D. Deng

发表

Comprehensively analyze the expression and prognostic role for ten-eleven translocations (TETs) in acute myeloid leukemia

Yan Huang, Jie Wei, Xunjun Huang, 2020, Translational cancer research.

Targeted agents for chronic myelogenous leukemia: will that be the end of allogeneic bone marrow transplantation for that disease?

P. Schwarzenberger, Rongrong Liu, Jie Yang, 2010, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Liproxstatin-1 induces cell cycle arrest, apoptosis, and caspase-3/GSDME-dependent secondary pyroptosis in K562 cells

Y. Dai, D. Deng, P. Cheng, 2022, International journal of oncology.

Alterations of anticoagulant proteins and soluble endothelial protein C receptor in thalassemia patients of Chinese origin.

Y. Lai, Zhenfang Liu, Yuling Xu, 2018, Thrombosis research.

M. Xiong, Z. Huang, Jie Wei, 2021, Annals of translational medicine.

Combination of CsA, MTX and low-dose, short-course mycophenolate mofetil for GVHD prophylaxis

P. Schwarzenberger, J. Yang, W. Li, 2009, Bone Marrow Transplantation.

Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D region

Jie Yan, F. Lin, A. Wei, 2021, Hematology.

A novel fibrinogen gamma-chain mutation, p. γAla327Val, causes structural abnormality of D region and ultimately leads to congenital dysfibrinogenemia

Jie Yan, F. Lin, A. Wei, 2020, bioRxiv.

Identification the prognostic value of glutathione peroxidases expression levels in acute myeloid leukemia.

Wenqi Wu, Zhenfang Liu, Xinran Liu, 2020, Annals of translational medicine.

Fas-670A>G polymorphism is not associated with an increased risk of acute myeloid leukemia development

Z. Mo, Xiaobo Yang, Bing Zhang, 2015, Biomedical reports.

Over-expression of miR-196b-5p is significantly associated with the progression of myelodysplastic syndrome

Y. Lai, Zhenfang Liu, D. Deng, 2017, International Journal of Hematology.

Anti-epidermal growth factor receptor monoclonal antibody-based therapy for metastatic colorectal cancer: a meta-analysis of the effect of PIK3CA mutations in KRAS wild-type patients

Z. Mo, A. Tan, Xiaobo Yang, 2014, Archives of medical science : AMS.

Polymorphisms in the methylenetetrahydrofolate reductase gene (MTHFR) are associated with susceptibility to adult acute myeloid leukemia in a Chinese population.

Z. Mo, Xiaobo Yang, Bing Zhang, 2015, Cancer epidemiology.

Analyzing the key gene expression and prognostics values for acute myeloid leukemia

Yan Huang, Y. Lai, Jie Wei, 2020, Translational cancer research.

Identification the prognostic value of glutathione peroxidases expression levels in acute myeloid leukemia

Wenqi Wu, Zhenfang Liu, Xinran Liu, 2020, Annals of translational medicine.

GSTT1 and GSTM1 polymorphisms predict treatment outcome for acute myeloid leukemia: a systematic review and meta-analysis

Z. Mo, Xiaobo Yang, Bing Zhang, 2014, Annals of Hematology.

Analysis of the genetic variants associated with recurrent thromboembolism in a patient with hemoglobin H disease following splenectomy: A case report

Rongrong Liu, Y. Lai, D. Deng, 2016, Biomedical reports.

Congenital dysfibrinogenaemia assessed by whole blood thromboelastography

F. Lin, L. Liao, A. Wei, 2018, International journal of laboratory hematology.

Abnormal fibrinogen with an Aα 16Arg → Cys substitution is associated with multiple cerebral infarctions

Jie Yan, F. Lin, L. Liao, 2018, Journal of Thrombosis and Thrombolysis.

Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His

Jie Yan, F. Lin, L. Liao, 2016, Medicine.

A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A release

Jie Yan, F. Lin, L. Liao, 2017, International Journal of Hematology.

Management of dysfibrinogenemia in pregnancy: A case report

Jie Yan, F. Lin, L. Liao, 2018, Journal of clinical laboratory analysis.

A novel fibrinogen gamma-chain mutation, p.Cys165Arg, causes disruption of the γ165Cys-Bβ227Cys disulfide bond and ultimately leads to hypofibrinogenemia.

Jie Yan, F. Lin, L. Liao, 2018, Thrombosis research.

Dysfibrinogenemia in a patient undergoing artificial abortion after misdiagnosis and review of the literature.

Jie Yan, F. Lin, L. Liao, 2015, Clinica chimica acta; international journal of clinical chemistry.

Fibrinogen Clauss and prothrombin time derived method ratio can differentiate dysfibrinogenemia from hypofibrinogenemia and hyperfibrinogenemia.

Jie Yan, F. Lin, L. Liao, 2020, Thrombosis research.

Combined use of Clauss and prothrombin time‐derived methods for determining fibrinogen concentrations: Screening for congenital dysfibrinogenemia

Jie Yan, F. Lin, L. Liao, 2018, Journal of clinical laboratory analysis.

[Analysis of a family with congenital dysfibrinogenemia caused by an Arg275His mutation in the gamma chain of fibrinogen].

Jie Yan, F. Lin, L. Liao, 2016, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Favorable prognosis of biallelic CEBPA gene mutations in acute myeloid leukemia patients: a meta‐analysis

Z. Mo, Y. Lai, Bing Zhang, 2015, European journal of haematology.

Analysis of the genetic variants associated with recurrent thromboembolism in a patient with hemoglobin H disease following splenectomy: A case report

Rongrong Liu, Y. Lai, D. Deng, 2016, Biomedical reports.

miR-639在骨髓增生异常综合征中的表达及其靶基因预测

D. Deng, Hongying Li, Xupai Zhang, 2017, Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi.

Targeted agents for chronic myelogenous leukemia: will that be the end of allogeneic bone marrow transplantation for that disease?

P. Schwarzenberger, Rongrong Liu, Jie Yang, 2010, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.