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Items: 1 to 20 of 43

1.

Diagnostic X-rays and risk of childhood leukaemia.

Bartley K, Metayer C, Selvin S, Ducore J, Buffler P.

Int J Epidemiol. 2010 Dec;39(6):1628-37. doi: 10.1093/ije/dyq162. Epub 2010 Oct 1.

2.

Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk.

Sherborne AL, Hosking FJ, Prasad RB, Kumar R, Koehler R, Vijayakrishnan J, Papaemmanuil E, Bartram CR, Stanulla M, Schrappe M, Gast A, Dobbins SE, Ma Y, Sheridan E, Taylor M, Kinsey SE, Lightfoot T, Roman E, Irving JA, Allan JM, Moorman AV, Harrison CJ, Tomlinson IP, Richards S, Zimmermann M, Szalai C, Semsei AF, Erdelyi DJ, Krajinovic M, Sinnett D, Healy J, Gonzalez Neira A, Kawamata N, Ogawa S, Koeffler HP, Hemminki K, Greaves M, Houlston RS.

Nat Genet. 2010 Jun;42(6):492-4. doi: 10.1038/ng.585. Epub 2010 May 9.

3.

APEX1 gene amplification and its protein overexpression in osteosarcoma: correlation with recurrence, metastasis, and survival.

Yang J, Yang D, Cogdell D, Du X, Li H, Pang Y, Sun Y, Hu L, Sun B, Trent J, Chen K, Zhang W.

Technol Cancer Res Treat. 2010 Apr;9(2):161-9.

PMID:
20218738
4.

Human apurinic/apyrimidinic endonuclease (APE1) is a prognostic factor in ovarian, gastro-oesophageal and pancreatico-biliary cancers.

Al-Attar A, Gossage L, Fareed KR, Shehata M, Mohammed M, Zaitoun AM, Soomro I, Lobo DN, Abbotts R, Chan S, Madhusudan S.

Br J Cancer. 2010 Feb 16;102(4):704-9. doi: 10.1038/sj.bjc.6605541. Epub 2010 Jan 19.

5.

Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia.

Papaemmanuil E, Hosking FJ, Vijayakrishnan J, Price A, Olver B, Sheridan E, Kinsey SE, Lightfoot T, Roman E, Irving JA, Allan JM, Tomlinson IP, Taylor M, Greaves M, Houlston RS.

Nat Genet. 2009 Sep;41(9):1006-10. doi: 10.1038/ng.430. Epub 2009 Aug 16.

6.

Germline genomic variants associated with childhood acute lymphoblastic leukemia.

Treviño LR, Yang W, French D, Hunger SP, Carroll WL, Devidas M, Willman C, Neale G, Downing J, Raimondi SC, Pui CH, Evans WE, Relling MV.

Nat Genet. 2009 Sep;41(9):1001-5. doi: 10.1038/ng.432. Epub 2009 Aug 16.

7.

Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood.

Novara F, Beri S, Bernardo ME, Bellazzi R, Malovini A, Ciccone R, Cometa AM, Locatelli F, Giorda R, Zuffardi O.

Hum Genet. 2009 Oct;126(4):511-20. doi: 10.1007/s00439-009-0689-7. Epub 2009 May 30.

8.

CYP1A1/2 haplotypes and lung cancer and assessment of confounding by population stratification.

Aldrich MC, Selvin S, Hansen HM, Barcellos LF, Wrensch MR, Sison JD, Kelsey KT, Buffler PA, Quesenberry CP Jr, Seldin MF, Wiencke JK.

Cancer Res. 2009 Mar 15;69(6):2340-8. doi: 10.1158/0008-5472.CAN-08-2576. Epub 2009 Mar 10.

9.

Repair of ionizing radiation-induced DNA double-strand breaks by non-homologous end-joining.

Mahaney BL, Meek K, Lees-Miller SP.

Biochem J. 2009 Feb 1;417(3):639-50. doi: 10.1042/BJ20080413. Review.

10.

Childhood leukaemia following medical diagnostic exposure to ionizing radiation in utero or after birth.

Wakeford R.

Radiat Prot Dosimetry. 2008;132(2):166-74. doi: 10.1093/rpd/ncn272. Epub 2008 Oct 15.

PMID:
18922822
11.

Subgroup-specific associations in the face of overall null results: should we rush in or fear to tread?

Weiss NS.

Cancer Epidemiol Biomarkers Prev. 2008 Jun;17(6):1297-9. doi: 10.1158/1055-9965.EPI-08-0144. No abstract available.

12.

DNA repair alterations in common pediatric malignancies.

Papaefthymiou MA, Giaginis CT, Theocharis SE.

Med Sci Monit. 2008 Jan;14(1):RA8-15. Review.

PMID:
18160950
13.

Non-homologous end-joining, a sticky affair.

van Gent DC, van der Burg M.

Oncogene. 2007 Dec 10;26(56):7731-40. Review.

PMID:
18066085
14.

DNA quantification of whole genome amplified samples for genotyping on a multiplexed bead array platform.

Hansen HM, Wiemels JL, Wrensch M, Wiencke JK.

Cancer Epidemiol Biomarkers Prev. 2007 Aug;16(8):1686-90.

15.
16.

Accuracy of multiplexed Illumina platform-based single-nucleotide polymorphism genotyping compared between genomic and whole genome amplified DNA collected from multiple sources.

Paynter RA, Skibola DR, Skibola CF, Buffler PA, Wiemels JL, Smith MT.

Cancer Epidemiol Biomarkers Prev. 2006 Dec;15(12):2533-6.

17.

Promoter SNPs in G1/S checkpoint regulators and their impact on the susceptibility to childhood leukemia.

Healy J, Bélanger H, Beaulieu P, Larivière M, Labuda D, Sinnett D.

Blood. 2007 Jan 15;109(2):683-92. Epub 2006 Sep 28.

18.

Leukemia and lymphoma: a cost of doing business for adaptive immunity.

Schlissel MS, Kaffer CR, Curry JD.

Genes Dev. 2006 Jun 15;20(12):1539-44. No abstract available.

19.

A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q.

Mathias RA, Gao P, Goldstein JL, Wilson AF, Pugh EW, Furbert-Harris P, Dunston GM, Malveaux FJ, Togias A, Barnes KC, Beaty TH, Huang SK.

BMC Genet. 2006 Jun 14;7:38.

20.

Polymorphisms in ERCC1 and susceptibility to childhood acute lymphoblastic leukemia in a Chinese population.

Wang SL, Zhao H, Zhou B, Chen YL, Zou Y, Zhu XF, Li QS, Han MZ, Yang RC, Han ZC.

Leuk Res. 2006 Nov;30(11):1341-5. Epub 2006 May 24.

PMID:
16723154

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