Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP50879.RAu1bFx0aqk6ZWemEhj7SZymNOgCnpXfngTgNPMCXZyKw130_assertion description "[ These findings suggest that TAP2*0103 may be closely associated with low serum ALT activity in HCV-infected Japanese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50879.RAu1bFx0aqk6ZWemEhj7SZymNOgCnpXfngTgNPMCXZyKw130_provenance.
- NP50884.RArncNGaUeRpcDfNp2Xi7sEeawhkC9OX3-UuYGJwJ9Jn8130_assertion description "[As TAP2*Bky2 had a strong linkage disequilibrium with DRB1*08032, TAP2*Bky2 or its haplotype with DRB1*08032 may be involved in SS-A/Ro antibody production not only in SS but also SLE patients, indicating that TAP2*Bky2 may be a susceptible gene not only to the disease of SS but also to the SS-A/Ro autoantibody production.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50884.RArncNGaUeRpcDfNp2Xi7sEeawhkC9OX3-UuYGJwJ9Jn8130_provenance.
- NP50887.RApuNrRrPozSKz7vqbvefOVuR7AXVqpYgU-q4T-w6cM5o130_assertion description "[Polymorphism of the TAP1 gene in Polish patients with psoriasis vulgaris.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50887.RApuNrRrPozSKz7vqbvefOVuR7AXVqpYgU-q4T-w6cM5o130_provenance.
- NP50893.RAnGjB8tfOgGiiyoNLuWGL8mndN5vZiL9U1cCVwjMsOkE130_assertion description "[Genetic epidemiology of juvenile idiopathic arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50893.RAnGjB8tfOgGiiyoNLuWGL8mndN5vZiL9U1cCVwjMsOkE130_provenance.
- NP50894.RAto7dzj3NuaulL34Rz5Y-0_nYmZAxIeG6HjsbeoIMtKg130_assertion description "[HLA-DRB1, TAP2/TAP1, and HLA-DPB1 haplotypes in Finnish juvenile idiopathic arthritis: more complexity within the MHC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50894.RAto7dzj3NuaulL34Rz5Y-0_nYmZAxIeG6HjsbeoIMtKg130_provenance.
- NP50898.RAgORAP7BZYvcL08k3dvMFP_MmYG8h2yx3ITZBcqzL6ko130_assertion description "[The association of TAP2*Bky2 was found with the antibody production to both 60 and 52kDa SS-A/Ro antigens. As TAP2*Bky2 had a strong linkage disequilibrium with DRB1*08032, TAP2*Bky2 or its haplotype with DRB1*08032 may be involved in SS-A/Ro antibody production not only in SS but also SLE patients, indicating that TAP2*Bky2 may be a susceptible gene not only to the disease of SS but also to the SS-A/Ro autoantibody production.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50898.RAgORAP7BZYvcL08k3dvMFP_MmYG8h2yx3ITZBcqzL6ko130_provenance.
- NP50900.RAutY_DoNZ5EVGTtrxN9-P8zTAcoOZhfgXDFFjX7N9AZY130_assertion description "[However, the G alleles of TAP1-1 and TAP1-2 were significantly more common than the A alleles in serositis of SLE patients (chi(2)=11.16 and P=0.004, chi(2)=8.10 and P=0.02, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50900.RAutY_DoNZ5EVGTtrxN9-P8zTAcoOZhfgXDFFjX7N9AZY130_provenance.
- NP50901.RAodVg3yjtd0eXzZScwD8_AwVePuINowOgz0HsuxuSwck130_assertion description "[ The TAP2 locus influences susceptibility to SLE in our patient group; however, it has no significant effect on the immune response or on the clinical course of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50901.RAodVg3yjtd0eXzZScwD8_AwVePuINowOgz0HsuxuSwck130_provenance.
- NP50905.RAqAgWGgHLqy7Z_9AkI0x_nC-GRRRw1wgsT2FPTi8TBPY130_assertion description "[TAP1 and TAP2 gene polymorphisms were associated with different subsets of SSc: TAP1*A/A genotype with anti-topo I-positive dcSSc (p = 0.01, p corrected = 0.04), TAP2*A1/C genotype with anti-topo I-positive lcSSc (p < 0.05), TAP2*Bky2 and *C alleles with anti-topo I-negative dcSSc (both p < 0.05), and TAP2*B/E genotype with anti-topo I-negative lcSSc (p = 0.004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50905.RAqAgWGgHLqy7Z_9AkI0x_nC-GRRRw1wgsT2FPTi8TBPY130_provenance.
- NP50910.RAn7tx33nlNLbQMtqYnnVQjR8y86fPoGSu9XPumAttDVs130_assertion description "[To examine the distribution of transporter associated with antigen processing (TAP) gene polymorphism in a southern Chinese population and the association between TAP gene polymorphism and predisposition to Graves disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50910.RAn7tx33nlNLbQMtqYnnVQjR8y86fPoGSu9XPumAttDVs130_provenance.
- NP50916.RAj2O0Y34z2Ovj6Xm84SUhYPifX7tTmtIjPdue1VefeRk130_assertion description "[ This study demonstrates an association of atopic dermatitis with HLA-A24 and TAP2*C alleles in Korean patients. Discrepancy with the previous reports might be related to different patient characteristics and ethnic variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50916.RAj2O0Y34z2Ovj6Xm84SUhYPifX7tTmtIjPdue1VefeRk130_provenance.
- NP50919.RAhRAk25BSq8l9csZIKH2C5rjw9tNUUMG_-Q0zfSmmroI130_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." NP50919.RAhRAk25BSq8l9csZIKH2C5rjw9tNUUMG_-Q0zfSmmroI130_provenance.
- NP50926.RAqdYWoIMnDL0IxMLo3cFlwLfZluLg0ABJgvuoK8Eb6yU130_assertion description "[ These data suggest that plasma TAFI antigen levels are genetically controlled. The T/T Thr325Ile polymorphism of the TAFI gene is associated with lower plasma levels of TAFI antigen and lower restenosis rates after PCI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50926.RAqdYWoIMnDL0IxMLo3cFlwLfZluLg0ABJgvuoK8Eb6yU130_provenance.
- NP50927.RAiyOdnwltRkjZ31e5uvb48h6wX9s96D8Hoy1kcTFYWrw130_assertion description "[The frequency of FXIIIA Leu34Leu in PE patients and]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50927.RAiyOdnwltRkjZ31e5uvb48h6wX9s96D8Hoy1kcTFYWrw130_provenance.
- NP50944.RAqD8josyNuC1ds6C4Qjtr62f-WwgBNDsUWCea0n49tRA130_assertion description "[The synapsin II gene is located on 3p25, a region that has been implicated to be associated with schizophrenia by genetic linkage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50944.RAqD8josyNuC1ds6C4Qjtr62f-WwgBNDsUWCea0n49tRA130_provenance.
- NP50948.RAryT9vfSic9rWDF0cxvJKPaWePen2yHuF6-ed2pFaE_A130_assertion description "[Recently, a new candidate gene (SYBL1) for BPAD has been described on Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50948.RAryT9vfSic9rWDF0cxvJKPaWePen2yHuF6-ed2pFaE_A130_provenance.
- NP50949.RAoNtSQuOpHMDhWlbMGZ3Ot6aFMScEYVKjhp-3fCUyhBE130_assertion description "[Recently, a new candidate gene (SYBL1) for BPAD has been described on Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50949.RAoNtSQuOpHMDhWlbMGZ3Ot6aFMScEYVKjhp-3fCUyhBE130_provenance.
- NP50959.RArfUft0RgZe1Z9sy6e-HZ9b8CcCrqP8Bfhlmsj93S660130_assertion description "[Of the 224 SNPs investigated, 20 potential candidates associated with CRC were identified, including IL6 -174G>C (g.22062318G>C), XRCC1 c.685 C>T (p.Arg194Trp), PPARGC1A g.92945042C>T (3'UTR 96516), GSTP1 c.342A>C (p.Ile105Val), GSTM1 c.573C>G (p.Lys173Asn), and SULT1A1 g.19934792G>A (p.Arg213His).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50959.RArfUft0RgZe1Z9sy6e-HZ9b8CcCrqP8Bfhlmsj93S660130_provenance.
- NP50961.RAoRK5a9sBRXgtPStzlkRVZSKUqMD4R3qnzrZRpaPZ6yQ130_assertion description "[In a multicenter case-control study, 490 colorectal cancer patients and 593 controls (433 matched case-control pairs) were genotyped for common polymorphisms in the cytochrome P450 (CYP1A1, CYP1A2, CYP1B1, CYP2A6, CYP2C9, CYP2C19 and CYP2D6), glutathione S-transferase (GSTM1, GSTP1 and GSTT1), sulfotransferase (SULT1A1 and SULT1A2), N-acetyl transferase 2 (NAT2), NAD(P)H:quinone oxidoreductase (NQO1), methylenetetrahydrofolate reductase (MTHFR), and microsomal epoxide hydrolase (EPHX1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50961.RAoRK5a9sBRXgtPStzlkRVZSKUqMD4R3qnzrZRpaPZ6yQ130_provenance.
- NP50962.RAh080TQVsGFURA9hHcxnGyqLqeVkI8lv-KjVURlJKctw130_assertion description "[Our results showed that the interaction between polymorphisms in CYP1B1 1294G and SULT1A1*2 may play a significant role on CRC in the Chinese population. Also, it is suggested that the association between cigarette smoking and CRC could be differentiated by the CYP1B1 1294G allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50962.RAh080TQVsGFURA9hHcxnGyqLqeVkI8lv-KjVURlJKctw130_provenance.
- NP50968.RAppOw712ydUdz18f2z4fS2sCb3p-nQaZAYTjrawu9LvA130_assertion description "[Study on the relationship between polymorphisms of genes (CYP17, CYP19 and SULT1A1) and susceptibility to breast cancer in Chinese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50968.RAppOw712ydUdz18f2z4fS2sCb3p-nQaZAYTjrawu9LvA130_provenance.
- NP50970.RAmea93Ch6YmXlRtkEL1evsmjAiB5qJjdIVUzYxRcMwMk130_assertion description "[Our data suggest that UGT1A1 but not SULT1A1 genotype might be important for breast cancer risk and phenotype in Russian women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50970.RAmea93Ch6YmXlRtkEL1evsmjAiB5qJjdIVUzYxRcMwMk130_provenance.
- NP50972.RArAvr_1obbH-_ATgnSKYWqR4fmhzJmPs4YUHK9POgkyM130_assertion description "[Sulfotransferase 1A1 (SULT1A1) polymorphism and breast cancer risk in Chinese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50972.RArAvr_1obbH-_ATgnSKYWqR4fmhzJmPs4YUHK9POgkyM130_provenance.
- NP50974.RAsbk_bHCRw0iyYOiP-rbnQkK13Cty3dvgjFFTkEmZdu8130_assertion description "[An analysis of 444 breast cancer patients and 227 controls revealed no effect of SULT1A1 genotype on the risk of breast cancer (P = 0.69); however, it did appear to influence the age of onset among early-onset affected patients (P = 0.04).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50974.RAsbk_bHCRw0iyYOiP-rbnQkK13Cty3dvgjFFTkEmZdu8130_provenance.
- NP50975.RAt2qcAKq_ntMYty55ZL02GYCjK1N5zsIRoCpR_04MJzk130_assertion description "[We have shown an association between tamoxifen and its metabolites and estrogen serum levels. An impact of CYP2C19 predicted activity on tamoxifen, as well as estrogen kinetics may partly explain the observed association between tamoxifen and its metabolites and estrogen serum levels. Since the role of estrogen levels during tamoxifen therapy is still a matter of debate further prospective studies to examine the effect of tamoxifen and estrogen kinetics on treatment outcome are warranted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50975.RAt2qcAKq_ntMYty55ZL02GYCjK1N5zsIRoCpR_04MJzk130_provenance.
- NP50979.RAqqWV-OzW_53LteXcae-lDhzombSrdnhWt8AiRs9Fl5c130_assertion description "[These findings suggest that individual susceptibility to bladder cancer may be modulated by GSTM1, GSTT1 and NAT2 polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50979.RAqqWV-OzW_53LteXcae-lDhzombSrdnhWt8AiRs9Fl5c130_provenance.
- NP50989.RAhEnymIh8fEijirwZc_JQPoQomSqeBrhNFgQlRinz73g130_assertion description "[The SULT1A1*2/*2 genotype in combination with the CYP3A5 heterozygous genotypes was associated with significantly increased risk for OC (AOR, 3.60; P=0.001) with the risk being even higher among smokers compared with non-smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50989.RAhEnymIh8fEijirwZc_JQPoQomSqeBrhNFgQlRinz73g130_provenance.
- NP50991.RAk-x3ApUKK8nI6ZdSdPmD82OzK_8Ui6YoNWnrIw6A29Y130_assertion description "[These results indicate that variations in SULT1A1 activity contributes to prostate cancer risk and the magnitude of the association may differ by ethnicity and be modified by meat consumption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50991.RAk-x3ApUKK8nI6ZdSdPmD82OzK_8Ui6YoNWnrIw6A29Y130_provenance.
- NP50992.RAox3tWs6tBwwe3w8XFbV8r2bVreTUQBgJUiFeMPrMumw130_assertion description "[Genetic polymorphism of the SULT1A1 gene, SULT1A1, was reported to be associated with risks of several cancers; however, one study showed no significant relation between SULT1A1 genotype with prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50992.RAox3tWs6tBwwe3w8XFbV8r2bVreTUQBgJUiFeMPrMumw130_provenance.
- NP50996.RAtGfvG9-_RSg0HTSkzVNUUJ3lzIpraxC0HGzzcu-ZR2s130_assertion description "[Our results, which are against the original hypothesis, demonstrate that the variant SULT1A1 638A allele is associated with susceptibility to lung cancer in relation to tobacco smoking.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50996.RAtGfvG9-_RSg0HTSkzVNUUJ3lzIpraxC0HGzzcu-ZR2s130_provenance.
- NP51000.RAom9tcgOrASOqfV1ZIkYx9Sf7u35cU-UolvIn_Ryi7EE130_assertion description "[Statistical analyses of histological types of lung cancer in comparison with the control individuals indicated a significant difference between SULT1A1 Arg(213)His polymorphism and SCC (p = 0.027) and other types of cancer (p = 0.037), except SMCC (p = 0.854).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51000.RAom9tcgOrASOqfV1ZIkYx9Sf7u35cU-UolvIn_Ryi7EE130_provenance.
- NP51001.RAva_beFO-4AEk-VdIRPgOZKuMGamc-yAC6_mMp29gVQw130_assertion description "[Polymorphisms of the AURKA (STK15/Aurora Kinase) Gene and Breast Cancer Risk (United States).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51001.RAva_beFO-4AEk-VdIRPgOZKuMGamc-yAC6_mMp29gVQw130_provenance.
- NP51005.RAiVKq6gN3ogXsx4qFDATiXOnun1fXPChk7T3J2bcIfAM130_assertion description "[, the F31I polymorphism in AURKA is not associated with a modified risk of breast cancer in BRCA1 and BRCA2 carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51005.RAiVKq6gN3ogXsx4qFDATiXOnun1fXPChk7T3J2bcIfAM130_provenance.
- NP51008.RApGTALfXCoBepV92n5MrmLVDyUhG_xOLmYyxxgXpurDU130_assertion description "[No significant association was observed between the polymorphism and metastasis and disease stage of the cancer. These findings suggest that the Phe31Ile polymorphism in Aurora A may be a genetic modifier for developing breast carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51008.RApGTALfXCoBepV92n5MrmLVDyUhG_xOLmYyxxgXpurDU130_provenance.
- NP51015.RAhHGW4G2zpVqFSe-h_T_L6Vbg6PXg_0Z7hA3erNsOKQQ130_assertion description "[To explore the relationship between the sequence variation of the promoter region (-1543 approximately -1160) of STK11 gene and the risk of developing Peutz-Jeghers syndrome (PJS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51015.RAhHGW4G2zpVqFSe-h_T_L6Vbg6PXg_0Z7hA3erNsOKQQ130_provenance.
- NP51018.RAhLk0kCPiJPuCf6lOj9NZ716CcRQ6tgI6hLezW8JMMtY130_assertion description "[ We identified a panel of novel SNPs in genes coding for proteins important in the T H 1/T H 2 cell differentiation. SNPs of the GATA3 gene showed an initial association to asthma-related phenotypes. Elucidation of the importance of the identified panel of SNPs in other T H 1/T H 2 mediated diseases will be of great interest.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51018.RAhLk0kCPiJPuCf6lOj9NZ716CcRQ6tgI6hLezW8JMMtY130_provenance.
- NP51021.RAmkCH4JRjuRIAnYEL3F_UOw2MlJJmEecmVZ4v_QQ41hM130_assertion description "[Replication of genetic association studies in asthma and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51021.RAmkCH4JRjuRIAnYEL3F_UOw2MlJJmEecmVZ4v_QQ41hM130_provenance.
- NP51025.RArSs9p1FpT0LjtWH-ZcwxkBMcOrEhbhDvr8dbzFzOc54130_assertion description "[ Tunisian persons carrying the P2/P2 genotype of the hsp70-2 gene may have an increased risk of obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51025.RArSs9p1FpT0LjtWH-ZcwxkBMcOrEhbhDvr8dbzFzOc54130_provenance.
- NP51036.RAuk92o9zJGpOXfKWFWaT1poeC8qjHD489hWCaMU9ZLk8130_assertion description "[In conclusion, this pilot identified SNPs as potential markers that could predict hepatitis B patient response. These observations may help guide future large-scale studies in examining host SNPs for their clinical utility in predicting IFN response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51036.RAuk92o9zJGpOXfKWFWaT1poeC8qjHD489hWCaMU9ZLk8130_provenance.
- NP51040.RAuukq6H6a__Tf1XdC29Y_9JwSWlBof-s7gKt3lvxBqAY130_assertion description "[The somatostatin receptor 5 (SSTR5) gene is a candidate gene for bipolar affective disorder (BPAD) as well as for other neuropsychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51040.RAuukq6H6a__Tf1XdC29Y_9JwSWlBof-s7gKt3lvxBqAY130_provenance.
- NP51048.RAp2RdvlMoJDCWF57uZI2UG-ZWRFccu0pdiJrVE6OuSwc130_assertion description "[Genetic variation in the growth hormone synthesis pathway in relation to circulating insulin-like growth factor-I, insulin-like growth factor binding protein-3, and breast cancer risk: results from the European prospective investigation into cancer and nutrition study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51048.RAp2RdvlMoJDCWF57uZI2UG-ZWRFccu0pdiJrVE6OuSwc130_provenance.
- NP51050.RAvZd0gCKUaXk2O-vwWrq1_me-zI7tTsRinx6VfkagoMs130_assertion description "[Genetic variation in the growth hormone synthesis pathway in relation to circulating insulin-like growth factor-I, insulin-like growth factor binding protein-3, and breast cancer risk: results from the European prospective investigation into cancer and nutrition study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51050.RAvZd0gCKUaXk2O-vwWrq1_me-zI7tTsRinx6VfkagoMs130_provenance.
- NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_assertion description "[Further studies are needed to explore contributions from other genetic factors such as rare variants in these genes and variation outside of these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_provenance.
- NP51054.RAiT7I0UuQeD478EOCggh_NqpJaqh7Krvhd8i8-RBgvBY130_assertion description "[Genetic variation in the growth hormone synthesis pathway in relation to circulating insulin-like growth factor-I, insulin-like growth factor binding protein-3, and breast cancer risk: results from the European prospective investigation into cancer and nutrition study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51054.RAiT7I0UuQeD478EOCggh_NqpJaqh7Krvhd8i8-RBgvBY130_provenance.
- NP51056.RAm49GiplyimxdjeruMnFzl8tEbzv6IwUyhrFx3YOh7pY130_assertion description "[Gain of chromosome arm 17q is associated with unfavourable prognosis in neuroblastoma, but does not involve mutations in the somatostatin receptor 2(SSTR2) gene at 17q24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51056.RAm49GiplyimxdjeruMnFzl8tEbzv6IwUyhrFx3YOh7pY130_provenance.
- NP51066.RAncGfIdRaB1acUUelJJlTzSq3wDz63Il9fU4sDzagZAI130_assertion description "[Determinants of variable response to simvastatin treatment: the role of common variants of SCAP, SREBF-1a and SREBF-2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51066.RAncGfIdRaB1acUUelJJlTzSq3wDz63Il9fU4sDzagZAI130_provenance.
- NP51068.RAjfwUb22Gzl-jbunCwx6LZoQpVmc9-Ol9Ta3duLg-am0130_assertion description "[These data suggest that the genetic mechanism(s) of carcinogenesis differs between the differentiated type and the undifferentiated type of gastric cancer and that K-ras mutations may be involved in the early stages of gastric carcinogenesis of the differentiated type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51068.RAjfwUb22Gzl-jbunCwx6LZoQpVmc9-Ol9Ta3duLg-am0130_provenance.
- NP51069.RAjwkVP5G_lKcYSgvw_IArUwINj4G6ezCuNqt0jHq1cv0130_assertion description "[The study indicated that 1784GC/CC genotypes of SREBP-2 were significantly related with the elevated concentrations of serum TC and LDL-C in hypercholesterolemic subjects, and further work is necessary to confirm the role of 1784G > C polymorphism of SREBP-2 gene in the development of hyperlipidemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51069.RAjwkVP5G_lKcYSgvw_IArUwINj4G6ezCuNqt0jHq1cv0130_provenance.
- NP51071.RAvP5I2meHlmu2_Mrx4j3BOkvLXx6Z658YI6YgGXPsIuU130_assertion description "[Analysis of the SREBF2 gene as a genetic risk factor for vascular dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51071.RAvP5I2meHlmu2_Mrx4j3BOkvLXx6Z658YI6YgGXPsIuU130_provenance.
- NP51074.RAokqbcESacWJn9JNhq_IeuKPDZ1vmsGiW7Puwb_W7KjY130_assertion description "[The objective of the study was to examine associations between SRD5A2 polymorphisms and measures of benign prostatic hyperplasia (BPH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51074.RAokqbcESacWJn9JNhq_IeuKPDZ1vmsGiW7Puwb_W7KjY130_provenance.
- NP51075.RAvqK_QKXYHQnnnuKvzUykQm2eanU_UPYXd0AKN76jceU130_assertion description "[ The authors obtained the first SNP data indicating that CYP17 and CYP1A1-1 play a role in the pathogenesis of fibroadenoma. Although the authors were not able to develop interaction models involving SNPs, they did provide evidence that CYP1A1 is a low-penetrance susceptibility gene with respect to breast carcinoma in a large series of Caucasian women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51075.RAvqK_QKXYHQnnnuKvzUykQm2eanU_UPYXd0AKN76jceU130_provenance.
- NP51077.RAmcpIjeS6fmpAZbosr063vpHh7QnGceS2m_y194V33t8130_assertion description "[ This study is the first to our knowledge focusing on Japanese women, suggesting that SRD5A2 polymorphisms might have an association with breast cancer risk. Further large-sample studies will be required to confirm the association and to assess any interactions with environmental factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51077.RAmcpIjeS6fmpAZbosr063vpHh7QnGceS2m_y194V33t8130_provenance.
- NP51079.RAov_zl2QeVB1xB0Dewm_-XtarWPvurnmBIxYjfRrzlys130_assertion description "[In an analysis combining data from 2 population-based case-control studies of postmenopausal breast cancer (1,296 cases and 1,055 controls) conducted in Washington State in 1997-1999 and 2000-2004, the authors evaluated how 51 single nucleotide polymorphisms in 7 progesterone-related genes (AKR1C1, AKR1C2, AKR1C3, CYP3A4, SRD5A1, SRD5A2, and PGR) influenced breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51079.RAov_zl2QeVB1xB0Dewm_-XtarWPvurnmBIxYjfRrzlys130_provenance.
- NP51081.RAg66oaINgM8w5rc5CP09xqIHRrLEGuysmYrGXrjLyors130_assertion description "[Longer (TA)n repeat but not A49T and V89L polymorphisms in SRD5A2 gene may confer prostate cancer risk in South Indian men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51081.RAg66oaINgM8w5rc5CP09xqIHRrLEGuysmYrGXrjLyors130_provenance.
- NP51082.RAkFS8QsuTZhJDnodVgJUgQA84uLNY0JbQueze9xvrmBI130_assertion description "[To estimate the prostate cancer risk conferred by individual single nucleotide polymorphisms (SNPs), SNP-SNP interactions, and/or cumulative SNP effects, we evaluated the association between prostate cancer risk and the genetic variants of 12 key genes within the steroid hormone pathway (CYP17, HSD17B3, ESR1, SRD5A2, HSD3B1, HSD3B2, CYP19, CYP1A1, CYP1B1, CYP3A4, CYP27B1, and CYP24A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51082.RAkFS8QsuTZhJDnodVgJUgQA84uLNY0JbQueze9xvrmBI130_provenance.
- NP51084.RAtAOO0rg9UOI0h4nzjPJ-cLbj77HwoL50APIPeuuhxU8130_assertion description "[PCR was used to examine the A49T polymorphisms of SRD5A2 gene in the tissues of prostate cancer resected from 112 patients (CaP group) and the specimens of benign prostate hyperplasia (BPH group) resected from 89 patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51084.RAtAOO0rg9UOI0h4nzjPJ-cLbj77HwoL50APIPeuuhxU8130_provenance.
- NP51100.RAmCwhnxg6lwcyhBC7lJUsh-ED1whmX0T9hZYAeHFR6QA130_assertion description "[These data suggest that OPN genotypes may influence MS development and progression due to their influence on OPN levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51100.RAmCwhnxg6lwcyhBC7lJUsh-ED1whmX0T9hZYAeHFR6QA130_provenance.
- NP51107.RApC_elKcj1WMmc-3D76fajst76At-HWsqE1WGuc92Ax4130_assertion description "[An osteopontin (SPP1) polymorphism is associated with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51107.RApC_elKcj1WMmc-3D76fajst76At-HWsqE1WGuc92Ax4130_provenance.
- NP51109.RAostzUql6KGNWHdCqkNUTEdE_Xk3__bUmwJTD-17hkcs130_assertion description "[This study provides a biologic relevance for OPN variants at the protein level, and suggests an influence of this gene on the IFN-alpha pathway in SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51109.RAostzUql6KGNWHdCqkNUTEdE_Xk3__bUmwJTD-17hkcs130_provenance.
- NP51113.RAoZf6c-bCcMVPREgeu4YPCTFdIo7HMYXGKhNIGs6zJBU130_assertion description "[Despite the biological plausibility of IgE-related mechanisms in asthma, very few of the tested candidates showed evidence of association with both wheeze and increased IgE levels. We were unable to confirm associations of the positional candidates DPP10 and PHF11 with wheeze, although our study had ample power to detect the expected associations of IL13 variants with IgE and SPINK5 variants with eczema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51113.RAoZf6c-bCcMVPREgeu4YPCTFdIo7HMYXGKhNIGs6zJBU130_provenance.
- NP51118.RAncjuDYEJcGqxiUcTM7S0-jVaL0BR6sZnq9DqhfoQHWs130_assertion description "[first recognized the association between mutations in the SPINK1 gene and chronic pancreatitis (CP), but the significance of SPINK1 gene mutation in pancreatitis and its relation to alcohol consumption remains unclear in Japan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51118.RAncjuDYEJcGqxiUcTM7S0-jVaL0BR6sZnq9DqhfoQHWs130_provenance.
- NP51122.RAiTf3GYFnqyMT-61pm_axtEpXz16tRQLwRgWKmMXuEd0130_assertion description "[One ACP patient (2.2%) was found to carry the most common mutation (N34S) of SPINK1 compared to none of the ALD patients (P=NS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51122.RAiTf3GYFnqyMT-61pm_axtEpXz16tRQLwRgWKmMXuEd0130_provenance.
- NP51124.RAv7urv7mfDEuQ75ukVEY7CNWFHh5nn7dPzJ2GjvhLU9Q130_assertion description "[Mutations in cystic fibrosis transmembrane conductance regulator (CFTR), in cationic trypsinogen (PRSS1) and in serine protease inhibitor Kazal type 1 (SPINK1) genes have been associated with chronic pancreatitis (alcohol related, idiopathic and hereditary).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51124.RAv7urv7mfDEuQ75ukVEY7CNWFHh5nn7dPzJ2GjvhLU9Q130_provenance.
- NP51126.RApKJ5cGm9LLadUBZXga9BhuJvwENA5rP5bqtDqeGYh3g130_assertion description "[This study shows that SPINK1 N34S and CFTR Q1352H mutations are uncommon and do not play an important role in chronic alcoholic pancreatitis in Korea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51126.RApKJ5cGm9LLadUBZXga9BhuJvwENA5rP5bqtDqeGYh3g130_provenance.
- NP51131.RAtCT-lJdjHzfaN32KCHsqGhEyTq0hX6-bJsOJ5S3HCcM130_assertion description "[Limited contribution of the SPINK1 N34S mutation to the risk and severity of alcoholic chronic pancreatitis: a report from the United States.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51131.RAtCT-lJdjHzfaN32KCHsqGhEyTq0hX6-bJsOJ5S3HCcM130_provenance.
- NP51135.RAnscfM4YajT07EeRp4yhk2uulJLCPDmmaHViC2k4tA9Q130_assertion description "[To test the hypothesis that calcium sensing receptor (CASR) polymorphisms are associated with chronic pancreatitis (CP), and to determine whether serine protease inhibitor Kazal 1type (SPINK1) N34S or alcohol are necessary co-factors in its etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51135.RAnscfM4YajT07EeRp4yhk2uulJLCPDmmaHViC2k4tA9Q130_provenance.
- NP51138.RAgXMv7T8t4aaMqzwNhVBV0257JjP_l8_88YsV_MDG1LQ130_assertion description "[Our study suggests, for the first time, that CASR mutation may be a risk for TCP, and that this risk may be further increased if there is an associated SPINK1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51138.RAgXMv7T8t4aaMqzwNhVBV0257JjP_l8_88YsV_MDG1LQ130_provenance.
- NP51140.RArhOjj4p7B5huVLlUyP2KmwoQ7Xhwi8XlaQIxC9j656s130_assertion description "[However, whether patients with mutations in other genes, such as the serine protease inhibitor Kazal type 1 (SPINK1) gene, are also at a higher risk of pancreatic cancer remains unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51140.RArhOjj4p7B5huVLlUyP2KmwoQ7Xhwi8XlaQIxC9j656s130_provenance.
- NP51145.RAu-sCGPczCdbfK1ZLVSuzIJ10xPBQ74pp7Sjc6WPWWcU130_assertion description "[Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51145.RAu-sCGPczCdbfK1ZLVSuzIJ10xPBQ74pp7Sjc6WPWWcU130_provenance.
- NP51146.RAnDMeKZl6fKvBN6kTRNL4f6UINApDeAeFKApLhpRagq8130_assertion description "[Asymptomatic cognitive impairment mostly affecting executive functions is present in SPG4 mutation carriers and is more frequent in those with missense mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51146.RAnDMeKZl6fKvBN6kTRNL4f6UINApDeAeFKApLhpRagq8130_provenance.
- NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_assertion description "[ This study is the first to show that polymorphisms of the SPARC gene are associated with susceptibility to, and clinical manifestations of, SSc and that they may also be functionally important in influencing SPARC expression in skin fibroblasts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_provenance.
- NP51149.RAjs3tyETR0glVL5s0d7nhjk65a-R_78FvXMmE3K5d21c130_assertion description "[In conclusion, mutations are frequently found in genes that control androgen action and metabolism, but are seldom found in genes active in the early phase of sex determination and differentiation. Mutations in AR, SRD5A2 or WT1 seem to be associated not only with hypospadias but also with micropenis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51149.RAjs3tyETR0glVL5s0d7nhjk65a-R_78FvXMmE3K5d21c130_provenance.
- NP51150.RAl-eAGSe9ntuGJNgzHMsGI7pW4iMyqG-qNAklmtLqS0g130_assertion description "[The sorted genes allow us to draw novel hypotheses for future studies of HCV infection to ultimately identify bona fide genes and their variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51150.RAl-eAGSe9ntuGJNgzHMsGI7pW4iMyqG-qNAklmtLqS0g130_provenance.
- NP51151.RAjO4HRxAwhbJ3-Nkq5OVR4rHSJNLuGzJMlmA_rHT5-Zs130_assertion description "[Genetic influence on cigarette-induced cardiovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51151.RAjO4HRxAwhbJ3-Nkq5OVR4rHSJNLuGzJMlmA_rHT5-Zs130_provenance.
- NP51159.RAjRlbOoULI4I3YKzAGAwXG11QxrMf2ZNB-UPW26HWWiA130_assertion description "[ The results suggest that manganese superoxide dismutase gene polymorphism is associated with exudative age-related macular degeneration. Microsomal epoxide hydrolase is another enzyme that may be associated with the disease. The exudative form of age-related macular degeneration may have genetic risk factors against oxidative stress and/or effects of xenobiotics. Further association studies in other polymorphic genes for xenobiotic-metabolizing enzymes are needed to elucidate the environmental-genetic interaction in the underlying cause of age-related macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51159.RAjRlbOoULI4I3YKzAGAwXG11QxrMf2ZNB-UPW26HWWiA130_provenance.
- NP51160.RAmGaVSlWq8AMwbUoO4r0eFytTyAYVes9QJ5KKe6lGjdg130_assertion description "[These data suggest a genetic role of MnSOD polymorphism in the development of age-related degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51160.RAmGaVSlWq8AMwbUoO4r0eFytTyAYVes9QJ5KKe6lGjdg130_provenance.
- NP51168.RAkSeB7cI-r_uDfVIVgnI-TyiphI5FgqL4dXvSiQy5ajk130_assertion description "[These findings suggest that individual susceptibility of bladder cancer may be modulated by MPO and MnSOD polymorphisms, and that the combination of genetic factors involved in oxidative stress response with environmental carcinogens may play an important role in bladder carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51168.RAkSeB7cI-r_uDfVIVgnI-TyiphI5FgqL4dXvSiQy5ajk130_provenance.
- NP51170.RAloaJeQIfd9gUCQ5iQW1fsMMUHOF_sffdLCHfb_wgdBI130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51170.RAloaJeQIfd9gUCQ5iQW1fsMMUHOF_sffdLCHfb_wgdBI130_provenance.
- NP51173.RAiW27xtloyKP13Q8_aaGrxwjTS1qG6RVvHeKEg8GEF1s130_assertion description "[ While these results need to be confirmed in other studies, they point to a possible role for genes involved in oxidative stress in the development of ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51173.RAiW27xtloyKP13Q8_aaGrxwjTS1qG6RVvHeKEg8GEF1s130_provenance.
- NP51177.RAp8Lt3QAcSrCY2hvMPbqfhiokhaUOVsK1TwSjDqLdrKg130_assertion description "[Our results are consistent with the hypothesis that women with higher SOD2 antioxidant activity may experience less treatment-related toxicity but shorter time to disease recurrence or death after breast cancer adjuvant chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51177.RAp8Lt3QAcSrCY2hvMPbqfhiokhaUOVsK1TwSjDqLdrKg130_provenance.
- NP51179.RAs09i_eZL19V4U5Pb9BL42-D4HxR7b81EFHEN20S-CMk130_assertion description "[Polymorphism (ALA16VAL) correlates with regional lymph node status in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51179.RAs09i_eZL19V4U5Pb9BL42-D4HxR7b81EFHEN20S-CMk130_provenance.
- NP51180.RAkZySZfxowgio4cMHcFAvFtLonwTNOcZKqL-E7sy-FUI130_assertion description "[Establishment of a multiplex ligation-dependent SNP genotyping method and its application in the detection of genes related to chemotherapeutic drugs in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51180.RAkZySZfxowgio4cMHcFAvFtLonwTNOcZKqL-E7sy-FUI130_provenance.
- NP51185.RAomWdGVZssQNBz3wzP9fRYPG8_2By_6-Qf58aYiIRfyE130_assertion description "[ Cirrhosis is more likely to develop in C282Y homozygotes with the GSTP1 Val/Val genotype than in those with non-Val/Val genotypes, which in part explains the variable phenotypic expression of HHC and highlights the central role of oxidative stress in its pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51185.RAomWdGVZssQNBz3wzP9fRYPG8_2By_6-Qf58aYiIRfyE130_provenance.
- NP51186.RAvQeDfHboAIilBCBPzFFXVl2Ur3Zj7Q02kszTWeae2TU130_assertion description "[ No association was found between the previously implicated polymorphisms of TNF-alpha, IL-10, CD14 and MnSOD, either individually or simultaneously, and the presence of established ALD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51186.RAvQeDfHboAIilBCBPzFFXVl2Ur3Zj7Q02kszTWeae2TU130_provenance.
- NP51187.RAhk5jr2l-pC3kfgg5WirEp-SVB09vypiD-zanHEXypbs130_assertion description "[ The excess of -697 variant in the promoter regulation region of the HTR2C gene may be a risk factor for the susceptibility to the occurrence of TD in Chinese male patients with schizophrenia. A combination of DRD3 variant allele (Gly) and MnSOD wild allele (Val) may increase the susceptibility to the development of TD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51187.RAhk5jr2l-pC3kfgg5WirEp-SVB09vypiD-zanHEXypbs130_provenance.
- NP51198.RAgAixWqbPEhP8zVwZNevkRuDLDBYoYIz_lcAoGn85JXI130_assertion description "[ CYP1A1 4887A may be a protective factor for the development of AS in Taiwan. However, MnSOD gene polymorphisms are not associated with the susceptibility to AS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51198.RAgAixWqbPEhP8zVwZNevkRuDLDBYoYIz_lcAoGn85JXI130_provenance.
- NP51200.RApU1HZWK6-nmcPpz-dwk1Ffjk04Pmp9opcqeH7O6zDbI130_assertion description "[ Simultaneous presence of CYP1A1 4889G and 4887A is associated with development of BD in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51200.RApU1HZWK6-nmcPpz-dwk1Ffjk04Pmp9opcqeH7O6zDbI130_provenance.
- NP51211.RAu_aW7HWJyhQSUpSaGTtBA4lJ8GzmSWl69t6TbLdLBNM130_assertion description "[Functional polymorphism of manganese superoxide dismutase (MnSOD) gene correlates with schizophrenia in Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51211.RAu_aW7HWJyhQSUpSaGTtBA4lJ8GzmSWl69t6TbLdLBNM130_provenance.
- NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_assertion description "[In patients with hereditary haemochromatosis, the MnSOD genotype affects the risk of cardiomyopathy related to iron overload and possibly to other known and unknown risk factors and could represent an iron toxicity modifier gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_provenance.
- NP51216.RAucR9piQkHrG5mPPM48QA0gDLqBiwn2AZfww_IUamZ5o130_assertion description "[Therefore, MnSOD 1183C polymorphisms may be a precipitating factor for the development of psoriatic arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51216.RAucR9piQkHrG5mPPM48QA0gDLqBiwn2AZfww_IUamZ5o130_provenance.
- NP51220.RAvQpfGx4PTJ4FX7S0elgJJj3icV7plVsZoF8qS5zJN8M130_assertion description "[ The present data suggest a role for CYP1B1 and CYP1A1 as new candidate genes in the etiology of CRC and confirm the carcinogenic role of aromatic amines metabolism for colorectum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51220.RAvQpfGx4PTJ4FX7S0elgJJj3icV7plVsZoF8qS5zJN8M130_provenance.
- NP51224.RAspGkLeQSXz_rTamBrLdSmZFM0T0vhXvmN53oqWmlS5A130_assertion description "[Manganese superoxide dismutase Ala16Val polymorphism is associated with the development of type 2 diabetes in Japanese-Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51224.RAspGkLeQSXz_rTamBrLdSmZFM0T0vhXvmN53oqWmlS5A130_provenance.
- NP51226.RAqFkftg578c_0JFHxisGTctsJgPx7lU4YsBiBGFOQAOc130_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." NP51226.RAqFkftg578c_0JFHxisGTctsJgPx7lU4YsBiBGFOQAOc130_provenance.
- NP51228.RAoLl4EBzMNP_6B2w5jLcbMr5by0QmoT0fdXsWlmzWrIM130_assertion description "[There were no associations between SOD1, SOD2 and CAT polymorphisms and PTDM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51228.RAoLl4EBzMNP_6B2w5jLcbMr5by0QmoT0fdXsWlmzWrIM130_provenance.
- NP51229.RAs3crGLgqfTpK70otBpdcITO96_Yj6loiRAogvZ5MO1M130_assertion description "[Amyotrophic lateral sclerosis and SOD1 gene: an overview.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51229.RAs3crGLgqfTpK70otBpdcITO96_Yj6loiRAogvZ5MO1M130_provenance.
- NP51230.RAoSQtG9y_PpqfffKGiuu956itifgpIMBxM5g17pFABK0130_assertion description "[Normal complement of motor units in asymptomatic familial (SOD1 mutation) amyotrophic lateral sclerosis carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51230.RAoSQtG9y_PpqfffKGiuu956itifgpIMBxM5g17pFABK0130_provenance.
- NP51238.RArVGGa_FJmQ_lwWP2SjazJFO48JN4JukJGCmj9q8gqig130_assertion description "[SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51238.RArVGGa_FJmQ_lwWP2SjazJFO48JN4JukJGCmj9q8gqig130_provenance.
- NP51241.RAgItE_J2luJALcsMhr9qn--Chi_FrqUjRhJjnCKhYedE130_assertion description "[Our findings suggest that SOAT1 gene may possibly be only a minor risk factor in AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51241.RAgItE_J2luJALcsMhr9qn--Chi_FrqUjRhJjnCKhYedE130_provenance.
- NP51242.RAtACxpAUIlqkrR0-pHYoK2vdFGYXohb_ebkg9WkygeHM130_assertion description "[PARK16, PARK8, and PARK1 loci but not BST1 were found to be associated with PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51242.RAtACxpAUIlqkrR0-pHYoK2vdFGYXohb_ebkg9WkygeHM130_provenance.
- NP51248.RAvJOVHf-cRDZEKUCisCAXKafGXPVQRDMliuJJb1Ob3oM130_assertion description "[Our genetic analysis suggests that CALB1 is associated with PD independently of SNCA, and that FGF20 is associated with PD synergistically with SNCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51248.RAvJOVHf-cRDZEKUCisCAXKafGXPVQRDMliuJJb1Ob3oM130_provenance.