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1

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

JING WANG, XUEFENG WANG, JING DAI, QIULAN DING, QIHUA FU, HONGLI WANG, LISONG SHEN, DAO LI

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 167 KB

english, 2009

2

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

Zhou, Jingyi, Ding, Qiulan, Wu, Wenman, Ouyang, Qi, Xie, Yinyin, Wu, Xi, Lu, Yeling, Dai, Jing, Liang, Qian, Wang, Hongli, Wang, Xuefeng, Hu, Yiqun

Journal:

Journal of Clinical Pathology

Année:

2017

Langue:

english

Fichier:

PDF, 2.56 MB

english, 2017

3

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

Ma, Siyu, Chen, Changming, Liang, Qian, Wu, Xi, Wang, Xuefeng, Wu, Wenman, Liu, Yan, Ding, Qiulan

Journal:

Orphanet Journal of Rare Diseases

Année:

2019

Langue:

english

Fichier:

PDF, 1.13 MB

english, 2019

4

Changes in Biomarkers of Coagulation, Fibrinolytic, and Endothelial Functions for Evaluating the Predisposition to Venous Thromboembolism in Patients With Hereditary Thrombophilia

Li, Lei, Gao, Lixia, Wu, Xi, Wu, Wenman, Ding, Qiulan, Wang, Xuefeng

Journal:

Clinical and Applied Thrombosis/Hemostasis

Année:

2020

Fichier:

PDF, 353 KB

2020

5

Access to functionalized 4-benzylidene-4H-benzo[d][1,3]thiazines via tandem addition-cyclization/cross-coupling reactions

Qiuping Ding, Xianjin Liu, Jinsheng Yu, Qiulan Zhang, Dan Wang, Banpeng Cao, Yiyuan Peng

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 414 KB

english, 2012

6

ChemInform Abstract: Access to Functionalized 4-Benzylidene-4H-benzo[d][1,3]thiazines via Tandem Addition-Cyclization/Cross-Coupling Reactions.

Qiuping Ding, Xianjin Liu, Jinsheng Yu, Qiulan Zhang, Dan Wang, Banpeng Cao, Yiyuan Peng

Journal:

Année:

2012

Fichier:

PDF, 41 KB

2012

7

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

Ding, Qiulan, Shen, Wei, Ye, Xu, Wu, Yingting, Wang, Xuefeng, Wang, Hongli

Journal:

Blood Cells, Molecules, and Diseases

Année:

2013

Langue:

english

Fichier:

PDF, 176 KB

english, 2013

8

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

Liang, Qian, Chen, Qiong, Ding, Qiulan, Wu, Fang, Wang, Xuefeng, Xi, Xiaodong, Wang, Hongli

Journal:

Thrombosis Research

Année:

2013

Langue:

english

Fichier:

PDF, 633 KB

english, 2013

9

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

Ding, Qiulan, Wang, Min, Xu, Guanqun, Ye, Xu, Xi, Xiaodong, Yu, Tingting, Wang, Xuefeng, Wang, Hongli

Journal:

Thrombosis Research

Année:

2013

Langue:

english

Fichier:

PDF, 800 KB

english, 2013

10

Characterization of the Heparin-Binding Site of the Protein Z-Dependent Protease Inhibitor

Yang, Likui, Ding, Qiulan, Huang, Xin, Olson, Steven T., Rezaie, Alireza R.

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 1.80 MB

english, 2012

11

Efficient AAV1–AAV2 Hybrid Vector for Gene Therapy of Hemophilia

Hauck, Bernd, Xu, Ray Ruian, Xie, Jing, Wu, Wenman, Ding, Qiulan, Sipler, Matthew, Wang, Hongli, Chen, Ling, Wright, J. Fraser, Xiao, Weidong

Journal:

Human Gene Therapy

Année:

2006

Langue:

english

Fichier:

PDF, 197 KB

english, 2006

12

Complete Correction of Hemophilia A with Adeno-Associated Viral Vectors Containing a Full-Size Expression Cassette

Lu, Hui, Chen, Lingxia, Wang, Jinhui, Huack, Bernd, Sarkar, Rita, Zhou, Shangzhen, Xu, Ray, Ding, Qiulan, Wang, Xuefeng, Wang, Hongli, Xiao, Weidong

Journal:

Human Gene Therapy

Année:

2008

Langue:

english

Fichier:

PDF, 100 KB

english, 2008

13

Identification of anti-moesin antibodies in the serums of patients with antiphospholipid syndrome

Lin, Xiaoyi, Liang, Qian, Lin, Lin, Ding, Qiulan, Wang, Xuefeng, Wang, Ying

Journal:

Thrombosis Research

Année:

2015

Langue:

english

Fichier:

PDF, 378 KB

english, 2015

14

High resolution single nucleotide polymorphism array reveals cryptic indicating information about myelodysplastic syndrome-related myeloid malignancies

Chi, Kun, Li, Yang, Ding, Qiulan, Xu, Lan, Chen, Yu, Wang, Xuefeng

Journal:

Leukemia and Lymphoma

Année:

2015

Langue:

english

Fichier:

PDF, 654 KB

english, 2015

15

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

Zhou, Jingyi, Ding, Qiulan, Chen, Yaopeng, Ouyang, Qi, Jiang, Linlin, Dai, Jing, Lu, Yeling, Wu, Xi, Liang, Qian, Wang, Hongli, Wang, Xuefeng

Journal:

Blood Cells, Molecules, and Diseases

Année:

2015

Langue:

english

Fichier:

PDF, 1.19 MB

english, 2015

16

The Enhancing Effects of the Light Chain on Heavy Chain Secretion in Split Delivery of Factor VIII Gene

Chen, Lingxia, Zhu, Fuxiang, Li, Juan, Lu, Hui, Jiang, Haiyan, Sarkar, Rita, Arruda, Valder R, Wang, Jinhui, Zhao, Jennifer, Pierce, Glenn F, Ding, Qiulan, Wang, Xuefeng, Wang, Hongli, Pipe, Steven W,

Journal:

Molecular Therapy

Année:

2007

Langue:

english

Fichier:

PDF, 195 KB

english, 2007

17

PML/RARα Fusion Protein Transactivates the Tissue Factor Promoter through a GAGC-Containing Element without Direct DNA Association

Jinsong Yan, Kankan Wang, Leiming Dong, Hongchen Liu, Weiqin Chen, Wenda Xi, Qiulan Ding, Nelly Kieffer, Jacques P. Caen, Saijuan Chen, Zhu Chen and Xiaodong Xi

Journal:

Proceedings of the National Academy of Sciences

Année:

2010

Langue:

english

Fichier:

PDF, 1.34 MB

english, 2010

18

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

Shao, Yanyan, Cao, Yanan, Lu, Yeling, Dai, Jing, Ding, Qiulan, Wang, Xuefeng, Xi, Xiaodong, Wang, Hongli

Journal:

Blood Cells, Molecules, and Diseases

Année:

2016

Langue:

english

Fichier:

PDF, 943 KB

english, 2016

19

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

Zhou, Jingyi, Xin, Yu, Ding, Qiulan, Jiang, Linlin, Chen, Yaopeng, Dai, Jing, Lu, Yeling, Wu, Xi, Liang, Qian, Wang, Hongli, Wang, Xuefeng

Journal:

Clinical and Experimental Pharmacology and Physiology

Année:

2016

Langue:

english

Fichier:

PDF, 501 KB

english, 2016

20

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

Ye, Xu, Feng, Ying, Ding, Qiulan, Dai, Jing, Wang, Xuefeng

Journal:

Blood Coagulation & Fibrinolysis

Année:

2011

Langue:

english

Fichier:

PDF, 185 KB

english, 2011

21

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

Yu, Tingting, Dai, Jing, Liu, Hongjing, Ding, Qiulan, Lu, Yelin, Wang, Hongli, Wang, Xuefeng, Fu, Qihua

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 94 KB

english, 2012

22

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

Xin, Yu, Zhou, Jingyi, Ding, Qiulan, Chen, Changming, Wu, Xi, Wang, Xuefeng, Wang, Hongli, Jiang, Xiaofeng

Journal:

Journal of Clinical Pathology

Année:

2017

Langue:

english

Fichier:

PDF, 455 KB

english, 2017

23

An exonic missense mutation c.28G>A is associated with weak B blood group by affecting RNA splicing of the ABO gene

Cai, Xiaohong, Qian, Chengrui, Wu, Wenman, Lei, Hang, Ding, Qiulan, Zou, Wei, Xiang, Dong, Wang, Xuefeng

Journal:

Transfusion (Elsevier)

Année:

2017

Langue:

english

Fichier:

PDF, 568 KB

english, 2017

24

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

Yu, Tingting, Dai, Jing, Liu, Hongjing, Wang, Jian, Ding, Qiulan, Wang, Hongli, Wang, Xuefeng, Fu, Qihua

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 182 KB

english, 2012

25

On box-perfect graphs

Ding, Guoli, Zang, Wenan, Zhao, Qiulan

Journal:

Journal of Combinatorial Theory, Series B

Année:

2017

Langue:

english

Fichier:

PDF, 1.27 MB

english, 2017

26

Evaluation of the new Chinese Disseminated Intravascular Coagulation Scoring System in critically ill patients: A multicenter prospective study

Wu, Yingying, Luo, Lili, Niu, Ting, Han, Yue, Feng, Ying, Ding, Qiulan, Huang, Ruibin, Zhang, Xiaohui, Feng, Jianming, Hou, Ming, Peng, Jun, Li, Yan, Zhou, Yuhong, Su, Lei, Yang, Linhua, Zhou, Zeping,

Journal:

Scientific Reports

Année:

2017

Langue:

english

Fichier:

PDF, 1.04 MB

english, 2017

27

Screening and functional exploration of prothrombin Arg596 related mutations in Chinese venous thromboembolism patients

Wu, Xi, Li, Lei, Ding, Qiulan, Wang, Xuefeng, Wu, Fang, Wu, Wenman

Journal:

Journal of Clinical Pathology

Année:

2018

Langue:

english

Fichier:

PDF, 1.33 MB

english, 2018

28

Rap1 deficiency-provoked paracrine dysfunction impairs immunosuppressive potency of mesenchymal stem cells in allograft rejection of heart transplantation

Ding, Yue, Liang, Xiaoting, Zhang, Yuelin, Yi, Li, Shum, Ho Cheung, Chen, Qiulan, Chan, Barbara P., Fan, Huimin, Liu, Zhongmin, Tergaonkar, Vinay, Qi, Zhongquan, Tse, Hung-fat, Lian, Qizhou

Journal:

Cell Death and Disease

Année:

2018

Langue:

english

Fichier:

PDF, 3.86 MB

english, 2018

29

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

Liang, Qian, Qin, Huanhuan, Ding, Qiulan, Xie, Xiaoling, Wu, Runhui, Wang, Hongli, Hu, Yiqun, Wang, Xuefeng

Journal:

Thrombosis and Haemostasis

Année:

2017

Langue:

english

Fichier:

PDF, 328 KB

english, 2017

30

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

Chen, Changming, Yang, Likui, Villoutreix, Bruno O., Wang, Xuefeng, Ding, Qiulan, Rezaie, Alireza R.

Journal:

Thrombosis and Haemostasis

Année:

2017

Langue:

english

Fichier:

PDF, 830 KB

english, 2017

31

Expression and functional characterisation of natural R147W and K150del variants of protein C in the Chinese population

Ding, Qiulan, Yang, Likui, Hassanian, Seyed, Rezaie, Alireza R.

Journal:

Thrombosis and Haemostasis

Année:

2013

Langue:

english

Fichier:

PDF, 1.19 MB

english, 2013

32

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

Wu, Xi, Ding, Qiulan, Wang, Xuefeng, Dai, Jing, Wu, Wenman

Journal:

BMC Medical Genetics

Année:

2018

Langue:

english

Fichier:

PDF, 412 KB

english, 2018

33

A Unique Feature of Iron Loss via Close Adhesion of Helicobacter pylori to Host Erythrocytes

Wang, Zhiwei, Zhang, Lijuan, Guo, Zhi, Liu, Lei, Ji, Jun, Zhang, Jianian, Chen, Xuehua, Liu, Bingya, Zhang, Jun, Ding, Qiulan, Wang, Xuefeng, Zhao, Wei, Zhu, Zhenggang, Yu, Yingyan, Glogauer, Michael

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 1.43 MB

english, 2012

34

Occurence of haemophilia A and B in a Chinese family with mosaicism of the F9 gene mutation in the HB index‘s maternal grandfather

Lu, Yeling, Xie, Bingshou, Ding, Qiulan, Dai, Jing, Xi, Xiaodong, Wang, Mingshan, Wang, Hongli, Wang, Xuefeng

Journal:

Thrombosis and Haemostasis

Année:

2010

Langue:

english

Fichier:

PDF, 85 KB

english, 2010

35

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

Liang, Qian, Xiang, Mingjie, Lu, Yeling, Ruan, Yufeng, Ding, Qiulan, Wang, Xuefeng, Xi, Xiaodong, Wang, Hongli

Journal:

Thrombosis and Haemostasis

Année:

2015

Langue:

english

Fichier:

PDF, 306 KB

english, 2015

36

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

You, Guoling, Chi, Kun, Lu, Yeling, Ding, Qiulan, Dai, Jing, Xi, Xiaodong, Wang, Hongli, Wang, Xuefeng

Journal:

Thrombosis and Haemostasis

Année:

2014

Langue:

english

Fichier:

PDF, 512 KB

english, 2014

37

Paradoxical bleeding and thrombotic episodes of dysprothrombinaemia due to a homozygous Arg382His mutation

Ding, Qiulan, Yang, Likui, Zhao, Xiaoqing, Wu, Wenman, Wang, Xuefeng, Rezaie, Alireza R.

Journal:

Thrombosis and Haemostasis

Année:

2017

Langue:

english

Fichier:

PDF, 566 KB

english, 2017

38

The missense Thr211Pro mutation in the factor X activation peptide of a bleeding patient causes molecular defect in the clotting cascade

Ding, Qiulan, Shen, Yiping, Yang, Likui, Wang, Xuefeng, Rezaie, Alireza

Journal:

Thrombosis and Haemostasis

Année:

2013

Langue:

english

Fichier:

PDF, 772 KB

english, 2013

39

A multicenter, prospective evaluation of the Chinese Society of Thrombosis and Hemostasis Scoring System for disseminated intravascular coagulation

Luo, Lili, Wu, Yingying, Niu, Ting, Han, Yue, Feng, Ying, Ding, Qiulan, Huang, Ruibin, Zhang, Xiaohui, Feng, Jianming, Hou, Ming, Peng, Jun, Li, Yan, Zhou, Yuhong, Su, Lei, Yang, Linhua, Zhou, Zeping,

Journal:

Thrombosis Research

Année:

2018

Langue:

english

Fichier:

PDF, 3.20 MB

english, 2018

40

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

Ding, Qiulan, Wu, Wenman, Fu, Qihua, Wang, Xuefeng, Hu, Yiqun, Wang, Hongli, Wang, Zhenyi

Journal:

Thrombosis and Haemostasis

Année:

2005

Langue:

english

Fichier:

PDF, 253 KB

english, 2005

41

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

Xie, Xiaoling, Chen, Changming, Liang, Qian, Wu, Xi, Wang, Xuefeng, Wu, Wenman, Ding, Qiulan

Journal:

Année:

2019

Fichier:

PDF, 948 KB

2019

42

An Unexpected Dynamic Binding Mode between Coagulation Factor X and Rivaroxaban Reveals Importance of Flexibility in Drug Binding

Qu, Si‐Ying, Xu, Qin, Wu, Wenman, Li, Fang, Li, Cheng‐Dong, Huang, Ran, Ding, Qiulan, Wei, Dong‐Qing

Journal:

Chemical Biology & Drug Design

Année:

2019

Langue:

english

Fichier:

PDF, 792 KB

english, 2019

43

Development of combine grain yield monitor system with self-feedback function

Changhua, Lu, Xiaofei, An, Hai, Ding, Weiqiang, Fu, Liwei, Li, Qiulan, Wu, Zhijun, Meng

Journal:

IFAC-PapersOnLine

Année:

2018

Langue:

english

Fichier:

PDF, 555 KB

english, 2018

44

Recombination in a Chinese haemophilia A family

Lu, Yeling, Wang, Xuefeng, Ding, Qiulan, Dai, Jing, Xi, Xiaodong, Wang, Hongli

Journal:

Année:

2008

Langue:

english

Fichier:

PDF, 1.15 MB

english, 2008

45

Ranking tournaments with no errors I: Structural description

Chen, Xujin, Ding, Guoli, Zang, Wenan, Zhao, Qiulan

Journal:

Journal of Combinatorial Theory, Series B

Année:

2019

Langue:

english

Fichier:

PDF, 1.47 MB

english, 2019

46

Ranking tournaments with no errors I: Structural description

Chen, Xujin, Ding, Guoli, Zang, Wenan, Zhao, Qiulan

Journal:

Journal of Combinatorial Theory, Series B

Année:

2019

Fichier:

PDF, 1.47 MB

2019

47

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

Wu, Xi, Dai, Jing, Xu, Xiaoqian, Li, Fang, Li, Lei, Lu, Yeling, Xu, Qin, Ding, Qiulan, Wu, Wenman, Wang, Xuefeng

Journal:

Arteriosclerosis Thrombosis and Vascular Biology

Année:

2019

Langue:

english

Fichier:

PDF, 1.45 MB

english, 2019

48

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

Wu, Xi, Dai, Jing, Xu, Xiaoqian, Li, Fang, Li, Lei, Lu, Yeling, Xu, Qin, Ding, Qiulan, Wu, Wenman, Wang, Xuefeng

Journal:

Arteriosclerosis Thrombosis and Vascular Biology

Année:

2019

Fichier:

PDF, 1.45 MB

2019

49

Ranking tournaments with no errors II: Minimax relation

Chen, Xujin, Ding, Guoli, Zang, Wenan, Zhao, Qiulan

Journal:

Journal of Combinatorial Theory, Series B

Année:

2019

Fichier:

PDF, 1.52 MB

2019

50

Gly197Arg mutation in protein C causes recurrent thrombosis in a heterozygous carrier

Lu, Yeling, Giri, Hemant, Villoutreix, Bruno O., Ding, Qiulan, Wang, Xuefeng, Rezaie, Alireza R.

Journal:

Journal of Thrombosis and Haemostasis

Année:

2020

Fichier:

PDF, 1.43 MB

2020