Chen W - Search Results

1

TRIM59 knockdown inhibits cell proliferation by down-regulating the Wnt/β-catenin signaling pathway in neuroblastoma.

Chen G, Chen W, Ye M, Tan W, Jia B. Chen G, et al. Among authors: chen w. Biosci Rep. 2019 Jan 18;39(1):BSR20181277. doi: 10.1042/BSR20181277. Print 2019 Jan 31. Biosci Rep. 2019. PMID: 30389710 Free PMC article.

2

Application of Heparin/Collagen-REDV Selective Active Interface on ePTFE Films to Enhance Endothelialization and Anticoagulation.

Shan Y, Jia B, Ye M, Shen H, Chen W, Zhang H. Shan Y, et al. Among authors: chen w. Artif Organs. 2018 Aug;42(8):824-834. doi: 10.1111/aor.13131. Epub 2018 Apr 18. Artif Organs. 2018. PMID: 29667205

3

Novel homozygous ataxia‑telangiectasia (A‑T) mutated gene mutation identified in a Chinese pedigree with A‑T.

Chen W, Liu S, Hu H, Chen G, Zhu S, Jia B, Sheng W, Huang G. Chen W, et al. Among authors: chen g. Mol Med Rep. 2019 Aug;20(2):1655-1662. doi: 10.3892/mmr.2019.10402. Epub 2019 Jun 20. Mol Med Rep. 2019. PMID: 31257506 Free PMC article.

4

High Prevalence of Unrecognized Congenital Heart Disease in School-Age Children in Rural China: A Population-Based Echocardiographic Screening Study.

Zhao Q, Chen H, Zhang G, Chen W, Jia B, Liu F, Ma X, Yan W, Niu C, Huang G. Zhao Q, et al. Among authors: chen w, chen h. Circulation. 2021 Dec 7;144(23):1896-1898. doi: 10.1161/CIRCULATIONAHA.121.056455. Epub 2021 Dec 6. Circulation. 2021. PMID: 34871107 Clinical Trial. No abstract available.

5

Hypermethylation-mediated down-regulation of lncRNA TBX5-AS1:2 in Tetralogy of Fallot inhibits cell proliferation by reducing TBX5 expression.

Ma J, Chen S, Hao L, Sheng W, Chen W, Ma X, Zhang B, Ma D, Huang G. Ma J, et al. Among authors: chen s, chen w. J Cell Mol Med. 2020 Jun;24(11):6472-6484. doi: 10.1111/jcmm.15298. Epub 2020 May 5. J Cell Mol Med. 2020. PMID: 32368852 Free PMC article.

6

CpG site hypomethylation at ETS1‑binding region regulates DLK1 expression in Chinese patients with Tetralogy of Fallot.

Tian G, He L, Gu R, Sun J, Chen W, Qian Y, Ma X, Yan W, Zhao Z, Xu Z, Suo M, Sheng W, Huang G. Tian G, et al. Among authors: chen w. Mol Med Rep. 2022 Mar;25(3):93. doi: 10.3892/mmr.2022.12609. Epub 2022 Jan 21. Mol Med Rep. 2022. PMID: 35059744 Free PMC article.

7

A novel ZIC3 gene mutation identified in patients with heterotaxy and congenital heart disease.

Li S, Liu S, Chen W, Yuan Y, Gu R, Song Y, Li J, Cao Y, Lin Y, Xu J, Wang H, Ma D, Ma X, Sheng W, Huang G. Li S, et al. Among authors: chen w. Sci Rep. 2018 Aug 17;8(1):12386. doi: 10.1038/s41598-018-30204-3. Sci Rep. 2018. PMID: 30120289 Free PMC article.

8

Long non-coding RNA SAP30-2:1 is downregulated in congenital heart disease and regulates cell proliferation by targeting HAND2.

Ma J, Chen S, Hao L, Sheng W, Chen W, Ma X, Zhang B, Ma D, Huang G. Ma J, et al. Among authors: chen s, chen w. Front Med. 2021 Feb;15(1):91-100. doi: 10.1007/s11684-020-0778-5. Epub 2020 Aug 19. Front Med. 2021. PMID: 32820380

9

WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation.

Hao L, Ma J, Wu F, Ma X, Qian M, Sheng W, Yan T, Tang N, Jiang X, Zhang B, Xiao D, Qian Y, Zhang J, Jiang N, Zhou W, Chen W, Ma D, Huang G. Hao L, et al. Among authors: chen w. Clin Transl Med. 2022 Jul;12(7):e941. doi: 10.1002/ctm2.941. Clin Transl Med. 2022. PMID: 35808830 Free PMC article.

10

DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome.

Liu S, Chen W, Zhan Y, Li S, Ma X, Ma D, Sheng W, Huang G. Liu S, et al. Among authors: chen w. Sci Rep. 2019 Apr 30;9(1):6683. doi: 10.1038/s41598-019-43109-6. Sci Rep. 2019. PMID: 31040315 Free PMC article.

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