Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP78770.RAqK4xATrR5iRR9LvGZvu2J6VOlMj5uAwRLVtzJFtv1nI130_assertion description "[Microarray-based mutation analysis of 183 Spanish families with Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78770.RAqK4xATrR5iRR9LvGZvu2J6VOlMj5uAwRLVtzJFtv1nI130_provenance.
- NP78775.RAsdf7aMLtCiy2HLV5hvCyER53bn948IfwRKHik8Ap9zE130_assertion description "[, this study suggests that KIR3DS1 may severe as AS susceptive genes to trigger continuous injury of arthrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78775.RAsdf7aMLtCiy2HLV5hvCyER53bn948IfwRKHik8Ap9zE130_provenance.
- NP78776.RAtpI7vYzRpZDvmGG_k6U8z5pC14ZUPmf1Q7Ji1jeLkdw130_assertion description "[KIR and HLA gene combinations in Vogt-Koyanagi-Harada disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78776.RAtpI7vYzRpZDvmGG_k6U8z5pC14ZUPmf1Q7Ji1jeLkdw130_provenance.
- NP78777.RAtNdfiRGT9A7aY-eQ4wbf5E2hB9KpSNhIQq6L3F1ervc130_assertion description "[Killer cell immunoglobulin-like receptor gene-cluster 3DS1-2DL5-2DS1-2DS5 predisposes susceptibility to Vogt-Koyanagi-Harada syndrome in Japanese individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78777.RAtNdfiRGT9A7aY-eQ4wbf5E2hB9KpSNhIQq6L3F1ervc130_provenance.
- NP78778.RAhjANObcyYbFOeI1bekgzhGpPK8wQ9_sNDzbq7riWEBs130_assertion description "[There may be a association between the polymorphism of KIR genes with SLE in North of China should be investigated further.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78778.RAhjANObcyYbFOeI1bekgzhGpPK8wQ9_sNDzbq7riWEBs130_provenance.
- NP78781.RAgF2vSkWtcKHTPK4xPNAiRLzmEGtHgqRGQy2b7HQc-pQ130_assertion description "[KIR genes and KIR ligands affect occurrence of acute GVHD after unrelated, 12/12 HLA matched, hematopoietic stem cell transplantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78781.RAgF2vSkWtcKHTPK4xPNAiRLzmEGtHgqRGQy2b7HQc-pQ130_provenance.
- NP78784.RAl6RTiID5V4QN00fZX6fXAGmmg1l4kh4untKm9YzANd8130_assertion description "[Multiple sclerosis associates with LILRA3 deletion in Spanish patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78784.RAl6RTiID5V4QN00fZX6fXAGmmg1l4kh4untKm9YzANd8130_provenance.
- NP78787.RAmQO0zNZv8e8I55bhdGdJEP7MXhA0riVnudEhxmSoa9o130_assertion description "[Activating killer cell immunoglobulin-like receptors 3DS1 and 2DS1 protect against developing the severe form of recurrent respiratory papillomatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78787.RAmQO0zNZv8e8I55bhdGdJEP7MXhA0riVnudEhxmSoa9o130_provenance.
- NP78791.RAgH9gE1_5buwKcY6gcRjrbQs3noZwacDGJuc5h2GXGj8130_assertion description "[There may be a association between the polymorphism of KIR genes with SLE in North of China should be investigated further.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78791.RAgH9gE1_5buwKcY6gcRjrbQs3noZwacDGJuc5h2GXGj8130_provenance.
- NP78793.RAuOrrcCz6PAHLHyCyrRFR9q-xRDEibMaO5mAYV_WFVZM130_assertion description "[A study of the killer cell immunoglobulin-like receptor gene KIR2DS1 in a Caucasoid Brazilian population with psoriasis vulgaris.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78793.RAuOrrcCz6PAHLHyCyrRFR9q-xRDEibMaO5mAYV_WFVZM130_provenance.
- NP78798.RAoxBC-uPIfnOJIcaD-RySOvoBGwMDLqh_pAk-FJtWsvE130_assertion description "[Our results indicate that RM could be associated with NK cell activation mediated by a profile rich in activating KIR genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78798.RAoxBC-uPIfnOJIcaD-RySOvoBGwMDLqh_pAk-FJtWsvE130_provenance.
- NP78806.RAo77frzDrPKFniGkH8fDyrkCrZRQ7-UbfmJnGQGKjXec130_assertion description "[The diversity of KIR gene in Chinese Northern Han population and the impact of donor KIR and patient HLA genotypes on outcome following HLA-identical sibling allogeneic hematopoietic stem cell transplantation for hematological malignancy in Chinese people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78806.RAo77frzDrPKFniGkH8fDyrkCrZRQ7-UbfmJnGQGKjXec130_provenance.
- NP78807.RAs3s5TH6mUYMdiRgbt4cltgSgUvyEG2SneqPt9gF8fvA130_assertion description "[Association between killer-cell immunoglobulin-like receptor genotypes and leprosy in Brazil.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78807.RAs3s5TH6mUYMdiRgbt4cltgSgUvyEG2SneqPt9gF8fvA130_provenance.
- NP78815.RAuBGNpDY14sasZeHgmsli-ipiFtxvu1q_Y4Kspxv-51Q130_assertion description "[High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78815.RAuBGNpDY14sasZeHgmsli-ipiFtxvu1q_Y4Kspxv-51Q130_provenance.
- NP78820.RAojDt-IkzvqpiMjLMCmh2jAPAuifk76p--84ihPqdR14130_assertion description "[Accordingly, in the present study we evaluated whether the pro-inflammatory polymorphisms of lipopolysaccaride-receptors, +896A/G Toll-Like Receptor (TLR4) and -260C/T CD14, are risk factors for AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78820.RAojDt-IkzvqpiMjLMCmh2jAPAuifk76p--84ihPqdR14130_provenance.
- NP78823.RAkuf-uypT7cH5SXFEh5wK_RKi-ck5rLS5JJ1mLGDczoE130_assertion description "[These results demonstrate a clear association between polymorphisms in the IRAK4 gene and serum IgE levels in patients with CRS and asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78823.RAkuf-uypT7cH5SXFEh5wK_RKi-ck5rLS5JJ1mLGDczoE130_provenance.
- NP78829.RAmCLFte1nWQXhceQUeNrl4LDiIqz5vgR8B1hfPSQJICg130_assertion description "[Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78829.RAmCLFte1nWQXhceQUeNrl4LDiIqz5vgR8B1hfPSQJICg130_provenance.
- NP78832.RAppca7e7j0gBy4MU2nrjE0GIp4uO8DMW62iEwk4BJvuk130_assertion description "[TT homozygotes are more common in adult patients with allergic rhinitis among the Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78832.RAppca7e7j0gBy4MU2nrjE0GIp4uO8DMW62iEwk4BJvuk130_provenance.
- NP78840.RApFsRm89gClikE5GiBMMnkCseDs6J4obetfnr6AX1SEk130_assertion description "[Individuals with the functional TRIB3 Q84R polymorphism are at risk for MetS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78840.RApFsRm89gClikE5GiBMMnkCseDs6J4obetfnr6AX1SEk130_provenance.
- NP78847.RAtdeEfdg05r9nBhFncfvYD_WhQInI8GNEUuFF3WMogSQ130_assertion description "[Candidate-gene testing for orphan limb-girdle muscular dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78847.RAtdeEfdg05r9nBhFncfvYD_WhQInI8GNEUuFF3WMogSQ130_provenance.
- NP78851.RAgklyUV9-w9PJF2D48EX1cEPixFk5yPp41HvG7x4z38o130_assertion description "[Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78851.RAgklyUV9-w9PJF2D48EX1cEPixFk5yPp41HvG7x4z38o130_provenance.
- NP78856.RAntMaZcgI2TXULR3eI-RYw-f9tdwR6qlM4CA8ttPIP_Y130_assertion description "[Association study between the pericentrin (PCNT) gene and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78856.RAntMaZcgI2TXULR3eI-RYw-f9tdwR6qlM4CA8ttPIP_Y130_provenance.
- NP78857.RAg3D80CtsdXXs3Bo_yUjkeWtGbnhGl4X26ZLm4wxUI24130_assertion description "[Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78857.RAg3D80CtsdXXs3Bo_yUjkeWtGbnhGl4X26ZLm4wxUI24130_provenance.
- NP78868.RAjSQv0US1N8tkYU1ejBHxGmCwbwYiUYnE7e_PpX2o3_0130_assertion description "[It has been reported that the CCR5-Delta32, CCR2-64I and SDF1-3'A polymorphisms have protective effects against HIV-1 infection and can delay the progression of AIDS in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78868.RAjSQv0US1N8tkYU1ejBHxGmCwbwYiUYnE7e_PpX2o3_0130_provenance.
- NP78869.RAsLuuhQ9mjbsKkj9O6SozdCb5q-rekGtJ1WCuAmgyETo130_assertion description "[Frequency of CCR5 Gene 32-bp deletion in Pakistani ethnic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78869.RAsLuuhQ9mjbsKkj9O6SozdCb5q-rekGtJ1WCuAmgyETo130_provenance.
- NP78871.RAtBUyCqdMmDqhMj-F7Zdx-ONbNs1YowZYNpGV1CAEbCY130_assertion description "[Impact of chemokine receptor CCR2 and CCR5 gene polymorphism on allograft outcome in North Indian renal transplant recipients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78871.RAtBUyCqdMmDqhMj-F7Zdx-ONbNs1YowZYNpGV1CAEbCY130_provenance.
- NP78878.RAgUNMRamGGetRjJQrAZUBuctDwlEm1_4cHnaZUrhQbL0130_assertion description "[The present study highlights that common variants of inflammatory cytokine genes exert a modest effect on risk of DN and a combination of risk alleles confer a substantial increased risk of nephropathy in type 2 diabetes among Asian Indians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78878.RAgUNMRamGGetRjJQrAZUBuctDwlEm1_4cHnaZUrhQbL0130_provenance.
- NP78881.RAg_79l6NabJLhIG0PLvux0_t3hiYXU81Icq7MFcBSPh8130_assertion description "[Is CCR5-Delta32 mutation associated with diabetic nephropathy in type 2 diabetes?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78881.RAg_79l6NabJLhIG0PLvux0_t3hiYXU81Icq7MFcBSPh8130_provenance.
- NP78884.RApzCZzcJl_2_cOFGSO7EATyfLP2rnYu1Y7RbVzwzEOU0130_assertion description "[The C-C chemokine receptor (CCR)5 gene has been associated with both parenchymal pulmonary sarcoidosis and perianal Crohn's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78884.RApzCZzcJl_2_cOFGSO7EATyfLP2rnYu1Y7RbVzwzEOU0130_provenance.
- NP78886.RArCY841n2K0JJjuoJAJ5O-uj41uK0vazUu_fe1xIfzV4130_assertion description "[Associations of NHL and NHL subtypes with polymorphisms and haplotypes in CCR5, CCR2, CCL5, CXCL12, and CX(3)CR(1) were explored in a pooled analysis of three case-control studies (San Francisco Bay Area, California; United Kingdom; total: cases N = 1610, controls N = 1992).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78886.RArCY841n2K0JJjuoJAJ5O-uj41uK0vazUu_fe1xIfzV4130_provenance.
- NP78888.RAqnSzI24f_7KaJ9Ro0Mj_4i-1HSXhLIvhimKHoUtsbJg130_assertion description "[Genetic deficiency of chemokine receptor CCR5 is a strong risk factor for symptomatic West Nile virus infection: a meta-analysis of 4 cohorts in the US epidemic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78888.RAqnSzI24f_7KaJ9Ro0Mj_4i-1HSXhLIvhimKHoUtsbJg130_provenance.
- NP78890.RAjRV8GJ6OH0rb5bmZqI38wqAtAufx-MD4pZaTKzvtjb4130_assertion description "[Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78890.RAjRV8GJ6OH0rb5bmZqI38wqAtAufx-MD4pZaTKzvtjb4130_provenance.
- NP78893.RAodsgtNmsQj-k2BotRiealiwMTjWsMN7ZoaU7uFwsG3k130_assertion description "[Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78893.RAodsgtNmsQj-k2BotRiealiwMTjWsMN7ZoaU7uFwsG3k130_provenance.
- NP78895.RAvoEeD1jZoFHUFbzax_ItEWOtIUTLuOp3R6y4klg2DXQ130_assertion description "[Therefore, we asked whether genetic variation within the ANGPTL4 gene contributes to prediabetic phenotypes, such as dyslipidemia, insulin resistance, or beta-cell dysfunction, in white subjects at an increased risk for type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78895.RAvoEeD1jZoFHUFbzax_ItEWOtIUTLuOp3R6y4klg2DXQ130_provenance.
- NP78896.RAgqqscTAy8MfEQDvQdLL3U_Fueg6GiSBNh7qhilLcGPk130_assertion description "[Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78896.RAgqqscTAy8MfEQDvQdLL3U_Fueg6GiSBNh7qhilLcGPk130_provenance.
- NP78906.RAry1uMn-aWDiV5FUZlz9QeHQpK5f8iQ5OoQlB3AJ_tLg130_assertion description "[Impact of chemokine receptor CCR2 and CCR5 gene polymorphism on allograft outcome in North Indian renal transplant recipients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78906.RAry1uMn-aWDiV5FUZlz9QeHQpK5f8iQ5OoQlB3AJ_tLg130_provenance.
- NP78910.RAmteSV6S7SkSLu5d2l5QJNrCIXAWtTELIgyFZKhpKV0w130_assertion description "[Associations of NHL and NHL subtypes with polymorphisms and haplotypes in CCR5, CCR2, CCL5, CXCL12, and CX(3)CR(1) were explored in a pooled analysis of three case-control studies (San Francisco Bay Area, California; United Kingdom; total: cases N = 1610, controls N = 1992).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78910.RAmteSV6S7SkSLu5d2l5QJNrCIXAWtTELIgyFZKhpKV0w130_provenance.
- NP78923.RAggZ3unwSx8gj3Q88KG4Aoq-x-OxshnS9VhnNRW1hZB8130_assertion description "[IFIH1-GCA-KCNH7 locus is not associated with genetic susceptibility to multiple sclerosis in French patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78923.RAggZ3unwSx8gj3Q88KG4Aoq-x-OxshnS9VhnNRW1hZB8130_provenance.
- NP78927.RAkANPKj6n_V8aFdX8YnP5xgHbp-J07M_bZcChykxsI_I130_assertion description "[Our findings suggest that HTR5A gene could play an important role in the pathogenesis of bipolar disorder in our population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78927.RAkANPKj6n_V8aFdX8YnP5xgHbp-J07M_bZcChykxsI_I130_provenance.
- NP78933.RAtVQC7KPjmNdsmzV7SVDLIofaRFBqx-VUZkR4v34LbrI130_assertion description "[PTEN identified as important risk factor of chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78933.RAtVQC7KPjmNdsmzV7SVDLIofaRFBqx-VUZkR4v34LbrI130_provenance.
- NP78935.RAraVlAeHEJa7d2zUPjPVPP8oPDoVIZPJbwJ_NnORO7E0130_assertion description "[Genetic association of the CHRNA6 and CHRNB3 genes with tobacco dependence in a nationally representative sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78935.RAraVlAeHEJa7d2zUPjPVPP8oPDoVIZPJbwJ_NnORO7E0130_provenance.
- NP78936.RAsI_OwfSUSkBKQ0gbkZBHZ-y4tlArgTa4MUuV9Ben4Fo130_assertion description "[A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78936.RAsI_OwfSUSkBKQ0gbkZBHZ-y4tlArgTa4MUuV9Ben4Fo130_provenance.
- NP78939.RAoCpYo4p8QlMY7cHtSdHoAk9alFBHIwiBwcv8oQGwlUQ130_assertion description "[Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerstrm test for nicotine dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78939.RAoCpYo4p8QlMY7cHtSdHoAk9alFBHIwiBwcv8oQGwlUQ130_provenance.
- NP78945.RAorN1qLKoxYOvMiY1kYQULy9be7qvIjq8uTG1VcTfvL4130_assertion description "[Explorative study to identify novel candidate genes related to oxaliplatin efficacy and toxicity using a DNA repair array.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78945.RAorN1qLKoxYOvMiY1kYQULy9be7qvIjq8uTG1VcTfvL4130_provenance.
- NP78948.RAtSliDrE4iSMezO6EGg08jcy8GJa7aGCwWRFpu7PnBok130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78948.RAtSliDrE4iSMezO6EGg08jcy8GJa7aGCwWRFpu7PnBok130_provenance.
- NP78949.RAolS9OLe3K1TAarIdTmfH7Nj7gL_VwTN5rlxzoncZ1oA130_assertion description "[High-order interactions among genetic polymorphisms in nucleotide excision repair pathway genes and smoking in modulating bladder cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78949.RAolS9OLe3K1TAarIdTmfH7Nj7gL_VwTN5rlxzoncZ1oA130_provenance.
- NP78952.RAs_4ztNwo_NE0e9vDGBffNqmmozvhBiYJcll2DF6-Y9M130_assertion description "[Significant allele frequency differences between schizophrenia cases and controls were observed at 4 tagSNPs located in the genes DRD5, HTR1B1, DBH, and TH1 (P<0.005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78952.RAs_4ztNwo_NE0e9vDGBffNqmmozvhBiYJcll2DF6-Y9M130_provenance.
- NP78955.RAn2UOisAjnAf_8c8t1MGiH5RNPm3ikzRMqIHh6JeJsBo130_assertion description "[Centrosome-related genes, genetic variation, and risk of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78955.RAn2UOisAjnAf_8c8t1MGiH5RNPm3ikzRMqIHh6JeJsBo130_provenance.
- NP78958.RAm1IK3b2pAZhhmjpHUJ_4bkD4D8lbfGybmPMoI5PFpbI130_assertion description "[Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78958.RAm1IK3b2pAZhhmjpHUJ_4bkD4D8lbfGybmPMoI5PFpbI130_provenance.
- NP78962.RAuLUcujxMFPZSkbXg3X2t4dZUPgJCVu3FHYGWDiKiw0o130_assertion description "[Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78962.RAuLUcujxMFPZSkbXg3X2t4dZUPgJCVu3FHYGWDiKiw0o130_provenance.
- NP78964.RApoPGQOucyUibhDSoMH3KnuvXfJRCIXW9fmvrATvw5Ds130_assertion description "[A recent genome-wide association (GWA) study of U.S. Caucasians suggested that eight single nucleotide polymorphisms (SNPs) in CTNNBL1 are associated with obesity and increased fat mass.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78964.RApoPGQOucyUibhDSoMH3KnuvXfJRCIXW9fmvrATvw5Ds130_provenance.
- NP78969.RApU7AwlWqTFT-q-QOnflfqFSa5wPFNMI-NLCwDEi1TQ4130_assertion description "[Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78969.RApU7AwlWqTFT-q-QOnflfqFSa5wPFNMI-NLCwDEi1TQ4130_provenance.
- NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs130_assertion description "[We examined associations between common germline genetic variation in 13 genes involved in cell cycle control (CCND1, CCND2, CCND3, CCNE1, CDK2 p33, CDK4, CDK6, CDKN1A p21, Cip1, CDKN1B p27, Kip1, CDKN2A p16, CDKN2B p15, CDKN2C p18, and CDKN2D p19) and survival among women diagnosed with invasive breast cancer participating in the SEARCH (Studies of Epidemiology and Risk factors in Cancer Heredity) breast cancer study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs130_provenance.
- NP78972.RAnsVJGivXpJyVGwUk9vnJWZ-mK5j78r40J6Y5Te55KTo130_assertion description "[Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78972.RAnsVJGivXpJyVGwUk9vnJWZ-mK5j78r40J6Y5Te55KTo130_provenance.
- NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_assertion description "[To assess the prevalence of different forms of OCA and different gene mutations among non-Hispanic Caucasian patients, we performed DNA sequence analysis of the four genes associated with `classical` OCA (TYR, OCA2, TYRP1, SLC45A2), the two principal genes associated with syndromic OCA (HPS1, HPS4), and a candidate OCA gene (SILV), in 121 unrelated, unselected non-Hispanic/Latino Caucasian patients carrying the clinical diagnosis of OCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_provenance.
- NP78983.RAtC-Ya5X3JVXf_u5c9MuTKyYIiKlIIwOfc4hdK09_9s0130_assertion description "[Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78983.RAtC-Ya5X3JVXf_u5c9MuTKyYIiKlIIwOfc4hdK09_9s0130_provenance.
- NP78989.RAqedIXgcP3qlToi_00fnszY_N5ZSxPG1AdI7KTVYfpgI130_assertion description "[Meta-analysis of genetic polymorphisms and gastric cancer risk: variability in associations according to race.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78989.RAqedIXgcP3qlToi_00fnszY_N5ZSxPG1AdI7KTVYfpgI130_provenance.
- NP78994.RAnt2bZilADxsqWh-hg0whYSKMLYa63P0YEIFwNSm33ak130_assertion description "[Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78994.RAnt2bZilADxsqWh-hg0whYSKMLYa63P0YEIFwNSm33ak130_provenance.
- NP78995.RAj5mYP1KYCRBRvxN9BSudcGJC563pW7OwK5i-smOpXkU130_assertion description "[Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78995.RAj5mYP1KYCRBRvxN9BSudcGJC563pW7OwK5i-smOpXkU130_provenance.
- NP79002.RAtO6L71VTmhNzOGrMCsbIe1S8xHurhXu7jshJ427MZdE130_assertion description "[PTEN identified as important risk factor of chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79002.RAtO6L71VTmhNzOGrMCsbIe1S8xHurhXu7jshJ427MZdE130_provenance.
- NP79006.RAqMwZiQ6Z_cZ-JomrvAzCsL-vO4-XX5Rk-fkscXcs2A4130_assertion description "[Recapitulation of two genomewide association studies on blood pressure and essential hypertension in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79006.RAqMwZiQ6Z_cZ-JomrvAzCsL-vO4-XX5Rk-fkscXcs2A4130_provenance.
- NP79018.RAgKb7_pW-fYkpmWsCLUlrBLw6gyYJx8boR-rCAr585bM130_assertion description "[A common haplotype of the GEMIN4 gene was associated with a significantly reduced risk of esophageal cancer (odds ratio, 0.65; 95% CI, 0.42-0.99).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79018.RAgKb7_pW-fYkpmWsCLUlrBLw6gyYJx8boR-rCAr585bM130_provenance.
- NP79019.RAq_lizrOGnzcfGJNym__elGEAp6Pd9BuJZSqUHMV_RFE130_assertion description "[Carboxypeptidase 4 gene variants and early-onset intermediate-to-high risk prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79019.RAq_lizrOGnzcfGJNym__elGEAp6Pd9BuJZSqUHMV_RFE130_provenance.
- NP79020.RAr2LJhub9kp7VTO130aCRUkZ6DC6M9mdoXT5Jqrn4XnI130_assertion description "[Ten non-synonymous single nucleotide polymorphisms (nsSNPs), which were recently associated with colorectal cancer risk in a comprehensive, array based study (AKAP9 M463I, DKK3 G335R, AMPD1 Q12X, LIPC L356F, PSMB9 V32I, THBS1 N700S, CA6 S90G, ASCC3 C1995S, DHX36 S416C and CPA4 G303C) were re-evaluated in the present study based on 626 German familial non-HNPCC colorectal cancer patients and 736 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79020.RAr2LJhub9kp7VTO130aCRUkZ6DC6M9mdoXT5Jqrn4XnI130_provenance.
- NP79026.RAp3UjgEngSeU2PBpDEsbvbHwOIYqvsCP-pTW-uadv-as130_assertion description "[A review of smoking behavior and smokers evidence (chemical modification, inducing nicotine metabolism, and individual variations by genotype: dopaminergic function and personality traits).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79026.RAp3UjgEngSeU2PBpDEsbvbHwOIYqvsCP-pTW-uadv-as130_provenance.
- NP79028.RAjfUYwritcQezZvTuHKooOdWS8G6hDQAvU9PwapOI_04130_assertion description "[Recent genome-wide association studies have identified 1q31 (RGS1), 2q11-12 (IL18RAP), 3p21 (CCR1/CCR3/CCR2), 3q25-26 (IL12A/SCHIP1), 3q28 (LPP), 4q27 (IL2/IL21), 6q25 (TAGAP) and 12q24 (SH2B3) as susceptibility regions for coeliac disease (CD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79028.RAjfUYwritcQezZvTuHKooOdWS8G6hDQAvU9PwapOI_04130_provenance.
- NP79039.RAghxRVcdoljwXUDA7oooZbz_qiRGFgiYA8UlLnBXLQck130_assertion description "[These results demonstrate a clear association between polymorphisms in the IRAK4 gene and serum IgE levels in patients with CRS and asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79039.RAghxRVcdoljwXUDA7oooZbz_qiRGFgiYA8UlLnBXLQck130_provenance.
- NP79044.RAt5QCHvYCsdVrTqdMLEJZdXkHYWPY9AwhedvxmxzNx08130_assertion description "[Toll-like receptor signaling pathway variants and prostate cancer mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79044.RAt5QCHvYCsdVrTqdMLEJZdXkHYWPY9AwhedvxmxzNx08130_provenance.
- NP79047.RAgUdEchJ_HJTwMqgUH9Tg2gwpSlFCCz4iek1M5sdiNoY130_assertion description "[Our results showed that SNPs in the TLR2, 4 and 9 genes were not significantly associated with susceptibility to BD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79047.RAgUdEchJ_HJTwMqgUH9Tg2gwpSlFCCz4iek1M5sdiNoY130_provenance.
- NP79051.RAtl9u8RUcMNyZ4zDWa8RO9YbWSpCwsGSM5YlXZ2kAkf8130_assertion description "[Toll-like receptor 8 polymorphism and coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79051.RAtl9u8RUcMNyZ4zDWa8RO9YbWSpCwsGSM5YlXZ2kAkf8130_provenance.
- NP79057.RAg0aCRp4pPMpa1_DfgLfJFyA-PWvpAyHRaJ1vXTB3waw130_assertion description "[Toll-like receptor signaling pathway variants and prostate cancer mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79057.RAg0aCRp4pPMpa1_DfgLfJFyA-PWvpAyHRaJ1vXTB3waw130_provenance.
- NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_assertion description "[HJV p.A310G polymorphism and two intronic variants were found, but none of these alterations were associated with digenic inheritance with the HFE gene. Our data indicate that HJV and HAMP functional mutations are not frequent in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance.
- NP79066.RAs4_fabGBPbvueVbFI-VKNG7Ud2Ke9Po4dII8wBim-lU130_assertion description "[The findings suggest a relation between aggrecan and symptomatic LDH, where symptomatic LDH has a lower tendency of allele repeats. In addition, this study observed an association between the distribution of aggrecan gene VNTR polymorphism and the expression of aggrecan in symptomatic LDH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79066.RAs4_fabGBPbvueVbFI-VKNG7Ud2Ke9Po4dII8wBim-lU130_provenance.
- NP79068.RAlezGnfED-HPvuwi6EyuzxEVcyYuijTtWhSbP_oJRE7c130_assertion description "[Association of IL-1F7 gene with susceptibility to human leukocyte antigen-B27 positive ankylosing spondylitis in Han Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79068.RAlezGnfED-HPvuwi6EyuzxEVcyYuijTtWhSbP_oJRE7c130_provenance.
- NP79072.RApB0TBbY1yf8NBdwLD9tVy6ktATcpAjM7uCb7bnn6u1A130_assertion description "[Single SNP associations noted in outbred Caucasian populations were not found in the Korean AS cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79072.RApB0TBbY1yf8NBdwLD9tVy6ktATcpAjM7uCb7bnn6u1A130_provenance.
- NP79073.RAiBNlMhFgU0ltLhgQ7sSQX3IKFH12JG99qvxZKjrtTdc130_assertion description "[Single SNP associations noted in outbred Caucasian populations were not found in the Korean AS cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79073.RAiBNlMhFgU0ltLhgQ7sSQX3IKFH12JG99qvxZKjrtTdc130_provenance.
- NP79080.RAlrVWaq_N1RP9rzhC8dHD8o2Td3raUrkw6-VpsRGN3TE130_assertion description "[These results show near-perfect replication and provide the first additional evidence that CLU, CR1, and PICALM are associated with the risk of LOAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79080.RAlrVWaq_N1RP9rzhC8dHD8o2Td3raUrkw6-VpsRGN3TE130_provenance.
- NP79091.RAhiB7nLqNYjoZuqSy-cbgx5R4nEn7v5INqqIOkx4l3uc130_assertion description "[Our study indicates interesting new candidate genes and functional pathways for further study and confirms earlier findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79091.RAhiB7nLqNYjoZuqSy-cbgx5R4nEn7v5INqqIOkx4l3uc130_provenance.
- NP79093.RAjO_iSZ1JtvI9A5aIDrh7yVAaaQBJGYVjtpoxetIqvwQ130_assertion description "[Polymorphisms in the folate/Hcy pathway are associated with tHcy and folate derivative levels. In African American and Caucasian women, different factors are associated with folate/Hcy phenotypes and may contribute to race-specific differences in the risks of a range of pregnancy-related pathologies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79093.RAjO_iSZ1JtvI9A5aIDrh7yVAaaQBJGYVjtpoxetIqvwQ130_provenance.
- NP79095.RAjGQGNTfKk-GMiAwp8pj3ZTjs6Uqr7vXX9NVd3z51Prs130_assertion description "[To explore the significance of Hey, the gene polymorphisms of methylenetetrahydrofolate reductase (MTHFR) C677 T and cystathionine beta- synthase (CBS844) ins68 in type 2 diabetes mellitus (DM) with coronary heart disease (CHD) in China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79095.RAjGQGNTfKk-GMiAwp8pj3ZTjs6Uqr7vXX9NVd3z51Prs130_provenance.
- NP79097.RAogIYSZJDEfLg8m1ue2LxEozeD2Y5qu331KrQrJy83Gc130_assertion description "[Homocysteine and cognitive impairment in Parkinson's disease: a biochemical, neuroimaging, and genetic study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79097.RAogIYSZJDEfLg8m1ue2LxEozeD2Y5qu331KrQrJy83Gc130_provenance.
- NP79100.RAi3PcMx35uz3fILNjTaj1A5phgP6wzkV0gS_E_8BTrWg130_assertion description "[PTEN identified as important risk factor of chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79100.RAi3PcMx35uz3fILNjTaj1A5phgP6wzkV0gS_E_8BTrWg130_provenance.
- NP79107.RAqapV4n05s-r7w3cq1T2p2ov6mvLZ7-lVyFhbHEjmKJg130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79107.RAqapV4n05s-r7w3cq1T2p2ov6mvLZ7-lVyFhbHEjmKJg130_provenance.
- NP79109.RAq2hN-48yDu7sJXJYGvfY8RE5BHoWaa1k4T-S3ekU05k130_assertion description "[Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79109.RAq2hN-48yDu7sJXJYGvfY8RE5BHoWaa1k4T-S3ekU05k130_provenance.
- NP79110.RAsx27hwqSazpxiqOXkif-mWNZ2PlVhfpGzM4JNvIHsPU130_assertion description "[Polymorphisms in CBR3 may explain interindividual and interethnic variability of doxorubicin pharmacokinetics and pharmacodynamics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79110.RAsx27hwqSazpxiqOXkif-mWNZ2PlVhfpGzM4JNvIHsPU130_provenance.
- NP79116.RAj2LjjmpR3XIEYHBUwyR4PPYiA9EbktaZ8Gb-qCSjItY130_assertion description "[Genetic susceptibility to respiratory syncytial virus bronchiolitis in preterm children is associated with airway remodeling genes and innate immune genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79116.RAj2LjjmpR3XIEYHBUwyR4PPYiA9EbktaZ8Gb-qCSjItY130_provenance.
- NP79121.RAnpq8jUgDSvDX1-3I0cPhH5xSTbK2nWwSmeaz7OtA60k130_assertion description "[A novel exonic variant (221delT) in the LGALS13 gene encoding placental protein 13 (PP13) is associated with preterm labour in a low risk population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79121.RAnpq8jUgDSvDX1-3I0cPhH5xSTbK2nWwSmeaz7OtA60k130_provenance.
- NP79133.RAqBPb_Z0stoe5G0ioAwl7McTulaM-rw7Wc1WJGUmx2Lo130_assertion description "[Catalase -262C>T polymorphism in systemic lupus erythematosus in Poland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79133.RAqBPb_Z0stoe5G0ioAwl7McTulaM-rw7Wc1WJGUmx2Lo130_provenance.
- NP79139.RAqX_oeSu3s8fFhYmcqU2B9UtdPCQj0h9YD6kCvAJFjo0130_assertion description "[PTEN identified as important risk factor of chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79139.RAqX_oeSu3s8fFhYmcqU2B9UtdPCQj0h9YD6kCvAJFjo0130_provenance.
- NP79140.RAokyI7zdRlW_8D0DwK1rdF8bUTbAwKwC93ZDW5ROqzqQ130_assertion description "[Genotype TT of the CAT -262C/T locus marked resistance to the COPD development in Russians (chi2 = 6.82; P = 0.0098; Pcor = = 0.0196; OR = 0.31; 95% CI, 0.119 to 0.77).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79140.RAokyI7zdRlW_8D0DwK1rdF8bUTbAwKwC93ZDW5ROqzqQ130_provenance.
- NP79143.RAue9dURHkSpfx--hYh9rS77PiMcas7-A8-eslQuVKP9o130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79143.RAue9dURHkSpfx--hYh9rS77PiMcas7-A8-eslQuVKP9o130_provenance.
- NP79146.RAtpC7xZFc9kQDW5D6gWNbmQLiVGSSULhYUfuLpAcufuo130_assertion description "[Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79146.RAtpC7xZFc9kQDW5D6gWNbmQLiVGSSULhYUfuLpAcufuo130_provenance.
- NP79147.RAsx4bFEolgX7D8iEUBvdQ3gGaJWsuNk8YhGo5lw6-Y9M130_assertion description "[A novel haplotype-sharing approach for genome-wide case-control association studies implicates the calpastatin gene in Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79147.RAsx4bFEolgX7D8iEUBvdQ3gGaJWsuNk8YhGo5lw6-Y9M130_provenance.
- NP79148.RAs05ekT5v64xoX-DOfw4lIt1zDmU3duAKkdVUtsyEjo4130_assertion description "[Using data from the National Institutes of Neurological disease and Stroke's (NINDS) study of Parkinson disease (PD), we recently reported that single nucleotide polymorphisms (SNPs) in a region containing the Calpastatin (CAST) gene were associated with PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79148.RAs05ekT5v64xoX-DOfw4lIt1zDmU3duAKkdVUtsyEjo4130_provenance.
- NP79152.RAoswyPzcC8W-kDmVONJENSxhx2oJH3x1lU2dfu8WzBA8130_assertion description "[Genetic variation in calcium-sensing receptor and risk for colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79152.RAoswyPzcC8W-kDmVONJENSxhx2oJH3x1lU2dfu8WzBA8130_provenance.
- NP79159.RAnMI-LyRnbv-XUB1sanWJW_u86gPXIP6HpG9Ot4hsUfE130_assertion description "[Further, individuals with the AG and AA genotypes of CASP9 Ex5 + 32 G > A also experienced a decreased risk of multiple myeloma (OR(AG) = 0.8, 95% CI = 0.5-1.3; OR(AA) = 0.5, 95% CI = 0.3-0.9; p-trend = 0.02).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79159.RAnMI-LyRnbv-XUB1sanWJW_u86gPXIP6HpG9Ot4hsUfE130_provenance.
- NP79160.RAiugqbsFLRxq6zGGHv5pmK7UuojRxnVVBv2p0a6pJ7as130_assertion description "[Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79160.RAiugqbsFLRxq6zGGHv5pmK7UuojRxnVVBv2p0a6pJ7as130_provenance.
- NP79166.RAtNeOSWIP9AOuZBdqNH1A8fJJdXa_ljUzGtbo8YUllpk130_assertion description "[PTEN identified as important risk factor of chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79166.RAtNeOSWIP9AOuZBdqNH1A8fJJdXa_ljUzGtbo8YUllpk130_provenance.
- NP79175.RAiqETygdJvTUpc8ADbx4CW56ChwGEoPULzIPGffOyakc130_assertion description "[We found association with CLL susceptibility and 22 haplotypes in APAF1, IL6, TNFRSF13B, IL16, CASP3, CCR7, LTA/TNF, BAX, BCL2, CXCL12, CASP10/CASP8, CASP1, CCL2, BAK1, and IL1A candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79175.RAiqETygdJvTUpc8ADbx4CW56ChwGEoPULzIPGffOyakc130_provenance.
- NP79176.RAi7kmparDaaPi62pOAYzUzji6DAaYIE_lEO5MHu83FbY130_assertion description "[These results suggested that the CASP8 -652 6N ins/del polymorphism is involved in etiology of bladder cancer and thus may be a marker for genetic susceptibility to bladder cancer in Chinese populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79176.RAi7kmparDaaPi62pOAYzUzji6DAaYIE_lEO5MHu83FbY130_provenance.