Zhu T - Search Results

1

Clinical characterization and the improved molecular diagnosis of autosomal dominant cone-rod dystrophy in patients with SCA7.

Zou X, Yao F, Li F, Wu S, Li H, Sun Z, Zhu T, Wei X, Li D, Sui R. Zou X, et al. Among authors: zhu t. Mol Vis. 2021 May 7;27:221-232. eCollection 2021. Mol Vis. 2021. PMID: 34012225 Free PMC article.

2

Ocular Features in Chinese Patients with Blau Syndrome.

Wu S, Zhong L, Sun Z, Zhu T, Song H, Sui R. Wu S, et al. Among authors: zhu t. Ocul Immunol Inflamm. 2020;28(1):79-85. doi: 10.1080/09273948.2019.1569239. Epub 2019 Feb 26. Ocul Immunol Inflamm. 2020. PMID: 30806112

3

TNFRSF21 mutations cause high myopia.

Pan H, Wu S, Wang J, Zhu T, Li T, Wan B, Liu B, Luo Y, Ma X, Sui R, Wang B. Pan H, et al. Among authors: zhu t. J Med Genet. 2019 Oct;56(10):671-677. doi: 10.1136/jmedgenet-2018-105684. Epub 2019 Jun 12. J Med Genet. 2019. PMID: 31189563

4

CLINICAL CHARACTERISTICS AND MOLECULAR GENETIC ANALYSIS OF A COHORT OF CHINESE PATIENTS WITH CHOROIDEREMIA.

Han X, Wu S, Li H, Zhu T, Wei X, Zhou Q, Sui R. Han X, et al. Among authors: zhu t. Retina. 2020 Nov;40(11):2240-2253. doi: 10.1097/IAE.0000000000002743. Retina. 2020. PMID: 31922496

5

Unilateral retinocytoma associated with a variant in the RB1 gene.

Wu S, Zou X, Sun Z, Zhu T, Wei X, Sui R. Wu S, et al. Among authors: zhu t. Mol Genet Genomic Med. 2020 Apr;8(4):e1156. doi: 10.1002/mgg3.1156. Epub 2020 Jan 29. Mol Genet Genomic Med. 2020. PMID: 31997559 Free PMC article.

6

Structural modeling, mutation analysis, and in vitro expression of usherin, a major protein in inherited retinal degeneration and hearing loss.

Yu D, Zou J, Chen Q, Zhu T, Sui R, Yang J. Yu D, et al. Among authors: zhu t. Comput Struct Biotechnol J. 2020 Jun 10;18:1363-1382. doi: 10.1016/j.csbj.2020.05.025. eCollection 2020. Comput Struct Biotechnol J. 2020. PMID: 32637036 Free PMC article.

7

USH2A variants in Chinese patients with Usher syndrome type II and non-syndromic retinitis pigmentosa.

Zhu T, Chen DF, Wang L, Wu S, Wei X, Li H, Jin ZB, Sui R. Zhu T, et al. Br J Ophthalmol. 2021 May;105(5):694-703. doi: 10.1136/bjophthalmol-2019-315786. Epub 2020 Jul 16. Br J Ophthalmol. 2021. PMID: 32675063

8

Detailed comparison of phenotype between male patients carrying variants in exons 1-14 and ORF15 of RPGR.

Zou X, Fang S, Wu S, Li H, Sun Z, Zhu T, Wei X, Sui R. Zou X, et al. Among authors: zhu t. Exp Eye Res. 2020 Sep;198:108147. doi: 10.1016/j.exer.2020.108147. Epub 2020 Jul 21. Exp Eye Res. 2020. PMID: 32702353

9

Variants at codon 838 in the GUCY2D gene result in different phenotypes of cone rod dystrophy.

Sun Z, Wu S, Zhu T, Li H, Wei X, Du H, Sui R. Sun Z, et al. Among authors: zhu t. Ophthalmic Genet. 2020 Dec;41(6):548-555. doi: 10.1080/13816810.2020.1807026. Epub 2020 Aug 18. Ophthalmic Genet. 2020. PMID: 32811265

10

Novel variants in PNPLA6 causing syndromic retinal dystrophy.

Wu S, Sun Z, Zhu T, Weleber RG, Yang P, Wei X, Pennesi ME, Sui R. Wu S, et al. Among authors: zhu t. Exp Eye Res. 2021 Jan;202:108327. doi: 10.1016/j.exer.2020.108327. Epub 2020 Oct 22. Exp Eye Res. 2021. PMID: 33141049 Free PMC article.

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