Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP52835.RAr8k_w2QF56Hq8e8dVLZe7xcRZNeox419yICS-rCLAds130_assertion description "[Alanine for proline substitution in the peroxisome proliferator-activated receptor gamma-2 (PPARG2) gene and the risk of incident myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52835.RAr8k_w2QF56Hq8e8dVLZe7xcRZNeox419yICS-rCLAds130_provenance.
- NP52840.RAhSh7lqmcNGlaBM_gXVoAhe0HGSe-HB9KIa7Dx870n7o130_assertion description "[ In MS, CC genotype was prone to lesion of carotid artery, but CT + TT may reduce lesion of carotid artery, which implicates that PPAR gamma C161-T may play a important role in carotid artery arteriosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52840.RAhSh7lqmcNGlaBM_gXVoAhe0HGSe-HB9KIa7Dx870n7o130_provenance.
- NP52848.RAm7-ZZ_84y0SSgdgf_3fj5rhjyHxG01jzRVMf8f_fcLM130_assertion description "[In the monogenic analysis, only the peroxisome proliferator-activated receptor delta (PPARD) gene was associated with obesity (OR = 1.43 1.04-1.97, p = 0.027).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52848.RAm7-ZZ_84y0SSgdgf_3fj5rhjyHxG01jzRVMf8f_fcLM130_provenance.
- NP52849.RAs1bjJL19ERowH-rdTuYq95Q465JYbMY45x8GHOmBB2M130_assertion description "[DNA from blood collected in 1989 was genotyped for 16 SNPs in 8 obesity-related genes: monoamine oxidase A (MAOA), lipoprotein lipase (LPL), paraoxonase 1 and 2 (PON1 and PON2), leptin receptor (LEPR), tumor necrosis factor-alpha (TNFalpha), and peroxisome proliferative activated receptor-gamma and -delta (PPARG and PPARD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52849.RAs1bjJL19ERowH-rdTuYq95Q465JYbMY45x8GHOmBB2M130_provenance.
- NP52855.RAqxNib5yIpJr4KlBE53SEXq2LgCgdZIxmzWM6kP6PNUM130_assertion description "[Our results suggest that POU2F1 is a candidate gene for AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52855.RAqxNib5yIpJr4KlBE53SEXq2LgCgdZIxmzWM6kP6PNUM130_provenance.
- NP52858.RAlPkkRFDoEetdk2vMceeaE_EjPj36AAV_NTfrhlEBItY130_assertion description "[A PON3 SNP (A99A) was identified and the effect of these four PON SNPs on HDL levels and CHD risk was examined in the prospective Northwick Park Heart Study II (NPHSII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52858.RAlPkkRFDoEetdk2vMceeaE_EjPj36AAV_NTfrhlEBItY130_provenance.
- NP52868.RAhk19XJu8Iz2b5LBIgNBU1y4cxZF3dtAStE_RJUpOsOc130_assertion description "[Interactions and associations of paraoxonase gene cluster polymorphisms with myocardial infarction in a Pakistani population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52868.RAhk19XJu8Iz2b5LBIgNBU1y4cxZF3dtAStE_RJUpOsOc130_provenance.
- NP52870.RAq7yLh0iVf3FVRygdcLesh6h7kPrIWDWckz9muaIJLT0130_assertion description "[In this study, we investigated the relationship between the C311S PON2 polymorphism and the prognosis of acute myocardial infarction (AMI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52870.RAq7yLh0iVf3FVRygdcLesh6h7kPrIWDWckz9muaIJLT0130_provenance.
- NP52876.RArrr_0dDacsKenR1Lx1M23NjztMam9lKdzPZSJb-aykg130_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." NP52876.RArrr_0dDacsKenR1Lx1M23NjztMam9lKdzPZSJb-aykg130_provenance.
- NP52878.RAl8ivZJCXY713e1w6S5gmd5v6qhikOmytsHROqz3rxzI130_assertion description "[Eleven polymorphisms of PON1, PON2 and PON3 gene were investigated for association with CHD in 474 male patients and 475 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52878.RAl8ivZJCXY713e1w6S5gmd5v6qhikOmytsHROqz3rxzI130_provenance.
- NP52879.RAtqU38Bn1uxzDv8Mdx1eIjKhQB0TEy8ps9yo-Ej6kE_M130_assertion description "[In contrast to traditional coronary risk factors, the PON1 M/L mutation can be considered predictive of protection against CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52879.RAtqU38Bn1uxzDv8Mdx1eIjKhQB0TEy8ps9yo-Ej6kE_M130_provenance.
- NP52885.RApt_eIU74pMPVk3UiXdDLISnD7HqnuJfBxBVpMONhMrU130_assertion description "[Polymorphisms in the PON gene cluster are associated with Alzheimer disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52885.RApt_eIU74pMPVk3UiXdDLISnD7HqnuJfBxBVpMONhMrU130_provenance.
- NP52892.RAr8ZDG_6BXTHab6XHyQe6Jbg4C3oeWViSLK9RApHQrTs130_assertion description "[Although advances have been made in research into the paraoxonase family and atherosclerosis, much more needs to be done.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52892.RAr8ZDG_6BXTHab6XHyQe6Jbg4C3oeWViSLK9RApHQrTs130_provenance.
- NP52899.RAlQw28eOvSOlwuG_PwNWMnVVNhsLPW68LR96jE6Z8L-A130_assertion description "[Results from this research that both PON2148 polymorphism and PON2311 polymorphism in neonates are significantly associated with preterm respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52899.RAlQw28eOvSOlwuG_PwNWMnVVNhsLPW68LR96jE6Z8L-A130_provenance.
- NP52907.RAvWt1Ea5DCjtsH3tKDBtg9ZAd8PX6Q-rSX6mcdGR-uXA130_assertion description "[The data show a large variability in allele frequencies, and, in particular, that PON1 allele distribution depends on membership to different geographic populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52907.RAvWt1Ea5DCjtsH3tKDBtg9ZAd8PX6Q-rSX6mcdGR-uXA130_provenance.
- NP52909.RAlvZ1ggD6Da4roB39f-lj48Hqxoge4Yqfxin-1SRYe98130_assertion description "[Genetic determinants of plasma HDL-cholesterol levels in familial hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52909.RAlvZ1ggD6Da4roB39f-lj48Hqxoge4Yqfxin-1SRYe98130_provenance.
- NP52910.RAvaSmHX0vYZSqYOVAAovf0q5r4Rynzkx-P3lUFLgK1WM130_assertion description "[Lipid profile, markers of LDL resistance to in vitro oxidation (lag-phase, oxidation rate and thiobarbituric acid-reactive substances), vitamin E content in LDL, PON1 activity and genotypes in both HCh and control subjects were determined at baseline.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52910.RAvaSmHX0vYZSqYOVAAovf0q5r4Rynzkx-P3lUFLgK1WM130_provenance.
- NP52919.RAuptuXpjG0sUb4U08HFOJ-v80Vt5yL9EPiHidZhzLp78130_assertion description "[We examined risk of multiple myeloma (MM) associated with variants in genes involved in metabolism and response to exogenous chemicals cytochrome P450 enzymes (CYP1B1, CYP2C9), epoxide hydrolase (EPHX1), paraoxonase 1 (PON1), arylhydrocarbon hydroxylase receptor (AHR), and NAD(P)H:quinone oxidoreductase (NQO1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52919.RAuptuXpjG0sUb4U08HFOJ-v80Vt5yL9EPiHidZhzLp78130_provenance.
- NP52929.RAgEs-706sX6j-aNRgILw1xdZZCxcvLbR67NL2s8LxYsk130_assertion description "[This study demonstrates that PON L55 homozygosity is an independent risk factor for autopsy-verified atherosclerosis in Finns.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52929.RAgEs-706sX6j-aNRgILw1xdZZCxcvLbR67NL2s8LxYsk130_provenance.
- NP52930.RAqo3EpHaM3KYBvlMC5ckcaH6FfLisjXseK7nS2wUhm8s130_assertion description "[We evaluated whether PON1 gene haplotypes influence the metabolic disturbances, presence of subclinical atherosclerosis, and virologic outcome associated with the infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52930.RAqo3EpHaM3KYBvlMC5ckcaH6FfLisjXseK7nS2wUhm8s130_provenance.
- NP52932.RAh50ytKq9CWxm5jjo8MUlWenhw_jQTEMiHq9E49VOQpo130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52932.RAh50ytKq9CWxm5jjo8MUlWenhw_jQTEMiHq9E49VOQpo130_provenance.
- NP52934.RAlFxpkUYSmc5mhGnb24Za7TPxQuSWzwislxkoow2ZHb8130_assertion description "[ There was a significant association between PON1 A632G polymorphism and MVA as well as VSA, but the impact of this on VSA and MVA is different in the Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52934.RAlFxpkUYSmc5mhGnb24Za7TPxQuSWzwislxkoow2ZHb8130_provenance.
- NP52935.RAn3nbNX3ZDy842Ku3obJoYydyzxaGRoi6uAhyyGNKb40130_assertion description "[The alpha-adducin 460trp variant (OR 0.73, 95% CI 0.59-0.91, P=0.006) and the cholesteryl ester transfer protein -629A variant (OR 0.82, 95% CI 0.68-0.97, P=0.025) were both associated with a significant protective effect on MI, as was the paraoxonase 1/paraoxonase 2 haplotype comprising met55 and gln192 in paraoxonase 1 and cys311 in paraoxonase 2 (OR 0.52, 95% CI 0.39-0.77, P=0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52935.RAn3nbNX3ZDy842Ku3obJoYydyzxaGRoi6uAhyyGNKb40130_provenance.
- NP52937.RAt5VBDpif5yFokx4arnBS3zS7W2FHuUtyRjxqLphyj1Q130_assertion description "[The risk of MI increases with advancing age, principally among subjects carrying the low-activity QQ genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52937.RAt5VBDpif5yFokx4arnBS3zS7W2FHuUtyRjxqLphyj1Q130_provenance.
- NP52938.RAhU-hRniGlVQaPLCXg7df9nS-OoVOeo4Ywdmq8f1QI0o130_assertion description "[PON1 polymorphism, diabetes mellitus, obesity, and risk of myocardial infarction: Modifying effect of diabetes mellitus and obesity on the association between PON1 polymorphism and myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52938.RAhU-hRniGlVQaPLCXg7df9nS-OoVOeo4Ywdmq8f1QI0o130_provenance.
- NP52942.RAuijyQdIRbbEhligLx__TClatXVrhNRs9A-vkJWfCKxw130_assertion description "[Association between paraoxonase-1 and paraoxonase-2 polymorphisms and the risk of acute myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52942.RAuijyQdIRbbEhligLx__TClatXVrhNRs9A-vkJWfCKxw130_provenance.
- NP52945.RAmIos1qSLJC6nrlPNHwjFVxRS2sRfTXMCFTXCVbtBtDY130_assertion description "[Gene polymorphisms of PON1 55 Met/Leu, PON2 148 Ala/Gly and MnSOD 9 Ala/Val seemed to involve in the morbidity of CHD by influencing the plasma activities of PON and MnSOD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52945.RAmIos1qSLJC6nrlPNHwjFVxRS2sRfTXMCFTXCVbtBtDY130_provenance.
- NP52950.RAuXNzk8fmbcos7i423zjyyT2mvgKtbChwI8ZxB2GpzwI130_assertion description "[There is no robust evidence that the PON1 Q192R polymorphism is associated with CHD risk in Caucasian women or men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52950.RAuXNzk8fmbcos7i423zjyyT2mvgKtbChwI8ZxB2GpzwI130_provenance.
- NP52952.RAl2HOIV6Dh95PIdRzpJ8S2_t6VsdvCmB5LFhrgB5XIXY130_assertion description "[Three polymorphisms in the PON1 (Leu55Met and Gln192Arg) and PON2 (Ser311Cys) genes have been shown to be associated with the risk of CAD in several European or European-derived populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52952.RAl2HOIV6Dh95PIdRzpJ8S2_t6VsdvCmB5LFhrgB5XIXY130_provenance.
- NP52953.RAu0HLoVLAB7TDOTpuc2k-ZuOMLXh7ogWJlD-2PQ_W1c4130_assertion description "[Published data on the association between paraoxonase1 (PON1) polymorphisms and coronary heart disease (CHD) have yielded controversial results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52953.RAu0HLoVLAB7TDOTpuc2k-ZuOMLXh7ogWJlD-2PQ_W1c4130_provenance.
- NP52955.RAqzELQgRD4LTkVN4gW5VXsF5qbTl5KE2BhOUsSqjL988130_assertion description "[ The PON1 102V allele appears to be associated with an increased risk for prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52955.RAqzELQgRD4LTkVN4gW5VXsF5qbTl5KE2BhOUsSqjL988130_provenance.
- NP52957.RAgYKoOkhEcix8N6QBLMTc9fy3UsIhLUI9nA5znoCg6yU130_assertion description "[Multiple logistic regression analysis with forward stepwise selection involving the PON1-192R allele and the environmental risk factors revealed that the most predictive independent risk factor for coronary spasm was the PON1-192R allele (significance=0.0016, OR=2.52), followed by cigarette smoking (significance=0.0007, OR=2.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52957.RAgYKoOkhEcix8N6QBLMTc9fy3UsIhLUI9nA5znoCg6yU130_provenance.
- NP52958.RAh91jspP5R8EMJ4U9Dkqpp7H8s2vFNBS2Mw0d7f_o8GI130_assertion description "[There was no difference in the prevalence of the PON1-R allele between those with early- or late-onset CAD (46.0% vs. 52.7%; p = 0.25).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52958.RAh91jspP5R8EMJ4U9Dkqpp7H8s2vFNBS2Mw0d7f_o8GI130_provenance.
- NP52967.RAm-dt7h5dEJFeYbuQl05_qDluQ-nc-loUtgjrnncHbaU130_assertion description "[Association between the paraoxonase-1 192Q>R allelic variant and coronary endothelial dysfunction in patients with early coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52967.RAm-dt7h5dEJFeYbuQl05_qDluQ-nc-loUtgjrnncHbaU130_provenance.
- NP52968.RAsOh1iT3HHvXZODQpeK3MasOE_1FCQ8CTC1-0RAOII4s130_assertion description "[Here, we report previously nonperceived interrelationships between expression variations and nucleotide polymorphisms of the chromosome 7q21-22 acetylcholinesterase-paraoxonase 1 (ACHE-PON1) locus with the trait- and state-anxiety measures of 461 healthy subjects from the Health, Risk Factors, Exercise Training, and Genetics Family Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52968.RAsOh1iT3HHvXZODQpeK3MasOE_1FCQ8CTC1-0RAOII4s130_provenance.
- NP52971.RAoyvk659dBJGyEvEqm_cLdcXvYpGggin-5c81reRpTY8130_assertion description "[These findings suggest that the PON1 -107T allele is independently associated with the risk of AIS, in addition to interacting with and potentiating the risk conferred by the Q192R polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52971.RAoyvk659dBJGyEvEqm_cLdcXvYpGggin-5c81reRpTY8130_provenance.
- NP52972.RAiXBu4R7VlwHlpulPEWNbVzf27aqPlYzIzuQD5lf4Zys130_assertion description "[In conclusion, PON1 genetic variations are associated with risk factors, severity, type and prognosis of stroke and oxidative stress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52972.RAiXBu4R7VlwHlpulPEWNbVzf27aqPlYzIzuQD5lf4Zys130_provenance.
- NP52973.RAgXqN36BCRgkxuJdcZnaMBNKUb1tQs5ixn-_nAp13JL8130_assertion description "[Mutations of genes encoding for endogenous modulators of the cholinergic system should merit further investigation as prognostic indicators of individual response to treatment in AD subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52973.RAgXqN36BCRgkxuJdcZnaMBNKUb1tQs5ixn-_nAp13JL8130_provenance.
- NP52974.RApCaScX4we5TjJ7da36RHXiqeS17eSbiYqyTTU5Ix4qw130_assertion description "[Polymorphisms in the PON gene cluster are associated with Alzheimer disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52974.RApCaScX4we5TjJ7da36RHXiqeS17eSbiYqyTTU5Ix4qw130_provenance.
- NP52976.RAjmCFWRAivgdcz9TKg2uTUW1J35Yo946NvoZL17kXdkc130_assertion description "[Our results indicate that Gln192Arg polymorphism in PON1 gene is associated with AD and PON1 R allele might be a protective factor for AD in Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52976.RAjmCFWRAivgdcz9TKg2uTUW1J35Yo946NvoZL17kXdkc130_provenance.
- NP52977.RAo0khvctNx8qObs8fmI4KccM2Pcey3YGChBel4cbmpg8130_assertion description "[Our results indicate that Gln192Arg polymorphism in the PON1 gene is associated with AD, and PON1 R allele might be a protective factor for AD in a Chinese Han ethnic population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52977.RAo0khvctNx8qObs8fmI4KccM2Pcey3YGChBel4cbmpg8130_provenance.
- NP52979.RAp3C_TIwbyVI9OTDUOfhuj-YFTqQSJJ-0wulyG1DqI9U130_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." NP52979.RAp3C_TIwbyVI9OTDUOfhuj-YFTqQSJJ-0wulyG1DqI9U130_provenance.
- NP52988.RAm2A_5Ze1oY9VzgkNBBbiu1v2djw7R7b0OnVlnVBDNh4130_assertion description "[ This association study suggested that lower plasma PON1 activity increased the risk of CHD in Chinese women, which may be mediated by the higher frequency of -107T allele in cases. Haplotype analyses indicated that there might be some synergistic effects between the PON1 -107C > T and PON2 S311C polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52988.RAm2A_5Ze1oY9VzgkNBBbiu1v2djw7R7b0OnVlnVBDNh4130_provenance.
- NP52998.RApc2G9XLIAy7tyeYqzPbATUi5rtVqgNsjT9Quh5IFP0c130_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." NP52998.RApc2G9XLIAy7tyeYqzPbATUi5rtVqgNsjT9Quh5IFP0c130_provenance.
- NP53004.RAo20ZlBb-8u8n8YiZ54l9Pae_2HLF2R_Ck_cqpDIKKgs130_assertion description "[Our results suggest that the M54L and Q192R polymorphisms are not major risk factors for PD in the Finnish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53004.RAo20ZlBb-8u8n8YiZ54l9Pae_2HLF2R_Ck_cqpDIKKgs130_provenance.
- NP53009.RAukV_EpsuYPYk3H05dBvgrWZ1HEhrxIcI10ZWKM03Yec130_assertion description "[The increase in risk we observed among PON1-55 variant carriers for specific organophosphates metabolized by PON1 underscores the importance of considering susceptibility factors when studying environmental exposures in Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53009.RAukV_EpsuYPYk3H05dBvgrWZ1HEhrxIcI10ZWKM03Yec130_provenance.
- NP53011.RAlbf48YmSLICAPLCUHqGAFih6vFcor01pzu7Wr9bLDK0130_assertion description "[ The changes in antioxidant status after tomato juice consumption seem to depend on the PON1-192 genotype. Healthy elderly, carrying the R-allele, could specifically reduce their higher cardiovascular risk by changing dietary habits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53011.RAlbf48YmSLICAPLCUHqGAFih6vFcor01pzu7Wr9bLDK0130_provenance.
- NP53014.RAmeOU2f6phgGQ5jQbOJmjsEDdz_mzeQePHx-MSK_UzD0130_assertion description "[We postulate that lower than expected PON1 enzyme activity within specific genotypes might explain the reported association between R and L alleles and the risk of developing AIS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53014.RAmeOU2f6phgGQ5jQbOJmjsEDdz_mzeQePHx-MSK_UzD0130_provenance.
- NP53015.RAiPkWOQTDxfjzwYsVl-3QRztRTI-sTp4bYM1E9JEKVlQ130_assertion description "[Paraoxonase 1 gene polymorphisms and dementia in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53015.RAiPkWOQTDxfjzwYsVl-3QRztRTI-sTp4bYM1E9JEKVlQ130_provenance.
- NP53017.RAsccrZ5CaDcu3AL9kJ41Mt7-MpaY3ruHFogAMZYzDfnU130_assertion description "[Paraoxonase activity and paraoxonase 1 gene polymorphism in patients with uremia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53017.RAsccrZ5CaDcu3AL9kJ41Mt7-MpaY3ruHFogAMZYzDfnU130_provenance.
- NP53019.RAjuM04A0rebSmNH8voI6cbsPHpBKlJ-wIpw3gyUnEPDk130_assertion description "[In conclusion, PON 1 (LL+ML) 55 but not PON 1 (Q/R) 192 or PON 2 (S/C) 311, appears to be an independent risk factor for increased carotid IMT i middle-aged women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53019.RAjuM04A0rebSmNH8voI6cbsPHpBKlJ-wIpw3gyUnEPDk130_provenance.
- NP53021.RAnzuYLHmys5ZU3CC3nW7eg3If3_vJSnxyP7aHnFpMOoY130_assertion description "[Paraoxonase-1 55/192 genotypes in schizophrenic patients and their relatives in Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53021.RAnzuYLHmys5ZU3CC3nW7eg3If3_vJSnxyP7aHnFpMOoY130_provenance.
- NP53025.RAsu_moymNjDgonIUJtjqQtPVnuwnmoB1Yv8cLgGOTB2E130_assertion description "[This study provides direct evidence for a mechanistic link between genetic determinants and activity of PON1 with systemic oxidative stress and prospective cardiovascular risk, indicating a potential mechanism for the atheroprotective function of PON1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53025.RAsu_moymNjDgonIUJtjqQtPVnuwnmoB1Yv8cLgGOTB2E130_provenance.
- NP53027.RAtm75FvZ6MLhYSbk-5jp0syqxmBvhkpP_F6byZSuK0zE130_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." NP53027.RAtm75FvZ6MLhYSbk-5jp0syqxmBvhkpP_F6byZSuK0zE130_provenance.
- NP53032.RApx_J6UMRH12rxReFtCMBwHR_G_JVT8HNOAS5IJW2Jh4130_assertion description "[An insertional polymorphism of the proopiomelanocortin gene is associated with fasting insulin levels in childhood obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53032.RApx_J6UMRH12rxReFtCMBwHR_G_JVT8HNOAS5IJW2Jh4130_provenance.
- NP53033.RAsbiuVCWtQvMXSOR1H7FiVBW6GTksqz2Vv3E6q0ozPHk130_assertion description "[To acquire more information relative to the course of obesity in conditions of food restriction in subjects carrying mutations in the melanocortin signaling pathway, 710 obese children (mean age: 9.5+/-2.1 yr; mean z-score body mass index: 3.63+/-1.6) were genotyped for the proopiomelanocortin (POMC) R236G substitution, a variant which has been associated to early onset obesity, by restriction fragment length polymorphism (RFLP) analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53033.RAsbiuVCWtQvMXSOR1H7FiVBW6GTksqz2Vv3E6q0ozPHk130_provenance.
- NP53036.RAukb_euMdB5Wb5Q-RhKyazhzlR_bB4HgcrJd-9vpCnRA130_assertion description "[In the present study, we therefore focused on dietary composition as a specific trait related to obesity and we determined whether genetic variations in leptin (LEP), LEP receptor (LEPR), adiponectin (ADIPOQ), IL-6 and pro-opiomelanocortin (POMC) underlie specific native food preferences and obesity-related anthropometric parameters.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53036.RAukb_euMdB5Wb5Q-RhKyazhzlR_bB4HgcrJd-9vpCnRA130_provenance.
- NP53051.RAqLhcGUqgoBGe8rp-kgJOAvsh95ZQjoqJ2x7vHzWge4E130_assertion description "[Our results demonstrate that POLG mutations account for a substantial proportion of patients (13%) with PEO and multiple mitochondrial DNA deletions and cause both clinically and genetically heterogeneous disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53051.RAqLhcGUqgoBGe8rp-kgJOAvsh95ZQjoqJ2x7vHzWge4E130_provenance.
- NP53065.RAlGXFy_X2uWPuJpzWdMdNFUbUmVEgVGL-k6H2f804Bu4130_assertion description "[Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53065.RAlGXFy_X2uWPuJpzWdMdNFUbUmVEgVGL-k6H2f804Bu4130_provenance.
- NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_assertion description "[ Intronic variants of the PLTP gene are significantly associated with obesity-related phenotypes. Considering the number and the relevance of candidate genes surrounding the PLTP locus and the absence of missense polymorphisms in the coding region, the associations could be mediated by a second gene allele in linkage disequilibrium with the marker locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_provenance.
- NP53069.RAqwV03Ia5hVwJdVxzD8PFMyjAZnnqLEuAf4FG1P2zgBY130_assertion description "[No associations between PLIN haplotypes and obesity risk were found in Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53069.RAqwV03Ia5hVwJdVxzD8PFMyjAZnnqLEuAf4FG1P2zgBY130_provenance.
- NP53075.RAhMv5pWZvcrvXPqNGBiAq0O5wDdo3HGJboXNu6aCajvU130_assertion description "[Association between mutation of phospholamban gene and dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53075.RAhMv5pWZvcrvXPqNGBiAq0O5wDdo3HGJboXNu6aCajvU130_provenance.
- NP53082.RAmLUVQOZAMftMmU2zzcloG5mkDtAkvRZumjehWy0chNI130_assertion description "[PLEKHA1-LOC387715-HTRA1 polymorphisms and exudative age-related macular degeneration in the French population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53082.RAmLUVQOZAMftMmU2zzcloG5mkDtAkvRZumjehWy0chNI130_provenance.
- NP53086.RAg6yibS8VuhBi_uxoN1NWtnh2QpRm61Hean9s1xk0rqU130_assertion description "[We conclude that neither gene accounts for the association signal we previously observed. As these are the only clear cut functional candidate genes in the region, identification of the putative susceptibility locus for RD on 15q will require more methodical non-hypothesis driven positional cloning approaches.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53086.RAg6yibS8VuhBi_uxoN1NWtnh2QpRm61Hean9s1xk0rqU130_provenance.
- NP53088.RAj2DOF8QQZtt39pROQeSeZjhPOnOVVK6N_SD-xTBnQ9k130_assertion description "[When analyzed according to presence or absence of different dinucleotide alleles, a PLCG1-8 repeat was more frequent among lithium responders vs controls. In line with Turecki et al., we also noticed a moderately over-representation of the PLCG1-5 repeat among the bipolar patients as compared to the controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53088.RAj2DOF8QQZtt39pROQeSeZjhPOnOVVK6N_SD-xTBnQ9k130_provenance.
- NP53089.RAgf1F6lgXyh1pr6Ui7Q1FNfxdF26FUgyn7zNwOSZgKPo130_assertion description "[ These findings generally do not support the hypothesis that genes associated with a prothrombotic state are risk factors among a subgroup of young people with stroke of undetermined cause. Except for the D tissue plasminogen activator allele, the findings also indicated that these genetic factors are unrelated, or only weakly related, to all ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53089.RAgf1F6lgXyh1pr6Ui7Q1FNfxdF26FUgyn7zNwOSZgKPo130_provenance.
- NP53090.RArxo-nNeaqomAgvHUBPouKAorM5EVXxEbj5mrC3sMGjc130_assertion description "[ The TPA -7351C/T polymorphism is an independent risk factor for lacunar stroke. The findings suggest that impaired fibrinolysis may play a role in the pathogenesis of lacunar stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53090.RArxo-nNeaqomAgvHUBPouKAorM5EVXxEbj5mrC3sMGjc130_provenance.
- NP53092.RAiIWczrYXeYQhQs09ssxFWllS4Nj8faXzaagWomIitd8130_assertion description "[Regulatory polymorphisms in extracellular matrix protease genes and susceptibility to rheumatoid arthritis: a case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53092.RAiIWczrYXeYQhQs09ssxFWllS4Nj8faXzaagWomIitd8130_provenance.
- NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_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." NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_provenance.
- NP53097.RAqiAeKf8RITKnEQEyEW1HLReTuOouaeNzLJry49jvL5Q130_assertion description "[Tissue-type plasminogen activator -7,351C/T enhancer polymorphism is associated with a first myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53097.RAqiAeKf8RITKnEQEyEW1HLReTuOouaeNzLJry49jvL5Q130_provenance.
- NP53100.RAueLsXxmvh-ax0Ily2DDW4vcAN-wfcErgFiLGUgYUJTw130_assertion description "[the ADAMDEC 1 haplotype may indicate an underlying mechanism for high FVIII levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53100.RAueLsXxmvh-ax0Ily2DDW4vcAN-wfcErgFiLGUgYUJTw130_provenance.
- NP53103.RAs5TWO6774jAhYkW_X-SjNGl8Z9oUiLSfDhhq5nrt61I130_assertion description "[This study was designed to investigate associations of t-PA and PAI-1 genes with clinical features of the patients with bleeding gastric ulcers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53103.RAs5TWO6774jAhYkW_X-SjNGl8Z9oUiLSfDhhq5nrt61I130_provenance.
- NP53111.RAktr6Bze5js85dnFkrX4rnAv-zp1962z5YVQFn-On5qY130_assertion description "[Schizophrenia: an association study targets phospholipase A2 genes as potential sites of susceptible genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53111.RAktr6Bze5js85dnFkrX4rnAv-zp1962z5YVQFn-On5qY130_provenance.
- NP53116.RAr6YrKB_O4Jh9_1NKXMj-D3PzMtB4wVEuZECvDAj3Uy0130_assertion description "[ The genetic mutation of plasma PAF-AH gene appear to be an independent risk factor for AAA. Our findings need to be confirmed in a larger, prospective study including patients from different populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53116.RAr6YrKB_O4Jh9_1NKXMj-D3PzMtB4wVEuZECvDAj3Uy0130_provenance.
- NP53123.RAiTsDjRQ6o7YKOzRlBoh-KLsGm6UfdYvdGtEIf_xF96Y130_assertion description "[Many loci in the cPLA2 family genes were associated with schizophrenic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53123.RAiTsDjRQ6o7YKOzRlBoh-KLsGm6UfdYvdGtEIf_xF96Y130_provenance.
- NP53127.RAnOHzBwsDVInl3G3mIcgUeoHNoZoP2KU8BCFJpfjAerY130_assertion description "[Schizophrenic subjects were found to have a significant excess of the A2/A2 homozygote relative to healthy control subjects]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53127.RAnOHzBwsDVInl3G3mIcgUeoHNoZoP2KU8BCFJpfjAerY130_provenance.
- NP53130.RAv7ETfKNtRqwqFHbja0ZCqogivwxm8lO1XNufollby0U130_assertion description "[BanI polymorphism of cytosolic phospholipase A2 gene is associated with age at onset in male patients with schizophrenia and schizoaffective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53130.RAv7ETfKNtRqwqFHbja0ZCqogivwxm8lO1XNufollby0U130_provenance.
- NP53131.RAmrY8sr8KWgkK6mi_5V-nNhsQ79Smu6KCVfDUX_ONVKU130_assertion description "[Low-penetrance genes and their involvement in colorectal cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53131.RAmrY8sr8KWgkK6mi_5V-nNhsQ79Smu6KCVfDUX_ONVKU130_provenance.
- NP53136.RAm20l6fJvOksfuokPw5GqrQa-zz1q3rvfNB3XT0H5vKA130_assertion description "[Secretory phospholipase A2 does not appear to be associated with phenotypic variation in familial adenomatous polyposis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53136.RAm20l6fJvOksfuokPw5GqrQa-zz1q3rvfNB3XT0H5vKA130_provenance.
- NP53139.RAhKnxUGqHar5J0jOuXtQHf1J8sxR1hjYppQsrfeZBTTY130_assertion description "[Gross PKHD1 deletions account for a detectable proportion of ARPKD cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53139.RAhKnxUGqHar5J0jOuXtQHf1J8sxR1hjYppQsrfeZBTTY130_provenance.
- NP53141.RAhGp1TL4mb_cE2XCvEQ_S21lrZx3u_W5XSvutkZEqRnc130_assertion description "[Liver pyruvate kinase polymorphisms are associated with type 2 diabetes in northern European Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53141.RAhGp1TL4mb_cE2XCvEQ_S21lrZx3u_W5XSvutkZEqRnc130_provenance.
- NP53142.RAv13dvO40hvKBVbscNHxQS5aNHGQjFzk1w8O91_rNqn4130_assertion description "[Type 2 diabetes susceptibility genes on chromosome 1q21-24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53142.RAv13dvO40hvKBVbscNHxQS5aNHGQjFzk1w8O91_rNqn4130_provenance.
- NP53143.RApDqyU1S8SB_E1_u6YKsesc16Q-AOPGKP5hGds4mdjU8130_assertion description "[A mutation in the RIEG1 gene associated with Peters' anomaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53143.RApDqyU1S8SB_E1_u6YKsesc16Q-AOPGKP5hGds4mdjU8130_provenance.
- NP53146.RAvFgz30E9IwveRHvJV83gdgewVoso8QUFBDwqTkdXf14130_assertion description "[We concluded that mutations in parkin gene are common in Chinese EOPD patients, and mainly are exon rearrangements, while mutation in PINK1 might be not common in Chinese EOPD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53146.RAvFgz30E9IwveRHvJV83gdgewVoso8QUFBDwqTkdXf14130_provenance.
- NP53158.RApoQSKhN_X7JK8ISAGEQfeATWnH79YgJ5nQi1ZXITcbw130_assertion description "[Association studies between common variants in prolyl isomerase Pin1 and the risk for late-onset Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53158.RApoQSKhN_X7JK8ISAGEQfeATWnH79YgJ5nQi1ZXITcbw130_provenance.
- NP53160.RAsgwMnvX9JWc4wWo7oFgYOxVdrQqWSBgUrMM8LgWij74130_assertion description "[PIN-1 promoter polymorphisms in mild cognitive impairment and susceptibility to Alzheimer's disease: a preliminary report.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53160.RAsgwMnvX9JWc4wWo7oFgYOxVdrQqWSBgUrMM8LgWij74130_provenance.
- NP53174.RAvbkdF-kCNOFRxeQTimCIk0yv3a9qqlIpi7lN8IjOK70130_assertion description "[Phosphatidyl-inositol-3-kinase alpha catalytic subunit mutation and response to neoadjuvant endocrine therapy for estrogen receptor positive breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53174.RAvbkdF-kCNOFRxeQTimCIk0yv3a9qqlIpi7lN8IjOK70130_provenance.
- NP53178.RAugH0tRv3fkiPqZHp7PxRZmKwBiISsZeoXLDvcTJ4o5s130_assertion description "[ SNP C8880T of pIgR is related with NPC susceptibility; pIgR gene may be associated to risk of NPC development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53178.RAugH0tRv3fkiPqZHp7PxRZmKwBiISsZeoXLDvcTJ4o5s130_provenance.
- NP53183.RAgTCX_UAWo6mF-87SWXmC0DQdVjjzhyiSdykNhhYXrsU130_assertion description "[ Our four major findings are the extreme rarity of CCHS, the improved recognition over time, the lack of effect of HSCR on the mortality rate, and the high frequency of PHOX2B mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53183.RAgTCX_UAWo6mF-87SWXmC0DQdVjjzhyiSdykNhhYXrsU130_provenance.
- NP53187.RAhYB18XFCwU16Z2o-cUku3I4HiAC8xpLx239zS6_WgC0130_assertion description "[Six asthma candidate genes, ADAM33, NPSR1, PHF11, DPP10, HLA-G, and CYFIP2, located at different chromosome regions have been positionally cloned following the reported linkage studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53187.RAhYB18XFCwU16Z2o-cUku3I4HiAC8xpLx239zS6_WgC0130_provenance.
- NP53188.RAsDXhE1cImipWUUE_zQB8V8RSGbjQK_JxLzYEtlahjHo130_assertion description "[Positional cloning and candidate gene studies in different Caucasian populations identified the gene encoding plant homeodomain zinc finger protein 11 (PHF11) to be associated with asthma and eczema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53188.RAsDXhE1cImipWUUE_zQB8V8RSGbjQK_JxLzYEtlahjHo130_provenance.
- NP53190.RAvFp7U4sF6FlhqC7O9-OqyP9SuiZyJoHKVIkjIdeXKZg130_assertion description "[These data suggest that prohibitin genotyping has value in assessing risk of breast cancer in women aged 50 years or younger with at least one first-degree relative with the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53190.RAvFp7U4sF6FlhqC7O9-OqyP9SuiZyJoHKVIkjIdeXKZg130_provenance.
- NP53193.RAl6Cj3OWWNYc2B9q2I2xc08QLWia837Gk3fFD5dMEBAs130_assertion description "[ These data suggest that genetic variants of both the ERbeta and the PGR may influence prolactin release.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53193.RAl6Cj3OWWNYc2B9q2I2xc08QLWia837Gk3fFD5dMEBAs130_provenance.
- NP53198.RAht2otMRYYdkqR-Xn-Tc_hrzBr3hEFhFLRTUX00k1yI8130_assertion description "[Additional studies of the +331C/T variant are warranted given the current finding and the equivocal results of previous studies. The +331 T allele has been shown to result in a reduced progesterone (P) receptor A to P receptor B ratio, and if the observed association with endometriosis is confirmed it would suggest that this ratio is important for this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53198.RAht2otMRYYdkqR-Xn-Tc_hrzBr3hEFhFLRTUX00k1yI8130_provenance.
- NP53202.RAjDP2aQb2VLbuRl0faXuZlXKt4T2d8fdSbMPjF5MO4j0130_assertion description "[Quantitative trait loci predicting circulating sex steroid hormones in men from the NCI-Breast and Prostate Cancer Cohort Consortium (BPC3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53202.RAjDP2aQb2VLbuRl0faXuZlXKt4T2d8fdSbMPjF5MO4j0130_provenance.
- NP53203.RAl48a4DI5nQrh-8F-9nYOVC4VxSo1qSxi1dTCW1Jjn7Y130_assertion description "[Investigation of hormone receptor genes in migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53203.RAl48a4DI5nQrh-8F-9nYOVC4VxSo1qSxi1dTCW1Jjn7Y130_provenance.
- NP53207.RAnfqbymlo0Lu5_8quLNUOTEdm38kJ0swnMQvPmXW25Ac130_assertion description "[Association of a progesterone receptor gene +331 G/A polymorphism with breast cancer risk: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53207.RAnfqbymlo0Lu5_8quLNUOTEdm38kJ0swnMQvPmXW25Ac130_provenance.
- NP53208.RAmj3DHdKq1ZI_zmphyD4zgh0D7Qf3rSt2BaxSSzJot20130_assertion description "[No association between a progesterone receptor gene promoter polymorphism (+331G>A) and breast cancer risk in Caucasian women: evidence from a literature-based meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53208.RAmj3DHdKq1ZI_zmphyD4zgh0D7Qf3rSt2BaxSSzJot20130_provenance.
- NP53210.RArW_S4_vFZz_9BNfZ1WvqTUM74Q_Urg5S1AstLqbZPIM130_assertion description "[Genetic polymorphisms in the EGFR (R521K) and estrogen receptor (T594T) genes, EGFR and ErbB-2 protein expression, and breast cancer risk in Tunisia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53210.RArW_S4_vFZz_9BNfZ1WvqTUM74Q_Urg5S1AstLqbZPIM130_provenance.
- NP53211.RAuYXgeKpJPz93W_aW9pmKAZW4xXem2qr8zxUry-5zInA130_assertion description "[Common germline polymorphisms in COMT, CYP19A1, ESR1, PGR, SULT1E1 and STS and survival after a diagnosis of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53211.RAuYXgeKpJPz93W_aW9pmKAZW4xXem2qr8zxUry-5zInA130_provenance.