The association of miR34b/c and TP53 gene polymorphisms with Wilms tumor risk in Chinese children
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Zhen Wang | Jing He | Jinhong Zhu | Haixia Zhou | Ju-xiang Wang | Yixiao Mo | Ji-Chen Ruan | Jiandong Shi | Xiao-kai Huang | Susu Lou | X. Tian | Jiandong Shi
[1] Jing He,et al. The association of RAN and RANBP2 gene polymerphisms with Wilms tumor risk in Chinese children , 2020, Journal of Cancer.
[2] Shuai Jiang. Special issue editorial: Recent progress of MicroRNA research in immunity. , 2019, Cancer letters.
[3] Jian Zhang,et al. Association between rs4938723 polymorphism and the risk of primary open‐angle glaucoma (POAG) in a Chinese population , 2019, Journal of cellular biochemistry.
[4] Jing He,et al. MYCN gene polymorphisms and Wilms tumor susceptibility in Chinese children , 2019, Journal of clinical laboratory analysis.
[5] H. Xia,et al. Association of miR-34b/c rs4938723 and TP53 Arg72Pro Polymorphisms with Neuroblastoma Susceptibility: Evidence from Seven Centers , 2019, Translational oncology.
[6] V. Rotter,et al. p53 balances between tissue hierarchy and anarchy , 2019, Journal of molecular cell biology.
[7] J. Soh,et al. Droplet digital PCR as a novel system for the detection of microRNA‑34b/c methylation in circulating DNA in malignant pleural mesothelioma. , 2019, International journal of oncology.
[8] N. Cho,et al. p53 expression status is associated with cancer-specific survival in stage III and high-risk stage II colorectal cancer patients treated with oxaliplatin-based adjuvant chemotherapy , 2019, British Journal of Cancer.
[9] H. Xia,et al. Association of KRAS and NRAS gene polymorphisms with Wilms tumor risk: a four-center case-control study , 2019, Aging.
[10] J. Kurie,et al. MiR-34a and miR-34b/c have distinct effects on the suppression of lung adenocarcinomas , 2019, Experimental & Molecular Medicine.
[11] P. Liu,et al. TP53 rs1042522 C>G polymorphism and Wilms tumor susceptibility in Chinese children: a four-center case–control study , 2019, Bioscience reports.
[12] S. Ghavami,et al. Association between miR‐34b/c rs4938723 polymorphism and risk of cancer: An updated meta‐analysis of 27 case‐control studies , 2018, Journal of cellular biochemistry.
[13] P. Radice,et al. Genetic and epigenetic analyses guided by high resolution whole-genome SNP array reveals a possible role of CHEK2 in Wilms tumour susceptibility , 2018, Oncotarget.
[14] H. Xia,et al. Base Excision Repair Gene Polymorphisms and Wilms Tumor Susceptibility , 2018, EBioMedicine.
[15] N. Phuong,et al. Methylation profiles of miR34 gene family in Vietnamese patients suffering from breast and lung cancers. , 2018, Molecular medicine reports.
[16] D. Canning. Re: Risk of Adverse Health and Social Outcomes up to 50 Years after Wilms Tumor: The British Childhood Cancer Survivor Study. , 2018, The Journal of urology.
[17] H. Xia,et al. Association of Common Genetic Variants in Pre-microRNAs and Neuroblastoma Susceptibility: A Two-Center Study in Chinese Children , 2018, Molecular therapy. Nucleic acids.
[18] Ying Zhu,et al. Exome-wide analyses identify low-frequency variant in CYP26B1 and additional coding variants associated with esophageal squamous cell carcinoma , 2018, Nature Genetics.
[19] M. Hashemi,et al. Association between Pri-miR-34b/c rs4938723 polymorphism and bladder cancer risk , 2017, Journal of biomedical research.
[20] T. Cai,et al. Genetic predisposition to lung cancer: comprehensive literature integration, meta-analysis, and multiple evidence assessment of candidate-gene association studies , 2017, Scientific Reports.
[21] Zhuorong Zhang,et al. The TP53 gene rs1042522 C>G polymorphism and neuroblastoma risk in Chinese children , 2017, Aging.
[22] H. Xia,et al. Association between TP53 gene Arg72Pro polymorphism and Wilms' tumor risk in a Chinese population. , 2017, OncoTargets and therapy.
[23] Jinhong Zhu,et al. BARD1 Gene Polymorphisms Confer Nephroblastoma Susceptibility , 2017, EBioMedicine.
[24] Xuejun Zhang,et al. pri-miR-34b/c rs4938723 polymorphism is associated with hepatocellular carcinoma risk: a case-control study in a Chinese population. , 2017, International journal of molecular epidemiology and genetics.
[25] Jiaoyuan Li,et al. Genetic variants in the regulatory region of SLC10A1 are not associated with the risk of hepatitis B virus infection and clearance. , 2016, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.
[26] James R. Anderson,et al. Association of Chromosome 1q Gain With Inferior Survival in Favorable-Histology Wilms Tumor: A Report From the Children's Oncology Group. , 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[27] H. Xia,et al. Association of potentially functional variants in the XPG gene with neuroblastoma risk in a Chinese population , 2016, Journal of cellular and molecular medicine.
[28] C. Shaw,et al. Mutations in the transcriptional repressor REST predispose to Wilms tumor , 2015, Nature Genetics.
[29] Shu Liu,et al. Association of p53 rs1042522, MDM2 rs2279744, and p21 rs1801270 polymorphisms with retinoblastoma risk and invasion in a Chinese population , 2015, Scientific Reports.
[30] V. Vaira,et al. Deregulation of MiR-34b/Sox2 Predicts Prostate Cancer Progression , 2015, PloS one.
[31] C. Peng,et al. Association between miR34b/c Polymorphism rs4938723 and Cancer Risk: A Meta-Analysis of 11 Studies including 6169 Cases and 6337 Controls , 2014, Medical science monitor : international medical journal of experimental and clinical research.
[32] S. Seal,et al. Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour , 2014, Nature Communications.
[33] C. Hother,et al. Diffuse large B-cell lymphoma with combined TP53 mutation and MIR34A methylation: Another “double hit” lymphoma with very poor outcome? , 2013, Oncotarget.
[34] E. Lerut,et al. p53 Immunohistochemistry expression in Wilms tumor: a prognostic tool in the detection of tumor aggressiveness. , 2013, The Journal of urology.
[35] H. Seuánez,et al. WT1, WTX and CTNNB1 mutation analysis in 43 patients with sporadic Wilms' tumor. , 2013, Oncology reports.
[36] A. Ashworth,et al. Molecular profiling reveals frequent gain of MYCN and anaplasia‐specific loss of 4q and 14q in wilms tumor , 2011, Genes, chromosomes & cancer.
[37] D. Jin,et al. Epigenetic inactivation of the MIR34B/C in multiple myeloma. , 2011, Blood.
[38] Hongbing Shen,et al. A potentially functional polymorphism in the promoter region of miR‐34b/c is associated with an increased risk for primary hepatocellular carcinoma , 2011, International journal of cancer.
[39] M. Stratton,et al. Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene , 2009, Journal of Medical Genetics.
[40] V. Huff,et al. Wilms tumor genetics: Mutations in WT1, WTX, and CTNNB1 account for only about one‐third of tumors , 2008, Genes, chromosomes & cancer.
[41] N. Nowak,et al. Fine structure analysis of the WT1 gene in sporadic Wilms tumors. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[42] B. Williams,et al. Mutations of the p53 tumor suppressor gene occur infrequently in Wilms' tumor. , 1994, Cancer research.
[43] N. Lemoine,et al. Aberrant expression of the tumour suppressor gene p53 is very frequent in Wilms' tumours , 1992, The Journal of pathology.