Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP45112.RAkddK5FAmPaufqVojkYNzXRxwtiJve4TLpfqS3T7PZgQ130_assertion description "[Additionally, due to the lack of large pedigrees suitable for linkage analysis, and since SMAD4 germline mutations have been reported in families with combined HHT and juvenile polyposis, we screened this gene and five other genes involved in the TGF-beta/BMP pathway in the patients without mutation of ENG or ACVRL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45112.RAkddK5FAmPaufqVojkYNzXRxwtiJve4TLpfqS3T7PZgQ130_provenance.
- NP45119.RApEf0RZ7ucqvY1x3DPAf1_0IvZ83bdz2wznA0EaFcuvA130_assertion description "[A Met299Val variant in the elongation of very long chain fatty acids-like 4 (ELOVL4) gene was significantly associated with ARM in the case-control allele (P=0.001), case-control genotype (P=0.001) and case-control family (P<0.0001) tests.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45119.RApEf0RZ7ucqvY1x3DPAf1_0IvZ83bdz2wznA0EaFcuvA130_provenance.
- NP45125.RAp-zgzsDjSVBANGK_3Otc-YuEWYEaeRCl-uiumDy1rlw130_assertion description "[one SNP of LOXL2 showed a significant association with IA individually, and we also detected a gene-gene interaction of LOXL2 with ELN/LIMK1, which may play an important role in susceptibility to IA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45125.RAp-zgzsDjSVBANGK_3Otc-YuEWYEaeRCl-uiumDy1rlw130_provenance.
- NP45130.RAqr5ISlDS7xWOpxP6beTlFWgHy1XLNP6WuemeNoljAJY130_assertion description "[These results suggest that common variants at HPC2/ELAC2 are associated with CaP risk in a sample unselected for family history or other factors associated with CaP risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45130.RAqr5ISlDS7xWOpxP6beTlFWgHy1XLNP6WuemeNoljAJY130_provenance.
- NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_assertion description "[ These results suggest that, in a European-American population, ELAC2 217L and RNASEL 541E are associated with metastatic sporadic disease. ELAC2 and RNASEL SNP analysis may prove useful in determining which patients are at risk for developing clinically significant prostate carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_provenance.
- NP45138.RAtpo50es6aMzZnu5v5EtgQULx85mLeaqZEQH6n7vs3-k130_assertion description "[These results confirm that the NE promoter region polymorphisms may influence in risk for lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45138.RAtpo50es6aMzZnu5v5EtgQULx85mLeaqZEQH6n7vs3-k130_provenance.
- NP45140.RAjmvL5-Ijdsbv7YJUmWJBQeQ2OdKWuJbMmy8WU6y7pLI130_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." NP45140.RAjmvL5-Ijdsbv7YJUmWJBQeQ2OdKWuJbMmy8WU6y7pLI130_provenance.
- NP45143.RAvqMw4gtijyLupiqgEd56eXLUVcRwEeflPAX2TI1h8AQ130_assertion description "[Frequency of mutations in the early growth response 2 gene associated with peripheral demyelinating neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45143.RAvqMw4gtijyLupiqgEd56eXLUVcRwEeflPAX2TI1h8AQ130_provenance.
- NP45145.RAq4lDbzZJMGVOoyZdahapArXofV2yw-7mOQKqav8PdSM130_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." NP45145.RAq4lDbzZJMGVOoyZdahapArXofV2yw-7mOQKqav8PdSM130_provenance.
- NP45148.RAkovs0vRQ4CeLlqJgiY3PiyxpV5dPdvpRy33AUU-ZL6U130_assertion description "[We prospectively investigated the outcome of personalized second-line treatment based on epidermal growth factor receptor (EGFR) gene status in previously treated patients with advanced non-small cell lung cancer (NSCLC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45148.RAkovs0vRQ4CeLlqJgiY3PiyxpV5dPdvpRy33AUU-ZL6U130_provenance.
- NP45165.RAg1eAzNmOh4-TzZlH97FgeHPeZN2uQSmJEoJeTrxIEME130_assertion description "[EGFR mutations and human papillomavirus in squamous cell carcinoma of tongue and tonsil.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45165.RAg1eAzNmOh4-TzZlH97FgeHPeZN2uQSmJEoJeTrxIEME130_provenance.
- NP45171.RAi_l7uZt0IcBW4Mb-CK_zvGbGp8gIDYtD6g22E7GnH7M130_assertion description "[Recently, an objective response rate of 12% was reported in a phase II study of cetuximab in patients with epidermal growth factor receptor (EGFR)-expressing metastatic colorectal cancer (mCRC) refractory to fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy (IMC-0144).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45171.RAi_l7uZt0IcBW4Mb-CK_zvGbGp8gIDYtD6g22E7GnH7M130_provenance.
- NP45174.RAh1O-5XSun-1xRMMofbo0QogBJ8wHnRrNODZGVAhKsd4130_assertion description "[A larger, multicenter study may help clarify these results and is also required to replicate our preliminary finding of an association between ADPKD and the EGFR polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45174.RAh1O-5XSun-1xRMMofbo0QogBJ8wHnRrNODZGVAhKsd4130_provenance.
- NP45176.RAl0eWATwwYCBGpXpR71X8HhfhMOhoDbpYgKRUXUtIK5o130_assertion description "[Modification of breast cancer risk in young women by a polymorphic sequence in the egfr gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45176.RAl0eWATwwYCBGpXpR71X8HhfhMOhoDbpYgKRUXUtIK5o130_provenance.
- NP45177.RAhVIGNMeG0_-U4vipLo_S-DKUmfIdkiMTQgQQZqBJ0-A130_assertion description "[On the other hand, the data demonstrate clearly for the first time an interaction between the length of a polymorphism in intron 1 of egfr as an inherited genetic factor and the frequency of egfr amplification, as an acquired genetic factor, both factors contributing to EGFR overexpression in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45177.RAhVIGNMeG0_-U4vipLo_S-DKUmfIdkiMTQgQQZqBJ0-A130_provenance.
- NP45181.RAqSFzTGkKQcD6Q2vMwCmRcgT0Cl25fSYZ287eZQiVA9M130_assertion description "[Genetic polymorphisms in the EGFR (R521K) and estrogen receptor (T594T) genes, EGFR and ErbB-2 protein expression, and breast cancer risk in Tunisia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45181.RAqSFzTGkKQcD6Q2vMwCmRcgT0Cl25fSYZ287eZQiVA9M130_provenance.
- NP45184.RAuxjO3l-uTmaUOBep9-p1NFdRQsigyLDDTnAO2YaY7dg130_assertion description "[Epidermal growth factor receptor and vascular endothelial growth factor receptor 2 are specific biomarkers in triple-negative breast cancer. Results from a controlled randomized trial with long-term follow-up.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45184.RAuxjO3l-uTmaUOBep9-p1NFdRQsigyLDDTnAO2YaY7dg130_provenance.
- NP45185.RAlwvretp_wBYSA_Bw3e19ft_HVNvFiG3Zf502tDHdLxs130_assertion description "[A polymorphic AC repeat in intron 1 of the EGFR gene was genotyped on 352 healthy individuals and 118 women with breast cancer sampled from the Kuwaiti and Tunisian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45185.RAlwvretp_wBYSA_Bw3e19ft_HVNvFiG3Zf502tDHdLxs130_provenance.
- NP45187.RAlPlcbLq7w8E-SMO5lScI3L0m0xH77oVLbw8ZmxywXeQ130_assertion description "[These results indicate that the molecular targeting therapy to EGFR may be a treatment for oral cavity cancer in the betel quid-chewing prevalent area.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45187.RAlPlcbLq7w8E-SMO5lScI3L0m0xH77oVLbw8ZmxywXeQ130_provenance.
- NP45188.RAu4aKlad7ZmyCLiQQby3P-_EHiJTTLBsgMv8caIYXaZk130_assertion description "[These results indicate that the molecular targeting therapy to EGFR may be a treatment for oral cavity cancer in the betel quid-chewing prevalent area.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45188.RAu4aKlad7ZmyCLiQQby3P-_EHiJTTLBsgMv8caIYXaZk130_provenance.
- NP45200.RAmLkYf4KNKi-DRxpi0lcFu4gsWnbjuzSdiad48hltUHA130_assertion description "[Migraine and epilepsy has been suggested to share disease mechanisms and therefore EFHC1 is an excellent candidate gene for migraine in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45200.RAmLkYf4KNKi-DRxpi0lcFu4gsWnbjuzSdiad48hltUHA130_provenance.
- NP45208.RAqanGPSOTrMYq_-tBIISE3cvT6EMx8k8pTNhd9Gz1oD4130_assertion description "[To further investigate the involvement of other genes, mutation analysis of the endothelin-B receptor (EDNRB) gene was performed in 52 unrelated sporadic HSCR patients, including 38 non-syndromic and 14 patients with HSCR and Down's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45208.RAqanGPSOTrMYq_-tBIISE3cvT6EMx8k8pTNhd9Gz1oD4130_provenance.
- NP45210.RApHfJNbN7mePqTVn5nkyI0795Kx1-J1ktaD7OK_clcdI130_assertion description "[A polymorphism in the endothelin-A receptor gene predicts survival in patients with idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45210.RApHfJNbN7mePqTVn5nkyI0795Kx1-J1ktaD7OK_clcdI130_provenance.
- NP45218.RAvsY1Vb-hwkQ9nB68Kpq7UhlGoGPo6AJPKtMIPxHlFB4130_assertion description "[Association of variants in angiotensin-converting enzyme and endothelin-1 genes with phototherapy in cutaneous T-cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45218.RAvsY1Vb-hwkQ9nB68Kpq7UhlGoGPo6AJPKtMIPxHlFB4130_provenance.
- NP45221.RAtr6gO8yForlLid2rQzPr3iCNaUIHhxwsXKY3oSL0oxM130_assertion description "[Molecular genetics of microvascular disease in diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45221.RAtr6gO8yForlLid2rQzPr3iCNaUIHhxwsXKY3oSL0oxM130_provenance.
- NP45222.RAha14QQM6VyveN680xCL3-Xt9ByEDk5z8CHOW_04_OKM130_assertion description "[Although a functional relevance of the EDN1 G-N haplotype itself remains unclear, the data demonstrate that genetic variation at the EDN1 locus has a significant effect on glomerular filtration but not on UAE in the general]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45222.RAha14QQM6VyveN680xCL3-Xt9ByEDk5z8CHOW_04_OKM130_provenance.
- NP45225.RAlzX-FSKymjNWNaCtYoOXlCl8z7R7VL1_ptUfw9TuJA8130_assertion description "[Higher AP level corresponding to 3-rd degree AH in the group of patients with burdened familial anamnesis was associated with carriage of Asn allele of polymorphic marker Lysl98Asn of EDN1 gene (OR 2.24 95% CI 1.20-4.18, p=0.008), 4a allele of polymorphic marker 4a/4b of NOS3 gene (OR 2.23 C/1.29-3.83, p=0.002), genotype ArgArg of polymorphic marker Glnl92Arg of PON1 gene (OR 6.14 C71.46-25.67, p=0.01), T allele of polymorphic marker of C825T gene GNB3 (OR 1.75 C/1.11-2.76, p=0.01) and genotype AA of polymorphic marker A(A153)G of AT2R1 gene (OR 2.61 C/11.29-5.34, p=0.005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45225.RAlzX-FSKymjNWNaCtYoOXlCl8z7R7VL1_ptUfw9TuJA8130_provenance.
- NP45230.RAokFZuRvsua8tapw55pNfY_0eLy1OJ0WFnql5h9TP8Xw130_assertion description "[ Individuals with a genetic predisposition for exaggerated vasoconstriction who also display low AM skills may be at particular risk for development of stress-induced EH. Such individuals may particularly benefit from anger management training.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45230.RAokFZuRvsua8tapw55pNfY_0eLy1OJ0WFnql5h9TP8Xw130_provenance.
- NP45231.RAiHAOEy8X317_AFnkRFzahl0abTYfSVDy-vcJIGvDogg130_assertion description "[ Our results suggest that genetic variation in the ETA receptor predicts survival in dilated cardiomyopathy patients, which might have important consequences for the identification of high-risk individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45231.RAiHAOEy8X317_AFnkRFzahl0abTYfSVDy-vcJIGvDogg130_provenance.
- NP45241.RApyeL5GGONMIakalCfZuyvnK5NAmZ3rpBJOthSypsTak130_assertion description "[Dystrobrevin binding protein 1 (DTNBP1) has been identified as putative schizophrenia susceptibility gene, but it remains unknown whether polymorphisms relate to altered cerebral structure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45241.RApyeL5GGONMIakalCfZuyvnK5NAmZ3rpBJOthSypsTak130_provenance.
- NP45244.RAj5Fy0xZt2kG1bUf3QUtp7XOEc4KdjVOxbBK9h2DiAMk130_assertion description "[Association analysis of the stratified sample showed a trend toward association of PIP4K2A SNPs rs1417374 and rs1409395 with schizophrenia in the DTNBP1 HRH positive families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45244.RAj5Fy0xZt2kG1bUf3QUtp7XOEc4KdjVOxbBK9h2DiAMk130_provenance.
- NP45246.RApqww6ow8L_Vdzy1ceOK80wFduUOhqsfnfPZKfeuAZbo130_assertion description "[Genetic variation in dysbindin 1 (DTNBP1) gene region tagged by SNP rs1018381 exhibits a linkage with cognitive deficits in patients with schizophrenia and healthy subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45246.RApqww6ow8L_Vdzy1ceOK80wFduUOhqsfnfPZKfeuAZbo130_provenance.
- NP45248.RAlMw5fYQEdiPoqgEpfDVBb-9ZCtoK2TMLibVMcG23VdY130_assertion description "[Several studies of the dystrobrevin-binding protein 1 gene (DTNBP1), neuregulin 1 (NRG1), D-amino-acid oxidase (DAO), DAO activator (DAOA, G72), and metabotropic glutamate receptor 3 (GRM3) genes have suggested an association between variants of these genes and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45248.RAlMw5fYQEdiPoqgEpfDVBb-9ZCtoK2TMLibVMcG23VdY130_provenance.
- NP45249.RAp8uhHoSrNvmO7ovfixR4fF6A-3J2q0mcAObLzt3rL0E130_assertion description "[We found a new schizophrenia risk and protective haplotypes in intron VII of DTNBP1; one of the most important candidate genes for this disorder, to-date.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45249.RAp8uhHoSrNvmO7ovfixR4fF6A-3J2q0mcAObLzt3rL0E130_provenance.
- NP45252.RAm6UDFHcwTE93kG55aC8reTnZ-eA9gXmW7DQmLnFGQjU130_assertion description "[Findings suggest that the human dysbindin gene may play a role in the susceptibility to bipolar affective disorder, which underscores a potentially important area of etiological overlap with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45252.RAm6UDFHcwTE93kG55aC8reTnZ-eA9gXmW7DQmLnFGQjU130_provenance.
- NP45262.RAkwefmX8ld6JRQ2_l1SJ6WedSD2Qqw2oQtFVXlOcA034130_assertion description "[Analysis of the CAG repeats in the SCA1 and B37 genes in schizophrenic and bipolar I disorder patients: tentative association between B37 and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45262.RAkwefmX8ld6JRQ2_l1SJ6WedSD2Qqw2oQtFVXlOcA034130_provenance.
- NP45264.RAnwVFt9M7JusAhP9dgraHgbXYEeUEIySzBCv4nWU22SA130_assertion description "[Our results suggest that the *2236C allele in the 3'UTR of the DRP-2 gene, or an unknown mutation in linkage disequilibrium with this allele, may reduce the susceptibility to schizophrenia, especially the paranoid subtype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45264.RAnwVFt9M7JusAhP9dgraHgbXYEeUEIySzBCv4nWU22SA130_provenance.
- NP45265.RApFaLmn87_GtTYZgyB0tX6oYRVOZc_eCJytia3pxWUx4130_assertion description "[The human dihydropyrimidinase-related protein 2 (DRP-2) gene on chromosome 8p21 is associated with paranoid-type schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45265.RApFaLmn87_GtTYZgyB0tX6oYRVOZc_eCJytia3pxWUx4130_provenance.
- NP45267.RAvNo_dePh-sL8xQreYs4BLYc9dy5I7WN5_CMc4klz1UE130_assertion description "[All candidate gene approaches continue to face the problem of relatively low power, given modest odds ratios for even the best replicated genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45267.RAvNo_dePh-sL8xQreYs4BLYc9dy5I7WN5_CMc4klz1UE130_provenance.
- NP45269.RAkSahH9LvGkobnxVnA5oL4KI3IT1mww1GvwmYBKWiaCk130_assertion description "[The DRD4 7-repeat (OR=1.34, 95% CI 1.23-1.45, P= 2 x 10(-12)) and 5-repeat (OR=1.68, 95% CI 1.17-2.41, P=0.005) alleles as well as the DRD5 148-bp allele (OR=1.34, 95% CI 1.21-1.49, P= 8 x 10(-8)) confer increased risk of ADHD, whereas the DRD4 4-repeat (OR=0.90, 95% CI 0.84-0.97, P=0.004) and DRD5 136-bp (OR=0.57, 95% CI 0.34-0.96, P=0.022) alleles have protective effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45269.RAkSahH9LvGkobnxVnA5oL4KI3IT1mww1GvwmYBKWiaCk130_provenance.
- NP45276.RAvN__tVO9k9bNi8iPXwzVXu1GC9ltfZixUbxhzeq-YLg130_assertion description "[These data suggest that the SNPs in DRD2 and AKT1 may influence the treatment response to risperidone in schizophrenia patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45276.RAvN__tVO9k9bNi8iPXwzVXu1GC9ltfZixUbxhzeq-YLg130_provenance.
- NP45279.RAoX9Xp-3q6CsVMUETIyawbSFNcQIyTw2NBkrWqzzxhgs130_assertion description "[Results of chi-square statistical analyses indicated that the allele distribution for migraine cases compared to controls was not significantly different for any of the three tested gene markers (chi2 = 0.1, P =.74 for DRD1; chi2 = 1.8, P =.18 for DRD3; and chi2 = 20.3, P =.08 for DRD5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45279.RAoX9Xp-3q6CsVMUETIyawbSFNcQIyTw2NBkrWqzzxhgs130_provenance.
- NP45290.RAgiOBWZUkxos4JsmLCxu4CRKWnsej-49VgD72m69wJPg130_assertion description "[To investigate the association of the 48 bp variable number tandem repeat (VNTR) polymorphism in the dopamine D4 receptor (DRD4) gene exon III with schizophrenia in Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45290.RAgiOBWZUkxos4JsmLCxu4CRKWnsej-49VgD72m69wJPg130_provenance.
- NP45291.RAv2DLz0d3VzIxw5kvCSoKDnaF6VxuhD7pDEho4QI3y0M130_assertion description "[Although the association is weak and should be considered tentative until other studies replicate it, this polymorphism provides a tool with the potential to examine whether DRD4 is related to susceptibility to and neuroleptic response in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45291.RAv2DLz0d3VzIxw5kvCSoKDnaF6VxuhD7pDEho4QI3y0M130_provenance.
- NP45293.RAoMMcLWTShPB6kFx-0qlsddk4d0sPMnNhYaFsyIPa0RU130_assertion description "[An association between a microsatellite polymorphism at the DRD5 gene and the liability to substance abuse: pilot study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45293.RAoMMcLWTShPB6kFx-0qlsddk4d0sPMnNhYaFsyIPa0RU130_provenance.
- NP45296.RAnLdBdOz8GV3Hu8AuZM6B9nZ9pz6rM0nv-3qr1tTT-bI130_assertion description "[ The allele frequency estimates for DRD4 provided here will contribute towards developing an informative database for this functionally relevant locus. This will prove useful when studying the association between genetic factors and pathogenesis of disease in Indian populations and will address the concern of biased results of association due to population admixtures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45296.RAnLdBdOz8GV3Hu8AuZM6B9nZ9pz6rM0nv-3qr1tTT-bI130_provenance.
- NP45302.RAqOXEO440agUBUNB46GP7AyLamLuJTzAfKTGx_kYvJRA130_assertion description "[In this study, we used a family-based association approach to investigate the implication of dopamine-related candidate genes, which had been previously reported as possibly associated with TS genes that encode for the dopamine receptors DRD2, DRD3 and DRD4, the dopamine transporter 1 (SLC6A3) and the monoamine oxidase-A (MAO-A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45302.RAqOXEO440agUBUNB46GP7AyLamLuJTzAfKTGx_kYvJRA130_provenance.
- NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_assertion description "[ The results suggests that the studied gene variants of type D2 dopamine receptors are not promising candidate genes for bipolar affective illness. We did not consider the family history of the examined subjects, and also the control group was not psychiatrically screened, which may contribute to the lack of significant results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_provenance.
- NP45313.RAg3m-66gIgdjnWGpbeoK2yScs4Adsk7knE9wv81CJL-I130_assertion description "[Results suggested that DRD4 L participants demonstrated significantly higher craving after consumption of alcohol as compared with the control beverage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45313.RAg3m-66gIgdjnWGpbeoK2yScs4Adsk7knE9wv81CJL-I130_provenance.
- NP45315.RAp0_v9gF75rBZuV6Qsqifwu1AIPshtHOiXpi8TCM-Yq8130_assertion description "[These findings extend previous work highlighting the significance of personality traits as a mediating factor between genetic susceptibility and substance use during the period of early experimental use.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45315.RAp0_v9gF75rBZuV6Qsqifwu1AIPshtHOiXpi8TCM-Yq8130_provenance.
- NP45317.RAjawqoLjvIox70-3mYTPSP2AgM2Qr_e3cZIV0E9S5O-A130_assertion description "[Trends were observed for interactions between the DRD4 gene and, among males, the MAOA gene and ADHD symptoms to predict smoking risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45317.RAjawqoLjvIox70-3mYTPSP2AgM2Qr_e3cZIV0E9S5O-A130_provenance.
- NP45318.RAmUZZcpedfw7H0mKCgKzZNJUoV2dhNIiOv-kh4rMJATw130_assertion description "[Interactions between prenatal exposure to smoking and variations in the DAT1 and DRD4 loci were observed in children with either the DSM-IV or population-defined ADHD combined subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45318.RAmUZZcpedfw7H0mKCgKzZNJUoV2dhNIiOv-kh4rMJATw130_provenance.
- NP45320.RAk_dHRAwKfxeVTVMMR5vnU3Yf3JAprm9Ae_9ki2q54GY130_assertion description "[The DRD4 7-repeat (OR=1.34, 95% CI 1.23-1.45, P= 2 x 10(-12)) and 5-repeat (OR=1.68, 95% CI 1.17-2.41, P=0.005) alleles as well as the DRD5 148-bp allele (OR=1.34, 95% CI 1.21-1.49, P= 8 x 10(-8)) confer increased risk of ADHD, whereas the DRD4 4-repeat (OR=0.90, 95% CI 0.84-0.97, P=0.004) and DRD5 136-bp (OR=0.57, 95% CI 0.34-0.96, P=0.022) alleles have protective effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45320.RAk_dHRAwKfxeVTVMMR5vnU3Yf3JAprm9Ae_9ki2q54GY130_provenance.
- NP45321.RArMgnuBXQpzUQrLucB3D-1Rk5MwGhMWFW9QfXoBwcHQ0130_assertion description "[On the other hand, DRD4 (OR = 1.26, p = 0.01) and DRD5 (OR = 1.4, p = 0.01) are significantly associated to ADHD according to the present meta-analysis, confirming previous ones.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45321.RArMgnuBXQpzUQrLucB3D-1Rk5MwGhMWFW9QfXoBwcHQ0130_provenance.
- NP45322.RAiGP0wKygySE0x-iBuni8o0bKcjhH5vBG2g12bq7TQJQ130_assertion description "[We present replicated evidence that polymorphisms in the DRD4 and DAT1 genes were associated with variation in intellectual functioning among children diagnosed as having ADHD, apart from severity of their symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45322.RAiGP0wKygySE0x-iBuni8o0bKcjhH5vBG2g12bq7TQJQ130_provenance.
- NP45330.RAojoMhqdCtQTrp_07ejXwsYnXz8hdIIcQp-fw0QhN-T4130_assertion description "[As part of our ongoing studies on the association between alcoholism and dopaminergic genes, we report herein a mutation analysis of the 14-3-3 eta chain gene (YWHAH) and an association study between alcoholism and the YWHAH and dopamine D4 receptor gene (DRD4) polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45330.RAojoMhqdCtQTrp_07ejXwsYnXz8hdIIcQp-fw0QhN-T4130_provenance.
- NP45346.RAqpIhYnLNZDcvknS4kuzHdEkb5kbLkntV_JRrs6l907I130_assertion description "[Association between different psychotic disorders and the DRD4 polymorphism, but no differences in the main ligand binding region of the DRD4 receptor protein compared to controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45346.RAqpIhYnLNZDcvknS4kuzHdEkb5kbLkntV_JRrs6l907I130_provenance.
- NP45357.RAv_6SFZcLGj6-dveeOZ6dTAMYWgfjW-_9GOkqdkc0FaE130_assertion description "[The Mantel-Haenszel pooled OR for SCZ among carriers of the DRD3 Ser9Gly homozygosity (Ser/Ser homozygotes and Gly/Gly homozygotes) of the nine Japanese studies was 1.16 (95% CI 0.97-1.39), pointing to a non-significant effect of the DRD3 Ser9Gly homozygosity as a risk factor for SCZ.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45357.RAv_6SFZcLGj6-dveeOZ6dTAMYWgfjW-_9GOkqdkc0FaE130_provenance.
- NP45359.RAokG66xdZ_ZcqLdRbhyv5s-lF-iLPVNwzUjOZ8Lmf8qs130_assertion description "[This study investigated whether single-nucleotide polymorphisms in the genes of dopamine receptors DRD1, DRD2, DRD3 and DRD4 are associated with antipsychotics-induced RLS in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45359.RAokG66xdZ_ZcqLdRbhyv5s-lF-iLPVNwzUjOZ8Lmf8qs130_provenance.
- NP45361.RApQF7nMWTuXo5htL4kmtPTPn9nJUwKb4qvf7tJT7Znt0130_assertion description "[Habit learning and the genetics of the dopamine D3 receptor: evidence from patients with schizophrenia and healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45361.RApQF7nMWTuXo5htL4kmtPTPn9nJUwKb4qvf7tJT7Znt0130_provenance.
- NP45370.RAvwhCYLs4-JP4Z8odjiJf7QWE83THnUacgcC504Atuj4130_assertion description "[Tardive dyskinesia is a chronic adverse effect of anti psychotic drugs, where association with a polymorphic site in the dopamine D3 receptor gene has been previously reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45370.RAvwhCYLs4-JP4Z8odjiJf7QWE83THnUacgcC504Atuj4130_provenance.
- NP45372.RAgyETdLdFgIC-Y2sxQJ8fe4vKfxpCHNjQx1ZVJ-VU6iU130_assertion description "[These findings support a small but significant contribution of the HT2CR and DRD3 to susceptibility to TD, which is additive in nature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45372.RAgyETdLdFgIC-Y2sxQJ8fe4vKfxpCHNjQx1ZVJ-VU6iU130_provenance.
- NP45379.RAun6Fonrei2eoUijEuyfj7CtbjfmhoOh7uTVTIoDYTEM130_assertion description "[Possible association between the dopamine D3 receptor gene and bipolar affective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45379.RAun6Fonrei2eoUijEuyfj7CtbjfmhoOh7uTVTIoDYTEM130_provenance.
- NP45382.RAq3qfLcJLkrkFSrk0s4T3yhGG83VHG3ZhVca_WCAVpsE130_assertion description "[Our results demonstrate that a varying sex distribution in the samples investigated might contribute to the heterogeneous results reported in association studies for candidate genes in alcoholism and, therefore, should be taken into account in future studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45382.RAq3qfLcJLkrkFSrk0s4T3yhGG83VHG3ZhVca_WCAVpsE130_provenance.
- NP45388.RAtxunGitRixdEKGRtpFuBny0vUMJ2vPHQPW4faRSCNvI130_assertion description "[Association study of dopamine D2, D3 receptor gene polymorphisms with motor fluctuations in PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45388.RAtxunGitRixdEKGRtpFuBny0vUMJ2vPHQPW4faRSCNvI130_provenance.
- NP45390.RAloQM1aTR0BJZJkYj_Ltasspl5khyT0QIJ1oikVEJZLE130_assertion description "[Pharmacogenetics of parkinsonism, rigidity, rest tremor, and bradykinesia in African-Caribbean inpatients: differences in association with dopamine and serotonin receptors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45390.RAloQM1aTR0BJZJkYj_Ltasspl5khyT0QIJ1oikVEJZLE130_provenance.
- NP45393.RAl5BL-mTY_uoat0V9R1VLTYp2homTvcqW8kb5qoDdoWU130_assertion description "[DRD3 Ser9Gly and HS1BP3 Ala265Gly are not associated with Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45393.RAl5BL-mTY_uoat0V9R1VLTYp2homTvcqW8kb5qoDdoWU130_provenance.
- NP45396.RAg8RQEwKrKuE0egI9Jn5cQfciV7r4yorZtUmaSzv95zQ130_assertion description "[An association was found between the presence of psychotic symptoms and aggressive behaviour and the DRD1 polymorphism and between the presence of psychosis, but not aggression, and the DRD3 polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45396.RAg8RQEwKrKuE0egI9Jn5cQfciV7r4yorZtUmaSzv95zQ130_provenance.
- NP45397.RApGbX8rRj8ZWOKvoFU5T8dYJW2JGBSpJrqT28uk5yMZI130_assertion description "[Our results suggest that genetic polymorphisms of DRD4 and DRD3 may well be associated with personality traits, and that conflicting findings to date may arise from the problem of phenotype definition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45397.RApGbX8rRj8ZWOKvoFU5T8dYJW2JGBSpJrqT28uk5yMZI130_provenance.
- NP45404.RAuMtxiD6DbhaMnRO_xbmXNoORswt-DByC8MKr00-0Xyo130_assertion description "[Although no DRD2 polymorphisms were associated with the risk of alcoholism, +32806C>T and Block2-ht1 showed associations (in dominant models) with both the state anxiety level scale (STAI-S) and the trait anxiety level scale (STAI-T) (P=0.004 and P=0.003, and P=0.01 and P=0.005, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45404.RAuMtxiD6DbhaMnRO_xbmXNoORswt-DByC8MKr00-0Xyo130_provenance.
- NP45411.RAoqL37mzLzIEzl0HeaT7NLgiotfK7QZtTLRCTxn57CzU130_assertion description "[These deficits were related to SNPs from 16 genes, several previously associated with schizophrenia risk and/or involved in normal central nervous system development, including AKT, PI3K, SLC6A4, DRD2, CHRM2, and ADORA2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45411.RAoqL37mzLzIEzl0HeaT7NLgiotfK7QZtTLRCTxn57CzU130_provenance.
- NP45415.RAnOP9GoaQofXxax71wF-lE-O6zvzkXkQrubDQMDYcBm8130_assertion description "[Because of the essential role dopamine D2 receptor (DRD2) in dopamine signaling, DRD2 gene has been regarded as one of the top candidate genes for SZ.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45415.RAnOP9GoaQofXxax71wF-lE-O6zvzkXkQrubDQMDYcBm8130_provenance.
- NP45420.RAluWP4qRGAzD2wm2B6VHKkrdLXBBiaEyCzXXCEYiOgOk130_assertion description "[Functional variants of the dopamine receptor D2 gene modulate prefronto-striatal phenotypes in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45420.RAluWP4qRGAzD2wm2B6VHKkrdLXBBiaEyCzXXCEYiOgOk130_provenance.
- NP45421.RAmSGNOWqGEjrfSinowyxjai97GrE_hTXIpTi4SRYInb8130_assertion description "[Candidate genes for alcohol dependence: a review of genetic evidence from human studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45421.RAmSGNOWqGEjrfSinowyxjai97GrE_hTXIpTi4SRYInb8130_provenance.
- NP45453.RAr8tHV2tSp-G2BadLaVdCoe0ZJPCbbwDUYUj1ubPiMqY130_assertion description "[We tested for gender-specific interactions between smoking and genetic polymorphisms of monoamine oxidase B (MAO-B) intron 13 (G or A allele), monoamine oxidase A (MAO-A) EcoRV (Yor N allele), and dopamine D2 recepor (DRD2) Taq1B (B1 or B2 allele) in a case-control study of 186 incident idiopathic Parkinson's disease (PD) cases and 296 age- and gender-matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45453.RAr8tHV2tSp-G2BadLaVdCoe0ZJPCbbwDUYUj1ubPiMqY130_provenance.
- NP45456.RAkPQ9XU6W5sjZ8U7huXVyOyy6Y5SBIdMpn69wG5Kp1KA130_assertion description "[Association of DRD3 and GRIN2B with impulse control and related behaviors in Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45456.RAkPQ9XU6W5sjZ8U7huXVyOyy6Y5SBIdMpn69wG5Kp1KA130_provenance.
- NP45457.RAp4CO4VltxtnMCjp1rBcFXkNUvR185CLqiJVgb00SQcA130_assertion description "[In this study, we used a family-based association approach to investigate the implication of dopamine-related candidate genes, which had been previously reported as possibly associated with TS genes that encode for the dopamine receptors DRD2, DRD3 and DRD4, the dopamine transporter 1 (SLC6A3) and the monoamine oxidase-A (MAO-A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45457.RAp4CO4VltxtnMCjp1rBcFXkNUvR185CLqiJVgb00SQcA130_provenance.
- NP45458.RAl3BbDEjgXhGvsgSSAKxaXoMNrWFV0opfAqz5Sg7mvjY130_assertion description "[Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45458.RAl3BbDEjgXhGvsgSSAKxaXoMNrWFV0opfAqz5Sg7mvjY130_provenance.
- NP45464.RAiOfIlcLeKXtY_fGkoaNqt5lzI7x4k-JNWlBEcgW2Z-g130_assertion description "[Therefore, the authors examined the association between the TaqI A polymorphism of the dopamine D(2) receptor gene (DRD(2)), which alters DRD(2) density and function, and the development of neuroleptic malignant syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45464.RAiOfIlcLeKXtY_fGkoaNqt5lzI7x4k-JNWlBEcgW2Z-g130_provenance.
- NP45471.RAjxcNRwbnZx3uqamZeKcqzlPjctemH-rZa-iGI7CKXcc130_assertion description "[Association of dopamine D2 receptor polymorphisms Ser311Cys and TaqIA with obesity or type 2 diabetes mellitus in Pima Indians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45471.RAjxcNRwbnZx3uqamZeKcqzlPjctemH-rZa-iGI7CKXcc130_provenance.
- NP45473.RApCsaF5QyKs-bB92MHNmWlJEv95lko97ZJrBRxoh9uvc130_assertion description "[This study provides support for an association between ADHD and polymorphisms in both NET1 and DRD1; polymorphisms in ten other candidate genes were not associated with ADHD. Because family-based and case-control methods gave divergent results, both should be used in genetic studies of ADHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45473.RApCsaF5QyKs-bB92MHNmWlJEv95lko97ZJrBRxoh9uvc130_provenance.
- NP45475.RAj_k5uuSe8Xk64VEBogM28i31w2-jGI5izkn5c9iP4wI130_assertion description "[Association of the calcyon gene (DRD1IP) with attention deficit/hyperactivity disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45475.RAj_k5uuSe8Xk64VEBogM28i31w2-jGI5izkn5c9iP4wI130_provenance.
- NP45480.RAruzmRNZE4gsPO5y3LYLkp7wVEglPiP3M0CehqPZBo5U130_assertion description "[These genetics data suggest that the analyzed polymorphisms of the dopamine genes may not be associated with RLS symptoms in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45480.RAruzmRNZE4gsPO5y3LYLkp7wVEglPiP3M0CehqPZBo5U130_provenance.
- NP45483.RAjAd7HsUTgMAuUIIa1eyjy-c712oW_pgRArjtwEywQ3A130_assertion description "[We conducted a pharmacogenetic study to evaluate whether variants in dopamine-related genes (DRD1-DRD5, AKT1 and GSK3beta) and serotonin receptor genes (HTR1A, HTR1B, HTR1D, HTR2A, HTR2C, HTR6 and HTR7) can be used to predict the efficacy of risperidone treatment for schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45483.RAjAd7HsUTgMAuUIIa1eyjy-c712oW_pgRArjtwEywQ3A130_provenance.
- NP45484.RAvSdRgu38Aa4mTo1ZGk0wGdXjre1rgAzQrvFLjGi3dFs130_assertion description "[Correlates of response to Olanzapine in a North Indian Schizophrenia sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45484.RAvSdRgu38Aa4mTo1ZGk0wGdXjre1rgAzQrvFLjGi3dFs130_provenance.
- NP45485.RAt8TiB6Yg50NrPEmxDlOqDK7hTVyxKTtBZfZIRh8abMA130_assertion description "[Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45485.RAt8TiB6Yg50NrPEmxDlOqDK7hTVyxKTtBZfZIRh8abMA130_provenance.
- NP45486.RAgbgSEGIPZUNmrwELiKGTHc2Fz9YIeO2IJq5LArNn77M130_assertion description "[Association of polymorphisms in the BDNF, DRD1 and DRD3 genes with tobacco smoking in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45486.RAgbgSEGIPZUNmrwELiKGTHc2Fz9YIeO2IJq5LArNn77M130_provenance.
- NP45489.RAh9bzlhT4eA2zUDeGbSeCTo456CDaxw2wF3Vb8wyC-aU130_assertion description "[An association between the DRD1 gene and bipolar I disorder (BP I) in the Sardinian population is suggested.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45489.RAh9bzlhT4eA2zUDeGbSeCTo456CDaxw2wF3Vb8wyC-aU130_provenance.
- NP45496.RAkehDyHxPHdAqCX9x9iDpxNESsLK04SGtKeSqZxdQ5DE130_assertion description "[Dopamine D1 receptor gene polymorphism is associated with essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45496.RAkehDyHxPHdAqCX9x9iDpxNESsLK04SGtKeSqZxdQ5DE130_provenance.
- NP45506.RAkvxBbV74-1V2N3bIC001JkI5IdNqclMJD0i35iaEhMQ130_assertion description "[Genetic variants in epigenetic genes and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45506.RAkvxBbV74-1V2N3bIC001JkI5IdNqclMJD0i35iaEhMQ130_provenance.
- NP45508.RAo9ERUhCVvZxVjHLUM0uSW3aEiIpvvojZYKouddSfDHM130_assertion description "[No significant associations with the risk of SLE were detected. However, further analyses of association with the risk of renal disorder among SLE patients revealed several positive associations. One promoter SNP (-1066G>C), +2630T>C (Ser145Ser), +6235G>C and one haplotype showed weak associations with the risk of nephritis among SLE patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45508.RAo9ERUhCVvZxVjHLUM0uSW3aEiIpvvojZYKouddSfDHM130_provenance.
- NP45511.RAlRPoF8G-Zs0930kQPY36oVeSpN-FTaDuOgnqY_rgPLw130_assertion description "[Analysis of genetic polymorphism of deoxyribonuclease I in Ovambo and Turk populations using a genotyping method.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45511.RAlRPoF8G-Zs0930kQPY36oVeSpN-FTaDuOgnqY_rgPLw130_provenance.
- NP45513.RAoa159WkPOJcGHhZMLkeZT_U1Xnw7JR7dk9ZTSeRPNM4130_assertion description "[The frequency of the homozygous minor allele (Arg/Arg) was much higher in patients who had the anti-RNP antibody (31.3%) than in patients who did not have this antibody (14.4%) (P=0.0006, OR=2.86). In addition, the A/T mutation in exon 2 of DNASE reported in two Japanese SLE patients was not present in SLE patients (n=350) or controls (n=330) in our Korean population which, combined with the results of previous reports, strongly suggests that the mutation is not present in three major ethnic]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45513.RAoa159WkPOJcGHhZMLkeZT_U1Xnw7JR7dk9ZTSeRPNM4130_provenance.
- NP45514.RAtZUuELNQKEwdipqBOU0jV1kpvLG3nbRfDgWQkDkw9mI130_assertion description "[The association of the Gln244Arg SNP with SLE susceptibility indicates that common polymorphisms in DNASEI play a role in the genetics of SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45514.RAtZUuELNQKEwdipqBOU0jV1kpvLG3nbRfDgWQkDkw9mI130_provenance.
- NP45515.RAhJoSA_8bfbA9pfJhzDKUJGqn06ivLy0hv12mfB8kSoE130_assertion description "[Study of DNASE I gene polymorphisms in systemic lupus erythematosus susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45515.RAhJoSA_8bfbA9pfJhzDKUJGqn06ivLy0hv12mfB8kSoE130_provenance.
- NP45518.RAij81CVwiiJ8B7PHofavA7Lf9KW-zjUOYlpXecwUEJ6g130_assertion description "[The data presented here provide further support for the association between schizophrenia and CAG repeat number polymorphism in SCA1 gene. The significant increase of the mean number of CAG repeats in schizophrenics was found also in the MJD1/SCA3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45518.RAij81CVwiiJ8B7PHofavA7Lf9KW-zjUOYlpXecwUEJ6g130_provenance.
- NP45521.RAtaO6YhznjTpUPR9PIGoEpKL4ssjksAZuM1Tc4IARYUw130_assertion description "[ These results emphazise the importance of screening for MD1 gene carriers among cataract patients, and further genetic counselling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45521.RAtaO6YhznjTpUPR9PIGoEpKL4ssjksAZuM1Tc4IARYUw130_provenance.
- NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_assertion description "[We found no strong evidence of association for any of these loci with AD in this population. While the possibility exists that the genes analysed are involved in AD (ie they have weak effects and/or are population specific), results reinforce the need for extensive replication studies if we are to be successful in defining true risk factors in complex diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_provenance.
- NP45533.RAte3fwKQHkJqUh0AJYw2qOc9MTxRLgUrHoHCGokbaSD0130_assertion description "[Evidence of transmission ratio distortion of DLG5 R30Q variant in general and implication of an association with Crohn disease in men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45533.RAte3fwKQHkJqUh0AJYw2qOc9MTxRLgUrHoHCGokbaSD0130_provenance.
- NP45535.RAoyZ4o1IZ96JOTBnzfQssDGJE-W304s238ORHisxhx_Y130_assertion description "[DLG5 has a gender-specific role in the susceptibility of pediatric CD. Specifically, the significant negative association found between DLG5 R30Q and CD in female children suggests DLG5 may have a protective effect in CD susceptibility for female children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45535.RAoyZ4o1IZ96JOTBnzfQssDGJE-W304s238ORHisxhx_Y130_provenance.