J. Dai

发表

Female hemophilia A heterozygous for a de novo frameshift and a novel missense mutation of factor VIII

Q. Ding, X-H Cai, X-F Wang, 2006, Journal of thrombosis and haemostasis : JTH.

Inactivated SARS-CoV-2 vaccine does not influence the profile of prothrombotic antibody nor increase the risk of thrombosis in a prospective Chinese cohort

J. Qu, Xinxin Zhang, J. Dai, 2021, Science Bulletin.

A rapid multifluorescent polymerase chain reaction for genetic counselling in Chinese haemophilia A families

X-F Wang, J. Dai, Y. Fang, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

Agent Targeting to P-selectin MR Molecular Imaging of Thrombus : Development and Application of a Gd-based Novel Contrast

Q. Ding, Hai-liang Ge, J. Dai, 2009 .

Genomic Analysis of Mycobacterium abscessus Complex Isolates from Patients with Pulmonary Infection in China

Yan Zhu, Jing Lu, J. Dai, 2022, Microbiology Spectrum.

Genomic Analysis of Mycobacterium abscessus Complex Isolates from Patients with Pulmonary Infection in China

Yan Zhu, Jing Lu, J. Dai, 2022, Microbiology spectrum.

Haemophilia A in two unrelated females due to F8 gene inversions combined with skewed inactivation of X chromosome

X. Xi, Q. Ding, J. Dai, 2009, Thrombosis and Haemostasis.

Characterisation of large F9 deletions in seven unrelated patients with severe haemophilia B

X. Wu, X. Xi, Q. Ding, 2014, Thrombosis and Haemostasis.

A case of factor XI deficiency caused by compound heterozygous F11 gene mutation

Jing Wang, Q. Ding, J. Dai, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

Homozygous protein C deficiency with late onset venous thrombosis: identification and in vitro expression study of a novel Pro275Ser mutation

Tingting Yu, Jian Wang, Q. Ding, 2012, Pathology.

Thromboelastography predicts risks of obstetric complication occurrence in (hypo)dysfibrinogenemia patients under non‐pregnant state

Q. Ding, J. Dai, Xue-feng Wang, 2016, Clinical and experimental pharmacology & physiology.

Dysfibrinogenemia-associated novel heterozygous mutation, Shanghai (FGA c.169_180+2 del), leads to N-terminal truncation of fibrinogen Aα chain and impairs fibrin polymerization

Wenman Wu, Yin-yin Xie, Q. Ding, 2016, Journal of Clinical Pathology.

Molecular basis of type I antithrombin deficiency in two women with recurrent venous thromboembolism in the first trimester of pregnancy.

X. Xi, Q. Ding, J. Dai, 2012, Blood cells, molecules & diseases.

Clinical features and molecular basis of 102 Chinese patients with congenital dysfibrinogenemia.

Q. Ding, J. Dai, Xue-feng Wang, 2015, Blood cells, molecules & diseases.

Maternal microchimerism protects hemophilia A patients from inhibitor development.

Wenman Wu, Zhenping Chen, R. Wu, 2020, Blood advances.

Impact of polymorphisms in genes involved in autoimmune disease on inhibitor development in Chinese patients with haemophilia A

Q. Ding, J. Dai, Xue-feng Wang, 2011, Thrombosis and Haemostasis.

Spectrum of F9 mutations in Chinese haemophilia B patients: identification of 20 novel mutations

Tingting Yu, Q. Ding, J. Dai, 2012, Pathology.

Spectrum and origin of mutations in sporadic cases of haemophilia A in China

X. Wu, Q. Ding, J. Dai, 2018, Haemophilia : the official journal of the World Federation of Hemophilia.

Recombination in a Chinese haemophilia A family.

X. Xi, Q. Ding, J. Dai, 2008, Pathology.

Characterization of large deletions in the F8 gene using multiple competitive amplification and the genome walking technique

X. Xi, X. Wang, Q. Ding, 2013, Journal of thrombosis and haemostasis : JTH.

The characteristics and spectrum of F9 mutations in Chinese sporadic haemophilia B pedigrees

Wenman Wu, Q. Ding, J. Dai, 2019, Haemophilia : the official journal of the World Federation of Hemophilia.

Characterisation and validation of a novel panel of the six short tandem repeats for genetic counselling in Chinese haemophilia A pedigrees

X. Xi, X. Wang, Q. Ding, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

Prevalence of the factor 8 gene intron 1 inversion in Chinese haemophiliacs and its application to carrier detection and prenatal diagnosis in haemophilia A families

X. Xi, X. Wang, Q. Ding, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.

Identification and characterisation of a novel aberrant pattern of intron 1 inversion with concomitant large insertion and deletion within the F8 gene

X. Xi, Q. Ding, J. Dai, 2014, Thrombosis and Haemostasis.

The prevalence of heterozygous F12 mutations in Chinese population and its relevance to incidents of thrombosis

Wenman Wu, Q. Ding, J. Dai, 2018, BMC Medical Genetics.

A novel mutation in a patient with congenital coagulation factor XII deficiency.

J. Dai, Ying Pang, Xue-feng Wang, 2008, Chinese medical journal.

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

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

Hereditary protein C deficiency: a case report.

Q. Ding, J. Dai, P. Jin, 2007, Pathology.

Prothrombin Arg541Trp Mutation Leads to Defective PC (Protein C) Pathway Activation and Constitutes a Novel Genetic Risk Factor for Venous Thrombosis

Lei Li, Wenman Wu, Q. Ding, 2019, Arteriosclerosis, thrombosis, and vascular biology.

Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia

X-H Cai, X-F Wang, J. Dai, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

[A heterozygous point mutation G13328A in antithrombin gene causes thrombosis].

Q. Ding, J. Dai, Q. Fu, 2005, Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi.

Genetic analysis of a pedigree with combined factor XII and factor XI deficiency

Q. Ding, J. Dai, X. Ye, 2011, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Clinical manifestations and mutation spectrum of 57 subjects with congenital factor XI deficiency in China.

X. Xi, Q. Ding, J. Dai, 2016, Blood cells, molecules & diseases.

Hereditary protein C deficiency caused by compound heterozygous mutants in two independent Chinese families

Hui Chen, Q. Ding, J. Dai, 2014, Pathology.

The status of carrier and prenatal diagnosis of haemophilia in China

X. Xi, Q. Ding, J. Dai, 2012, Haemophilia.

[Intron 1 and 22 inversions in factor VIII gene in patients with haemophilia A].

Q. Ding, J. Dai, Tan Li, 2009, Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi.

Identification of a novel splicing mutation in the fibrinogen Aα chain gene leading to hypofibrinogenaemia in a Chinese pedigree

X. Wang, X. Xi, Q. Ding, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

CD36 mediates SARS-CoV-2-envelope-protein-induced platelet activation and thrombosis

Junling Liu, J. Dai, Chengde Yang, 2023, Nature communications.

[Inherited afibrinogenemia caused by compound heterozygous mutations in the beta beta-chain of fibrinogen].

J. Dai, Q. Fu, R. Zhou, 2005, Zhongguo shi yan xue ye xue za zhi.

Using a minigene approach to characterize a novel splice site mutation in human F7 gene causing inherited factor VII deficiency in a Chinese pedigree

X. Wang, X. Xi, Q. Ding, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

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.

Structural and functional characterization of novel F7 mutations identified in Chinese factor VII‐deficient patients

Wenman Wu, Q. Ding, J. Dai, 2023, British journal of haematology.

Impact of polymorphisms in genes involved in autoimmune disease on inhibitor development in Chinese patients with haemophilia A

Q. Ding, J. Dai, Hongli Wang, 2011, Thrombosis and Haemostasis.