Ding Q - Search Results

1

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

Ding Q, Yang L, Hassanian SM, Rezaie AR. Ding Q, et al. Thromb Haemost. 2013 Apr;109(4):614-24. doi: 10.1160/TH12-10-0760. Epub 2013 Feb 7. Thromb Haemost. 2013. PMID: 23389250 Free PMC article.

2

Characterization of the heparin-binding site of the protein z-dependent protease inhibitor.

Yang L, Ding Q, Huang X, Olson ST, Rezaie AR. Yang L, et al. Among authors: ding q. Biochemistry. 2012 May 15;51(19):4078-85. doi: 10.1021/bi300353c. Epub 2012 May 2. Biochemistry. 2012. PMID: 22540147 Free PMC article.

3

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

Ding Q, Shen Y, Yang L, Wang X, Rezaie AR. Ding Q, et al. Thromb Haemost. 2013 Jul;110(1):53-61. doi: 10.1160/TH13-03-0184. Epub 2013 May 16. Thromb Haemost. 2013. PMID: 23677006 Free PMC article.

4

Protein C Thr315Ala variant results in gain of function but manifests as type II deficiency in diagnostic assays.

Ding Q, Yang L, Dinarvand P, Wang X, Rezaie AR. Ding Q, et al. Blood. 2015 Apr 9;125(15):2428-34. doi: 10.1182/blood-2014-12-617274. Epub 2015 Feb 4. Blood. 2015. PMID: 25651845 Free PMC article.

5

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

Ding Q, Yang L, Zhao X, Wu W, Wang X, Rezaie AR. Ding Q, et al. Thromb Haemost. 2017 Feb 28;117(3):479-490. doi: 10.1160/TH16-10-0750. Epub 2016 Dec 15. Thromb Haemost. 2017. PMID: 27975099 Free PMC article.

6

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

Chen C, Yang L, Villoutreix BO, Wang X, Ding Q, Rezaie AR. Chen C, et al. Among authors: ding q. Thromb Haemost. 2017 Jun 28;117(7):1358-1369. doi: 10.1160/TH17-01-0043. Epub 2017 Apr 13. Thromb Haemost. 2017. PMID: 28405673 Free PMC article.

7

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

Liang Q, Qin H, Ding Q, Xie X, Wu R, Wang H, Hu Y, Wang X. Liang Q, et al. Among authors: ding q. Thromb Haemost. 2017 Jul 26;117(8):1534-1548. doi: 10.1160/TH16-10-0794. Epub 2017 May 24. Thromb Haemost. 2017. PMID: 28536718

8

Clinical Manifestation and Mutation Spectrum of 53 Unrelated Pedigrees with Protein S Deficiency in China.

Li L, Wu X, Wu W, Ding Q, Cai X, Wang X. Li L, et al. Among authors: ding q. Thromb Haemost. 2019 Mar;119(3):449-460. doi: 10.1055/s-0038-1677031. Epub 2019 Jan 22. Thromb Haemost. 2019. PMID: 30669159

9

Ile73Asn mutation in protein C introduces a new N-linked glycosylation site on the first EGF-domain of protein C and causes thrombosis.

Lu Y, Mehta-D'souza P, Biswas I, Villoutreix BO, Wang X, Ding Q, Rezaie AR. Lu Y, et al. Among authors: ding q. Haematologica. 2020 Jun;105(6):1712-1722. doi: 10.3324/haematol.2019.227033. Epub 2019 Aug 8. Haematologica. 2020. PMID: 31399531 Free PMC article.

10

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

Lu Y, Giri H, Villoutreix BO, Ding Q, Wang X, Rezaie AR. Lu Y, et al. Among authors: ding q. J Thromb Haemost. 2020 May;18(5):1141-1153. doi: 10.1111/jth.14777. Epub 2020 Apr 9. J Thromb Haemost. 2020. PMID: 32078247 Free PMC article.

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