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Critical Reviews™ in Eukaryotic Gene Expression

Publication de 6  numéros par an

ISSN Imprimer: 1045-4403

ISSN En ligne: 2162-6502

The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two preceding years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) IF: 1.6 To calculate the five year Impact Factor, citations are counted in 2017 to the previous five years and divided by the source items published in the previous five years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) 5-Year IF: 2.2 The Immediacy Index is the average number of times an article is cited in the year it is published. The journal Immediacy Index indicates how quickly articles in a journal are cited. Immediacy Index: 0.3 The Eigenfactor score, developed by Jevin West and Carl Bergstrom at the University of Washington, is a rating of the total importance of a scientific journal. Journals are rated according to the number of incoming citations, with citations from highly ranked journals weighted to make a larger contribution to the eigenfactor than those from poorly ranked journals. Eigenfactor: 0.00058 The Journal Citation Indicator (JCI) is a single measurement of the field-normalized citation impact of journals in the Web of Science Core Collection across disciplines. The key words here are that the metric is normalized and cross-disciplinary. JCI: 0.33 SJR: 0.345 SNIP: 0.46 CiteScore™:: 2.5 H-Index: 67

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ABCB1 Polymorphisms and Childhood Acute Lymphoblastic Leukemia Risk: A Meta-Analysis

Volume 27, Numéro 2, 2017, pp. 173-181
DOI: 10.1615/CritRevEukaryotGeneExpr.2017019077
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RÉSUMÉ

The association between ATP-binding cassette subfamily B member 1 (ABCB1) C3435T and C1236T polymorphisms and the risk for childhood acute lymphoblastic leukemia (ALL) is inconclusive. We conducted a meta-analysis of all published studies to determine the association of ABCB1 C3435T and C1236T polymorphisms and pediatric ALL risk. A systematic retrieval of relevant publications from the PubMed and Web of Science databases was performed. Data were calculated and statistical analysis was performed using STATA version 12.0 software. Metaanalysis results showed no significant association between C3435T polymorphism and pediatric ALL risk (TT vs. CC: odds ratio [OR] = 1.20, 95% confidence interval [CI] = 0.95–1.52; CT vs. CC: OR = 1.00, 95% CI = 0.82–1.23; the dominant model: OR = 1.07, 95% CI = 0.89–1.29; the recessive model: OR = 1.17, 95% CI = 0.84–1.62). Similarly, there was no association found for the C1236T polymorphism (TT vs. CC: OR = 1.18, 95% CI= 0.82–1.70; CT vs. CC: OR = 1.08, 95% CI = 0.80–1.45; the dominant model: OR = 1.10, 95% CI= 0.83–1.46; the recessive model: OR = 0.98, 95% CI = 0.61–1.58). Similar results were observed in the subgroup analyses on ethnicity and Hardy–Weinberg equilibrium. The present meta-analysis found no evidence for ABCB1 C3435T and C1236T polymorphisms as risk factors for pediatric ALL.

CITÉ PAR
  1. Li Yang, He Li-Ru, Gao Ying, Zhou Ning-Ning, Liu Yurong, Zhou Xin-Ke, Liu Ji-Fang, Guan Xin-Yuan, Ma Ning-Fang, Xie Dan, CHD1L contributes to cisplatin resistance by upregulating the ABCB1–NF-κB axis in human non-small-cell lung cancer, Cell Death & Disease, 10, 2, 2019. Crossref

  2. Liu Wei, Li Yan, Zhao Zhenhui, Li Xun, Clinical relevance of multi-drug resistance gene C3435T polymorphism in diffuse large B-cell lymphoma in Xinjiang, Medicine, 99, 35, 2020. Crossref

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