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10篇 您的检索式:作者名="DARLENE C"
    题名 作者 年代 出处 被引量
1Heterozygous em- bryonicstem cell lines derived from nonhuman pri- mate parthenotes显示文摘Vikas D Lisa C Darlene P 2008Stem Cells2008,26,:1
2The efficacy of thyroidectomy for Graves' disease a meta-analysis 显示文摘Tapash K Charle C Darlene M 2002J Surg Res2002,90,2:1
3The efficacy of thyroideetomy for Graves' disease:a meta-analysis显示文摘Tapash K Charle C Darlene M 2002J Surg Res2002,90,2:1
4The efficacy of thyroideetomy for Graves' disease:a meta-analysis显示文摘Tapash K Charle C Darlene M 0,,02:1
5Examining the sructure of the Revised Accept- ance Disability Scale 显示文摘Darlene AG Donald C 2007J Rehabi12007,73,3:1
6Accurate assessment of particle counts in liquids显示文摘John G E Darlene C S Robert D L 1995Lubrication Engineer1995,51,3:1
7The econom- ics of illeginntare activicies: Further evidence 显示文摘MIXON J FRANKLIN G DARLENE C 1996The Joumal of Sociocconomics1996,,3:1
8Postsurgical pain syndromes: Chronic pain after hysterectomy and cesarean sec- tion显示文摘Darlene C Recker D O Patricia M 2011Reg Anesth Pain Med2011,15,3:1
9Expression of tissue factor pathway inhibitor in human fetal and placental tissues显示文摘Cynthia S E Darlene A C Rbert D C 2000Early Human Development2000,59,:1
10Analysis of 12 variants in the development of gastric and colorectal cancers显示文摘AIM To evaluate the relation between 12 polymorphisms and the development of gastric cancer(GC) and colorectal cancer(CRC).METHODS In this study,we included 125 individuals with GC diagnosis,66 individuals with CRC diagnosis and 475 cancer-free individuals. All participants resided in the North region of Brazil and authorized the use of their samples. The 12 polymorphisms(in CASP8,CYP2 E1,CYP19 A1,IL1 A,IL4,MDM2,NFKB1,PAR1,TP53,TYMS,UGT1 A1 and XRCC1 genes) were genotyped in a single PCR for each individual,followed by fragment analysis. To avoid misinterpretation due to population substructure,we applied a previously developed set of 61 ancestryinformative markers that can also be genotyped by multiplex PCR. The statistical analyses were performed in Structure v.2.3.4,R environment and SPSS v.20.RESULTS After statistical analyses with the control of confounding factors,such as genetic ancestry,three markers(rs79071878 in IL4,rs3730485 in MDM2 and rs28362491 in NFKB1) were positively associated with the development of GC. One of these markers(rs28362491) and the marker in the UGT1 A1 gene(rs8175347) were positively associated with the development of CRC. Therefore,we investigated whether the joint presence of the deleterious alleles of each marker could affect the development of cancer and we obtained positive results in all analyses. Carriers of the combination of alleles RP1 + DEL(rs79071878 and rs28361491,respectively) are at 10-times greater risk of developing GC than carriers of other combinations. Similarly,carriers of the combination of DEL + RARE(rs283628 and rs8175347) are at about 12-times greater risk of developing CRC than carriers of other combinations.CONCLUSION These findings are important for the comprehension of gastric and CRC development,particularly in highly admixed populations,such as the Brazilian population.Giovanna C Cavalcante Marcos AT Amador Andre M Ribeiro dos Santos Darlen C Carvalho Roberta B Andrade Esdras EB Pereira Marianne R Fernandes Danielle F Costa Ney PC Santos Paulo P Assumpcao Andrea Ribeiro dos Santos Sidney Santos 2017World Journal of Gastroenterology2017,23,48:0
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