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https://www.selleckchem.com/products/mt-802.html This study was conducted to evaluate the relationship between the p73 G4C14-to-A4T14 polymorphism (hereafter, G4C14-to-A4T14) and lung cancer risk. The studies on the relationship between G4C14-A4T14 and lung cancer risk published as of November 5, 2018, were comprehensively searched in PubMed, Embase, the Cochrane Library, the Chinese Wanfang database, China National Knowledge Infrastructure (CNKI), and China Biology Medicine (CBM). The last update was on May 24, 2019. Statistical analysis was performed using Stata 12.0. The association between G4C14-A4T14 and lung cancer risk was analyzed in nine studies. The findings indicate no association between G4C14-to-A4T14 and lung cancer risk (allele model OR=0.90, 95% CI 0.73-1.11, I =86.0%, P=.330; dominant model OR=0.93, 95% CI 0.74-1.17, I =82.6%, P=.551; recessive model OR=0.75, 95% CI 0.50-1.13, I =75.2%, P=.165; homozygote model OR=0.74, 95% CI 0.47-1.17, I =79.6%, P=.199; heterozygote model OR=0.98, 95% CI 0.80-1.21, I =75.8%, P=.879). The heterogeneity between subgroups by cancer types and genotyping method was significantly reduced. After the deletion of suspected duplicates, no association was found between G4C14-to-A4T14 and lung cancer susceptibility. Our meta-analysis confirms that G4C14-to-A4T14 is not significantly related to lung cancer risk. Our meta-analysis confirms that G4C14-to-A4T14 is not significantly related to lung cancer risk. Bone marrow graft cell content impacts engraftment potential after allogeneic hematopoietic cell transplantation (alloHCT). Surrogates, such as intraoperative total nucleated cell count (ioTNC), are of unclear utility in predicting final graft characteristics. In addition, demographic and clinical factors may influence graft cellular profile and recipient engraftment. We retrospectively reviewed marrow harvests at our institution performed between 2009 and 2019. During this time, an ioTNC was measured after 50% of the proje

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