Chen X - Search Results

1

Lactylation-driven FTO targets CDK2 to aggravate microvascular anomalies in diabetic retinopathy.

Chen X, Wang Y, Wang JN, Zhang YC, Zhang YR, Sun RX, Qin B, Dai YX, Zhu HJ, Zhao JX, Zhang WW, Ji JD, Yuan ST, Shen QD, Liu QH. Chen X, et al. EMBO Mol Med. 2024 Feb;16(2):294-318. doi: 10.1038/s44321-024-00025-1. Epub 2024 Jan 31. EMBO Mol Med. 2024. PMID: 38297099 Free PMC article.

2

Targeted sequencing of 179 genes associated with hereditary retinal dystrophies and 10 candidate genes identifies novel and known mutations in patients with various retinal diseases.

Chen X, Zhao K, Sheng X, Li Y, Gao X, Zhang X, Kang X, Pan X, Liu Y, Jiang C, Shi H, Chen X, Rong W, Chen LJ, Lai TY, Liu Y, Wang X, Yuan S, Liu Q, Vollrath D, Pang CP, Zhao C. Chen X, et al. Among authors: chen lj. Invest Ophthalmol Vis Sci. 2013 Mar 1;54(3):2186-97. doi: 10.1167/iovs.12-10967. Invest Ophthalmol Vis Sci. 2013. PMID: 23462753

3

Maternal germline mosaicism of kinesin family member 21A (KIF21A) mutation causes complex phenotypes in a Chinese family with congenital fibrosis of the extraocular muscles.

Liu G, Chen X, Sun X, Liu H, Zhao K, Chang Q, Pan X, Wang X, Yuan S, Liu Q, Zhao C. Liu G, et al. Among authors: chen x. Mol Vis. 2014 Jan 6;20:15-23. eCollection 2014. Mol Vis. 2014. PMID: 24426772 Free PMC article.

4

[Targeted sequencing identifies a hotspot mutation SNRNP200 p.S1087L correlates with novel phenotypes in retinitis pigmentosa].

Chen X, Gao X, Zhao KX, Pan XY, Zhang XM, Wang XY, Yuan ST, Liu QH, Zhao C. Chen X, et al. Zhonghua Yan Ke Za Zhi. 2013 Dec;49(12):1104-10. Zhonghua Yan Ke Za Zhi. 2013. PMID: 24499697 Chinese.

5

Knocking Down Snrnp200 Initiates Demorphogenesis of Rod Photoreceptors in Zebrafish.

Liu Y, Chen X, Qin B, Zhao K, Zhao Q, Staley JP, Zhao C. Liu Y, et al. Among authors: chen x. J Ophthalmol. 2015;2015:816329. doi: 10.1155/2015/816329. Epub 2015 Jun 2. J Ophthalmol. 2015. PMID: 26137319 Free PMC article.

6

MicroRNA-184 promotes differentiation of the retinal pigment epithelium by targeting the AKT2/mTOR signaling pathway.

Jiang C, Qin B, Liu G, Sun X, Shi H, Ding S, Liu Y, Zhu M, Chen X, Zhao C. Jiang C, et al. Among authors: chen x. Oncotarget. 2016 Aug 9;7(32):52340-52353. doi: 10.18632/oncotarget.10566. Oncotarget. 2016. PMID: 27418134 Free PMC article.

7

A large family with inherited optic disc anomalies: a correlation between a new genetic locus and complex ocular phenotypes.

Wang D, Pan X, Ji J, Gu S, Sun X, Jiang C, Xia W, Qiu Z, Kang X, Ding S, Liu Q, Chen X, Lu F, Zhao C. Wang D, et al. Among authors: chen x. Sci Rep. 2017 Aug 10;7(1):7799. doi: 10.1038/s41598-017-07730-7. Sci Rep. 2017. PMID: 28798362 Free PMC article.

8

LncRNA ZNF503-AS1 promotes RPE differentiation by downregulating ZNF503 expression.

Chen X, Jiang C, Qin B, Liu G, Ji J, Sun X, Xu M, Ding S, Zhu M, Huang G, Yan B, Zhao C. Chen X, et al. Cell Death Dis. 2017 Sep 7;8(9):e3046. doi: 10.1038/cddis.2017.382. Cell Death Dis. 2017. PMID: 28880276 Free PMC article.

9

c-Jun-mediated microRNA-302d-3p induces RPE dedifferentiation by targeting p21^Waf1/Cip1.

Jiang C, Xie P, Sun R, Sun X, Liu G, Ding S, Zhu M, Yan B, Liu Q, Chen X, Zhao C. Jiang C, et al. Among authors: chen x. Cell Death Dis. 2018 May 1;9(5):451. doi: 10.1038/s41419-018-0481-5. Cell Death Dis. 2018. PMID: 29670082 Free PMC article.

10

CRB2 mutation causes autosomal recessive retinitis pigmentosa.

Chen X, Jiang C, Yang D, Sun R, Wang M, Sun H, Xu M, Zhou L, Chen M, Xie P, Yan B, Liu Q, Zhao C. Chen X, et al. Among authors: chen m. Exp Eye Res. 2019 Mar;180:164-173. doi: 10.1016/j.exer.2018.12.018. Epub 2018 Dec 26. Exp Eye Res. 2019. PMID: 30593785

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