Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP48780.RAmVWdZ3U49OOnLuI5jtCJ68lll9ldQMc5phMZENjsSqo130_assertion description "[We investigated the associations between hypertension status and the genotypes of four single nucleotide polymorphism (SNP) sites in four hypertension-related genes (Angiotensinogen AGT, Angiotensin I Converting Enzyme ACE, Angiotensinogen II receptor, subtype 1 AGTR1, and Alpha 1-Antichymotrypsin ACT or SERPINA3), in an African American sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48780.RAmVWdZ3U49OOnLuI5jtCJ68lll9ldQMc5phMZENjsSqo130_provenance.
- NP48781.RAsvB2gWAVg8nQ64wxQzJzI7OiSSiOBBpZdwM0g_CP14w130_assertion description "[Angiotensin II type 1 receptor polymorphisms and susceptibility to hypertension: a HuGE review.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48781.RAsvB2gWAVg8nQ64wxQzJzI7OiSSiOBBpZdwM0g_CP14w130_provenance.
- NP48787.RAvoH5KO5TvUjdpLZ2hFO_BpTeTdJejSC1eBAAMLveG6A130_assertion description "[There is no association between between ATIR gene A1166/C polymorphism and occurrence of early-onset CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48787.RAvoH5KO5TvUjdpLZ2hFO_BpTeTdJejSC1eBAAMLveG6A130_provenance.
- NP48794.RAtC0nWFH85uE2asa29WzV8AT5cWNtxkdJJcB6ZYAtXWA130_assertion description "[This study suggests possible interactions between genes from the RA, bradykinin, and fibrinolytic systems on the risk of cardiovascular disease, extending previous research that has demonstrated that interactions among genes from these systems influence plasma concentrations of both t-PA and PAI-1. Further explorations of these interactions are needed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48794.RAtC0nWFH85uE2asa29WzV8AT5cWNtxkdJJcB6ZYAtXWA130_provenance.
- NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_assertion description "[Thus the presence of 1166C allele of AGTR1 and 2350G allele of ACE can be considered as predisposing factors for LVH development in EH. In contrast, association of studied polymorphisms with presence or LVH degree was not detected in patients with arterial hypertension combined with DM2. This may indicate another structure of genetic component of predisposition to LVH in different causes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_provenance.
- NP48809.RAm3XArPQIUALD7XXf_OV-V7IWonaMsOv_462A8aTaQ3Y130_assertion description "[This study suggests that genetic control of RAS activity correlates with production of anti-HLA antibodies, possibly explaining the relationship to chronic allograft outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48809.RAm3XArPQIUALD7XXf_OV-V7IWonaMsOv_462A8aTaQ3Y130_provenance.
- NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_assertion description "[To detect the relation of the risk factors of primary VUR with the genetic polymorphism, the distribution of ACE, AT1 and AT2 genotypes after stratification by risk factors was also studied in the primary VUR patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_provenance.
- NP48824.RAkT_d-aDoUmDUlWLOmDva_vvJ84OGh0VDIpg9a_SuhTc130_assertion description "[In conclusion, Susceptibility to develop cough is associated with a genetic variant of the bradykinin B2 receptor promoter; thus, it may be possible to identify those patients who will develop this adverse reaction to ACE inhibitors in advance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48824.RAkT_d-aDoUmDUlWLOmDva_vvJ84OGh0VDIpg9a_SuhTc130_provenance.
- NP48826.RAl9PXEPS26qhyVyz1nuj-S7-6QF1hG_2hCxP8pHQF3aE130_assertion description "[In the presence of other coexisting risk factors the AGTR1 A(1166)C but not the NOS3 G(894)T polymorphism increased the risk of stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48826.RAl9PXEPS26qhyVyz1nuj-S7-6QF1hG_2hCxP8pHQF3aE130_provenance.
- NP48836.RArLTwH78k4nyvjIRJM_1vf0kV7gXS1WJM8oDQVH0ymU4130_assertion description "[It was the aim of this study, therefore, to investigate the involvement of the ACE insertion/deletion (I/D), AT1 receptor 1166 A->C and AGT M235T polymorphisms as predisposing factors for myocardial infarction (MI) in 195 young South African Indians (</= 45 years).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48836.RArLTwH78k4nyvjIRJM_1vf0kV7gXS1WJM8oDQVH0ymU4130_provenance.
- NP48839.RAoLguOIG1MK9Lw2pAQvRmoCGU-N6_TDWY9-uw7b-pBU4130_assertion description "[Angiotensin II type-I receptor and ACE polymorphisms and risk of myocardial infarction in men and women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48839.RAoLguOIG1MK9Lw2pAQvRmoCGU-N6_TDWY9-uw7b-pBU4130_provenance.
- NP48840.RAq-16gBJ0VHMRQhBadub3lvl1awTj8ESyN72Ko9pRS-Q130_assertion description "[An interactive effect on MI risk was found between ACE-DD and AGT1R-AA genotypes (odds ratio OR=2, 95% CI= 1-3.9), between ACE-DD and angiotensinogen-TT genotypes (OR = 2.7, 95% CI = 1-7.3), as well as among ACE-DD, angiotensinogen-TT, and AGT1R-AA genotypes (OR=4.8, 95% CI = 1-22.8).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48840.RAq-16gBJ0VHMRQhBadub3lvl1awTj8ESyN72Ko9pRS-Q130_provenance.
- NP48841.RAvauTcOVtxmb73VELVO0h0bbyjjtsxiD7omJeoJ1B40s130_assertion description "[Polymorphisms in RAAS genes can be important in the onset of a first AMI in young patients (ACE, CYP11B2 polymorphisms), but not in the disease progression after a long follow-up period. Larger collaborative studies are needed to confirm these results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48841.RAvauTcOVtxmb73VELVO0h0bbyjjtsxiD7omJeoJ1B40s130_provenance.
- NP48844.RAngKtQsibM8YpgYy674hdtxVmjx3I3NoiYQqyQcI2VWA130_assertion description "[ Delete polymorphism of A1166-C gene is associated with DN in type 2 diabetes mellitus. It is suggested that detection of significant AGTIR-A1166-C polymorphism is of help for preventing DN in type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48844.RAngKtQsibM8YpgYy674hdtxVmjx3I3NoiYQqyQcI2VWA130_provenance.
- NP48853.RAmBLQV9fNmHOocGgdAEx68O4UaS9HbJ70WP2O3C5YlCQ130_assertion description "[To determine whether angiotensin-converting enzyme (ACE) gene, angiotensinogen (AGT) gene and angiotensin II receptor 1 (AT1R) gene are implicated in Chinese essential hypertension (EH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48853.RAmBLQV9fNmHOocGgdAEx68O4UaS9HbJ70WP2O3C5YlCQ130_provenance.
- NP48856.RAmz5OLtIgJSSEwxRZpQLt49tNk9ntj78qEVCvvJZiZ0A130_assertion description "[Angiotensin II type 1 receptor gene polymorphism is associated with the severity but not prevalence of coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48856.RAmz5OLtIgJSSEwxRZpQLt49tNk9ntj78qEVCvvJZiZ0A130_provenance.
- NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_assertion description "[Six SNPs that were discovered and were associated with CAD may help in explaining the molecular basis of the disorder and the susceptibility to coronary atherosclerosis. It can also help identify early prediction, prevention and therapy for CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_provenance.
- NP48865.RAiLAJB0M1OzTu82zXcF1Z4HBQp18STKTy43zRQ_bLki4130_assertion description "[To better understand the relationship between angiotensinogen (AGT) genetic variation and essential hypertension, AGT genotypes and haplotypes were tested for association with hypertensive endophenotypes and essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48865.RAiLAJB0M1OzTu82zXcF1Z4HBQp18STKTy43zRQ_bLki4130_provenance.
- NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_assertion description "[Our research data showed that the polymorphisms of all the four genes might be associated with hypertension in the Kazakhs group of Xinjiang while there might be interactions existed in AGT, ACE, AGE and CHO.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_provenance.
- NP48869.RAqCInOl-OyKTUO-zz9EN0oqrQrtPveV31pYFDKoxwK50130_assertion description "[In 194 hypertensives and 304 controls of Hellenic origin, the possible association between the (CA)n repeat polymorphism of angiotensinogen (AGT), the 250 bp insertion/deletion (I/D) of angiotensin-converting enzyme (ACE), the tetranucleotide repeat polymorphism (TCTG)n of renin, and the (CT)n repeat polymorphism of the natriuretic peptide receptor A (NPRA) and hypertension was assessed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48869.RAqCInOl-OyKTUO-zz9EN0oqrQrtPveV31pYFDKoxwK50130_provenance.
- NP48870.RAv1TC36G6vyzk0iW4zzwYcL84gIeWFnEPKINPuksMNCs130_assertion description "[Angiotensinogen T174M and M235T variants and hypertension in the Hani and Yi minority groups of China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48870.RAv1TC36G6vyzk0iW4zzwYcL84gIeWFnEPKINPuksMNCs130_provenance.
- NP48877.RAic5eId4Bcj27yhtasyuLZ4SP3Wp7-EIoYb1v8_-ct9k130_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." NP48877.RAic5eId4Bcj27yhtasyuLZ4SP3Wp7-EIoYb1v8_-ct9k130_provenance.
- NP48884.RAqPxdgF2PdPaSCocmGHFy6S0G7c2JEnLIo8Pbc8Am1LM130_assertion description "[Left-ventricular hypertrophy caused by exercise training is exacerbated in homozygous TT individuals with angiotensinogen polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48884.RAqPxdgF2PdPaSCocmGHFy6S0G7c2JEnLIo8Pbc8Am1LM130_provenance.
- NP48894.RAiPZlJraAmEkkFY4WrxU-cyt8070zEcF5PS04FnRK4kw130_assertion description "[The data hereby provide further support for the association between angiotensinogen M235T polymorphism and CAD severity independently of other cardiovascular risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48894.RAiPZlJraAmEkkFY4WrxU-cyt8070zEcF5PS04FnRK4kw130_provenance.
- NP48904.RAqSSE6MGT1C1VRxrnTgLEHMIDAb3FJnUUd618Iu4QvdA130_assertion description "[We could only establish a role for the AT1R 1166A/C polymorphism in restenosis after PCI. However, significant gene-gene interaction was suggested for the ACE gene and the HO-1 promotor. The RAS and HO-1 relation in restenosis merits further investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48904.RAqSSE6MGT1C1VRxrnTgLEHMIDAb3FJnUUd618Iu4QvdA130_provenance.
- NP48905.RAvboyO77T-mtP87149omPlW4K2dMr4neGZZySmA7oFTw130_assertion description "[ AT1 receptor genotypes could influence arterial ageing in hypertensive subjects. These results also show that the association between genotypes and arterial stiffness may manifest itself later in life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48905.RAvboyO77T-mtP87149omPlW4K2dMr4neGZZySmA7oFTw130_provenance.
- NP48910.RAsnakhybcN3CeR_7vuVam74UeX3_r6sbX8croxxsHbv4130_assertion description "[We examined 118 CKD patients and 98 control subjects for the occurrence of common polymorphisms in angiotensin converting enzyme insertion/deletion (ACE; I/D), angiotensinogen (AGT; M235T), chymase (CMA; -1903G>A), angiotensin receptor type-1 (AGTR1-1166A>C), methylene tetrahydrofolate reductase (MTHFR; 677C>T), nephrin (NPHS1; R1160X) and podocin (NPHS2; R291W and R229Q).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48910.RAsnakhybcN3CeR_7vuVam74UeX3_r6sbX8croxxsHbv4130_provenance.
- NP48916.RArDHFH5bSiZeFpNwiJ-yd_hCaHASBcyvq7ImW_KS1Sck130_assertion description "[Synergistic effect between apolipoprotein E and angiotensinogen gene polymorphisms in the risk for early myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48916.RArDHFH5bSiZeFpNwiJ-yd_hCaHASBcyvq7ImW_KS1Sck130_provenance.
- NP48919.RArNIc-h_HLh5TbTDEDFf7dfsiN5F-UXrcd2KUieuUj-8130_assertion description "[Genotypic interactions of renin-angiotensin system genes in myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48919.RArNIc-h_HLh5TbTDEDFf7dfsiN5F-UXrcd2KUieuUj-8130_provenance.
- NP48920.RAmS7vIpQuVvkTt4ERLYRXlY9DYDrsfZtvS0bnims-dm4130_assertion description "[A study of three candidate genes for pre-eclampsia in a Sinhalese population from Sri Lanka.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48920.RAmS7vIpQuVvkTt4ERLYRXlY9DYDrsfZtvS0bnims-dm4130_provenance.
- NP48921.RAjKw9dNqjPqv9P04DeGeaaG0zpPxGdQrA6ABSuH5qWws130_assertion description "[Genetic analysis of the angiotensinogen gene in pre-eclampsia: study of german women and review of the literature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48921.RAjKw9dNqjPqv9P04DeGeaaG0zpPxGdQrA6ABSuH5qWws130_provenance.
- NP48925.RAhSZ4skfwmjPIF2mtyZTcurK9oJKQbQTIS92vAckJXDg130_assertion description "[The result indicates that the AGT M235T polymorphism and the ACE intron 16 polymorphism play no significant role in preeclampsia observed in Korean women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48925.RAhSZ4skfwmjPIF2mtyZTcurK9oJKQbQTIS92vAckJXDg130_provenance.
- NP48931.RAq2yU7hLDCrRXfwUfFXdBIGZfhtc1awh1Lo9540OlkvU130_assertion description "[Effect of ACE gene polymorphism on age at renal death in polycystic kidney disease in Japan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48931.RAq2yU7hLDCrRXfwUfFXdBIGZfhtc1awh1Lo9540OlkvU130_provenance.
- NP48938.RApOw4x6hf56AixIWJuEKu8HW1nd68WboKs5xYfLmVGUk130_assertion description "[Polymorphisms in AGT1R and AGT genes are associated with renal dysfunction and CHD in type 2 diabetes and further support the important role of the RAS in these complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48938.RApOw4x6hf56AixIWJuEKu8HW1nd68WboKs5xYfLmVGUk130_provenance.
- NP48941.RAr1AnZC6OJFkrL4iKD2Mfoix8iW5D2BvlJsGfEJ2X9YY130_assertion description "[To investigate predictive genetic markers for diabetic nephropathy, we studied the genetic polymorphisms of angiotensin-converting enzyme (ACE) and angiotensinogen (AGN) in Japanese subjects with non-insulin-dependent diabetes mellitus (NIDDM) with and without nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48941.RAr1AnZC6OJFkrL4iKD2Mfoix8iW5D2BvlJsGfEJ2X9YY130_provenance.
- NP48947.RAiHUZ8APRu_Sx69ylZ5BaLt318y80nUnipdMLloj0EFs130_assertion description "[Polymorphisms within the angiotensinogen gene (GT-repeat) and the risk of stroke in pediatric patients with sickle cell disease: a case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48947.RAiHUZ8APRu_Sx69ylZ5BaLt318y80nUnipdMLloj0EFs130_provenance.
- NP48948.RAmp04FIfEb9zk7GBZ9xyJIetjWrlIe_AAm7rC7RkDnnI130_assertion description "[The I/D polymorphism of ACE gene may be one of the risk factors and susceptible genetic markers for ischemic stroke with essential hypertension in Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48948.RAmp04FIfEb9zk7GBZ9xyJIetjWrlIe_AAm7rC7RkDnnI130_provenance.
- NP48949.RAodLib78TCR1ei_fGni-A9pg5rxPTUodfRtIcXKYa2oE130_assertion description "[Association of the T174M and M235T polymorphisms of the angiotensinogen gene with myocardial ischemia in the Russian population of the city of Moscow.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48949.RAodLib78TCR1ei_fGni-A9pg5rxPTUodfRtIcXKYa2oE130_provenance.
- NP48951.RAtkI2dhD0lX8dXeEokAFgmJ_QqftXOSfCjpd_h7I4UTs130_assertion description "[ It follows that the examined polymorphisms in the genes for ACE, angiotensinogen, and ET-1 could participate in the etiopathogenesis of atopic diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48951.RAtkI2dhD0lX8dXeEokAFgmJ_QqftXOSfCjpd_h7I4UTs130_provenance.
- NP48957.RAge5g6QGh4KEgY0DdJX7vTntkciJv75yTKl3wUgfolv8130_assertion description "[Angiotensinogen and angiotensin converting enzyme gene polymorphisms and the risk of bipolar affective disorder in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48957.RAge5g6QGh4KEgY0DdJX7vTntkciJv75yTKl3wUgfolv8130_provenance.
- NP48960.RAkB8mJzauGb475GZ7aykWyRUJ6-i9hZ-qsm9ku-dX09s130_assertion description "[Angiotensinogen and angiotensin converting enzyme gene polymorphisms and the risk of bipolar affective disorder in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48960.RAkB8mJzauGb475GZ7aykWyRUJ6-i9hZ-qsm9ku-dX09s130_provenance.
- NP48968.RAlLiX64mhFYxzwPzlZnAZCQMHkzxfjySmAd2crQQTXoU130_assertion description "[Analysis of glycogen debranching enzyme (debrancher) cDNA from a patient with glycogen storage disease type III revealed a deletion of 124 base pairs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48968.RAlLiX64mhFYxzwPzlZnAZCQMHkzxfjySmAd2crQQTXoU130_provenance.
- NP48969.RAupJq1Emc7Qv4aTiQkTM4PB0OjvIp5TFchsjYZEnpSHI130_assertion description "[A novel polymorphism in the promoter of the RAGE gene is associated with non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48969.RAupJq1Emc7Qv4aTiQkTM4PB0OjvIp5TFchsjYZEnpSHI130_provenance.
- NP48978.RAhDHtsxrtLpviKHl6XwmuApGHrVe6269xvw6ajjirwgg130_assertion description "[It is suggested that increase of IMT and formation of plaque are risk factors in patients aged 50 or above with hypertension, and that careful observation of the carotid artery will be effective for early detection of arteriosclerosis, and to predict the symptoms thereof.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48978.RAhDHtsxrtLpviKHl6XwmuApGHrVe6269xvw6ajjirwgg130_provenance.
- NP48981.RAqCx7hKZFsvXbFVNfZ95BlpYs_1Fbzu77xQuHOvhlAU4130_assertion description "[There is evidence to implicate adrenoceptor genes in hypertension, although future studies designed to investigate epistatic and gene-environment interactions would allow more solid conclusions to be drawn about the role of these genes in hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48981.RAqCx7hKZFsvXbFVNfZ95BlpYs_1Fbzu77xQuHOvhlAU4130_provenance.
- NP48983.RAmA8pbLQjgqGeGfWq-tSKk9IuGBzjfIzWlPOu7Mp8WXk130_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." NP48983.RAmA8pbLQjgqGeGfWq-tSKk9IuGBzjfIzWlPOu7Mp8WXk130_provenance.
- NP48984.RAumAWpFFOhlQj_qa8sLBDviur_hotZ_p5DYER1b1MIAE130_assertion description "[Therefore, we studied adrenergic receptor genes alpha1d (ADRA1d), beta2 (ADRB2) and beta3 (ADRB3), and IL-4/IL-4 receptor genes in patients with interstitial cystitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48984.RAumAWpFFOhlQj_qa8sLBDviur_hotZ_p5DYER1b1MIAE130_provenance.
- NP48989.RAizHO-hQUmK9b30TPriEL3KZkyRAbaNkGI4ZHVK_vO6k130_assertion description "[The Trp64Arg polymorphism of ADRB3 warrants consideration, along with other polymorphisms involved in the development of obesity, for tailor-made prevention of obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48989.RAizHO-hQUmK9b30TPriEL3KZkyRAbaNkGI4ZHVK_vO6k130_provenance.
- NP48990.RAquOtnFA2uhRjfg_jtt7BwA3kHMRQUJvOlO5yymp5v3s130_assertion description "[beta(3) Adrenergic receptor polymorphism and obesity-related phenotypes in hypertensive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48990.RAquOtnFA2uhRjfg_jtt7BwA3kHMRQUJvOlO5yymp5v3s130_provenance.
- NP48993.RAjTO3cLgqC3KyVw59o6L_ZWMIutKDL06ehUoqVywOaVQ130_assertion description "[Association of beta 3-adrenergic receptor gene with obesity in patients with type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48993.RAjTO3cLgqC3KyVw59o6L_ZWMIutKDL06ehUoqVywOaVQ130_provenance.
- NP49013.RAjdUHB_Yeusx_o3KQSz5cvOAKyFnzyBAjKdF3NIkiDWg130_assertion description "[ Estrogen receptor alpha polymorphisms, but not beta3-adrenergic receptor gene, may be associated with a risk of endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49013.RAjdUHB_Yeusx_o3KQSz5cvOAKyFnzyBAjKdF3NIkiDWg130_provenance.
- NP49023.RAtTlnil-N4LZBD99RGc2FXjN7R-xGRGrLMzjnzqMzQJI130_assertion description "[Common genetic variation of beta1- and beta2-adrenergic receptor and response to four classes of antihypertensive treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49023.RAtTlnil-N4LZBD99RGc2FXjN7R-xGRGrLMzjnzqMzQJI130_provenance.
- NP49025.RAr7WZCYsuOSJ7qJN_M0QmE5UhIRmID-dHE7RTgz61SJg130_assertion description "[Beta-2 adrenergic receptor gene polymorphisms Gln27Glu, Arg16Gly and Thr164Ile were suggested to have an effect in heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49025.RAr7WZCYsuOSJ7qJN_M0QmE5UhIRmID-dHE7RTgz61SJg130_provenance.
- NP49027.RAhrht0rpVvKQNmYaSohKoOibKM5qU_IDvpu_QtXgUYwU130_assertion description "[Impact of beta-2 Thr164Ile and combined beta-adrenergic receptor polymorphisms on prognosis in a cohort of heart failure outpatients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49027.RAhrht0rpVvKQNmYaSohKoOibKM5qU_IDvpu_QtXgUYwU130_provenance.
- NP49030.RAnCrrFBg20JFXqFe-qcZCKf-j0OFtL_payCHGU2RVAM0130_assertion description "[In this prospective study, we found no association between five functional betaAR polymorphisms and survival in patients with stable CHF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49030.RAnCrrFBg20JFXqFe-qcZCKf-j0OFtL_payCHGU2RVAM0130_provenance.
- NP49035.RAvo9YAQjz1kdZWMfekv3nWWYhQ9A6RY2yblQmByEugDM130_assertion description "[The significant associations between certain gene variants with concentration variations in serum C-reactive protein and homocysteine among adult women need to be confirmed in further genetic association studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49035.RAvo9YAQjz1kdZWMfekv3nWWYhQ9A6RY2yblQmByEugDM130_provenance.
- NP49043.RAhbsOeJTnmqdBDQVzFmjsgbEDZiZKYwoNTOPMD03A17o130_assertion description "[Beta 2-Adrenergic receptor polymorphisms, especially homozygous arginine 16, were associated with higher serum IgE levels in children with asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49043.RAhbsOeJTnmqdBDQVzFmjsgbEDZiZKYwoNTOPMD03A17o130_provenance.
- NP49048.RAnRPDWcIXk6Kfjid8cE3yuxfVcasLjAiow65zY4a2kc8130_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." NP49048.RAnRPDWcIXk6Kfjid8cE3yuxfVcasLjAiow65zY4a2kc8130_provenance.
- NP49052.RAicsBlcMFVKyriIsKcn_MvOWGd0l9qkhdTBeFq54FvOA130_assertion description "[Our results showed that the 27Glu allele of the ADRB2 gene appears to be a risk factor for abdominal obesity among male subjects, specially among those with lower HDL-cholesterol levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49052.RAicsBlcMFVKyriIsKcn_MvOWGd0l9qkhdTBeFq54FvOA130_provenance.
- NP49053.RApVYwKzDlo80ldmAKHZOpERUzvKP7Wmpw8rk56M0uxG0130_assertion description "[The present results suggest that a particular population such as lumberjacks, sharing the same environment, could help target genes involved in complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49053.RApVYwKzDlo80ldmAKHZOpERUzvKP7Wmpw8rk56M0uxG0130_provenance.
- NP49054.RAvngXgE9Q9WwHe1Xju3_QtDUcHzi2SVrPisLerGBWt2U130_assertion description "[Effects of novel capsinoid treatment on fatness and energy metabolism in humans: possible pharmacogenetic implications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49054.RAvngXgE9Q9WwHe1Xju3_QtDUcHzi2SVrPisLerGBWt2U130_provenance.
- NP49055.RApqlV4QsnJVKF-SHThVV1gyccp6sh-1Xfb0h5qLpZy1U130_assertion description "[Augmented muscle vasodilatory responses in obese children with Glu27 beta-2-adrenoceptor polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49055.RApqlV4QsnJVKF-SHThVV1gyccp6sh-1Xfb0h5qLpZy1U130_provenance.
- NP49057.RAlv4HzSDa5TWCqkftJQxOBVH63mj57RGQxcjVStiR9TA130_assertion description "[Candidate genes and growth curves for adiposity in African- and European-American youth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49057.RAlv4HzSDa5TWCqkftJQxOBVH63mj57RGQxcjVStiR9TA130_provenance.
- NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_assertion description "[Together, our findings suggest that the presence of beta2AR gene polymorphisms may be inconclusive in the susceptibility to MS or in the clinical characteristics of Japanese patients with MS and, therefore, need further studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_provenance.
- NP49070.RAm57BI2mIfSvAnFZaLppopHbP3d-APVeD1JGuBHZpZPc130_assertion description "[The Gly16-->Arg16 and Gln27-->Glu27 polymorphisms of beta2-adrenergic receptor are associated with metabolic syndrome in men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49070.RAm57BI2mIfSvAnFZaLppopHbP3d-APVeD1JGuBHZpZPc130_provenance.
- NP49071.RAktMB86hpAkXFSpHHdF4Mf4a9E687GSz8xGtBGNgi2-s130_assertion description "[The presence of the Glu27 and Arg64 polymorphisms of the ADRB2 and ADRB3 genes are not directly related to indices of the metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49071.RAktMB86hpAkXFSpHHdF4Mf4a9E687GSz8xGtBGNgi2-s130_provenance.
- NP49078.RAqJfhgWTc14wIzHpKOmRAzMNI_TvQDxeF8OCyFLOKAmY130_assertion description "[Association of polymorphisms in the beta2-adrenoreceptor gene with higher levels of parasitic infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49078.RAqJfhgWTc14wIzHpKOmRAzMNI_TvQDxeF8OCyFLOKAmY130_provenance.
- NP49081.RAgWf1Z5Ypiyl70yTntCh2r3AHLq9OjE0-3Oy-w9pF9jU130_assertion description "[Our goal was to determine whether the polymorphisms Arg389Gly (rs1801253) and Ser49Gly (rs1801252) of the ADRB1 gene were associated with essential hypertension in Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49081.RAgWf1Z5Ypiyl70yTntCh2r3AHLq9OjE0-3Oy-w9pF9jU130_provenance.
- NP49083.RArPKPPVf6QuLill86hxe1dZkNLwR6GN8BeqbRboa8wjk130_assertion description "[beta(1)-Adrenergic receptor polymorphism was associated with different blood pressure responses to metoprolol therapy in patients with essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49083.RArPKPPVf6QuLill86hxe1dZkNLwR6GN8BeqbRboa8wjk130_provenance.
- NP49096.RAuGkbgQH_Nd4cWWR0zp4cK2uYMzUDIxAaWK5HQigBs-Q130_assertion description "[ The alpha2CDel322-325 and beta1Arg389 receptors act synergistically to increase the risk of heart failure in blacks. Genotyping at these two loci may be a useful approach for identification of persons at risk for heart failure or its progression, who may be candidates for early preventive measures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49096.RAuGkbgQH_Nd4cWWR0zp4cK2uYMzUDIxAaWK5HQigBs-Q130_provenance.
- NP49099.RAj4MGFgmkqNOKdpzufUPgM1_6wFJxB8mGVgTNiZdV56I130_assertion description "[Beta-1-adrenergic receptor gene in major depression: influence on antidepressant treatment response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49099.RAj4MGFgmkqNOKdpzufUPgM1_6wFJxB8mGVgTNiZdV56I130_provenance.
- NP49100.RAscd06kxUag8GVpbeAw9FZVjiAI4KMDxroBg2I4cDd-k130_assertion description "[ Heart failure patients with the Arg389Arg genotype and Gly49 carriers had greater improvements in LV remodeling from beta-blocker treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49100.RAscd06kxUag8GVpbeAw9FZVjiAI4KMDxroBg2I4cDd-k130_provenance.
- NP49103.RAswoJQNnT0550zv7ogcSNn9FDa8mWwrjV3OR3ydX0FxY130_assertion description "[Carriers of the ADRB1 Arg389 allele (heterozygotes+homozygotes) had an approximately 3.5-fold increased risk for MI than Gly389 homozygotes (OR=3.59, 95% CI=0.96-13.47, P=0.045).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49103.RAswoJQNnT0550zv7ogcSNn9FDa8mWwrjV3OR3ydX0FxY130_provenance.
- NP49106.RAs1scayg-9KQbuYXleXukixUn93qcSnWCzIUtER_Ee-Q130_assertion description "[Effects of novel capsinoid treatment on fatness and energy metabolism in humans: possible pharmacogenetic implications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49106.RAs1scayg-9KQbuYXleXukixUn93qcSnWCzIUtER_Ee-Q130_provenance.
- NP49110.RAo-DR2T1KUCcZbr0CWeXwJ0E-fkwPxCWUDsIH1TqYgsk130_assertion description "[beta2-adrenergic receptor polymorphisms and salbutamol-stimulated energy expenditure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49110.RAo-DR2T1KUCcZbr0CWeXwJ0E-fkwPxCWUDsIH1TqYgsk130_provenance.
- NP49116.RAjB6TNM3NpFCPMsS-x5phSI9htNlxseTiOCkvxqzaV0M130_assertion description "[ For the first time, we show that beta(2)-adrenoceptor polymorphisms significantly influence the relationship between heart rate and cardiac adrenergic drive in CHF, but do not affect the rate of norepinephrine release from sympathetic nerve terminals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49116.RAjB6TNM3NpFCPMsS-x5phSI9htNlxseTiOCkvxqzaV0M130_provenance.
- NP49127.RAswXTQkqIg-FeDPD_X15WgiXufDUM831WtctroIb4j4M130_assertion description "[Resting sympathetic nerve activity is related to age, sex and arterial pressure but not to 2-adrenergic receptor subtype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49127.RAswXTQkqIg-FeDPD_X15WgiXufDUM831WtctroIb4j4M130_provenance.
- NP49133.RAoOAPoFMOB-jaWJJInZN3BRV_eK9Cz5Gf9_7YPAu9CBs130_assertion description "[There is evidence to implicate adrenoceptor genes in hypertension, although future studies designed to investigate epistatic and gene-environment interactions would allow more solid conclusions to be drawn about the role of these genes in hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49133.RAoOAPoFMOB-jaWJJInZN3BRV_eK9Cz5Gf9_7YPAu9CBs130_provenance.
- NP49142.RAr0sF9b75dSYZP5CVt5-TUGJkCn9AGAJOA-UUbW91-wo130_assertion description "[Our results suggest that the ADRA2A gene might have a small effect on ADHD susceptibility or that this gene might modulate the severity of the disorder. They are also consistent with the noradrenergic theories of ADHD, suggesting a role for the alpha2A adrenergic receptors in the disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49142.RAr0sF9b75dSYZP5CVt5-TUGJkCn9AGAJOA-UUbW91-wo130_provenance.
- NP49143.RAkNOjS3t_ymeFHQLrOwrpvUR0YNIOjSWz-XqM4AhmmPE130_assertion description "[This study aimed to investigate the association between this ADRA2A polymorphism and attention-deficit/hyperactivity disorder-inattentive type (ADHD-I) in a nonreferred sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49143.RAkNOjS3t_ymeFHQLrOwrpvUR0YNIOjSWz-XqM4AhmmPE130_provenance.
- NP49146.RAixjcLKzukRvx7TTnluU3qUAOJFlcfSlhUTluFCMeSsY130_assertion description "[Patients One hundred six patients consecutively diagnosed as having ADHD were genotyped for the ADRA2A -1291 C>G polymorphism and were included in the analyses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49146.RAixjcLKzukRvx7TTnluU3qUAOJFlcfSlhUTluFCMeSsY130_provenance.
- NP49147.RAgaz3sL9INyqDD3Zd57dBZvtK8d6eh0SaHw22cW-66qw130_assertion description "[Personality mediation of genetic effects on Attention-Deficit/Hyperactivity Disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49147.RAgaz3sL9INyqDD3Zd57dBZvtK8d6eh0SaHw22cW-66qw130_provenance.
- NP49149.RAvoFH2PSnU5ueAcEwstXTOfrK6cFpdgIKYarbonrpM1I130_assertion description "[Possible association of the alpha-2A-adrenergic receptor gene with response time variability in attention deficit hyperactivity disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49149.RAvoFH2PSnU5ueAcEwstXTOfrK6cFpdgIKYarbonrpM1I130_provenance.
- NP49156.RAv3Haojqvuu2_HwvEBRku0G2OchKuIhvclavGTIv2T_U130_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." NP49156.RAv3Haojqvuu2_HwvEBRku0G2OchKuIhvclavGTIv2T_U130_provenance.
- NP49160.RAmtB4wQTmJw10JVPKhAo_2Baf4x2wGE2lkrijdjKJI-g130_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." NP49160.RAmtB4wQTmJw10JVPKhAo_2Baf4x2wGE2lkrijdjKJI-g130_provenance.
- NP49165.RAvYU5AxZKobNo_Y8Pf-2uisAPk3E7sn_gX_gMB220IKA130_assertion description "[There is evidence to implicate adrenoceptor genes in hypertension, although future studies designed to investigate epistatic and gene-environment interactions would allow more solid conclusions to be drawn about the role of these genes in hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49165.RAvYU5AxZKobNo_Y8Pf-2uisAPk3E7sn_gX_gMB220IKA130_provenance.
- NP49173.RAuMEctwwwDORCrmIqiwViJ7ArCXqGGEnCXlqdnL7POS0130_assertion description "[Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49173.RAuMEctwwwDORCrmIqiwViJ7ArCXqGGEnCXlqdnL7POS0130_provenance.
- NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_assertion description "[ The adenosine-related gene variants do not appear to alter susceptibility to the disease in this group of essential hypertensives. However, involvement of these genes and the adenosine system cannot be conclusively excluded from essential hypertension pathogenesis as other gene variants may still be involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_provenance.
- NP49176.RAiI98n7_1jExJquySEq5zAOJh8BeBYYZ4YNzmtStGFKo130_assertion description "[Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49176.RAiI98n7_1jExJquySEq5zAOJh8BeBYYZ4YNzmtStGFKo130_provenance.
- NP49180.RAl_BY2UpxjQnnG8HWIV470MsZGLXH0ETyzi3_ARXDlPM130_assertion description "[Genetic variation in adiponectin receptor 1 and adiponectin receptor 2 is associated with type 2 diabetes in the Old Order Amish.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49180.RAl_BY2UpxjQnnG8HWIV470MsZGLXH0ETyzi3_ARXDlPM130_provenance.
- NP49188.RAubSGTd12F1ysNJDm6EMdgKartEOKSYIUxqOrJ2-fCn8130_assertion description "[our data indicate significant associations between ADIPOR1 haplotypes and diabetes risk but do not support a relation between ADIPOR2 variability and the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49188.RAubSGTd12F1ysNJDm6EMdgKartEOKSYIUxqOrJ2-fCn8130_provenance.
- NP49192.RAmURxCFD3Yd9GTiBxiMijV9UCnzIhlA3KOY1tviD7MuM130_assertion description "[Association studies between ADIPOR1 genetic variants and predisposition to type 2 diabetes (DM2) have provided contradictory results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49192.RAmURxCFD3Yd9GTiBxiMijV9UCnzIhlA3KOY1tviD7MuM130_provenance.
- NP49197.RAh7ZlfzKh0fjPylBe5hHpYlyfCFVq26KydHzxhKR7TbI130_assertion description "[ These preliminary results suggest that ADH4 may play a role in the etiology of alcohol dependence. The association requires further study and replication but is functionally plausible and has a large effect size.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49197.RAh7ZlfzKh0fjPylBe5hHpYlyfCFVq26KydHzxhKR7TbI130_provenance.
- NP49198.RAq1fsINCJs0qegJ3yegafjGPI_AZyPOMEnbf9JHHeIEA130_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." NP49198.RAq1fsINCJs0qegJ3yegafjGPI_AZyPOMEnbf9JHHeIEA130_provenance.
- NP49209.RAiWKlr8fKzx32Mad3TXMZbKTTskYif0AfOEy6ehKBya8130_assertion description "[The goal of this study was to determine whether any associations exist between the ADH2, ADH3, and ALDH2 polymorphisms and alcohol dependence in a group of Native Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49209.RAiWKlr8fKzx32Mad3TXMZbKTTskYif0AfOEy6ehKBya8130_provenance.
- NP49212.RApxFp-VkO58q3OM7QAbQomUqbf4ML7oyd_MLdMrqQrTM130_assertion description "[for ADH1B and ADH1C genotypes among men and women were similar.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49212.RApxFp-VkO58q3OM7QAbQomUqbf4ML7oyd_MLdMrqQrTM130_provenance.
- NP49213.RApdQad0Vm9_UxPRDnRhTTEwKH17qYnLhNx79-htqvj40130_assertion description "[We compared the frequencies of polymorphisms in ten genes that have been hypothesized to have a role in risk of EC (CYP1A1, CYP2A6, CYP2E1, GSTM1, GSTP1, GSTT1, ADH2, ADH3, ALDH2, and O6-MGMT) among three Iranian ethnic groups with highly varying rates of EC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49213.RApdQad0Vm9_UxPRDnRhTTEwKH17qYnLhNx79-htqvj40130_provenance.
- NP49215.RAo7X1dG0ga9hd2P-DSdRyyUJrckh58rGz_iQEC_Bh_MM130_assertion description "[Our data did not show that ADH3 genotypes had a significantly independent effect on the risk of HNSCC, nor did they modify the risks increased by alcohol or tobacco consumption and high-risk human papillomavirus infection. However, participants with ADH3(1-2) genotype were associated with poorer survival compared with those who had the other two ADH3 genotypes and a higher rate of recurrence than participants with ADH3(1-1) genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49215.RAo7X1dG0ga9hd2P-DSdRyyUJrckh58rGz_iQEC_Bh_MM130_provenance.
- NP49218.RAl1hkPLiIH4L68jwBhLOzk4-GXAlj_Nt9i1XVF6Xfs0M130_assertion description "[Role of epoxide hydrolase, NAD(P)H:quinone oxidoreductase, cytochrome P450 2E1 or alcohol dehydrogenase genotypes in susceptibility to colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49218.RAl1hkPLiIH4L68jwBhLOzk4-GXAlj_Nt9i1XVF6Xfs0M130_provenance.
- NP49222.RAiqc5SUzz3A2xdN13oNLfsOz314zn3kmBDMirrgiB514130_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." NP49222.RAiqc5SUzz3A2xdN13oNLfsOz314zn3kmBDMirrgiB514130_provenance.