Zhou Z - Search Results

1

Identification of gross deletions in FBN1 gene by MLPA.

Yang H, Ma Y, Luo M, Zhao K, Zhang Y, Zhu G, Sun X, Luo F, Wang L, Shu C, Zhou Z. Yang H, et al. Among authors: zhou z. Hum Genomics. 2018 Oct 4;12(1):46. doi: 10.1186/s40246-018-0178-y. Hum Genomics. 2018. PMID: 30286810 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: zhou z. 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: zhou z. 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

Genetic testing of 248 Chinese aortopathy patients using a panel assay.

Yang H, Luo M, Fu Y, Cao Y, Yin K, Li W, Meng C, Ma Y, Zhang J, Fan Y, Shu C, Chang Q, Zhou Z. Yang H, et al. Among authors: zhou z. Sci Rep. 2016 Sep 9;6:33002. doi: 10.1038/srep33002. Sci Rep. 2016. PMID: 27611364 Free PMC article.

5

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: zhou z. Thromb Res. 2016 Dec;148:125-127. doi: 10.1016/j.thromres.2016.11.003. Epub 2016 Nov 6. Thromb Res. 2016. PMID: 27846449

6

Common Variant in Glycoprotein Ia Increases Long-Term Adverse Events Risk After Coronary Artery Bypass Graft Surgery.

Liu H, Xu Z, Gu H, Li W, Chen W, Sun C, Zhao K, Teng X, Zhang H, Jiang L, Hu S, Zhou Z, Zheng Z. Liu H, et al. Among authors: zhou z. J Am Heart Assoc. 2016 Nov 23;5(12):e004496. doi: 10.1161/JAHA.116.004496. J Am Heart Assoc. 2016. PMID: 27881421 Free PMC article.

7

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: zhou z. 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

8

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: zhou z. 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.

9

Vascular Ehlers-Danlos Syndrome With a Novel Missense COL3A1 Mutation Present With Pulmonary Complications and Iliac Arterial Dissection.

Gu G, Yang H, Cui L, Fu Y, Li F, Zhou Z, Zheng Y. Gu G, et al. Among authors: zhou z. Vasc Endovascular Surg. 2018 Feb;52(2):138-142. doi: 10.1177/1538574417745432. Epub 2017 Dec 7. Vasc Endovascular Surg. 2018. PMID: 29216800 Review.

10

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: zhou z. Respir Res. 2018 May 9;19(1):87. doi: 10.1186/s12931-018-0789-9. Respir Res. 2018. PMID: 29743074 Free PMC article.

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