Hongli Wang

发表

A novel Alu-mediated 61-kb deletion of the von Willebrand factor (VWF) gene whose breakpoints co-locate with putative matrix attachment regions.

D. Cooper, N. Chuzhanova, F. Xie, 2006, Blood cells, molecules & diseases.

Six novel missense mutations causing factor X deficiency and application of thrombin generation test.

X. Xi, Q. Ding, Xue-feng Wang, 2013, Thrombosis research.

Efficient AAV1-AAV2 hybrid vector for gene therapy of hemophilia.

Wenman Wu, J. F. Wright, W. Xiao, 2006, Human gene therapy.

Enterovirus D68 virus-like particles expressed in Pichia pastoris potently induce neutralizing antibody responses and confer protection against lethal viral infection in mice

Chao Zhang, Wei Zhang, Qingwei Liu, 2018, Emerging Microbes & Infections.

Enhanced factor VIII heavy chain for gene therapy of hemophilia A.

X. Yang, R. Sarkar, Jinhui Wang, 2009, Molecular therapy : the journal of the American Society of Gene Therapy.

The enhancing effects of the light chain on heavy chain secretion in split delivery of factor VIII gene.

R. Sarkar, Juan Li, Xiao Xiao, 2007, Molecular therapy : the journal of the American Society of Gene Therapy.

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.

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.

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.

Dominant factor XI deficiency caused by mutations in the factor XI catalytic domain.

T. Dang, Wenman Wu, J. Meijers, 2004, Blood.

Clinical and genetic features of protein C deficiency in 23 unrelated Chinese patients.

Q. Ding, Xue-feng Wang, Hongli Wang, 2013, Blood cells, molecules & diseases.

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.

A novel fibrinogen Bβ chain frameshift mutation in a patient with severe congenital hypofibrinogenaemia

H. Ni, R. Zhou, Z. Zhai, 2006, Thrombosis and Haemostasis.

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.

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

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

Gene therapy for hemophilia B mediated by recombinant adeno-associated viral vector with hFIXR338A, a high catalytic activity mutation of human coagulation factor IX

Zhijian Wu, D. Lu, Hongli Wang, 2001, Science in China Series C: Life Sciences.

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.

Recombination in a Chinese haemophilia A family.

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

catalytic domain Dominant factor XI deficiency caused by mutations in the factor XI

T. Dang, Wenman Wu, J. Meijers, 2004 .

Molecular basis and thrombotic manifestations of antithrombin deficiency in 15 unrelated Chinese patients.

Tingting Yu, X. Xi, Q. Ding, 2013, Thrombosis research.

Identification of a novel splicing mutation in the fibrinogen gamma chain gene leading to dysfibrinogenaemia in a Chinese pedigree

Huayun Chen, Xiaobo Hu, Xue-feng Wang, 2015, Pathology.

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

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

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.

Characterisation and quantification of F8 transcripts of ten putative splice site mutations

X. Xi, Q. Ding, Xue-feng Wang, 2014, Thrombosis and Haemostasis.

Complete correction of hemophilia A with adeno-associated viral vectors containing a full-size expression cassette.

R. Sarkar, Jinhui Wang, W. Xiao, 2008, Human gene therapy.

Molecular and clinical profile of VWD in a large cohort of Chinese population: application of next generation sequencing and CNVplex® technique

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

[Type I antithrombin deficiency due to 13389G deletion in antithrombin gene].

Q. Ding, Q. Fu, Hongli Wang, 2002, Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi.

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.

Novel aberrant splicings caused by a splice site mutation (IVS1a+5g>a) in F7 gene

Wenman Wu, Q. Ding, Q. Fu, 2005, Thrombosis and Haemostasis.

[Gene diagnosis of hemophilia B by multiple STR analysis].

Yi Fang, Hongli Wang, H. Chu, 2002, Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi.

Maternal chromosome 4 heterodisomy/isodisomy and Bβ chain Trp323X mutation resulting in severe hypodysfibrinogenaemia

Yiping Shen, X. Xi, Q. Ding, 2012, Thrombosis and Haemostasis.

Type I coagulation factor V deficiency caused by compound heterozygous mutation of F5 gene

X. Wang, Z. Wang, Q. Ding, 2003, Haemophilia : the official journal of the World Federation of Hemophilia.

一个遗传性凝血因子XIII缺陷症家系的基因诊断

Q. Ding, Hongli Wang, Yun Shen, 2015, Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi.

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.