Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP48720.RAentB8NNJxavRhYxFPMc8WTUQpUCPNXSAPRSrRwISt8E130_assertion description "[Genetic variation and antioxidant response gene expression in the bronchial airway epithelium of smokers at risk for lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48720.RAentB8NNJxavRhYxFPMc8WTUQpUCPNXSAPRSrRwISt8E130_provenance.
- NP48721.RAYOaQUsszYqmF3pX8T3JZ76tNCyQo_5HF5t-TQ0pbioI130_assertion description "[ Polymorphisms in HSD3B1, CYP19, AKR1C3 genes may be associated with an enlarged prostate in older men. These data provide insights into genes that should be examined further for their potential role in the pathogenesis of BPH. (c) 2005 Wiley-Liss, Inc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48721.RAYOaQUsszYqmF3pX8T3JZ76tNCyQo_5HF5t-TQ0pbioI130_provenance.
- NP48722.RAYwRlhXYVUX5D3LEgGc9uEIXznCl_ucdZb46STVT0SrA130_assertion description "[ SNP-71G is a functional polymorphism that may contribute to testosterone excess in a subset of PCOS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48722.RAYwRlhXYVUX5D3LEgGc9uEIXznCl_ucdZb46STVT0SrA130_provenance.
- NP48727.RAT-XjNx5XFAQLpb7yH1rf9IdtMeGlnscH4UGAz7F5XsM130_assertion description "[Aldose reductase (AC)n gene polymorphism and susceptibility to diabetic retinopathy in Type 2 diabetes in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48727.RAT-XjNx5XFAQLpb7yH1rf9IdtMeGlnscH4UGAz7F5XsM130_provenance.
- NP48732.RASYqAHh7u_PTvqkbSeXc8Lg_UQX-0gkd-o8vWvrH_2Ng130_assertion description "[Diabetic retinopathy: Validation study of ALR2, RAGE, iNOS and TNFB gene variants in a south Indian cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48732.RASYqAHh7u_PTvqkbSeXc8Lg_UQX-0gkd-o8vWvrH_2Ng130_provenance.
- NP48735.RARzoGPZhtU0IskkuTiBLTRgdLpcFT1MmO1M0KGhZyhXE130_assertion description "[C-106T polymorphism of AKR1B1 is associated with diabetic nephropathy and erythrocyte aldose reductase content in Japanese subjects with type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48735.RARzoGPZhtU0IskkuTiBLTRgdLpcFT1MmO1M0KGhZyhXE130_provenance.
- NP48737.RASJ2j9SRPpRRzMbxccfSqqdYQTfcyqSNacv8ipxhKuMg130_assertion description "[Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48737.RASJ2j9SRPpRRzMbxccfSqqdYQTfcyqSNacv8ipxhKuMg130_provenance.
- NP48738.RAX9m2KQ0KFg1QJzO6UWjg44Ttjv3z3rP3rDEYHHHshXo130_assertion description "[Polymorphisms at +49A/G and CT60 sites in the 3' UTR of the CTLA-4 gene and APECED-related AIRE gene mutations analysis in sporadic idiopathic hypoparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48738.RAX9m2KQ0KFg1QJzO6UWjg44Ttjv3z3rP3rDEYHHHshXo130_provenance.
- NP48739.RAa0yGIInLBwvr_4kzSL9hJzbLrEZWJjR0oI6TvaP_THc130_assertion description "[Correlation between activation-induced cytidine deaminase gene polymorphism and atopic asthma and plasma IgE in adult.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48739.RAa0yGIInLBwvr_4kzSL9hJzbLrEZWJjR0oI6TvaP_THc130_provenance.
- NP48744.RAWi4kmR9m5VPOPV4CPsFgFY78yy5TxXdMzu1KeNMvwLI130_assertion description "[Estrogen metabolism-related genes and breast cancer risk: the multiethnic cohort study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48744.RAWi4kmR9m5VPOPV4CPsFgFY78yy5TxXdMzu1KeNMvwLI130_provenance.
- NP48750.RAUCQGE9dsJOyz-YiNKjnpNfSKFO3Tstjs3K81-ual3fo130_assertion description "[Endometriosis is associated with the AHSG gene polymorphism in Korean women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48750.RAUCQGE9dsJOyz-YiNKjnpNfSKFO3Tstjs3K81-ual3fo130_provenance.
- NP48753.RAdAjKP4XYIHEyZzrwcarf0XsQjqYL_J5IxAMK3DUROYE130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48753.RAdAjKP4XYIHEyZzrwcarf0XsQjqYL_J5IxAMK3DUROYE130_provenance.
- NP48755.RAXbD5J_T4W8ORmUmjvXu-QHyMojxIXcKzdjRfLo0CJf8130_assertion description "[Association of micropenis with Pro185Ala polymorphism of the gene for aryl hydrocarbon receptor repressor involved in dioxin signaling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48755.RAXbD5J_T4W8ORmUmjvXu-QHyMojxIXcKzdjRfLo0CJf8130_provenance.
- NP48758.RAZP5L3xLLFkR-Csty2b8QGhN69vjr_9mpyNlNH5K3NMk130_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." NP48758.RAZP5L3xLLFkR-Csty2b8QGhN69vjr_9mpyNlNH5K3NMk130_provenance.
- NP48760.RAYd9TJWhBAx2GC40wN0zMK4kKQ1e4NsKSrxGQO-utT-M130_assertion description "[This analysis showed that the C4599A polymorphism was associated with hypertension in women (p=0.0058), but not in men. Moreover, this female-specific association was pronounced in premenopausal women. The female-specific association may be helpful in conducting further molecular and biological studies on the relationship among sex, the renin-angiotensin system, and hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48760.RAYd9TJWhBAx2GC40wN0zMK4kKQ1e4NsKSrxGQO-utT-M130_provenance.
- NP48769.RAUU4i0EsTzbywZutwdVZ1KHNcP-AwWwBfewa_tZlPRg8130_assertion description "[We conclude that genetic polymorphisms of RAS components are not independent prognostic indicators of renal scarring in patients with VUR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48769.RAUU4i0EsTzbywZutwdVZ1KHNcP-AwWwBfewa_tZlPRg8130_provenance.
- NP48771.RAUSV4P9Ujhey4SzPtitZMU9aydQe3acUa-GcRBG67T1I130_assertion description "[Also, in the case of combination of ACE and AT2 gene, the combination of ACE II genotype and AT2 A-1332G transition occurs infrequently in primary VUR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48771.RAUSV4P9Ujhey4SzPtitZMU9aydQe3acUa-GcRBG67T1I130_provenance.
- NP48777.RARaY987jqy8Xz4-n79CfU-TP1ZQU58HmCxoNHc5ovARc130_assertion description "[Studies were searched from the Chinese Biomedicine Database, the China National Knowledge Infrastructure platform, Pubmed and Medline, using the search terms 'hypertension', 'angiotensin II type 1 receptor', 'AT(1)R', 'polymorphism', 'China' and 'Chinese', without limiting to any specific language.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48777.RARaY987jqy8Xz4-n79CfU-TP1ZQU58HmCxoNHc5ovARc130_provenance.
- NP48778.RATfecXP1kLbjuIj7GseTGO1Kzc-iNKkvg7b-orcqDoZI130_assertion description "[Relationship study of angiotensin II type 1 receptor gene A1166C polymorphism, food consumption and behavior on hypertension in Kazakh group, Xinjiang.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48778.RATfecXP1kLbjuIj7GseTGO1Kzc-iNKkvg7b-orcqDoZI130_provenance.
- NP48783.RAR_FolBPWrvAUuariMyU62SB-xeGpKySHowU8D3Ed0VA130_assertion description "[We studied the effects of the angiotensinogen T174M and M235T, angiotensin converting enzyme insertion/deletion (ACE I/D), and angiotensin II receptor 1 (AT1R) A1166C gene polymorphisms on the risk of hypertension among Hispanics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48783.RAR_FolBPWrvAUuariMyU62SB-xeGpKySHowU8D3Ed0VA130_provenance.
- NP48785.RAZioFWrvVPRpxpIcTauWMtPNKgBhNhG1y19oCds8xEuE130_assertion description "[Data on the association of the ACE I/D and AT1R A1166C polymorphisms with hypertension are conflicting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48785.RAZioFWrvVPRpxpIcTauWMtPNKgBhNhG1y19oCds8xEuE130_provenance.
- NP48793.RAT6BXFMMK_0tkn-EENpangAPohks1dB8DYIfLkNWYMcM130_assertion description "[Pharmacological effects of lipid-lowering drugs recapitulate with a larger amplitude the phenotypic effects of common variants within their target genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48793.RAT6BXFMMK_0tkn-EENpangAPohks1dB8DYIfLkNWYMcM130_provenance.
- NP48799.RAdLacV1cQHAkq4O8eO1kryjifnlPmYt7WqyAFxLpS5G4130_assertion description "[ An increasing number of risk alleles are associated with an elevated risk for CAD. An analysis of multiple polymorphisms, some several hundred, each with a small impact, may allow improved assessment of the individual genetic burden for CAD. Larger studies are needed to prove this hypothesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48799.RAdLacV1cQHAkq4O8eO1kryjifnlPmYt7WqyAFxLpS5G4130_provenance.
- NP48802.RATDnhT5-XN_eOsuym9Hj-CSPbdvT9-RvYZyM6F4OzsRY130_assertion description "[These results indicate that susceptibility to faster progression to ESRD is associated with the AT1R A1166C polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48802.RATDnhT5-XN_eOsuym9Hj-CSPbdvT9-RvYZyM6F4OzsRY130_provenance.
- NP48804.RAUH6kgUQSaWZ4s5h-vHWN9hHbApIRyzJ9l3--SpZzAHU130_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." NP48804.RAUH6kgUQSaWZ4s5h-vHWN9hHbApIRyzJ9l3--SpZzAHU130_provenance.
- NP48816.RAbUWCCA3Nq_YutFvWMs4xVjE-tj4WWbo9rCbHICQo3d8130_assertion description "[We studied the association between the M235T polymorphism of the angiotensinogen gene (AGT) and the C573T polymorphism of the angiotensin II type 1 receptor (AT1R) and blood pressure, carotid atherosclerosis and cerebrovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48816.RAbUWCCA3Nq_YutFvWMs4xVjE-tj4WWbo9rCbHICQo3d8130_provenance.
- NP48818.RAUOGOosnEnQGYam7dPURI1nHpDYG8hlx3XPjiOD-53eE130_assertion description "[These data suggest that genetic polymorphisms in the renin-angiotensin system are associated with renal phenotypes in the general population, but that many associations differ across racial/ethnic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48818.RAUOGOosnEnQGYam7dPURI1nHpDYG8hlx3XPjiOD-53eE130_provenance.
- NP48819.RAWKgLpNCagHHSFsW27ONbnTP323aeKDjYlUsQic9_g6M130_assertion description "[Common polymorphisms in genes responsible for vascular function, inflammation, and oxidative stress appear to modify associations between proximity to major roadways and LVM. Further understanding of how genes modify effects of air pollution on CVD may help guide research efforts into specific mechanistic pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48819.RAWKgLpNCagHHSFsW27ONbnTP323aeKDjYlUsQic9_g6M130_provenance.
- NP48820.RAQteye_yspaZq9VgFKJrV-tlFaipTgrLdjoVv3j0nrCE130_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." NP48820.RAQteye_yspaZq9VgFKJrV-tlFaipTgrLdjoVv3j0nrCE130_provenance.
- NP48821.RAWCEPN7jdnTKsIzu7yAggTx8QZOUWhit8MCOW-j7ob8o130_assertion description "[Polymorphisms of the renin-angiotensin system genes predict progression of subclinical coronary atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48821.RAWCEPN7jdnTKsIzu7yAggTx8QZOUWhit8MCOW-j7ob8o130_provenance.
- NP48822.RAT3cJtedaXxVH0_dM7gY2ePkYfkVSaMkOHZpsIKNH7BA130_assertion description "[Early sign of atherosclerosis in slow coronary flow and relationship with angiotensin-converting enzyme I/D polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48822.RAT3cJtedaXxVH0_dM7gY2ePkYfkVSaMkOHZpsIKNH7BA130_provenance.
- NP48828.RAf8a3hCGCfGsa2yuYMqXOWNDSEGRkId1og1jJxylKKYE130_assertion description "[ AT1R gene contributes to the development of essential hypertensive, but not to the incidence of BI in the hypertensive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48828.RAf8a3hCGCfGsa2yuYMqXOWNDSEGRkId1og1jJxylKKYE130_provenance.
- NP48835.RAbbV76TXlNdjsKiYYUVZ6jgSIyZUKT0luOZS3RoKN3LU130_assertion description "[Although there have been several association studies of angiotensin II type 1 receptor (AT1R, A/C1166) gene polymorphism in clinical endpoints such as myocardial infarction (MI), hypertension, aortic stiffness, and left ventricular mass, the relationship between AT1R polymorphism and biventricular function in acute anterior MI has not been studied before.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48835.RAbbV76TXlNdjsKiYYUVZ6jgSIyZUKT0luOZS3RoKN3LU130_provenance.
- NP48838.RAW1M_FS43s0sDvmBgh8BPZos2o8yhKktAsPupJw7Um9g130_assertion description "[The allelic frequencies of angiotensin II type I receptor C and angiotensin II type 2 receptor A were significantly higher in the acute myocardial infarction subjects than in the control subjects, and this tendency was more significant in the younger patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48838.RAW1M_FS43s0sDvmBgh8BPZos2o8yhKktAsPupJw7Um9g130_provenance.
- NP48842.RAUIo4iPAb8mVN7JL23gO3NCMbK_gQ73o7ulgjyJolNL0130_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." NP48842.RAUIo4iPAb8mVN7JL23gO3NCMbK_gQ73o7ulgjyJolNL0130_provenance.
- NP48843.RAYjUXHPocqbv9Hwhu4r72K2Jv1HaD3gZGd5kPAWgmJfE130_assertion description "[SNPs Met235Thr in angiotensinogen, T>C (-344) in aldosterone synthase, and G>A (-1903) in chymase genes are significantly associated with diabetic chronic renal insufficiency in Indian patients and warrant replication in larger sample sets. Use of such markers for prediction of susceptibility to diabetes specific renal disease in the ethnically Indian popula]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48843.RAYjUXHPocqbv9Hwhu4r72K2Jv1HaD3gZGd5kPAWgmJfE130_provenance.
- NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_assertion description "[ These results suggest that the AGT and AT1 receptor genes are not major genetic determinants of hypertension associated with NIDDM in this population, although we can not exclude the possibility that these loci make a minor contribution in a polygenic context.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_provenance.
- NP48847.RAbj-uQjdplx_X6C4r3XSE00CrPlH5z6uzYk47HhBYeBo130_assertion description "[The risk of diabetes due to thiazide use was not increased among AGTR1 1166 CC homozygous subjects and less increased among GNB3 T allele carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48847.RAbj-uQjdplx_X6C4r3XSE00CrPlH5z6uzYk47HhBYeBo130_provenance.
- NP48854.RAYj3Sx1C6vy-dPDJQ38_Men89ZWc4RafBAKwjYwAWy6c130_assertion description "[To investigate whether angiotensinogen(AGT) M235T, angiotensin II type I receptor(AT(1)R) gene A1166C and angiotensin converting enzyme(ACE) gene I/D polymorphism are implicated in human essential hypertension(HT) in Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48854.RAYj3Sx1C6vy-dPDJQ38_Men89ZWc4RafBAKwjYwAWy6c130_provenance.
- NP48867.RAbJS9vhVQdav9dBpxY1PowQGJNSegQVemv6MMyXVtS_4130_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." NP48867.RAbJS9vhVQdav9dBpxY1PowQGJNSegQVemv6MMyXVtS_4130_provenance.
- NP48873.RASEU_IBRauvGnrvOOXBoa7CfwB-pVBV9SYzl8Tx_jUVA130_assertion description "[It was found that specific gene combinations are involved in the CAS development and determine variation in the pathogenetically important quantitative traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48873.RASEU_IBRauvGnrvOOXBoa7CfwB-pVBV9SYzl8Tx_jUVA130_provenance.
- NP48887.RAW8U_eksnUhmhlEIN-8e4sTf-obl8uPxOD2xpLF2wLO0130_assertion description "[Susceptibility for ESRD and faster progression to ESRD are linked with the AGT genotype in diabetic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48887.RAW8U_eksnUhmhlEIN-8e4sTf-obl8uPxOD2xpLF2wLO0130_provenance.
- NP48890.RAdlqyo8mKUMk8Bus0i-zFEpS50UmTL4akgC5shK66Oqg130_assertion description "[Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48890.RAdlqyo8mKUMk8Bus0i-zFEpS50UmTL4akgC5shK66Oqg130_provenance.
- NP48892.RATHCSf8r8zBfII1qFHAITCqoZwaP6y-LsuFhOBOdCiyQ130_assertion description "[Endothelial nitric oxide synthase and angiotensinogen gene polymorphism in coronary artery diseases in Egypt.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48892.RATHCSf8r8zBfII1qFHAITCqoZwaP6y-LsuFhOBOdCiyQ130_provenance.
- NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_assertion description "[To investigate the role of haplotypes formed by these polymorphisms for angiotensinogen levels we examined blood pressure, coronary artery disease (CAD), myocardial infarction (MI), and AGT genotypes and haplotypes in 2,575 patients with angiographically documented CAD and 731 individuals in whom CAD had been ruled out by angiography.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance.
- NP48895.RAadfmlggydhKJc9aZxtPXUog-TO7GuW2Wc8_KAuqSxto130_assertion description "[The frequencies of ACE-DD genotype and ACE-D allele were much higher in DN(+) group than in DN (-) group (0.25 vs 0.05, 0.47 vs 0.29, respectively), so were the frequencies of TT genotype and T allele in AGT-M235T (0.73 vs 0.54, 0.85 vs 0.68, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48895.RAadfmlggydhKJc9aZxtPXUog-TO7GuW2Wc8_KAuqSxto130_provenance.
- NP48907.RAchb13wUQCNsyPRLQ3Zka1aJM2ZWshJuXIlWjkxl9nOk130_assertion description "[Our results suggest that in the Polish population the AT1R gene polymorphism might be associated with increased susceptibility to chronic renal diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48907.RAchb13wUQCNsyPRLQ3Zka1aJM2ZWshJuXIlWjkxl9nOk130_provenance.
- NP48911.RAWzdpMLwpq71yZylIgiFKNMtxPTR7ga8MDHIni0mXMMo130_assertion description "[Angiotensinogen M235T genotype predicts progression in chronic renal allograft dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48911.RAWzdpMLwpq71yZylIgiFKNMtxPTR7ga8MDHIni0mXMMo130_provenance.
- NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_assertion description "[ The high MetS prevalence in Oji-Cree adults, especially women, is consistent with their high risk of T2DM and CHD. Functional polymorphisms in three candidate genes for plasma lipoproteins and blood pressure were associated with MetS in adult Oji-Cree. Furthermore, several female adolescents met the adult MetS criteria, suggesting that the genesis of MetS begins in youth, especially among aboriginal females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_provenance.
- NP48917.RAdPjtpVtddQkEf_QYCSL1x5NaBmAAIZ3WzHTeuF4zkeg130_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." NP48917.RAdPjtpVtddQkEf_QYCSL1x5NaBmAAIZ3WzHTeuF4zkeg130_provenance.
- NP48928.RAUoKGUX8CFLtq8EcHz3hJXTrLALN9M_Q9-OjB87hTrcY130_assertion description "[, we found an association between the angiotensinogen variant 235T and preeclampsia as well as an interaction between the variant 235T and the two other genes studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48928.RAUoKGUX8CFLtq8EcHz3hJXTrLALN9M_Q9-OjB87hTrcY130_provenance.
- NP48932.RAZ_k8s36P5-kkR0HLL0lVJZTV0hzJ7_R7Zz4X7vxveO4130_assertion description "[The molecular variant M235T of the AGT gene is significantly associated with essential hypertension in this population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48932.RAZ_k8s36P5-kkR0HLL0lVJZTV0hzJ7_R7Zz4X7vxveO4130_provenance.
- NP48933.RAXc5pgpU39S43TtfP1oaFFCKX_sqmb8761L8HWnJB7y4130_assertion description "[To investigate whether angiotensinogen(AGT) M235T, angiotensin II type I receptor(AT(1)R) gene A1166C and angiotensin converting enzyme(ACE) gene I/D polymorphism are implicated in human essential hypertension(HT) in Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48933.RAXc5pgpU39S43TtfP1oaFFCKX_sqmb8761L8HWnJB7y4130_provenance.
- NP48934.RAcZSCMvpFgHyzyvdl63HE74jIpy7K5t4N9AzB1fsvvKA130_assertion description "[T+31C polymorphism of angiotensinogen gene and essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48934.RAcZSCMvpFgHyzyvdl63HE74jIpy7K5t4N9AzB1fsvvKA130_provenance.
- NP48937.RARplQau0xUAB0FG3UEyzaT7tZHPGbtayPpt_2AHv03h4130_assertion description "[Gender-dependent effect of ACE I/D and AGT M235T polymorphisms on the progression of urinary albumin excretion in Taiwanese with type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48937.RARplQau0xUAB0FG3UEyzaT7tZHPGbtayPpt_2AHv03h4130_provenance.
- NP48944.RAdgAGlU5cg4zgBm53ON4zM0VFlLKNBbCf-8yS6RDh2o4130_assertion description "[The independent risk conferred by genetic variants encoding pathways such as inflammation and lipid metabolism, not adequately reflected by conventional biomarkers, may identify high-risk individuals for intensified control of modifiable risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48944.RAdgAGlU5cg4zgBm53ON4zM0VFlLKNBbCf-8yS6RDh2o4130_provenance.
- NP48952.RAZB0KcAwCmC_gwi9pmN_ta3XBgDcIE_IGbt9CRfCeYPc130_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." NP48952.RAZB0KcAwCmC_gwi9pmN_ta3XBgDcIE_IGbt9CRfCeYPc130_provenance.
- NP48955.RAc6DzzWEKVcV0sQTc8gqKCPagjE5zWoGzZ2xGK1W9mxE130_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." NP48955.RAc6DzzWEKVcV0sQTc8gqKCPagjE5zWoGzZ2xGK1W9mxE130_provenance.
- NP48958.RAa0eXKNLLBfi3LivoDFJen8DJEV_xeZoIWDlNUDviH0Y130_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." NP48958.RAa0eXKNLLBfi3LivoDFJen8DJEV_xeZoIWDlNUDviH0Y130_provenance.
- NP48961.RAWKQNeB1AiP7C0GU70KaIWs2UrPx-L7HHpIZnPSh1AiY130_assertion description "[Association between an agouti-related protein gene polymorphism and anorexia nervosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48961.RAWKQNeB1AiP7C0GU70KaIWs2UrPx-L7HHpIZnPSh1AiY130_provenance.
- NP48962.RAYGyHnVUVA3PlIDtv9Ushea-Zui193NgJADtnw2PDUcQ130_assertion description "[Family trios analysis of common polymorphisms in the obestatin/ghrelin, BDNF and AGRP genes in patients with Anorexia nervosa: association with subtype, body-mass index, severity and age of onset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48962.RAYGyHnVUVA3PlIDtv9Ushea-Zui193NgJADtnw2PDUcQ130_provenance.
- NP48973.RATdDil8aeAfkMdSu37V57u32s3imZrq42ZNlLk6QBe1M130_assertion description "[Variants in the advanced glycosylation end product-specific receptor (AGER) gene have been associated with diabetic vasculopathy, however their role in the pathogenesis of insulin resistance and type 2 diabetes mellitus (T2DM) are uncertain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48973.RATdDil8aeAfkMdSu37V57u32s3imZrq42ZNlLk6QBe1M130_provenance.
- NP48976.RAe0P6rxryMXXD89Pt6ffAtdfUam2iWaGHk_pk57UeA8I130_assertion description "[To investigate the genotype of Arg389Gly polymorphism in beta(1)-adrenergic receptor gene(beta(1)-AR), Arg16Gly polymorphism in beta(2)-adrenergic receptor gene (beta(2)-AR) and Trp64Arg polymorphism in beta(3)-adrenergic receptor gene (beta(3)-AR) in the high risk population of hypertension and analyze the role of the genes in the pathogenesis of essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48976.RAe0P6rxryMXXD89Pt6ffAtdfUam2iWaGHk_pk57UeA8I130_provenance.
- NP48977.RAerDVoXz4XzUC2pwegVTQ8YAjTaiPybNxXo3wzHc_t94130_assertion description "[The thiazide-sensitive Na(+)-Cl(-) cotransporter gene, C1784T, and adrenergic receptor-beta3 gene, T727C, may be gene polymorphisms susceptible to the antihypertensive effect of thiazide diuretics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48977.RAerDVoXz4XzUC2pwegVTQ8YAjTaiPybNxXo3wzHc_t94130_provenance.
- NP48980.RATUf-KLF5ILKN2oEk28ZEDu1hjCFxqn6MRZmSf6nNSeA130_assertion description "[Genetic factors are relevant and independent determinants of antihypertensive drug effects in a multiracial population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48980.RATUf-KLF5ILKN2oEk28ZEDu1hjCFxqn6MRZmSf6nNSeA130_provenance.
- NP48987.RAU4sy5q9cQBUnx5k62Jj1FMzlobpupQIkPALu9J7VMPw130_assertion description "[Some studies indicate that the Trp64Arg polymorphism in the gene encoding the beta3-adrenergic receptor (ADRB3) is associated with obesity, insulin resistance and earlier onset of type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48987.RAU4sy5q9cQBUnx5k62Jj1FMzlobpupQIkPALu9J7VMPw130_provenance.
- NP48992.RAZiZRByBdHsJ818eMxj-HvLqpladrofQVG_zlNdVYdWI130_assertion description "[Mutation of beta 3-adrenergic-receptor gene and the response to dietary intervention in obese children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48992.RAZiZRByBdHsJ818eMxj-HvLqpladrofQVG_zlNdVYdWI130_provenance.
- NP48998.RAWUQ7WShd9VVY1CQEUMMrIJfCrxnC6zN5KTB0dYnUE7w130_assertion description "[Association of beta3-adrenergic receptor gene polymorphism with insulin resistance in Japanese-American men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48998.RAWUQ7WShd9VVY1CQEUMMrIJfCrxnC6zN5KTB0dYnUE7w130_provenance.
- NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_assertion description "[Variants located within the gene TCF7L2 are strongly associated with T2D but not with MS, providing support to previous evidence indicating that polymorphisms at the TCF7L2 gene increase T2D risk. In contrast, the non-synonymous ADRB3 rs4994 polymorphism is associated with T2D and MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance.
- NP49010.RAQdEkOQ3pKLCbUQpXjnJYSFbqUcaxOmk7rzrNtqiHLCg130_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." NP49010.RAQdEkOQ3pKLCbUQpXjnJYSFbqUcaxOmk7rzrNtqiHLCg130_provenance.
- NP49011.RAdxW1QRzrJVc7h4MB4revA4fr2t-Djont5prFBGAYCA4130_assertion description "[, genetic variation may modify the magnitude of the beneficial effects of PA on characteristics of the metabolic syndrome in persons with IGT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49011.RAdxW1QRzrJVc7h4MB4revA4fr2t-Djont5prFBGAYCA4130_provenance.
- NP49012.RAaB4JjFhAk7cjgGXNQJgUv7D2hZlukKel3Bj4ZGW9XwU130_assertion description "[The prevalence of the Arg allele of the Trp64Arg polymorphism in the beta3-adrenergic receptor gene may contribute to the susceptibility to endometrial cancer among obese/overweight individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49012.RAaB4JjFhAk7cjgGXNQJgUv7D2hZlukKel3Bj4ZGW9XwU130_provenance.
- NP49018.RAXej_2mEHR0EhxkL90aaGX6xQDFzB3hEb7HGMV8hyujU130_assertion description "[There was significant association between the C659G polymorphism of ADRB2 gene and essential hypertension in Xinjiang Kazakans suggesting a role of ADRB2 gene C659G polymorphism in the development of hypertension in Xinjiang Kazakans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49018.RAXej_2mEHR0EhxkL90aaGX6xQDFzB3hEb7HGMV8hyujU130_provenance.
- NP49022.RAV-6Yx8x8xgLDTTOLo3TEVhUmjqtnswLM2SsyD1qcs0w130_assertion description "[A46G and C79G polymorphisms in the 2-adrenergic receptor gene (ADRB2) and essential hypertension risk: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49022.RAV-6Yx8x8xgLDTTOLo3TEVhUmjqtnswLM2SsyD1qcs0w130_provenance.
- NP49028.RATcDHqPro3CUf7exg-68mc5ekdHLb8bRiIeqrJB7Lhrc130_assertion description "[Ile164 variant of beta2-adrenoceptor does not influence outcome in heart failure but may interact with beta blocker treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49028.RATcDHqPro3CUf7exg-68mc5ekdHLb8bRiIeqrJB7Lhrc130_provenance.
- NP49031.RAZpI2oCm14TghzYqGudaDf5pQaRYEhwA4JF8X7wRIX44130_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." NP49031.RAZpI2oCm14TghzYqGudaDf5pQaRYEhwA4JF8X7wRIX44130_provenance.
- NP49032.RAWAkFf4ABTkK7NbcaKj34MkUB9CPangSGt_L0mos1Qco130_assertion description "[ Patients prescribed beta-blocker therapy after an ACS have differential survival associated with their ADRB2 genotypes. Further assessment of the benefits of beta-blocker therapy in high-risk genotype groups may be warranted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49032.RAWAkFf4ABTkK7NbcaKj34MkUB9CPangSGt_L0mos1Qco130_provenance.
- NP49034.RAUAHhBJePWK3U1rMOjYklkzxGi8ekmXbDL_ngr8j6noI130_assertion description "[Beta-adrenergic receptor polymorphisms: cardiovascular disease associations and pharmacogenetics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49034.RAUAHhBJePWK3U1rMOjYklkzxGi8ekmXbDL_ngr8j6noI130_provenance.
- NP49037.RAbctxuEmeSAl_Vchm452xzrRk_YEJh-Z5tPjkZSmdFUA130_assertion description "[The study aimed to determine the association between these two ADRB2 SNPs, their haplotypes and the phenotypes in Thai asthmatic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49037.RAbctxuEmeSAl_Vchm452xzrRk_YEJh-Z5tPjkZSmdFUA130_provenance.
- NP49038.RAVn4Wh7U_7wXlWka2EaftboI7Hi-Q_ZsEGVXxD8EcMvs130_assertion description "[Fifty-three mild-to-moderate asthmatics were genotyped for four genetic polymorphisms of four genes: beta2-adrenergic receptor (ADRB2), adenylate cyclase 9 (ADCY9), neurokinin receptor 2 (NK2R) and T-box 21 (TBX21).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49038.RAVn4Wh7U_7wXlWka2EaftboI7Hi-Q_ZsEGVXxD8EcMvs130_provenance.
- NP49040.RAXCHYqwyTxpYOiSJPV8mV8MMhziVes4w5uArkqoNfTnw130_assertion description "[Asthmatic patients with the Arg/Arg genotype at codon 16 of ADRB2 achieve better asthma control with long-term regular use of combined budesonide and formoterol treatment, suggesting that the ADRB2 genotype may dictate choice of treatment strategy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49040.RAXCHYqwyTxpYOiSJPV8mV8MMhziVes4w5uArkqoNfTnw130_provenance.
- NP49041.RAZ1mcyZsy9A-lBe18ZtR32W5OiBDVpjalkCt38hwyAIk130_assertion description "[In subjects with persistent asthma, the ADRB2 Arg16Gly polymorphism does not alter lung function responses to SAL or FSC over the 12 hour dosing interval following acute and chronic dosing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49041.RAZ1mcyZsy9A-lBe18ZtR32W5OiBDVpjalkCt38hwyAIk130_provenance.
- NP49044.RAQoVfZojMxjYI2mpEekgxa9rQqpEmF2yNQQmnlzqdwTw130_assertion description "[In study 2, the frequency of asthma exacerbations (15 9% of 168 Gly/Gly, 13 8% of 169 Gly/Arg, and 6 9% of 67 Arg/Arg participants) and other study endpoints were closely similar for all ADRB2 genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49044.RAQoVfZojMxjYI2mpEekgxa9rQqpEmF2yNQQmnlzqdwTw130_provenance.
- NP49047.RAZDHy5s_OdrUIWIOCtm6_kfzYNuN7b0EdZEYDgcVF4ho130_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." NP49047.RAZDHy5s_OdrUIWIOCtm6_kfzYNuN7b0EdZEYDgcVF4ho130_provenance.
- NP49050.RAZGuFS5-w71aA4Pbv5-DbY0GUx781xfxwkW3NwMeKbgY130_assertion description "[TV watching modifies obesity risk linked to the 27Glu polymorphism of the ADRB2 gene in girls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49050.RAZGuFS5-w71aA4Pbv5-DbY0GUx781xfxwkW3NwMeKbgY130_provenance.
- NP49059.RAZg0Hbj09-VMgjAE6uTUCGuK0mnCj3jqRjny4tWC_VUI130_assertion description "[Beta(2)-adrenergic receptor gene variation and hypertension in subjects with type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49059.RAZg0Hbj09-VMgjAE6uTUCGuK0mnCj3jqRjny4tWC_VUI130_provenance.
- NP49060.RAXHvCsphnDsyWHlkfuSfNVZDH0bPjbRjM-sRB2JPxk0E130_assertion description "[The independent risk conferred by genetic variants encoding pathways such as inflammation and lipid metabolism, not adequately reflected by conventional biomarkers, may identify high-risk individuals for intensified control of modifiable risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49060.RAXHvCsphnDsyWHlkfuSfNVZDH0bPjbRjM-sRB2JPxk0E130_provenance.
- NP49067.RAcVeMWm7Jv1Thnkc1yCKMJOdN78x4uII3od1begxyAFM130_assertion description "[Relationship of beta2-adrenergic receptor polymorphism with obesity in type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49067.RAcVeMWm7Jv1Thnkc1yCKMJOdN78x4uII3od1begxyAFM130_provenance.
- NP49072.RATT65yZhvTYQ38SqrH3TwjEtI5M-TLv7-qQX-xhKDzwo130_assertion description "[these findings suggest that the genotypes and haplotypes of ADRB2 may influence parameters of the metabolic syndrome in Korean adolescents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49072.RATT65yZhvTYQ38SqrH3TwjEtI5M-TLv7-qQX-xhKDzwo130_provenance.
- NP49073.RAf0Kk-aEx7MzSqk_YA7BWuFvvllSteU1UXQQuoAzgyfU130_assertion description "[Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49073.RAf0Kk-aEx7MzSqk_YA7BWuFvvllSteU1UXQQuoAzgyfU130_provenance.
- NP49077.RAcaGkG2nJOesj5AhQ7h95je0SbzAGbaWa8WtEhib01xg130_assertion description "[ The polymorphism at position 27 was associated with decreased airway responsiveness in the study population and the polymorphism at position 16 was associated with increased wheeze during respiratory infection, but neither was associated with physician-diagnosed asthma or any of the other variables considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49077.RAcaGkG2nJOesj5AhQ7h95je0SbzAGbaWa8WtEhib01xg130_provenance.
- NP49079.RAX_l1ITtt4Zztl6ZOXOH7B-vknrutMDAx-tpUymUCdbk130_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." NP49079.RAX_l1ITtt4Zztl6ZOXOH7B-vknrutMDAx-tpUymUCdbk130_provenance.
- NP49085.RAfVe5ncvuiQpZ4j7LfWwai_Tm_LRw8Jfewiud3ommj-g130_assertion description "[Our data suggest that individuals homozygous for the Arg389 allele of the beta(1)-adrenergic receptor gene are at increased risk to develop hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49085.RAfVe5ncvuiQpZ4j7LfWwai_Tm_LRw8Jfewiud3ommj-g130_provenance.
- NP49087.RAQ821iUUBd2S8H_YsvQ7QC649K-v8B5VfCnOfw3A2u4A130_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." NP49087.RAQ821iUUBd2S8H_YsvQ7QC649K-v8B5VfCnOfw3A2u4A130_provenance.
- NP49088.RAQY2gqhhNGOrgy7Y2_HUJAy9xK8VV-M2_F9itt5akKjA130_assertion description "[Genetic factors are relevant and independent determinants of antihypertensive drug effects in a multiracial population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49088.RAQY2gqhhNGOrgy7Y2_HUJAy9xK8VV-M2_F9itt5akKjA130_provenance.
- NP49089.RAW0dkR0im2Y3UKPAZcQBN3qLJ-tL2q_m3Quyqg7w1B0U130_assertion description "[A total of 226 patients with end-stage HF (ejection fraction 35%) were genotyped for the two (1)AR SNPs and the three (2)AR SNPs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49089.RAW0dkR0im2Y3UKPAZcQBN3qLJ-tL2q_m3Quyqg7w1B0U130_provenance.
- NP49092.RAQMt_3hD9k2G4a3ZHQ6qgUIRal4vg1pJFJ8GW2V8ICNM130_assertion description "[We tested the hypothesis that polymorphisms at codons 389 (Arg389Gly) and 49 (Ser49Gly) of the beta(1)-adrenergic receptor would be associated with differences in initial tolerability of beta-blocker therapy in patients with heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49092.RAQMt_3hD9k2G4a3ZHQ6qgUIRal4vg1pJFJ8GW2V8ICNM130_provenance.
- NP49095.RAXimQySjZwC3uv8NXLPKDsoccExjbHa7-UhIQXVhw4bo130_assertion description "[Role of beta adrenergic receptor polymorphisms in heart failure: systematic review and meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49095.RAXimQySjZwC3uv8NXLPKDsoccExjbHa7-UhIQXVhw4bo130_provenance.
- NP49097.RAao0yOu4pcXgmLnfQNsIszo39loj0TWxdaN8_xbMGOuI130_assertion description "[A novel missense mution in the beta(1)-adrenergic receptor gene was associated with a decreased mortality risk in patients with congestive heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49097.RAao0yOu4pcXgmLnfQNsIszo39loj0TWxdaN8_xbMGOuI130_provenance.
- NP49098.RAf8DVhSAEGWITzaPC44yRLZ1__Y6h0vfyfhgLMa25qdU130_assertion description "[To evaluate the effect of ADRB1 Arg389Gly (1165 CG), Ser49Gly (145 AG), and ADRB2 Gly16Arg (46 GA), Gln27Glu (79 CG) genotypes on survival among patients discharged with prescribed beta-blockers after an acute coronary syndrome (ACS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49098.RAf8DVhSAEGWITzaPC44yRLZ1__Y6h0vfyfhgLMa25qdU130_provenance.