Gao X - Search Results

1

[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. Among authors: gao x. Zhonghua Yan Ke Za Zhi. 2013 Dec;49(12):1104-10. Zhonghua Yan Ke Za Zhi. 2013. PMID: 24499697 Chinese.

2

[Gene mapping and analysis of candidate genes in a Chinese family with autosomal dominant congenital coralliform cataract].

Ju H, Zhao KX, Wang LM, Wang YC, Ying M, Gao X. Ju H, et al. Among authors: gao x. Zhonghua Yan Ke Za Zhi. 2012 Aug;48(8):713-7. Zhonghua Yan Ke Za Zhi. 2012. PMID: 23141511 Chinese.

3

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: gao x. Invest Ophthalmol Vis Sci. 2013 Mar 1;54(3):2186-97. doi: 10.1167/iovs.12-10967. Invest Ophthalmol Vis Sci. 2013. PMID: 23462753

4

Mutation analysis of pre-mRNA splicing genes in Chinese families with retinitis pigmentosa.

Pan X, Chen X, Liu X, Gao X, Kang X, Xu Q, Chen X, Zhao K, Zhang X, Chu Q, Wang X, Zhao C. Pan X, et al. Among authors: gao x. Mol Vis. 2014 Jun 2;20:770-9. eCollection 2014. Mol Vis. 2014. PMID: 24940031 Free PMC article.

5

Molecular genetic testing in clinical diagnostic assessments that demonstrate correlations in patients with autosomal recessive inherited retinal dystrophy.

Liu X, Xiao J, Huang H, Guan L, Zhao K, Xu Q, Zhang X, Pan X, Gu S, Chen Y, Zhang J, Shen Y, Jiang H, Gao X, Kang X, Sheng X, Chen X, Zhao C. Liu X, et al. Among authors: gao x. JAMA Ophthalmol. 2015 Apr;133(4):427-36. doi: 10.1001/jamaophthalmol.2014.5831. JAMA Ophthalmol. 2015. PMID: 25611614

6

Targeted next-generation sequencing reveals novel EYS mutations in Chinese families with autosomal recessive retinitis pigmentosa.

Chen X, Liu X, Sheng X, Gao X, Zhang X, Li Z, Li H, Liu Y, Rong W, Zhao K, Zhao C. Chen X, et al. Among authors: gao x. Sci Rep. 2015 Mar 10;5:8927. doi: 10.1038/srep08927. Sci Rep. 2015. PMID: 25753737 Free PMC article.

7

Variants identified by next-generation sequencing cause endoplasmic reticulum stress in Rhodopsin-associated retinitis pigmentosa.

Wang Y, Chen X, Gao X, Zhao A, Zhao C, Chen X. Wang Y, et al. Among authors: gao x. BMC Ophthalmol. 2021 Oct 19;21(1):371. doi: 10.1186/s12886-021-02110-2. BMC Ophthalmol. 2021. PMID: 34666717 Free PMC article.

8

The short-term effects of blood donation on the ocular parameters including blood flow of the retina and choroid in healthy people using OCT- angiography.

Yu M, Sun X, Zeng F, Gao X, Li Z, Yuan G, Wang T. Yu M, et al. Among authors: gao x. BMC Ophthalmol. 2023 Jun 12;23(1):259. doi: 10.1186/s12886-023-03002-3. BMC Ophthalmol. 2023. PMID: 37303035 Free PMC article.

9

Understanding the role of corneal biomechanics-associated genetic variants by bioinformatic analyses.

Sun X, Gao X, Mu BK, Wang Y. Sun X, et al. Among authors: gao x. Int Ophthalmol. 2022 Mar;42(3):981-988. doi: 10.1007/s10792-021-02081-9. Epub 2021 Oct 12. Int Ophthalmol. 2022. PMID: 34642840

10

Circ-ADAM9 Promotes High Glucose-Induced Retinal Pigment Epithelial Cell Injury in DR via Regulating miR-338-3p/CARM1 Axis.

Liang Z, Lu C, Feng T, Gao X, Tu Y, Yang W, Wang Y. Liang Z, et al. Among authors: gao x. J Ophthalmol. 2022 Jan 20;2022:2522249. doi: 10.1155/2022/2522249. eCollection 2022. J Ophthalmol. 2022. PMID: 35096421 Free PMC article.

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