Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP44739.RArJvL-f7g1GmzzymiHXl9wajUBLb1LaYB_-97es8Mpl4130_assertion description "[Polymorphisms in estrogen related genes may modify the protective effect of isoflavones against prostate cancer risk in Japanese men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44739.RArJvL-f7g1GmzzymiHXl9wajUBLb1LaYB_-97es8Mpl4130_provenance.
- NP44744.RAjSMCxei76kAZVIM0gIi4Vqv5MlMc-2vmYktef3t0eP8130_assertion description "[We investigated the association between the ER- gene (ESR1) PvuII and XbaI and ER- gene (ESR2) RsaI and Alul polymorphisms and the idiopathic male infertility in Iranian males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44744.RAjSMCxei76kAZVIM0gIi4Vqv5MlMc-2vmYktef3t0eP8130_provenance.
- NP44748.RAnI6Sp8qgYlJH-_p6COj2MMroobtJR9BaSwdgcrRkqQY130_assertion description "[Investigation of hormone receptor genes in migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44748.RAnI6Sp8qgYlJH-_p6COj2MMroobtJR9BaSwdgcrRkqQY130_provenance.
- NP44761.RAsL2IU16PZ3ATkCSqj56zhBxNSu0s1iLVq4KzA-xRQA8130_assertion description "[Estrogen receptor gene polymorphisms and the genetics of osteoporosis: a HuGE review.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44761.RAsL2IU16PZ3ATkCSqj56zhBxNSu0s1iLVq4KzA-xRQA8130_provenance.
- NP44762.RAmRG_Stf9dvbwgxyJBUkIe7LfLu2VgfyXkW0aDfWmcfI130_assertion description "[We investigated the relationships of PvuII and XbaI polymorphisms of the estrogen receptor alpha (ER-alpha) gene, lifestyle factors with speed of sound at the calcaneus (calcaneal SOS) and osteoporosis in a population-based study of 140 healthy postmenopausal women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44762.RAmRG_Stf9dvbwgxyJBUkIe7LfLu2VgfyXkW0aDfWmcfI130_provenance.
- NP44765.RAuKEZ8VaxkzyBOHAMDXdYXuftWHNo-jfU9hYyZ9BWTbU130_assertion description "[We found that genes previously identified by their association with subclinical features of knee OA or progression were also associated with clinical knee OA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44765.RAuKEZ8VaxkzyBOHAMDXdYXuftWHNo-jfU9hYyZ9BWTbU130_provenance.
- NP44769.RAuGzZZIAixEAFAXuLdpdIylO8v0auh_1DQp9VmFgxF8M130_assertion description "[Our work has excluded the association of the ESRalpha Pvu II and Xb I polymorphism with severe preeclampsia in a Southwest Chinese population, although this polymorphism may be associated with the systolic blood pressure level in the normal pregnant women]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44769.RAuGzZZIAixEAFAXuLdpdIylO8v0auh_1DQp9VmFgxF8M130_provenance.
- NP44770.RAhmNXO2BtbH8mQHr8hjNM5gCq6Jbx2YNHZlATJBqM0NQ130_assertion description "[Association between estrogen receptor alpha (ESR1) gene polymorphisms and severe preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44770.RAhmNXO2BtbH8mQHr8hjNM5gCq6Jbx2YNHZlATJBqM0NQ130_provenance.
- NP44776.RAlnmsNR4q-JdZgULGIHV32jrPtCzeOiW1-ZZgONwwW8Y130_assertion description "[Distinct association of gene polymorphisms of estrogen receptor and vitamin D receptor with lumbar spondylosis in post-menopausal women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44776.RAlnmsNR4q-JdZgULGIHV32jrPtCzeOiW1-ZZgONwwW8Y130_provenance.
- NP44779.RAtzWcUBHZ5uVj2p8v7WsZ_FHGwBHzWhOC4jIF0g9IxSM130_assertion description "[ These data suggest that genetic variants of both the ERbeta and the PGR may influence prolactin release.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44779.RAtzWcUBHZ5uVj2p8v7WsZ_FHGwBHzWhOC4jIF0g9IxSM130_provenance.
- NP44781.RAlzJ7DLEQz6gwjtrVmzK8VRCDYd-1hppQCV5fDO7t1cw130_assertion description "[The -351A/G ESR1 polymorphism might be associated with MI, but not with extreme longevity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44781.RAlzJ7DLEQz6gwjtrVmzK8VRCDYd-1hppQCV5fDO7t1cw130_provenance.
- NP44787.RAjSJslMkLnvuvdzWE8vzMF7ITSdZB-76ZEb5y7HPS-RQ130_assertion description "[ Urolithiasis among men appears to be associated with AR gene CAG repeat and ER gene TA repeat polymorphisms, whereas there was no significant association among female stone patients. These sex hormone receptors seem to be related to the higher incidence of stone formation among men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44787.RAjSJslMkLnvuvdzWE8vzMF7ITSdZB-76ZEb5y7HPS-RQ130_provenance.
- NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_assertion description "[ We have demonstrated that the PvuII polymorphism in the ORalpha gene is related to both the presence of AS in postmenopausal women and to lipid levels in adolescent females, suggesting that this polymorphism may influence the risk of AS partly by affecting lipid levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_provenance.
- NP44792.RAvbdcuF5Ij8wVkp35qrh0k9FuJntkyvyMGgbWcywgnsA130_assertion description "[Association of polymorphism of human alpha oestrogen receptor gene with coronary artery disease in men: a necropsy study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44792.RAvbdcuF5Ij8wVkp35qrh0k9FuJntkyvyMGgbWcywgnsA130_provenance.
- NP44793.RAlLzNLduzkzDrBtXwq2DTJVs3HkE_9Y9JcMwtuQptgRw130_assertion description "[To investigate the association between sequence variants in the promoter region of the oestrogen receptor-alpha (ER-alpha) gene and the angiographic severity of coronary artery disease (CAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44793.RAlLzNLduzkzDrBtXwq2DTJVs3HkE_9Y9JcMwtuQptgRw130_provenance.
- NP44795.RAq-Wj-3PEDTfFSkQZXSIglUpbaII5KPw8heG7rSr3qhc130_assertion description "[Gender-specific effect of estrogen receptor-1 gene polymorphisms in coronary artery disease and its angiographic severity in Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44795.RAq-Wj-3PEDTfFSkQZXSIglUpbaII5KPw8heG7rSr3qhc130_provenance.
- NP44796.RAoDSt_YKYRP2IAmN8gU9vxta96vlRP6TY504ZX72fiJw130_assertion description "[We did not observe an association between ESR1 PvuII and XbaI gene polymorphisms with CAD in the risk of CAD in an Iranian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44796.RAoDSt_YKYRP2IAmN8gU9vxta96vlRP6TY504ZX72fiJw130_provenance.
- NP44798.RAqd-OwJsWJuU-aFAw16HE1YiNtagN0dD7zVnuGztqgys130_assertion description "[Sequence variants in the estrogen receptor alpha gene (ESR1) may alter the atheroprotective effects of estrogens, and be associated with the severity of coronary artery disease (CAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44798.RAqd-OwJsWJuU-aFAw16HE1YiNtagN0dD7zVnuGztqgys130_provenance.
- NP44803.RAlRHae0bB3i2FJbeZ66nOhygX7I8pfsfHzYQhK0qQiF8130_assertion description "[The TC patients exhibited a significantly higher frequency of the liver glutathione-S-transferase GST1*0 allele, whereas the GST1*2 frequency was two times higher in the control subjects than in the TC patients (0.2522 and 0.0953, respectively). The TC and control groups showed statistically significant differences in the frequencies of the following]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44803.RAlRHae0bB3i2FJbeZ66nOhygX7I8pfsfHzYQhK0qQiF8130_provenance.
- NP44804.RAjn4xpZ7dzT9Wk6G3Wdwyd1jQLqvn-iPwlX47GDiVsck130_assertion description "[Interindividual variation in nucleotide excision repair genes and risk of endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44804.RAjn4xpZ7dzT9Wk6G3Wdwyd1jQLqvn-iPwlX47GDiVsck130_provenance.
- NP44808.RAh3wKJ5pW3lpa8pFbvWnXVg68uaLxYe6ZGHGH7ezeMek130_assertion description "[XPA A23G polymorphism is associated with the elevated response to platinum-based chemotherapy in advanced non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44808.RAh3wKJ5pW3lpa8pFbvWnXVg68uaLxYe6ZGHGH7ezeMek130_provenance.
- NP44813.RAm4y-qoUuyzXEEBIZNmuuAt6-A4msZgOjcAXeesDy5Q8130_assertion description "[Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44813.RAm4y-qoUuyzXEEBIZNmuuAt6-A4msZgOjcAXeesDy5Q8130_provenance.
- NP44815.RArRnNoXYGTntA8-WnjCpJ0OqKZr2-oYz3YX_Ls--JpIc130_assertion description "[We conclude that these genes do not have an important role in protection against colorectal carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44815.RArRnNoXYGTntA8-WnjCpJ0OqKZr2-oYz3YX_Ls--JpIc130_provenance.
- NP44821.RAnqe5_OeudHf4LSvO3X5FtHzDTSXELk3wbiRVJDrZEZY130_assertion description "[We investigated the association of urinary bladder cancer with genetic polymorphisms in the xeroderma pigmentosum complementation group C (XPC), group D (XPD) and group G (XPG), X-ray repair cross-complementing group 1 (XRCC1) and group 3 (XRCC3), Nijmegen breakage syndrome 1 (NBS1), cyclin D1, methylene-tetrahydrofolate reductase (MTHFR), NAD(P)H dehydrogenase quinone 1 (NQO1), H-ras and glutathione S-transferase theta 1 (GSTT1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44821.RAnqe5_OeudHf4LSvO3X5FtHzDTSXELk3wbiRVJDrZEZY130_provenance.
- NP44825.RAtlJSIajD1xY8pXolNuic8azzSHoaJTqw5gBPu9HYBhM130_assertion description "[Bladder cancer and polymorphisms of DNA repair genes (XRCC1, XRCC3, XPD, XPG, APE1, hOGG1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44825.RAtlJSIajD1xY8pXolNuic8azzSHoaJTqw5gBPu9HYBhM130_provenance.
- NP44827.RAg-OMIecd1ImXPYHeLFXnwpSdKgWoz2K9yNKv8PutLz4130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44827.RAg-OMIecd1ImXPYHeLFXnwpSdKgWoz2K9yNKv8PutLz4130_provenance.
- NP44838.RAp3nrbqXp_-0moEhMwo6fSvQFMMEuZfZq2EmgDo2FlWE130_assertion description "[Polygenic model of DNA repair genetic polymorphisms in human breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44838.RAp3nrbqXp_-0moEhMwo6fSvQFMMEuZfZq2EmgDo2FlWE130_provenance.
- NP44843.RAurHRu4xQmtRiCCoLfBi8yJCT7V7gRyQhD_RI3eCffW8130_assertion description "[Comprehensive screen of genetic variation in DNA repair pathway genes and postmenopausal breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44843.RAurHRu4xQmtRiCCoLfBi8yJCT7V7gRyQhD_RI3eCffW8130_provenance.
- NP44845.RAsHoWVKyF1oTiEX__mrJ5ElCfg7UQyFy50YBJxpth9pw130_assertion description "[We analyzed 13 polymorphisms in seven DNA repair genes belonging to different repair pathways X-ray repair cross-complementing group 1 (XRCC1): 26304C>T, 26651A>G, 28152A>G; xeroderma pigmentosum-D (XPD): 23591A>G, 35931A>C; excision repair complementing defective in Chinese hamster, group 1 (ERCC1): 19007C>T; XRCC3: 4541T>C, 17893A>G, 18067C>T; proliferating cell nuclear antigen (PCNA): 6084G>C; ERCC4: 30028C>T, 30147A>G; and XRCC2-31479A>G in 317 incident bladder cancer patients and 317 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44845.RAsHoWVKyF1oTiEX__mrJ5ElCfg7UQyFy50YBJxpth9pw130_provenance.
- NP44848.RAsum5bDI9VjGEFpzEH5jKY_Unrxi1V-Ga47a221qPvks130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44848.RAsum5bDI9VjGEFpzEH5jKY_Unrxi1V-Ga47a221qPvks130_provenance.
- NP44852.RApq-Vuj3lD8UK46AhsL_V08UUluBdU8yGferxiezIv2M130_assertion description "[Genotyping of polymorphisms of XRCC1 (Arg194Trp and Arg399Gln), OGG1 (Ser326Cys and Arg229Gln), ERCC2 Lys751Gln, ERCC4 Ser662Pro, and ERCC5 His1104Asp was performed and used to evaluate breast cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44852.RApq-Vuj3lD8UK46AhsL_V08UUluBdU8yGferxiezIv2M130_provenance.
- NP44855.RApwQmX0sM16bTeq54xkeMslYaqIU4i8Xm5D5kGkgeQvk130_assertion description "[Interactive effect was also observed between ERCC4 genotype and body mass idnex (BMI) for the breast cancer risk; the ERCC4 C allele containing genotypes posed a 1.7-fold (95% CI: 0.96-2.93) breast cancer risk in obese women (BMI>25 kg/m(2)) with a borderline significance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44855.RApwQmX0sM16bTeq54xkeMslYaqIU4i8Xm5D5kGkgeQvk130_provenance.
- NP44858.RAqi0MSrZEtBSeQ4POkknqcckoW4priC5arnDdJiEDY2A130_assertion description "[our data provide persuasive evidence against an overall association between invasive breast cancer risk and ERCC4 rs744154, TNF rs361525, CASP10 rs13010627, PGR rs1042838, and BID rs8190315 genotypes among women of European descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44858.RAqi0MSrZEtBSeQ4POkknqcckoW4priC5arnDdJiEDY2A130_provenance.
- NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_assertion description "[We conclude that the malignant phenotype probably results from a summation of polymorphic nucleotide excision repair genes showing opposing effects (an increased risk of XPC versus a protective effect of XPD). The protective effect of the homozygous variant of XRCC1 Arg399Gln for GERD and BE suggests that base excision repair alterations may occur early in progression to EADC, likely in response to GERD-induced endogenous oxidative or inflammatory DNA damage. As GERD and BE are highly prevalent in the general population, this protective effect may well explain why only a fraction of individuals with GERD and BE progress into invasive EADC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_provenance.
- NP44871.RAqTQz1NhtZZ3Dey8y3opmlI-2xPEnq6U6cHGLGl73sBE130_assertion description "[Selected genetic polymorphisms in MGMT, XRCC1, XPD, and XRCC3 and risk of head and neck cancer: a pooled analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44871.RAqTQz1NhtZZ3Dey8y3opmlI-2xPEnq6U6cHGLGl73sBE130_provenance.
- NP44877.RAukui608PA-1mN7AXCqFt8jczj-IpRBWaOgFkBFNa4CQ130_assertion description "[A pharmacogenetic approach may be a useful strategy for personalizing and optimizing chemotherapy in mCRC patients and deserves confirmation in additional prospective studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44877.RAukui608PA-1mN7AXCqFt8jczj-IpRBWaOgFkBFNa4CQ130_provenance.
- NP44879.RAveBCAuR3xrEI-Q8HN5cDDFHqKW7qZgGkOpLYm6RNAI8130_assertion description "[First-line therapy with oxaliplatin, irinotecan and capecitabine is efficient and well-tolerated. The GSTP1 polymorphism A>G status was significantly associated with ORR and PFS in mCRC treated with this triplet therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44879.RAveBCAuR3xrEI-Q8HN5cDDFHqKW7qZgGkOpLYm6RNAI8130_provenance.
- NP44882.RAs7uZH0NhTXIkAQA6K0MlqOJxcutkfP2YutlIGFY4d5g130_assertion description "[Common polymorphisms in the XPD and hOGG1 genes are not associated with the risk of colorectal cancer in a Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44882.RAs7uZH0NhTXIkAQA6K0MlqOJxcutkfP2YutlIGFY4d5g130_provenance.
- NP44888.RAivd10DrOPs5uUMGgLV4FsqLHRo6wFntfsN6iscw27Hk130_assertion description "[In conclusion, the APE1 Asp148Glu polymorphism is highly predictive for lung cancer, and cumulative cigarette smoking modifies the associations between the XRCC1 Arg399Gln and the XPD Lys751Gln polymorphisms and lung cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44888.RAivd10DrOPs5uUMGgLV4FsqLHRo6wFntfsN6iscw27Hk130_provenance.
- NP44890.RAkQTX_4oPmuPx44oAGHZBK3YOavKaIZLCqlu9FiOOwGQ130_assertion description "[Haplotype analysis including three previously studied polymorphisms (ERCC1 Asn118Asn, ERCC2 Arg156Arg, and ERCC2 Lys751Gln) revealed that a haplotype consisting of ERCC1Asn118Asn(G)-ERCC2 Arg156Arg(C)-ERCC2 Asp312Asn(G)-ERCC2 Lys751Gln(C) was marginally associated with an increased risk of lung cancer (OR = 3.61, 95% CI = 1.00-13.06, P = 0.04).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44890.RAkQTX_4oPmuPx44oAGHZBK3YOavKaIZLCqlu9FiOOwGQ130_provenance.
- NP44896.RAh0i9I5lgLV8elIH4AO6j6XaoM9CbsqDVbFUrXsg0ZoU130_assertion description "[ Cytokine gene polymorphisms predicted clinical outcome for advanced melanoma patients who received biochemotherapy. The combined effects of multiple genetic polymorphisms may provide more accurate prognostic information. Additional independent studies are needed to confirm these pilot findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44896.RAh0i9I5lgLV8elIH4AO6j6XaoM9CbsqDVbFUrXsg0ZoU130_provenance.
- NP44897.RAjlblQLCz2buHN6nFUJuxL1LLKcQ1Lj9lSHn28GjCRQk130_assertion description "[Moreover, the number of the observed XPD at-risk genotypes (i.e., 312Asn/Asn+Asn/Asp and 751Gln/Gln+Lys/Gln) was associated with cutaneous melanoma risk in a dose-response manner (OR, 1.47; 95% CI, 0.97-2.23 for one at-risk genotype; OR, 1.83; 95% CI, 1.29-2.61 for two at-risk genotypes; P(trend) < 0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44897.RAjlblQLCz2buHN6nFUJuxL1LLKcQ1Lj9lSHn28GjCRQk130_provenance.
- NP44902.RApCqZPQeWtpiCq2ZlCZN1wFvCUej5bGAJ2X0_HSQSQa8130_assertion description "[Our data suggested variant (AA) of ERCC2 312 AA genotype to be associated with high risk of tumor recurrence and reduced recurrence free survival in superficial bladder cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44902.RApCqZPQeWtpiCq2ZlCZN1wFvCUej5bGAJ2X0_HSQSQa8130_provenance.
- NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_assertion description "[For other polymorphisms included in this study, NBS1 Glu185Gln, XPD Lys751Gln, XPG Asp1104His, XRCC1 Arg399Gln, XRCC3 Thr241Met, cyclin D1 Pro242Pro, MTHFR Ala222Val and Glu429Ala, NQO1 Arg139Trp and Pro187Ser, no significant differences for genotype distributions and allele frequencies between the bladder cancer cases and the controls were observed in the present study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44908.RAp-09OdEx61vTtsfqBEK7V1bKWKDB4jueR3nqtG9ersU130_provenance.
- NP44916.RAvTePqakstX5xRl56bk5FI20Tx3z4p1ST5SlGsEtRenk130_assertion description "[However, when the intra group risk was compared, the risk due to the XPD polymorphic genotypes Lys/Gln or Gln/Gln was significantly lower among familial breast cancer patients compared to sporadic breast cancer patients OR = 0.61; 95%CI = 0.39-0.94; p value = 0.024) whereas the risk implied by XRCC1 variant genotype was not significantly different between the familial and nonfamilial groups of breast cancer patients OR = 0.97; 95%CI = 0.63-1.49; p value = 0.882.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44916.RAvTePqakstX5xRl56bk5FI20Tx3z4p1ST5SlGsEtRenk130_provenance.
- NP44918.RAuS2UahlvPTc2Ry83EQgopFrcLCU89t4eraBwB01d40M130_assertion description "[No associations were found between ERCC2/XPD Arg156Arg and risk of breast cancer (AA/AC versus CC: OR = 0.79, 95% CI = 0.49-1.28, P = 0.33; AA versus CC: OR = 0.89, 95% CI = 0.49-1.63, P = 0.72; AC versus CC: OR = 0.74, 95% CI = 0.44-1.24, P = 0.25).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44918.RAuS2UahlvPTc2Ry83EQgopFrcLCU89t4eraBwB01d40M130_provenance.
- NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_assertion description "[In a nested case-control study of breast cancer in US radiologic technologists exposed to low levels of ionizing radiation (858 cases, 1,083 controls), we examined whether risk of breast cancer conferred by radiation was modified by nucleotide excision gene polymorphisms ERCC2 (XPD) rs13181, ERCC4 (XPF) rs1800067 and rs1800124, ERCC5 (XPG) rs1047769 and rs17655; and ERCC6 rs2228526.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44921.RAu6CUwgtoWxv1X_opLB-mlEmZZt2CCQhA897YW0T7jzU130_provenance.
- NP44924.RAsRHQl1V2BgJpSDtHrCMl4dwjOZdTw7lO9bHz5okcgAM130_assertion description "[The genotype frequency for heterozygote A/C in XPC exon 15 and T/C in XRCC3 exon 7, homozygote A/A in XPD exon 10 were significantly different between BC group and control group in Chinese population (P<0.05, OR=1.47, 95% CI, 1.00-2.16 for A/C in XPC exon 15; P<0.05, OR=1.79, 95% CI, 0.98-3.26 for T/C in XRCC3 exon 7; P<0.05, OR=0.51, 95% CI, 0.27-0.94 for G/A in XPD exon 10).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44924.RAsRHQl1V2BgJpSDtHrCMl4dwjOZdTw7lO9bHz5okcgAM130_provenance.
- NP44925.RAl0liIKwEASktN3fnSw5ONgKgv7bus70anAEtzBhlyvc130_assertion description "[Although no significant association was observed between the genetic polymorphisms and the risk of breast cancer, women with both ERCC2 A allele- and ERCC4 C allele-containing genotypes showed a 2.6-fold risk (95% CI: 1.02-6.48) of breast cancer compared to women concurrently carrying the ERCC2 GG and ERCC4 TT genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44925.RAl0liIKwEASktN3fnSw5ONgKgv7bus70anAEtzBhlyvc130_provenance.
- NP44927.RApZn7B9WSh1j4RDVdy1XLv4Jg-ygToxG5xW4fEm8Y9vY130_assertion description "[Specific polymorphisms may influence clinical outcomes of AGC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44927.RApZn7B9WSh1j4RDVdy1XLv4Jg-ygToxG5xW4fEm8Y9vY130_provenance.
- NP44930.RAvdH0S0BGaT-sauYJlhD2C2vZzjH-ECexKn5C2aGaGdE130_assertion description "[ Genetic variations in cytokine and DNA repair genes contribute to susceptibility to HBV-related HCC. Smoking increased such genetic susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44930.RAvdH0S0BGaT-sauYJlhD2C2vZzjH-ECexKn5C2aGaGdE130_provenance.
- NP44931.RAjOwTlOaIHQFJ_7-Cl1WpmbqVBTD9-dF--H5CbB7z0hE130_assertion description "[ These results suggested that alterations in GLTSCR1 (or a closely linked gene) were associated with the development and progression of oligodendroglioma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44931.RAjOwTlOaIHQFJ_7-Cl1WpmbqVBTD9-dF--H5CbB7z0hE130_provenance.
- NP44933.RAn4f_T39aqTZ63oOGrzhe7qmjUHGVb9KG5DbTXx1rN4Q130_assertion description "[Detection of ERCC1 118 polymorphisms in non-small-cell lung cancer by an improved fluorescence polarization assay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44933.RAn4f_T39aqTZ63oOGrzhe7qmjUHGVb9KG5DbTXx1rN4Q130_provenance.
- NP44944.RAnIs9584IYf4dNRbKJLM_1cSoKij2fWMxIMHu1vVwTIM130_assertion description "[While it cannot be ruled out that the present findings are due to chance, the present results are consistent with previous findings that XPD Arg156Arg is a weak risk factor for basal cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44944.RAnIs9584IYf4dNRbKJLM_1cSoKij2fWMxIMHu1vVwTIM130_provenance.
- NP44945.RAk1t0D_21JlmaZJ3fWbaHeaBLmtk6sG9rbeIhGfMBrzw130_assertion description "[To evaluate the effect of excision repair cross-complementing group 1 (ERCC1) and X-ray cross-complementing group 1 (XRCC1) gene polymorphisms on treatment outcome in patients receiving oxaliplatin-based regimens for metastatic colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44945.RAk1t0D_21JlmaZJ3fWbaHeaBLmtk6sG9rbeIhGfMBrzw130_provenance.
- NP44947.RApiX1GXbHYEEaOh-qdd6rMuZ2U3EBL1BpYrxME-FWp6c130_assertion description "[The ERCC1-118 and MTHFR C677T polymorphisms were associated with progression and severe diarrhoea, respectively, after FOLFOX treatment in mCRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44947.RApiX1GXbHYEEaOh-qdd6rMuZ2U3EBL1BpYrxME-FWp6c130_provenance.
- NP44948.RAvy8I3ywzeSjbnaKLBLVvcJOmF5qN39ChpfcwPBDM7mA130_assertion description "[Our results suggest that the ASE-1 G-21A, RAI IVS1 A4364G and ERCC1 Asn118Asn polymorphisms and the previously identified haplotype are not associated with risk of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44948.RAvy8I3ywzeSjbnaKLBLVvcJOmF5qN39ChpfcwPBDM7mA130_provenance.
- NP44950.RAjg6eI_mLrH8NnBD6tOGWoYl81WRqVob8EuekOZvJCVY130_assertion description "[The aim of our study was to assess whether the polymorphism of the nucleotide excision repair enzyme, excision repair cross-complementing rodent repair deficiency, complementation group 1 (ERCC1), had an effect on the tumor response in patients treated with standard chemotherapy regimens for a metastatic colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44950.RAjg6eI_mLrH8NnBD6tOGWoYl81WRqVob8EuekOZvJCVY130_provenance.
- NP44951.RAsYC05mnyQxQY5p3ix2DLVynOLQhie8hgQ3SHRSlzepA130_assertion description "[ERCC1 gene polymorphism as a predictor for clinical outcome in advanced colorectal cancer patients treated with platinum-based chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44951.RAsYC05mnyQxQY5p3ix2DLVynOLQhie8hgQ3SHRSlzepA130_provenance.
- NP44953.RAgw8h0Zv5bY0MFBPNiwZU7ZRW8kHTcubZKkwdyoIc8Q4130_assertion description "[A pharmacogenetic approach may be a useful strategy for personalizing and optimizing chemotherapy in mCRC patients and deserves confirmation in additional prospective studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44953.RAgw8h0Zv5bY0MFBPNiwZU7ZRW8kHTcubZKkwdyoIc8Q4130_provenance.
- NP44957.RAn-d9xUE63JprebENEFmFNtvS96QP4QTEbNfItK0vWPg130_assertion description "[these findings provide support for the influence of genetic variation in NER on bladder cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44957.RAn-d9xUE63JprebENEFmFNtvS96QP4QTEbNfItK0vWPg130_provenance.
- NP44959.RAmYyA0uqf3B8SgIo13YxmUCpLps7U6VP7zwD6-tInzG8130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44959.RAmYyA0uqf3B8SgIo13YxmUCpLps7U6VP7zwD6-tInzG8130_provenance.
- NP44962.RAnHzDLhJWwsFEDyBTUuwQ8KtArMUS6hmYt53YN3Xjo6A130_assertion description "[PTGS2 and ERCC5 were associated with stomach cancer risk in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44962.RAnHzDLhJWwsFEDyBTUuwQ8KtArMUS6hmYt53YN3Xjo6A130_provenance.
- NP44964.RAoEVvz8NECrXqopTFy2AG2vwt6oZY99mk79GBbrdvjc0130_assertion description "[Polymorphisms in nucleotide excision repair genes, polycyclic aromatic hydrocarbon-DNA adducts, and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44964.RAoEVvz8NECrXqopTFy2AG2vwt6oZY99mk79GBbrdvjc0130_provenance.
- NP44969.RAhz5OKm1ik123DiB-4xQu7WMq15OlijAFD_FCPkGYeQs130_assertion description "[Using a multivariate model, the presence of polymorphic variants in DNA-repair genes are powerful prognosis factors and response to cisplatin predictors among SCCHN patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44969.RAhz5OKm1ik123DiB-4xQu7WMq15OlijAFD_FCPkGYeQs130_provenance.
- NP44974.RAmS2OtSvxdL7ms05pzf46iwa3eowqZ8FVjrEXHNMC6NY130_assertion description "[ This study is one of the first comprehensive mutational analyses of major genes in a specific signaling pathway in a sizeable cohort of lung adenocarcinomas. Our results suggest the majority of gain-of-function mutations within kinase genes in the EGFR signaling pathway have already been identified. Our findings also implicate FGFR4 in the pathogenesis of a subset of lung adenocarcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44974.RAmS2OtSvxdL7ms05pzf46iwa3eowqZ8FVjrEXHNMC6NY130_provenance.
- NP44977.RAhqVB5vxbKPFBqqOKHuYFc6CvrXTmzlezb-ALTJE2BRk130_assertion description "[we have confirmed the role of EGFR gene mutation as predictor of response to EGFR TKIs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44977.RAhqVB5vxbKPFBqqOKHuYFc6CvrXTmzlezb-ALTJE2BRk130_provenance.
- NP44982.RAgrQHV9OBzdPV4sDgZoh1ib-dU_UWTpLPC8etfyC-tQM130_assertion description "[Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44982.RAgrQHV9OBzdPV4sDgZoh1ib-dU_UWTpLPC8etfyC-tQM130_provenance.
- NP44984.RAgt592OGhP4NWmLnki6sNbcl0GzBSU6EqtR5zMyrkQLk130_assertion description "[These new findings suggest that observed associations between NRG1 and schizophrenia may be mediated through functional interaction not just with ERBB4, but with other members of the NRG and ERBB families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44984.RAgt592OGhP4NWmLnki6sNbcl0GzBSU6EqtR5zMyrkQLk130_provenance.
- NP44996.RAgAh7DKQEdy1EAsGntcSCYcUkHtII4Fh0CtWmKP-5FFU130_assertion description "[HER2 polymorphisms and breast cancer in Tunisian women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44996.RAgAh7DKQEdy1EAsGntcSCYcUkHtII4Fh0CtWmKP-5FFU130_provenance.
- NP44997.RAlCBl79nrdCeESX0pjeA0g64tfnFaWVCcUgZm_5-Zmc8130_assertion description "[Association between HER2, TOP2A, and response to anthracycline-based preoperative chemotherapy in high-risk primary breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44997.RAlCBl79nrdCeESX0pjeA0g64tfnFaWVCcUgZm_5-Zmc8130_provenance.
- NP45000.RAoCCNEl3uZkqN00kpNU1KueJFzBgG9jHPJAbUELje8c8130_assertion description "[Common genetic variants in the BRAF and KRAS oncogenes may be important in the prediction of survival in patients with invasive epithelial ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45000.RAoCCNEl3uZkqN00kpNU1KueJFzBgG9jHPJAbUELje8c8130_provenance.
- NP45001.RAvfDLfoh2twOZx7rB-Wwiq2J6KvgqHVm7syPRCsukYyA130_assertion description "[We found no evidence of disease association for SNPs in BRAF, KRAS, ERBB2 and PIK3CA when OC was considered as a single disease phenotype; but after stratification by histological subtype, we found borderline evidence of association for SNPs in KRAS and BRAF with mucinous OC and in ERBB2 and PIK3CA with endometrioid OC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45001.RAvfDLfoh2twOZx7rB-Wwiq2J6KvgqHVm7syPRCsukYyA130_provenance.
- NP45003.RAlmGObUQifncXFGpeBvDA9B01tG4SuuGSAh6ekYr0gSQ130_assertion description "[This study used a case-control design to assess the predictive value of 3 polymorphisms in VDR (TaqI and FokI) and HER-2 (Val655Ile) to determine the risk of developing PRCa in patients with BPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45003.RAlmGObUQifncXFGpeBvDA9B01tG4SuuGSAh6ekYr0gSQ130_provenance.
- NP45005.RApm7BVnaZ5wBV4kO38jSjW741wQVl7lJ8heqg2fTlNq0130_assertion description "[To investigate both whether the risk of gastric cancer is associated with the Ile/Val single nucleotide polymorphism (SNP) of human epidermal growth factor receptor-2 (HER-2) transmembrane domain-coding region at codon 655 and the suggested existence of HER-2 expression in gastric cancer cases in a Turkish patient group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45005.RApm7BVnaZ5wBV4kO38jSjW741wQVl7lJ8heqg2fTlNq0130_provenance.
- NP45012.RAg3sJRWBfsFvYM9BTdqR50lj8jkAzpYVyksdQehHZ92o130_assertion description "[Familial erythrocytosis (familial polycythemia) inherited as an autosomal dominant trait has recently been reported to be associated with mutations in the gene encoding the erythropoietin receptor (EpoR) in a small number of families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45012.RAg3sJRWBfsFvYM9BTdqR50lj8jkAzpYVyksdQehHZ92o130_provenance.
- NP45013.RAkkLTxtQWJqt096SUlKk_CP7TeMpR3MKZ-7-JR3yh8dE130_assertion description "[ These data suggest an intriguing and possibly novel role for sEH in the pathogenesis of atherosclerosis, which deserves additional investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45013.RAkkLTxtQWJqt096SUlKk_CP7TeMpR3MKZ-7-JR3yh8dE130_provenance.
- NP45015.RAsg3Eao3OKhx7njupqWDj3i-MWRWsg9BgI-uL8R9YL3g130_assertion description "[We genotyped 2,065 Atherosclerosis Risk in Communities study participants (1,085 incident CHD cases, 980 non-cases) for 10 previously identified polymorphisms in EPHX2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45015.RAsg3Eao3OKhx7njupqWDj3i-MWRWsg9BgI-uL8R9YL3g130_provenance.
- NP45016.RAgJFAQbzOkUghzzZ3ipbwpGk8KKeIF-XkoQSXeOrhn50130_assertion description "[Sequence variation in the soluble epoxide hydrolase gene and subclinical coronary atherosclerosis: interaction with cigarette smoking.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45016.RAgJFAQbzOkUghzzZ3ipbwpGk8KKeIF-XkoQSXeOrhn50130_provenance.
- NP45018.RAr9gA1g7uaN55YHksxwBXE2yZ61au1ViCkGG3GplsArs130_assertion description "[Smokers with any variant allele of EPHX1 were at increased risk for CRC, as were individuals with any variant allele of CYP1A1 together with any variant allele of EPHX1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45018.RAr9gA1g7uaN55YHksxwBXE2yZ61au1ViCkGG3GplsArs130_provenance.
- NP45020.RAmz1F65Vg5ZzizcnfCaNjpErZXVZK0fBg5jaWSdgP8Lo130_assertion description "[Red meat intake, doneness, polymorphisms in genes that encode carcinogen-metabolizing enzymes, and colorectal cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45020.RAmz1F65Vg5ZzizcnfCaNjpErZXVZK0fBg5jaWSdgP8Lo130_provenance.
- NP45035.RAkkn4PE-SM-XwV7HtgT9we8iQ6_Kyvubw4amczgoRm0k130_assertion description "[Genetic polymorphisms of MPO, GSTT1, GSTM1, GSTP1, EPHX1 and NQO1 as risk factors of early-onset lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45035.RAkkn4PE-SM-XwV7HtgT9we8iQ6_Kyvubw4amczgoRm0k130_provenance.
- NP45040.RAlmcC5gGZXjop1kvgN0ebWjJUA_0bNYJ6gLICs3PYkAE130_assertion description "[Using the odds ratio as a measure of association, we did not observe elevated risks of CL/P associated with either allelic comparison. This suggests that when mothers smoke periconceptionally, their infants having these alleles at either (or both) loci were not at substantially increased risk for CL/P compared to infants with the wild-type alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45040.RAlmcC5gGZXjop1kvgN0ebWjJUA_0bNYJ6gLICs3PYkAE130_provenance.
- NP45048.RAnZM8bD_yz18nttQzEysr24XEoGJyHW19StZiY4FdrbU130_assertion description "[Cluster analysis may identify meaningful disease subtypes and/or groups of related phenotypic variables even in a highly selected group of severe emphysema subjects, and may be useful for genetic association studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45048.RAnZM8bD_yz18nttQzEysr24XEoGJyHW19StZiY4FdrbU130_provenance.
- NP45059.RAqOhzvb6OFNW-pODTofWpuNu3JuV9EM8dThjFgZViKgw130_assertion description "[Present case-control study evaluated the influence of EPHX1 genetic variations on squamous cell esophageal cancer (ESCC) susceptibility in 107 patients and 320 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45059.RAqOhzvb6OFNW-pODTofWpuNu3JuV9EM8dThjFgZViKgw130_provenance.
- NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_assertion description "[We investigated whether polymorphisms in the gene for microsomal epoxide hydrolase (mEPHX), an enzyme involved in this protective process, had any bearing on individual susceptibility to the development of chronic obstructive pulmonary disease (COPD) and emphysema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_provenance.
- NP45063.RAm5csW-_HpVGuO3AbJlcQHnU0RUYv1elPBz9uvUf5AR4130_assertion description "[genetic variation in surfactant protein B is associated with chronic obstructive pulmonary disease susceptibility and exacerbation frequency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45063.RAm5csW-_HpVGuO3AbJlcQHnU0RUYv1elPBz9uvUf5AR4130_provenance.
- NP45070.RAqe_hDPOFFRsyq57nn58_AwdCefTFh_MBxjd92My-5Co130_assertion description "[Polymerase chain reaction-restriction fragment length polymorphism-based genotyping assays were used to determine the frequency of polymorphisms in EPHX1 (exons 3 and 4), NQO1 (exon 6), GSTM1 (deletion), GSTP1 (exon 5), and GSTT1 (deletion) in a case-control study comprised of 238 patients with breast cancer and 313 healthy individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45070.RAqe_hDPOFFRsyq57nn58_AwdCefTFh_MBxjd92My-5Co130_provenance.
- NP45072.RApuk0a1OBAtdRYY0sruQyvZ2HcoS_bpcOoe87zD0XtHA130_assertion description "[Breast cancer: a candidate gene approach across the estrogen metabolic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45072.RApuk0a1OBAtdRYY0sruQyvZ2HcoS_bpcOoe87zD0XtHA130_provenance.
- NP45074.RAkA-ueultMmYx26ngseHsyEE7lKwDDf1EJv5VMu_xbx0130_assertion description "[ The use of two intragenic SNPs jointly in haplotype analysis of association demonstrated that the genetically determined low-activity haplotype C-A (His113-His139) was significantly less frequent in women with placental abruption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45074.RAkA-ueultMmYx26ngseHsyEE7lKwDDf1EJv5VMu_xbx0130_provenance.
- NP45076.RAqqfQItNO7wU_trSey6qAa8YzXrL9nvGEl7Dbrvm1rbg130_assertion description "[CYP1A1, CYP2E1, GSTM1, GSTT1, EPHX1 exons 3 and 4, and NAT2 polymorphisms, smoking, consumption of alcohol and fruit and vegetables and risk of head and neck cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45076.RAqqfQItNO7wU_trSey6qAa8YzXrL9nvGEl7Dbrvm1rbg130_provenance.
- NP45081.RApZHivEmEeP4KJ2JS9Z176OzIxQm5hsAG37RO1qb6klQ130_assertion description "[Interindividual variations in DNA adduct levels assessed by analysis of multiple genetic polymorphisms in smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45081.RApZHivEmEeP4KJ2JS9Z176OzIxQm5hsAG37RO1qb6klQ130_provenance.
- NP45083.RAmiSi4M7Ee5xQByF4fERyb-0Z1GE-S6yTq72ryve47Sk130_assertion description "[The outcomes of the present study show that molecular epidemiology approaches (i.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45083.RAmiSi4M7Ee5xQByF4fERyb-0Z1GE-S6yTq72ryve47Sk130_provenance.
- NP45088.RAt2-h8_cSMJjKJuxUhb5zopO73zA9iEsq7bRex0eVKlY130_assertion description "[A case-control study was done to determine the association between glutathione S-transferase M1 (GSTM1), GSTT1, GSTP1, EPHX1, and p53 codon 72 polymorphisms as risk factors in 120 adult acute myeloid leukemia (AML) cases and 202 healthy controls by polymerase chain reaction-restriction fragment length polymorphism techniques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45088.RAt2-h8_cSMJjKJuxUhb5zopO73zA9iEsq7bRex0eVKlY130_provenance.
- NP45089.RAoI3FeMMyPX1CgwP27PG7gaZ6y-Ud-SZ5SuYrpRDsZIY130_assertion description "[The results suggest that the proposed EPHX-mediated bioactivation of components of cigarette smoke to mutagenic forms is unlikely to be involved in the etiology of ovarian cancer in general but that a greater rate of EPHX-mediated detoxification may decrease the risk of endometrioid ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45089.RAoI3FeMMyPX1CgwP27PG7gaZ6y-Ud-SZ5SuYrpRDsZIY130_provenance.
- NP45090.RAuiVf7TqyvaSSEQTBaqGqsp_qzBEqdya4fkAhYy9keA8130_assertion description "[To characterize cytochrome P4501A1 (CYP1A1), glutathione S-transferases (GSTs) and microsomal epoxide hydrolase (mEH) polymorphisms in Chinese esophageal cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45090.RAuiVf7TqyvaSSEQTBaqGqsp_qzBEqdya4fkAhYy9keA8130_provenance.
- NP45093.RAhE4Wbi0hU62Np8ihJ_n6VRkHCBM-i80Jv12WLnjo3Ak130_assertion description "[Plasma cell membrane glycoprotein-1 K121Q polymorphism in preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45093.RAhE4Wbi0hU62Np8ihJ_n6VRkHCBM-i80Jv12WLnjo3Ak130_provenance.
- NP45095.RAq1cN9Pwz_1mp_Wa6Gwj3aSjJUGLVrsvweep4_z1RKX0130_assertion description "[This suggests that impaired insulin signaling is of etiologic importance in PCOS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45095.RAq1cN9Pwz_1mp_Wa6Gwj3aSjJUGLVrsvweep4_z1RKX0130_provenance.
- NP45104.RAj55u2c7mRvyqKgVwQQq1dGPz-1Xb7wOwZVan4Uhcixg130_assertion description "[Our data suggest that patients with T2D carrying the ENPP1 Q121 variant are at increased risk of decreased GFR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45104.RAj55u2c7mRvyqKgVwQQq1dGPz-1Xb7wOwZVan4Uhcixg130_provenance.
- NP45107.RAnr3YzM2iohOg1gs1uj9ejqVIRicADuNpdDCs_0LTB8Y130_assertion description "[We analyzed two independent series of cardiovascular patients at a defined end-point of atherosclerotic vascular disease (those having suffered myocardial infarction) for the PC-1 K121Q mutation by a newly developed mutagenic separated PCR assay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45107.RAnr3YzM2iohOg1gs1uj9ejqVIRicADuNpdDCs_0LTB8Y130_provenance.