Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP83601.RAqm9gh0cY0-_1waDNugxQY2GGxY0_P0eFSYvZ-JEGVbs130_assertion description "[These results suggest that CACNA1C may be associated with secondary hyperparathyroidism. In addition, the haplotype-based approach may be useful to screen for key molecules associated with complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83601.RAqm9gh0cY0-_1waDNugxQY2GGxY0_P0eFSYvZ-JEGVbs130_provenance.
- NP83605.RAv04YJZFoS9Vfxk0alY8edpbVuR88eRRURoh2tN104ag130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83605.RAv04YJZFoS9Vfxk0alY8edpbVuR88eRRURoh2tN104ag130_provenance.
- NP83615.RAp04zdozKpwN-GGl8j4ZvhA87uuaTOo7lslokqyk6DQo130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83615.RAp04zdozKpwN-GGl8j4ZvhA87uuaTOo7lslokqyk6DQo130_provenance.
- NP83616.RArUZ_934e8nJLpdhp_2-x5gXrpAk_KnsG8Oor0D049fc130_assertion description "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83616.RArUZ_934e8nJLpdhp_2-x5gXrpAk_KnsG8Oor0D049fc130_provenance.
- NP83618.RAlNkdmuOKWmcKTYnaA7r5xbAOq7X71L5CsX4cfXEFznc130_assertion description "[A118G polymorphism of OPRM1 gene is associated with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83618.RAlNkdmuOKWmcKTYnaA7r5xbAOq7X71L5CsX4cfXEFznc130_provenance.
- NP83625.RAtcBBicnHzo9ApdCsTOdVZKLR0BeLPFes_RqcohcdPRw130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83625.RAtcBBicnHzo9ApdCsTOdVZKLR0BeLPFes_RqcohcdPRw130_provenance.
- NP83627.RAu4oN6SFXjaQcF3-XmmOVkx_Qu6eyBXiX1Vs-iCLOTbY130_assertion description "[Despite the small sample size, this novel analysis method identified an sMRI component including brain areas previously reported to be abnormal in schizophrenia and an associated genetic component containing several putative schizophrenia risk genes. Thus, we identified multiple genes potentially underlying specific structural brain abnormalities in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83627.RAu4oN6SFXjaQcF3-XmmOVkx_Qu6eyBXiX1Vs-iCLOTbY130_provenance.
- NP83630.RAmUN0o83WD1TSKe4thh1NvxFD8GSaEP53oob-B7geDB0130_assertion description "[Although there were no significant (P > 0.05) differences in the frequencies of genotypes or alleles of APE1, XRCC1, XPD, XPG, and HOGG1 genes between patients and controls, the frequency of the XRCC3 Thr/Thr genotype was significantly greater in endometriosis patients compared with controls (P = 0.005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83630.RAmUN0o83WD1TSKe4thh1NvxFD8GSaEP53oob-B7geDB0130_provenance.
- NP83631.RAla5t1CDtixorXEd4-_OBErSgwlfUAnSiBt_5l-vfZrc130_assertion description "[The association of polymorphisms in DNA base excision repair genes XRCC1, OGG1 and MUTYH with the risk of childhood acute lymphoblastic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83631.RAla5t1CDtixorXEd4-_OBErSgwlfUAnSiBt_5l-vfZrc130_provenance.
- NP83639.RAj7Z2va9eMaUwULggslbN_Iuv8r3nz2OUpBfRqt3oFDo130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83639.RAj7Z2va9eMaUwULggslbN_Iuv8r3nz2OUpBfRqt3oFDo130_provenance.
- NP83647.RAp8IPCTOjSvBnFSQgStbay0fUDZvFvQwO7wNOTZCa1Mk130_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." NP83647.RAp8IPCTOjSvBnFSQgStbay0fUDZvFvQwO7wNOTZCa1Mk130_provenance.
- NP83654.RAsoK4GzLqMJCDMPxvgps_f3w8-Phg2qnvGJR98XuKL8k130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83654.RAsoK4GzLqMJCDMPxvgps_f3w8-Phg2qnvGJR98XuKL8k130_provenance.
- NP83666.RAtmDwFEppfoy4Ax8lbBFZO08yiVMV7LYgV-DkCdj5gJc130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83666.RAtmDwFEppfoy4Ax8lbBFZO08yiVMV7LYgV-DkCdj5gJc130_provenance.
- NP83670.RAtNzWUqx_z-TwWglP0H7qBYPsbAiA4gyqAY9eh1YbEcQ130_assertion description "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83670.RAtNzWUqx_z-TwWglP0H7qBYPsbAiA4gyqAY9eh1YbEcQ130_provenance.
- NP83671.RAlfoG4PR0iekBsj6UnoNchXAju5wVWIA17f6npixoVVI130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83671.RAlfoG4PR0iekBsj6UnoNchXAju5wVWIA17f6npixoVVI130_provenance.
- NP83680.RAjSiMg2EjB556uvsSwF_kCYVNuKGl7rLgKcHeEucFJAs130_assertion description "[Altogether, ASK1-PEX7 haplotypes and MAP2K2 genotype variations explain 6.3% additional variance in AO for HD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83680.RAjSiMg2EjB556uvsSwF_kCYVNuKGl7rLgKcHeEucFJAs130_provenance.
- NP83683.RAqUDyGW7Yltw1v4oBdIWxzLoChALIUlpCn4g-CRaTlD0130_assertion description "[Use of expression data and the CGEMS genome-wide breast cancer association study to identify genes that may modify risk in BRCA1/2 mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83683.RAqUDyGW7Yltw1v4oBdIWxzLoChALIUlpCn4g-CRaTlD0130_provenance.
- NP83684.RAsbLKuMkTvhgSs4xmgZi68cxjOEgSLeOPmPKOxbPaLF8130_assertion description "[Two putatively functional single nucleotide polymorphisms of choline-metabolizing genes, PEMT -774G>C (rs12325817) and CHDH +432G>T (rs12676), were also found be related to breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83684.RAsbLKuMkTvhgSs4xmgZi68cxjOEgSLeOPmPKOxbPaLF8130_provenance.
- NP83686.RAmAwPjYhj-UFTrnmyy6l98NM9UBGlMzY29LMliwY8bso130_assertion description "[Opioid neuropeptide genotypes in relation to heroin abuse: dopamine tone contributes to reversed mesolimbic proenkephalin expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83686.RAmAwPjYhj-UFTrnmyy6l98NM9UBGlMzY29LMliwY8bso130_provenance.
- NP83688.RAhWs6NvvvMJnsdc40w-WGSl8uvdts8EzlFvMhvgq-GU4130_assertion description "[PDE4D and ALOX5AP genetic variants and risk for Ischemic Cerebrovascular Disease in Sweden.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83688.RAhWs6NvvvMJnsdc40w-WGSl8uvdts8EzlFvMhvgq-GU4130_provenance.
- NP83689.RAo39lLpqWlJTkxu5NbDVdGaVkqPRMgdFt24K_hAPgy8Q130_assertion description "[We conclude that PDCD1 is unlikely to be a major susceptibility gene for T1DM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83689.RAo39lLpqWlJTkxu5NbDVdGaVkqPRMgdFt24K_hAPgy8Q130_provenance.
- NP83690.RAu2uzmIqvX_YJZxjVGfwZ5d90GQStXnqiG-P6DNrtVh4130_assertion description "[NF1 gene and neurofibromatosis 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83690.RAu2uzmIqvX_YJZxjVGfwZ5d90GQStXnqiG-P6DNrtVh4130_provenance.
- NP83691.RAlApAUEYJ280z_2ZBpH54wFybMKonVyKNRFaCUPxKafM130_assertion description "[Aryl hydrocarbon receptor nuclear translocator-like (BMAL1) is associated with susceptibility to hypertension and type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83691.RAlApAUEYJ280z_2ZBpH54wFybMKonVyKNRFaCUPxKafM130_provenance.
- NP83693.RAs717pjcTQcaLwCKz2iEnSmwNtoiO0t88e7jaurHl_bA130_assertion description "[Association of missense variants of the PRKC, apoptosis, WT1, regulator (PAWR) gene with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83693.RAs717pjcTQcaLwCKz2iEnSmwNtoiO0t88e7jaurHl_bA130_provenance.
- NP83694.RAsberSx3H2KhGQ9-KcN4JsQYx7V-NGNp1TePdyr5Z7So130_assertion description "[Parkin polymorphisms in progressive supranuclear palsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83694.RAsberSx3H2KhGQ9-KcN4JsQYx7V-NGNp1TePdyr5Z7So130_provenance.
- NP83696.RAm8pJwvfPzHJe0tTDL11gmNnjU8wMr5OAqQZ7RFhSAKg130_assertion description "[The PAI-1 4G/5G gene polymorphism and ischemic stroke: an association study and meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83696.RAm8pJwvfPzHJe0tTDL11gmNnjU8wMr5OAqQZ7RFhSAKg130_provenance.
- NP83701.RAqFX-9IHYl37Sa-VlL83owcUbj_almhfboNenJmRlgDE130_assertion description "[Single nucleotide polymorphism (SNP) mapping was performed on an 865-kb candidate region (D6S1683-D6S265) in 166 Tasmanian MS families, and seven candidate genes ubiquitin D (UBD), olfactory receptor 2H3 (OR2H3), gamma-aminobutyric acid B receptor 1 (GABBR1), myelin oligodendrocyte glycoprotein (MOG), HLA-F, HLA complex group 4 (HCG4) and HLA-G were resequenced.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83701.RAqFX-9IHYl37Sa-VlL83owcUbj_almhfboNenJmRlgDE130_provenance.
- NP83702.RAvhnT1baTU8taMTMWNz_WNV8Kcv2qD4SWn9-6H-vgUdU130_assertion description "[These findings suggest that genetic variants of the OPRL1 gene play a role in alcohol dependence in the Scandinavian population, warranting further investigation at the OPRL1 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83702.RAvhnT1baTU8taMTMWNz_WNV8Kcv2qD4SWn9-6H-vgUdU130_provenance.
- NP83704.RAs_SoSN-ByYF7tCfLxvIVaJfKZpRF_h0htZS0IhciDKg130_assertion description "[A regulatory variation in OPRK1, the gene encoding the kappa-opioid receptor, is associated with alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83704.RAs_SoSN-ByYF7tCfLxvIVaJfKZpRF_h0htZS0IhciDKg130_provenance.
- NP83719.RAqRQmLXR4_73Q7XOCJU3Yyi65K3eLk6_yIjmWq_CrtRI130_assertion description "[There is a lack of association between the allelic variants studied and the risk of developing allergic asthma and rhinitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83719.RAqRQmLXR4_73Q7XOCJU3Yyi65K3eLk6_yIjmWq_CrtRI130_provenance.
- NP83724.RAqiro4pA7RnsRJnPXoHBfCPP_nVmaXqcLoSCmxBSRjV0130_assertion description "[N-acetyl transferase-2 and bladder cancer risk: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83724.RAqiro4pA7RnsRJnPXoHBfCPP_nVmaXqcLoSCmxBSRjV0130_provenance.
- NP83730.RAuTh5wwjzWq1TE2K3IAQ4f0WaVuw3-BafImaO7J-NMDg130_assertion description "[the performance of the two multiplex mutation assays was superior to direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83730.RAuTh5wwjzWq1TE2K3IAQ4f0WaVuw3-BafImaO7J-NMDg130_provenance.
- NP83732.RAo6IQasp7t_lklfOcyBPA9uwFMgufJ3jPrAhnLZXhiWM130_assertion description "[Activating point mutations of genes of the RAS family (KRAS, HRAS and NRAS genes) are frequently found in carcinomas, but their prevalence in sarcomas varies considerably among ethnic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83732.RAo6IQasp7t_lklfOcyBPA9uwFMgufJ3jPrAhnLZXhiWM130_provenance.
- NP83733.RAk7oijd5JVo4-1l1RvATQvbwV3ZZEP063HI3NUgyceX4130_assertion description "[While confirming the negative effect of KRAS mutations on outcome after cetuximab, we show that BRAF, NRAS, and PIK3CA exon 20 mutations are significantly associated with a low response rate. Objective response rates could be improved by additional genotyping of BRAF, NRAS, and PIK3CA exon 20 mutations in a KRAS wild-type population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83733.RAk7oijd5JVo4-1l1RvATQvbwV3ZZEP063HI3NUgyceX4130_provenance.
- NP83735.RAhaWMJWUS98iKTY2d2-Wy1nrzNMdusu9yRJlgIIeZMiQ130_assertion description "[Our study demonstrates that mutations in each part of the EGFR pathway were associated with different clinicopathologic features in patients with NSCLCs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83735.RAhaWMJWUS98iKTY2d2-Wy1nrzNMdusu9yRJlgIIeZMiQ130_provenance.
- NP83736.RAvRUk2YWu1IPQaGjlyRMUWV3494MEgOj7qoMvfqfDixQ130_assertion description "[We studied a series of 53 CMML samples including 31 cases of myeloproliferative form (MP-CMML) and 22 cases of myelodysplastic forms (MD-CMML) using array-comparative genomic hybridisation (aCGH) and sequencing of 13 candidate genes including ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, PTPN11, RUNX1, TET2 and WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83736.RAvRUk2YWu1IPQaGjlyRMUWV3494MEgOj7qoMvfqfDixQ130_provenance.
- NP83738.RAka0k0eJ5Pnean0sq6FyVq1q0qG0dMGZ7jxcMy2E17uI130_assertion description "[Our results demonstrated the effectiveness and robustness of our CNV-association analysis and provided an alternative avenue for discovering new associated loci of human diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83738.RAka0k0eJ5Pnean0sq6FyVq1q0qG0dMGZ7jxcMy2E17uI130_provenance.
- NP83740.RAqgWLUY7y4gaeDSDQ5F624aNZwG1WxhV1r7ngAYWvP38130_assertion description "[Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83740.RAqgWLUY7y4gaeDSDQ5F624aNZwG1WxhV1r7ngAYWvP38130_provenance.
- NP83743.RAhg7bmsZw-qFXkfXMkD-ovqZ0f6dOvOkLCTLRABUz3qM130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83743.RAhg7bmsZw-qFXkfXMkD-ovqZ0f6dOvOkLCTLRABUz3qM130_provenance.
- NP83752.RAkEp_VtHXT8yumoPqh6wGMRSohS0BN3DjmWZmqdxlwg0130_assertion description "[Although these 6 genes may be involved in the pathogenesis of GC-induced ocular hypertension, it does not appear that major heritable risk alleles in these genes are responsible for the development of GC-induced ocular hypertension or POAG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83752.RAkEp_VtHXT8yumoPqh6wGMRSohS0BN3DjmWZmqdxlwg0130_provenance.
- NP83759.RAiyERbLXhduI2kf303LerG7LKdNA6Wa5_ocJ6H4QWG9w130_assertion description "[We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83759.RAiyERbLXhduI2kf303LerG7LKdNA6Wa5_ocJ6H4QWG9w130_provenance.
- NP83768.RAhPYPP_SBFICkdP-NAgUZ4KkvVLmH7KKRyTb9UX_Y5CI130_assertion description "[Nuclear receptor rev-erb-{alpha} circadian gene variants and lithium carbonate prophylaxis in bipolar affective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83768.RAhPYPP_SBFICkdP-NAgUZ4KkvVLmH7KKRyTb9UX_Y5CI130_provenance.
- NP83769.RApEJSCuYFdckPLa3KARlr1xyAXBuRveXwuLHkTpDOHUg130_assertion description "[Nuclear receptor rev-erb-{alpha} circadian gene variants and lithium carbonate prophylaxis in bipolar affective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83769.RApEJSCuYFdckPLa3KARlr1xyAXBuRveXwuLHkTpDOHUg130_provenance.
- NP83776.RAgw-zUXXY2v1tXDXmULfazo2EbPJH4tntl6VvW-JkHuU130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83776.RAgw-zUXXY2v1tXDXmULfazo2EbPJH4tntl6VvW-JkHuU130_provenance.
- NP83780.RAqeYubbATVshCWohYZFS0_ZTXG54bsstJCCSC3Og6SV8130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83780.RAqeYubbATVshCWohYZFS0_ZTXG54bsstJCCSC3Og6SV8130_provenance.
- NP83802.RAg1FtRfknTHxUTUYq_hNXbtRJpEy5lEnBU-Ipkvsl3kA130_assertion description "[Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83802.RAg1FtRfknTHxUTUYq_hNXbtRJpEy5lEnBU-Ipkvsl3kA130_provenance.
- NP83806.RAgSywT0fa9Y7fS1vmrt9-VqwRuTFrKkpQzaEQD4cCd2Y130_assertion description "[The results demonstrated that genetic variation in KCNJ11, BDNF, PFKP, PTER and SEC16B were associated with SGA and support the concept that genetic factors associated with obesity and/or type 2 diabetes are more prevalent in those born SGA compared to those born AGA. We have previously determined that environmental factors are associated with differences in birthweight in the ABC study and now we have demonstrated a significant genetic contribution, suggesting that the interaction between genetics and the environment are important.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83806.RAgSywT0fa9Y7fS1vmrt9-VqwRuTFrKkpQzaEQD4cCd2Y130_provenance.
- NP83808.RAn7VUdk6pd15LvjshL8RIsbmeZSt0cGtys_xSf-6KrGc130_assertion description "[CNVs in a single subject with TOF occurred at six loci, two that encode known (NOTCH1, JAG1) disease-associated genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83808.RAn7VUdk6pd15LvjshL8RIsbmeZSt0cGtys_xSf-6KrGc130_provenance.
- NP83809.RApbOsFcO05GBaWkR5Wpcagl91rdK3nQx_vKj5IDpZlxE130_assertion description "[We report a novel association between the fetal ADCY5 type 2 diabetes risk allele and decreased birthweight, and confirm in meta-analyses associations between decreased birthweight and the type 2 diabetes risk alleles of HHEX-IDE and CDKAL1. No strong general effect on birthweight can be ascribed to the 25 common type 2 diabetes risk alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83809.RApbOsFcO05GBaWkR5Wpcagl91rdK3nQx_vKj5IDpZlxE130_provenance.
- NP83815.RAlHl6cMR6c0dWkI6E_G3-9BDYgbRldDEJZjn5N5RCtuo130_assertion description "[Our results do not show any influence of the two polymorphisms, VNTR in intron 4 and Glu298Asp of the eNOS gene, on early pregnancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83815.RAlHl6cMR6c0dWkI6E_G3-9BDYgbRldDEJZjn5N5RCtuo130_provenance.
- NP83817.RAqGvMgLWqt8WZaGyBcn58xEt2S_AVduId88Z9iv26OEs130_assertion description "[Several laboratories, including ours, have shown that variants in NOS3 (the gene encoding eNOS) are overrepresented in individuals with altitude-related illnesses such as high altitude pulmonary edema (HAPE) and acute mountain sickness (AMS), suggesting that NOS3 genotypes contribute to altitude tolerance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83817.RAqGvMgLWqt8WZaGyBcn58xEt2S_AVduId88Z9iv26OEs130_provenance.
- NP83819.RAn_QJIgwunmph9Zchfl2pfjs96vug1i_4uYxAp57XSVk130_assertion description "[The results from this exploratory case-control study show the lack of an association between MTHFR, factor II G20210A, factor V G1691A, NOS3, intron 4 VNTR, and APOE epsilon4 gene polymorphisms and the development of spontaneous cervical artery dissection. Our findings contribute towards a better understanding of the genetic risk factors associated with spontaneous cervical artery dissection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83819.RAn_QJIgwunmph9Zchfl2pfjs96vug1i_4uYxAp57XSVk130_provenance.
- NP83828.RAoLzMd2dDxw3CgQSZBLs_svipfI7U9Tee7M2mQ9ZxXpY130_assertion description "[The role of polymorphic variants of gene of inducible NO-synthase NOS2 in brain infarction in patients with acute ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83828.RAoLzMd2dDxw3CgQSZBLs_svipfI7U9Tee7M2mQ9ZxXpY130_provenance.
- NP83833.RAmYqVcYbRTMdARNjZgggIGEb1u9_N_C6CHz2A9N0Nk4U130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83833.RAmYqVcYbRTMdARNjZgggIGEb1u9_N_C6CHz2A9N0Nk4U130_provenance.
- NP83841.RAqhQhfw1KzAEBBpYmG_SZm2HG3qCdOhwmel30S9IWj2Q130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83841.RAqhQhfw1KzAEBBpYmG_SZm2HG3qCdOhwmel30S9IWj2Q130_provenance.
- NP83844.RAjXNuj3tAFrM2SBaWiHzvvgT1xrkggnKh_ZOaHecsXUg130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83844.RAjXNuj3tAFrM2SBaWiHzvvgT1xrkggnKh_ZOaHecsXUg130_provenance.
- NP83846.RAjAdXKKDxvtbIjei8AJOEyMKtHccYbCG15auhHJV0kuY130_assertion description "[Common single nucleotide polymorphisms in immunoregulatory genes and multiple myeloma risk among women in Connecticut.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83846.RAjAdXKKDxvtbIjei8AJOEyMKtHccYbCG15auhHJV0kuY130_provenance.
- NP83848.RAo72JWA1qzhz14tyor3s1e5SNQOfC1VWP48naLUTBzm8130_assertion description "[The results of the present study do not provide evidence for the association between the NFKBIL1 exon 4 polymorphism and MS predisposition in the investigated Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83848.RAo72JWA1qzhz14tyor3s1e5SNQOfC1VWP48naLUTBzm8130_provenance.
- NP83857.RAsvmUO4Gl6ldaYPFORKMKFyODMiH1qt6OQg91RXbYyko130_assertion description "[IkappaBalpha promoter polymorphisms in patients with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83857.RAsvmUO4Gl6ldaYPFORKMKFyODMiH1qt6OQg91RXbYyko130_provenance.
- NP83858.RAko5iCaH5Y3V7gz_uXbvIoGlNks124-YtGqX4oBzfESs130_assertion description "[We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83858.RAko5iCaH5Y3V7gz_uXbvIoGlNks124-YtGqX4oBzfESs130_provenance.
- NP83861.RAhidixqSLb4BOaL5BbCjcVdnkfdA0y39uShSXGBfpbYQ130_assertion description "[A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83861.RAhidixqSLb4BOaL5BbCjcVdnkfdA0y39uShSXGBfpbYQ130_provenance.
- NP83866.RAjxkq-ehE-0flmIKN5VW_prrXyZ-dI6tW6a4tUGC6oBk130_assertion description "[We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83866.RAjxkq-ehE-0flmIKN5VW_prrXyZ-dI6tW6a4tUGC6oBk130_provenance.
- NP83879.RAmMNSgc2U_yDRHBiL7kUbBdJcrE5XlYYIiMU5UyGyq4U130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83879.RAmMNSgc2U_yDRHBiL7kUbBdJcrE5XlYYIiMU5UyGyq4U130_provenance.
- NP83882.RAi3C0qsUPI9f5jAMPm4o2n1RoqnsdsssAEesqIMNUWIc130_assertion description "[Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83882.RAi3C0qsUPI9f5jAMPm4o2n1RoqnsdsssAEesqIMNUWIc130_provenance.
- NP83883.RAvEoz-11O06Snr7pLG3ajUy05yL1oIWJEEyr58q5bIOQ130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83883.RAvEoz-11O06Snr7pLG3ajUy05yL1oIWJEEyr58q5bIOQ130_provenance.
- NP83891.RArOM3RuIPsCtj717RYvXKXD8a8QBojoLk9uRvAIdQFvc130_assertion description "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83891.RArOM3RuIPsCtj717RYvXKXD8a8QBojoLk9uRvAIdQFvc130_provenance.
- NP83892.RAgQZr3SrCRTarf6SUQ8yHH7bVD0hS6j7C6za6PZFApaI130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83892.RAgQZr3SrCRTarf6SUQ8yHH7bVD0hS6j7C6za6PZFApaI130_provenance.
- NP83898.RAm0jgezyWgPpGAgPHXW4-mt2owBov2CNd5FRBa65HynE130_assertion description "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83898.RAm0jgezyWgPpGAgPHXW4-mt2owBov2CNd5FRBa65HynE130_provenance.
- NP83900.RAsX8JzLN1w9IPJsPwz2yjOlQ-jJtId_lQZDW5-uD5_ls130_assertion description "[Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83900.RAsX8JzLN1w9IPJsPwz2yjOlQ-jJtId_lQZDW5-uD5_ls130_provenance.
- NP83902.RAiuaiZBMgWILjpf3zx_k9l6yCNARh2_tbZLNpLS3hwlw130_assertion description "[A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83902.RAiuaiZBMgWILjpf3zx_k9l6yCNARh2_tbZLNpLS3hwlw130_provenance.
- NP83903.RAvm7ji3lj_KJxjXNdDwZGMVazOJEzk_Spp1epsdUcxbM130_assertion description "[To investigate the association of the rs4149601 polymorphisms of neural precursor cell expressed developmentally downregulated 4-like gene (NEDD4L) and obesity in Xinjiang Kazakh population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83903.RAvm7ji3lj_KJxjXNdDwZGMVazOJEzk_Spp1epsdUcxbM130_provenance.
- NP83907.RApeaQeJWu6Z2szMEjJCPtRNDF0SoKOuDabS-tUdIM_dE130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83907.RApeaQeJWu6Z2szMEjJCPtRNDF0SoKOuDabS-tUdIM_dE130_provenance.
- NP83912.RAlsVpHyDLrwLetZCrfUhYgfY6pEa24nQTQcqu-jru8xw130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83912.RAlsVpHyDLrwLetZCrfUhYgfY6pEa24nQTQcqu-jru8xw130_provenance.
- NP83915.RAp5OMKz2agBGP_Z3K0jcAycCSl1zyIHJhezwbKukRo_Y130_assertion description "[The findings are consistent with our hypothesis that variability in genes involved in steroidogenesis and estrogen metabolism may alter the risk of developing endometrial cancer, suggesting that they may be useful as biomarkers for genetic susceptibility to endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83915.RAp5OMKz2agBGP_Z3K0jcAycCSl1zyIHJhezwbKukRo_Y130_provenance.
- NP83916.RAgx_6lhP-0BQvQhpJmxLbAQ2b7Y2AzN0nRAaUvb2mCEs130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83916.RAgx_6lhP-0BQvQhpJmxLbAQ2b7Y2AzN0nRAaUvb2mCEs130_provenance.
- NP83917.RAuY0KAVHbd6zTFLKn_6iWIVfVwJYtGGiD5SB6ESVgd-o130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83917.RAuY0KAVHbd6zTFLKn_6iWIVfVwJYtGGiD5SB6ESVgd-o130_provenance.
- NP83923.RAm_pXcSWrpO3w9lnhI9tZUGKGUEOBwAuVU9nHP6LuEno130_assertion description "[Variation within DNA repair pathway genes and risk of multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83923.RAm_pXcSWrpO3w9lnhI9tZUGKGUEOBwAuVU9nHP6LuEno130_provenance.
- NP83927.RAlp9ych6jFiDXqInMlDJtiHs6VdTbQxrRmbEyDTb7bdc130_assertion description "[Analysis of genetic predisposition to pulmonary tuberculosis in native Russians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83927.RAlp9ych6jFiDXqInMlDJtiHs6VdTbQxrRmbEyDTb7bdc130_provenance.
- NP83932.RAkIqu8KUoolY9mtJ9Al8PeW3yXu9JvKdzBx5FJLz4Nf4130_assertion description "[Our results indicate that MYT1L may be a potential risk gene for MDD in the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83932.RAkIqu8KUoolY9mtJ9Al8PeW3yXu9JvKdzBx5FJLz4Nf4130_provenance.
- NP83934.RAoM8H_DyX8lRCpBwby9v63cVyK1h4WumAJ-G4xN74pCo130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83934.RAoM8H_DyX8lRCpBwby9v63cVyK1h4WumAJ-G4xN74pCo130_provenance.
- NP83935.RAnXYT9NqOfrIPt-jzynqscvluPHcKPsgqEyZKWkYV62o130_assertion description "[Genetic variation and antioxidant response gene expression in the bronchial airway epithelium of smokers at risk for lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83935.RAnXYT9NqOfrIPt-jzynqscvluPHcKPsgqEyZKWkYV62o130_provenance.
- NP83939.RAtWTb4b_djqH6xg2A8fOR4dhn7Q9p_qsI6zeww4PVnJQ130_assertion description "[We designed a custom resequencing chip that can detect known and new sequence changes in 90 retinal disease genes using a new high-throughput strategy with a high sensitivity and specificity for one tenth of the cost of conventional direct sequencing. The developed amplification strategy allows for the pooling of multiple patients with non-overlapping phenotypes, enabling many patients to be analyzed simultaneously in a fast and cost-effective manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83939.RAtWTb4b_djqH6xg2A8fOR4dhn7Q9p_qsI6zeww4PVnJQ130_provenance.
- NP83948.RAoDIp0yZHDiZNWk9ySoklRGlCJx7mmhjqt1v7arfJu0k130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83948.RAoDIp0yZHDiZNWk9ySoklRGlCJx7mmhjqt1v7arfJu0k130_provenance.
- NP83957.RAikquoyr86u4CRLKpHjPMAZsIIps-Mds0PpVfkE50PUc130_assertion description "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83957.RAikquoyr86u4CRLKpHjPMAZsIIps-Mds0PpVfkE50PUc130_provenance.
- NP83965.RAohzyYfq8GQa_z4_QZphxANDMQw10g3btfM7rmieDKdg130_assertion description "[We screened the exons, splice sites, and predicted promoters of 24 bilateral congenital idiopathic clubfoot patients and 24 matched controls in MYH 1, 2, 3, and 8 via sequence-based analysis, and screened an additional 76 patients in each discovered SNP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83965.RAohzyYfq8GQa_z4_QZphxANDMQw10g3btfM7rmieDKdg130_provenance.
- NP83970.RAhStk9VoD_NPN7v0J-_bmWRkab5f1CqZYQhMoQK0ae0E130_assertion description "[There is genetic heterogeneity in CRC associations in Americans of African versus European descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83970.RAhStk9VoD_NPN7v0J-_bmWRkab5f1CqZYQhMoQK0ae0E130_provenance.
- NP83972.RAutOiWRbzbFgs33fsiWcrMJljP44e4kwzfT3DdBQKdCQ130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83972.RAutOiWRbzbFgs33fsiWcrMJljP44e4kwzfT3DdBQKdCQ130_provenance.
- NP83977.RAjPKGfqWcrkJ1mldcDzYF4Ugf7i1QQrSJcmEmrZvVNrQ130_assertion description "[Adding SNPs previously associated with fasting glucose, insulin, lipids or obesity to a genetic risk score for type 2 diabetes significantly increases the power to discriminate between people with and without clinically manifest type 2 diabetes compared with a model including only conventional type 2 diabetes loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83977.RAjPKGfqWcrkJ1mldcDzYF4Ugf7i1QQrSJcmEmrZvVNrQ130_provenance.
- NP83980.RAqK3klxNIbWhoyn0ikp7-p7V4HWZNY9yVUEyjP5KGu_4130_assertion description "[The association of polymorphisms in DNA base excision repair genes XRCC1, OGG1 and MUTYH with the risk of childhood acute lymphoblastic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83980.RAqK3klxNIbWhoyn0ikp7-p7V4HWZNY9yVUEyjP5KGu_4130_provenance.
- NP83982.RArh6F0rHhJEff5uWFnYpGNXBooOsIHc9sBsbmpLBTaCM130_assertion description "[Polymorphisms in the base excision repair pathway and graft-versus-host disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83982.RArh6F0rHhJEff5uWFnYpGNXBooOsIHc9sBsbmpLBTaCM130_provenance.
- NP83986.RAsyApNX6iRqzgkKDI-oH5jYHbh2AP1X4RkOq0K33e10k130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83986.RAsyApNX6iRqzgkKDI-oH5jYHbh2AP1X4RkOq0K33e10k130_provenance.
- NP83988.RAnh_DpBsNDaxgUy9KTNT19aX_gMD0E4HJ2fPYAaNGB7c130_assertion description "[Polygenic association with total homocysteine in the post-folic acid fortification era: the CARDIA study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83988.RAnh_DpBsNDaxgUy9KTNT19aX_gMD0E4HJ2fPYAaNGB7c130_provenance.
- NP83993.RAs_meJQyrdMNkcfAYZv2s2YpN5akKC-s88ZnLx8ncD3k130_assertion description "[These studies identify single locus associations with preterm birth for both maternal and fetal genotypes in two populations of European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83993.RAs_meJQyrdMNkcfAYZv2s2YpN5akKC-s88ZnLx8ncD3k130_provenance.
- NP84000.RAnn_oiM-LYvWy1zut8Fke3uKQP-oNDzwypx5iwJO8MUg130_assertion description "[The potential influence of Cys-Gly on this phenotype is novel, and of considerable interest given that it has been linked to altered spontaneous activity and sedation in an animal model. Cys-Gly is a recognised ligand at the N-methyl-D-aspartatic acid (NMDA) subclass of glutamate receptor, a system associated with depression. In addition, the C677T-MTHFR association adds further support to existing findings underscoring the potential role of folate in depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84000.RAnn_oiM-LYvWy1zut8Fke3uKQP-oNDzwypx5iwJO8MUg130_provenance.
- NP84001.RAq2x4WXQq93NhPn2g_STcl4zVHU2l_7lRH1TTPouj5ks130_assertion description "[The results demonstrated that genetic variation in KCNJ11, BDNF, PFKP, PTER and SEC16B were associated with SGA and support the concept that genetic factors associated with obesity and/or type 2 diabetes are more prevalent in those born SGA compared to those born AGA. We have previously determined that environmental factors are associated with differences in birthweight in the ABC study and now we have demonstrated a significant genetic contribution, suggesting that the interaction between genetics and the environment are important.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84001.RAq2x4WXQq93NhPn2g_STcl4zVHU2l_7lRH1TTPouj5ks130_provenance.
- NP84003.RApGooKs4TW0v_HRaSs81EsKUf3WAwWiOswQFiYcqWhjQ130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84003.RApGooKs4TW0v_HRaSs81EsKUf3WAwWiOswQFiYcqWhjQ130_provenance.
- NP84009.RAs8hXCTllGwUgBAl2EKSm8hffF2pKD3VAbgHXIcNeP1s130_assertion description "[Association of methylenetetrahydrofolate reductase (MTHFR 677C>T and 1298A>C) polymorphisms and haplotypes with silent brain infarction and homocysteine levels in a Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84009.RAs8hXCTllGwUgBAl2EKSm8hffF2pKD3VAbgHXIcNeP1s130_provenance.
- NP84015.RAsbDak2xf_J8DuDKqWx4QeFWsOioxuLsDGgHSqDHg6RU130_assertion description "[Methylenetetrahydrofolate reductase correction of reducatase polymorphism and asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84015.RAsbDak2xf_J8DuDKqWx4QeFWsOioxuLsDGgHSqDHg6RU130_provenance.
- NP84016.RAsUV5-Z_GpGImJHEfyT193UoacAQGNPNmSoLFmuPbIRE130_assertion description "[The detection of somatic mutations in rectal cancer tumors led us to re-evaluate the utility of the tests performed in blood samples for these polymorphisms in rectal cancer. Furthermore, studies aimed at assessing the influence of pharmacogenetic markers in treatment response performed in blood samples should take into account the particular pattern of hypermutability present in each tumor type. We hypothesize that different patterns of hypermutability present in each tumor type would be related to the different results in association studies related to response to the treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84016.RAsUV5-Z_GpGImJHEfyT193UoacAQGNPNmSoLFmuPbIRE130_provenance.
- NP84020.RAhZuH8ypmYL1YAjWenpDA927pPjBwD0Dfn6RJBrK3Brc130_assertion description "[These studies identify single locus associations with preterm birth for both maternal and fetal genotypes in two populations of European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84020.RAhZuH8ypmYL1YAjWenpDA927pPjBwD0Dfn6RJBrK3Brc130_provenance.