Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP49623.RApAH_NeKf6CX_30a9f-o6u12c-n7Upin3TEragQLFXNY130_assertion description "[Association of the ACE gene I/D polymorphism with insulin sensitivity depends on the presence of additional macroangiopathic risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49623.RApAH_NeKf6CX_30a9f-o6u12c-n7Upin3TEragQLFXNY130_provenance.
- NP49624.RAqcJfI6jdkz7YZyltb6FtuGpAz5pT1BU5hHLPmjur-bU130_assertion description "[ These data suggest that the I/D polymorphism is not associated with risk factors for CHD in overweight sedentary women; however, women who are homozygous for the D allele of the ACE gene are more insulin sensitive, whereas women who are homozygous for the I allele of the ACE gene have greater insulin resistance and potential risk for type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49624.RAqcJfI6jdkz7YZyltb6FtuGpAz5pT1BU5hHLPmjur-bU130_provenance.
- NP49640.RAiI_TaQMgoHkSkcq_GAsEhL1ZlOiD1EaC84Tbbx-SVq0130_assertion description "[The ACE gene could serve as the visceral damage indicator in SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49640.RAiI_TaQMgoHkSkcq_GAsEhL1ZlOiD1EaC84Tbbx-SVq0130_provenance.
- NP49648.RAnKJgnPogMqsieg-KE3mXL3HeIqFESPpoP-trGp_32w0130_assertion description "[The ACE gene could serve as the visceral damage indicator in SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49648.RAnKJgnPogMqsieg-KE3mXL3HeIqFESPpoP-trGp_32w0130_provenance.
- NP49651.RAq7ryyzxVyyBa0ycZ-X2sMWz2DP8S3-Iw-z8KmiZOn64130_assertion description "[Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49651.RAq7ryyzxVyyBa0ycZ-X2sMWz2DP8S3-Iw-z8KmiZOn64130_provenance.
- NP49658.RAr0gqAav4Co_ivY1E0rUSMuKgJ9zRLz5LSlJuM-Ti87w130_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." NP49658.RAr0gqAav4Co_ivY1E0rUSMuKgJ9zRLz5LSlJuM-Ti87w130_provenance.
- NP49662.RAv3V6qZbDIafKDP2Au80MpE55WQKQMBJKPbepUEwEKmE130_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." NP49662.RAv3V6qZbDIafKDP2Au80MpE55WQKQMBJKPbepUEwEKmE130_provenance.
- NP49672.RAkDg6kPOfvzJjgfZLepgfeYkT1ppXdamrcreDhEZa64Y130_assertion description "[SNP -11377 G/C in the proximal promoter region of the APM1 gene contributes to the development of T2DM in Han nationality but may not be a functional SNP in the APM1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49672.RAkDg6kPOfvzJjgfZLepgfeYkT1ppXdamrcreDhEZa64Y130_provenance.
- NP49677.RAvico4y1tpfBtVmKN6PiT26lZSaI4Tkpnpq6K_piysnQ130_assertion description "[Multivariable logistic regression analysis with adjustment for age, body mass index, and smoking status revealed that the T-->G (3' UTR) polymorphism of the thrombospondin 2 gene (THBS2), the -603A-->G polymorphism of the coagulation factor III gene (F3), and the G-->T (intron 2) polymorphism of the adipocyte, C1Q, and collagen domain containing (adiponectin) gene (ADIPOQ) were significantly associated with the prevalence of type 2 diabetes mellitus in men, and that the A-->G (Arg160Gly) polymorphism of the paraoxonase 1 gene (PON1) was significantly associated with this condition in women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49677.RAvico4y1tpfBtVmKN6PiT26lZSaI4Tkpnpq6K_piysnQ130_provenance.
- NP49680.RAmDZv8j6_u8qsBvgKuChWwi3a0rrY0LMCwYdiv1b5NEs130_assertion description "[In our population, genetic variants in the adiponectin gene influenced plasma adiponectin levels, and one of them was associated with hypertension. This study has provided further evidence for a role of adiponectin in the development of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49680.RAmDZv8j6_u8qsBvgKuChWwi3a0rrY0LMCwYdiv1b5NEs130_provenance.
- NP49682.RAhEVwTq2wfisU_yeeiFXxzA9rTYJh6Yy6caZHLDvyiqU130_assertion description "[Associations between two single nucleotide polymorphisms of adiponectin gene and coronary artery diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49682.RAhEVwTq2wfisU_yeeiFXxzA9rTYJh6Yy6caZHLDvyiqU130_provenance.
- NP49695.RAoYcHe2FQ3vg8xHuekaxPYY6WulZ1of63jV9jOzlHqsg130_assertion description "[In conclusion, the allele-specific differential expression of this common polymorphism could be responsible for its biological effects observed in this and the other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49695.RAoYcHe2FQ3vg8xHuekaxPYY6WulZ1of63jV9jOzlHqsg130_provenance.
- NP49700.RAodgXsdPH1-mg8ON-HWWZNY9R72NQgw4DmK89uVPvzGo130_assertion description "[Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49700.RAodgXsdPH1-mg8ON-HWWZNY9R72NQgw4DmK89uVPvzGo130_provenance.
- NP49701.RAsAIfwGrjUEavdqzcCLcE1hA0KmcVwKGHhFVQCQctnaY130_assertion description "[Our study observed further hypoadiponectinemia and IR in NAFLD with metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49701.RAsAIfwGrjUEavdqzcCLcE1hA0KmcVwKGHhFVQCQctnaY130_provenance.
- NP49704.RAmqmrXf9pyloLDfqivjqYIroTc6ixU0gMuXLuFS3Iut8130_assertion description "[These gene variants were detected in either homozygous or compound heterozygous form in 7% of the study population. Additionally, the frequency of the 625G>A allele in the Hispanic population (30%) was significantly higher than that of the African-American (9%) and Asian (13%) subpopulations. A previously unreported variant, IVS 5 (-10) C>T, was identified in three African-American newborns (0.3%). The C(4)-acylcarnitine concentration in blood spots was significantly higher in subjects homozygous for the 625A variant when compared to those homozygous for the wild type (p<0.0001). However, none of the observed genotypes was associated with a concentration of C(4)-acylcarnitine that would be consistent with a biochemical diagnosis of SCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49704.RAmqmrXf9pyloLDfqivjqYIroTc6ixU0gMuXLuFS3Iut8130_provenance.
- NP49709.RAlqmsh-tYBTIwIgV32IVCchbuQLcpfqycWNT23ves9jw130_assertion description "[Polymorphism of the ACE Gene in dialysis patients: overexpression of DD genotype in type 2 diabetic end-stage renal failure patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49709.RAlqmsh-tYBTIwIgV32IVCchbuQLcpfqycWNT23ves9jw130_provenance.
- NP49712.RAhj2x57BDHD6xhAjApjSLb41dsW_WOJcd5O8363mlzuM130_assertion description "[ We concluded that blood group O/secretors (Se/Se) and O/Le(a-b-) were associated with childhood asthma, and may act as one of the predominant factors for environmental triggers of allergy for asthmatic children in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49712.RAhj2x57BDHD6xhAjApjSLb41dsW_WOJcd5O8363mlzuM130_provenance.
- NP49714.RAuJf4GsZUHN6pWxrn8A6nSe_bhNKpN_zO8fDGuHFzoeg130_assertion description "[This is a descriptive study which contributes to the knowledge of the genetic structure of Mexican population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49714.RAuJf4GsZUHN6pWxrn8A6nSe_bhNKpN_zO8fDGuHFzoeg130_provenance.
- NP49715.RAoS3xzJq2YZWsWwHyQQ5Zvkc3JSfv5oHdqKPQOFvY-wE130_assertion description "[Coronary atherosclerosis and blood groups of ABO system in women (own data and review).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49715.RAoS3xzJq2YZWsWwHyQQ5Zvkc3JSfv5oHdqKPQOFvY-wE130_provenance.
- NP49718.RAsjoCuCbntgBlKhlIyj-kBg1lMnahYvYQ5ZMkZDMQqPE130_assertion description "[except for the ABO blood group, none of the polymorphisms studied contribute strongly to the thrombotic risk in FV Leiden homozygotes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49718.RAsjoCuCbntgBlKhlIyj-kBg1lMnahYvYQ5ZMkZDMQqPE130_provenance.
- NP49719.RApxlUufBRUV_G30huJxW-IsXVYEGWWcWyjZIXZyLgNiY130_assertion description "[Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49719.RApxlUufBRUV_G30huJxW-IsXVYEGWWcWyjZIXZyLgNiY130_provenance.
- NP49720.RArc5fg3PcUgo2-FSyhM0ZPG57tXDvjGuoRpkcndk4aoA130_assertion description "[ The data and case application demonstrated that ABO typing by oligonucleotide probe arrays was a useful technique for paternity testing and individual identification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49720.RArc5fg3PcUgo2-FSyhM0ZPG57tXDvjGuoRpkcndk4aoA130_provenance.
- NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_assertion description "[Corresponding positions of nonhuman primates have G and C, suggesting that the Se(375) allele is one of the ancestral alleles, reflecting the early human migration from Africa to New Guinea and the long isolation of Dani populations from neighboring populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_provenance.
- NP49725.RAvxP1OoS2ZVqAoDpby4gFrdVHzr22fxVQJyACD8LwKh0130_assertion description "[The number of different O alleles in population samples varied greatly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49725.RAvxP1OoS2ZVqAoDpby4gFrdVHzr22fxVQJyACD8LwKh0130_provenance.
- NP49729.RAuUedOrf2ybSLXFTt4QqjL6j41OLFq59esJrD4E5stA8130_assertion description "[Genetic variation in ABC G5/G8 and NPC1L1 impact cholesterol response to plant sterols in hypercholesterolemic men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49729.RAuUedOrf2ybSLXFTt4QqjL6j41OLFq59esJrD4E5stA8130_provenance.
- NP49739.RAl8mEMxZstaaEbjkTx-a1j3RovVwDItsU8FDI0cR7dZ0130_assertion description "[Our data support the notion that ABCG5/G8 genetic variants modulate plasma lipids concentrations in patients with FH and confirm that this effect could be influenced by smoking. Therefore, these results suggest that gene-environmental interactions can affect the clinical phenotype of FH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49739.RAl8mEMxZstaaEbjkTx-a1j3RovVwDItsU8FDI0cR7dZ0130_provenance.
- NP49741.RAhjfLqQF4OWRakTJlO5EuvkDAiLGFkc_A7f7Q00ZLd0A130_assertion description "[ABCG5/G8 polymorphisms and markers of cholesterol metabolism: systematic review and meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49741.RAhjfLqQF4OWRakTJlO5EuvkDAiLGFkc_A7f7Q00ZLd0A130_provenance.
- NP49746.RAvLPjXv2rJYnbu7oB_n0dAAEL1etpNfKnrbGYjEkMSqc130_assertion description "[These data suggest that BCRP is a candidate RCC susceptibility gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49746.RAvLPjXv2rJYnbu7oB_n0dAAEL1etpNfKnrbGYjEkMSqc130_provenance.
- NP49750.RAtABwLjOptlf-wyPvqijpTRMMwzJOCVInyXpS2XTAocw130_assertion description "[Metabolic control in type 2 diabetes is associated with sulfonylurea receptor-1 (SUR-1) but not with KCNJ11 polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49750.RAtABwLjOptlf-wyPvqijpTRMMwzJOCVInyXpS2XTAocw130_provenance.
- NP49753.RApSJj7StEpnT9c-30Oo-oAYUW1mJt7OWUw5-AO3jQljc130_assertion description "[Neither the exon 16 nor the exon 18 ABCC8 variants were associated with diabetes (1.04 0.91-1.18, P = 0.57; 0.93 0.71-1.23, P = 0.63, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49753.RApSJj7StEpnT9c-30Oo-oAYUW1mJt7OWUw5-AO3jQljc130_provenance.
- NP49759.RAo-zD-JsGv5o8KRsIWpccF5zD4-OSVZDG38RbG0o9j8k130_assertion description "[Influence of leukotriene pathway polymorphisms on response to montelukast in asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49759.RAo-zD-JsGv5o8KRsIWpccF5zD4-OSVZDG38RbG0o9j8k130_provenance.
- NP49769.RAnaec9BnKEHkysFttldjxu_IBVvFNJ4EZjXdXwho0RQs130_assertion description "[The use of two intragenic SNPs in both single locus and haplotype analyses of association suggests that the BSEP gene is a susceptibility gene in intrahepatic cholestasis of pregnancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49769.RAnaec9BnKEHkysFttldjxu_IBVvFNJ4EZjXdXwho0RQs130_provenance.
- NP49772.RAuuF6VEvoahVcUPOXV5DCwT1j96X2xZIY-_OBpsbflSY130_assertion description "[ABCB1 allele polymorphism is associated with virological efficacy in nave HIV-infected patients on HAART containing nonboosted PIs but not boosted PIs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49772.RAuuF6VEvoahVcUPOXV5DCwT1j96X2xZIY-_OBpsbflSY130_provenance.
- NP49773.RAqAdZR2Mucq3nI6gH4mnhoCXQ7rxI7dy9AjDx5n8Pq7I130_assertion description "[ABCB1 polymorphisms and the concentrations of lopinavir and ritonavir in blood, semen and saliva of HIV-infected men under antiretroviral therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49773.RAqAdZR2Mucq3nI6gH4mnhoCXQ7rxI7dy9AjDx5n8Pq7I130_provenance.
- NP49775.RAkuqVkg-5hBiu-fpZ-tJWgLyb_cSODikiK9tk-aQw-Ok130_assertion description "[Relatively frequent CYP2B6 polymorphisms may predict decreased plasma efavirenz exposure in patients of African descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49775.RAkuqVkg-5hBiu-fpZ-tJWgLyb_cSODikiK9tk-aQw-Ok130_provenance.
- NP49785.RAosUiw6YXJiPVHchVb-qvaiiQcTrY-6p17XRh7VYsYao130_assertion description "[ An MDR1 haplotype containing SNPs e21/2677T and e26/3435T protects against PD in ethnic Chinese, compatible with the observation of a recent positive selection of the T alleles of these 2 SNPs in this ethnic population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49785.RAosUiw6YXJiPVHchVb-qvaiiQcTrY-6p17XRh7VYsYao130_provenance.
- NP49788.RAgESVs7lpuVdjlZam1in7qtAJYJCNNOgY9fUUPyafRAA130_assertion description "[In conclusion, and other drug transporters represent plausible candidates as Parkinson's disease risk genes. Larger studies are required to confirm this role in the etiology of Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49788.RAgESVs7lpuVdjlZam1in7qtAJYJCNNOgY9fUUPyafRAA130_provenance.
- NP49790.RAnOgz9xkxWuJeZMoBTbQeqy2fA13rWhEkE0GVqWTEGYQ130_assertion description "[However, the distribution of c.3435C/T differed significantly between PD patients exposed to pesticides compared to those non-exposed (odds ratio=4.74; confidence interval=1.009; 22.306); p=0.047), suggesting that common MDR1 variants might influence the risk to develop PD in conjunction with exposure to pesticides.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49790.RAnOgz9xkxWuJeZMoBTbQeqy2fA13rWhEkE0GVqWTEGYQ130_provenance.
- NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_assertion description "[ Based on these results, we conclude that homozygosity for the ABCB1 2677T (S893) allele is associated with reduced risk of chronic renal dysfunction among liver transplantation patients receiving an immunosuppressive regimen containing CNIs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_provenance.
- NP49797.RAlu7hLczt27XYsEBgbdIemN5c-GZRX11hD0Tuh7o3dJI130_assertion description "[Pharmacogenetics and cardiovascular disease: impact on drug response and applications to disease management.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49797.RAlu7hLczt27XYsEBgbdIemN5c-GZRX11hD0Tuh7o3dJI130_provenance.
- NP49800.RAuX2l7Ox__0Y5SUHtnijoEIoxfwCm0dgj6s4XgcMlovU130_assertion description "[Our findings suggest that MDR1 2677G-->T/A and 3435C-->T polymorphisms can be used to predict treatment response to VC chemotherapy in NSCLC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49800.RAuX2l7Ox__0Y5SUHtnijoEIoxfwCm0dgj6s4XgcMlovU130_provenance.
- NP49802.RApDw7iPHB5HkzhOYBKLpCoi7JJ-GVlf_ysI0VOskBwzQ130_assertion description "[Differences in allelic distribution for genes involved in paclitaxel disposition or DNA repair were observed between Japanese and US patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49802.RApDw7iPHB5HkzhOYBKLpCoi7JJ-GVlf_ysI0VOskBwzQ130_provenance.
- NP49804.RAhFouFijLYDP97wyArekvtBEIK8CVj2g75l-KCjtnsKA130_assertion description "[Germline genetic variations in drug action pathways predict clinical outcomes in advanced lung cancer treated with platinum-based chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49804.RAhFouFijLYDP97wyArekvtBEIK8CVj2g75l-KCjtnsKA130_provenance.
- NP49811.RArjRXirIw1WqnQBq_AnyXLZ1qN4dDK7djeD-dfnJac44130_assertion description "[Among children enrolled in the Northern California Childhood Leukemia Study, we examined the susceptibility conferred by MDR1 single nucleotide polymorphisms (SNP) and predicted haplotypes and whether they modify the association between indoor insecticide exposure and risk of childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49811.RArjRXirIw1WqnQBq_AnyXLZ1qN4dDK7djeD-dfnJac44130_provenance.
- NP49818.RAvVU7GO0cGB-5A8ThhtjUs--EBNjNcQyh_sQ9UCLNKxo130_assertion description "[We have investigated the association between polymorphisms related to antiepileptic drug metabolism (CYP2C9, CYP2C19, and UGT), transport (ABCB1), and targets (SCN1A) both in a crude analysis and after adjusting by clinical factors associated with drug-resistance, and stratifying by patient age or aetiology of epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49818.RAvVU7GO0cGB-5A8ThhtjUs--EBNjNcQyh_sQ9UCLNKxo130_provenance.
- NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_assertion description "[We performed a meta-analysis to evaluate the association between ABCB1 C3435T polymorphisms and the prevalence of epilepsy, including all relevant human studies (until June 2009), in which patients with or without epilepsy had undergone genotyping for the ABCB1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_provenance.
- NP49821.RAtZBv58q2VABzaLzTVL3hdPJnI4aOdfLnM_eGp1lRkrM130_assertion description "[Analysis of genotype and haplotype effects of ABCB1 (MDR1) polymorphisms in the risk of medically refractory epilepsy in an Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49821.RAtZBv58q2VABzaLzTVL3hdPJnI4aOdfLnM_eGp1lRkrM130_provenance.
- NP49823.RAmC-Cu5sWIArAk9lGYLxVSEF2ppV8yjQORBbG3tvY-xw130_assertion description "[Our study did not support any significant association between the MDR1 (C3435T) polymorphism and resistance to CBZ in epilepsy patients from Turkey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49823.RAmC-Cu5sWIArAk9lGYLxVSEF2ppV8yjQORBbG3tvY-xw130_provenance.
- NP49829.RAg9HgGaobLQJC8nKIbLeS3FDZ-1iQ2OUIssNadTLepBE130_assertion description "[Sequential influences of leukemia-specific and genetic factors on p-glycoprotein expression in blasts from 817 patients entered into the National Cancer Research Network acute myeloid leukemia 14 and 15 trials.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49829.RAg9HgGaobLQJC8nKIbLeS3FDZ-1iQ2OUIssNadTLepBE130_provenance.
- NP49830.RAupfcsI2xHACYGGDwr-XFjxWWDmYIV8qmOnxZbXCi0F8130_assertion description "[The aim of the study was to evaluate the influence of the MDR1 C3435T polymorphism on the therapeutic response in 23 patients treated with cetuximab plus irinotecan for irinotecan refractory liver metastatic colorectal cancer considering their KRAS status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49830.RAupfcsI2xHACYGGDwr-XFjxWWDmYIV8qmOnxZbXCi0F8130_provenance.
- NP49833.RAiZq9Lcfm707x07hm8dNrCpD0u8Zwssa3L-8cK0yY4dg130_assertion description "[No association between MDR1 (ABCB1) 2677G>T and 3435C>T polymorphism and sporadic colorectal cancer among Bulgarian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49833.RAiZq9Lcfm707x07hm8dNrCpD0u8Zwssa3L-8cK0yY4dg130_provenance.
- NP49855.RApALzCeEqtfeWijXvsF-gzNlcthZuRU49FPHFB5N8CC8130_assertion description "[Breast cancer patients initiating TEC (including docetaxel, epirubicin, and cyclophosphamide) treatment were genotyped for CYP3A4, CYP3A5, and ABCB1 to identify variability factors of side effects for docetaxel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49855.RApALzCeEqtfeWijXvsF-gzNlcthZuRU49FPHFB5N8CC8130_provenance.
- NP49862.RAlVgQAabQ8gp2_qKoC6HdxIYsC_dUsE_dhT_H0AYVLHE130_assertion description "[Transfection of the breast cancer cell line MCF-7 and its doxorubicin-selected variant MCF-7/ADR by either C/EBPbeta or C/EBPbeta-LIP (a dominant-negative form of C/EBPbeta) confirmed their roles in the activation or repression of the endogenous, chromosomally embedded MDR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49862.RAlVgQAabQ8gp2_qKoC6HdxIYsC_dUsE_dhT_H0AYVLHE130_provenance.
- NP49868.RAqi0Fj2uqYY1VWtbAusT4-Xw8xCeaOwGnFDMkPzwXzxE130_assertion description "[Our results suggest that homozygosity for 3435T alleles of ABCB1 is a risk factor for occurrence of nortriptyline-induced postural hypotension (OR = 1.37, P = 0.042, 95% CI 1.01-1.86).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49868.RAqi0Fj2uqYY1VWtbAusT4-Xw8xCeaOwGnFDMkPzwXzxE130_provenance.
- NP49869.RArL68InhhDrJAc8sSf_nx1jdmv05tOWwehuehBJjehgE130_assertion description "[While this study does not definitively exclude ABCA4 from contributing to a small or moderate fraction of ARM, it adds to the body of evidence suggesting that ABCA4 is not a major susceptibility gene for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49869.RArL68InhhDrJAc8sSf_nx1jdmv05tOWwehuehBJjehgE130_provenance.
- NP49879.RAkyMukDkNO5F1231pZrmn7BTeZrjH1ps98zrBe6bFctc130_assertion description "[These findings show that several common genetic variants influence the lipid phenotype and the CAD risk in FH heterozygotes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49879.RAkyMukDkNO5F1231pZrmn7BTeZrjH1ps98zrBe6bFctc130_provenance.
- NP49881.RAmTVF5NBEcMHsy3I79yI2bKDXzR4Jz2GWitQ0UZhwAqk130_assertion description "[Interestingly, the effect of TLR4, APOE and ABCA1 variants on AMD susceptibility was opposite to that of association with atherosclerosis risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49881.RAmTVF5NBEcMHsy3I79yI2bKDXzR4Jz2GWitQ0UZhwAqk130_provenance.
- NP49886.RAk91AIVzeySDAMLGLOMZYandKeHhHg3ubK1QqAXOIDVY130_assertion description "[Since altered cholesterol metabolism is also involved in Alzheimer's disease (AD), the effects of two ABCA1 polymorphisms (G-395C promoter polymorphism (rs 2246293) and exonic R219K) on the risk of AD in 241 AD patients and 294 non-demented controls, and on CSF cholesterol and 24S-hydroxycholesterol in 74 AD patients and 42 non-demented controls were investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49886.RAk91AIVzeySDAMLGLOMZYandKeHhHg3ubK1QqAXOIDVY130_provenance.
- NP49887.RAmg9FgEyxKPocgVU-YaeX8HQhkcFBDGWonqu0HZNZ6q0130_assertion description "[However, together with the reported associations of AD with APOE, CYP46A1 and ABCA1, the present result adds a very significant support for the role of cholesterol and phospholipid homeostasis in AD and a rationale for testing novel cholesterol homeostasis-related therapeutic strategies in AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49887.RAmg9FgEyxKPocgVU-YaeX8HQhkcFBDGWonqu0HZNZ6q0130_provenance.
- NP49889.RAnLERiq0FkMqyh-DPctwTjObaw3ubz18LBa6GQy3i3h4130_assertion description "[Epistasis between intracellular cholesterol trafficking-related genes (NPC1 and ABCA1) and Alzheimer's disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49889.RAnLERiq0FkMqyh-DPctwTjObaw3ubz18LBa6GQy3i3h4130_provenance.
- NP49898.RArTp3nL072F_8n-8A9g-siwuOE8YvfBnig3mV1dSu-Mw130_assertion description "[Investigation of ABCA1 C69T and G-191C polymorphisms in coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49898.RArTp3nL072F_8n-8A9g-siwuOE8YvfBnig3mV1dSu-Mw130_provenance.
- NP49899.RAtaC5ES0Vs4rbTM4PnBINNVyua3oTPBURmtEFoDin4rY130_assertion description "[No significant association was found between cardiovascular endpoints and ABCA1 gene A2589G and G3456C genotypes in this study population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49899.RAtaC5ES0Vs4rbTM4PnBINNVyua3oTPBURmtEFoDin4rY130_provenance.
- NP49900.RAvCuLbf6yRxpAB5ZTsKCEi5IQGkAgiLUkPW6iWK041FA130_assertion description "[A geographical heterogeneity of environmental and genetic risk factors related to the development of coronary artery disease exists in Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49900.RAvCuLbf6yRxpAB5ZTsKCEi5IQGkAgiLUkPW6iWK041FA130_provenance.
- NP49901.RAjlqlN24cad6UqyahM_L37Bwi0qlE8M3zgSJG6CohnpY130_assertion description "[We determined the presence of the R219K variant in the ABCA1 gene by polymerase chain reaction (PCR) and restriction analysis in 301 patients with and without CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49901.RAjlqlN24cad6UqyahM_L37Bwi0qlE8M3zgSJG6CohnpY130_provenance.
- NP49906.RAknewfgQjYPu0EcAPwbsTLi9_0L7zBRzK9q6Pm3aKJKI130_assertion description "[ABCA1 gene polymorphisms but not haplotypes are involved in the variability of plasma ApoA1 and the susceptibility to coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49906.RAknewfgQjYPu0EcAPwbsTLi9_0L7zBRzK9q6Pm3aKJKI130_provenance.
- NP49907.RApbgeWSldZl06jRcBHBF6BTlfaniWEqFNUMNaK7fivjs130_assertion description "[The -191G/C SNP in the promoter region of ABCA1 is associated with increased CAD and the C allele may relate to the stability of CAD without detectable changes in plasma lipids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49907.RApbgeWSldZl06jRcBHBF6BTlfaniWEqFNUMNaK7fivjs130_provenance.
- NP49913.RAgbGL7jP0jnXrPerKzPON5HVFxe9z8TqFNEqj81ECTdE130_assertion description "[We show that 3 of 6 nonsynonymous SNPs in ABCA1 predict risk of IHD in the general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49913.RAgbGL7jP0jnXrPerKzPON5HVFxe9z8TqFNEqj81ECTdE130_provenance.
- NP49920.RAuDgVSmsdUk-f8lrlVlenUuLzcaLlTcCdX_WlLEq5GtY130_assertion description "[Alpha-2-macroglobulin (A2M) deletion polymorphism was recently reported to be associated with Alzheimer's disease (AD) in a way comparable to apolipoprotein E (APOE) polymorphism in a family-based study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49920.RAuDgVSmsdUk-f8lrlVlenUuLzcaLlTcCdX_WlLEq5GtY130_provenance.
- NP49923.RAux7XJ-QcriJUarQ3FDJGYAkwa2uJSgGN1jF-b6ivpX0130_assertion description "[Association between haplotype -88G/25G in A2M with Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49923.RAux7XJ-QcriJUarQ3FDJGYAkwa2uJSgGN1jF-b6ivpX0130_provenance.
- NP49925.RAtwNuBk-k6XVFM9RPtH6S4EHT5SsU5MZFWxWZMk-Miig130_assertion description "[An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49925.RAtwNuBk-k6XVFM9RPtH6S4EHT5SsU5MZFWxWZMk-Miig130_provenance.
- NP49930.RAmhdkf1-B6EH_QnGbyRra776TT1HNNZALKExNptrlJyk130_assertion description "[Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49930.RAmhdkf1-B6EH_QnGbyRra776TT1HNNZALKExNptrlJyk130_provenance.
- NP49932.RAh2hjn5sNfp4eHVY3mYWfMA2VjQiI6yubZmU7qHqqNX4130_assertion description "[A haplotype comprising SNPs in two proinflammatory cytokines, tumor necrosis factor-alpha and lymphotoxin-alpha (rs1800629, rs361525, rs1799724, rs909253, and rs2239704), increased non-Hodgkin lymphoma risk overall (OR, 1.31; 95% CI, 1.06-1.63; P = 0.01) and notably for diffuse large B cell (OR, 1.64; 95% CI, 1.23-2.19; P = 0.0007).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49932.RAh2hjn5sNfp4eHVY3mYWfMA2VjQiI6yubZmU7qHqqNX4130_provenance.
- NP49938.RAq6ld49GNd7h3V93Rd0s9JXIoZdT0Fh9rYtvCSwCpwFA130_assertion description "[This TNF-alpha polymorphism is associated with clinical features of disease including progression. There is clear evidence of TNF-alpha overexpression and bioactivity with neutrophilic inflammation. The polymorphism is likely to be a factor that influences a COPD disease phenotype and its progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49938.RAq6ld49GNd7h3V93Rd0s9JXIoZdT0Fh9rYtvCSwCpwFA130_provenance.
- NP49941.RAnotrnnza9YyFHgxhRbJ-jkVxXFi9Y8TuGL-Dh6Ka8kY130_assertion description "[Tumour necrosis factor gene polymorphisms are associated with COPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49941.RAnotrnnza9YyFHgxhRbJ-jkVxXFi9Y8TuGL-Dh6Ka8kY130_provenance.
- NP49942.RAnUOAnxaBp-uuxlv9G9auyUbT6R5m6rYzNkFeLvnNe7c130_assertion description "[Genotype frequencies of the 5 SNPs showed no significant difference between the COPD and DB patient groups and the healthy smokers group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49942.RAnUOAnxaBp-uuxlv9G9auyUbT6R5m6rYzNkFeLvnNe7c130_provenance.
- NP49943.RApS03B-lsnx8OxXrZPiUukODdchJ27O67sqHZ4dMvUxM130_assertion description "[Common genetic variants in the interleukin-6 and chitotriosidase genes are associated with the risk for serious infection in children undergoing therapy for acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49943.RApS03B-lsnx8OxXrZPiUukODdchJ27O67sqHZ4dMvUxM130_provenance.
- NP49946.RAh-fZTqEk1k4YvSmI9deC70cAiJ6g4E8azE0IPenFFQ8130_assertion description "[In order to investigate functionally important genes of the tumor necrosis factor alpha (TNFalpha) pathway we studied the frequency of DNA polymorphisms in the interleukin 6 (IL6), the TNFalpha, and the TNFalpha receptor 1 (TNFR1) genes in 264 sporadic German PD patients and in 183 age and sex matched German healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49946.RAh-fZTqEk1k4YvSmI9deC70cAiJ6g4E8azE0IPenFFQ8130_provenance.
- NP49947.RAqLkJGBD0kbXuAdn_7Af2grjU6IR_lS3ECr3KJ9lij9Y130_assertion description "[In the present study, we investigated the genetic polymorphisms of the IL10 (-1082 and -519) and TNF (-308) genes in relation to the risk of PD, and their associations with age of PD onset in a group of 316 patients, divided into two subgroups: Group 1: patients with early onset PD (EOPD), i.e.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49947.RAqLkJGBD0kbXuAdn_7Af2grjU6IR_lS3ECr3KJ9lij9Y130_provenance.
- NP49948.RAkDyLZJL2pk-mCU_kqfV8LdKurALHbYFWzFhvn7MV2nI130_assertion description "[Tumor necrosis factor gene polymorphisms in patients with sporadic Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49948.RAkDyLZJL2pk-mCU_kqfV8LdKurALHbYFWzFhvn7MV2nI130_provenance.
- NP49962.RAv9frFnj3hp_vAAlz3uBbPAimjq8TIknjtvIbm3CNsj4130_assertion description "[Identification of two independent risk factors for lupus within the MHC in United Kingdom families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49962.RAv9frFnj3hp_vAAlz3uBbPAimjq8TIknjtvIbm3CNsj4130_provenance.
- NP49965.RAuG9V4hR1w_ixGFFh3JIaUJuRvmnja8oH0zkqbksecug130_assertion description "[Frequency of TNF-alpha-308 GA genotype was significantly higher in the sepsis group than in the control group and TNF-alpha-308GA and IL-10-592CC genotypes were related to poor outcome of sepsis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49965.RAuG9V4hR1w_ixGFFh3JIaUJuRvmnja8oH0zkqbksecug130_provenance.
- NP49967.RAoOIH5k-C6m-88balXIK9qB0e2vdqsutitYRerODOP74130_assertion description "[To investigate the relation of the biallelic Nco1 restriction fragment length polymorphism in the first intron of the tumor necrosis factor (TNF) beta gene with the development of severe sepsis in multiply injured patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49967.RAoOIH5k-C6m-88balXIK9qB0e2vdqsutitYRerODOP74130_provenance.
- NP49968.RArCnW82rg4wENlb9_ZGp6XMfIDpzjnqapJC3oYyL5xkk130_assertion description "[Association of tumor necrosis factor microsatellites TNF with the susceptibility to and outcome of postoperative severe sepsis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49968.RArCnW82rg4wENlb9_ZGp6XMfIDpzjnqapJC3oYyL5xkk130_provenance.
- NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_assertion description "[The result suggests that this variation has a strong association with AS in males and females. No similar reports about the association between AS and the T mutation allele have been acquired. Therefore, our hypothesis can be supported by our results on the whole and the -850C-->T mutation allele in the region on promoter of TNFalphagene is likely one of susceptible genes to AS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49974.RAiDLqW7f7aHczXJ6EWZY_LMtCaHIOSttDPpWD9FfKSGI130_provenance.
- NP49975.RAllHYfrMs_mUv4uiihVCY42xrJv2utnozpySAMQ6EtgM130_assertion description "[Higher LPS-stimulated TNF-alpha mRNA levels in peripheral blood mononuclear cells from Chinese ankylosing spondylitis patients with -308G/A polymorphism in promoter region of tumor necrosis factor: association with distinct A33/B58/Cw10 haplotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49975.RAllHYfrMs_mUv4uiihVCY42xrJv2utnozpySAMQ6EtgM130_provenance.
- NP49978.RAhLXSQcYPPF-1iQmyUHjFSnhZP3U_oKe3xIEZWQ3lEpo130_assertion description "[Lack of a strong association between HLA class II, tumour necrosis factor and transporter associated with antigen processing gene polymorphisms and virological response to alpha-interferon treatment in patients with chronic hepatitis C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49978.RAhLXSQcYPPF-1iQmyUHjFSnhZP3U_oKe3xIEZWQ3lEpo130_provenance.
- NP49981.RAlVlFDZp9RDU37fZr3TLzlLwZJCtdD_iMMvSTDUHMh5w130_assertion description "[Polymorphisms in the interleukin-10, tumor necrosis factor-alpha, and transforming growth factor-beta1 genes in chronic hepatitis C patients treated with interferon and ribavirin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49981.RAlVlFDZp9RDU37fZr3TLzlLwZJCtdD_iMMvSTDUHMh5w130_provenance.
- NP49984.RAlcPPLx0GmwqFr7krgBRh5P28ze4Dd2G1gBcUSy_6to4130_assertion description "[Tumor necrosis factor alpha promoter polymorphisms at position -308 in Taiwanese chronic hepatitis C patients treated with interferon-alpha.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49984.RAlcPPLx0GmwqFr7krgBRh5P28ze4Dd2G1gBcUSy_6to4130_provenance.
- NP49989.RAljdOrxmuw13Tv5Z7t0AHVq8FmRwYfPMdonDoZbefutI130_assertion description "[Tumour necrosis factor alpha -308G->A polymorphism is not associated with response to TNFalpha blockers in Caucasian patients with rheumatoid arthritis: systematic review and meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49989.RAljdOrxmuw13Tv5Z7t0AHVq8FmRwYfPMdonDoZbefutI130_provenance.
- NP49994.RAujRSQCMgOmxZVhmvLd4g5bm_TV6u48i_1fV9WsgWFS8130_assertion description "[Tumor necrosis factor-alpha -308 promoter polymorphism contributes independently to HLA alleles in the severity of rheumatoid arthritis in Mexicans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49994.RAujRSQCMgOmxZVhmvLd4g5bm_TV6u48i_1fV9WsgWFS8130_provenance.
- NP49998.RAo174_w1xqDf6UAYNRvifCLy2F3qc1dR85RU_GYGgXbA130_assertion description "[The combined effects of TNFalpha-308, IL-6 -174 and IL-10 -1082 variant alleles may be more decisive to induce functional differences and modify the risk for AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49998.RAo174_w1xqDf6UAYNRvifCLy2F3qc1dR85RU_GYGgXbA130_provenance.
- NP50002.RAovtXrW7maVDK7DmN9Hh54m8dAaauW9Wib0qdTbF9OP8130_assertion description "[To evaluate the association between promoter region polymorphisms in the TNF-alpha and IL-10 genes and risk of late-onset AD in older white subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50002.RAovtXrW7maVDK7DmN9Hh54m8dAaauW9Wib0qdTbF9OP8130_provenance.
- NP50005.RAh7Ehz25ZTYTO1o7jjOE38iLI91dhCOYBVHrR_ghAnOY130_assertion description "[Logistic regression analysis indicated that the possession of the T allele significantly increased the risk of Alzheimer's disease associated with carriage of the apolipoprotein E epsilon4 allele (odds ratio 2.73 1.68-4.44 for those with apolipoprotein E epsilon4 but no TNF-alpha T, vs 4.62 2.38-8.96 for those with apolipoprotein E epsilon4 and TNF-alpha T; p=0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50005.RAh7Ehz25ZTYTO1o7jjOE38iLI91dhCOYBVHrR_ghAnOY130_provenance.
- NP50006.RAgBtuCDWoId2HzDfiWpusX1dmzLXzkwOa7aMhdo6-Xwc130_assertion description "[Cytokine polymorphisms and Alzheimer disease: possible associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50006.RAgBtuCDWoId2HzDfiWpusX1dmzLXzkwOa7aMhdo6-Xwc130_provenance.
- NP50008.RAqW1Bk5SHICQaiJbxbqHG1MvJIdEuC0TIDpjzRgO08oQ130_assertion description "[No associations were identified between SNPs in the promoter regions of the IL-1beta, IL-6, or TNFalpha proinflammatory cytokines genes or the TGFbeta1 and VEGF genes and susceptibility to CP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50008.RAqW1Bk5SHICQaiJbxbqHG1MvJIdEuC0TIDpjzRgO08oQ130_provenance.
- NP50010.RArd4zZtmTUh2QbCLqQNl6zRAkV0h1q0UvAw17A7uQK2Q130_assertion description "[The aims of the current investigation were to determine whether functional polymorphisms in the tumor necrosis factor-alpha (TNF-alpha) gene at positions -308 and -238; in the transforming growth factor-beta 1 (TGF-beta(1)) gene at positions -509, +869 (codon 10), and +915 (codon 25); in the interleukin-10 (IL-10) gene at position -1082; and in the intron 1 of the interferon-gamma (IFN-gamma) gene at position +874 are associated with alcoholic chronic pancreatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50010.RArd4zZtmTUh2QbCLqQNl6zRAkV0h1q0UvAw17A7uQK2Q130_provenance.
- NP50011.RAkivdE7bEMiCf_9gtBm4bDgGoQIGH_GMmXON3iGbwm5M130_assertion description "[One hundred eleven men with African American ancestry were tested for G6PD deficiency (Type A-202/376) and for the cytokine gene promoter polymorphisms of IL-10 (-1082 G/A, -819 T/C, and -592 A/C), tumor necrosis factor (TNF)-alpha (-308 G/A), transforming growth factor (TGF)-beta1 (C/T codon 10 and C/G codon 25), IL-6 (-174 G/C), and interferon (IFN)-gamma (+874 A/T).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50011.RAkivdE7bEMiCf_9gtBm4bDgGoQIGH_GMmXON3iGbwm5M130_provenance.
- NP50014.RAuXCr9Jemo9aLlTwPZP-07h7HJ6yLRcPzgHEMsFmyIzw130_assertion description "[ The strongest association in this predominantly white population with SLE was between HLA-DR3 and anti-La, which seemed to account for any associations with TNFalpha alleles on an extended DR3 haplotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50014.RAuXCr9Jemo9aLlTwPZP-07h7HJ6yLRcPzgHEMsFmyIzw130_provenance.
- NP50026.RAnldl1lfYjdrj4SGTTdySnEhqJynJxnUtRo5a-U41jkg130_assertion description "[Polymorphisms in immunoregulatory genes may influence susceptibility to preterm birth or premature rupture of membranes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50026.RAnldl1lfYjdrj4SGTTdySnEhqJynJxnUtRo5a-U41jkg130_provenance.
- NP50027.RApM_JMboOx7yP16ZXWKr7-Xw6yEgS2LH3SvVYUoUIkh8130_assertion description "[Juvenile idiopathic arthritis genetics - what's new? What's next?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50027.RApM_JMboOx7yP16ZXWKr7-Xw6yEgS2LH3SvVYUoUIkh8130_provenance.