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PUBMED FOR HANDHELDS

Journal Abstract Search


294 related items for PubMed ID: 17081685

  • 1. Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer.
    Darvishi K, Sharma S, Bhat AK, Rai E, Bamezai RN.
    Cancer Lett; 2007 May 08; 249(2):249-55. PubMed ID: 17081685
    [Abstract] [Full Text] [Related]

  • 2. Mitochondrial genetic background modifies breast cancer risk.
    Bai RK, Leal SM, Covarrubias D, Liu A, Wong LJ.
    Cancer Res; 2007 May 15; 67(10):4687-94. PubMed ID: 17510395
    [Abstract] [Full Text] [Related]

  • 3. Germline HVR-II mitochondrial polymorphisms associated with breast cancer in Tunisian women.
    Yacoubi Loueslati B, Troudi W, Cherni L, Rhomdhane KB, Mota-Vieira L.
    Genet Mol Res; 2010 Aug 31; 9(3):1690-700. PubMed ID: 20812191
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  • 4. Mitochondrial DNA mutations in breast cancer tissue and in matched nipple aspirate fluid.
    Zhu W, Qin W, Bradley P, Wessel A, Puckett CL, Sauter ER.
    Carcinogenesis; 2005 Jan 31; 26(1):145-52. PubMed ID: 15375011
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  • 5. Genetic polymorphism of manganese superoxide dismutase (MnSOD) and breast cancer susceptibility.
    Kocabaş NA, Sardaş S, Cholerton S, Daly AK, Elhan AH, Karakaya AE.
    Cell Biochem Funct; 2005 Jan 31; 23(1):73-6. PubMed ID: 15386537
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  • 6. Genetic variation in transforming growth factor-beta1 gene associated with increased risk of esophageal squamous cell carcinoma.
    Wei YS, Xu QQ, Wang CF, Pan Y, Liang F, Long XK.
    Tissue Antigens; 2007 Dec 31; 70(6):464-9. PubMed ID: 17990985
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  • 7. p53 genotypes and haplotypes associated with risk of breast cancer.
    Buyru N, Altinisik J, Demokan S, Dalay N.
    Cancer Detect Prev; 2007 Dec 31; 31(3):207-13. PubMed ID: 17574348
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  • 8. Potential influence of interleukin-1 haplotype IL-1 beta-511*T-IL-1RN*1 in conferring low risk to middle third location of esophageal cancer: a case-control study.
    Upadhyay R, Jain M, Kumar S, Ghoshal UC, Mittal B.
    Hum Immunol; 2008 Mar 31; 69(3):179-86. PubMed ID: 18396210
    [Abstract] [Full Text] [Related]

  • 9. Concomitant presence of mutations in mitochondrial genome and p53 in cancer development - a study in north Indian sporadic breast and esophageal cancer patients.
    Gochhait S, Bhatt A, Sharma S, Singh YP, Gupta P, Bamezai RN.
    Int J Cancer; 2008 Dec 01; 123(11):2580-6. PubMed ID: 18792899
    [Abstract] [Full Text] [Related]

  • 10. [Polymorphism of the mitochondrial microsatellite 303-315 in breast cancer in Tunisia].
    Yacoubi-Loueslati B, Troudi W, Baccar A, Cherni L, Rhomdhane KB, Elgaaied AB.
    Bull Cancer; 2009 Mar 01; 96(3):337-42. PubMed ID: 19318312
    [Abstract] [Full Text] [Related]

  • 11. Can mitochondrial DNA mutations in circulating white blood cells and serum be used to detect breast cancer?
    Losanoff JE, Zhu W, Qin W, Mannello F, Sauter ER.
    Breast; 2008 Oct 01; 17(5):540-2. PubMed ID: 18571924
    [Abstract] [Full Text] [Related]

  • 12. Association of p53 polymorphisms with breast cancer: a case-control study in Slovak population.
    Franeková M, Zúbor P, Stanclová A, Dussan CA, Bohusová T, Galo S, Dobrota D, Kajo K, Péc M, Racay P.
    Neoplasma; 2007 Oct 01; 54(2):155-61. PubMed ID: 17319790
    [Abstract] [Full Text] [Related]

  • 13. The Amerindian mtDNA haplogroup B2 enhances the risk of HPV for cervical cancer: de-regulation of mitochondrial genes may be involved.
    Guardado-Estrada M, Medina-Martínez I, Juárez-Torres E, Roman-Bassaure E, Macías L, Alfaro A, Alcántara-Vázquez A, Alonso P, Gomez G, Cruz-Talonia F, Serna L, Muñoz-Cortez S, Borges-Ibañez M, Espinosa A, Kofman S, Berumen J.
    J Hum Genet; 2012 Apr 01; 57(4):269-76. PubMed ID: 22357541
    [Abstract] [Full Text] [Related]

  • 14. Genetic variation in TP53 and risk of breast cancer in a population-based case control study.
    Sprague BL, Trentham-Dietz A, Garcia-Closas M, Newcomb PA, Titus-Ernstoff L, Hampton JM, Chanock SJ, Haines JL, Egan KM.
    Carcinogenesis; 2007 Aug 01; 28(8):1680-6. PubMed ID: 17449902
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  • 20. Mitochondrial DNA polymorphisms associated with longevity in a Finnish population.
    Niemi AK, Hervonen A, Hurme M, Karhunen PJ, Jylhä M, Majamaa K.
    Hum Genet; 2003 Jan 01; 112(1):29-33. PubMed ID: 12483296
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