Shen T - Search Results

1

Comprehensive mutation analysis by whole-exome sequencing in 41 Chinese families with Leber congenital amaurosis.

Chen Y, Zhang Q, Shen T, Xiao X, Li S, Guan L, Zhang J, Zhu Z, Yin Y, Wang P, Guo X, Wang J, Zhang Q. Chen Y, et al. Among authors: shen t. Invest Ophthalmol Vis Sci. 2013 Jun 26;54(6):4351-7. doi: 10.1167/iovs.13-11606. Invest Ophthalmol Vis Sci. 2013. PMID: 23661368

2

Detection of CRB1 mutations in families with retinal dystrophy through phenotype-oriented mutational screening.

Li S, Shen T, Xiao X, Guo X, Zhang Q. Li S, et al. Among authors: shen t. Int J Mol Med. 2014 Apr;33(4):913-8. doi: 10.3892/ijmm.2014.1655. Epub 2014 Feb 12. Int J Mol Med. 2014. PMID: 24535598

3

Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing.

Xu Y, Guan L, Shen T, Zhang J, Xiao X, Jiang H, Li S, Yang J, Jia X, Yin Y, Guo X, Wang J, Zhang Q. Xu Y, et al. Among authors: shen t. Hum Genet. 2014 Oct;133(10):1255-71. doi: 10.1007/s00439-014-1460-2. Epub 2014 Jun 18. Hum Genet. 2014. PMID: 24938718

4

Mutation analysis of Leber congenital amaurosis‑associated genes in patients with retinitis pigmentosa.

Shen T, Guan L, Li S, Zhang J, Xiao X, Jiang H, Yang J, Guo X, Wang J, Zhang Q. Shen T, et al. Mol Med Rep. 2015 Mar;11(3):1827-32. doi: 10.3892/mmr.2014.2894. Epub 2014 Nov 7. Mol Med Rep. 2015. PMID: 25377065

5

KIF21A mutation in two Chinese families with congenital fibrosis of the extraocular muscles type 1 and 3.

Chen J, Ye Q, Deng D, Yan J, Lin H, Shen T, Lin Y. Chen J, et al. Among authors: shen t. Mol Med Rep. 2016 Oct;14(4):3145-51. doi: 10.3892/mmr.2016.5624. Epub 2016 Aug 11. Mol Med Rep. 2016. PMID: 27513105 Free PMC article.

6

Missense mutation in the PAX6 gene can cause a complex mild variable phenotype predominated by concomitant strabismus.

Shen T, Qiu X, Lin X, Lin J, Li X, Chen Q, Pan L, Wang Z, Shen H, Zhang Q, Yan J. Shen T, et al. Among authors: shen h. Ophthalmic Genet. 2022 Feb;43(1):88-96. doi: 10.1080/13816810.2021.1961283. Epub 2021 Aug 3. Ophthalmic Genet. 2022. PMID: 34344282

7

Intermediate filaments in the medial rectus muscles in patients with concomitant exotropia.

Shen T, Lin J, Li X, Deng D. Shen T, et al. Int Ophthalmol. 2020 Feb;40(2):403-410. doi: 10.1007/s10792-019-01197-3. Epub 2019 Oct 19. Int Ophthalmol. 2020. PMID: 31630292

8

Long-term therapeutic outcome of ophthalmic complications following endoscopic sinus surgery.

Wu H, Shen T, Chen J, Yan J. Wu H, et al. Among authors: shen t. Medicine (Baltimore). 2016 Sep;95(38):e4896. doi: 10.1097/MD.0000000000004896. Medicine (Baltimore). 2016. PMID: 27661034 Free PMC article.

9

Lateral rectus muscle differentiation potential in paralytic esotropia patients.

Xia Q, Ling X, Wang Z, Shen T, Chen M, Mao D, Ma X, Ning J, Zhang H, Chen D, Gu Q, Shen H, Yan J. Xia Q, et al. Among authors: shen h, shen t. BMC Ophthalmol. 2021 May 27;21(1):235. doi: 10.1186/s12886-021-01994-4. BMC Ophthalmol. 2021. PMID: 34044792 Free PMC article.

10

Newly developed abnormal head position and secondary esotropia after strabismus surgery for children with intermittent exotropia.

Shen T, Kang Y, Lin X, Wu H, Yan J. Shen T, et al. Int Ophthalmol. 2022 Oct;42(10):2965-2972. doi: 10.1007/s10792-021-02173-6. Epub 2022 Jan 27. Int Ophthalmol. 2022. PMID: 35083599

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