Qin X - Search Results

1

[Genetic diagnosis and bioinformatic analysis of a pedigree with inherited factor VII deficiency].

Guo Z, Guo J, Wu R, Zhang Y, Qin X, Liu X, Yang L. Guo Z, et al. Among authors: qin x. Zhonghua Xue Ye Xue Za Zhi. 2015 Feb;36(2):163-5. doi: 10.3760/cma.j.issn.0253-2727.2015.02.018. Zhonghua Xue Ye Xue Za Zhi. 2015. PMID: 25778897 Free PMC article. Chinese. No abstract available.

2

[Screening and analysis of coagulation factor VIII inhibitor in patients with hemophilia A].

Zhang AL, Yang LH, Liu XE, Zhao H, Zhang JH, Dong CX, Qi XL, Qin XY. Zhang AL, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2011 Aug;19(4):968-70. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2011. PMID: 21867625 Chinese.

3

[Expressions of Th17 cells and interleukin 17 in patients with primary immune thrombocytopenia and their clinical significance].

Duan XJ, Yang LH, Zhang L, Ren FG, Zhang RJ, Chen JF, Qin XY, Liang HZ. Duan XJ, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2012 Oct;20(5):1154-7. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2012. PMID: 23114138 Chinese.

4

[Detection of intron 22 inversion of factor VIII gene in severe hemophilia A patients].

Guo ZP, Chen JF, Qin XY, Zhang YF, Yang LH. Guo ZP, et al. Zhonghua Xue Ye Xue Za Zhi. 2013 Nov;34(11):918-21. doi: 10.3760/cma.j.issn.0253-2727.2013.11.002. Zhonghua Xue Ye Xue Za Zhi. 2013. PMID: 24294844 Chinese.

5

[Study on the correlation between FcγR IIIA-158V/F single nucleotide polymorphisms and adult primary immune thrombocytopenia].

Guo Z, Chen J, Zhang W, Zhang Y, Qin X, Yang L. Guo Z, et al. Among authors: qin x. Zhonghua Xue Ye Xue Za Zhi. 2014 Mar;35(3):242-4. doi: 10.3760/cma.j.issn.0253-2727.2014.03.015. Zhonghua Xue Ye Xue Za Zhi. 2014. PMID: 24666494 Chinese. No abstract available.

6

Hemophilia care in China: review of care for 417 hemophilia patients from 11 treatment centers in Shanxi Province.

Zhao H, Yang L, Long C, Guo Y, Wu R, Liu X, Qin X, Liang H, Duan Z. Zhao H, et al. Among authors: qin x. Expert Rev Hematol. 2015 Aug;8(4):543-50. doi: 10.1586/17474086.2015.1043263. Epub 2015 May 6. Expert Rev Hematol. 2015. PMID: 25948487

7

Spectrum of Molecular Defects in 216 Chinese Families With Hemophilia A: Identification of Noninversion Mutation Hot Spots and 42 Novel Mutations.

Guo Z, Yang L, Qin X, Liu X, Zhang Y. Guo Z, et al. Among authors: qin x. Clin Appl Thromb Hemost. 2018 Jan;24(1):70-78. doi: 10.1177/1076029616687848. Epub 2017 Jan 5. Clin Appl Thromb Hemost. 2018. PMID: 28056528 Free PMC article. Clinical Trial.

8

Molecular mechanism of a novel Ser362Asn mutation causing inherited FX deficiency in a Chinese family.

Zhang X, Chen K, Wang G, Zhang C, Zhao B, Liu X, Qin X, Yang L. Zhang X, et al. Among authors: qin x. Int J Hematol. 2020 Jul;112(1):8-16. doi: 10.1007/s12185-020-02877-y. Epub 2020 Apr 13. Int J Hematol. 2020. PMID: 32285359

9

Identification of five novel variants of haemophilia B in 32 patients in Shanxi province, China.

Zhang X, Wang G, Chen K, Zhang C, Qin X, Zhang Y, Liu X, Yang L. Zhang X, et al. Among authors: qin x. Haemophilia. 2020 Jul;26(4):e217-e219. doi: 10.1111/hae.14007. Epub 2020 Apr 20. Haemophilia. 2020. PMID: 32311179 No abstract available.

10

[Altered Splicing in Stable Cell Strains Expressing Mini-hF9 Gene with Nonsense Mutation].

Wang G, Sun WW, Zhu LK, Ma YC, Zhang XL, Zhang JH, Ren J, Qin XY, Yang LH, Chai BF. Wang G, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021 Feb;29(1):228-232. doi: 10.19746/j.cnki.issn.1009-2137.2021.01.037. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021. PMID: 33554825 Chinese.

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