170
[PubMed - indexed for MEDLINE]
15.

DNA damage and repair in gastric cancer--a correlation with the hOGG1 and RAD51 genes polymorphisms.

Poplawski T, Arabski M, Kozirowska D, Blasinska-Morawiec M, Morawiec Z, Morawiec-Bajda A, Klupińska G, Jeziorski A, Chojnacki J, Blasiak J.

Mutat Res. 2006 Oct 10;601(1-2):83-91. Epub 2006 Jul 14.

PMID:
16843501
[PubMed - indexed for MEDLINE]
16.

Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease.

Agostinho Lde A, Rocha CF, Medina-Acosta E, Barboza HN, da Silva AF, Pereira SP, da Silva Idos S, Paradela ER, Figueiredo AL, Nogueira Ede M, Alvarenga RM, Hernan Cabello P, dos Santos SR, Paiva CL.

J Hum Genet. 2012 Dec;57(12):796-803. doi: 10.1038/jhg.2012.120. Epub 2012 Oct 11. Erratum in: J Hum Genet. 2012 Dec;57(12):810.

PMID:
23051704
[PubMed - indexed for MEDLINE]
17.

Age at onset in Huntington's disease: replication study on the associations of ADORA2A, HAP1 and OGG1.

Taherzadeh-Fard E, Saft C, Wieczorek S, Epplen JT, Arning L.

Neurogenetics. 2010 Oct;11(4):435-9. doi: 10.1007/s10048-010-0248-3. Epub 2010 May 30.

PMID:
20512606
[PubMed - indexed for MEDLINE]
18.

Repair of oxidative DNA damage is delayed in the Ser326Cys polymorphic variant of the base excision repair protein OGG1.

Kershaw RM, Hodges NJ.

Mutagenesis. 2012 Jul;27(4):501-10. doi: 10.1093/mutage/ges012. Epub 2012 Mar 25.

PMID:
22451681
[PubMed - indexed for MEDLINE]
Free Article
19.

hOGG1 Ser326Cys polymorphism and G:C-to-T:A mutations: no evidence for a role in tobacco-related non small cell lung cancer.

Hu YC, Ahrendt SA.

Int J Cancer. 2005 Apr 10;114(3):387-93.

PMID:
15551330
[PubMed - indexed for MEDLINE]
20.

[Huntington's disease: clinical and molecular genetics].

Warita H, Shiro Y, Kashihara K, Abe K.

Nihon Rinsho. 1999 Apr;57(4):896-9. Review. Japanese.

PMID:
10222786
[PubMed - indexed for MEDLINE]

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