Zhang W - Search Results

1

Whole exome sequencing reveals a stop-gain mutation of PKD2 in an autosomal dominant polycystic kidney disease family complicated with aortic dissection.

Zhang W, Han Q, Liu Z, Zhou W, Cao Q, Zhou W. Zhang W, et al. BMC Med Genet. 2018 Jan 30;19(1):19. doi: 10.1186/s12881-018-0536-6. BMC Med Genet. 2018. PMID: 29378535 Free PMC article.

2

Bismuthoxyiodide nanoflakes/titania nanotubes arrayed p-n heterojunction and its application for photoelectrochemical bioanalysis.

Zhao WW, Liu Z, Shan S, Zhang WW, Wang J, Ma ZY, Xu JJ, Chen HY. Zhao WW, et al. Sci Rep. 2014 Mar 21;4:4426. doi: 10.1038/srep04426. Sci Rep. 2014. PMID: 24651880 Free PMC article.

3

Effect of lipid-modifying therapy on long-term mortality after abdominal aortic aneurysm repair: a systemic review and meta-analysis.

Zhang W, Liu Z, Liu C. Zhang W, et al. World J Surg. 2015 Mar;39(3):794-801. doi: 10.1007/s00268-014-2858-7. World J Surg. 2015. PMID: 25385163 Review.

4

SDF1-3'A polymorphism is associated with size but not occurrence of abdominal aortic aneurysm in a Chinese population.

Zhang W, Liu Z, Zhou M, Yi L, Liu C. Zhang W, et al. J Vasc Surg. 2016 Aug;64(2):479-483. doi: 10.1016/j.jvs.2015.01.059. Epub 2015 Mar 19. J Vasc Surg. 2016. PMID: 25800732 Free article.

5

Plasma microRNAs serve as potential biomarkers for abdominal aortic aneurysm.

Zhang W, Shang T, Huang C, Yu T, Liu C, Qiao T, Huang D, Liu Z, Liu C. Zhang W, et al. Clin Biochem. 2015 Oct;48(15):988-92. doi: 10.1016/j.clinbiochem.2015.04.016. Epub 2015 Apr 25. Clin Biochem. 2015. PMID: 25916817

6

A Novel Mutation of SMAD3 Identified in a Chinese Family with Aneurysms-Osteoarthritis Syndrome.

Zhang W, Zhou M, Liu C, Liu C, Qiao T, Huang D, Ran F, Wang W, Liu C, Liu Z. Zhang W, et al. Biomed Res Int. 2015;2015:968135. doi: 10.1155/2015/968135. Epub 2015 Jun 29. Biomed Res Int. 2015. PMID: 26221609 Free PMC article.

7

Identification of a missense mutation of COL3A1 in a Chinese family with atypical Ehlers-Danlos syndrome using targeted next-generation sequencing.

Zhang W, Han Q, Zhou M, Ran F, Qiao T, Yi L, Liu C, Liu Z. Zhang W, et al. Mol Med Rep. 2017 Feb;15(2):936-940. doi: 10.3892/mmr.2016.6082. Epub 2016 Dec 29. Mol Med Rep. 2017. PMID: 28035354 Free PMC article.

8

Exome sequencing identified a novel SMAD2 mutation in a Chinese family with early onset aortic aneurysms.

Zhang W, Zeng Q, Xu Y, Ying H, Zhou W, Cao Q, Zhou W. Zhang W, et al. Clin Chim Acta. 2017 May;468:211-214. doi: 10.1016/j.cca.2017.03.007. Epub 2017 Mar 7. Clin Chim Acta. 2017. PMID: 28283438

9

Whole exome sequencing identifies FBN1 mutations in two patients with early‑onset type B aortic dissection.

Han Q, Zhang W, Liu C, Zhou M, Ran F, Yi L, Sun X, Liu Z. Han Q, et al. Among authors: zhang w. Mol Med Rep. 2017 Nov;16(5):6620-6625. doi: 10.3892/mmr.2017.7410. Epub 2017 Aug 31. Mol Med Rep. 2017. PMID: 28901506 Free PMC article.

10

Familial early-onset deep venous thrombosis associated with a novel HRG mutation.

Luo J, Zhang W, Zeng Q, Zhou W, Cao Q, Zhou W. Luo J, et al. Among authors: zhang w. Eur J Med Genet. 2018 Feb;61(2):68-71. doi: 10.1016/j.ejmg.2017.10.019. Epub 2017 Nov 7. Eur J Med Genet. 2018. PMID: 29108964

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