Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP65763.RAv6GayskULk2dhcv3zgHlJBWrB-oWa8vs-PN4c5KCK7Q130_assertion description "[Differences between rare allele carriage rates of CP and healthy groups regarding MMP-2, MMP-9 and MMP-12 gene polymorphisms were not significant (p>0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65763.RAv6GayskULk2dhcv3zgHlJBWrB-oWa8vs-PN4c5KCK7Q130_provenance.
- NP65765.RAr7IEYwIUYwAz9kblXIs-Abri70SDZMoeyNqGjpbby6s130_assertion description "[The study findings support a role for MMP-9, but not MMP-2, in the pathogenesis of intracranial aneurysms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65765.RAr7IEYwIUYwAz9kblXIs-Abri70SDZMoeyNqGjpbby6s130_provenance.
- NP65767.RAseM-Rx5LBgvQnU5FRlXtgJwdRsUQy9cVd1PJC3cct4s130_assertion description "[Matrix metalloproteinase-9 gene -1562C/T polymorphism mitigates preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65767.RAseM-Rx5LBgvQnU5FRlXtgJwdRsUQy9cVd1PJC3cct4s130_provenance.
- NP65768.RAvjh8KoL1v9W0qqIT2fQnkz6cQ5_CwYyM2jPhzSNOd7I130_assertion description "[Interleukin-4 -590 (C>T), toll-like receptor-2 +2258 (G>A) and matrix metalloproteinase-9 -1562 (C>T) polymorphisms in pre-eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65768.RAvjh8KoL1v9W0qqIT2fQnkz6cQ5_CwYyM2jPhzSNOd7I130_provenance.
- NP65773.RAmdebwl8ezeEtmsLqmfWkXvyFRej8UHRGDzifKEwvRSA130_assertion description "[Matrix metalloproteinase polymorphisms and bladder cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65773.RAmdebwl8ezeEtmsLqmfWkXvyFRej8UHRGDzifKEwvRSA130_provenance.
- NP65776.RAqWwvJunByctPnR_RQyA-tOXDaWY-LPhiPx4nKagVMGs130_assertion description "[For MMP-2, MMP-3, MMP-9, MMP-12, and TIMP-1 polymorphisms there were no clear associations with aneurysm growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65776.RAqWwvJunByctPnR_RQyA-tOXDaWY-LPhiPx4nKagVMGs130_provenance.
- NP65777.RAuma4PjcZCcWk-EeWft1h7EL775naZLHt4YctVEIBtf4130_assertion description "[In light to recently found contribution of factors associated with angiogenesis, thrombosis and inflammation to carcinogenesis, we investigated the possible association of metalloproteinase-9 (MMP-9) with increased risk of oral cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65777.RAuma4PjcZCcWk-EeWft1h7EL775naZLHt4YctVEIBtf4130_provenance.
- NP65784.RAsGxFYZ5t_wtviG76glHdD4PuwSFrcn8Ctipe5wkVS98130_assertion description "[A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65784.RAsGxFYZ5t_wtviG76glHdD4PuwSFrcn8Ctipe5wkVS98130_provenance.
- NP65787.RAq3xgE7xBtooDLhNO3uScGm6bVg85iZrE7vZzcVAMmaA130_assertion description "[The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65787.RAq3xgE7xBtooDLhNO3uScGm6bVg85iZrE7vZzcVAMmaA130_provenance.
- NP65788.RAtOB8z-0QvJHtTxidn1ZofVF2vEfChfvocd5ZpZZ58NE130_assertion description "[Mismatch repair polymorphisms and the risk of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65788.RAtOB8z-0QvJHtTxidn1ZofVF2vEfChfvocd5ZpZZ58NE130_provenance.
- NP65790.RAkP0mpX4q3kEjfD6nM7ORmjL0C1SDyGNbFjrGEUmNu9U130_assertion description "[we find some evidence that common variants in mismatch repair genes may contribute to survival of patients with colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65790.RAkP0mpX4q3kEjfD6nM7ORmjL0C1SDyGNbFjrGEUmNu9U130_provenance.
- NP65793.RAiiG6BT3A24jQSg3lxwx0HO7EfLcaXyLOA40bCf5cnxA130_assertion description "[Polymorphisms in XPD, XPC and the risk of death in patients with urinary bladder neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65793.RAiiG6BT3A24jQSg3lxwx0HO7EfLcaXyLOA40bCf5cnxA130_provenance.
- NP65798.RAiuE4o4WrNeUsfXAv-_AFTGCp5BwjcEP0GpPKceG_soQ130_assertion description "[Considering this importance, we decided to investigate several highly mutative parts of mtDNA for point mutations as MT-LTI (tRNA(Leucine1(UUA/G))), MT-NDI (NADH Dehydrogenase subunit 1), MT-COII (Cytochrome c oxidase subunit II), MT-TK (tRNA(Lysine)), MT-ATP8 (ATP synthase subunit F0 8) and MT-ATP6 (ATP synthase subunit F0 6) in 20 Iranian MS patients and 80 age-matched control subjects by PCR and automated DNA sequencing to evaluate any probable point mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65798.RAiuE4o4WrNeUsfXAv-_AFTGCp5BwjcEP0GpPKceG_soQ130_provenance.
- NP65799.RAjrrIk-dFwb8vZJUvgZfbdRDKonW4oJIzvNamwHWVz3Y130_assertion description "[Considering this importance, we decided to investigate several highly mutative parts of mtDNA for point mutations as MT-LTI (tRNA(Leucine1(UUA/G))), MT-NDI (NADH Dehydrogenase subunit 1), MT-COII (Cytochrome c oxidase subunit II), MT-TK (tRNA(Lysine)), MT-ATP8 (ATP synthase subunit F0 8) and MT-ATP6 (ATP synthase subunit F0 6) in 20 Iranian MS patients and 80 age-matched control subjects by PCR and automated DNA sequencing to evaluate any probable point mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65799.RAjrrIk-dFwb8vZJUvgZfbdRDKonW4oJIzvNamwHWVz3Y130_provenance.
- NP65806.RAhp6xZaFz5CeTBsotJl_rkCGh0eGk-CMrej1PNQZcrbw130_assertion description "[This study suggests that multivitamin supplement use may modify the association between folate pathway genes and colorectal cancer risk in a post-folic-acid-supplemented population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65806.RAhp6xZaFz5CeTBsotJl_rkCGh0eGk-CMrej1PNQZcrbw130_provenance.
- NP65810.RAk_hx8V4zIvxZSkg7FcLTg1nw9XLGAWrjpSaGhAP6icE130_assertion description "[objective: We determined the frequency of aberrant methylation of HIC1 and RASSF1A gene promoters and their association with methylene tetrahydrofolate dehydrogenase (MTHFD1) G1958A polymorphism and major clinical and pathological features of breast cancer in Iranian women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65810.RAk_hx8V4zIvxZSkg7FcLTg1nw9XLGAWrjpSaGhAP6icE130_provenance.
- NP65811.RAjE00F-hiiPzpayQucZkXCfZORtKCMsqZrP6ybbp-dUc130_assertion description "[Polymorphic variants of folate metabolizing genes (C677T and A1298C MTHFR, C1420T SHMT1 and G1958A MTHFD) are not associated with the risk of breast cancer in West Siberian Region of Russia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65811.RAjE00F-hiiPzpayQucZkXCfZORtKCMsqZrP6ybbp-dUc130_provenance.
- NP65813.RAorzRsp1Aprhrc-TyUfjk8eBUoH6OhnRDyqOcWt94sCc130_assertion description "[By analysis of a large number of subjects and a more specific patient selection, we showed the first genetic evidence that MTHFR C677T, MS A2756G and MTRR A66G genotypes were independently associated with male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65813.RAorzRsp1Aprhrc-TyUfjk8eBUoH6OhnRDyqOcWt94sCc130_provenance.
- NP65820.RAi_jtKKc22utIfsQTEuujsp6Qm65-AjleuBFeFlijwlQ130_assertion description "[We examined the association of a single nucleotide polymorphism (SNP) at position 677 in the MTHFR gene on GvHD outcomes in allogeneic HSCT patients administered MTX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65820.RAi_jtKKc22utIfsQTEuujsp6Qm65-AjleuBFeFlijwlQ130_provenance.
- NP65821.RAsXKc6mfTbMytGdJerA0vt1mCF9hcUSQRxLTAbDpYmrM130_assertion description "[No association was observed between the C677T polymorphism and the outcome parameters for any of the different genotypes studied here.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65821.RAsXKc6mfTbMytGdJerA0vt1mCF9hcUSQRxLTAbDpYmrM130_provenance.
- NP65825.RAipEfOeDVkXeixfZ6CS7fo9iHm6VyOAwYK_KuxOxz3dQ130_assertion description "[Significance of factor V, prothrombin, MTHFR, and PAI-1 genotypes in childhood cerebral thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65825.RAipEfOeDVkXeixfZ6CS7fo9iHm6VyOAwYK_KuxOxz3dQ130_provenance.
- NP65826.RAmEZ4LrjRs97OZwyphPscy1lCcXNrCI2ZCwn-eyWVct8130_assertion description "[There was no association between MTHFR C677T, A1298C, MTRR A66G, TS 2R-->3R and 6-bp deletion/insertion polymorphisms and MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65826.RAmEZ4LrjRs97OZwyphPscy1lCcXNrCI2ZCwn-eyWVct8130_provenance.
- NP65828.RAgO8AtUy2r_skf6FsGn4q-5Hpr6_9LhuMFidJeqkynzk130_assertion description "[Methylenetetrahydrofolate reductase genotype does not play a role in multiple myeloma pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65828.RAgO8AtUy2r_skf6FsGn4q-5Hpr6_9LhuMFidJeqkynzk130_provenance.
- NP65831.RAn7M-LuOMNj3hmMbl7qIlk8XEm3ttJfQaP7nmZYDvT6c130_assertion description "[Impact of air pollution and genotype variability on DNA damage in Prague policemen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65831.RAn7M-LuOMNj3hmMbl7qIlk8XEm3ttJfQaP7nmZYDvT6c130_provenance.
- NP65832.RAmarsgQA2U0t64otLphGgjNwfSzs_7cxO3U3cGS65iBs130_assertion description "[Oxidative damage to biological macromolecules in Prague bus drivers and garagemen: impact of air pollution and genetic polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65832.RAmarsgQA2U0t64otLphGgjNwfSzs_7cxO3U3cGS65iBs130_provenance.
- NP65841.RArJF1b76WuY6Q_p2_YruroONefM2oNu_tddEd9F-4lHw130_assertion description "[MtSNPs T3394C in NADH dehydrogenase subunit 1 (ND1), G4491A in ND2, T16189C and T16519C were found with significantly higher frequency in patients with T2DM than in the controls (T16189C, p = 0.0045; T16519C, p < 0.0001; T3394C, p = 0.0015; G4491A, p = 0.0015).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65841.RArJF1b76WuY6Q_p2_YruroONefM2oNu_tddEd9F-4lHw130_provenance.
- NP65845.RAoBaQz024tw99mIakQ7uWSMYM0pgrxvwDH4196h1IoqA130_assertion description "[The analysis presented here provides evidence that there is an association between G11778A and G3460A with haplogroup J (including J1 and J2) and W, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65845.RAoBaQz024tw99mIakQ7uWSMYM0pgrxvwDH4196h1IoqA130_provenance.
- NP65850.RAlUvAy8B9dmlXqaezLQEi2uUMrq8gTbEHgWMzTLBQN24130_assertion description "[Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65850.RAlUvAy8B9dmlXqaezLQEi2uUMrq8gTbEHgWMzTLBQN24130_provenance.
- NP65851.RAmANKQzb9RvjMm7yipaRWFHFYVjwJk9evdkmc4FDIo6U130_assertion description "[A rapid and reliable detection system for identifying mitochondrial polymorphisms and haplotypes was developed based on hybridization probe technology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65851.RAmANKQzb9RvjMm7yipaRWFHFYVjwJk9evdkmc4FDIo6U130_provenance.
- NP65853.RAnApSieaQ_r_LdxnV8RpVf3VOc2rrmYCZzEPoZWIpxPk130_assertion description "[The present results suggest that the ND2-237 Leu/Met polymorphism modulates the effects of coffee consumption on hypertension risk in middle-aged Japanese men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65853.RAnApSieaQ_r_LdxnV8RpVf3VOc2rrmYCZzEPoZWIpxPk130_provenance.
- NP65855.RAphXyMf1XKSrQ2kewZMtPq2IJEcosW-qLs4bQ3idA5UI130_assertion description "[In contrast, the frequency of C5178A in ND2 and A10398G in ND3 was higher in the controls than in patients with T2DM (C5178A, p = 0.014; A10398G, p = 0.0011).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65855.RAphXyMf1XKSrQ2kewZMtPq2IJEcosW-qLs4bQ3idA5UI130_provenance.
- NP65861.RAgr4I8T52GnYndj6eehCxkP1AyfzO2jG5YnxhE4_67cQ130_assertion description "[The three LHON primary mutations are rare in general Chinese populations. The optimized MAS-PCR assay provides an easier, faster and more cost-effective method for detection of the three LHON primary mutations, making it practical for clinical diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65861.RAgr4I8T52GnYndj6eehCxkP1AyfzO2jG5YnxhE4_67cQ130_provenance.
- NP65865.RAsXix8sR2D24PRPyxN_I3ITcCc0X1mTI5SASMQ_LdLPw130_assertion description "[Is polymorphism of CALM1 gene or growth hormone receptor gene associated with susceptibility to adolescent idiopathic scoliosis?.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65865.RAsXix8sR2D24PRPyxN_I3ITcCc0X1mTI5SASMQ_LdLPw130_provenance.
- NP65884.RAkevZWASneV5HqWYuEBNktZMK3u5eJlSgsK14OWsg4ZQ130_assertion description "[These data do not support the hypothesis that genetic variation in genes involved in the metabolism of folate are implicated in the etiology of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65884.RAkevZWASneV5HqWYuEBNktZMK3u5eJlSgsK14OWsg4ZQ130_provenance.
- NP65885.RAkTM4dUVG18t6ZbXeRK6Av6ei2roHEOpdXhKhqX9x7_A130_assertion description "[We analysed common genetic polymorphisms of 5,10-methylenetetrahydrofolate reductase (MTHFR), thymidylate synthase (TS), methionine synthase (MS) and methionine synthase reductase (MTRR) in 68 children with ALL and 258 healthy controls to investigate their influence on the risk for ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65885.RAkTM4dUVG18t6ZbXeRK6Av6ei2roHEOpdXhKhqX9x7_A130_provenance.
- NP65891.RAk48dz7HPL321Fp2uv4--VOBEVaAY3BxazR3yDzY1D5A130_assertion description "[Polymorphisms of methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR), and thymidylate synthase (TYMS) in multiple myeloma risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65891.RAk48dz7HPL321Fp2uv4--VOBEVaAY3BxazR3yDzY1D5A130_provenance.
- NP65897.RAq2VeB3nLBWy2ay5UMUEWYHYj8Leo2XnLDxyDOUNfxkM130_assertion description "[The present study indicates the association of the mitochondrial G1888A variant with Type 2 diabetes and insulin resistance in Caucasian-Brazilian patients from southern Brazil. However, further studies are required to confirm its effects on mitochondrial function and the role of these effects on the pathogenesis of Type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65897.RAq2VeB3nLBWy2ay5UMUEWYHYj8Leo2XnLDxyDOUNfxkM130_provenance.
- NP65901.RAq1OcGpYJjWv6UqoUbm5Ra-DwUY8u_hNHvg_05lSJNdQ130_assertion description "[By analysis of a large number of subjects and a more specific patient selection, we showed the first genetic evidence that MTHFR C677T, MS A2756G and MTRR A66G genotypes were independently associated with male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65901.RAq1OcGpYJjWv6UqoUbm5Ra-DwUY8u_hNHvg_05lSJNdQ130_provenance.
- NP65906.RAoFTBk9nrqjOCaHKi5PWTzKAPzNQ3g2b07Ew_GtGs66I130_assertion description "[Methionine-dependence phenotype in the de novo pathway in BRCA1 and BRCA2 mutation carriers with and without breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65906.RAoFTBk9nrqjOCaHKi5PWTzKAPzNQ3g2b07Ew_GtGs66I130_provenance.
- NP65908.RAqRcUAJlUvJ8U7ezwDxU9uIn-JqLrpHI_FOWBPKs0vVk130_assertion description "[MTRR A66G polymorphism and breast cancer risk: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65908.RAqRcUAJlUvJ8U7ezwDxU9uIn-JqLrpHI_FOWBPKs0vVk130_provenance.
- NP65913.RAiTvH2lGOZfS2yioBR0oSeYznDVcUXPvBCAyz_IKQCXw130_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." NP65913.RAiTvH2lGOZfS2yioBR0oSeYznDVcUXPvBCAyz_IKQCXw130_provenance.
- NP65918.RAsIDSdn6zbT0N-5UvPhbpVnf39WkcUOIUJq38kLHMP2M130_assertion description "[One-carbon metabolism-related gene polymorphisms and risk of head and neck squamous cell carcinoma: case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65918.RAsIDSdn6zbT0N-5UvPhbpVnf39WkcUOIUJq38kLHMP2M130_provenance.
- NP65920.RAoxdh5T3ojqwxGlZD4M5Vu9veomuFtP-zBEhfkO0qST8130_assertion description "[Mitochondrial and nuclear gene mutations in the type 2 diabetes patients of Coimbatore population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65920.RAoxdh5T3ojqwxGlZD4M5Vu9veomuFtP-zBEhfkO0qST8130_provenance.
- NP65925.RAhp7Tm2V2UqpGMeST4L42Fxs9ovPDGm6QW5cwB6YIVKI130_assertion description "[Type 2 diabetes in China is associated with several mitochondrial gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65925.RAhp7Tm2V2UqpGMeST4L42Fxs9ovPDGm6QW5cwB6YIVKI130_provenance.
- NP65936.RAjVLt2MNdHHeDd_K0OC9f9WGyrsLDXnjllNJTPApQjqk130_assertion description "[Germline mutations and polymorphic variants in MMR, E-cadherin and MYH genes associated with familial gastric cancer in Jiangsu of China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65936.RAjVLt2MNdHHeDd_K0OC9f9WGyrsLDXnjllNJTPApQjqk130_provenance.
- NP65937.RAntvqoF-l8yteLHkvE9sn9oI_H-HYuVuYFnFuHM02FdQ130_assertion description "[Mutation analysis of the MYH gene in unrelated Czech APC mutation-negative polyposis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65937.RAntvqoF-l8yteLHkvE9sn9oI_H-HYuVuYFnFuHM02FdQ130_provenance.
- NP65942.RAo3IHmrbTwCA-gUq5-qvQSvYgE88RnE6ylkqK2IOy_IU130_assertion description "[Our results and those of the meta-analysis (>2000 CD patients and 4000 control individuals) question the role of MYO9B at the CELIAC4 locus as a disease-causing gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65942.RAo3IHmrbTwCA-gUq5-qvQSvYgE88RnE6ylkqK2IOy_IU130_provenance.
- NP65945.RAmuGAXwVwQuxDwT0rUzrfyd05u8KQ63O7zRGsCNTyDjY130_assertion description "[Myocilin seems to be a very strong candidate for explaining some of the pathophysiological pathways leading to the development of both glaucoma and high myopia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65945.RAmuGAXwVwQuxDwT0rUzrfyd05u8KQ63O7zRGsCNTyDjY130_provenance.
- NP65946.RAiDpW-7bMMpQyVJhEk6LfS8YDxD_KDNycQGclEvnJJLM130_assertion description "[Our results suggest that MYOC polymorphisms have a very low, or possibly negligible, influence on high myopia susceptibility in subjects of European ethnicity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65946.RAiDpW-7bMMpQyVJhEk6LfS8YDxD_KDNycQGclEvnJJLM130_provenance.
- NP65947.RAvAcG7uA13qXaWgELrv3ILv3Jpg3yNVE--eSiaG293ok130_assertion description "[Mutation analysis of NANOS3 in 80 Chinese and 88 Caucasian women with premature ovarian failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65947.RAvAcG7uA13qXaWgELrv3ILv3Jpg3yNVE--eSiaG293ok130_provenance.
- NP65951.RAkIpq6rUnRx4sQzxEUfJ6MpHVnFpmD236_8u_S06CQBo130_assertion description "[Detoxication gene polymorphism and susceptibility to sporadic motor neuron disease in Russian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65951.RAkIpq6rUnRx4sQzxEUfJ6MpHVnFpmD236_8u_S06CQBo130_provenance.
- NP65952.RAgBzW2XhIluJpiIKwHD3hnvdsIAhWJrx-7nFOKPPCtuw130_assertion description "[Detoxication gene polymorphism and susceptibility to sporadic motor neuron disease in Russian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65952.RAgBzW2XhIluJpiIKwHD3hnvdsIAhWJrx-7nFOKPPCtuw130_provenance.
- NP65953.RAtQJU3Tcgp6fPI78C8rViiNj9ve6ViZn4LojgSaTWItE130_assertion description "[the increase of nasopharyngeal carcinoma risk in Tunisia seems to be associated with GSTM10/0 and NAT2*6/6 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65953.RAtQJU3Tcgp6fPI78C8rViiNj9ve6ViZn4LojgSaTWItE130_provenance.
- NP65955.RAmnbz1sH9d9jvGZkTaUUcGloagTMUEM5hOUsywDSALDc130_assertion description "[The role of CYP1A1, GSTM1, GSTT1, EPHX1, and NAT2 genotypes in susceptibility to malignant mesothelioma (MM) was compared in two case-control studies, previously conducted in two countries where different types of asbestos fibers have been used Hirvonen et al., 1995.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65955.RAmnbz1sH9d9jvGZkTaUUcGloagTMUEM5hOUsywDSALDc130_provenance.
- NP65956.RApVe-qH8duC8qNE5QFJ55ncT_JbzuAhhgmUxFCFua7L0130_assertion description "[Inherited variation in carcinogen-metabolizing enzymes and risk of colorectal polyps.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65956.RApVe-qH8duC8qNE5QFJ55ncT_JbzuAhhgmUxFCFua7L0130_provenance.
- NP65957.RAnTuPr4f7BtKItyzHJHwdZ-SLoI3xVeBWNiIevQ6ujH4130_assertion description "[Meat intake, heterocyclic amine exposure, and metabolizing enzyme polymorphisms in relation to colorectal polyp risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65957.RAnTuPr4f7BtKItyzHJHwdZ-SLoI3xVeBWNiIevQ6ujH4130_provenance.
- NP65967.RAjSfXi9yjdaCJQ9KfkdbC8M6jaIQedGNwMy4fmnebX3A130_assertion description "[The relationship between Helicobacter pylori infection and promoter polymorphism of the Nrf2 gene in chronic gastritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65967.RAjSfXi9yjdaCJQ9KfkdbC8M6jaIQedGNwMy4fmnebX3A130_provenance.
- NP65968.RAvZ7R2nh0uA_wKO3S2074rLSy2YHkpc_TSv7me4NOyag130_assertion description "[The FCRL3 polymorphisms associated with rheumatoid arthritis in a Japanese population are not associated per se with rheumatoid arthritis in a Spanish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65968.RAvZ7R2nh0uA_wKO3S2074rLSy2YHkpc_TSv7me4NOyag130_provenance.
- NP65973.RAvqyloRkxqlVVi8d07V6AMtq7Hy1QIskpURPgu-wE8N0130_assertion description "[NF-kappaB1 and NF-kappaBIalpha genes might be susceptible genes for melanoma risk and functional polymorphisms of these genes might be biological predictors for melanoma progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65973.RAvqyloRkxqlVVi8d07V6AMtq7Hy1QIskpURPgu-wE8N0130_provenance.
- NP65974.RAh5bIoTGgsYpQoLDavpl86B5poO5mm3JyYyVDQL0WUfg130_assertion description "[A total of 122 TB patients and 166 healthy controls (N = 166) negative for human immunodeficiency virus infection were examined for IL1B-511 and +3,953, TAP1 and TAP2 and IKBL+738 polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65974.RAh5bIoTGgsYpQoLDavpl86B5poO5mm3JyYyVDQL0WUfg130_provenance.
- NP65981.RAnZA8axX0n1s5idv2PZPWmAdw-Jj_Ni8CFdVWiGjXkf0130_assertion description "[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65981.RAnZA8axX0n1s5idv2PZPWmAdw-Jj_Ni8CFdVWiGjXkf0130_provenance.
- NP65982.RAvrEH9ut5_Yd7jINAifJ-RYgtsBb_N1-FewI8fF_9wi8130_assertion description "[The NKX3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65982.RAvrEH9ut5_Yd7jINAifJ-RYgtsBb_N1-FewI8fF_9wi8130_provenance.
- NP65999.RAmaVIJTlTq5y-i0twPVXVGFD1iocUXCxVxPOBVAg_1bM130_assertion description "[Thirteen single nucleotide polymorphisms (SNPs) from 10 oxidative stress genes (AKR1A1, AKR1C1, CYBA, GPX, MPO, NOS2A, NOS3, OGG1, PPARG and SOD2) were genotyped in 1172 NHL cases and 982 population-based controls from a USA multicenter case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65999.RAmaVIJTlTq5y-i0twPVXVGFD1iocUXCxVxPOBVAg_1bM130_provenance.
- NP66006.RAqXVWvl3KrwQo10uCyxAX4JtIr5esMr7tp0Zm8kMIGd8130_assertion description "[We have identified significant differences in the (AAAT)(n) and (CCTTT)(n) polymorphisms in Asian diabetics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66006.RAqXVWvl3KrwQo10uCyxAX4JtIr5esMr7tp0Zm8kMIGd8130_provenance.
- NP66008.RApDF_XkyOJsbVvOW7sJWUnw916GrlgFtBhLy0C33Ufv4130_assertion description "[Genetic variants of nNOS, but not iNOS, may be biomarkers for susceptibility to CM, and the risk of CM associated with sunburns and moles may be modulated by nNOS variant genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66008.RApDF_XkyOJsbVvOW7sJWUnw916GrlgFtBhLy0C33Ufv4130_provenance.
- NP66012.RAhoKgzpLpxVbScldUPwVA1NqqgCbQRWLnJjkmq-GXxZU130_assertion description "[Results suggest that the (CCTTT)n NOS2 microsatellite may influence bladder cancer risk and aggressiveness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66012.RAhoKgzpLpxVbScldUPwVA1NqqgCbQRWLnJjkmq-GXxZU130_provenance.
- NP66019.RAlG8vawQoq6HeBvsq7VvsJmg0BQgEkkAtbvT9YL1ZyJ8130_assertion description "[An intron 4 VNTR polymorphism of the endothelial nitric oxide synthase gene is associated with early-onset colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66019.RAlG8vawQoq6HeBvsq7VvsJmg0BQgEkkAtbvT9YL1ZyJ8130_provenance.
- NP66022.RAmX2wLFMDk2xkD9aVSBYEvt-k7NPXsB1lODRWdsbjndM130_assertion description "[Endothelial nitric oxide synthase G894T (Glu298Asp) polymorphism was predictive of glycemic status in a 5-year prospective study of Chinese subjects with impaired glucose tolerance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66022.RAmX2wLFMDk2xkD9aVSBYEvt-k7NPXsB1lODRWdsbjndM130_provenance.
- NP66025.RArl-JVwem7hnNqjpsbHUk01DC0doCNq4P0dnM9J5wnAo130_assertion description "[Stromelysin-1 5A/6A and eNOS T-786C polymorphisms, MTHFR C677T and A1298C mutations, and cigarette-cannabis smoking: a pilot, hypothesis-generating study of gene-environment pathophysiological associations with Buerger's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66025.RArl-JVwem7hnNqjpsbHUk01DC0doCNq4P0dnM9J5wnAo130_provenance.
- NP66032.RAox9yB1maBcLlqxjn4GSC0Nztj-77Ckz4kSMh65raRZM130_assertion description "[Metabolic background determines the importance of NOS3 polymorphisms in restenosis after percutaneous coronary intervention: A study in patients with and without the metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66032.RAox9yB1maBcLlqxjn4GSC0Nztj-77Ckz4kSMh65raRZM130_provenance.
- NP66034.RAlWaloXGH1hZbR9_o58qAvYwityvK5ln8HbUVc0iFH5s130_assertion description "[specific NOS3 SNPs and haplotypes were associated with inter-individual variation in ABI, a non-invasive marker of peripheral arterial disease, in replicate subsets of hypertensive subjects. These findings motivate further investigation of the role of NOS3 variants in determining susceptibility to peripheral arterial disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66034.RAlWaloXGH1hZbR9_o58qAvYwityvK5ln8HbUVc0iFH5s130_provenance.
- NP66035.RAmaUru8T8TLd2FLPFwc9AKboEuRDqQ6zghPrLJPmTb3Q130_assertion description "[Effects of endothelial nitric oxide synthase, interleukin-6 gene polymorphisms and asymmetric dimethylarginine levels on risk factors and lesion sites in peripheral artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66035.RAmaUru8T8TLd2FLPFwc9AKboEuRDqQ6zghPrLJPmTb3Q130_provenance.
- NP66039.RAuKRXOG0GOlV7qeOd1yog9tPOVghZyp-vPRcPRaCc3E8130_assertion description "[NOTCH1 and FBXW7 mutations were not predictive of outcome in the overall cohort of adult patients with T-lymphoblastic leukemia, but there was a trend towards a favorable prognostic impact of NOTCH1-FBXW7 mutations in the small subgroup of patients with low-risk ERG/BAALC expression status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66039.RAuKRXOG0GOlV7qeOd1yog9tPOVghZyp-vPRcPRaCc3E8130_provenance.
- NP66042.RAu34KG5Ol96MmzbsQ2jeyjeFUbvMVjRc271COHNg8SXI130_assertion description "[Polymorphisms in genes involved in neurodevelopment may be associated with altered brain morphology in schizophrenia: preliminary evidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66042.RAu34KG5Ol96MmzbsQ2jeyjeFUbvMVjRc271COHNg8SXI130_provenance.
- NP66044.RAm0BWRFWdL4qwrFVsHRrRHuD39lqRS8fp72ruBhVckKc130_assertion description "[Association of Per1 and Npas2 with autistic disorder: support for the clock genes/social timing hypothesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66044.RAm0BWRFWdL4qwrFVsHRrRHuD39lqRS8fp72ruBhVckKc130_provenance.
- NP66045.RAucUIV8gtxwlw0lK1UrTdDGUqui4tOyWQA5-dwnOiUlc130_assertion description "[Non-synonymous polymorphisms in the circadian gene NPAS2 and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66045.RAucUIV8gtxwlw0lK1UrTdDGUqui4tOyWQA5-dwnOiUlc130_provenance.
- NP66046.RAphXL9KNO0ycjlYBrjEiV2U0knv_bBGrmkZhi0JWhnPI130_assertion description "[The circadian gene NPAS2 is a novel prognostic biomarker for breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66046.RAphXL9KNO0ycjlYBrjEiV2U0knv_bBGrmkZhi0JWhnPI130_provenance.
- NP66052.RAjZJlQlwwdoNv4Jo76mcvt3BoJPt8NhH9b63i6kSuRrw130_assertion description "[Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66052.RAjZJlQlwwdoNv4Jo76mcvt3BoJPt8NhH9b63i6kSuRrw130_provenance.
- NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_assertion description "[First, two thirds of nephrotic syndrome manifesting in the first year of life can be explained by mutations in 4 genes only (NPHS1, NPHS2, WT1, or LAMB2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_provenance.
- NP66056.RAqCKeSyPjNjccfSC7np3jc6V9opd9uWGqmzTHlMQp5Ak130_assertion description "[In conclusion, podocin mutations do not appear to be a major cause of SRNS in Greek children, although the study cohort was small.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66056.RAqCKeSyPjNjccfSC7np3jc6V9opd9uWGqmzTHlMQp5Ak130_provenance.
- NP66057.RAvkAmOLuTPd41iYbF3Nmund1HHzPjad05QjKG5eM-NSk130_assertion description "[Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66057.RAvkAmOLuTPd41iYbF3Nmund1HHzPjad05QjKG5eM-NSk130_provenance.
- NP66058.RAkiFBLjE7c-_lKkMalSyymnSu5kWAldaGNxm2H_71fkc130_assertion description "[NPHS2 mutations in children with steroid-resistant nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66058.RAkiFBLjE7c-_lKkMalSyymnSu5kWAldaGNxm2H_71fkc130_provenance.
- NP66059.RApwV6C64T4qbMepN7Nhu1DBJ4ca2sZk-JZLBP9IPLlRA130_assertion description "[In Chinese children with steroid-resistant nephrotic syndrome (SRNS), it was reported that NPHS2 mutation was detected in 4.3%, which was lower than that in Caucasians (10-30%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66059.RApwV6C64T4qbMepN7Nhu1DBJ4ca2sZk-JZLBP9IPLlRA130_provenance.
- NP66063.RAipmYomedqBNUgGgF83hkOHShpMBZPj_DFBXD0xhPph4130_assertion description "[Association between the T-381C polymorphism of the brain natriuretic peptide gene and risk of type 2 diabetes in human populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66063.RAipmYomedqBNUgGgF83hkOHShpMBZPj_DFBXD0xhPph4130_provenance.
- NP66064.RAnpDFUtYQwCmgyCNGJkDdUWlLEOGqHIAkMg78Dh44ucU130_assertion description "[A recent study reported an association between the brain natriuretic peptide (BNP) promoter T-381C polymorphism (rs198389) and protection against type 2 diabetes (T2D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66064.RAnpDFUtYQwCmgyCNGJkDdUWlLEOGqHIAkMg78Dh44ucU130_provenance.
- NP66065.RAlN5Y3mvfhcsKBZ7wC0VYMgtHbgX91fIKAbtuBcZG0IY130_assertion description "[These results support a susceptibility locus for asthma and related phenotypes on chromosome 7, and are in agreement with recent reports suggesting that a common susceptibility factor for atopic manifestations in asthma is likely conferred by the locus containing the GPR154 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66065.RAlN5Y3mvfhcsKBZ7wC0VYMgtHbgX91fIKAbtuBcZG0IY130_provenance.
- NP66074.RAsq98AhgjUZoplcqW4cpNay8jHUcMVBiAlxqj0799LIE130_assertion description "[To study the relationship between neuropeptide Y2 receptor (NPY2R) gene rs1047214 polymorphism and obesity or metabolic syndrome in Chinese children and adolescents, in order to provide theoretical evidence for obesity control.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66074.RAsq98AhgjUZoplcqW4cpNay8jHUcMVBiAlxqj0799LIE130_provenance.
- NP66076.RAkRUWRQKGkQmYXm7NixbLCHP_LLn-oq7QnTq1zGqYKzE130_assertion description "[No association of sequence variants in the neuropeptide Y2 receptor (NPY2R) gene with early onset obesity in Germans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66076.RAkRUWRQKGkQmYXm7NixbLCHP_LLn-oq7QnTq1zGqYKzE130_provenance.
- NP66079.RAif-aSHjTTUd2KAFvl10DlGm6dlpBxwwv_Po_gV7NGLY130_assertion description "[Association of neuropeptide Y receptor Y5 polymorphisms with dyslipidemia in Mexican Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66079.RAif-aSHjTTUd2KAFvl10DlGm6dlpBxwwv_Po_gV7NGLY130_provenance.
- NP66082.RAjJKn9cW4QeEj0OYWTr-LppgiCLtOKjcDqmXx6uZRcP8130_assertion description "[We evaluated associations between non-Hodgkin's lymphoma and 15 variants in AHR, CYP1A1, CYP1A2, CYP1B1, CYP2C9, CYP2E1, GSTP1, GSTM3, EPHX1, NQO1, and PON1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66082.RAjJKn9cW4QeEj0OYWTr-LppgiCLtOKjcDqmXx6uZRcP8130_provenance.
- NP66102.RAkA79h4_wUYQ0stA9iJCAMtcFqwgvyNvAISwyBvL2Tzc130_assertion description "[Common genetic variation in Neuregulin 3 (NRG3) influences risk for schizophrenia and impacts NRG3 expression in human brain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66102.RAkA79h4_wUYQ0stA9iJCAMtcFqwgvyNvAISwyBvL2Tzc130_provenance.
- NP66104.RApr6sRJPyYNqBwquFkzCmuTHqLiMat8yn0esv_lOf6tg130_assertion description "[Our findings implicating the MHC region are consistent with an immune component to schizophrenia risk, whereas the association with NRGN and TCF4 points to perturbation of pathways involved in brain development, memory and cognition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66104.RApr6sRJPyYNqBwquFkzCmuTHqLiMat8yn0esv_lOf6tg130_provenance.
- NP66106.RAg0KoKykKYhjso_uI7sxR-_4eDKDW7vPsNm4knyTP35k130_assertion description "[An investigation of the neurotrophic factor genes GDNF, NGF, and NT3 in susceptibility to ADHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66106.RAg0KoKykKYhjso_uI7sxR-_4eDKDW7vPsNm4knyTP35k130_provenance.
- NP66108.RAisbqkGQY7KGr5gVO6HKMsP-EcOvFdifSNy2C0dOdmxc130_assertion description "[Individually, three SNPs were associated with alcohol dependence and alcohol abuse (AD) (P-value from 0.0019 to 0.0059, significance level was set at P<or=0.01 corrected for multiple testing), whereas a common 18 locus haplotype within the largest LD block of NTRK2, a 119-kb region containing the 5' flanking region and exons 1-15, was marginally overrepresented in control subjects compared to AD individuals (global P=0.057).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66108.RAisbqkGQY7KGr5gVO6HKMsP-EcOvFdifSNy2C0dOdmxc130_provenance.
- NP66113.RArBbRsgoTUPzdzArIwWNqv8f9RMwxCk5oSJkE69v7ZCw130_assertion description "[Vegetables- and antioxidant-related nutrients, genetic susceptibility, and non-Hodgkin lymphoma risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66113.RArBbRsgoTUPzdzArIwWNqv8f9RMwxCk5oSJkE69v7ZCw130_provenance.
- NP66114.RAgZMiy8-m2RhMaLo0r6_cMVsznaiS1fWCHx4HDsR-zGw130_assertion description "[Influence of polymorphisms at loci encoding DNA repair proteins on cancer susceptibility and G2 chromosomal radiosensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66114.RAgZMiy8-m2RhMaLo0r6_cMVsznaiS1fWCHx4HDsR-zGw130_provenance.
- NP66116.RAuXDJFCyhmrlHw_LOD4HFRyU1evRsGUqSLtJAv9hXd2k130_assertion description "[The results suggested that the asbestos occupational exposure might induce DNA damage and the augment on susceptivity of H2O2 oxidation and the fall of the capacity of repairing DNA damage might be one of the mechanisms to induce asbestosis among subjects with the Cys allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66116.RAuXDJFCyhmrlHw_LOD4HFRyU1evRsGUqSLtJAv9hXd2k130_provenance.
- NP66120.RArTOmyC8g4gN4Xqilx2aXT8txuErm2k_OBMX2tB_m_cw130_assertion description "[BER gene polymorphisms (OGG1 Ser326Cys and XRCC1 Arg194Trp) and modulation of DNA damage due to pesticides exposure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66120.RArTOmyC8g4gN4Xqilx2aXT8txuErm2k_OBMX2tB_m_cw130_provenance.
- NP66136.RAjP4QHwgSnO_S70IFzHZZ1AnXWgAK_mbA6uuLlfA-3QM130_assertion description "[Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66136.RAjP4QHwgSnO_S70IFzHZZ1AnXWgAK_mbA6uuLlfA-3QM130_provenance.
- NP66140.RAv3mvrSLyZ5mD-d7mgj4rhpTBYfzmSANR5EDjRK4R7kw130_assertion description "[However, inconsistent SNP-level results suggest that further studies will be needed to determine the mechanism by which ORMDL3 predisposes to asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66140.RAv3mvrSLyZ5mD-d7mgj4rhpTBYfzmSANR5EDjRK4R7kw130_provenance.