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194 related items for PubMed ID: 19176223
1. The p21 codon 31*C- and DRD2 codon 313*T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma. Hsieh YY, Chang CC, Bau DT, Tsai FJ, Tsai CH, Chen CP. Fertil Steril; 2009 Mar; 91(3):869-77. PubMed ID: 19176223 [Abstract] [Full Text] [Related]
2. X-ray repair cross-complementing group 4 (XRCC4) promoter -1394( *)T-related genotype, but not XRCC4 codon 247/intron 3 or xeroderma pigmentosum group D codon 312, 751/promoter -114, polymorphisms are correlated with higher susceptibility to myoma. Hsieh YY, Chang CC, Bau DT, Yeh LS, Tsai FJ, Tsai CH. Fertil Steril; 2008 Oct; 90(4 Suppl):1417-23. PubMed ID: 18177646 [Abstract] [Full Text] [Related]
3. Tumor necrosis factor-alpha-308 promoter and p53 codon 72 gene polymorphisms in women with leiomyomas. Hsieh YY, Chang CC, Tsai FJ, Lin CC, Yeh LS, Tsai CH. Fertil Steril; 2004 Oct; 82 Suppl 3():1177-81. PubMed ID: 15474092 [Abstract] [Full Text] [Related]
4. XRCC1 399 Arg-related genotype and allele, but not XRCC1 His107Arg, XRCC1 Trp194Arg, KCNQ2, AT1R, and hOGG1 polymorphisms, are associated with higher susceptibility of endometriosis. Hsieh YY, Chang CC, Chen SY, Chen CP, Lin WH, Tsai FJ. Gynecol Endocrinol; 2012 Apr; 28(4):305-9. PubMed ID: 22084859 [Abstract] [Full Text] [Related]
5. Nasopharyngeal carcinoma and genetic polymorphisms of DNA repair enzymes XRCC1 and hOGG1. Cho EY, Hildesheim A, Chen CJ, Hsu MM, Chen IH, Mittl BF, Levine PH, Liu MY, Chen JY, Brinton LA, Cheng YJ, Yang CS. Cancer Epidemiol Biomarkers Prev; 2003 Oct; 12(10):1100-4. PubMed ID: 14578150 [Abstract] [Full Text] [Related]
6. hOGG1 Ser326Cys and XRCC1 Arg399Gln polymorphisms associated with chronic obstructive pulmonary disease. Yang SF, Xu YJ, Xie JG, Zhang ZX. Chin Med J (Engl); 2009 Apr 20; 122(8):960-6. PubMed ID: 19493423 [Abstract] [Full Text] [Related]
7. Polymorphism of the p53 tumor suppressor gene is associated with susceptibility to uterine leiomyoma. Denschlag D, Bettendorf H, Watermann D, Keck C, Tempfer C, Pietrowski D. Fertil Steril; 2005 Jul 20; 84(1):162-6. PubMed ID: 16009172 [Abstract] [Full Text] [Related]
8. T allele for VEGF-460 gene polymorphism at 5'-untranslated region is associated with higher susceptibility of leiomyoma. Hsieh YY, Chang CC, Tsai FJ, Lin CC, Tsai CH. Biochem Genet; 2008 Jun 20; 46(5-6):356-61. PubMed ID: 18256925 [Abstract] [Full Text] [Related]
9. Estrogen receptor alpha-351 XbaI*G and -397 PvuII*C-related genotypes and alleles are associated with higher susceptibilities of endometriosis and leiomyoma. Hsieh YY, Wang YK, Chang CC, Lin CS. Mol Hum Reprod; 2007 Feb 20; 13(2):117-22. PubMed ID: 17121748 [Abstract] [Full Text] [Related]
10. Insulin-like growth factors II exon 9 and E-cadherin-Pml I but not myeloperoxidase promoter-463, urokinase-ApaL I nor xeroderma pigmentosum polymorphisms are associated with higher susceptibility to leiomyoma. Hsieh YY, Chang CC, Wang YK, Hsu KH, Chen CP, Hsu CM, Tsai FJ. Anticancer Res; 2010 Jun 20; 30(6):2203-8. PubMed ID: 20651370 [Abstract] [Full Text] [Related]
11. Single nucleotide polymorphisms in base-excision repair genes hOGG1, APE1 and XRCC1 do not alter risk of Alzheimer's disease. Parildar-Karpuzoğlu H, Doğru-Abbasoğlu S, Hanagasi HA, Karadağ B, Gürvit H, Emre M, Uysal M. Neurosci Lett; 2008 Sep 19; 442(3):287-91. PubMed ID: 18672023 [Abstract] [Full Text] [Related]
12. The dopamine receptor D2 genotype is associated with hyperprolactinemia. Hansen KA, Zhang Y, Colver R, Tho SP, Plouffe L, McDonough PG. Fertil Steril; 2005 Sep 19; 84(3):711-8. PubMed ID: 16169407 [Abstract] [Full Text] [Related]
13. Single nucleotide polymorphism in DNA base excision repair genes XRCC1 and hOGG1 and the risk of endometrial carcinoma in the Polish population. Romanowicz-Makowska H, Smolarz B, Houli A, Szyłło K. Pol J Pathol; 2011 Sep 19; 62(2):89-94. PubMed ID: 21866464 [Abstract] [Full Text] [Related]
14. XRCC1 polymorphism and lung cancer risk. Schneider J, Classen V, Helmig S. Expert Rev Mol Diagn; 2008 Nov 19; 8(6):761-80. PubMed ID: 18999926 [Abstract] [Full Text] [Related]
15. Four novel single nucleotide polymorphisms within the promoter region of p53 gene and their associations with uterine leiomyoma. Hsieh YY, Wang JP, Lin CS. Mol Reprod Dev; 2007 Jul 19; 74(7):815-20. PubMed ID: 17186536 [Abstract] [Full Text] [Related]
16. DNA repair gene hOGG1 codon 326 and XRCC1 codon 399 polymorphisms and bladder cancer risk in a Japanese population. Arizono K, Osada Y, Kuroda Y. Jpn J Clin Oncol; 2008 Mar 19; 38(3):186-91. PubMed ID: 18272472 [Abstract] [Full Text] [Related]
17. NAT2, XRCC1 and hOGG1 polymorphisms, cigarette smoking, alcohol consumption and risk of upper aerodigestive tract cancer. Marques CR, Da Silva TM, De Albuquerque DM, Chaves MS, Marques Filho MF, Oliveira JS, Di Pietro G, Sousa SM, Simões AL, Rios-Santos F. Anticancer Res; 2014 Jun 19; 34(6):3217-24. PubMed ID: 24922697 [Abstract] [Full Text] [Related]
18. The progesterone receptor gene polymorphism, PROGINS, may be a factor related to the development of uterine fibroids. Gomes MT, Castro Rde A, Villanova FE, da Silva ID, Baracat EC, de Lima GR, Girão MJ. Fertil Steril; 2007 May 19; 87(5):1116-21. PubMed ID: 17224149 [Abstract] [Full Text] [Related]
19. Angiotensin I-converting enzyme insertion-related genotypes and allele are associated with higher susceptibility of endometriosis and leiomyoma. Hsieh YY, Lee CC, Chang CC, Wang YK, Yeh LS, Lin CS. Mol Reprod Dev; 2007 Jul 19; 74(7):808-14. PubMed ID: 17186537 [Abstract] [Full Text] [Related]
20. DNA repair gene XPD and XRCC1 polymorphisms and the risk of childhood acute lymphoblastic leukemia. Batar B, Güven M, Bariş S, Celkan T, Yildiz I. Leuk Res; 2009 Jun 19; 33(6):759-63. PubMed ID: 19101034 [Abstract] [Full Text] [Related] Page: [Next] [New Search]