Chen Q - Search Results

1

Novel LTBP3 mutations associated with thoracic aortic aneurysms and dissections.

Zhu G, Luo M, Chen Q, Zhang Y, Zhao K, Zhang Y, Shu C, Yang H, Zhou Z. Zhu G, et al. Among authors: chen q. Orphanet J Rare Dis. 2021 Dec 14;16(1):513. doi: 10.1186/s13023-021-02143-2. Orphanet J Rare Dis. 2021. PMID: 34906192 Free PMC article.

2

Genetic testing of 10 patients with features of Loeys-Dietz syndrome.

Luo M, Yang H, Yin K, Chen Q, Zhang J, Fan Y, Zhou Z, Chang Q. Luo M, et al. Among authors: chen q. Clin Chim Acta. 2016 May 1;456:144-148. doi: 10.1016/j.cca.2016.02.005. Epub 2016 Feb 11. Clin Chim Acta. 2016. PMID: 26877057

3

Genetic testing of the FBN1 gene in Chinese patients with Marfan/Marfan-like syndrome.

Yang H, Luo M, Chen Q, Fu Y, Zhang J, Qian X, Sun X, Fan Y, Zhou Z, Chang Q. Yang H, et al. Among authors: chen q. Clin Chim Acta. 2016 Aug 1;459:30-35. doi: 10.1016/j.cca.2016.05.021. Epub 2016 May 24. Clin Chim Acta. 2016. PMID: 27234404

4

A novel PROS1 mutation, c.74dupA, was identified in a protein S deficiency family.

Zhang Y, Yang H, Chen Q, Yu J, Chen X, Liu S, Gao G, Song Y, Zhou Z. Zhang Y, et al. Among authors: chen q, chen x. Thromb Res. 2016 Dec;148:125-127. doi: 10.1016/j.thromres.2016.11.003. Epub 2016 Nov 6. Thromb Res. 2016. PMID: 27846449

5

Reversible MRI findings in a case of acute intermittent porphyria with a novel mutation in the porphobilinogen deaminase gene.

Yang J, Yang H, Chen Q, Hua B, Zhu T, Zhao Y, Yu X, Zhu H, Zhou Z. Yang J, et al. Among authors: chen q. Blood Cells Mol Dis. 2017 Mar;63:21-24. doi: 10.1016/j.bcmd.2016.12.005. Epub 2016 Dec 18. Blood Cells Mol Dis. 2017. PMID: 28011390

6

Clinical and Laboratory Features of Acute Porphyria: A Study of 36 Subjects in a Chinese Tertiary Referral Center.

Yang J, Chen Q, Yang H, Hua B, Zhu T, Zhao Y, Zhu H, Yu X, Zhang L, Zhou Z. Yang J, et al. Among authors: chen q. Biomed Res Int. 2016;2016:3927635. doi: 10.1155/2016/3927635. Epub 2016 Nov 29. Biomed Res Int. 2016. PMID: 28025645 Free PMC article. Clinical Trial.

7

Genetic analyses in a cohort of 191 pulmonary arterial hypertension patients.

Yang H, Zeng Q, Ma Y, Liu B, Chen Q, Li W, Xiong C, Zhou Z. Yang H, et al. Among authors: chen q. Respir Res. 2018 May 9;19(1):87. doi: 10.1186/s12931-018-0789-9. Respir Res. 2018. PMID: 29743074 Free PMC article.

8

Perioperative urinary thromboxane metabolites and outcome of coronary artery bypass grafting: a nested case-control study.

Liu H, Xu Z, Sun C, Chen Q, Bao N, Chen W, Zhou Z, Wang X, Zheng Z. Liu H, et al. Among authors: chen q, chen w. BMJ Open. 2018 Aug 30;8(8):e021219. doi: 10.1136/bmjopen-2017-021219. BMJ Open. 2018. PMID: 30166295 Free PMC article.

9

Exosomal miR-423-5p mediates the proangiogenic activity of human adipose-derived stem cells by targeting Sufu.

Xu F, Xiang Q, Huang J, Chen Q, Yu N, Long X, Zhou Z. Xu F, et al. Among authors: chen q. Stem Cell Res Ther. 2019 Mar 21;10(1):106. doi: 10.1186/s13287-019-1196-y. Stem Cell Res Ther. 2019. PMID: 30898155 Free PMC article.

10

Reversible splenial lesion syndrome (RESLES) due to acute intermittent porphyria with a novel mutation in the hydroxymethylbilane synthase gene.

Yang J, Han F, Chen Q, Zhu T, Zhao Y, Yu X, Zhu H, Cao J, Li X. Yang J, et al. Among authors: chen q. Orphanet J Rare Dis. 2020 Apr 19;15(1):98. doi: 10.1186/s13023-020-01375-y. Orphanet J Rare Dis. 2020. PMID: 32306994 Free PMC article.

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