Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP48291.RAeccvY5oq6pyQx_4q4ps6XaZhfC9jqZxAE6mJeBHQKAo130_assertion description "[Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48291.RAeccvY5oq6pyQx_4q4ps6XaZhfC9jqZxAE6mJeBHQKAo130_provenance.
- NP48292.RAUPnbM7qxxU_pl65MC40PJQtLdY2kSlEYfJvGU52qlCI130_assertion description "[Postprandial triglyceride levels in familial combined hyperlipidemia. The role of apolipoprotein E and lipoprotein lipase polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48292.RAUPnbM7qxxU_pl65MC40PJQtLdY2kSlEYfJvGU52qlCI130_provenance.
- NP48297.RAeXctTuSMlBhbM4VQLTtcQXzybwmYelw58URj0agXF-s130_assertion description "[We studied the effect of APOE and APOC1 genes on magnetic resonance imaging measures in a sample of 50 subjects with age-associated memory impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48297.RAeXctTuSMlBhbM4VQLTtcQXzybwmYelw58URj0agXF-s130_provenance.
- NP48299.RAXhlYfpeBIVmGpHu4w-u9Wl8Tp9-tRQNu5hiAv-18Qv0130_assertion description "[Association of a novel 3-amino acid deletion mutation of apolipoprotein E (Apo E Tokyo) with lipoprotein glomerulopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48299.RAXhlYfpeBIVmGpHu4w-u9Wl8Tp9-tRQNu5hiAv-18Qv0130_provenance.
- NP48301.RAX5xoQhvtMFvntzf3m9S8jVtgwlDRJ2V5Sj9MOi5tnI0130_assertion description "[However, analysis of apoE genotypes as a function of stroke subtype revealed that the apoE4 allele was significantly more common in those patients with macroangiopathy-associated CVD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48301.RAX5xoQhvtMFvntzf3m9S8jVtgwlDRJ2V5Sj9MOi5tnI0130_provenance.
- NP48306.RAad6vCKK00t-AzKZT6HFUSrGZ0AVvJQYEdDsX42VKptU130_assertion description "[Our findings suggest that genetic effects may differ between small and large vessel subtypes, although the evidence base is small.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48306.RAad6vCKK00t-AzKZT6HFUSrGZ0AVvJQYEdDsX42VKptU130_provenance.
- NP48315.RAbnlNlVRaTKjazzwyhxoPFkl9jxDx7dt71DShC3T1pzo130_assertion description "[Polymorphisms in the apolipoprotein E (Apo E) gene have been associated with lipid levels, carotid intima media thickness (CCA-IMT), inflammation and cardiovascular disease (CVD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48315.RAbnlNlVRaTKjazzwyhxoPFkl9jxDx7dt71DShC3T1pzo130_provenance.
- NP48316.RAZcn2RmLwPwcfXXEiP2gm8HT0JDovlh0aFvEOW-FnVkY130_assertion description "[Apolipoprotein E, cardiovascular disease and cognitive function in aging women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48316.RAZcn2RmLwPwcfXXEiP2gm8HT0JDovlh0aFvEOW-FnVkY130_provenance.
- NP48322.RAWKPiVHhUzkPGbN7Ckve_qDVJCc8ISjhhrXQCNE7u76M130_assertion description "[Association between apolipoprotein E epsilon4 and sleep-disordered breathing in adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48322.RAWKPiVHhUzkPGbN7Ckve_qDVJCc8ISjhhrXQCNE7u76M130_provenance.
- NP48326.RAcFXA_dFXvzJGTsWph4lpNbQbRwoRoO798weozZ4-fL4130_assertion description "[Apolipoprotein E in temporal lobe epilepsy: a case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48326.RAcFXA_dFXvzJGTsWph4lpNbQbRwoRoO798weozZ4-fL4130_provenance.
- NP48330.RAbVlj_QwCy_rnPfV74UR__UsZDVZplhdMPHCihtR2s28130_assertion description "[Each method suggested that the -352G allele frequency is higher for EOAD in the eastern Finnish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48330.RAbVlj_QwCy_rnPfV74UR__UsZDVZplhdMPHCihtR2s28130_provenance.
- NP48351.RAajLxmaK8gEQhxWzw8DnmiXUPyHSqw35armLbsTpwyFc130_assertion description "[Exact localization of the familial dysbetalipoproteinemia associated HpaI restriction site in the promoter region of the APOC1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48351.RAajLxmaK8gEQhxWzw8DnmiXUPyHSqw35armLbsTpwyFc130_provenance.
- NP48353.RAePdIW1Zo19YIljuQ4b0fYAetNKDUkf3gdgPjVWF362w130_assertion description "[Individual coronary risk might be related to the presence of a critical accumulation detrimental polymorphisms]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48353.RAePdIW1Zo19YIljuQ4b0fYAetNKDUkf3gdgPjVWF362w130_provenance.
- NP48354.RAU8lQZNKh9v9XZx8R8JxUYmqQpglsS_-r448sOp8Ya3Y130_assertion description "[Ins/Del, XbaI, and EcoRI polymorphic sites of the apolipoprotein B (apo B) gene were studied in 67 patients with CHD and in 67 age-matched healthy individuals selected from a population of Brazilians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48354.RAU8lQZNKh9v9XZx8R8JxUYmqQpglsS_-r448sOp8Ya3Y130_provenance.
- NP48361.RAf74aCGIGEj3KzZEs_rHCu6F4yJkfvGQ0V8Dda0cSQRI130_assertion description "[Polymorphisms in genes encoding proteins in the lipid metabolism are associated with the response to antihypertensive treatment in a drug specific pattern.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48361.RAf74aCGIGEj3KzZEs_rHCu6F4yJkfvGQ0V8Dda0cSQRI130_provenance.
- NP48362.RAbibWKSloGn5jmZHOfRCYLs11Tdmc7F8Qi5rANdyucJM130_assertion description "[Future studies on single nucleotide polymorphisms in larger samples are needed to further investigate the possible contribution of the APOB gene to essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48362.RAbibWKSloGn5jmZHOfRCYLs11Tdmc7F8Qi5rANdyucJM130_provenance.
- NP48365.RAVpB14rJptvHI81dQfe2HNKWShCiC-0k1WYxbF_6tec4130_assertion description "[Autosomal dominant hypercholesterolemia (ADH) is caused by mutations in the genes coding for the low-density lipoprotein receptor (LDLR), apolipoprotein B-100 (APOB), or proprotein convertase subtilisin/kexin type 9 (PCSK9).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48365.RAVpB14rJptvHI81dQfe2HNKWShCiC-0k1WYxbF_6tec4130_provenance.
- NP48372.RAYqJ2xDAX8r-P9KjWrchVJkESKCVGVRZvsrnBPCLqE4k130_assertion description "[Genetic screening protocol for familial hypercholesterolemia which includes splicing defects gives an improved mutation detection rate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48372.RAYqJ2xDAX8r-P9KjWrchVJkESKCVGVRZvsrnBPCLqE4k130_provenance.
- NP48373.RAVExDXwf3NXkZQkQs40klDQYdl5DgootK2YyXh_2DF9A130_assertion description "[Associations between five polymorphisms representing four lipid transport gene loci and dyslipidemia were demonstrated in this German population. It is possible that predisposition to dyslipidemia in Germany involves a particular selection of polymorphic loci, which are different from those identified in other European countries.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48373.RAVExDXwf3NXkZQkQs40klDQYdl5DgootK2YyXh_2DF9A130_provenance.
- NP48375.RASw0NsyYxgn_noa9NELbL9lBjrivpv7mp2NnHpOLvBL8130_assertion description "[CAD patients with two HVE-36 alleles and no HVE-32 alleles (the two most common forms) had significantly higher concentrations of LDL-cholesterol, apolipoprotein B, and triglycerides, and significantly lower values of HDL-cholesterol and apolipoprotein AI than the control group (p < 0.01 for all comparisons).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48375.RASw0NsyYxgn_noa9NELbL9lBjrivpv7mp2NnHpOLvBL8130_provenance.
- NP48381.RARMhb7POPvv5ta6BE2RlfdI7U_1KGmDxupOsRTeazd8I130_assertion description "[This study identifies the apolipoprotein B gene polymorphism associated with coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48381.RARMhb7POPvv5ta6BE2RlfdI7U_1KGmDxupOsRTeazd8I130_provenance.
- NP48382.RAfe6FYp1EsboFsmmpk1GxdSFtRBnQn0bvvBZ_ibt060s130_assertion description "[Genetic variations of the apolipoprotein B gene in Turkish patients with coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48382.RAfe6FYp1EsboFsmmpk1GxdSFtRBnQn0bvvBZ_ibt060s130_provenance.
- NP48383.RAegLzEfN3LaOnFla3Bl1sR7YcaXbSKppIlCxALY_x8uY130_assertion description "[ variation in LIPC (hepatic lipase) gene associates with clinical outcomes in Italian patients with established CAD. Further studies on the LIPC gene in CAD patients are warranted, in particular looking at the possible influences on clinical outcomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48383.RAegLzEfN3LaOnFla3Bl1sR7YcaXbSKppIlCxALY_x8uY130_provenance.
- NP48384.RAV8gMZagDIZTs4X9brAqXCHThokuMUlnkSsSqRvIoGqo130_assertion description "[ The alleles for apo e4, XbaI x(+), 3'VNTR-B may be the important genetic markers of Han CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48384.RAV8gMZagDIZTs4X9brAqXCHThokuMUlnkSsSqRvIoGqo130_provenance.
- NP48390.RASQ6lBNHG8BNUHpKRIOL-CwpXKpHebBRqkybrzDPxtZ4130_assertion description "[Our findings show that APOB gene, encoding one of the main components of lipid metabolism system, is involved into the diabetic polyneuropathy development in type 1 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48390.RASQ6lBNHG8BNUHpKRIOL-CwpXKpHebBRqkybrzDPxtZ4130_provenance.
- NP48394.RAaaMFB7IUbYLNEuR4s-sTttvjwrXK60FFJhkSx5e3uIE130_assertion description "[Apolipoprotein B gene polymorphisms in people in the east Mediterranean area of Turkey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48394.RAaaMFB7IUbYLNEuR4s-sTttvjwrXK60FFJhkSx5e3uIE130_provenance.
- NP48406.RAYSBN_N41ulyfSpoeXbydgJuQBQM1AoG71XVO3z5VtdU130_assertion description "[Apolipoprotein B signal peptide polymorphism and plasma LDL-cholesterol response to low-calorie diet.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48406.RAYSBN_N41ulyfSpoeXbydgJuQBQM1AoG71XVO3z5VtdU130_provenance.
- NP48413.RAZiWxEspIobVyINZk1HjgfPGxdKQDD6hvYNpzPhd-A78130_assertion description "[These results suggest that genetic variations at LPL and ApoB loci are among the factors contributing to the variability in response to lipid parameters to therapy in Type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48413.RAZiWxEspIobVyINZk1HjgfPGxdKQDD6hvYNpzPhd-A78130_provenance.
- NP48418.RAVXpizqwJfNSjijGJTC8eUd0YHuNSy2Dftx_vggGUwac130_assertion description "[Although a comparable healthy Israeli population study is needed for more precise interpretation of these results, frequency differences in these polymorphic alleles--associated with lipid metabolism, renin-angiotensin system and leukocyte adhesion mechanism--between CVD patients and healthy individuals nevertheless implicate these candidate genes as predisposing for CVD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48418.RAVXpizqwJfNSjijGJTC8eUd0YHuNSy2Dftx_vggGUwac130_provenance.
- NP48428.RAS3jDugcfNPjPAhisWhvAlZ7erOVXorBoRShrZmE2HeM130_assertion description "[Some polymorphisms in the apolipoprotein B gene are associated with peripheral arterial disease, coronary artery disease and risk of myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48428.RAS3jDugcfNPjPAhisWhvAlZ7erOVXorBoRShrZmE2HeM130_provenance.
- NP48430.RAdOOAPHG9ZON_sq0YeLBoFLcdVKCYinSoU80nz_juXlU130_assertion description "[Exploration of multilocus effects in a highly polymorphic gene, the apolipoprotein (APOB) gene, in relation to plasma apoB levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48430.RAdOOAPHG9ZON_sq0YeLBoFLcdVKCYinSoU80nz_juXlU130_provenance.
- NP48438.RAax61-jzZzZ5y4XEyRFvzHLYv6d2IUQP4wJIH39HIlRI130_assertion description "[Some common polymorphisms and haplotypes in APOA5 are closely associated with FCH in Hong Kong Chinese, and these differ from those found in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48438.RAax61-jzZzZ5y4XEyRFvzHLYv6d2IUQP4wJIH39HIlRI130_provenance.
- NP48439.RAbB2T8GSgLL1g3WPizNGxKaeNKKOlGolsxwuKMwSnv2s130_assertion description "[ The association is found between the Hae III polymorphism and CHD, There is a significant correlation between the CC genotype of the APOA5 and the levels of plasma high density lipoprotein-cholosteal in the CHD group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48439.RAbB2T8GSgLL1g3WPizNGxKaeNKKOlGolsxwuKMwSnv2s130_provenance.
- NP48441.RAbkvJscPpSLA8-JGvI0xlxPagSZ6Fc5mygXqWeAbooj8130_assertion description "[Individual coronary risk might be related to the presence of a critical accumulation detrimental polymorphisms]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48441.RAbkvJscPpSLA8-JGvI0xlxPagSZ6Fc5mygXqWeAbooj8130_provenance.
- NP48444.RAc7eryAyh61BteDZJSiSCZxO4Ds7OVNSXCwQQNza3ZJg130_assertion description "[ Our data suggest that the APOA-IV gene polymorphisms investigated are associated with obesity-related traits. The effects of X*2 and 347Ser variants on BMI and the 360His variant on waist circumference depended on smoking status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48444.RAc7eryAyh61BteDZJSiSCZxO4Ds7OVNSXCwQQNza3ZJg130_provenance.
- NP48453.RAXOwGYvEJsXYLrbHA0_jQ4Mpq2J7G9lGLr2An6-e1OmM130_assertion description "[No significant association between apoB XbaI polymorphism and carotid IMT was found. However, serum total and LDL cholesterol and apoB concentrations were significantly different among apoB genotype groups (p<0.001 for all traits). The apoA-I/C-III/A-IV SstI polymorphism is associated with carotid IMT in young Finns.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48453.RAXOwGYvEJsXYLrbHA0_jQ4Mpq2J7G9lGLr2An6-e1OmM130_provenance.
- NP48457.RAZiq0KNBN1Sbetzb8iZDG6wN5mrn5R-Y6tOLgxdB075Y130_assertion description "[ Our data suggest that the APOA-IV gene polymorphisms investigated are associated with obesity-related traits. The effects of X*2 and 347Ser variants on BMI and the 360His variant on waist circumference depended on smoking status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48457.RAZiq0KNBN1Sbetzb8iZDG6wN5mrn5R-Y6tOLgxdB075Y130_provenance.
- NP48465.RAVlxqlLf9BqLSQO1yurSBjVYanQmUtfZYE7RJkG2hEIo130_assertion description "[Therefore, the present study aimed to elucidate the relationship of four single nucleotide polymorphisms (SNPs) in the Apo11q cluster, namely the -75G>A, +83C>T SNPs in the APOA1 gene, the Sac1 SNP in the APOC3 gene and the S19W variant in the APOA5 gene to plasma lipids and CAD in 190 affected sibling pairs (ASPs) belonging to Asian Indian families with a strong CAD history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48465.RAVlxqlLf9BqLSQO1yurSBjVYanQmUtfZYE7RJkG2hEIo130_provenance.
- NP48466.RAZ-Js1ls9v_1eF_1nyLF6VZ-ANlFmL2IDBex5wsQ8RtQ130_assertion description "[the APOAII rs5082 polymorphism appears to be cardioprotective in this representative Caucasian Australian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48466.RAZ-Js1ls9v_1eF_1nyLF6VZ-ANlFmL2IDBex5wsQ8RtQ130_provenance.
- NP48471.RAWv2iHVtm0uTCC69kIeo-fg6Sde8Ull4QY7q0UGodpG8130_assertion description "[A novel haplotype in ApoAI-CIII-AIV gene region is detrimental to Northwest Indians with coronary heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48471.RAWv2iHVtm0uTCC69kIeo-fg6Sde8Ull4QY7q0UGodpG8130_provenance.
- NP48482.RAVo-d-pSTgHp7g7yoZfBwTDnR2wNV0xXi8NJFeJI7Bn4130_assertion description "[Two newly identified SNPs in the APO AI-CIII intergenic region are strongly associated with familial combined hyperlipidaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48482.RAVo-d-pSTgHp7g7yoZfBwTDnR2wNV0xXi8NJFeJI7Bn4130_provenance.
- NP48485.RAfiNcVK_oHlDjAHqsOmXFtT0XBohH0s8omYvsMwLY5QE130_assertion description "[Some common polymorphisms and haplotypes in APOA5 are closely associated with FCH in Hong Kong Chinese, and these differ from those found in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48485.RAfiNcVK_oHlDjAHqsOmXFtT0XBohH0s8omYvsMwLY5QE130_provenance.
- NP48491.RAbqv1M9VYB1E2N-gM-ULRZ51vt9vEk6rSXFUbHWITbGc130_assertion description "[ Pending confirmation in prospective studies, the AA genotype of the MspI polymorphism of the Apo AI gene, within the Apo A-I/C-III/A-IV cluster, seems to be a risk factor for Type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48491.RAbqv1M9VYB1E2N-gM-ULRZ51vt9vEk6rSXFUbHWITbGc130_provenance.
- NP48493.RAZNMcpaDFoPZuJ41liNkEkEzP5IWlVCYL3NMnlrbiNrU130_assertion description "[Deoxyribonucleic acid polymorphism of the apoprotein AI-CIII-AIV gene cluster and coronary heart disease in non-insulin-dependent diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48493.RAZNMcpaDFoPZuJ41liNkEkEzP5IWlVCYL3NMnlrbiNrU130_provenance.
- NP48494.RATWM2r_yYkM98Lq38rG0MQrIw0vKi95Y-YNF_X51Gw_s130_assertion description "[DNA restriction polymorphisms of the apolipoprotein AI-CIII-AIV gene cluster: a genetic determinant of atherosclerosis in type 2 (non-insulin-dependent) diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48494.RATWM2r_yYkM98Lq38rG0MQrIw0vKi95Y-YNF_X51Gw_s130_provenance.
- NP48503.RAfi6198W7fy9DYvNFS2JYaYWcn_-xzeiiij7wpjRRZ4c130_assertion description "[Apolipoprotein A1 gene polymorphism (G-75A and C+83T) in patients with myocardial infarction: a pilot study in a north Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48503.RAfi6198W7fy9DYvNFS2JYaYWcn_-xzeiiij7wpjRRZ4c130_provenance.
- NP48504.RAbbjbWzyfEh8trwM0aOLo0mzjw0PKXXc_1ahBpOwbGW4130_assertion description "[No significant association between apoB XbaI polymorphism and carotid IMT was found. However, serum total and LDL cholesterol and apoB concentrations were significantly different among apoB genotype groups (p<0.001 for all traits). The apoA-I/C-III/A-IV SstI polymorphism is associated with carotid IMT in young Finns.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48504.RAbbjbWzyfEh8trwM0aOLo0mzjw0PKXXc_1ahBpOwbGW4130_provenance.
- NP48505.RAbjohrorcnui6Kxkbesnjf-KDiRyp_IASdDxcpnoKmFc130_assertion description "[These frequencies were compared to frequencies found in other world populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48505.RAbjohrorcnui6Kxkbesnjf-KDiRyp_IASdDxcpnoKmFc130_provenance.
- NP48512.RASIQeAFGONGR-YiLiyNAFoCjayU95JirPMMine8Jww0Q130_assertion description "[Homozygous carriers of the APEX1 148Glu variant had an increased risk (OR, 2.13; 95% CI, 0.96-4.74), whereas persons with the XRCC1 399Gln allele had a decreased risk (OR, 0.60; 95% CI, 0.35-1.02) of lung cancer compared with wild-type carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48512.RASIQeAFGONGR-YiLiyNAFoCjayU95JirPMMine8Jww0Q130_provenance.
- NP48515.RAedJ18TdnGJ_lO7qJGjIvSlzfFDnOScWo8ghk0HoZhHk130_assertion description "[A statistically significant interaction of current smoking status with APE1 Asp148Glu polymorphism was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48515.RAedJ18TdnGJ_lO7qJGjIvSlzfFDnOScWo8ghk0HoZhHk130_provenance.
- NP48517.RAfwYpWMyT9mdEjG_D51YNe46r_exbzFWUblg744KHALs130_assertion description "[Base excision repair genes and risk of lung cancer among San Francisco Bay Area Latinos and African-Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48517.RAfwYpWMyT9mdEjG_D51YNe46r_exbzFWUblg744KHALs130_provenance.
- NP48519.RAf7nEk0SbSf4CeTDi16fcYdGMkw7bCSTBGPn06ibOvyk130_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." NP48519.RAf7nEk0SbSf4CeTDi16fcYdGMkw7bCSTBGPn06ibOvyk130_provenance.
- NP48520.RAVTB33GUZkz8V4kCN5TPlT-XNxKj6PRxahRyjQjdKAeY130_assertion description "[The effect associated with the substitution of adenine (A) for guanidine (G) in the promoter region of the apolipoprotein AI gene (-75 bp) with plasma apo AI and high-density lipoprotein (HDL) levels was investigated in the European Atherosclerosis Research Study (EARS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48520.RAVTB33GUZkz8V4kCN5TPlT-XNxKj6PRxahRyjQjdKAeY130_provenance.
- NP48527.RARG1cwYQ7QUMmiHSIJkwgBD_z26-0X76hYT9RbuueQ68130_assertion description "[Association between single-nucleotide polymorphisms of selected genes involved in the response to DNA damage and risk of colon, head and neck, and breast cancers in a Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48527.RARG1cwYQ7QUMmiHSIJkwgBD_z26-0X76hYT9RbuueQ68130_provenance.
- NP48529.RARlrvRsRLZbWUCabkYC7e24zg9K3TZLGYk2Q9tCNo0jc130_assertion description "[Thus, while the TTR V30M mutation is required for disease in Portuguese patients, different genetic factors may govern the age of onset as well as the occurrence of anticipation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48529.RARlrvRsRLZbWUCabkYC7e24zg9K3TZLGYk2Q9tCNo0jc130_provenance.
- NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_assertion description "[Genomic DNA, which was extracted from peripheral blood lymphocytes of 22 FAP patients and the normal colon tissues of 43 sporadic colorectal cancers, were examined for mutations in exon15 of the APC gene by using PCR-TNT T7 Quick Coupled Tanscription/Translation System.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_provenance.
- NP48535.RAQ2BohA3Y-tEr-P9tEhAc8uoRS_IZmTZ97G3XuQ7aTb4130_assertion description "[We aimed to examine the interaction between the D1822V polymorphism of the APC gene and dietary intake in persons with CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48535.RAQ2BohA3Y-tEr-P9tEhAc8uoRS_IZmTZ97G3XuQ7aTb4130_provenance.
- NP48536.RAXPo6-Fwebc3_4Vjyceyq8vtfG2tPOZoCrL8A0MqUFWc130_assertion description "[Although relatively high folate intake was not associated with overall colorectal cancer risk, it reduced the risk of APC(-)colon tumors in men (RR 0.58, 95% CI 0.32-1.05, P(trend) = 0.06 for the highest vs. lowest tertile of folate intake).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48536.RAXPo6-Fwebc3_4Vjyceyq8vtfG2tPOZoCrL8A0MqUFWc130_provenance.
- NP48540.RAfVByRLRTQ8Sf8ooTFiCfgLW5MYLTQcazs_KNb-7qKJw130_assertion description "[Gene-environment interactions in pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48540.RAfVByRLRTQ8Sf8ooTFiCfgLW5MYLTQcazs_KNb-7qKJw130_provenance.
- NP48544.RAb63-r16MyvxwSBHiPB4Km1qnINpJwOlLJotu9L3MS-c130_assertion description "[ Adenomatous polyposis patients without a family history are usually diagnosed with symptoms, and at a later age. Phenotypically, they are similar to those with a family history. However, germline APC mutations are detected far less frequently in patients without a family history. A small percentage of these cases may be secondary to biallelic germline MYH mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48544.RAb63-r16MyvxwSBHiPB4Km1qnINpJwOlLJotu9L3MS-c130_provenance.
- NP48545.RAf7Ve2V3hMIQXYcQeEbJk2hYokgsxEJ2nV7qRrkgy5ds130_assertion description "[Our data indicate that the genotype/phenotype correlations in Argentinean patients are similar to those observed in other populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48545.RAf7Ve2V3hMIQXYcQeEbJk2hYokgsxEJ2nV7qRrkgy5ds130_provenance.
- NP48546.RAZNqEz49hfCiz6Twjw42T6A_vLaei9afFBNUxw0LIvZc130_assertion description "[We identified three common coding region variants, but none were over-represented in the patient samples, indicating that MYH variants are unlikely to predispose significantly to the risk of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48546.RAZNqEz49hfCiz6Twjw42T6A_vLaei9afFBNUxw0LIvZc130_provenance.
- NP48547.RAfLOuNzMqL2OIVHrai6PFQH5Dn_4C4JlhfA_w6Wzdmz4130_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." NP48547.RAfLOuNzMqL2OIVHrai6PFQH5Dn_4C4JlhfA_w6Wzdmz4130_provenance.
- NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_assertion description "[While germline mutations in the adenomatous polyposis coli (APC) gene cause the hereditary colon cancer syndrome (familial adenomatous polyposis (FAP)), the role of common germline APC variants in sporadic adenomatous polyposis remains unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_provenance.
- NP48556.RAS-RQ6tLagWByb9w8Sr2f0S0R36GwOZutnPAn8rUFF3I130_assertion description "[APC gene mutations causing familial adenomatous polyposis in Polish patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48556.RAS-RQ6tLagWByb9w8Sr2f0S0R36GwOZutnPAn8rUFF3I130_provenance.
- NP48571.RAYFx-eFZi7_PU-FTnWO0ZlVeJSP3ziajUXeJJGvCrJdU130_assertion description "[The human FE65 gene: genomic structure and an intronic biallelic polymorphism associated with sporadic dementia of the Alzheimer type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48571.RAYFx-eFZi7_PU-FTnWO0ZlVeJSP3ziajUXeJJGvCrJdU130_provenance.
- NP48573.RAYbUy7CWq_yYcZiiGl9rptTCgXdMUeEAJEv1vIJ7f73Q130_assertion description "[Meta-analysis of genetic variability in the beta-amyloid production, aggregation and degradation metabolic pathways and the risk of Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48573.RAYbUy7CWq_yYcZiiGl9rptTCgXdMUeEAJEv1vIJ7f73Q130_provenance.
- NP48575.RAf-OodQV6-KYcUyMOXqX118Qcve0M3zy5ajVa-G0YiP4130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48575.RAf-OodQV6-KYcUyMOXqX118Qcve0M3zy5ajVa-G0YiP4130_provenance.
- NP48577.RATIrzhcTPzRcyX1OLmIQP76G_FeLyIvwuPdKJI0K2gYk130_assertion description "[c954C-->T polymorphism in the Fe65L2 gene is associated with early-onset Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48577.RATIrzhcTPzRcyX1OLmIQP76G_FeLyIvwuPdKJI0K2gYk130_provenance.
- NP48583.RAY2HtAFvu8M7dJPn6OHDQNflAZoT7QQAoIwMplLsKTdM130_assertion description "[Adenosine monophosphate deaminase-1 genotyping should be further explored in CAD for prognostic, mechanistic and therapeutic insights.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48583.RAY2HtAFvu8M7dJPn6OHDQNflAZoT7QQAoIwMplLsKTdM130_provenance.
- NP48585.RAbWo_yYWZvUcnA6qa6O9R1cN4e-tLN9NaS4w975SQMdg130_assertion description "[The role of a common adenosine monophosphate deaminase (AMPD)-1 polymorphism in outcomes of ischemic and nonischemic heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48585.RAbWo_yYWZvUcnA6qa6O9R1cN4e-tLN9NaS4w975SQMdg130_provenance.
- NP48589.RAW7I3hNVen779RTEIYINa3TBvDzEycFGS56NrbleJHDs130_assertion description "[These results suggest that sequence variants in AMACR may be associated with CaP risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48589.RAW7I3hNVen779RTEIYINa3TBvDzEycFGS56NrbleJHDs130_provenance.
- NP48590.RAc2QT9vxFk_HdgtKXJ9CDDESHeMRlZ9ATwNfL1UG3l6k130_assertion description "[This study, performed in a relatively genetically homogenous Tasmanian population, provides further evidence for a significant association between variants within the AMACR gene and prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48590.RAc2QT9vxFk_HdgtKXJ9CDDESHeMRlZ9ATwNfL1UG3l6k130_provenance.
- NP48607.RAcJlPt26RcEb_yGArjYcU03swJPUSdNDd-WkyyP3Zf_I130_assertion description "[, haplotype B of the ALOX5AP gene is associated with an increased risk of MI in a large German study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48607.RAcJlPt26RcEb_yGArjYcU03swJPUSdNDd-WkyyP3Zf_I130_provenance.
- NP48609.RAVYLlJF8DxKb_BQh_N9Dq1PhVC9-AsGaca4MWHcukieo130_assertion description "[Variants of the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) gene have been implicated as a risk factor for stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48609.RAVYLlJF8DxKb_BQh_N9Dq1PhVC9-AsGaca4MWHcukieo130_provenance.
- NP48635.RAYkPTcuU0Tki95gaKUdOADT7i3Ojpyx6cCrcVCf4eBjc130_assertion description "[Evidence of epistasis between the catechol-O-methyltransferase and aldehyde dehydrogenase 3B1 genes in paranoid schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48635.RAYkPTcuU0Tki95gaKUdOADT7i3Ojpyx6cCrcVCf4eBjc130_provenance.
- NP48639.RAS3Xd7zdxF9HoBJteD6t0AfDtdKuB8Zh7AKVZ4_NJRb4130_assertion description "[A potential pharmacogenetic classification of acetaldehydism and alcoholism for alcoholics carrying the different ALDH2 genotypes is proposed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48639.RAS3Xd7zdxF9HoBJteD6t0AfDtdKuB8Zh7AKVZ4_NJRb4130_provenance.
- NP48641.RAd_IunmPTw8UtQy5SCvFkzH7Ol0Awqjj1DvtSXX4pMo4130_assertion description "[This study provides a baseline for future research into the role of the ALDH2 locus in alcoholism in Indian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48641.RAd_IunmPTw8UtQy5SCvFkzH7Ol0Awqjj1DvtSXX4pMo4130_provenance.
- NP48643.RAVGkI2ZWZGNYclMXvf-C8RnaeLQCjhB_1sRJSmTwbnKs130_assertion description "[To test for the possible association between mitochondrial aldehyde dehydrogenase (ALDH2) promoter polymorphism and alcoholism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48643.RAVGkI2ZWZGNYclMXvf-C8RnaeLQCjhB_1sRJSmTwbnKs130_provenance.
- NP48652.RAdFbm0ZWkpc10ESbARmqrgglidpnuhKRzDcdkMgSgi0U130_assertion description "[The present findings suggest that one of the genetic factors that may be related to probable AUD among Thai males living in the north-east is the ADH2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48652.RAdFbm0ZWkpc10ESbARmqrgglidpnuhKRzDcdkMgSgi0U130_provenance.
- NP48657.RAXee5c2DphySJuzU8C87G7CkADtN16tt5Z741qFdmjI0130_assertion description "[The prevalences of heterozygous ALDH2*1/*2 plus homozygous ALDH2*2/*2 in patients with alcoholic cirrhosis (7.1%) and alcoholics without evidence of liver disease (3.8%) were significantly lower than that in nondrinkers (45.3%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48657.RAXee5c2DphySJuzU8C87G7CkADtN16tt5Z741qFdmjI0130_provenance.
- NP48659.RAZKZho0hgxuj9yWBEXtrw77xoA-CHP5H3-X06R3aynUk130_assertion description "[Alcohol, ALDH2, and esophageal cancer: a meta-analysis which illustrates the potentials and limitations of a Mendelian randomization approach.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48659.RAZKZho0hgxuj9yWBEXtrw77xoA-CHP5H3-X06R3aynUk130_provenance.
- NP48660.RAYpO2XhtxBf72l2ToSt8gZOjdkWV8pz-f08cbcj99ttE130_assertion description "[Inactive ALDH2 encoded by ALDH2*1/2*2 and the low-activity form of alcohol dehydrogenase (ADH)-2 encoded by ADH2*1/2*1 enhance the risk for esophageal cancer in Japanese light to heavy drinkers, a significant association that emphasizes the importance of screening tests for inactive ALDH2 based on alcohol flushing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48660.RAYpO2XhtxBf72l2ToSt8gZOjdkWV8pz-f08cbcj99ttE130_provenance.
- NP48663.RATNbcKwdPfc8_dBn9hYXZot14WRj-q4ew6Un-73ysPIY130_assertion description "[Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48663.RATNbcKwdPfc8_dBn9hYXZot14WRj-q4ew6Un-73ysPIY130_provenance.
- NP48665.RAZvJeiSbJBzaA81iFQvSItYydYSqRVvr20PAkAY5jRoM130_assertion description "[Compared with individuals carrying both ALDH2 G/G and ADH2 A/A alleles and with a cumulative amount of alcohol consumption <2.5 (kg * years), drinkers carrying both ALDH2 A and ADH2 G alleles and with a cumulative amount of alcohol consumption > or =2.5 (kg * years) showed a significantly elevated risk of esophageal cancer (OR=53.15, 95% CI: 4.24-666.84).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48665.RAZvJeiSbJBzaA81iFQvSItYydYSqRVvr20PAkAY5jRoM130_provenance.
- NP48668.RAVnWYGdXXklQYxKcSutPymSz41N7fUVkZHyDGjBUFDW8130_assertion description "[To date, there have been no complaints from the participants, indicating that the announcement of polymorphism genotypes may be accepted differently from that of hereditary disease genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48668.RAVnWYGdXXklQYxKcSutPymSz41N7fUVkZHyDGjBUFDW8130_provenance.
- NP48671.RAfo7GxCDJxESFfcWDG0ig36D07Z7qIeZrfZ2AcLjQFxs130_assertion description "[ Although the present results should be replicated in other study populations for confirmation, the present results suggest that SLC12A1 may contribute to hypertension in Japanese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48671.RAfo7GxCDJxESFfcWDG0ig36D07Z7qIeZrfZ2AcLjQFxs130_provenance.
- NP48679.RAW9EDYg5zQ04yRcwuNI6ufRMpH71O0T7P9yCiBTi3_0Y130_assertion description "[ The present data suggest a role for CYP1B1 and CYP1A1 as new candidate genes in the etiology of CRC and confirm the carcinogenic role of aromatic amines metabolism for colorectum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48679.RAW9EDYg5zQ04yRcwuNI6ufRMpH71O0T7P9yCiBTi3_0Y130_provenance.
- NP48681.RAb9ZkomD2469vBiq153RZK8PEuah8KDtAQyVJMXHqHuw130_assertion description "[Low-penetrance genes and their involvement in colorectal cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48681.RAb9ZkomD2469vBiq153RZK8PEuah8KDtAQyVJMXHqHuw130_provenance.
- NP48685.RAUKprSCJvx0lQA1F1T10555XUuLLgurPUnBF1vs32P3w130_assertion description "[Screening of 214 single nucleotide polymorphisms in 44 candidate cancer susceptibility genes: a case-control study on gastric and colorectal cancers in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48685.RAUKprSCJvx0lQA1F1T10555XUuLLgurPUnBF1vs32P3w130_provenance.
- NP48689.RAakPZ0Nd2wGSD-WCCZ8qcSaeoIf2dSQ14mmgYNYvsquo130_assertion description "[genetic polymorphism of the ALDH2 gene influences the risk of developing alcoholic pancreatitis in Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48689.RAakPZ0Nd2wGSD-WCCZ8qcSaeoIf2dSQ14mmgYNYvsquo130_provenance.
- NP48691.RAayepFThYzWXVfL3-wray1NrVEIhFfed1CcejUx_SMxA130_assertion description "[This study integrates epidemiological and clinical data as well as genetic markers along major pathogenic pathways of PTD. The findings from this study should improve our understanding of genetic influences on PTD and gene-environment interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48691.RAayepFThYzWXVfL3-wray1NrVEIhFfed1CcejUx_SMxA130_provenance.
- NP48694.RAR_jtZPetM-Z28z9OZ71ymKHPf-LYmYG3_dw8Mrxwt6U130_assertion description "[These polymorphisms do not seem to govern progression from mild chronic atrophic gastritis to advanced precancerous gastric lesions, but the effects of smoking may be accentuated in individuals carrying variants of CYP2E1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48694.RAR_jtZPetM-Z28z9OZ71ymKHPf-LYmYG3_dw8Mrxwt6U130_provenance.
- NP48696.RAW81Ya63iy6b1idDOueaoQElVRMbZNvRPRWU2KZijF1Q130_assertion description "[ALDH2/ADH2 polymorphism associated with vasculopathy and neuropathy in type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48696.RAW81Ya63iy6b1idDOueaoQElVRMbZNvRPRWU2KZijF1Q130_provenance.
- NP48702.RAWKZh8Mukgt8zq7w7hSqHaqPuNefs3tjaXvJBIM77ixQ130_assertion description "[In stratified analyses, log BPb concentration was not associated with odds of ET in individuals with two ALAD-1 alleles (OR=2.69; 95% CI=0.61--11.82), but in individuals with an ALAD-2 allele, BPb concentration was significantly associated with odds of ET (OR=80.29; 95% CI=3.08--2,096.36).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48702.RAWKZh8Mukgt8zq7w7hSqHaqPuNefs3tjaXvJBIM77ixQ130_provenance.
- NP48704.RARZsvUzQvhEShE4io3jbtlp1SR1KrKDCjDcKZAcdzVTM130_assertion description "[The allele frequencies of C13298, T13348, T13847, T15096, and C15762 alleles were 21.3%, 2.3%. 82.1%, 62.5%, and 1.1%, respectively. All five mutations were detected by both DHPLC and direct DNA sequencing. No previously reported missense ALAD mutations were found in this Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48704.RARZsvUzQvhEShE4io3jbtlp1SR1KrKDCjDcKZAcdzVTM130_provenance.
- NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_assertion description "[Although our results indicate that lead may be implicated in meningioma risk in genetically susceptible individuals, these results need to be interpreted with caution given the small numbers of exposed cases with a variant genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_provenance.
- NP48710.RARjz-T6ohk_-m6mchKOCBTrOYTblkORdNzEvVwzci2uo130_assertion description "[Our findings did not confirm the association of AKT1 SNP2/3/4 TCG haplotype with the risk of schizophrenia as reported in the original study but showed the evidence of association with a different haplotype, AKT1 five-SNP AGCAG haplotype, with the risk of schizophrenia in Iranian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48710.RARjz-T6ohk_-m6mchKOCBTrOYTblkORdNzEvVwzci2uo130_provenance.
- NP48711.RAfvlCB_OlhuoW10chVlaM6QCpx7XPa9JgnjE8AgtIWUs130_assertion description "[Five single-nucleotide polymorphisms, rs3803300, rs1130214, rs3730358, rs2498799 and rs2494732, at the genomic region of AKT1 have been reported to be significantly associated with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48711.RAfvlCB_OlhuoW10chVlaM6QCpx7XPa9JgnjE8AgtIWUs130_provenance.
- NP48717.RAeLnfcTWWR2q-XpadaKkVxyfY2waMmkD4rErJZMzK7vQ130_assertion description "[Among GSTM1 null homozygotes, those who consumed green tea daily had a non-significant reduction in risk compared with non-consumers. Green tea consumption had no effect among OGG1 Ser(326) homozygotes or GSTM1 carriers. In addition, AKR1C3 genotype did not modulate the effect of green tea consumption. The chemopreventive effects of green tea in this population may be restricted to individuals who are particularly susceptible to oxidative stress and oxidative DNA damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48717.RAeLnfcTWWR2q-XpadaKkVxyfY2waMmkD4rErJZMzK7vQ130_provenance.