Changming Chen

发表

Complex recombination with deletion in the F8 and duplication in the TMLHE mediated by int22h copies during early embryogenesis

Wenman Wu, Q. Ding, Xue-feng Wang, 2017, Thrombosis and Haemostasis.

Gly74Ser mutation in protein C causes thrombosis due to a defect in protein S-dependent anticoagulant function

B. Villoutreix, Q. Ding, A. Rezaie, 2017, Thrombosis and Haemostasis.

Factor IX alteration p.Arg338Gln (FIX Shanghai) potentiates FIX clotting activity and causes thrombosis

Wenman Wu, Q. Ding, C. A. Valencia, 2020, Haematologica.

A pericentric inversion of chromosome X disrupting F8 and resulting in haemophilia A

Q. Ding, Xue-feng Wang, Hongli Wang, 2017, Journal of Clinical Pathology.

Phenotype and genotype of FXIII deficiency in two unrelated probands: identification of a novel F13A1 large deletion mediated by complex rearrangement

Wenman Wu, Q. Ding, Yan Liu, 2019, Orphanet journal of rare diseases.

The novel mutation p.Asp315Tyr causes severe hemophilia B by impairing coagulation factor IX expression.

Wenman Wu, Hongying Wei, Changming Chen, 2020, Thrombosis research.

AccuCopy quantification combined with pre-amplification of long-distance PCR for fast analysis of intron 22 inversion in haemophilia A.

Xue-feng Wang, Zhengwen Jiang, Q. Ding, 2016, Clinica chimica acta; international journal of clinical chemistry.

Characterization of two large duplications of F9 associated with mild and severe haemophilia B, respectively

Wenman Wu, Q. Ding, Xue-feng Wang, 2019, Haemophilia : the official journal of the World Federation of Hemophilia.

Unraveling the molecular basis underlying nine putative splice site variants of von Willebrand factor

Wenman Wu, Q. Ding, J. Dai, 2021, Human mutation.

Effects of 14 F9 synonymous codon variants on hemophilia B expression: Alteration of splicing along with protein expression

Wenman Wu, Q. Ding, Xue-feng Wang, 2022, Human mutation.

Unexpected Dynamic Binding May Rescue the Binding Affinity of Rivaroxaban in a Mutant of Coagulation Factor X

Q. Ding, Changming Chen, Zhi-Li Zhang, 2022, Frontiers in Molecular Biosciences.

Circulating RBP4 Increase and Its Diagnosis of Chronic Kidney Disease.

Changming Chen, C. Xun, Yong Zhao, 2018, Annals of clinical and laboratory science.

The Disulfide Bond between Cys22 and Cys27 in the Protease Domain Modulate Clotting Activity of Coagulation Factor X

Lei Li, Dongqing Wei, Mingzhu Zhao, 2019, Thrombosis and Haemostasis.

Coagulation and Fibrinolysis Gly 74 Ser mutation in protein C causes thrombosis due to a defect in protein S-dependent anticoagulant function

B. Villoutreix, Q. Ding, A. Rezaie, 2017 .

Activation of Platelet mTORC2/Akt Pathway by Anti-β2GP1 Antibody Promotes Thrombosis in Antiphospholipid Syndrome

Junling Liu, J. Dai, Chengde Yang, 2023, Arteriosclerosis, thrombosis, and vascular biology.