Xu Y - Search Results

1

Patient-specific mutations impair BESTROPHIN1's essential role in mediating Ca²⁺-dependent Cl^- currents in human RPE.

Li Y, Zhang Y, Xu Y, Kittredge A, Ward N, Chen S, Tsang SH, Yang T. Li Y, et al. Among authors: xu y. Elife. 2017 Oct 24;6:e29914. doi: 10.7554/eLife.29914. Elife. 2017. PMID: 29063836 Free PMC article.

2

Laser-Induced Photic Injury Phenocopies Macular Dystrophy.

Zhang L, Zheng A, Nie H, Bhavsar KV, Xu Y, Sliney DH, Trokel SL, Tsang SH. Zhang L, et al. Among authors: xu y. Ophthalmic Genet. 2016;37(1):59-67. doi: 10.3109/13816810.2015.1059458. Ophthalmic Genet. 2016. PMID: 26927809 Free PMC article.

3

Reprogramming towards anabolism impedes degeneration in a preclinical model of retinitis pigmentosa.

Zhang L, Justus S, Xu Y, Pluchenik T, Hsu CW, Yang J, Duong JK, Lin CS, Jia Y, Bassuk AG, Mahajan VB, Tsang SH. Zhang L, et al. Among authors: xu y. Hum Mol Genet. 2016 Oct 1;25(19):4244-4255. doi: 10.1093/hmg/ddw256. Epub 2016 Aug 11. Hum Mol Genet. 2016. PMID: 27516389 Free PMC article.

4

CRISPR applications in ophthalmologic genome surgery.

Cabral T, DiCarlo JE, Justus S, Sengillo JD, Xu Y, Tsang SH. Cabral T, et al. Among authors: xu y. Curr Opin Ophthalmol. 2017 May;28(3):252-259. doi: 10.1097/ICU.0000000000000359. Curr Opin Ophthalmol. 2017. PMID: 28141764 Free PMC article. Review.

5

Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia.

Toral MA, Velez G, Boudreault K, Schaefer KA, Xu Y, Saffra N, Bassuk AG, Tsang SH, Mahajan VB. Toral MA, et al. Among authors: xu y. Mol Genet Genomic Med. 2017 Feb 26;5(3):202-209. doi: 10.1002/mgg3.266. eCollection 2017 May. Mol Genet Genomic Med. 2017. PMID: 28546991 Free PMC article.

6

Electroretinography Reveals Difference in Cone Function between Syndromic and Nonsyndromic USH2A Patients.

Sengillo JD, Cabral T, Schuerch K, Duong J, Lee W, Boudreault K, Xu Y, Justus S, Sparrow JR, Mahajan VB, Tsang SH. Sengillo JD, et al. Among authors: xu y. Sci Rep. 2017 Sep 11;7(1):11170. doi: 10.1038/s41598-017-11679-y. Sci Rep. 2017. PMID: 28894305 Free PMC article.

7

CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa: A Brief Methodology.

Wu WH, Tsai YT, Justus S, Cho GY, Sengillo JD, Xu Y, Cabral T, Lin CS, Bassuk AG, Mahajan VB, Tsang SH. Wu WH, et al. Among authors: xu y. Methods Mol Biol. 2018;1715:191-205. doi: 10.1007/978-1-4939-7522-8_13. Methods Mol Biol. 2018. PMID: 29188514 Free PMC article.

8

Elabela promotes the retinal angiogenesis by inhibiting ferroptosis during the vaso-obliteration phase in mouse oxygen-induced retinopathy model.

Wang J, Zhang Q, Chen E, Zhao P, Xu Y. Wang J, et al. Among authors: xu y. FASEB J. 2022 May;36(5):e22257. doi: 10.1096/fj.202101785RRR. FASEB J. 2022. PMID: 35471770

9

Ophthalmic findings and a novel CTC1 gene mutation in coats plus syndrome: a case report.

Liang T, Zhang X, Xu Y, Zhao P. Liang T, et al. Among authors: xu y. Ophthalmic Genet. 2021 Feb;42(1):79-83. doi: 10.1080/13816810.2020.1827443. Epub 2020 Oct 9. Ophthalmic Genet. 2021. PMID: 33034244

10

Identification of immune-related endoplasmic reticulum stress genes in proliferative diabetic retinopathy using bioinformatics analysis.

Chen H, Chen E, Liu M, Wang J, Yin J, Zhao P, Xu Y. Chen H, et al. Among authors: xu y. Front Endocrinol (Lausanne). 2024 Aug 30;15:1341206. doi: 10.3389/fendo.2024.1341206. eCollection 2024. Front Endocrinol (Lausanne). 2024. PMID: 39280014 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

73,307 results

Search Page

Filters