Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP47269.RAkSv9oHpkqiY0sMzTCR41oJPyM-w-c9kT7l6Wnid_shk130_assertion description "[Leukocyte trafficking, regulated by chemokine ligands and their receptors, involves in the pathogenesis of graft-versus-host disease (GVHD) including CC ligand 5 (CCL5) or CC receptor 5 (CCR5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47269.RAkSv9oHpkqiY0sMzTCR41oJPyM-w-c9kT7l6Wnid_shk130_provenance.
- NP47272.RAnZLNc0yJxVZrbo9jO53yu4J_b7v6QRQYxY4-FzosH6g130_assertion description "[Intriguingly, homozygosity for the RA associated DNASE2 -1066 G allele had an additive effect on the disease susceptibility conferred by the wt allele of CCR5 (OR = 2.24, P = 0.0051 for carrier of both RA associated alleles)]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47272.RAnZLNc0yJxVZrbo9jO53yu4J_b7v6QRQYxY4-FzosH6g130_provenance.
- NP47278.RAiU3-kzWKZnE-NntfKXY6ITs1miQchvJ3Tv9wsGzbUj4130_assertion description "[This study finding provide a strong evidence that Eotaxin 1 Thr23Thr homozygote has a protective effect on asthma and significantly decreases plasma Eotaxin 1 concentrations in asthmatics in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47278.RAiU3-kzWKZnE-NntfKXY6ITs1miQchvJ3Tv9wsGzbUj4130_provenance.
- NP47281.RAgS5P4zpG-96g1XKXKIdNPbaZKr1QZoI0ULdoeANC43k130_assertion description "[CCR5Delta32 polymorphism effects on CCR5 expression, patterns of immunopathology and disease course in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47281.RAgS5P4zpG-96g1XKXKIdNPbaZKr1QZoI0ULdoeANC43k130_provenance.
- NP47283.RAiYFKHBPdLUu-HELXuOOqQSsktiy8VkvDeGQs10InjXs130_assertion description "[Thus, specific cyclin D1 isoforms are associated with discrete forms of breast cancer and high cyclin D1b protein levels hold prognostic potential.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47283.RAiYFKHBPdLUu-HELXuOOqQSsktiy8VkvDeGQs10InjXs130_provenance.
- NP47284.RAvzPIzjYWAIcoEabYP_0h1G0UVIQvUP24S9pcvYO92S0130_assertion description "[Breast cancer and cyclin D1 gene polymorphism in Turkish women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47284.RAvzPIzjYWAIcoEabYP_0h1G0UVIQvUP24S9pcvYO92S0130_provenance.
- NP47287.RAt5GrPcAM7ZLDWWeBAhCd1DcaJLE4_jDlT6UfjaM8abY130_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." NP47287.RAt5GrPcAM7ZLDWWeBAhCd1DcaJLE4_jDlT6UfjaM8abY130_provenance.
- NP47291.RAsybeLHenvmCYGfCBaeOnqznVOQNoXE3ir2bqB2JoPq8130_assertion description "[No statistical significance was observed between CCND1 AG genotype and tumour grades. While the functional significance of the observed segregation of the CCND1 A/G polymorphism and tumour grade is unclear, our data suggest that CCND1 allele frequencies and genotype distributions show significant differences between tumour grades in sporadic pituitary adenomas. Since CCND1 genotype may be determined by analysis of peripheral blood samples it may provide a useful predictive marker for those tumours likely to show invasive behaviour. This may be clinically useful in indicating which tumours should receive adjunctive treatment (e.g. radiotherapy) immediately after surgical resection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47291.RAsybeLHenvmCYGfCBaeOnqznVOQNoXE3ir2bqB2JoPq8130_provenance.
- NP47299.RAgel3JaKd6anteSFnQRXB2WBj9COhbr50xNM7_dRK6UY130_assertion description "[Our data suggest that CD1 A870 background may be imparting aggressive phenotype to EAC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47299.RAgel3JaKd6anteSFnQRXB2WBj9COhbr50xNM7_dRK6UY130_provenance.
- NP47300.RAoUW38kq9jBnu7lEXGwr9tEp0WbRF493golymQaHJg8E130_assertion description "[We did not find a correlation among the polymorphism of CCND1 A870G and colorectal cancer risk or between this polymorphism and lifestyle habits, diet, or follow-up.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47300.RAoUW38kq9jBnu7lEXGwr9tEp0WbRF493golymQaHJg8E130_provenance.
- NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_assertion description "[Polymorphisms in the 2 cell-cycle control genes Aurora A and Cyclin D1 have previously been associated with changes in the age of onset of colorectal cancer in persons harboring germline mutations in DNA mismatch repair genes associated with hereditary nonpolyposis colorectal cancer (HNPCC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_provenance.
- NP47302.RAvUFUb7n8qGaDCN8RQzYBKBX1qaO28YijrjjmSKrcaRc130_assertion description "[However, the CCND1 G870A polymorphism may modify the protective effect of postmenopausal hormone use on the development of CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47302.RAvUFUb7n8qGaDCN8RQzYBKBX1qaO28YijrjjmSKrcaRc130_provenance.
- NP47304.RAvf4V_06ewYi4YaFc89EM5Zl1nC7_pbHMaZcpr067YxQ130_assertion description "[Cyclin D1 and epidermal growth factor polymorphisms associated with survival in patients with advanced colorectal cancer treated with Cetuximab.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47304.RAvf4V_06ewYi4YaFc89EM5Zl1nC7_pbHMaZcpr067YxQ130_provenance.
- NP47307.RAquJhqyebI6m0ElHzhE6Uo9KSKBCXAzVInbzHbmnJ7rE130_assertion description "[Despite the relevance of both pathways in the pathogenesis of the disease, and the fact that this is indeed the first study that considers these pathways as a candidate-gene selection approach, our study does not present any evidence of the presence of low-penetrance variants for the selected markers in any of the considered genes in our cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47307.RAquJhqyebI6m0ElHzhE6Uo9KSKBCXAzVInbzHbmnJ7rE130_provenance.
- NP47311.RAn0gcy9JKRUHLtxMuQm6AoHQcd-55F9YfJY89evUY5eU130_assertion description "[Independent pharmacogenomic determinants associated with treatment outcome were identified in subsets of Taiwanese ALL patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47311.RAn0gcy9JKRUHLtxMuQm6AoHQcd-55F9YfJY89evUY5eU130_provenance.
- NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_assertion description "[: These data suggest that the CCND1 variant A allele may be a genetic susceptibility factor with a recessive or gene dose effect for the onset of sporadic RCC. More extensive and larger studies are required to clarify whether the CCND1 genotype is more specifically involved in the onset of a histological subset of RCC or RCC at a younger age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_provenance.
- NP47329.RAqyVRZrUfpaK8znkMqIpOOBIvjDToQQBZ4U6FI7954C8130_assertion description "[Polymorphisms in cyclin D1 gene and hepatocellular carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47329.RAqyVRZrUfpaK8znkMqIpOOBIvjDToQQBZ4U6FI7954C8130_provenance.
- NP47331.RAkPpI-WjN1pc2sPpTuHzAXaq-v8SKX3Xq2tXRoORr7PY130_assertion description "[Effects of cyclin D1 (CCND1) polymorphism on susceptibility to lung cancer in a North Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47331.RAkPpI-WjN1pc2sPpTuHzAXaq-v8SKX3Xq2tXRoORr7PY130_provenance.
- NP47338.RAt_-doKbrvi1W6MpU6ZDrDX8KJxGyZGS-34QpUHZmoSM130_assertion description "[Polymorphism within the cyclin D1 gene is associated with prognosis in patients with squamous cell carcinoma of the head and neck.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47338.RAt_-doKbrvi1W6MpU6ZDrDX8KJxGyZGS-34QpUHZmoSM130_provenance.
- NP47341.RApFGbc4mdBVaBEMagiBFY082dsTsIVgFd86vScsg-r3k130_assertion description "[These results are in agreement with previous findings in the Swedish and Sardinian populations and reinforce the possibility of a role for chemokines in MS pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47341.RApFGbc4mdBVaBEMagiBFY082dsTsIVgFd86vScsg-r3k130_provenance.
- NP47343.RAvFq21C-FLMRj6adNeL2g3gZA0KYKgLPluzWW1UPAdDI130_assertion description "[Association analysis of monocyte chemotactic protein-3 (MCP3) polymorphisms with asthmatic phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47343.RAvFq21C-FLMRj6adNeL2g3gZA0KYKgLPluzWW1UPAdDI130_provenance.
- NP47347.RAqxH-aDVZVUGIu-_DOwHOnbUGh1G_ksItw44rFjF26zk130_assertion description "[The MCP-1 -2518G variant in homozygous form appears as a genetic risk factor for severe CAD. This genotype is associated with elevated Lp(a) levels in patients. Individuals homozygous for CCR2-64I or CCR5Delta32 mutations are at reduced risk for severe CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47347.RAqxH-aDVZVUGIu-_DOwHOnbUGh1G_ksItw44rFjF26zk130_provenance.
- NP47348.RAoRDKVtOXFOPCjVbThddQYRjGYX-dD_g_pLeawxEDSpw130_assertion description "[The frequency and distribution of genotypes of the -28(C/G) RANTES gene polymorphism were significantly different between the 2 groups (p < 0.001), and the RANTES -28G allele was significantly more frequent in patients with SLE than in healthy controls (23.9% vs 11%; p = 0.006, OR 2.37, 95% CI 1.25-4.28).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47348.RAoRDKVtOXFOPCjVbThddQYRjGYX-dD_g_pLeawxEDSpw130_provenance.
- NP47350.RAkXQH29ISPXggJjtUp7xCJBuuFmPzWJ06laKQd5wIsQs130_assertion description "[These results suggest that the tested functional variation of RANTES, IL-8, IL-1alpha, and MCP-1 genes do not confer a relevant role in the susceptibility or severity of SLE in the Spanish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47350.RAkXQH29ISPXggJjtUp7xCJBuuFmPzWJ06laKQd5wIsQs130_provenance.
- NP47352.RAidRwlkZMkuRvM6HTyIx1YpoNxjj2Wi89cdGXKYeDelY130_assertion description "[In conclusion, RANTES haplotypes might contribute to the polygenic interaction between HCV and the host immune system and could help to risk stratify patients prior to antiviral therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47352.RAidRwlkZMkuRvM6HTyIx1YpoNxjj2Wi89cdGXKYeDelY130_provenance.
- NP47361.RAqCk0c7fbyhEfcztfSHMOuF-r4lqxYwvaYHhjJk90zMU130_assertion description "[This meta-analysis suggested that RANTES gene -403G/A polymorphism would be a risk factor among atopic asthma patients. To further evaluate gene-to-gene and gene-to-environment interactions on RANTES polymorphisms and asthma risk, more studies with thousands of patients are required.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47361.RAqCk0c7fbyhEfcztfSHMOuF-r4lqxYwvaYHhjJk90zMU130_provenance.
- NP47368.RAm_DJLQzTB9octmOXTaYjLyroYAOPhfVp3JjpJmMDiOA130_assertion description "[CCL5 and CCR5 genotypes modify clinical, radiological and pathological features of multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47368.RAm_DJLQzTB9octmOXTaYjLyroYAOPhfVp3JjpJmMDiOA130_provenance.
- NP47376.RAm_C5B9h6QlSM1utvEKiMMzdjrGjVPAhUYqf16-qqSCE130_assertion description "[The study results indicated that the -403 and -28 alleles in the RANTES promoter region belong to the predictor gene set for allergic rhinitis and could be used in genomic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47376.RAm_C5B9h6QlSM1utvEKiMMzdjrGjVPAhUYqf16-qqSCE130_provenance.
- NP47378.RAnEcoqMAUUWyxRrfSJeJBywrVCYMVh0tBUKwgYGIGEuI130_assertion description "[Considering that this might affect sarcoidosis, we studied polymorphism of the RANTES gene in 114 patients with sarcoidosis and 136 healthy control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47378.RAnEcoqMAUUWyxRrfSJeJBywrVCYMVh0tBUKwgYGIGEuI130_provenance.
- NP47379.RAjNidWg_c8e9IU_Xz1a20nodwfP0HQ7ANi3NX9XKjiY4130_assertion description "[To evaluate the effect of RANTES gene promoter polymorphism and RANTES receptor (CCR5 gene) promoter polymorphism on diabetic nephropathy in Japanese type 2 diabetic subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47379.RAjNidWg_c8e9IU_Xz1a20nodwfP0HQ7ANi3NX9XKjiY4130_provenance.
- NP47383.RAgoDICejisqSoX2NZTgZm95SK58SPio9yiP1BmJ93f4E130_assertion description "[Our results suggest that the polymorphisms of the eotaxin gene family are associated with the susceptibility of asthma and Eotaxin-3 might play the critical role for the recruitment of eosinophils and the maintenance of IgE levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47383.RAgoDICejisqSoX2NZTgZm95SK58SPio9yiP1BmJ93f4E130_provenance.
- NP47384.RAuzh_M0A4WJmhvrkTE3fZDIMzCkt6b57ccxpVzZ59rLA130_assertion description "[Single nucleotide polymorphism of eotaxin-3 +2497 is associated with the asthma susceptibility, peripheral eosinophil counts and total levels of plasma IgE in adult population from Hubei province, and polymorphism of +77 is associated with peripheral eosinophil counts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47384.RAuzh_M0A4WJmhvrkTE3fZDIMzCkt6b57ccxpVzZ59rLA130_provenance.
- NP47390.RAk1MpykWv0eIj12adX9j72pS0aP9IOpE48sxPVLnHbSY130_assertion description "[Our results strongly suggest that the polymorphisms of eotaxin-3 might be associated with susceptibility to RA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47390.RAk1MpykWv0eIj12adX9j72pS0aP9IOpE48sxPVLnHbSY130_provenance.
- NP47393.RAureQ2_p1NO60lciTPafecdtTwQgzGM-D6MpTbCAkygE130_assertion description "[The GG genotype and the G allele of the MCP-1 gene polymorphism were significantly more common in the AD group than in control individuals (P<0.0001) A logistic regression analysis indicated that the GG genotype was an independent risk factor for AD in our population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47393.RAureQ2_p1NO60lciTPafecdtTwQgzGM-D6MpTbCAkygE130_provenance.
- NP47398.RAsL8i5fi8dOxQvsDFcB_cyvp8QVeai0MWdBKJyudoAWs130_assertion description "[The aim of this study was to evaluate the relevance of functional genetic variations of RANTES, IL-8, IL-1alpha, and MCP-1 for systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47398.RAsL8i5fi8dOxQvsDFcB_cyvp8QVeai0MWdBKJyudoAWs130_provenance.
- NP47399.RAnRPZ3QdGPpPTbEP6F2fyAIHHFILlK3ve0W7fp4fFmNA130_assertion description "[In conclusion, our study suggests a possible role of the polymorphisms CCR5-Delta32, RANTES -403, and MCP-2 Q46K in the outcome of HCV infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47399.RAnRPZ3QdGPpPTbEP6F2fyAIHHFILlK3ve0W7fp4fFmNA130_provenance.
- NP47401.RAqPSPuZWs9P9jjU6KBUoQ_f6l-QdCqWlTl2EWWrBeNEg130_assertion description "[ Proinflammatory genetic profiles are significantly more common in subjects with stroke history. Synergistic effects between proinflammatory genotypes might be potential markers for cerebrovascular diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47401.RAqPSPuZWs9P9jjU6KBUoQ_f6l-QdCqWlTl2EWWrBeNEg130_provenance.
- NP47404.RAmFOiB8hYcW8-fPLmWxTDKlcsoxbOYZoZdcyuaYdTWfk130_assertion description "[Polymorphism in CC-chemokine ligand 2 associated with tuberculosis in Zambia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47404.RAmFOiB8hYcW8-fPLmWxTDKlcsoxbOYZoZdcyuaYdTWfk130_provenance.
- NP47405.RAkvw7weuDbe4_0Bwy7NLCmG5JN6iB1PCN9ammvtmVKQw130_assertion description "[These findings suggest that persons bearing the MCP-1 genotype GG produce high concentrations of MCP-1, which increases the risk of active TB infection in Chongqing Han people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47405.RAkvw7weuDbe4_0Bwy7NLCmG5JN6iB1PCN9ammvtmVKQw130_provenance.
- NP47407.RAgRkE0h5uN6EI-IvyVJQDrIWWmCyC_hXPsoFSbTJLpT8130_assertion description "[ RANTES A-403 was associated with CAD independently from conventional risk factors and CRP or fibrinogen as inflammatory biomarkers. The association was enhanced in smokers and ACS, conditions where platelet activation and inflammation predominate. RANTES A-403 may increase genetic susceptibility to CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47407.RAgRkE0h5uN6EI-IvyVJQDrIWWmCyC_hXPsoFSbTJLpT8130_provenance.
- NP47409.RAnpBBgtqi6CDWhfMi0TjiZSb9jet7OHkUzhJec03bQsI130_assertion description "[The MCP-1 -2518G variant in homozygous form appears as a genetic risk factor for severe CAD. This genotype is associated with elevated Lp(a) levels in patients. Individuals homozygous for CCR2-64I or CCR5Delta32 mutations are at reduced risk for severe CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47409.RAnpBBgtqi6CDWhfMi0TjiZSb9jet7OHkUzhJec03bQsI130_provenance.
- NP47411.RAulkMXy9exgh--4J-ie1fuTH4iayKgrBsmfP-NTq_K2U130_assertion description "[A monocyte chemoattractant protein-1 gene polymorphism is not associated with coronary artery disease in a Han Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47411.RAulkMXy9exgh--4J-ie1fuTH4iayKgrBsmfP-NTq_K2U130_provenance.
- NP47421.RAixlNRVjDUlltrZaD2d8k0W7jmziI8RyWpy3yIL_HOGc130_assertion description "[Though the utility for prediction of disease susceptibility of the studied polymorphisms in chemokine genes is in general not robust, we have found that polymorphisms in chemokine genes can influence the outcome of patients with idiopathic immune-mediated posterior segment uveitis. These associations require further analysis in other groups of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47421.RAixlNRVjDUlltrZaD2d8k0W7jmziI8RyWpy3yIL_HOGc130_provenance.
- NP47425.RArD72wzx-RYznRhRYF9jbhcedzqcelG8nFJoly0ydCy0130_assertion description "[Genetic polymorphisms within CCL2 gene are associated with susceptibility neither to SSc nor to specific disease phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47425.RArD72wzx-RYznRhRYF9jbhcedzqcelG8nFJoly0ydCy0130_provenance.
- NP47429.RAuidkB6j7x-VBmMkcvIuSqInzKC5--6_yZ352O4HJKJE130_assertion description "[Genetic variants of CC chemokine genes in experimental autoimmune encephalomyelitis, multiple sclerosis and rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47429.RAuidkB6j7x-VBmMkcvIuSqInzKC5--6_yZ352O4HJKJE130_provenance.
- NP47432.RAt9YGwj-ERGKl1zaFufGpMCWjJjQZX0u7FKbsjxtd_Q8130_assertion description "[Association of serum MCP-1 concentration and MCP-1 polymorphism with insulin resistance in Japanese individuals with obese type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47432.RAt9YGwj-ERGKl1zaFufGpMCWjJjQZX0u7FKbsjxtd_Q8130_provenance.
- NP47438.RAhalu3sIDG60Bq-ProWvnp_2HP_h4q7kA6LA56zZcgA0130_assertion description "[Although the allele frequency of MCP-1 promoter -2518 polymorphism is not likely to be the reason for the elevated serum MCP-1 level in Korean patients with Behcet's disease, it is possible that proinflammatory factors induced in patients' serum cause stronger activation of MCP-1 expression from the G-type promoter, as well as increased incidence of uveitis and gastric ulcer, among carriers of the G-allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47438.RAhalu3sIDG60Bq-ProWvnp_2HP_h4q7kA6LA56zZcgA0130_provenance.
- NP47441.RAtcMd5lxd8-EZMsBZ84O6uEJFEkFQ_bmgeE4lAUeAP0c130_assertion description "[We detected weak but reproducible association with markers in several genes, in proximity to susceptibility loci found in previous GWAS studies of bipolar disorder. Further work is required to study their localization, expression, and regulation and international meta-analytic efforts will help to further elucidate their role.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47441.RAtcMd5lxd8-EZMsBZ84O6uEJFEkFQ_bmgeE4lAUeAP0c130_provenance.
- NP47445.RAroBv60Zvzb1owYUwRDTAj-FwN4r-ogMohf6Z9coahQo130_assertion description "[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47445.RAroBv60Zvzb1owYUwRDTAj-FwN4r-ogMohf6Z9coahQo130_provenance.
- NP47448.RAl9ZhNdY5jxrSuaenqamAjQl0yPbYSr3N4kSnt9dLxQo130_assertion description "[Allelic frequency of the MCP-1 promoter -2518 polymorphism in the Korean population and in Korean patients with rheumatoid arthritis, systemic lupus erythematosus and adult-onset Still's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47448.RAl9ZhNdY5jxrSuaenqamAjQl0yPbYSr3N4kSnt9dLxQo130_provenance.
- NP47453.RAsprjEoCs3mh3iFT868M9xsmxfHr-f1L7IhuA5bMO-eE130_assertion description "[TARC/CCL17 may be a useful serological marker and may facilitate an assessment of the degree of disease activity in SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47453.RAsprjEoCs3mh3iFT868M9xsmxfHr-f1L7IhuA5bMO-eE130_provenance.
- NP47461.RAlctykTeJootcBF4LqXpk4Rrm2LVYumIohSVGZNo4Y4s130_assertion description "[Expression of eotaxin by human lung epithelial cells: induction by cytokines and inhibition by glucocorticoids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47461.RAlctykTeJootcBF4LqXpk4Rrm2LVYumIohSVGZNo4Y4s130_provenance.
- NP47462.RAsxtlaiEbQR0mUhdHUQORkRRPM5QZGHmt7s5UrPaZ4K8130_assertion description "[Eotaxin gene SNPs in the promoter and exon regions are not associated with susceptibility to AD, but two of them in the promoter region are associated with phenotype of AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47462.RAsxtlaiEbQR0mUhdHUQORkRRPM5QZGHmt7s5UrPaZ4K8130_provenance.
- NP47475.RAimuJooOPzhNiUnzzH0-473B64fvaSJiAebvzxiUpQ6A130_assertion description "[None of the other variations found were associated with PD, but a 2-marker haplotype (rs1800855/rs1800857) in the CCKAR gene protected women against PD (P=0.004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47475.RAimuJooOPzhNiUnzzH0-473B64fvaSJiAebvzxiUpQ6A130_provenance.
- NP47478.RAg04h43drnQDYaO2WGadQfPsweNPy1zWA0i1YW5XDDXw130_assertion description "[We speculated that alterations in the CCK-AR lead to an increase in dopamine release, which may in turn constitute a predisposition in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47478.RAg04h43drnQDYaO2WGadQfPsweNPy1zWA0i1YW5XDDXw130_provenance.
- NP47480.RAlRgGFW2Am99V0jEnXwwt0oloBRcL8bXgZAX9JnvCOOY130_assertion description "[The CCK-A receptor gene possibly associated with auditory hallucinations in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47480.RAlRgGFW2Am99V0jEnXwwt0oloBRcL8bXgZAX9JnvCOOY130_provenance.
- NP47486.RAnMnmJxWdEOxemEHC48gFXNYUPeipkm_x-t9_cKdxzks130_assertion description "[Deteriorating gallbladder contractions, possibly induced by alterations in the CCK-AR gene, as well as CCK-AR gene polymorphism, promoted gallstone formation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47486.RAnMnmJxWdEOxemEHC48gFXNYUPeipkm_x-t9_cKdxzks130_provenance.
- NP47489.RAgV1okHFfmyNyL2hKVwuCyzGf6PgIzIF9GKVlOdGr0kU130_assertion description "[While our family-based tests seem to support the CCK involvement in schizophrenia, no definite conclusion can be drawn based on such a small sample size.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47489.RAgV1okHFfmyNyL2hKVwuCyzGf6PgIzIF9GKVlOdGr0kU130_provenance.
- NP47490.RApd3h5A6ludTLnl-lgL5OfX1wND3Bds7GvLrCJCp7dd0130_assertion description "[These findings suggest that the novel STR or a nearby variant may confer susceptibility to the development of panic disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47490.RApd3h5A6ludTLnl-lgL5OfX1wND3Bds7GvLrCJCp7dd0130_provenance.
- NP47491.RAjEVgUcaoFvmVNCCV_CGRgnsuS_CJw-9ETBSm0lPH16U130_assertion description "[Cholecystokinin- and cholecystokinin-B-receptor gene polymorphisms in panic disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47491.RAjEVgUcaoFvmVNCCV_CGRgnsuS_CJw-9ETBSm0lPH16U130_provenance.
- NP47497.RAv2B19QgVW5LMADVPud6LKHMyB-Mp-KWQMGZP_G0rM9s130_assertion description "[Polymorphism or mutations in the CCK receptors may be involved in type 2 diabetes mellitus and obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47497.RAv2B19QgVW5LMADVPud6LKHMyB-Mp-KWQMGZP_G0rM9s130_provenance.
- NP47504.RAj712TG5lm5-gb6xwAnwPucXG58I9MBOO8WbinIVYt80130_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." NP47504.RAj712TG5lm5-gb6xwAnwPucXG58I9MBOO8WbinIVYt80130_provenance.
- NP47508.RAiHLiki0FJ3VqYiScGYJRUrn5PlKbTSPQ64k7vtwfR2A130_assertion description "[We report the results of molecular neonatal screening for homocystinuria (cystathionine beta-synthase deficiency) in neonates of Qatari origin, developed in conjunction with a novel biochemical screening approach.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47508.RAiHLiki0FJ3VqYiScGYJRUrn5PlKbTSPQ64k7vtwfR2A130_provenance.
- NP47509.RAuZbXD5e6MnhRjs-ocAiNXB5e_NgID76OZidzyMS6LXA130_assertion description "[Our data indicate that homocystinuria due to cystathionine beta-synthase deficiency is a frequently unrecognized disorder resulting in a high risk of thromboembolic events.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47509.RAuZbXD5e6MnhRjs-ocAiNXB5e_NgID76OZidzyMS6LXA130_provenance.
- NP47520.RAkQ-BcN6DJv09wxjKELmZ3fHTqfmxL1ozSXP11yWC5Q4130_assertion description "[We found that two single nucleotide polymorphisms in the cystathionine beta synthase (CBS) gene, 699C --> T and 1080T --> C, are associated with decreased risk of CAD and increased responsiveness to the tHcy lowering effects of folic acid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47520.RAkQ-BcN6DJv09wxjKELmZ3fHTqfmxL1ozSXP11yWC5Q4130_provenance.
- NP47521.RApFg7vP0X4-I-VeELbHHZpd4TiduHhWZ3FuUFmBgbBw8130_assertion description "[, the coincidence of clinical and biochemical effects of a common c.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47521.RApFg7vP0X4-I-VeELbHHZpd4TiduHhWZ3FuUFmBgbBw8130_provenance.
- NP47527.RAtsvWo1PT8ScNsjKF2ezS0Y4H3DOe5zUkku4IWVCk4Z0130_assertion description "[We found modest evidence for an association with a variant in the cav-1 gene and risk of overall PC and aggressive PC, which merits further study. We found no evidence that higher post-treatment serum cav-1 is associated with risk of aggressive PC or adverse PC outcomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47527.RAtsvWo1PT8ScNsjKF2ezS0Y4H3DOe5zUkku4IWVCk4Z0130_provenance.
- NP47533.RAkhdpaASKhuFC5emBAx4f_cSsS_cbJrNQSp0-Nfr3QOM130_assertion description "[Oxidative stress-related genotypes, fruit and vegetable consumption and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47533.RAkhdpaASKhuFC5emBAx4f_cSsS_cbJrNQSp0-Nfr3QOM130_provenance.
- NP47536.RAtCvt3YUJ32suoL4Pj_57nJBSXEhngfVVgPOrixa7ouQ130_assertion description "[On this evidence, these markers were not associated with DPN in the sample examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47536.RAtCvt3YUJ32suoL4Pj_57nJBSXEhngfVVgPOrixa7ouQ130_provenance.
- NP47547.RAv7VuVcRmSxLVo6gsXkudvQp0AbDvwPdbEzMvnOsUcwg130_assertion description "[Genetic polymorphisms of GSTT1, GSTM1, GSTP1, MnSOD, and catalase in nonhereditary chronic pancreatitis: evidence of xenobiotic stress and impaired antioxidant capacity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47547.RAv7VuVcRmSxLVo6gsXkudvQp0AbDvwPdbEzMvnOsUcwg130_provenance.
- NP47549.RAteZWyXWQwBw08g4TiGHr_1LXexHCjnXOQIwVmuuRBsE130_assertion description "[Our data suggest that genetic variations in the promoter region of catalase gene influence the susceptibility to essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47549.RAteZWyXWQwBw08g4TiGHr_1LXexHCjnXOQIwVmuuRBsE130_provenance.
- NP47552.RAjJl_0nPZM6HF6T8U-1E_0QltnnsV4QD0jeo1PLtN7Yc130_assertion description "[Our previous study in an isolated population showed an association between a genetic variant in the catalase gene (CAT) and essential hypertension (EH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47552.RAjJl_0nPZM6HF6T8U-1E_0QltnnsV4QD0jeo1PLtN7Yc130_provenance.
- NP47555.RAv6rMnwatam1WUwg-bj8MswIeb0RFWj_AQqUpyIwwLIk130_assertion description "[Nucleotide substitution C1167T in the catalase gene and position of nearby polymorphic markers DS11S907 and D11S2008 are connected with development of diabetes mellitus type 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47555.RAv6rMnwatam1WUwg-bj8MswIeb0RFWj_AQqUpyIwwLIk130_provenance.
- NP47556.RAi5n-zs3n9FCcdZ3JPQYzACEp-vV6l-lG2ks9ZdfAs28130_assertion description "[Support Vector Machine based feature selection method in this research found novel association between combinations of SNPs and T2D in a Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47556.RAi5n-zs3n9FCcdZ3JPQYzACEp-vV6l-lG2ks9ZdfAs28130_provenance.
- NP47557.RAqKJTJSqsDJ2noy4709UGNPotn_iyWgCva5dKYp7fcaE130_assertion description "[Our results highlight the potential of microarray-based technology for SNP genotyping in pharmacogenetics.(1)]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47557.RAqKJTJSqsDJ2noy4709UGNPotn_iyWgCva5dKYp7fcaE130_provenance.
- NP47560.RAkB8j6II0MQy22OGKS_hohLJlacqa4gCrzomBAGvOjFo130_assertion description "[Effects of the lactase 13910 C/T and calcium-sensor receptor A986S G/T gene polymorphisms on the incidence and recurrence of colorectal cancer in Hungarian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47560.RAkB8j6II0MQy22OGKS_hohLJlacqa4gCrzomBAGvOjFo130_provenance.
- NP47562.RAj1cRE0_ewvgpkmUoASDw4gNq50SPJyK1StUnwFP7VSs130_assertion description "[Genetic variation in the retinoid X receptor and calcium-sensing receptor and risk of colorectal cancer in the Colon Cancer Family Registry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47562.RAj1cRE0_ewvgpkmUoASDw4gNq50SPJyK1StUnwFP7VSs130_provenance.
- NP47563.RAiAkM8_btb7CsZ_hVnDIKj3TTma7BTA3y85dSjVNDb34130_assertion description "[These findings strongly favour a recommendation for MEN1 and CASR genotyping of patients with multiglandular FIHP, irrespective of urinary calcium excretion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47563.RAiAkM8_btb7CsZ_hVnDIKj3TTma7BTA3y85dSjVNDb34130_provenance.
- NP47571.RArAgrNkKpiTlOhiEcYI2a3Fr24JUt2NF2M8ShieMHcmM130_assertion description "[Studies of association of the CASQ1 rs2275703 polymorphism in relation to type 2 diabetes and related quantitative metabolic traits among 7,088 Danish whites.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47571.RArAgrNkKpiTlOhiEcYI2a3Fr24JUt2NF2M8ShieMHcmM130_provenance.
- NP47572.RAiOoABCGIMBAGn3eDp9CGqzhHKnJn6kg2UYn4RX8Vo8g130_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." NP47572.RAiOoABCGIMBAGn3eDp9CGqzhHKnJn6kg2UYn4RX8Vo8g130_provenance.
- NP47573.RAsFxJyAisT9raeylLmPNKrtcpScnwtg7KwJDC7sXVWts130_assertion description "[Familial hypocalciuric hypercalcemia associated with mutation in the human Ca(2+)-sensing receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47573.RAsFxJyAisT9raeylLmPNKrtcpScnwtg7KwJDC7sXVWts130_provenance.
- NP47575.RAtoSKIikhsvh1hLm1rbN_EVF75O_b11ow16C_zt72RDc130_assertion description "[ We observed that polymorphisms in FasL/Fas system and caspase-9 influence the response to infliximab in luminal and fistulizing Crohn's disease. The strongest association was seen between the Fas ligand -843 TT genotype and non-response. Concomitant mercaptopurine/azathioprine therapy, however, was able to overcome the effect of unfavourable genotypes in luminal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47575.RAtoSKIikhsvh1hLm1rbN_EVF75O_b11ow16C_zt72RDc130_provenance.
- NP47577.RApTSTZpO8SHjjO5lvF-9d4ByBVsy6KSvWwQSz4Yeux1Q130_assertion description "[To our knowledge, this is the first study to disclose a synergism between fat intake and SNPs in apoptotic genes in modulating disease activity in CD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47577.RApTSTZpO8SHjjO5lvF-9d4ByBVsy6KSvWwQSz4Yeux1Q130_provenance.
- NP47578.RAsk74aoeXuvb5BXqZ3uHI0jUDVPL-TkiwICxwpSjeu5Q130_assertion description "[Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47578.RAsk74aoeXuvb5BXqZ3uHI0jUDVPL-TkiwICxwpSjeu5Q130_provenance.
- NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_assertion description "[our data provide persuasive evidence against an overall association between invasive breast cancer risk and ERCC4 rs744154, TNF rs361525, CASP10 rs13010627, PGR rs1042838, and BID rs8190315 genotypes among women of European descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_provenance.
- NP47581.RAg37KK5MJwbYQDvIEH6XivKwCXFAItz34oc8An0t8-l0130_assertion description "[Risks of breast cancer associated with low-penetrance susceptibility polymorphisms do not vary significantly with these ten established environmental risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47581.RAg37KK5MJwbYQDvIEH6XivKwCXFAItz34oc8An0t8-l0130_provenance.
- NP47584.RAgDWHhjgOITusFAOgJRdReWIgdtOP3FgNcS7-XYcS_OE130_assertion description "[Association of breast cancer susceptibility variants with risk of pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47584.RAgDWHhjgOITusFAOgJRdReWIgdtOP3FgNcS7-XYcS_OE130_provenance.
- NP47586.RAj9rWlrygOWgLxTEvVe89QLFR-Lk_tXP7dBI2i9rL_nI130_assertion description "[This study confirms that susceptibility variants in FGFR2, TOX3 and MAP3K1 and on chromosome 8q are all associated with increased risk of cancer in individuals with a family history of breast cancer, whereas CASP8 is protective in this context.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47586.RAj9rWlrygOWgLxTEvVe89QLFR-Lk_tXP7dBI2i9rL_nI130_provenance.
- NP47588.RAldUzKgVQsUkrDIhgCX99-3hpMyuqtulTtewpzF_fB5w130_assertion description "[CASP8 polymorphisms, estrogen and progesterone receptor status, and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47588.RAldUzKgVQsUkrDIhgCX99-3hpMyuqtulTtewpzF_fB5w130_provenance.
- NP47594.RAn5GccOvlNzAD275Uar0gjyreP5JrlSA5V1uSH2Yc6Ks130_assertion description "[A deletion in CART is not associated with type 2 diabetes, but may contribute to dyslipidemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47594.RAn5GccOvlNzAD275Uar0gjyreP5JrlSA5V1uSH2Yc6Ks130_provenance.
- NP47595.RArIU2Kht8WOYolCdZ3BTdX5hYDk2-uyomfRd4k0dpbis130_assertion description "[In all, the 16 replicated and newly discovered loci, in addition to the three coding NOD2 variants, accounted for 11.2% of the total genetic variance for CD risk in the AJ population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47595.RArIU2Kht8WOYolCdZ3BTdX5hYDk2-uyomfRd4k0dpbis130_provenance.
- NP47608.RAtekGp6GvOzFuQW1aF-VOTD9po4yQ1sdDHIeED-3a9Ks130_assertion description "[Tumor necrosis factor (TNF) and lymphotoxin-alpha (LTA) polymorphisms and risk of non-Hodgkin lymphoma in the InterLymph Consortium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47608.RAtekGp6GvOzFuQW1aF-VOTD9po4yQ1sdDHIeED-3a9Ks130_provenance.
- NP47610.RAq0Zpx7oe4d9NokxYSPn3-YQ0klLZugo5JSDc2BAQ3PQ130_assertion description "[The NOD2 3020insC mutation and the risk of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47610.RAq0Zpx7oe4d9NokxYSPn3-YQ0klLZugo5JSDc2BAQ3PQ130_provenance.
- NP47611.RAiX-wsreiM65gfq7VD7i4_mG6UE0gg4v8REk3yLHslxE130_assertion description "[NOD2 3020insC alone is not sufficient for colorectal cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47611.RAiX-wsreiM65gfq7VD7i4_mG6UE0gg4v8REk3yLHslxE130_provenance.
- NP47615.RAkab2s711NFrjGQI0iQqDYmEveIlBpaUrpR9beGaIbsE130_assertion description "[Colorectal cancers from patients with NOD2 3020insC and TNFalpha-1031T/T constitutional changes are mostly right-sided disease (OR=2.21, p=0.03) with a tendency to higher stages (OR=2.41, p=0.06), increased number of associated polyps (OR=1.77, p=0.16) and later age of average age of disease onset (p=0.039).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47615.RAkab2s711NFrjGQI0iQqDYmEveIlBpaUrpR9beGaIbsE130_provenance.
- NP47617.RAhFR0jWQstQq5Fek2xzw7FmiHGOQXDyo6Dvi-6sHgqxU130_assertion description "[But, we report a significant disease contribution of CARD15 for CRC patients with very early disease manifestation, mainly driven by variant R702W.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47617.RAhFR0jWQstQq5Fek2xzw7FmiHGOQXDyo6Dvi-6sHgqxU130_provenance.
- NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_assertion description "[The CARD15 R702W variant might be a predisposing factor to sporadic CRC in Portugal, particularly in patients under 60-years old and in female patients. This susceptibility appears to be linked with germline CARD15 mutations. Nevertheless, we have found no evidence that CARD15 mutations predict the pathologic characteristics of CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_provenance.
- NP47620.RAkKxsVBq3auWj6guNb8LtmowVhmoSiRokv-fmFjx2XsE130_assertion description "[Nosocomial sepsis and polymorphism of the NOD-2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47620.RAkKxsVBq3auWj6guNb8LtmowVhmoSiRokv-fmFjx2XsE130_provenance.
- NP47621.RAm-kt87x50mIdRBWB9AuWXWV-P3K3z0Hh6m7LUr_3LxE130_assertion description "[The overall influence of the investigated polymorphisms on the development of preterm delivery seems moderate, since only the maternal IL6-174G genotype was associated with preterm birth and none of the polymorphisms were associated with intrauterine infection as the cause of preterm birth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47621.RAm-kt87x50mIdRBWB9AuWXWV-P3K3z0Hh6m7LUr_3LxE130_provenance.
- NP47625.RAhmBHbvPrkgn9nWi7TvGqZExQWq-9Ys-fU38z8KmXOaI130_assertion description "[Antibody response to this new panel of serological markers was associated with complicated disease phenotype, NOD2/CARD15 genotype, and a need for surgery in this eastern European IBD cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47625.RAhmBHbvPrkgn9nWi7TvGqZExQWq-9Ys-fU38z8KmXOaI130_provenance.