Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP48399.RAvwUI55WgrFre__Hq1mU4puD3Cpngn3WoCmSM4BPP_zM130_assertion description "[An attempt was made to associate the insertion-deletion (Ins/Del) polymorphism of the apolipoprotein B gene (apoB) with obesity and to identify alleles and genotypes predisposing to this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48399.RAvwUI55WgrFre__Hq1mU4puD3Cpngn3WoCmSM4BPP_zM130_provenance.
- NP48400.RAsBSsGwe_tzG86Zj8Lhz-X0WrCjV3qR9PCrMjB6C3B50130_assertion description "[Our study confirms in the obese subjects, results published in the general litterature, and shows that the apoB has an important role in the metabolism of plasma lipids and most particulary its gene variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48400.RAsBSsGwe_tzG86Zj8Lhz-X0WrCjV3qR9PCrMjB6C3B50130_provenance.
- NP48403.RAuQTT5ilgg3GTARxXF9QAPWDkENN_IkTviQVoAn-lkkI130_assertion description "[ApoB-100 gene EcoRI polymorphism. Relations to plasma lipoprotein changes associated with abdominal visceral obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48403.RAuQTT5ilgg3GTARxXF9QAPWDkENN_IkTviQVoAn-lkkI130_provenance.
- NP48404.RAlf9ttxyCuqRkAAM7DUQObrEyi2HolTPiyjEmCX-JNS4130_assertion description "[APOB XbaI and EcoRI restriction sites may serve as potential genetic markers affecting BMI, serum protein and lipid profiles in children from Guangxi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48404.RAlf9ttxyCuqRkAAM7DUQObrEyi2HolTPiyjEmCX-JNS4130_provenance.
- NP48411.RAo62Kr26jeWzZAcPmU27PwWa_fDCOdtsckoCvHNm4EeM130_assertion description "[Phenotype-genotype interactions on renal function in type 2 diabetes: an analysis using structural equation modelling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48411.RAo62Kr26jeWzZAcPmU27PwWa_fDCOdtsckoCvHNm4EeM130_provenance.
- NP48414.RAg2kLtpjApFE0--p4vdGVxZfmasDvV3ULWbbPlrPqtYg130_assertion description "[Genetic variation may modify the risk of death on dialysis. SNPs in proximity to genes regulating vascular extracellular matrix, cardiac ventricular repolarization, and smoking cessation are associated with dialysis survival in AAs with T2D. These results warrant replication in other cohorts and races.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48414.RAg2kLtpjApFE0--p4vdGVxZfmasDvV3ULWbbPlrPqtYg130_provenance.
- NP48415.RAgMokhB8BibNtWVfANIegxWz5f-19tnQ-BNsNAsSlsC8130_assertion description "[Apolipoprotein B-100 XbaI gene polymorphism in gallbladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48415.RAgMokhB8BibNtWVfANIegxWz5f-19tnQ-BNsNAsSlsC8130_provenance.
- NP48419.RAumVyEoCtSXoaHdAs9Xvsjou-7mgcbBCzHngGQYwqIyU130_assertion description "[Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48419.RAumVyEoCtSXoaHdAs9Xvsjou-7mgcbBCzHngGQYwqIyU130_provenance.
- NP48420.RArCiqwEjC1KQl9A5r-8AihZoDudAcS3oM1ZrrA5vOKGs130_assertion description "[Genome-wide association analysis of the FHS data detected two new gene regions with genome-wide significance, detected epistatic SNP effects on TC and HDL-C with the significance of suggestive linkage in seven pairs of gene regions, and confirmed some previously reported gene regions associated with TC and HDL-C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48420.RArCiqwEjC1KQl9A5r-8AihZoDudAcS3oM1ZrrA5vOKGs130_provenance.
- NP48422.RAkxY3yBUSrBNVVp6pe25TSIvnlkCPqAxra8nwqhK-OfY130_assertion description "[Genetic analysis of a kindred with familial hypobetalipoproteinemia. Evidence for two separate gene defects: one associated with an abnormal apolipoprotein B species, apolipoprotein B-37; and a second associated with low plasma concentrations of apolipoprotein B-100.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48422.RAkxY3yBUSrBNVVp6pe25TSIvnlkCPqAxra8nwqhK-OfY130_provenance.
- NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_assertion description "[There was no effect of genotype on the response of these parameters to gemfibrozil treatment. These results shed new light on the role of APOA5 variants in TG metabolism and CHD risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48434.RAvpSDSkb0xgH3QVc-8JLpEVBkg78pT2AHtELg3CxkvZU130_provenance.
- NP48435.RAt0cbBA57392jfi6_dfl590JQ_HoJ9UvVfDPKk9oVzJw130_assertion description "[In logistic regression models adjusted for age, gender, presence of diabetes, BMI, smoking, LDL-C, HDL-C and hypertension a significantly increased risk of developing CAD was found in patients carrying the apoA5-1131C allele, suggesting that this allele variant is an independent genetic risk factor for CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48435.RAt0cbBA57392jfi6_dfl590JQ_HoJ9UvVfDPKk9oVzJw130_provenance.
- NP48440.RAqzr5F9skHJjG7-17CPjVYbwDK9b-A270I18TwNhZQrI130_assertion description "[Our results emphasize the need to account for complex multi-gene influences and interactions when assessing the molecular pathology of multifactorial medical entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48440.RAqzr5F9skHJjG7-17CPjVYbwDK9b-A270I18TwNhZQrI130_provenance.
- NP48442.RAoP2zh7-YO3GnkJiFJQyPcAX-JvrxNiVid1kNccC_o2k130_assertion description "[Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48442.RAoP2zh7-YO3GnkJiFJQyPcAX-JvrxNiVid1kNccC_o2k130_provenance.
- NP48443.RAoaJ8jzwhLAUJSkdFwTLaGSdoXkFlzBw_tJmIf6-0N-s130_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." NP48443.RAoaJ8jzwhLAUJSkdFwTLaGSdoXkFlzBw_tJmIf6-0N-s130_provenance.
- NP48446.RAt9bIp_CoUxyMw7XJcf4u9mWT-6_MNYV0gT3ZoC9NHk4130_assertion description "[ The response of the biological variables to a urate-lowering diet was mainly influenced by diet. Changes in triglycerides were also influenced by the apolipoprotein AI XmnI polymorphism (p = 0.04), suggesting a gene-diet interaction (p = 0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48446.RAt9bIp_CoUxyMw7XJcf4u9mWT-6_MNYV0gT3ZoC9NHk4130_provenance.
- NP48450.RArc2KkvrtuNzd-hl7lziyibq4a1LjdnmmJkA6pNnK970130_assertion description "[Apolipoprotein A-IV genetic polymorphism and its impact on quantitative traits in normoglycemic and non-insulin-dependent diabetic Hispanics from the San Luis Valley, Colorado.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48450.RArc2KkvrtuNzd-hl7lziyibq4a1LjdnmmJkA6pNnK970130_provenance.
- NP48451.RAmcK0KiKHO1gThBl5vFhuqS_SrNmtdOAGQCiHiDNOqSw130_assertion description "[The risk of MI was particularly high in obese NIDDM patients with the apoA-IV 1-2 phenotype: 5.1 (2.4-11.2) times that in obese apoA-IV 1-1 NIDDM patients and 7.7 (3.6-16.7) times that in lean nondiabetic people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48451.RAmcK0KiKHO1gThBl5vFhuqS_SrNmtdOAGQCiHiDNOqSw130_provenance.
- NP48455.RAhoZoZAH9p4YdX-7C4cPuFoXjDvDIirtxSZOJiKoBuqI130_assertion description "[Genetic and environmental factors affecting the response to statin therapy in patients with molecularly defined familial hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48455.RAhoZoZAH9p4YdX-7C4cPuFoXjDvDIirtxSZOJiKoBuqI130_provenance.
- NP48458.RAosdSe5nZnzInpblcwshd_66iCCxB7-PLuKSpInHsxck130_assertion description "[ These data suggest a role for apoA-IV in fat storage or mobilization and that genetic variations in the apoA-IV gene may play a role in the development of obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48458.RAosdSe5nZnzInpblcwshd_66iCCxB7-PLuKSpInHsxck130_provenance.
- NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_assertion description "[Together with previous studies our results indicate that the relation between apo(a) genotypes, Lp(a) levels, and CHD may be heterogeneous across ethnic groups and that it depends on the genetic architecture of the Lp(a) trait in a given population whether an association of K-IV-2 repeat length with CHD exists or not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48459.RAvIZrbbJYcvKBwpXYLJcjp3AFlAyBSid4pBqxBwfMEK4130_provenance.
- NP48460.RAs_95Xw4J5fiumXh4G0Xwk1CSgmOF2i83BXwKEIo3mrs130_assertion description "[Our results highlight the potential of microarray-based technology for SNP genotyping in pharmacogenetics.(1)]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48460.RAs_95Xw4J5fiumXh4G0Xwk1CSgmOF2i83BXwKEIo3mrs130_provenance.
- NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_assertion description "[Both approaches (association analysis and gametic disequilibrium) revealed the same gene combinations contributing to the CAD risk factors. NOS3 and APOA1 markers were in gametic disequilibrium in the patients and both of them were associated with LDL. F13 and AGT were associated with systolic and diastolic blood pressure and two-locus gametic disequilibrium between F13 and AGT polymorphisms observed in the patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_provenance.
- NP48463.RAg_J1iL3WxxUmCXEYd3EddRLKK9wssS19QBMto0zeUd4130_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." NP48463.RAg_J1iL3WxxUmCXEYd3EddRLKK9wssS19QBMto0zeUd4130_provenance.
- NP48469.RAqL8J2dQMBoTKdTgAHkDxR4vT4BD2EDlYB_h-9qN5tLU130_assertion description "[Role of apolipoproteins E and A-I: epistatic villains of triglyceride mediation in coronary heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48469.RAqL8J2dQMBoTKdTgAHkDxR4vT4BD2EDlYB_h-9qN5tLU130_provenance.
- NP48477.RAnKFKw65Zsqa3w_q1vNPavwKgBWIL63hiTtE_YBjZDJc130_assertion description "[ Our study confirms that multiple stenting, diabetes and multivessel disease are powerful predictors of restenosis after intracoronary stent implantation. On the contrary, lipoprotein(a) and apolipoprotein(a) polymorphism do not appear to be reliable markers of restenosis in patients with stent implantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48477.RAnKFKw65Zsqa3w_q1vNPavwKgBWIL63hiTtE_YBjZDJc130_provenance.
- NP48480.RAlED0Ll8X1jiPr5UX1b6yiZX9QPzaP9_MK0iLApkcMC0130_assertion description "[ Our results suggest that changes from G to A at the -75 bp site and from C to T or G to A at the +83 bp site do increase circulating levels of apo A1 and HDL-C. And those individuals with these changes are likely to have a lower risk of developing CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48480.RAlED0Ll8X1jiPr5UX1b6yiZX9QPzaP9_MK0iLApkcMC0130_provenance.
- NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_assertion description "[While these effects can be attributed to the presence of the M2 and S2 minor alleles, these results suggest that the importance of specific allelic haplotypes may be greater than single genotypic effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_provenance.
- NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_assertion description "[An intronic single nucleotide polymorphism in ABCA1 and the APOE epsilon3 allele are associated with reduced LDLc lowering by statins and identify individuals who may be resistant to maximal LDLc lowering by statins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48486.RAmlyn1eMbEZMC_ptEpXKbx8fePApF0X5VvzilCt3k89Q130_provenance.
- NP48487.RAiKm-WCAO8ZT4X_ZFVtKu0oHPUzEEgt_9g5_HjUtVEqE130_assertion description "[We conclude that the expression of at least one apo(a) isoform may interact with other pathogenic mechanisms involved in controlling the age at onset of AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48487.RAiKm-WCAO8ZT4X_ZFVtKu0oHPUzEEgt_9g5_HjUtVEqE130_provenance.
- NP48490.RAngh3qLvgWTKx7gaknKS_PaJx1g-jp9bfk2XUU-h7hFk130_assertion description "[ The response of the biological variables to a urate-lowering diet was mainly influenced by diet. Changes in triglycerides were also influenced by the apolipoprotein AI XmnI polymorphism (p = 0.04), suggesting a gene-diet interaction (p = 0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48490.RAngh3qLvgWTKx7gaknKS_PaJx1g-jp9bfk2XUU-h7hFk130_provenance.
- NP48496.RAoGcaBKng75PblWiJGP_lAo-UKmHH6LsKlAoIoXuC3pY130_assertion description "[Association of lipoprotein lipase D9N polymorphism with myocardial infarction in type 2 diabetes: the genetics, outcomes, and lipids in type 2 diabetes (GOLD) study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48496.RAoGcaBKng75PblWiJGP_lAo-UKmHH6LsKlAoIoXuC3pY130_provenance.
- NP48502.RAkPR2zohg2JGgTncOTO9_3msXIVI1h71pDjXeR96TK7c130_assertion description "[Influence of cholesteryl ester transfer protein, peroxisome proliferator-activated receptor alpha, apolipoprotein E, and apolipoprotein A-I polymorphisms on high-density lipoprotein cholesterol, apolipoprotein A-I, lipoprotein A-I, and lipoprotein A-I:A-II concentrations: the Prospective Epidemiological Study of Myocardial Infarction study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48502.RAkPR2zohg2JGgTncOTO9_3msXIVI1h71pDjXeR96TK7c130_provenance.
- NP48507.RArz9pEFFxQ6aa4xk7CBp2GDUfw9ybwx3BSnFs6ndavsA130_assertion description "[ Gouty patients have an altered allelic distribution in the apolipoprotein AI-CIII-AIV cluster, which could lead to changes in levels of lipoproteins. This is not caused by a single mutation but rather by a combination of different mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48507.RArz9pEFFxQ6aa4xk7CBp2GDUfw9ybwx3BSnFs6ndavsA130_provenance.
- NP48511.RAn4mI0J5bwHufyqZ_fIxVgnoHVwXGhxUixMd7nZ_lf0c130_assertion description "[To investigate association between APE1/Ref-1 polymorphisms and lung cancer risk in Chinese populations, we first genotyped three variants of APE1/Ref-1 and found a -141 T-to-G variant (rs1760944) in the promoter associated with decreased risk of lung cancer odds ratio (OR) = 0.62 for GG; P=0.043.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48511.RAn4mI0J5bwHufyqZ_fIxVgnoHVwXGhxUixMd7nZ_lf0c130_provenance.
- NP48513.RAnW2e_vVnt9HOyF2gTFKAbHec-bO1_5E6iCHXTgYQ8Lg130_assertion description "[Comprehensive analysis of DNA repair gene polymorphisms and survival in patients with early stage non-small-cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48513.RAnW2e_vVnt9HOyF2gTFKAbHec-bO1_5E6iCHXTgYQ8Lg130_provenance.
- NP48526.RAlDLUOkpUrWWsohehf4ZtfYc1r774dG03JVOLM8OhMtI130_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." NP48526.RAlDLUOkpUrWWsohehf4ZtfYc1r774dG03JVOLM8OhMtI130_provenance.
- NP48537.RAgLaZSVi_jRNa5GTu1-0Hw7OFat3V-4ei-1xgAnbmzKQ130_assertion description "[We also investigated presence and the frequency of the most common APC gene mutations and APC E1317Q and I1307K germ-line variants in Croatian colorectal cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48537.RAgLaZSVi_jRNa5GTu1-0Hw7OFat3V-4ei-1xgAnbmzKQ130_provenance.
- NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_assertion description "[Despite the relevance of both pathways in the pathogenesis of the disease, and the fact that this is indeed the first study that considers these pathways as a candidate-gene selection approach, our study does not present any evidence of the presence of low-penetrance variants for the selected markers in any of the considered genes in our cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_provenance.
- NP48543.RAgpynCtF3G2f6zyMQlsBinAdyb_3MThQLeMvu2ZZLlFQ130_assertion description "[The results reveal that MYH accounts for 16 percent of polyposis patients without germline mutations in the APC gene and that it does not appear to be a modifier gene in FAP patients diagnosed with APC germline mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48543.RAgpynCtF3G2f6zyMQlsBinAdyb_3MThQLeMvu2ZZLlFQ130_provenance.
- NP48549.RAndywJMkDF-OxKda1x37ZWkPCTnXRxmqq67WPrhvIPP4130_assertion description "[Colorectal polyps in carriers of the APC I1307K polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48549.RAndywJMkDF-OxKda1x37ZWkPCTnXRxmqq67WPrhvIPP4130_provenance.
- NP48551.RAvzT65jWkxn-TTzZ8ooTjXJquYkijHe11k_ysQTfLQtU130_assertion description "[The APC variants I1307K and E1317Q are associated with colorectal tumors, but not always with a family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48551.RAvzT65jWkxn-TTzZ8ooTjXJquYkijHe11k_ysQTfLQtU130_provenance.
- NP48557.RAt2HELVh8ugf7xz5T9Iiuaw3wYYDluTOGCU4JVpDZZ10130_assertion description "[Familial adenomatous polyposis (FAP) is an autosomal dominant-inherited colorectal cancer syndrome, caused by germline mutations in the APC gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48557.RAt2HELVh8ugf7xz5T9Iiuaw3wYYDluTOGCU4JVpDZZ10130_provenance.
- NP48558.RAnNs7xMtkzYffaTvvNzq7Q7Ak0PJd4CRTcYgMmtfxB8g130_assertion description "[Familial adenomatous polyposis is an autosomal dominant disease characterised by predisposition to colon polyposis and colorectal cancer and caused by germline mutations in the APC gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48558.RAnNs7xMtkzYffaTvvNzq7Q7Ak0PJd4CRTcYgMmtfxB8g130_provenance.
- NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_assertion description "[The severe phenotype should be considered when counselling FAP families in which attenuated FAP is excluded and in which a causative APC mutation has not been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_provenance.
- NP48561.RAuCcL_Xiz-mjchZmoUbEefHfoMpjdJLAI8_Bg6NYgF8o130_assertion description "[Familial adenomatous polyposis, an autosomal-dominantly inherited colorectal cancer predisposition syndrome, is caused by germ-line mutations in the adenomatous polyposis coli (APC) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48561.RAuCcL_Xiz-mjchZmoUbEefHfoMpjdJLAI8_Bg6NYgF8o130_provenance.
- NP48562.RAn-iIRjNrv5NvfYr7P-_6v58QpvBM05lMw76OwFHQCng130_assertion description "[Cranial desmoid tumor associated with homozygous inactivation of the adenomatous polyposis coli gene in a 2-year-old girl with familial adenomatous polyposis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48562.RAn-iIRjNrv5NvfYr7P-_6v58QpvBM05lMw76OwFHQCng130_provenance.
- NP48564.RArXLYQ9PJC3KLmIZYOQVqdnomlxG8znheOcipMzUgJGc130_assertion description "[Association of APC gene mutations and histological characteristics of colorectal adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48564.RArXLYQ9PJC3KLmIZYOQVqdnomlxG8znheOcipMzUgJGc130_provenance.
- NP48565.RAg3HHiP_1kWA-aGS92dL6XOT4k4dMbfoRiEBTxFq_jYA130_assertion description "[Analysis of candidate genes in occurrence and growth of colorectal adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48565.RAg3HHiP_1kWA-aGS92dL6XOT4k4dMbfoRiEBTxFq_jYA130_provenance.
- NP48567.RAjqCJH4jqGgeP0efvJRQqrlMK8mKAGvCwEwhDO6InsK8130_assertion description "[Mutations or allelic loss of the adenomatous polyposis coli (APC) gene have therefore been implied in the pathogenesis of nasopharyngeal angiofibroma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48567.RAjqCJH4jqGgeP0efvJRQqrlMK8mKAGvCwEwhDO6InsK8130_provenance.
- NP48576.RAkttOaCae6nKl1dfGCN-j_l3SBDrvaMEIEbZIH_R81Hk130_assertion description "[Analysis of APBB2 gene polymorphisms in sporadic Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48576.RAkttOaCae6nKl1dfGCN-j_l3SBDrvaMEIEbZIH_R81Hk130_provenance.
- NP48578.RAhUqrMdAq6GM-_GcRM1he78oX_qIfLzmNAemjwNMHt4g130_assertion description "[Allelic imbalance of 12q22-23 associated with APAF-1 locus correlates with poor disease outcome in cutaneous melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48578.RAhUqrMdAq6GM-_GcRM1he78oX_qIfLzmNAemjwNMHt4g130_provenance.
- NP48579.RAn7HnoHHXVR1hZCXKT2FIHslrvvq48WpJYVvkTRVAkF0130_assertion description "[The sorted genes allow us to draw novel hypotheses for future studies of HCV infection to ultimately identify bona fide genes and their variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48579.RAn7HnoHHXVR1hZCXKT2FIHslrvvq48WpJYVvkTRVAkF0130_provenance.
- NP48580.RAvFvNqPIz4PdK6OP7BfTRJgg8jQoGtvUM89vCy24Nucs130_assertion description "[Genomic variations in the locus for aminopeptidase N:a putative cellular receptor for SARS-CoV spike glycoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48580.RAvFvNqPIz4PdK6OP7BfTRJgg8jQoGtvUM89vCy24Nucs130_provenance.
- NP48584.RAjEObfl8k8xtoVZc1Pc9R5UDtjqhpsZ49tuzWSetVeUs130_assertion description "[The presence of the C34T mutation in AMPD1 gene appears to be protective against acute heart failure in cardiac donors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48584.RAjEObfl8k8xtoVZc1Pc9R5UDtjqhpsZ49tuzWSetVeUs130_provenance.
- NP48586.RAu2f2asNkzfYJlZl2aavfilbATEiCY-oyTpZC2fNNgt8130_assertion description "[ The AMPD1 C34T polymorphism influences transplant-free cardiovascular survival in the setting of ischemic left ventricular dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48586.RAu2f2asNkzfYJlZl2aavfilbATEiCY-oyTpZC2fNNgt8130_provenance.
- NP48598.RAqmw1SOLcOMT0BrajWofj9rD8CX4cwk6A1mTeV-pZnMk130_assertion description "[Polymorphisms in candidate asthma genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48598.RAqmw1SOLcOMT0BrajWofj9rD8CX4cwk6A1mTeV-pZnMk130_provenance.
- NP48602.RAnkzYSxz7Z5TM1B5BG1d39YjKFI6g7dTOF4ffbStUW8A130_assertion description "[Leukotrienes play an important role in allergic and inflammatory diseases, but reports on the involvement of arachidonate 5-lipoxygenase-activating protein (ALOX5AP) and leukotriene A(4) hydrolase (LTA4H) in asthma have been inconclusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48602.RAnkzYSxz7Z5TM1B5BG1d39YjKFI6g7dTOF4ffbStUW8A130_provenance.
- NP48605.RAsiKd0y7bPTFcUv9dcF79V_b8T2_0Dm0OhWceNY4NBpY130_assertion description "[ The hypothesis that ALOX5AP contributes to susceptibility for MI was validated in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48605.RAsiKd0y7bPTFcUv9dcF79V_b8T2_0Dm0OhWceNY4NBpY130_provenance.
- NP48608.RAkjAGrvbXMxGx7hZJnBoTktveaxIY8ESTthJizIUH2oI130_assertion description "[ The present study suggests that sequence variants in the ALOX5AP gene are significantly associated with stroke, particularly in males. Variants in the PDE4D gene are not a major risk factor for stroke in individuals from central Europe. Population differences in allele and haplotype frequencies as well as LD structure may contribute to the observed differences between populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48608.RAkjAGrvbXMxGx7hZJnBoTktveaxIY8ESTthJizIUH2oI130_provenance.
- NP48614.RAs30aCG2WyHc9ZCuKQVwQg7nH7HsbASwDjuuYavNiIO4130_assertion description "[To characterize ALOX5 mRNA expression and cysteinyl-leukotriene production by eosinophils from individuals bearing ALOX5 promoter deletional variants and their association with the severity of childhood asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48614.RAs30aCG2WyHc9ZCuKQVwQg7nH7HsbASwDjuuYavNiIO4130_provenance.
- NP48617.RAmtrgzxk4nzTdmI9wtMkfGco0uozxdSg5xFQy7G58uGA130_assertion description "[It was confirmed that ALOX5 promoter polymorphisms have a clear influence in montelukast response in atopic moderate persistent asthma patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48617.RAmtrgzxk4nzTdmI9wtMkfGco0uozxdSg5xFQy7G58uGA130_provenance.
- NP48621.RArwqmdto0SGdDncDV99H6eyDEZdHVxjyss1CWVnz5UlA130_assertion description "[The current results suggested that polymorphisms of LOX genes may act independently or with other factors to affect the risk of colorectal adenoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48621.RArwqmdto0SGdDncDV99H6eyDEZdHVxjyss1CWVnz5UlA130_provenance.
- NP48624.RAuzlVWDNik_IwQuYOruQunQIG97lMuE754TIXQsZELX8130_assertion description "[Using a pathway-based approach, we also detected statistical evidence for interactions among ALOX5, ALOX5AP and LTA4H using RNA expression data from a collection of freshly harvested human aortas with varying degrees of atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48624.RAuzlVWDNik_IwQuYOruQunQIG97lMuE754TIXQsZELX8130_provenance.
- NP48625.RAkwPHTOCUABwjhTGViKhFppWcqo28HThn5XkKwgf1wFA130_assertion description "[We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48625.RAkwPHTOCUABwjhTGViKhFppWcqo28HThn5XkKwgf1wFA130_provenance.
- NP48631.RAhScRZiJ8rnJrM34PlnYWQHYBDrXPSAvUwPpEQ1bVWk4130_assertion description "[Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDOA(Arg303X/Cys338Tyr).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48631.RAhScRZiJ8rnJrM34PlnYWQHYBDrXPSAvUwPpEQ1bVWk4130_provenance.
- NP48632.RAiF73qCsEQB-GwaAc-Ppxd7OwYTdZg6feclxXeeW5xkg130_assertion description "[Mutations of the gene (GDB symbol ALDH10) were recently identified in three SLS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48632.RAiF73qCsEQB-GwaAc-Ppxd7OwYTdZg6feclxXeeW5xkg130_provenance.
- NP48633.RArywGhGySsUr5ucmZxAqsDHJFv7L2eqzQJTNSb13-Nak130_assertion description "[The Sjgren-Larsson syndrome gene is close to D17S805 as determined by linkage analysis and allelic association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48633.RArywGhGySsUr5ucmZxAqsDHJFv7L2eqzQJTNSb13-Nak130_provenance.
- NP48636.RAq2aBGFwu_CBRoNWdyz2wy37-q2ZVNwqpAtpux-9OsuA130_assertion description "[These data suggest that higher SSADH activity is associated with higher intelligence across the general population. The effect is small, with each allele having an effect size translating to about 1.5 IQ points.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48636.RAq2aBGFwu_CBRoNWdyz2wy37-q2ZVNwqpAtpux-9OsuA130_provenance.
- NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_assertion description "[The present findings suggest that the COMT and ALDH3 combination may be the most common type involved in predisposing to schizophrenia. Since the combination blocks the whole pathways for the breakdown of DA and noradrenaline, it is very likely to play a central role in developing paranoid schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_provenance.
- NP48640.RAlOeyRa9kXHK9PuL6HUmoy2xOcn51bbCo26WdGFAowFU130_assertion description "[Variant alleles of aldehyde dehydrogenase (ALDH2) and alcohol dehydrogenase (ADH1B) genes are prevalent in individuals of Asian heritage and have been associated with an increased level of response to alcohol and a decreased risk for alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48640.RAlOeyRa9kXHK9PuL6HUmoy2xOcn51bbCo26WdGFAowFU130_provenance.
- NP48642.RAsrFQLVjnzAsTYfRmVpxyCBGgplPetBXbuGPd9CP0uVc130_assertion description "[Pharmacokinetic and pharmacodynamic basis for partial protection against alcoholism in Asians, heterozygous for the variant ALDH2*2 gene allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48642.RAsrFQLVjnzAsTYfRmVpxyCBGgplPetBXbuGPd9CP0uVc130_provenance.
- NP48645.RAl9XY9ouBa2EkygOPRz6HGPq_jg9KD4c5Y-jKKgEMV7E130_assertion description "[We recruited 579 Han Chinese individuals in Taiwan, intending to examine the alcoholism-protection effects of different ADH1B and ALDH2 genotypes with or without antisocial personality disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48645.RAl9XY9ouBa2EkygOPRz6HGPq_jg9KD4c5Y-jKKgEMV7E130_provenance.
- NP48646.RAhNnqlIYdfpdtHtPeg05l3AbM01YjWORJPDc8Il8XuNE130_assertion description "[Genotype and allele frequencies of ALDH2 G1951A SNP in familial or non-familial alcoholic patients differ from normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48646.RAhNnqlIYdfpdtHtPeg05l3AbM01YjWORJPDc8Il8XuNE130_provenance.
- NP48648.RAt97f6FFIzNJvE3iac6vWe_o7jdxI2pi-KdFlWGvbiHk130_assertion description "[Candidate genes for alcohol dependence: a review of genetic evidence from human studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48648.RAt97f6FFIzNJvE3iac6vWe_o7jdxI2pi-KdFlWGvbiHk130_provenance.
- NP48649.RAi-UGtGEwTFHNybuOC-BO6D8BUDuUZUA5S54n_abFjUw130_assertion description "[ Individuals heterozygous for ALDH2*2 exhibit strong alcohol hypersensitivity caused by persistent accumulation of large amounts of acetaldehyde, but homozygosity for ADH2*2 is not dependent upon this pathway against alcoholism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48649.RAi-UGtGEwTFHNybuOC-BO6D8BUDuUZUA5S54n_abFjUw130_provenance.
- NP48654.RAq-Mz7aiPthQmQaJqzIF2foy7YTJfwc5uwvlj3wVakIo130_assertion description "[The present study shows that AUD was more directly and strongly associated with alcohol drinking than with alcohol metabolizing enzymes among male Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48654.RAq-Mz7aiPthQmQaJqzIF2foy7YTJfwc5uwvlj3wVakIo130_provenance.
- NP48656.RAs5iycUV4eMwxUidsfr3EmSlgEvESXsz6AqlWMll5VS0130_assertion description "[this study showed the strong effect of ADH2 His(47)Arg polymorphism on habitual drinking regardless of ALDH2 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48656.RAs5iycUV4eMwxUidsfr3EmSlgEvESXsz6AqlWMll5VS0130_provenance.
- NP48670.RAt288Rgg1CEoyR7Y6YDZwO6ftinPD33Nq-3TxIMHqSrA130_assertion description "[We carried out a meta-analysis of ALDH2 and head and neck cancer searching for relevant studies on Medline and Embase up to January 31, 2008, and investigated the consistency between the expected odds ratio (OR) among drinkers from the largest pooled analysis among never smokers and the observed OR from this meta-analysis by an interaction test.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48670.RAt288Rgg1CEoyR7Y6YDZwO6ftinPD33Nq-3TxIMHqSrA130_provenance.
- NP48672.RArOdSrabuM5Ij5f9CYEHhLXWArD32UB3jTsVIET4tK0w130_assertion description "[Although several candidate SNP relevant to hypertension and those influencing AC and BNP were identified, our middle-sized GWAS indicated that there is no master gene in Japanese people that profoundly affects BP-related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48672.RArOdSrabuM5Ij5f9CYEHhLXWArD32UB3jTsVIET4tK0w130_provenance.
- NP48674.RAq_2CBj5QLQEn6Q0x_cZLWjQDD9gl7YsDHUoQkxzan0g130_assertion description "[Genetic differences in ethanol metabolizing enzymes and blood pressure in Japanese alcohol consumers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48674.RAq_2CBj5QLQEn6Q0x_cZLWjQDD9gl7YsDHUoQkxzan0g130_provenance.
- NP48683.RAorfnt_gS7vwtQ5jcyA_E4H06o-5_wQ2eS5v55As692I130_assertion description "[To examine associations between the risk of colorectal cancer and the CD36 gene A52C polymorphism according to the ALDH2 gene Glu487Lys polymorphism and drinking habit, a hospital-based case-control study was conducted with 128 colorectal cancer cases and 238 cancer-free controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48683.RAorfnt_gS7vwtQ5jcyA_E4H06o-5_wQ2eS5v55As692I130_provenance.
- NP48684.RAm4Oh5ZtttawmO6R0tTrjAr-lAW61t9IBWO2DEedkQuY130_assertion description "[Alcohol dehydrogenase and aldehyde dehydrogenase polymorphisms and colorectal cancer: the Fukuoka Colorectal Cancer Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48684.RAm4Oh5ZtttawmO6R0tTrjAr-lAW61t9IBWO2DEedkQuY130_provenance.
- NP48686.RAuGrGK6EG02pYxlclfHS4x1gwKcwdCKQZTs7579419gw130_assertion description "[Polymorphisms of the ADH2 and ALDH2 genes are significantly associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48686.RAuGrGK6EG02pYxlclfHS4x1gwKcwdCKQZTs7579419gw130_provenance.
- NP48687.RAhj95lkSPAMyja53F1o5s702RS6MkiTdK2si-k58jwbA130_assertion description "[A novel polymorphism rs1329149 of CYP2E1 and a known polymorphism rs671 of ALDH2 of alcohol metabolizing enzymes are associated with colorectal cancer in a southwestern Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48687.RAhj95lkSPAMyja53F1o5s702RS6MkiTdK2si-k58jwbA130_provenance.
- NP48690.RAhn6DUEKatuV3dlI2un0HzAVaKrtA5r0RHPLShYrfG8Y130_assertion description "[On analysis of ADH2 and ALDH2 gene polymorphisms an association was found between ADH2*2 allele and alcoholic CP, and the ADH2*2/2*2 genotype had a tendency to increase the risk of developing pancreatic pseudocyst.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48690.RAhn6DUEKatuV3dlI2un0HzAVaKrtA5r0RHPLShYrfG8Y130_provenance.
- NP48693.RApPogcS0J0xfTIV8XGo3vnFy4Xh6dgEIRkn-anI3zza8130_assertion description "[ The gene polymorphism of ALDH is close to ALD. The allele of ALDH2*2 may be a negative risk factor for the developing of ALD]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48693.RApPogcS0J0xfTIV8XGo3vnFy4Xh6dgEIRkn-anI3zza8130_provenance.
- NP48698.RAuKzlOXS5XXj6RTI4qMjTLkZaUYl9gwfZfDmbCpeisY8130_assertion description "[ These results suggest that the Mae III polymorphisms of the ADH2 gene may be associated not only with susceptibility to alcoholic liver cirrhosis, but also with the development of alcoholism in Japanese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48698.RAuKzlOXS5XXj6RTI4qMjTLkZaUYl9gwfZfDmbCpeisY8130_provenance.
- NP48707.RAiMqYAO3gG2nKdCrwDjhU9YUPo5byXTIQDrPo5NeMciI130_assertion description "[We found an association between SNPs in the AKT1 gene and total Lewis score measuring obstetric complications in female patients with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48707.RAiMqYAO3gG2nKdCrwDjhU9YUPo5byXTIQDrPo5NeMciI130_provenance.
- NP48712.RAnnJfWXDthXuiZ1m4StvXoDQEEpcgvuDMzlAopFgCKds130_assertion description "[Our study provides support for the theory that AKT1 is a susceptibility gene for Japanese schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48712.RAnnJfWXDthXuiZ1m4StvXoDQEEpcgvuDMzlAopFgCKds130_provenance.
- NP48713.RAj7mWYeKx6glM70mb4DgI3sJn7sQJijqjv2YNipEPeWg130_assertion description "[Specifically, we present convergent evidence for a decrease in AKT1 protein levels and levels of phosphorylation of GSK3beta at Ser9 in the peripheral lymphocytes and brains of individuals with schizophrenia; a significant association between schizophrenia and an AKT1 haplotype associated with lower AKT1 protein levels; and a greater sensitivity to the sensorimotor gating-disruptive effect of amphetamine, conferred by AKT1 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48713.RAj7mWYeKx6glM70mb4DgI3sJn7sQJijqjv2YNipEPeWg130_provenance.
- NP48714.RAo2r-WYtTYRO0yTFnurXTc3fIfAYpnJD2Tle7UCnRYbE130_assertion description "[Our data suggest complex epistatic effects implicating an NRG1 molecular pathway in cognitive brain function and the pathogenesis of schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48714.RAo2r-WYtTYRO0yTFnurXTc3fIfAYpnJD2Tle7UCnRYbE130_provenance.
- NP48719.RAoY_QjYK3YXAH7JozBuYEsZaoNzQIKqAcYk44Nan6deo130_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." NP48719.RAoY_QjYK3YXAH7JozBuYEsZaoNzQIKqAcYk44Nan6deo130_provenance.
- NP48724.RAk_YBoBhbJyAP2QH8tcOkt1gVoBsLca1uK3kTpN5Itkc130_assertion description "[The association of aldose reductase gene (AKR1B1) polymorphisms with diabetic neuropathy in adolescents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48724.RAk_YBoBhbJyAP2QH8tcOkt1gVoBsLca1uK3kTpN5Itkc130_provenance.
- NP48726.RAmXUn8TSUrTpV_g474sT85HiiC_19oBKYzT2MTmGi0VM130_assertion description "[Recent experimental data suggest that a microsatellite polymorphism at 5' end of the aldose reductase gene may be associated with the development of diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48726.RAmXUn8TSUrTpV_g474sT85HiiC_19oBKYzT2MTmGi0VM130_provenance.
- NP48730.RAnA2ppZTSzK22LCJ6QL7_afA_Gcx7RaVUTi7sF3NhLzI130_assertion description "[In Chilean adults, the frequency of the C(-106)T polymorphism of the ALR2 gene was similar to that reported by others. Type-2 diabetics with the CC genotype were more susceptible for developing retinopathy as a result of chronic hyperglycemia than those with the CT or TT genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48730.RAnA2ppZTSzK22LCJ6QL7_afA_Gcx7RaVUTi7sF3NhLzI130_provenance.
- NP48747.RAh3FbAFGK_1fMCOTuYandrkIxZRZrhSXwP9zyuH0On40130_assertion description "[We investigated the Lys554 allele in 386 individuals of various ethnic origins and found the]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48747.RAh3FbAFGK_1fMCOTuYandrkIxZRZrhSXwP9zyuH0On40130_provenance.
- NP48748.RAlfUvvPhIX-Pt2lIZjtLH1zsKXkl8rZ352AaZRDE0iZU130_assertion description "[In conclusion, the results from our study suggest that the AhR Lys554Arg polymorphism may be a genetic susceptibility factor for breast cancer, whereas CYP1A2*1F, which is a potentially functional single nucleotide polymorphism, may not be related to breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48748.RAlfUvvPhIX-Pt2lIZjtLH1zsKXkl8rZ352AaZRDE0iZU130_provenance.
- NP48761.RAkLuN_5BRT8qJGrX9eIG0ZQCCfGFereRBWx4bTpfn7dM130_assertion description "[ The AGTR2 A1675G polymorphism might be involved in the development of essential hypertension in male Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48761.RAkLuN_5BRT8qJGrX9eIG0ZQCCfGFereRBWx4bTpfn7dM130_provenance.
- NP48762.RAth4sOKKnaMu7AAgeVQyEj1rhIaa2jiAA6dUoFgkWcSI130_assertion description "[ Our data indicate that the X-chromosomal located +1675 G/A-polymorphism of the AT2-R gene is associated with LV structure in young male humans with early structural changes of the heart due to arterial hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48762.RAth4sOKKnaMu7AAgeVQyEj1rhIaa2jiAA6dUoFgkWcSI130_provenance.