Chen WX - Search Results

1

Circ_0002295 facilitated myocardial fibrosis progression through the miR-1287/CXCR2 axis.

Ma GB, Chen WX, Zhan FJ, Xie WJ, Chen RW, Chen H, Ye WL, Jiang Y, Xu JP. Ma GB, et al. Among authors: chen wx, chen rw, chen h. Clin Exp Pharmacol Physiol. 2023 Dec;50(12):944-953. doi: 10.1111/1440-1681.13819. Epub 2023 Sep 9. Clin Exp Pharmacol Physiol. 2023. PMID: 37688444

2

Silencing of the CrkL gene reverses the doxorubicin resistance of K562/ADR cells through regulating PI3K/Akt/MRP1 signaling.

Yu J, Chen WX, Xie WJ, Chen RW, Lin DQ, You WW, Ye WL, Zhang HQ, Lin DH, Xu JP. Yu J, et al. Among authors: chen wx, chen rw. J Clin Lab Anal. 2021 Aug;35(8):e23817. doi: 10.1002/jcla.23817. Epub 2021 Jun 11. J Clin Lab Anal. 2021. PMID: 34114685 Free PMC article.

3

The Hippo Signaling Core Components YAP and TAZ as New Prognostic Factors in Lung Cancer.

Jiang Y, Xie WJ, Chen RW, You WW, Ye WL, Chen H, Chen WX, Xu JP. Jiang Y, et al. Among authors: chen wx, chen rw, chen h. Front Surg. 2022 Mar 21;9:813123. doi: 10.3389/fsurg.2022.813123. eCollection 2022. Front Surg. 2022. PMID: 35388363 Free PMC article. Review.

4

Genotype GG of rs895819 Functional Polymorphism Within miR-27a Might Increase Genetic Susceptibility to Colorectal Cancer in Han Chinese Population.

Jiang Y, Lin DH, Xu JP, Chen WX, Zheng SJ, Song L. Jiang Y, et al. Among authors: chen wx. J Clin Lab Anal. 2016 Jul;30(4):351-5. doi: 10.1002/jcla.21862. Epub 2015 Aug 24. J Clin Lab Anal. 2016. PMID: 26302683 Free PMC article.

5

Targeted Next-Generation Sequencing Newly Identifies Mutations in Exostosin-1 and Exostosin-2 Genes of Patients with Multiple Osteochondromas.

Guo X, Lin M, Shi T, Yan W, Chen W. Guo X, et al. Tohoku J Exp Med. 2017 Jul;242(3):173-181. doi: 10.1620/tjem.242.173. Tohoku J Exp Med. 2017. PMID: 28690282 Free article.

6

A novel splice mutation induces exon skipping of the EXT1 gene in patients with hereditary multiple exostoses.

Guo X, Lin M, Yan W, Chen W, Hong G. Guo X, et al. Int J Oncol. 2019 Mar;54(3):859-868. doi: 10.3892/ijo.2019.4688. Epub 2019 Jan 16. Int J Oncol. 2019. PMID: 30664192 Free PMC article.

7

[Analysis of a multiple osteochondroma case caused by novel splice mutation (c.1164+1G to A) of EXT1 gene].

Guo X, Chen W, Lin M, Shi T, Huang D, Wang Z. Guo X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Jun 10;34(3):411-415. doi: 10.3760/cma.j.issn.1003-9406.2017.03.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28604967 Chinese.

8

RYR3 Variants Are Potentially Associated With Idiopathic (Non-Lesional) Partial Epilepsy/Susceptibility of Seizures, Toward Understanding the Gene-Disease Association by Genetic Dependent Nature.

Tian Y, Hou YQ, Zhai QX, Song XW, Li BM, Wang J, Ji JJ, Liao YT, Chen WX, Li B, Liao WP. Tian Y, et al. Among authors: chen wx. Am J Med Genet B Neuropsychiatr Genet. 2025 Jan 22:e33023. doi: 10.1002/ajmg.b.33023. Online ahead of print. Am J Med Genet B Neuropsychiatr Genet. 2025. PMID: 39840699

9

CF₂H-synthon enables asymmetric radical difluoroalkylation for synthesis of chiral difluoromethylated amines.

Liu P, He Y, Jiang CH, Ren WR, Jin RX, Zhang T, Chen WX, Nie X, Wang XS. Liu P, et al. Among authors: chen wx. Nat Commun. 2025 Jan 11;16(1):599. doi: 10.1038/s41467-025-55912-z. Nat Commun. 2025. PMID: 39799146 Free PMC article.

10

Daily sodium intake and constipation in US adult males: an uncommon negative association revealed by national health and nutrition examination survey data from the United States (2005-2010).

Peng XF, Yang H, Chen WX, Yu M, Wang DC. Peng XF, et al. Among authors: chen wx. BMC Gastroenterol. 2025 Jan 6;25(1):1. doi: 10.1186/s12876-024-03543-x. BMC Gastroenterol. 2025. PMID: 39757154 Free PMC article.

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