Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP80053.RAgMfUr31-l7Nqh_lICPVrBkkwZYWnFtpYd3n8VNkpZ2E130_assertion description "[Severe obesity in Han Chinese was associated with 3 novel common SNPs for ESR1 and PPARgamma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80053.RAgMfUr31-l7Nqh_lICPVrBkkwZYWnFtpYd3n8VNkpZ2E130_provenance.
- NP80059.RAjo3tZrzeLG9kNyf17H0eWtbl1VnjepfEBZ0WmM-EwQU130_assertion description "[Genetic risk factors for renal failure among north Indian ESRD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80059.RAjo3tZrzeLG9kNyf17H0eWtbl1VnjepfEBZ0WmM-EwQU130_provenance.
- NP80062.RAgNGRrdYTYfH65jP4fgI5160Wl-FaEbiHy6p5XiLBOxk130_assertion description "[Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80062.RAgNGRrdYTYfH65jP4fgI5160Wl-FaEbiHy6p5XiLBOxk130_provenance.
- NP80064.RAtt1MPdb130TisKgvAmgb3u7n1LWL6p3UAi33VEmEcSM130_assertion description "[Polymorphisms of the UCP2 gene are associated with proliferative diabetic retinopathy in patients with diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80064.RAtt1MPdb130TisKgvAmgb3u7n1LWL6p3UAi33VEmEcSM130_provenance.
- NP80066.RAsSI5tz-7O4mDYAzjcUiIoayLMkklbphGFVjdRqwekx4130_assertion description "[The objective of this study was to evaluate the association of PPARG coactivator1 alpha (PPARGC1A), peroxisome proliferator activated receptor gamma (PPARG), and uncoupling protein1 (UCP1) gene polymorphisms with the metabolic syndrome (MS) in an Asian Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80066.RAsSI5tz-7O4mDYAzjcUiIoayLMkklbphGFVjdRqwekx4130_provenance.
- NP80067.RAkvFkoRIS1s_Ljemb5JyYx-Km9LXT0dR5NzgvL7yXEyw130_assertion description "[Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80067.RAkvFkoRIS1s_Ljemb5JyYx-Km9LXT0dR5NzgvL7yXEyw130_provenance.
- NP80068.RArasqlyytKSvvLcHVZ3VvOxWpJsKYBuXo4J2S6919YNQ130_assertion description "[Severe obesity in Han Chinese was associated with 3 novel common SNPs for ESR1 and PPARgamma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80068.RArasqlyytKSvvLcHVZ3VvOxWpJsKYBuXo4J2S6919YNQ130_provenance.
- NP80081.RAt1f0xmeRdvEbflz98gqh3ZvNXwZWMFAhJcRimb_ySj0130_assertion description "[By themselves, a single or double CGG deletion is unlikely to pose biologic significance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80081.RAt1f0xmeRdvEbflz98gqh3ZvNXwZWMFAhJcRimb_ySj0130_provenance.
- NP80082.RAgh2EASI71McLngy-6lVcQ5zDxy-iBI3Tq9nlrdzUzsc130_assertion description "[we provide evidence for a role of genetic variation in complement genes, particularly C5 and C9, and NHL risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80082.RAgh2EASI71McLngy-6lVcQ5zDxy-iBI3Tq9nlrdzUzsc130_provenance.
- NP80086.RAgVgFQGPNhYRviKdWDPTqm54X00yzs2oEZA67E249pOg130_assertion description "[Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80086.RAgVgFQGPNhYRviKdWDPTqm54X00yzs2oEZA67E249pOg130_provenance.
- NP80099.RAuB7Y3r4LwAtFukYg0r-lhQd6-3qMOzFPosg23R9fTmY130_assertion description "[Mutations in TYR were found in 26% of patients, while OCA2 and MATP caused OCA in 15% and 3%, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80099.RAuB7Y3r4LwAtFukYg0r-lhQd6-3qMOzFPosg23R9fTmY130_provenance.
- NP80102.RAupk0iq-QFC4M-ATpgQeuMjEpmSyBI6ghFh6jA410wT4130_assertion description "[PTEN identified as important risk factor of chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80102.RAupk0iq-QFC4M-ATpgQeuMjEpmSyBI6ghFh6jA410wT4130_provenance.
- NP80103.RAv_W7zKrTQ12qFROzggGdZhJqGsWDbITqpqP-ERHT-fQ130_assertion description "[Examination of association to autism of common genetic variationin genes related to dopamine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80103.RAv_W7zKrTQ12qFROzggGdZhJqGsWDbITqpqP-ERHT-fQ130_provenance.
- NP80105.RAudXYPa_IR6igqmAyVo_UXcVXhn7pLyZkGLOL0uVPfIA130_assertion description "[In both the Los Angeles and Guangxi studies, low-activity genotypes (reduced enzymatic activities) of methylenetetrahydrofolate reductase (MTHFR) and high-activity genotypes (enhanced enzymatic activities) of thymidylate synthase (TYMS), both of which discourage the misincorporation of uracil into DNA, were shown to be associated with a reduced risk for HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80105.RAudXYPa_IR6igqmAyVo_UXcVXhn7pLyZkGLOL0uVPfIA130_provenance.
- NP80108.RAnUMu1DNBIAYEQYZhTpHW-WE2yBhMFjsId-WebEU1DUg130_assertion description "[Correlation between thymidylate synthase protein expression and gene polymorphism with clinicopathological parameters in colorectal carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80108.RAnUMu1DNBIAYEQYZhTpHW-WE2yBhMFjsId-WebEU1DUg130_provenance.
- NP80109.RAvysiVOJDNpmzXYpkfFP4FVez_goD5Bp18d4I40UnsN0130_assertion description "[We describe a robust RFLP genotyping technique that employs size discrimination by capillary electrophoresis to genotype the TYMS TSER*3 G>C SNP. The technique also allows identification of a 6-bp insertion in the 3R allele, and we report the allelic frequencies for two uncommon TSER alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80109.RAvysiVOJDNpmzXYpkfFP4FVez_goD5Bp18d4I40UnsN0130_provenance.
- NP80112.RAtO_g90JShFR9nOnkBXvYuY00L1Dd64CdtnimkZoOKEE130_assertion description "[Thymidylate synthase genotypes and tumour regression in stage II/III rectal cancer patients after neoadjuvant fluorouracil-based chemoradiation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80112.RAtO_g90JShFR9nOnkBXvYuY00L1Dd64CdtnimkZoOKEE130_provenance.
- NP80114.RAn1BLTZegbeI_cGq-wNulBOMuQbkwlVUJ96OH_bkm3UA130_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." NP80114.RAn1BLTZegbeI_cGq-wNulBOMuQbkwlVUJ96OH_bkm3UA130_provenance.
- NP80115.RAqdygQkDkWajC4I-f4XVoa3ct19BNHHultZJf088w4dw130_assertion description "[Pretreatment blood samples from 60 patients with locally advanced T3 rectal tumors were analyzed for thymidylate synthase, epidermal growth factor receptor Sp1-216, and epidermal growth factor A61G gene polymorphisms by polymerase chain reaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80115.RAqdygQkDkWajC4I-f4XVoa3ct19BNHHultZJf088w4dw130_provenance.
- NP80116.RAqTj02WetbEsAxcyh3oypxv24priO-3Dh5F1R945J6O4130_assertion description "[The combined MTHFR 677TT/MTR 2756AA genotype was associated with increased DS risk (P=0.034), and the combined MTHFR 1298AC/TYMS 2R/2R genotype with reduced risk (P=0.003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80116.RAqTj02WetbEsAxcyh3oypxv24priO-3Dh5F1R945J6O4130_provenance.
- NP80120.RArFDwKDc7L2iCplppps9-36iyrVxsxImXZj6FTDodHCE130_assertion description "[Association of thymidylate synthase gene with endometrial cancer risk in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80120.RArFDwKDc7L2iCplppps9-36iyrVxsxImXZj6FTDodHCE130_provenance.
- NP80122.RAiwUVZXvKKV2Olsw__OxRWM5JkQMf3EG3iipgobKvvGo130_assertion description "[PTEN identified as important risk factor of chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80122.RAiwUVZXvKKV2Olsw__OxRWM5JkQMf3EG3iipgobKvvGo130_provenance.
- NP80127.RAr8rNbdgHYIA_h5QaBjidDWL1m49uWnkPiDU52Lr-a-E130_assertion description "[Multiple sclerosis susceptibility alleles in African Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80127.RAr8rNbdgHYIA_h5QaBjidDWL1m49uWnkPiDU52Lr-a-E130_provenance.
- NP80131.RAvvgk1Dj1JyXVR2xaY5RF02lQTDjrWMt4O-kt3QvF-2c130_assertion description "[We have demonstrated that several SNPs are associated with survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80131.RAvvgk1Dj1JyXVR2xaY5RF02lQTDjrWMt4O-kt3QvF-2c130_provenance.
- NP80132.RAul9bq3VuTwvXNvQZ-dfQw9PQDRd-dmRtcWoHDuE0pLU130_assertion description "[All together, our results show that genome wide patterns of alteration differ between EGFR and KRAS mutated lung ADC, describe two models of oncogenic cooperation involving either EGFR mutation and CDKN2A deletion or cyclin amplification and TP53 inactiva]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80132.RAul9bq3VuTwvXNvQZ-dfQw9PQDRd-dmRtcWoHDuE0pLU130_provenance.
- NP80140.RAuKcJHF5MTDR6maanqXIbEnidPVSrkwrSLWYBB3ft1lI130_assertion description "[In the present study we chose to investigate 7 genes involved in the synthesis, degradation and transportation of RA, ALDH1A1, ALDH1A2, ALDH1A3, CYP26A1, CYP26B1, CYP26C1 and Transthyretin (TTR), for their roles in the development of schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80140.RAuKcJHF5MTDR6maanqXIbEnidPVSrkwrSLWYBB3ft1lI130_provenance.
- NP80143.RAgYFVMEdEYBGphZzwrmDcSrxeBH5-45Lx9u9PV93Yj-o130_assertion description "[Genetic variation of the TUB gene was associated with both body composition and macronutrient intake, suggesting that TUB might influence eating behavior.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80143.RAgYFVMEdEYBGphZzwrmDcSrxeBH5-45Lx9u9PV93Yj-o130_provenance.
- NP80147.RAlEqDvGyArlGcST5XeQvdQHS3B0xGvcZP21zdEoLF6hw130_assertion description "[The aim of the present study was to investigate the mutation/variant of thyrotropin receptor (TSHR) and thyroid transcription factor-1 (TTF-1) genes in Chinese children with congenital hypothyroidism (CH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80147.RAlEqDvGyArlGcST5XeQvdQHS3B0xGvcZP21zdEoLF6hw130_provenance.
- NP80150.RAraOBViwXKHwO7cRiybr0VJYRIQIV6b0U-g-1VvIwUR4130_assertion description "[Low TSPY1 copy number is a new risk factor for male infertility with potential clinical consequences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80150.RAraOBViwXKHwO7cRiybr0VJYRIQIV6b0U-g-1VvIwUR4130_provenance.
- NP80153.RAit5OYc4uIYL3xKmoEUHoMy8qkW8bVGmAdqedwOQwnA8130_assertion description "[In Japan, TSHR mutations are relatively common among patients with CH, and a founder mutation (p.R450H) accounts for about 70% of mutants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80153.RAit5OYc4uIYL3xKmoEUHoMy8qkW8bVGmAdqedwOQwnA8130_provenance.
- NP80156.RAgeiF8Vi1eYRIQHzngxlIrDs0DXLdNilDxmCo1hl0An8130_assertion description "[In two large populations of elderly subjects, neither serum thyroid parameters nor polymorphisms in the type 2 deiodinase and the TSH receptor, were associated with blood pressure or the presence of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80156.RAgeiF8Vi1eYRIQHzngxlIrDs0DXLdNilDxmCo1hl0An8130_provenance.
- NP80169.RAlJ_72wMLSd93c0pKgqXLQIu7El2vgd3-hpTA0CFbwfU130_assertion description "[Additional studies are necessary to elucidate the conflicting results obtained for the DEFB1, IL4, and C1INH polymorphisms and their role in susceptibility to and severity of meningococcal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80169.RAlJ_72wMLSd93c0pKgqXLQIu7El2vgd3-hpTA0CFbwfU130_provenance.
- NP80176.RAq6jSL6ml2tPuEu2BWSvRSdaRjvQPrpjONUCQ-tFF2Fo130_assertion description "[These results demonstrate a clear association between polymorphisms in the IRAK4 gene and serum IgE levels in patients with CRS and asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80176.RAq6jSL6ml2tPuEu2BWSvRSdaRjvQPrpjONUCQ-tFF2Fo130_provenance.
- NP80178.RAsntefDisJAvKB0tmVLyCQZoZS4AseBJcgaextUO8LZI130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80178.RAsntefDisJAvKB0tmVLyCQZoZS4AseBJcgaextUO8LZI130_provenance.
- NP80182.RAgSuUq_nCTh8KcJBpi6sesMG6PW8ILpJI4jY3-piPuis130_assertion description "[we provide additional evidence for the role of genetic variation in TNF and LTA SNPs and haplotypes with risk of NHL and also provide some of the first preliminary evidence for an association of genetic variation in NFKB1, a downstream target of TNF sig]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80182.RAgSuUq_nCTh8KcJBpi6sesMG6PW8ILpJI4jY3-piPuis130_provenance.
- NP80183.RAgVKzZpS5DMC3gVg9OT1W9LDY7W4Fkuvfk5xdtwifWKw130_assertion description "[Genetic contributions to the development of retinopathy of prematurity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80183.RAgVKzZpS5DMC3gVg9OT1W9LDY7W4Fkuvfk5xdtwifWKw130_provenance.
- NP80192.RAshRZ8QZL-RcKxEXtJNw-wW7Hxau0SkHE9X8NTQYj-qQ130_assertion description "[Combining imaging and genetic data from a GWAS identified genes related to forebrain development and stress response, already implicated in schizophrenic dysfunction, as affecting prefrontal efficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80192.RAshRZ8QZL-RcKxEXtJNw-wW7Hxau0SkHE9X8NTQYj-qQ130_provenance.
- NP80194.RAh9mh2azO8TBRs2u3vm01eOdh7xVZMqG2cfr9iM7hB1A130_assertion description "[Determination of genetic predisposition to patent ductus arteriosus in preterm infants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80194.RAh9mh2azO8TBRs2u3vm01eOdh7xVZMqG2cfr9iM7hB1A130_provenance.
- NP80195.RApB3_GrqQn07mEyk7LioFUQtIv1aVD7gOrlUEVWXOD3A130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80195.RApB3_GrqQn07mEyk7LioFUQtIv1aVD7gOrlUEVWXOD3A130_provenance.
- NP80206.RAr2-DiOOu9QD2nEke-d67Qcr-diVyU6Ottfvzqejhn5c130_assertion description "[Sixteen single nucleotide polymorphisms (SNPs) (CYP3A4*1B A>G, CYP3A5*3 G>A, GSTP1 313 A>G, GSTM1 deletion, GSTT1 deletion, MDR1 exon 21 G>T/A, MDR1 exon 26 C>T, MTHFR 677 C>T, MTHFR 1298 A>C, NR3C1 1088 A>G, RFC 80 G>A, TPMT 238 G>C, TPMT 460 G>A, TPMT 719 A>G, VDR intron 8 G>A, VDR FokI T>C) that have been implicated in the pharmacogenetics of ALL therapy were analyzed by TotalPlex amplification and SNP genotyping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80206.RAr2-DiOOu9QD2nEke-d67Qcr-diVyU6Ottfvzqejhn5c130_provenance.
- NP80208.RAntOuuQbzcHlHDMGx2Oa9aIS2JZlgiYsK0YBoeeZDXnI130_assertion description "[Thiopurine S-methyltransferase (TPMT) gene polymorphism in Brazilian children with acute lymphoblastic leukemia: association with clinical and laboratory data.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80208.RAntOuuQbzcHlHDMGx2Oa9aIS2JZlgiYsK0YBoeeZDXnI130_provenance.
- NP80210.RAtGxUgw7IdPgvJljJnWFXhyNF5fQZiwUXJihGJjXv_RM130_assertion description "[SNaPshot method for TPMT polymorphism analysis works faster with the potential for high throughput.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80210.RAtGxUgw7IdPgvJljJnWFXhyNF5fQZiwUXJihGJjXv_RM130_provenance.
- NP80211.RAjWgRMRsRiZfDg4V7QRi58DjEOGflshJ8KlIw-nque4c130_assertion description "[Independent pharmacogenomic determinants associated with treatment outcome were identified in subsets of Taiwanese ALL patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80211.RAjWgRMRsRiZfDg4V7QRi58DjEOGflshJ8KlIw-nque4c130_provenance.
- NP80215.RAukhytvtM5Jhh_iMlRjkU743qnerymDFAeU075lccsSg130_assertion description "[Impact of the heterozygous TPMT*1/*3C genotype on azathioprine-induced myelosuppression in kidney transplant recipients in Thailand.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80215.RAukhytvtM5Jhh_iMlRjkU743qnerymDFAeU075lccsSg130_provenance.
- NP80242.RAqQh6GgVWsghQEiPHP6upXx0QOILwOl3q6pn4spyWps4130_assertion description "[Explorative study to identify novel candidate genes related to oxaliplatin efficacy and toxicity using a DNA repair array.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80242.RAqQh6GgVWsghQEiPHP6upXx0QOILwOl3q6pn4spyWps4130_provenance.
- NP80244.RAvnIXOS7zzIo9wTNP5oe8FtUKVu2bsTi7g_S6LGr13w8130_assertion description "[TP53 gene mutation is frequent in patients with acute myeloid leukemia and complex karyotype, and is associated with very poor prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80244.RAvnIXOS7zzIo9wTNP5oe8FtUKVu2bsTi7g_S6LGr13w8130_provenance.
- NP80245.RAgtKMkFxrp2Mlpm2zRoGGgaIDMsAyuo3WUq8ve9CzW2A130_assertion description "[We comprehensively analyzed the FLT3, cKIT, N-RAS, C/EBPA, AML1, MLL, NPM1, and TP53 mutations in 144 newly diagnosed de novo AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80245.RAgtKMkFxrp2Mlpm2zRoGGgaIDMsAyuo3WUq8ve9CzW2A130_provenance.
- NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_assertion description "[These point towards a variety of candidate genes that could contribute to the pathogenesis of minimally differentiated acute myeloid leukemia, including the tumor suppressor genes TP53 and NF1, and reinforced the importance of RUNX1 in this leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_provenance.
- NP80248.RAiUDLhNNQhuxLwQNUhXO62gCMcLuPDS1j61maTtFpXG4130_assertion description "[A case-control study was done to determine the association between glutathione S-transferase M1 (GSTM1), GSTT1, GSTP1, EPHX1, and p53 codon 72 polymorphisms as risk factors in 120 adult acute myeloid leukemia (AML) cases and 202 healthy controls by polymerase chain reaction-restriction fragment length polymorphism techniques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80248.RAiUDLhNNQhuxLwQNUhXO62gCMcLuPDS1j61maTtFpXG4130_provenance.
- NP80254.RAu9EoTR2s2ztbRRtHf8rPMwZCr7WDgblYOd9koVUoPW4130_assertion description "[Monoallelic TP53 inactivation is associated with poor prognosis in chronic lymphocytic leukemia: results from a detailed genetic characterization with long-term follow-up.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80254.RAu9EoTR2s2ztbRRtHf8rPMwZCr7WDgblYOd9koVUoPW4130_provenance.
- NP80270.RAkPrAyP9n4yelzlLVqOtJIZ2QNTBat_C5dgLYQKCAv6c130_assertion description "[The PPP2R5E gene is identified as harboring genetic variants that can affect human cancer and are possibly under evolutionary selection pressure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80270.RAkPrAyP9n4yelzlLVqOtJIZ2QNTBat_C5dgLYQKCAv6c130_provenance.
- NP80288.RAlLq52WZeTyDrh8pQbt8eH6QqcVTlYLS3XFjCWMATziM130_assertion description "[Interaction of P53 Arg72Pro and MDM2 T309G polymorphisms and their associations with risk of gastric cardia cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80288.RAlLq52WZeTyDrh8pQbt8eH6QqcVTlYLS3XFjCWMATziM130_provenance.
- NP80290.RAppCmz4EALz8O_qLDr97ZSOOqMHi-CgxGxOGi8bpEH3Q130_assertion description "[A p53 genetic polymorphism of gastric cancer: difference between early gastric cancer and advanced gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80290.RAppCmz4EALz8O_qLDr97ZSOOqMHi-CgxGxOGi8bpEH3Q130_provenance.
- NP80301.RAvbRoU3uNiPUGhVY9PL5SLm7IITQ-4yrMFd356nI8zY8130_assertion description "[Association of genetic polymorphisms, mRNA expression of p53 and p21 with chronic benzene poisoning in a chinese occupational population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80301.RAvbRoU3uNiPUGhVY9PL5SLm7IITQ-4yrMFd356nI8zY8130_provenance.
- NP80303.RAjIgCb47CMYvaTUcSvOG3f5oygHhZGqTbHIjk1Gt6yYQ130_assertion description "[Explorative study to identify novel candidate genes related to oxaliplatin efficacy and toxicity using a DNA repair array.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80303.RAjIgCb47CMYvaTUcSvOG3f5oygHhZGqTbHIjk1Gt6yYQ130_provenance.
- NP80305.RApfZePelAk0TRwmm6zL1SuHXSyVgEUdRnP7L9n35_1iY130_assertion description "[Different p53 mutation patterns in colorectal tumors from smokers and nonsmokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80305.RApfZePelAk0TRwmm6zL1SuHXSyVgEUdRnP7L9n35_1iY130_provenance.
- NP80314.RAqYM0sstHIe0_B_2O2C_0X_cTC-OR9bJqjEOa26tL384130_assertion description "[The findings suggest that polymorphisms of MDM2 and TP53 genes may be genetic modifier for developing NPC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80314.RAqYM0sstHIe0_B_2O2C_0X_cTC-OR9bJqjEOa26tL384130_provenance.
- NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_assertion description "[To investigate its relevance in childhood acute lymphoblastic leukemia (ALL) susceptibility, we genotyped 114 cases and 414 newborn controls from Wales (UK) for polymorphisms in TP53 (R72P), its negative regulator MDM2 (single-nucleotide polymorphism SNP309, rs2279744), and selected HLA complex genes whose products interact with TP53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_provenance.
- NP80321.RAmEfGNb0MjBg1z-rhdTrnzvpgfRttKwcW_p3Oma1VFpY130_assertion description "[Analysis of candidate genes in occurrence and growth of colorectal adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80321.RAmEfGNb0MjBg1z-rhdTrnzvpgfRttKwcW_p3Oma1VFpY130_provenance.
- NP80329.RAq6c3OxzVmqG6V9uUueyWgd3NJXlsXqt-bQEq2YKfZaE130_assertion description "[We identified and then confirmed through replication two new genetic loci for SLE: a promoter-region allele associated with reduced expression of BLK and increased expression of C8orf13 and variants in the ITGAM-ITGAX region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80329.RAq6c3OxzVmqG6V9uUueyWgd3NJXlsXqt-bQEq2YKfZaE130_provenance.
- NP80337.RAjAUdY_YGZTIwEVI92zJ0lq191hu5zr7JKYzHxFIOlmo130_assertion description "[Relationship between sex, shape, and substrate in hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80337.RAjAUdY_YGZTIwEVI92zJ0lq191hu5zr7JKYzHxFIOlmo130_provenance.
- NP80338.RAvgPYd3gQ6O6-FbK3_p6I-kcfoaFA1LwhI6fakmUzHtI130_assertion description "[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80338.RAvgPYd3gQ6O6-FbK3_p6I-kcfoaFA1LwhI6fakmUzHtI130_provenance.
- NP80341.RAuXfSQvH9zYkEATBMUTQ98ahHxbHWbVxP2Mbg8GUlwW0130_assertion description "[The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80341.RAuXfSQvH9zYkEATBMUTQ98ahHxbHWbVxP2Mbg8GUlwW0130_provenance.
- NP80357.RAuxZq3y-DeVUvAn67GeOp4Chg8eaSbkLB1l34XWy107g130_assertion description "[In this study, we tested 27 genes (ACE, BDNF, CH25H, CHRNB2, CST3, CTSD, DAPK1, GALP, hCG2039140, IL1B, LMNA, LOC439999, LOC651924, MAPT, MTHFR, MYH13, PCK1, PGBD1, PRNP, PSEN1, SORCS1, SORL1, TF, TFAM, TNK1, GWA_14q32.13, and GWA_7p15.2), all showing significant association with AD risk in the AlzGene meta-analyses, in a large collection of family-based samples comprised of 4,180 subjects from over 1,300 pedigrees.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80357.RAuxZq3y-DeVUvAn67GeOp4Chg8eaSbkLB1l34XWy107g130_provenance.
- NP80363.RAmpBH88Q6ArumZf-tBcOJNkndbZ8huB1Y1f0LjMlI3i8130_assertion description "[Four SNPs in the TERT and POT1 genes were significantly related with overall breast cancer risk. This initial analysis provides valuable clues for further exploration of the biological role of telomere pathway genes in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80363.RAmpBH88Q6ArumZf-tBcOJNkndbZ8huB1Y1f0LjMlI3i8130_provenance.
- NP80372.RAlWA3pbN_r5-wzD6ccnJOk3k1jtJKQu4DG780pw8Btdo130_assertion description "[PTEN identified as important risk factor of chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80372.RAlWA3pbN_r5-wzD6ccnJOk3k1jtJKQu4DG780pw8Btdo130_provenance.
- NP80373.RAmjFdhEQ4yb5_8VVwimPsarEVckd9DYl73ER9bgfUB2U130_assertion description "[The -509C/T polymorphism of transforming growth factor-beta1 is associated with increased risk for development of chronic idiopathic neutropenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80373.RAmjFdhEQ4yb5_8VVwimPsarEVckd9DYl73ER9bgfUB2U130_provenance.
- NP80376.RAjTiTKeSZoVUwiOQfljwg4FjWLqZx0RB4XsLe1MlP1Ms130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80376.RAjTiTKeSZoVUwiOQfljwg4FjWLqZx0RB4XsLe1MlP1Ms130_provenance.
- NP80380.RAnhAQDFFPTy7Cnb9EWlogk4rgXty34TcSD2iSBB-m6m0130_assertion description "[Association of BANK1 and TNFSF4 with systemic lupus erythematosus in Hong Kong Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80380.RAnhAQDFFPTy7Cnb9EWlogk4rgXty34TcSD2iSBB-m6m0130_provenance.
- NP80382.RArGQdTnMhL60UWI43cKJ_RQR7uiGY0MqsIjGLn8mVwPA130_assertion description "[Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80382.RArGQdTnMhL60UWI43cKJ_RQR7uiGY0MqsIjGLn8mVwPA130_provenance.
- NP80383.RAvgzyuf1GZHsGTQGmmke7dqPFIK0V2qQmADsViGGykGA130_assertion description "[A single-nucleotide polymorphism of the TNFSF4 gene is associated with systemic lupus erythematosus in Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80383.RAvgzyuf1GZHsGTQGmmke7dqPFIK0V2qQmADsViGGykGA130_provenance.
- NP80386.RAhpeOR42lesTtpEUyoK0TbC0nGf1QE4x9ElpQg-FwZi8130_assertion description "[Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80386.RAhpeOR42lesTtpEUyoK0TbC0nGf1QE4x9ElpQg-FwZi8130_provenance.
- NP80394.RAkjhaBTXQWjMMNzVJTKpoZTqEZCWymRrdASAs-85iT6s130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80394.RAkjhaBTXQWjMMNzVJTKpoZTqEZCWymRrdASAs-85iT6s130_provenance.
- NP80399.RAm2ZtCD5w_Ijc5xwy555p3DHREVeaE0Mf_WkpReccieQ130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80399.RAm2ZtCD5w_Ijc5xwy555p3DHREVeaE0Mf_WkpReccieQ130_provenance.
- NP80402.RAozJYlaF8sKDbliWVR5XElcBpZcUY1dgJ-k0pGHaN-JU130_assertion description "[Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80402.RAozJYlaF8sKDbliWVR5XElcBpZcUY1dgJ-k0pGHaN-JU130_provenance.
- NP80405.RAoIvg9C_IoztwiqUquAUf9CjPmnxZAD4xqMqbR8tb7xY130_assertion description "[To test whether polymorphisms in IL-1, NF-KB, FAS, and FASL genes are associated with risk of silicosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80405.RAoIvg9C_IoztwiqUquAUf9CjPmnxZAD4xqMqbR8tb7xY130_provenance.
- NP80406.RAro6UPtTD8tFXbDlj_sMP7iXWsSXaHmbxYyLupQKVNPk130_assertion description "[the consistency of these findings suggests that Fas promoter genetic variants may be related to sarcoidosis disease risk in AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80406.RAro6UPtTD8tFXbDlj_sMP7iXWsSXaHmbxYyLupQKVNPk130_provenance.
- NP80418.RAkYDbxmTJLeofA7GAH47n11n-1Hi8BVk85PrSso2YnOI130_assertion description "[The present study validated the hypothesis that the Fas 670 G variant may have an influencing role in preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80418.RAkYDbxmTJLeofA7GAH47n11n-1Hi8BVk85PrSso2YnOI130_provenance.
- NP80422.RAh4uxHEn5BufCfoJ7_-sHwT3gRcsKwKNk2gB-mdYv4Nk130_assertion description "[In this large UK cohort, we have found strong association of the CD40 gene with susceptibility to RA, and weaker evidence for association with RA in the CCL21 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80422.RAh4uxHEn5BufCfoJ7_-sHwT3gRcsKwKNk2gB-mdYv4Nk130_provenance.
- NP80428.RAj79IydluNmu_qNsS5ytMZe0Bz78TQ4U1eSQEiaiEnb0130_assertion description "[However, neither the allele frequency of CD40 nor the smoking and clinical stages in CD40 -1C/T genotypes frequency had significant differences between the COPD patients and control.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80428.RAj79IydluNmu_qNsS5ytMZe0Bz78TQ4U1eSQEiaiEnb0130_provenance.
- NP80429.RAtUFoehHG7uATWBmh-XepVQ5bBqwn9o02O5LuomSLTUE130_assertion description "[Analysis of candidate genes on chromosome 20q12-13.1 reveals evidence for BMI mediated association of PREX1 with type 2 diabetes in European Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80429.RAtUFoehHG7uATWBmh-XepVQ5bBqwn9o02O5LuomSLTUE130_provenance.
- NP80433.RAlr9xS9_QXIJd24ZZYEPKHZtiYfbeB87vdEbdLY820O0130_assertion description "[A potential role of TNFR gene polymorphisms in autoimmune thyroid diseases in the Tunisian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80433.RAlr9xS9_QXIJd24ZZYEPKHZtiYfbeB87vdEbdLY820O0130_provenance.
- NP80435.RAqeZsFMOHUGZZ3YI0BOlq1KMDHCAeh3ZZRlSYQPMTFSQ130_assertion description "[Multiple genetic factors in olanzapine-induced weight gain in schizophrenia patients: a cohort study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80435.RAqeZsFMOHUGZZ3YI0BOlq1KMDHCAeh3ZZRlSYQPMTFSQ130_provenance.
- NP80437.RArDWaUXpkcSEG6NnL7fEp87fBpMK4ckhDMCepRx3dzaM130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80437.RArDWaUXpkcSEG6NnL7fEp87fBpMK4ckhDMCepRx3dzaM130_provenance.
- NP80438.RApb_fqrJtYjfKjUziRr5CtiZ9l62-Uc4fhRPwohsojRw130_assertion description "[No genetic association between tumour necrosis factor receptor II 196R polymorphism and Japanese sporadic Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80438.RApb_fqrJtYjfKjUziRr5CtiZ9l62-Uc4fhRPwohsojRw130_provenance.
- NP80439.RAnKM7D61ENNIQZ7-viWpYhoPCJdFrDN34_yYWB4SoArM130_assertion description "[Does the simultaneous tumor necrosis factor receptor 2, tumor necrosis factor promoter gene polymorphism represent a higher risk for alcoholic liver disease?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80439.RAnKM7D61ENNIQZ7-viWpYhoPCJdFrDN34_yYWB4SoArM130_provenance.
- NP80447.RAn1pwlRZKtg2G6cLPgRcwTKcEci1xfCD_n555bH4KThI130_assertion description "[To investigate four functionally relevant polymorphisms in the tumor necrosis factor receptor 2-encoding gene, tumor necrosis factor receptor superfamily member 1B, for association with tuberculosis susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80447.RAn1pwlRZKtg2G6cLPgRcwTKcEci1xfCD_n555bH4KThI130_provenance.
- NP80451.RAsH_3d1tFkaDQdzCTXlfpX-udfmZt8HN1FRoD9OagoA8130_assertion description "[Lung cancer susceptibility model based on age, family history and genetic variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80451.RAsH_3d1tFkaDQdzCTXlfpX-udfmZt8HN1FRoD9OagoA8130_provenance.
- NP80453.RAsV__d9YHyrBRkJcAQ88nA716zITR--57Dqfn7Q3isD0130_assertion description "[When numeric scores were assigned to both the SNP and demographic data, and sequentially combined by a simple algorithm in a risk model, the composite score was found to be linearly related to lung cancer risk with a bimodal distribution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80453.RAsV__d9YHyrBRkJcAQ88nA716zITR--57Dqfn7Q3isD0130_provenance.
- NP80456.RAtQspNzdMVz9qw3G3piEy3ZRAfq-1UxrgpltLAWKWGcY130_assertion description "[A potential role of TNFR gene polymorphisms in autoimmune thyroid diseases in the Tunisian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80456.RAtQspNzdMVz9qw3G3piEy3ZRAfq-1UxrgpltLAWKWGcY130_provenance.
- NP80457.RAnnEgVkGsvLyfpZ-ZERUlaL0AWJIYFowXuxIv6Sr2WtE130_assertion description "[we provide additional evidence for the role of genetic variation in TNF and LTA SNPs and haplotypes with risk of NHL and also provide some of the first preliminary evidence for an association of genetic variation in NFKB1, a downstream target of TNF sig]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80457.RAnnEgVkGsvLyfpZ-ZERUlaL0AWJIYFowXuxIv6Sr2WtE130_provenance.
- NP80461.RAjbXBIb8unYsnSBOdl4URj50mBbwZbj1bIfjhnUH4u4Y130_assertion description "[Association between polymorphisms in tumor necrosis factor (TNF) and TNF receptor genes and circulating TNF, soluble TNF receptor levels, and bone mineral density in postmenopausal Korean women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80461.RAjbXBIb8unYsnSBOdl4URj50mBbwZbj1bIfjhnUH4u4Y130_provenance.
- NP80466.RArEzGJ389kbfApE5irX-1K0Li0UNh6OxSsj37s7fJZ6k130_assertion description "[The primary interest in the MSGB concept resides in its capacity to integrate cumulative genetic contributions to MS risk. This analysis underlines the high variability of family load with known common variants. This novel approach can be extended to other genetically complex diseases. Despite the emphasis on assembling large case-control datasets, multigenerational, multiaffected families remain an invaluable resource for advancing the understanding of the genetic architecture of complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80466.RArEzGJ389kbfApE5irX-1K0Li0UNh6OxSsj37s7fJZ6k130_provenance.
- NP80467.RArLtkmlOtuLhM8AgAFB9d6N-2mK15UukLANJyJDogaZ8130_assertion description "[Late-onset tumor necrosis factor receptor-associated periodic syndrome in multiple sclerosis patients carrying the TNFRSF1A R92Q mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80467.RArLtkmlOtuLhM8AgAFB9d6N-2mK15UukLANJyJDogaZ8130_provenance.
- NP80468.RAitvEvCc_7URqbM1Idp8hfPsKocI9dJ6Sqn7LC2sioQo130_assertion description "[PTEN identified as important risk factor of chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80468.RAitvEvCc_7URqbM1Idp8hfPsKocI9dJ6Sqn7LC2sioQo130_provenance.
- NP80472.RAoRUF5QgbegEuytwInEDMYfF-yXpH8YjKsuhB1VgK8xs130_assertion description "[The TNFSF10 (rs1131532) polymorphism was identified as a possible prognostic factor of survival in patients with operated invasive breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80472.RAoRUF5QgbegEuytwInEDMYfF-yXpH8YjKsuhB1VgK8xs130_provenance.
- NP80474.RAkO4sHUcPqjJtK6nbR7fqF5OUg_8E5k3wOFvUacT_E94130_assertion description "[The purpose of this study was to evaluate the role of osteoprotegerin gene (OPG) polymorphisms as genetic modifiers in the etiology of prostate cancer (PCa) and disease progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80474.RAkO4sHUcPqjJtK6nbR7fqF5OUg_8E5k3wOFvUacT_E94130_provenance.
- NP80475.RAt1dGs0T8MqZT0WQ-nOPuPJGEhJzo20_X_ezsskgPrKk130_assertion description "[Clinical significance of tumor necrosis factor receptor superfamily member 11b polymorphism in prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80475.RAt1dGs0T8MqZT0WQ-nOPuPJGEhJzo20_X_ezsskgPrKk130_provenance.
- NP80477.RAnkBI8VjRvRV2FGD38BZP_bTNe83cfJ3_kxBkqfnLYVs130_assertion description "[The combinations of polymorphisms in vitamin D receptor, osteoprotegerin and tumour necrosis factor superfamily member 11 genes are associated with bone mineral density.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80477.RAnkBI8VjRvRV2FGD38BZP_bTNe83cfJ3_kxBkqfnLYVs130_provenance.
- NP80481.RArh-bEkYE4_awcKG1m7_TL0r63jp-c5FYX8a4OcTy4X0130_assertion description "[Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80481.RArh-bEkYE4_awcKG1m7_TL0r63jp-c5FYX8a4OcTy4X0130_provenance.