Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP66146.RAghsm7BdfavDYgrszfAhvTeHvjYqw3VPVdsOJi1tdF7k130_assertion description "[P2RX7: A bipolar and unipolar disorder candidate susceptibility gene?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66146.RAghsm7BdfavDYgrszfAhvTeHvjYqw3VPVdsOJi1tdF7k130_provenance.
- NP66150.RAm_4R2GsVmsi4sntSPgbN2TLPa7NBGzqcOKqNj13y0qU130_assertion description "[the A1513C polymorphism in the P2X7R gene is related to the occurrence of infections and survival after allogeneic stem cell transplantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66150.RAm_4R2GsVmsi4sntSPgbN2TLPa7NBGzqcOKqNj13y0qU130_provenance.
- NP66154.RAroskL_xm_iktTiMQWs1gc-C5_mY69h_MzZq3eSNmtjs130_assertion description "[Fine-mapping and candidate gene investigation within the PARK10 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66154.RAroskL_xm_iktTiMQWs1gc-C5_mY69h_MzZq3eSNmtjs130_provenance.
- NP66155.RAuccPGmCYIc-VpT4f_JvIIHBSzAKEpBjdVyrWX_W3AZU130_assertion description "[Patients with Parkin or PINK1 mutations benefit from subthalamic nucleus deep brain stimulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66155.RAuccPGmCYIc-VpT4f_JvIIHBSzAKEpBjdVyrWX_W3AZU130_provenance.
- NP66156.RAjsPUcU1s0tFLV1sjj_x_vV_habOSm9jcoOxKg_6wP2Y130_assertion description "[In order to examine the association of common genetic variation in the base-excision repair (BER) pathway with bladder cancer risk, we analyzed 43 single nucleotide polymorphisms (SNPs) in 12 BER genes (OGG1, MUTYH, APEX1, PARP1, PARP3, PARP4, XRCC1, POLB, POLD1, PCNA, LIG1, and LIG3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66156.RAjsPUcU1s0tFLV1sjj_x_vV_habOSm9jcoOxKg_6wP2Y130_provenance.
- NP66157.RAkyjyjxwl3tvXUQsrO3uacqJoaPf_K5Uco9_IErH1gfw130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66157.RAkyjyjxwl3tvXUQsrO3uacqJoaPf_K5Uco9_IErH1gfw130_provenance.
- NP66160.RAq8WQ3DZVSEWURJ7sgwWVEnGQYshg_8rF1LnY6p2LFLI130_assertion description "[DNA repair single-nucleotide polymorphisms in colorectal cancer and their role as modifiers of the effect of cigarette smoking and alcohol in the Singapore Chinese Health Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66160.RAq8WQ3DZVSEWURJ7sgwWVEnGQYshg_8rF1LnY6p2LFLI130_provenance.
- NP66163.RAsyAmtXQapYNDNPloMZvZ-5vi3h7SeffQnprEafYjucQ130_assertion description "[To this end, we screened all PARP-1 exons, 7.1kb of intron-exon junction and 1.0-kb promoter sequences in 83 French patients with breast cancer and 100 controls by direct sequencing of genomic DNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66163.RAsyAmtXQapYNDNPloMZvZ-5vi3h7SeffQnprEafYjucQ130_provenance.
- NP66166.RApBy8F4WGHYQvubl2Y_WT7ioNR5JdQu8ZvFsrF7y3pNE130_assertion description "[In order to examine the association of common genetic variation in the base-excision repair (BER) pathway with bladder cancer risk, we analyzed 43 single nucleotide polymorphisms (SNPs) in 12 BER genes (OGG1, MUTYH, APEX1, PARP1, PARP3, PARP4, XRCC1, POLB, POLD1, PCNA, LIG1, and LIG3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66166.RApBy8F4WGHYQvubl2Y_WT7ioNR5JdQu8ZvFsrF7y3pNE130_provenance.
- NP66167.RAu6EZ6e1wcSohXJyLsbcSSIt95CzcSpr2GhAGtQrlDeM130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66167.RAu6EZ6e1wcSohXJyLsbcSSIt95CzcSpr2GhAGtQrlDeM130_provenance.
- NP66168.RAtwwVOg4metKym7bHe9X6XvmHtQVLWuHHZu5h48hOVHQ130_assertion description "[Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66168.RAtwwVOg4metKym7bHe9X6XvmHtQVLWuHHZu5h48hOVHQ130_provenance.
- NP66172.RAuDUFlco07mjiOlFWOBcbByQ5qRQoSJlh8mFZxQVXD_s130_assertion description "[Visfatin genotypes may account for insulin resistance and levels of lipid profile that may cause by different visfatin expression between genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66172.RAuDUFlco07mjiOlFWOBcbByQ5qRQoSJlh8mFZxQVXD_s130_provenance.
- NP66175.RAonAC1roqihzw2HNIUAhZMvjd4sAXj5cKeRSs3kyBGyM130_assertion description "[Candidate gene association study of insulin signaling genes and Alzheimer's disease: evidence for SOS2, PCK1, and PPARgamma as susceptibility loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66175.RAonAC1roqihzw2HNIUAhZMvjd4sAXj5cKeRSs3kyBGyM130_provenance.
- NP66177.RAiV2KuG4960_-MsM1PPMdFvGAqhrQm6pPQI2JJ6TH6qo130_assertion description "[Association studies of 22 candidate SNPs with late-onset Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66177.RAiV2KuG4960_-MsM1PPMdFvGAqhrQm6pPQI2JJ6TH6qo130_provenance.
- NP66181.RAi6RcjXYNYyCEFKXQuMrg4BZ7nhqkJvSSTeax3C1jJ8M130_assertion description "[PCM1 and schizophrenia: a replication study in the Northern Swedish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66181.RAi6RcjXYNYyCEFKXQuMrg4BZ7nhqkJvSSTeax3C1jJ8M130_provenance.
- NP66185.RAoHx-f3ziHcy38my1Lwd9jt0HtIaybKvq4AEQn0FDOrk130_assertion description "[We observed a weak protective effect of PD1.3A allele for MI (odds ratio: 0.78, 95% confidence interval: 0.61-0.98).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66185.RAoHx-f3ziHcy38my1Lwd9jt0HtIaybKvq4AEQn0FDOrk130_provenance.
- NP66191.RArVWyjj2WEr8czPTEIZhJkJqULsT0unWc8_X0aHRUhUM130_assertion description "[These results suggest that the rs1862214 polymorphism in PDCD5 is predictive for lung cancer risk and prognosis, and that PDCD5 may represent a novel tumor suppressor gene influencing lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66191.RArVWyjj2WEr8czPTEIZhJkJqULsT0unWc8_X0aHRUhUM130_provenance.
- NP66195.RAmMHMEJ1Fp9StZj5odfQv0L8i9D_zfVRLdq834xhR3tg130_assertion description "[Multivariable logistic regression analysis with adjustment for age, sex, body mass index, and the prevalence of smoking, hypertension, diabetes mellitus, and hypercholesterolemia revealed that the 677C-->T (Ala222Val) polymorphism of MTHFR, the 1595C-->G (Ser447Stop) polymorphism of LPL, and the -108/3G-->4G polymorphism of IPF1 were significantly associated with the prevalence of myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66195.RAmMHMEJ1Fp9StZj5odfQv0L8i9D_zfVRLdq834xhR3tg130_provenance.
- NP66196.RAnfGibYHVGsGLiX_ecEnWnZYqXjG5rGxI3Pkj33Yvr3w130_assertion description "[Association of gene polymorphisms with myocardial infarction in individuals with or without conventional coronary risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66196.RAnfGibYHVGsGLiX_ecEnWnZYqXjG5rGxI3Pkj33Yvr3w130_provenance.
- NP66198.RAk07OdH_eiCxVWveqL2gwQhrmVckhCoEdcJdXjyUpsdA130_assertion description "[Association of the kappa-opioid system with alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66198.RAk07OdH_eiCxVWveqL2gwQhrmVckhCoEdcJdXjyUpsdA130_provenance.
- NP66199.RAvFikgjTblTV-8-NX-NnVb5gZrFUB8wwqXyVGSv6wlOE130_assertion description "[Human clock, PER1 and PER2 polymorphisms: lack of association with cocaine dependence susceptibility and cocaine-induced paranoia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66199.RAvFikgjTblTV-8-NX-NnVb5gZrFUB8wwqXyVGSv6wlOE130_provenance.
- NP66202.RAoPZjfbOlfHEbCZ1_w1VWBgN64sVwHzs4e_I1W_Robrw130_assertion description "[Suggestive evidence for association of the circadian genes PERIOD3 and ARNTL with bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66202.RAoPZjfbOlfHEbCZ1_w1VWBgN64sVwHzs4e_I1W_Robrw130_provenance.
- NP66205.RArPanGVwxRDqMiBIMScxg2lYDazn6HgS2imgfErDQ4X4130_assertion description "[Association of the 54-nucleotide repeat polymorphism of hPer3 with heroin dependence in Han Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66205.RArPanGVwxRDqMiBIMScxg2lYDazn6HgS2imgfErDQ4X4130_provenance.
- NP66210.RAq8TxI973ntLXyrMoaPnpEL6TlGXZAq2i4fbmvzRvon8130_assertion description "[When expression of PTEN and mutations of KRAS, BRAF and PIK3CA are concomitantly ascertained, up to 70% of mCRC patients unlikely to respond to anti-EGFR therapies can be identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66210.RAq8TxI973ntLXyrMoaPnpEL6TlGXZAq2i4fbmvzRvon8130_provenance.
- NP66217.RAl8MA3-fHuVeMP24EoFuJigbVELljOPjvdYhWIr8KWAw130_assertion description "[Our study demonstrates that mutations in each part of the EGFR pathway were associated with different clinicopathologic features in patients with NSCLCs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66217.RAl8MA3-fHuVeMP24EoFuJigbVELljOPjvdYhWIr8KWAw130_provenance.
- NP66222.RAp_Poue24CumjjopSTVhm-RNadKX16gaTDbhbAhPUzDo130_assertion description "[Despite this apparent paradox, our data may therefore suggest involvement of PIP4K2A in schizophrenia in those families for whom genetic variation in DTNBP1 appears also to be a risk factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66222.RAp_Poue24CumjjopSTVhm-RNadKX16gaTDbhbAhPUzDo130_provenance.
- NP66224.RAn6eKoDIxHtnnne4W6SdCFOj5UcwvsZiFPAMRCQAh0Cg130_assertion description "[The association of the F279 loss of function variant with the reduced risk of CVD supports the concept that Lp-PLA(2) plays a proatherogenic and causative role in CVD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66224.RAn6eKoDIxHtnnne4W6SdCFOj5UcwvsZiFPAMRCQAh0Cg130_provenance.
- NP66226.RAk6rWyigKuEdanTbXbPaxtD-TkLZEARgf5L7NqFhBKrA130_assertion description "[Association studies between the plasmin genes and late-onset Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66226.RAk6rWyigKuEdanTbXbPaxtD-TkLZEARgf5L7NqFhBKrA130_provenance.
- NP66227.RAi8kzuET4HCe2yPyuhyR1cDXSRTTd90BYwfjwY-3bvuA130_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." NP66227.RAi8kzuET4HCe2yPyuhyR1cDXSRTTd90BYwfjwY-3bvuA130_provenance.
- NP66230.RAm2dycMWnFwNKl1C33G4huhVONhvnachrICaDgS8SqHE130_assertion description "[Is urokinase gene 3'-UTR polymorphism associated with prostate cancer?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66230.RAm2dycMWnFwNKl1C33G4huhVONhvnachrICaDgS8SqHE130_provenance.
- NP66231.RAjke0O1drbr5hOek9eqQ0jWTvPZXD_WUR_zfXi2PSVlQ130_assertion description "[Coding region polymorphisms in T cell signal transduction genes. Prevalence and association to development of multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66231.RAjke0O1drbr5hOek9eqQ0jWTvPZXD_WUR_zfXi2PSVlQ130_provenance.
- NP66236.RAvseja74CLGA53r-0zLoyNJ1H7XJJMsNa9e05XKIDPyM130_assertion description "[The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66236.RAvseja74CLGA53r-0zLoyNJ1H7XJJMsNa9e05XKIDPyM130_provenance.
- NP66238.RAhNDkbrFB8EuSykFhrh5v21lHxZAlouBzdd-mxvLHl3Y130_assertion description "[Obese Southern Europeans carrying the 148M allele have increased indices of liver damage uncoupled from proxy measures of insulin resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66238.RAhNDkbrFB8EuSykFhrh5v21lHxZAlouBzdd-mxvLHl3Y130_provenance.
- NP66249.RAizfY8l6wXtXEDyT31_eQGmc3exuaoXZZtGjPT2CeRFg130_assertion description "[Although the overall effect of DNA repair genes in colorectal cancer etiology seems limited, their influence in the response to chemotherapy and prognosis may be more relevant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66249.RAizfY8l6wXtXEDyT31_eQGmc3exuaoXZZtGjPT2CeRFg130_provenance.
- NP66254.RAm9yAsaH3xlyIuynjo0sAA8lx0RlufYoLgHRSxGRhgKI130_assertion description "[POLG1 polyglutamine tract variants associated with Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66254.RAm9yAsaH3xlyIuynjo0sAA8lx0RlufYoLgHRSxGRhgKI130_provenance.
- NP66257.RAuQguk88MsN-z9pPEZaCOXaz0etZGaZSCL06rwXR5itg130_assertion description "[Polymorphisms in genes regulating the HPA axis associated with empirically delineated classes of unexplained chronic fatigue.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66257.RAuQguk88MsN-z9pPEZaCOXaz0etZGaZSCL06rwXR5itg130_provenance.
- NP66264.RAvq9jVpQIjDHyVZ_b2liYtrkXuciGAk8_HvRUo8gQk5g130_assertion description "[Higher AP level corresponding to 3-rd degree AH in the group of patients with burdened familial anamnesis was associated with carriage of Asn allele of polymorphic marker Lysl98Asn of EDN1 gene (OR 2.24 95% CI 1.20-4.18, p=0.008), 4a allele of polymorphic marker 4a/4b of NOS3 gene (OR 2.23 C/1.29-3.83, p=0.002), genotype ArgArg of polymorphic marker Glnl92Arg of PON1 gene (OR 6.14 C71.46-25.67, p=0.01), T allele of polymorphic marker of C825T gene GNB3 (OR 1.75 C/1.11-2.76, p=0.01) and genotype AA of polymorphic marker A(A153)G of AT2R1 gene (OR 2.61 C/11.29-5.34, p=0.005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66264.RAvq9jVpQIjDHyVZ_b2liYtrkXuciGAk8_HvRUo8gQk5g130_provenance.
- NP66265.RApHIqb1Zq0iHr-5sCt5KvsmDwZKbjL_EcEfG_NJDS5F0130_assertion description "[Further examination of these genes and their relationships with cardiometabolic disease could foster development of pharmacogenetic guidelines aimed to prevent increases in fasting glucose during antihypertensive treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66265.RApHIqb1Zq0iHr-5sCt5KvsmDwZKbjL_EcEfG_NJDS5F0130_provenance.
- NP66269.RAmfh_ONvcFk385jM1-m1kilUd-6YZpuz36zp_oJkGHMo130_assertion description "[Therefore, polymorphisms of genes encoding endogenous free-radical scavenging systems, such as paraoxonase 1 (PON1), and anti-glycation defences, such as glyoxalase I (GI), could influence susceptibility to MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66269.RAmfh_ONvcFk385jM1-m1kilUd-6YZpuz36zp_oJkGHMo130_provenance.
- NP66287.RAvIZdPmGxfRvUDgWaymU5sz71Ct5xf64_s5a5N9XpjC8130_assertion description "[Peroxisome proliferator-activated corrected receptor-gamma2 corrected Pro12Ala, interaction with alcohol intake and NSAID use, in relation to risk of breast cancer in a prospective study of Danes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66287.RAvIZdPmGxfRvUDgWaymU5sz71Ct5xf64_s5a5N9XpjC8130_provenance.
- NP66294.RAhnkOpQkIQ636V9g_jBNZpc0a38kJE5Ek-bDdHLr4-B8130_assertion description "[Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66294.RAhnkOpQkIQ636V9g_jBNZpc0a38kJE5Ek-bDdHLr4-B8130_provenance.
- NP66296.RAvbwOzOwwkfkG8faRDd1SR9wc5W_lNyPt9fgi0TKrHGA130_assertion description "[We found that SNPs in ERCC1 and iASPP were associated with response to chemotherapy or combined chemotherapy and radiotherapy in NSCLC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66296.RAvbwOzOwwkfkG8faRDd1SR9wc5W_lNyPt9fgi0TKrHGA130_provenance.
- NP66299.RAgdfXZ9nYboSoRs3EGwIyLl_0FJeuJe4idnkuDEa8g7c130_assertion description "[The combined evidence from reduced DARPP-32 expression in the dorsolateral prefrontal cortex (DLPFC) in schizophrenic patients and from abnormalities in mice with a genetic deletion of DARPP-32 or with point mutations in phosphorylation sites of DARPP-32 suggested that it would be worthwhile to investigate the association between DARPP-32 and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66299.RAgdfXZ9nYboSoRs3EGwIyLl_0FJeuJe4idnkuDEa8g7c130_provenance.
- NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_assertion description "[Recent work on DAOA, PPP1R1B, and APOL1 suggests that these genes present common alleles associated to increase risk of schizophrenia but conferring an overall selective advantage, related to better cognitive performance (DAOA and PPP1R1B) or protection against pathogens (APOL1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_provenance.
- NP66303.RAlbImNE28hZ2DZPaRvEFUazg3xOG9k7hPsxgp6yNbb2k130_assertion description "[Genetic variants in epigenetic genes and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66303.RAlbImNE28hZ2DZPaRvEFUazg3xOG9k7hPsxgp6yNbb2k130_provenance.
- NP66305.RAu-jQjILQjAoEu4JZyaQC1zKDWUG16jdpSB7Z11kg_OA130_assertion description "[A frequent polymorphism, A91V (C to T transition at position 272), may impair processing of perforin protein to the active form, and has been suggested to increase susceptibility to childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66305.RAu-jQjILQjAoEu4JZyaQC1zKDWUG16jdpSB7Z11kg_OA130_provenance.
- NP66317.RAmU16cac9615TklKhB8IjMBt34keXZQNou-zKKyGMN9M130_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." NP66317.RAmU16cac9615TklKhB8IjMBt34keXZQNou-zKKyGMN9M130_provenance.
- NP66320.RAqgZjgIp6G7mX5hNZtwtEBVmzvpBswZu6TVelEi5ONR0130_assertion description "[Our study shows that there is no significant difference in the genotype, allele and haplotype frequencies of PRNP codon 129 and 219 polymorphisms between Korean VaD patients and normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66320.RAqgZjgIp6G7mX5hNZtwtEBVmzvpBswZu6TVelEi5ONR0130_provenance.
- NP66323.RAloqKz31A3kmAl_Un_AmO3z8g4gaSoZysRenYLGetNPo130_assertion description "[We have progressively analysed three studies of coronary heart disease (CHD) for a variant in EPCR (Ser219Gly).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66323.RAloqKz31A3kmAl_Un_AmO3z8g4gaSoZysRenYLGetNPo130_provenance.
- NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_assertion description "[None of the patients with sEPCR levels below 100 ng/ml carried the A3 haplotype, while patients with elevated sEPCR levels carried the A3 haplotype either in a heterozygous or homozygous state. Our study confirms that there is a strong association between A3 haplotype and elevated sEPCR levels. We suggest that elevated sEPCR levels might increase the risk of stroke at pediatric age when compared to controls. Studies with large series of patients are warranted to confirm this hypothesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_provenance.
- NP66330.RAsocOSn7HYRgCsJrCp3wO8_TKWOle6CGTTJGgzbV5Dsw130_assertion description "[We screened RHO, PRPF31, RP1, and IMPDH1 and identified causative mutations in 4% of isolated and 2% of adRP patients from India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66330.RAsocOSn7HYRgCsJrCp3wO8_TKWOle6CGTTJGgzbV5Dsw130_provenance.
- NP66331.RAnkCfumIOXCJ_Rm6tTXU3aZCYMWQaACLsRKjk5Zt-zpY130_assertion description "[A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66331.RAnkCfumIOXCJ_Rm6tTXU3aZCYMWQaACLsRKjk5Zt-zpY130_provenance.
- NP66334.RAmBNv6-L_017sorSusuAxGOuBX9UHP4d6i4SobsXO7fw130_assertion description "[Genetic association between polymorphisms of Pen2 gene and late onset Alzheimer's disease in the North Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66334.RAmBNv6-L_017sorSusuAxGOuBX9UHP4d6i4SobsXO7fw130_provenance.
- NP66338.RAthCxsGbo2VzxGoqRjYrfHzuB8LeUXTgom5A2Aqbmw8g130_assertion description "[Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66338.RAthCxsGbo2VzxGoqRjYrfHzuB8LeUXTgom5A2Aqbmw8g130_provenance.
- NP66345.RAoLsUzsA0Nh2iRfYh9JAMY8AuA_7K_QmaxLDi5H4Gp5Y130_assertion description "[Association of prostaglandin E synthase 2 (PTGES2) Arg298His polymorphism with type 2 diabetes in two German study populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66345.RAoLsUzsA0Nh2iRfYh9JAMY8AuA_7K_QmaxLDi5H4Gp5Y130_provenance.
- NP66346.RArzIiDvVpvttLB90k-xOiKLCFUlMCKnpB2LTiMCfsmP0130_assertion description "[Prostacyclin synthase and arachidonate 5-lipoxygenase polymorphisms and risk of colorectal polyps.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66346.RArzIiDvVpvttLB90k-xOiKLCFUlMCKnpB2LTiMCfsmP0130_provenance.
- NP66355.RAiQ0liIuMHfaZW9FnxCY_K9EFlGLoR9US-VaEPAhlY9c130_assertion description "[Functional polymorphisms in the cyclooxygenase 2 (COX-2) gene and risk of breast cancer in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66355.RAiQ0liIuMHfaZW9FnxCY_K9EFlGLoR9US-VaEPAhlY9c130_provenance.
- NP66357.RAjA_lV4G3HrYgiyEZV1koKDt8c_NdiyaTO3NgAi4zRr8130_assertion description "[Our data suggest that the FAS 1377G>A and IL10 592C>A polymorphisms could modify disease-free and overall survival in women with lymph node-positive breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66357.RAjA_lV4G3HrYgiyEZV1koKDt8c_NdiyaTO3NgAi4zRr8130_provenance.
- NP66358.RAtgb_tWCJKrGY7Y5aOZGxVAImhQ-BPv-HsvgOFnt474Q130_assertion description "[Current evidence on the relationship between polymorphisms in the COX-2 gene and breast cancer risk: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66358.RAtgb_tWCJKrGY7Y5aOZGxVAImhQ-BPv-HsvgOFnt474Q130_provenance.
- NP66359.RArzNnzS_tNR_YIBsmSUiEAznoiwCzloVtL9oqOuRBUWk130_assertion description "[The TNFSF10 (rs1131532) polymorphism was identified as a possible prognostic factor of survival in patients with operated invasive breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66359.RArzNnzS_tNR_YIBsmSUiEAznoiwCzloVtL9oqOuRBUWk130_provenance.
- NP66361.RApv_RAKuR18XbVshmv_MLX88q51ozntgvYiVlqdMpSNY130_assertion description "[Our results suggest that the COX-2 Val511Ala SNP does not antagonize the effect of NSAIDs on colon cancer risk and provides support that NSAID use and the COX-2 Val511Ala SNP may contribute to a reduced risk of colon cancer among African Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66361.RApv_RAKuR18XbVshmv_MLX88q51ozntgvYiVlqdMpSNY130_provenance.
- NP66364.RAhcZ_oL5Sz0uhOJV0nbD1854zUoUomlqeZvxnpbtzbTo130_assertion description "[Stratified analysis indicated that an elevated risk of GC was observed in subjects carrying the AA genotype and Helicobacter pylori infection (OR, 3.88; 95% CI: 1.46-10.34) or smoking (OR, 7.02; 95% CI: 2.19-22.48), and a high expression of COX-2 was found in subjects with AA genotype (OR, 1.84; 95% CI: 1.09-3.10) compared with GG genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66364.RAhcZ_oL5Sz0uhOJV0nbD1854zUoUomlqeZvxnpbtzbTo130_provenance.
- NP66366.RAtqV-6RWiwWASxWdHH9oZl4iNoOkYUC74dEeHFNxxJdc130_assertion description "[These results suggest that COX-2 genotyping might be useful in predicting the risk and severity of RA in individuals without the SE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66366.RAtqV-6RWiwWASxWdHH9oZl4iNoOkYUC74dEeHFNxxJdc130_provenance.
- NP66368.RAiZUasiG_8ma4gMe0MW5TxT1BJytkradcijwmYKit5qk130_assertion description "[Association of the 3050G>C polymorphism in the cyclooxygenase 2 gene with systemic sarcoidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66368.RAiZUasiG_8ma4gMe0MW5TxT1BJytkradcijwmYKit5qk130_provenance.
- NP66369.RAkt9dF6bunepHqDWmnPpKK6Vw-fNkUBYT0x7fCs4mHQ0130_assertion description "[These results suggest that the -765G --> C polymorphism of COX-2 does not play a significant role in the development of SLE in a Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66369.RAkt9dF6bunepHqDWmnPpKK6Vw-fNkUBYT0x7fCs4mHQ0130_provenance.
- NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_assertion description "[COX-2 common variants -765G-->C and -1195A-->G appear to be associated with risk of NMSC, although in different ways in the SCC and BCC subgroups, indicating that environmental and genetic risk factors may play different roles in the outcome leading to these two phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_provenance.
- NP66379.RAieX1Z1O78gxMM9wfCDafGGCHu5TdR3FCRliLom22rs8130_assertion description "[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66379.RAieX1Z1O78gxMM9wfCDafGGCHu5TdR3FCRliLom22rs8130_provenance.
- NP66384.RAniRlYruw77e16mTXhQ-RWRXCZ3vEb5Ak2HVb2vp_fbI130_assertion description "[The non-synonymous C1858T substitution in the PTPN22 gene is associated with susceptibility to the severe forms of alopecia areata.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66384.RAniRlYruw77e16mTXhQ-RWRXCZ3vEb5Ak2HVb2vp_fbI130_provenance.
- NP66387.RAm165DmHuNBwse80JmyRBwLrrFHbtcPm1pi5zZ_7OBAc130_assertion description "[Stepwise logistic regression analysis (controlled for the confounding effects of sex and race) showed that the PTPN22 CT/TT genotype was associated with a significantly higher risk of SSc compared with the CC genotype (for patients with SSc, OR 1.64, 95% CI 1.2-2.2; for ACA-positive patients with SSc, OR 1.63, 95% CI 1.0-2.6; for anti-topo I antibody-positive SSc, OR 2.33, 95% CI 1.5-3.7).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66387.RAm165DmHuNBwse80JmyRBwLrrFHbtcPm1pi5zZ_7OBAc130_provenance.
- NP66388.RAl7oJnlKKa6N9cBscXa2Mmm0p6yQb7usq83wsIDgBHo4130_assertion description "[We then conducted a meta-analysis of the most recent studies of SSc in order to verify the association or lack of association between the PTPN22 1858C>T variant and SSc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66388.RAl7oJnlKKa6N9cBscXa2Mmm0p6yQb7usq83wsIDgBHo4130_provenance.
- NP66396.RApXIUq-DPQ6-yPdJGFrOAtaiyv8If9QQSOTXjgG32A34130_assertion description "[Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66396.RApXIUq-DPQ6-yPdJGFrOAtaiyv8If9QQSOTXjgG32A34130_provenance.
- NP66399.RAt8s7h3TlYvYz7JYLCAezQl5pnjRaMeBuBYAcVuOMgZE130_assertion description "[these findings provide support for the influence of genetic variation in NER on bladder cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66399.RAt8s7h3TlYvYz7JYLCAezQl5pnjRaMeBuBYAcVuOMgZE130_provenance.
- NP66400.RArA86cw2aZXsWf64yM2Eq0EOxLlq9VQsWzoJpftkTg3o130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66400.RArA86cw2aZXsWf64yM2Eq0EOxLlq9VQsWzoJpftkTg3o130_provenance.
- NP66411.RArXdaRnuiBxkyCEEHtvMdSZ0GMyi9LAjoqBHjtj7OIRs130_assertion description "[Breast cancer risk is associated with the genes encoding the DNA double-strand break repair Mre11/Rad50/Nbs1 complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66411.RArXdaRnuiBxkyCEEHtvMdSZ0GMyi9LAjoqBHjtj7OIRs130_provenance.
- NP66412.RAlv6czc_dxA8vuXP8C8KmefA1W_WeIpn0yuqTvIpRo6s130_assertion description "[Haplotypic variation in MRE11, RAD50 and NBS1 and risk of non-Hodgkin's lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66412.RAlv6czc_dxA8vuXP8C8KmefA1W_WeIpn0yuqTvIpRo6s130_provenance.
- NP66413.RAq-QtRHFM7Nteba4lkxffdPWhpyK5QXDtXUtr2HYYbnU130_assertion description "[Although four variants, two in RAD50 and two in NBS1, showed association results suggestive of an effect on NHL, they were not significant after correction for multiple tests.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66413.RAq-QtRHFM7Nteba4lkxffdPWhpyK5QXDtXUtr2HYYbnU130_provenance.
- NP66414.RAhqasIp7FBTrcoHR2zuhHm6Rrk537WNWI4_CkEXEmo2A130_assertion description "[DNA damage and repair in gastric cancer--a correlation with the hOGG1 and RAD51 genes polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66414.RAhqasIp7FBTrcoHR2zuhHm6Rrk537WNWI4_CkEXEmo2A130_provenance.
- NP66415.RAhImbLA1oE9A8fsts9sdh29vF5ABYzCYeOb1iIYnp5W0130_assertion description "[RAD51 homologous recombination repair gene haplotypes and risk of acute myeloid leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66415.RAhImbLA1oE9A8fsts9sdh29vF5ABYzCYeOb1iIYnp5W0130_provenance.
- NP66416.RAr41cEh-wELNJpuu8ocwOFNJZTiZT1qW5qv-hIq822kY130_assertion description "[The DNA repair gene RAD51 (135G/C-5' UTR) polymorphism also increases t-AML risk, and when combined analysis was performed on both RAD51 and HLX1 variant alleles, a synergistic 9.5-fold increase (95% CI, 2.22-40.64) in the risk of t-AML was observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66416.RAr41cEh-wELNJpuu8ocwOFNJZTiZT1qW5qv-hIq822kY130_provenance.
- NP66418.RAnkP224159SbkprKu6KvI6S-B_PTcTh_CcTSWYHRjI-E130_assertion description "[Significant effect of homologous recombination DNA repair gene polymorphisms on pancreatic cancer survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66418.RAnkP224159SbkprKu6KvI6S-B_PTcTh_CcTSWYHRjI-E130_provenance.
- NP66425.RAguEtxCmzwtMLQ7roHbf1qNldZPcdjrPn9xq9EMqRuHQ130_assertion description "[Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66425.RAguEtxCmzwtMLQ7roHbf1qNldZPcdjrPn9xq9EMqRuHQ130_provenance.
- NP66431.RApn5AcDE_8p7B9dkxjK966TCIkuS7Wtd8vugkxO1TgCU130_assertion description "[Experimental and clinical evidences suggest that renin-angiotensin-aldosterone system (RAAS) has a crucial role in diabetic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66431.RApn5AcDE_8p7B9dkxjK966TCIkuS7Wtd8vugkxO1TgCU130_provenance.
- NP66433.RAgNqnvnqac4LFQmlPnUw5ddoYirtzPrtaJ-uQdltggMk130_assertion description "[we found no significant evidence that genetic variants in FOLR1, GGH, FPGS and SLC19A1 are associated with the risk of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66433.RAgNqnvnqac4LFQmlPnUw5ddoYirtzPrtaJ-uQdltggMk130_provenance.
- NP66435.RAtLBM9t0N3WDPmW2C8FAw-j0c7UFJMPF5tB4xIOQwdM8130_assertion description "[Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66435.RAtLBM9t0N3WDPmW2C8FAw-j0c7UFJMPF5tB4xIOQwdM8130_provenance.
- NP66437.RAvk8_YfI3o4nMkW56o7RvDsTxUPB-HgCQPqVxwc5teRs130_assertion description "[The C to G substitution at position -391 in the RGS2 promoter increases RGS2 expression in adipocytes and is associated with the metabolic syndrome in white European men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66437.RAvk8_YfI3o4nMkW56o7RvDsTxUPB-HgCQPqVxwc5teRs130_provenance.
- NP66445.RAt6paKUrD5WPqFlFhDBCJ0MWX0SHojMaWLH737UfVsW0130_assertion description "[Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66445.RAt6paKUrD5WPqFlFhDBCJ0MWX0SHojMaWLH737UfVsW0130_provenance.
- NP66448.RAh_XIefz4LODJpwnH79wVR1LJW-3jbbi71Jw-wqqZJNk130_assertion description "[it was found that oxygen radical generation occurred within carcinoma cells, but the role of polymorphism of specific genes in the development of breast cancer should be evaluated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66448.RAh_XIefz4LODJpwnH79wVR1LJW-3jbbi71Jw-wqqZJNk130_provenance.
- NP66449.RAvp7430Fr9MQZXbQ5IyfUdVoAHNNW0NZux1yQB-8JOFI130_assertion description "[Hence we found an important association between polymorphisms in the S100A8 gene and periodontitis in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66449.RAvp7430Fr9MQZXbQ5IyfUdVoAHNNW0NZux1yQB-8JOFI130_provenance.
- NP66455.RArCavvMttv6WsmXJZy7PodxAqfy2jXaQkBiACoHQtOhQ130_assertion description "[Gastrointestinal symptoms in families of patients with an SCN5A-encoded cardiac channelopathy: evidence of an intestinal channelopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66455.RArCavvMttv6WsmXJZy7PodxAqfy2jXaQkBiACoHQtOhQ130_provenance.
- NP66456.RAqNN-IMzNywn1p0bR9v5Q5_SxHuy8_WIdVQmkMeGwKfo130_assertion description "[Association of pre-eclampsia with the R563Q mutation of the beta-subunit of the epithelial sodium channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66456.RAqNN-IMzNywn1p0bR9v5Q5_SxHuy8_WIdVQmkMeGwKfo130_provenance.
- NP66457.RAjeaa7GZ-T1JOqrLJrG2TyTjz94Rx-JimirGR5Pqok0Q130_assertion description "[The prime candidates for genetic modifiers in CF are elements of host defence such as the TNFalpha receptor and of ion transport such as the amiloride-sensitive epithelial sodium channel ENaC, both of which are encoded side by side on 12p13 (TNFRSF1A, SCNN1A) and 16p12 (SCNN1B, SCNN1G).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66457.RAjeaa7GZ-T1JOqrLJrG2TyTjz94Rx-JimirGR5Pqok0Q130_provenance.
- NP66467.RAjaPdPBTx3IfGC6iMHdV4SE5-mgBHf1y_BPA4zCJLW6E130_assertion description "[Role of S128R polymorphism of E-selectin in colon metastasis formation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66467.RAjaPdPBTx3IfGC6iMHdV4SE5-mgBHf1y_BPA4zCJLW6E130_provenance.
- NP66469.RAua_JXU1w9nRwxxDFWKFryI2WAvfIUtXHi3L8PhOFzuE130_assertion description "[E-selectin S128R polymorphism leads to severe asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66469.RAua_JXU1w9nRwxxDFWKFryI2WAvfIUtXHi3L8PhOFzuE130_provenance.
- NP66470.RAlYn9q8i5qgpcTTKLa5rH4nHMF8O-a-fNYsvr3QijDvQ130_assertion description "[Our findings indicate therefore that the risk of acquiring CAD in patients with DM2 increases significantly in the presence of the 128R mutant allele of the E-selectin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66470.RAlYn9q8i5qgpcTTKLa5rH4nHMF8O-a-fNYsvr3QijDvQ130_provenance.
- NP66471.RApFIFFLSdD1S4ntWfXR4kK8KKpeGJdCh45a2QLBocJDk130_assertion description "[Association between the Phe206Leu polymorphism of L-selectin and brucellosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66471.RApFIFFLSdD1S4ntWfXR4kK8KKpeGJdCh45a2QLBocJDk130_provenance.
- NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_assertion description "[However, individuals with AATD phenotypes had a higher risk of developing squamous cell lung cancer then those with non-deficient AAT variants (OR = 4.51, 95% CI = 1.66-12.29).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_provenance.
- NP66483.RAljF93yS2zhHm9P3zHUdpCpnJivmW6OSRKvfgrkApy0Y130_assertion description "[This provides further evidence for the involvement of genetic variations of MEGSIN in the pathogenesis of IgAN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66483.RAljF93yS2zhHm9P3zHUdpCpnJivmW6OSRKvfgrkApy0Y130_provenance.
- NP66485.RAuquIzI91AiZB6PpTYrqRYOqJezeB1Y3tQDusogjLrNw130_assertion description "[267G/A in megsin gene is associated with IgAN susceptibility. AG and AA genotypes are the risk factors of pathogenesis of IgAN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66485.RAuquIzI91AiZB6PpTYrqRYOqJezeB1Y3tQDusogjLrNw130_provenance.
- NP66491.RAmN6NhyDUjbSi3vB2gFQKqkVE3fe-6ZlqokstWb4xrDo130_assertion description "[To determine the prevalence of polymorphisms in the plasminogen activator inhibitor-1 (PAI-1) promoter 4G/5G polymorphisms in Chinese Han population and to investigate whether they are associated with pulmonary thromboembolism (PTE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66491.RAmN6NhyDUjbSi3vB2gFQKqkVE3fe-6ZlqokstWb4xrDo130_provenance.
- NP66493.RAsFoq2M8fGDCuUzbqY_Gq_Wb9DZt1sPlIj8E80v8-YRs130_assertion description "[Plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism and endometriosis. Influence of PAI-1 polymorphism on PAI-1 antigen and mRNA expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66493.RAsFoq2M8fGDCuUzbqY_Gq_Wb9DZt1sPlIj8E80v8-YRs130_provenance.