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Results: 1 to 20 of 115

Similar articles for PubMed (Select 20719408)

1.

No association between DNA repair gene XRCC1 and amyotrophic lateral sclerosis.

Fang F, Umbach DM, Xu Z, Ye W, Sandler DP, Taylor JA, Kamel F.

Neurobiol Aging. 2012 May;33(5):1015.e25-6. doi: 10.1016/j.neurobiolaging.2010.07.004. Epub 2010 Aug 16.

2.

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.

Laaksovirta H, Peuralinna T, Schymick JC, Scholz SW, Lai SL, Myllykangas L, Sulkava R, Jansson L, Hernandez DG, Gibbs JR, Nalls MA, Heckerman D, Tienari PJ, Traynor BJ.

Lancet Neurol. 2010 Oct;9(10):978-85. doi: 10.1016/S1474-4422(10)70184-8.

3.

Association study between XRCC1 gene polymorphisms and sporadic amyotrophic lateral sclerosis.

Coppedè F, Migheli F, Lo Gerfo A, Fabbrizi MR, Carlesi C, Mancuso M, Corti S, Mezzina N, del Bo R, Comi GP, Siciliano G, Migliore L.

Amyotroph Lateral Scler. 2010;11(1-2):122-4. doi: 10.3109/17482960903220297.

PMID:
19707910
4.

Genome-wide analysis of the heritability of amyotrophic lateral sclerosis.

Keller MF, Ferrucci L, Singleton AB, Tienari PJ, Laaksovirta H, Restagno G, Chiò A, Traynor BJ, Nalls MA.

JAMA Neurol. 2014 Sep;71(9):1123-34. doi: 10.1001/jamaneurol.2014.1184. Erratum in: JAMA Neurol. 2014 Oct;71(10):1328.

PMID:
25023141
5.

Single-nucleotide polymorphism rs6690993 in FGGY is not associated with amyotrophic lateral sclerosisin a large Chinese cohort.

Cai B, Tang L, Zhang N, Fan D.

Neurobiol Aging. 2014 Jun;35(6):1512.e3-4. doi: 10.1016/j.neurobiolaging.2013.12.018. Epub 2013 Dec 27.

PMID:
24439956
6.

Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.

van Blitterswijk M, Blokhuis A, van Es MA, van Vught PW, Rowicka PA, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH.

Neurobiol Aging. 2012 Aug;33(8):1845.e1-3. doi: 10.1016/j.neurobiolaging.2012.01.007. Epub 2012 Feb 11.

PMID:
22330174
7.

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.

Shatunov A, Mok K, Newhouse S, Weale ME, Smith B, Vance C, Johnson L, Veldink JH, van Es MA, van den Berg LH, Robberecht W, Van Damme P, Hardiman O, Farmer AE, Lewis CM, Butler AW, Abel O, Andersen PM, Fogh I, Silani V, Chiò A, Traynor BJ, Melki J, Meininger V, Landers JE, McGuffin P, Glass JD, Pall H, Leigh PN, Hardy J, Brown RH Jr, Powell JF, Orrell RW, Morrison KE, Shaw PJ, Shaw CE, Al-Chalabi A.

Lancet Neurol. 2010 Oct;9(10):986-94. doi: 10.1016/S1474-4422(10)70197-6. Erratum in: Lancet Neurol. 2011 Mar;10(3):205.

8.

DNA repair XRCC1 Arg399Gln polymorphism is associated with the risk of development of end-stage renal disease.

Trabulus S, Guven GS, Altiparmak MR, Batar B, Tun O, Yalin AS, Tunckale A, Guven M.

Mol Biol Rep. 2012 Jun;39(6):6995-7001. doi: 10.1007/s11033-012-1529-8.

PMID:
22302399
9.

Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis.

Bogaert E, Goris A, Van Damme P, Geelen V, Lemmens R, van Es MA, van den Berg LH, Sleegers K, Verpoorten N, Timmerman V, De Jonghe P, Van Broeckhoven C, Traynor BJ, Landers JE, Brown RH Jr, Glass JD, Al-Chalabi A, Shaw CE, Birve A, Andersen PM, Slowik A, Tomik B, Melki J, Robberecht W, Van Den Bosch L.

Neurobiol Aging. 2012 Feb;33(2):418-20. doi: 10.1016/j.neurobiolaging.2010.03.007. Epub 2010 Apr 20.

10.

Screening of VCP mutations in Chinese amyotrophic lateral sclerosis patients.

Zou ZY, Liu MS, Li XG, Cui LY.

Neurobiol Aging. 2013 May;34(5):1519.e3-4. doi: 10.1016/j.neurobiolaging.2012.10.002. Epub 2012 Oct 24.

PMID:
23102936
11.

Mutation analysis of PFN1 in familial amyotrophic lateral sclerosis patients.

Daoud H, Dobrzeniecka S, Camu W, Meininger V, Dupré N, Dion PA, Rouleau GA.

Neurobiol Aging. 2013 Apr;34(4):1311.e1-2. doi: 10.1016/j.neurobiolaging.2012.09.001. Epub 2012 Oct 10.

PMID:
23062600
12.

A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS.

Wills AM, Cronin S, Slowik A, Kasperaviciute D, Van Es MA, Morahan JM, Valdmanis PN, Meininger V, Melki J, Shaw CE, Rouleau GA, Fisher EM, Shaw PJ, Morrison KE, Pamphlett R, Van den Berg LH, Figlewicz DA, Andersen PM, Al-Chalabi A, Hardiman O, Purcell S, Landers JE, Brown RH Jr.

Neurology. 2009 Jul 7;73(1):16-24. doi: 10.1212/WNL.0b013e3181a18674. Epub 2009 Mar 25.

13.

Whole-genome association studies of sporadic amyotrophic lateral sclerosis: are retroelements involved?

Mougeot JL, Richardson-Milazi S, Brooks BR.

Trends Mol Med. 2009 Apr;15(4):148-58. doi: 10.1016/j.molmed.2009.02.005. Epub 2009 Mar 21.

PMID:
19332388
14.

H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis.

van Rheenen W, Diekstra FP, van Doormaal PT, Seelen M, Kenna K, McLaughlin R, Shatunov A, Czell D, van Es MA, van Vught PW, van Damme P, Smith BN, Waibel S, Schelhaas HJ, van der Kooi AJ, de Visser M, Weber M, Robberecht W, Hardiman O, Shaw PJ, Shaw CE, Morrison KE, Al-Chalabi A, Andersen PM, Ludolph AC, Veldink JH, van den Berg LH.

Neurobiol Aging. 2013 May;34(5):1517.e5-7. doi: 10.1016/j.neurobiolaging.2012.07.020. Epub 2012 Oct 11.

PMID:
23063643
15.

Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis.

Xiao S, Sato C, Kawarai T, Goodall EF, Pall HS, Zinman LH, Robertson J, Morrison K, Rogaeva E.

Neurobiol Aging. 2008 Aug;29(8):1279-82. Epub 2007 Mar 23.

PMID:
17383054
16.

Analysis of the C9orf72 hexanucleotide repeat expansion in Korean patients with familial and sporadic amyotrophic lateral sclerosis.

Jang JH, Kwon MJ, Choi WJ, Oh KW, Koh SH, Ki CS, Kim SH.

Neurobiol Aging. 2013 Apr;34(4):1311.e7-9. doi: 10.1016/j.neurobiolaging.2012.09.004. Epub 2012 Oct 22.

PMID:
23088937
17.

[Correlations of single nucleotide polymorphisms of DNA repair gene XRCC1 to risk of colorectal cancer].

Jin MJ, Chen K, Zhang Y, Zhang W, Liu B, Zhang YJ.

Ai Zheng. 2007 Mar;26(3):274-9. Chinese.

PMID:
17355790
18.

No association of five candidate genetic variants with amyotrophic lateral sclerosis in a Chinese population.

Chen Y, Zeng Y, Huang R, Yang Y, Chen K, Song W, Zhao B, Li J, Yuan L, Shang HF.

Neurobiol Aging. 2012 Nov;33(11):2721.e3-5. doi: 10.1016/j.neurobiolaging.2012.06.004. Epub 2012 Jul 15.

PMID:
22795786
19.

Whole-genome analysis of sporadic amyotrophic lateral sclerosis.

Dunckley T, Huentelman MJ, Craig DW, Pearson JV, Szelinger S, Joshipura K, Halperin RF, Stamper C, Jensen KR, Letizia D, Hesterlee SE, Pestronk A, Levine T, Bertorini T, Graves MC, Mozaffar T, Jackson CE, Bosch P, McVey A, Dick A, Barohn R, Lomen-Hoerth C, Rosenfeld J, O'connor DT, Zhang K, Crook R, Ryberg H, Hutton M, Katz J, Simpson EP, Mitsumoto H, Bowser R, Miller RG, Appel SH, Stephan DA.

N Engl J Med. 2007 Aug 23;357(8):775-88. Epub 2007 Aug 1.

20.
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