Huang XF - Search Results

1

Single-cell RNA sequencing reveals new subtypes of lens superficial tissue in humans.

Zhu MC, Hu W, Lin L, Yang QW, Zhang L, Xu JL, Xu YT, Liu JS, Zhang MD, Tong XY, Zhu KY, Feng K, Feng Y, Su JZ, Huang XF, Li J. Zhu MC, et al. Among authors: huang xf. Cell Prolif. 2023 Nov;56(11):e13477. doi: 10.1111/cpr.13477. Epub 2023 Apr 14. Cell Prolif. 2023. PMID: 37057399 Free PMC article.

2

Unique presentation of congenital cataract concurrent with microcornea, microphthalmia plus posterior capsule defect in monozygotic twins caused by a novel GJA8 mutation.

Zhang H, Chen Z, He K, Chang P, Zhao Y, Huang X, Li J, Jin Z, Zhao YE. Zhang H, et al. Eye (Lond). 2019 Apr;33(4):686-689. doi: 10.1038/s41433-018-0277-y. Epub 2018 Nov 29. Eye (Lond). 2019. PMID: 30498267 Free PMC article. No abstract available.

3

Causal Relationships Between Glycemic Traits and Myopia.

Li FF, Zhu MC, Shao YL, Lu F, Yi QY, Huang XF. Li FF, et al. Among authors: huang xf. Invest Ophthalmol Vis Sci. 2023 Mar 1;64(3):7. doi: 10.1167/iovs.64.3.7. Invest Ophthalmol Vis Sci. 2023. PMID: 36867130 Free PMC article.

4

Whole exome sequencing reveals genetic predisposition in a large family with retinitis pigmentosa.

Wu J, Chen L, Tam OS, Huang XF, Pang CP, Jin ZB. Wu J, et al. Among authors: huang xf. Biomed Res Int. 2014;2014:302487. doi: 10.1155/2014/302487. Epub 2014 Jun 30. Biomed Res Int. 2014. PMID: 25101269 Free PMC article.

5

Depletion of miR-96 Delays, But Does Not Arrest, Photoreceptor Development in Mice.

Xiang L, Zhang J, Rao FQ, Yang QL, Zeng HY, Huang SH, Xie ZX, Lv JN, Lin D, Chen XJ, Wu KC, Lu F, Huang XF, Chen Q. Xiang L, et al. Among authors: huang xf, huang sh. Invest Ophthalmol Vis Sci. 2022 Apr 1;63(4):24. doi: 10.1167/iovs.63.4.24. Invest Ophthalmol Vis Sci. 2022. PMID: 35481839 Free PMC article.

6

Dysregulated Arginine Metabolism Is Linked to Retinal Degeneration in Cep250 Knockout Mice.

Xiang L, Yang QL, Xie BT, Zeng HY, Ding LJ, Rao FQ, Yan T, Lu F, Chen Q, Huang XF. Xiang L, et al. Among authors: huang xf. Invest Ophthalmol Vis Sci. 2023 Sep 1;64(12):2. doi: 10.1167/iovs.64.12.2. Invest Ophthalmol Vis Sci. 2023. PMID: 37656476 Free PMC article.

7

Genotype-phenotype correlation and mutation spectrum in a large cohort of patients with inherited retinal dystrophy revealed by next-generation sequencing.

Huang XF, Huang F, Wu KC, Wu J, Chen J, Pang CP, Lu F, Qu J, Jin ZB. Huang XF, et al. Among authors: huang f. Genet Med. 2015 Apr;17(4):271-8. doi: 10.1038/gim.2014.138. Epub 2014 Nov 6. Genet Med. 2015. PMID: 25356976 Free article.

8

SLC7A14 linked to autosomal recessive retinitis pigmentosa.

Jin ZB, Huang XF, Lv JN, Xiang L, Li DQ, Chen J, Huang C, Wu J, Lu F, Qu J. Jin ZB, et al. Among authors: huang xf, huang c. Nat Commun. 2014 Mar 27;5:3517. doi: 10.1038/ncomms4517. Nat Commun. 2014. PMID: 24670872 Free PMC article.

9

Clinical and genetic analyses reveal novel pathogenic ABCA4 mutations in Stargardt disease families.

Lin B, Cai XB, Zheng ZL, Huang XF, Liu XL, Qu J, Jin ZB. Lin B, et al. Among authors: huang xf. Sci Rep. 2016 Oct 14;6:35414. doi: 10.1038/srep35414. Sci Rep. 2016. PMID: 27739528 Free PMC article.

10

Correlation of serum amyloid A levels, clinical manifestations, treatment, and disease activity in patients with acute anterior uveitis.

Dai ML, Fan S, Li Z, Yu X, Lin D, Huang XF, Wang Y. Dai ML, et al. Among authors: huang xf. Eye (Lond). 2020 Sep;34(9):1672-1678. doi: 10.1038/s41433-019-0740-4. Epub 2019 Dec 16. Eye (Lond). 2020. PMID: 31844164 Free PMC article.

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