Liu X - Search Results

1

Targeted next generation sequencing identified novel mutations in RPGRIP1 associated with both retinitis pigmentosa and Leber's congenital amaurosis in unrelated Chinese patients.

Huang H, Wang Y, Chen H, Chen Y, Wu J, Chiang PW, Fan N, Su Y, Deng J, Chen D, Li Y, Zhang X, Zhang M, Liang S, Banerjee S, Qi M, Liu X. Huang H, et al. Among authors: liu x. Oncotarget. 2017 May 23;8(21):35176-35183. doi: 10.18632/oncotarget.17052. Oncotarget. 2017. PMID: 28456785 Free PMC article.

2

A novel MYOC heterozygous mutation identified in a Chinese Uygur pedigree with primary open-angle glaucoma.

Cai SP, Muhemaiti P, Yin Y, Cheng H, Di Ya A, Keyimu M, Cao X, Fan N, Jiang L, Yan N, Zhou X, Wang Y, Liu X. Cai SP, et al. Among authors: liu x. Mol Vis. 2012;18:1944-51. Epub 2012 Jul 18. Mol Vis. 2012. PMID: 22876119 Free PMC article.

3

Studies of a pedigree with limbal dermoid cyst.

Zhu J, Cheng HB, Fan N, Liu CM, Yu WH, Chen XM, Liu XY. Zhu J, et al. Int J Ophthalmol. 2012;5(5):641-3. doi: 10.3980/j.issn.2222-3959.2012.05.20. Epub 2012 Oct 18. Int J Ophthalmol. 2012. PMID: 23166879 Free PMC article.

4

Single nucleotide polymorphism of MYOC affected the severity of primary open angle glaucoma.

Zhou XM, Yin Y, Fan N, Cheng HB, Li XH, Wang Y, Yu WH, Cai SP, Liu XY. Zhou XM, et al. Int J Ophthalmol. 2013 Jun 18;6(3):264-8. doi: 10.3980/j.issn.2222-3959.2013.03.02. Print 2013. Int J Ophthalmol. 2013. PMID: 23826516 Free PMC article.

5

Novel compound heterozygous mutations identified in ADAMTSL4 gene in a Chinese family with isolated ectopia lentis.

Zhou XM, Wang Y, Zhao L, Yu WH, Fan N, Yan NH, Su Q, Liang YQ, Wang Y, Li LP, Cai SP, Jonas JB, Liu XY. Zhou XM, et al. Acta Ophthalmol. 2015 Feb;93(1):e91-2. doi: 10.1111/aos.12399. Epub 2014 May 7. Acta Ophthalmol. 2015. PMID: 24802351 Free article. No abstract available.

6

Neuroprotective effects of C3 exoenzyme in excitotoxic retinopathy.

Wang Y, Wang Y, Yang Q, Guo L, Yin Y, Fan N, Zhou X, Cai SP, Kaufman PL, Liu X. Wang Y, et al. Among authors: liu x. Exp Eye Res. 2014 Aug;125:128-34. doi: 10.1016/j.exer.2014.05.018. Epub 2014 Jun 11. Exp Eye Res. 2014. PMID: 24928315 Free PMC article.

7

Mutational Analysis of the TYR and OCA2 Genes in Four Chinese Families with Oculocutaneous Albinism.

Wang Y, Wang Z, Chen M, Fan N, Yang J, Liu L, Wang Y, Liu X. Wang Y, et al. Among authors: liu x, liu l. PLoS One. 2015 Apr 28;10(4):e0125651. doi: 10.1371/journal.pone.0125651. eCollection 2015. PLoS One. 2015. PMID: 25919014 Free PMC article.

8

A novel mutation in fibrillin-1 gene identified in a Chinese family with marfan syndrome.

Liu DL, Cao JH, Yang J, He F, Wang Y, Fan N, Liu XY. Liu DL, et al. Int J Clin Exp Med. 2015 May 15;8(5):7419-24. eCollection 2015. Int J Clin Exp Med. 2015. PMID: 26221284 Free PMC article.

9

Ocular Blood Flow and Normal Tension Glaucoma.

Fan N, Wang P, Tang L, Liu X. Fan N, et al. Among authors: liu x. Biomed Res Int. 2015;2015:308505. doi: 10.1155/2015/308505. Epub 2015 Oct 19. Biomed Res Int. 2015. PMID: 26558263 Free PMC article. Review.

10

Effects of Latanoprost and Bimatoprost on the Expression of Molecules Relevant to Ocular Inflow and Outflow Pathways.

Li X, He F, Gabelt BT, Wang Y, Cai S, Cao J, Fan N, Kaufman PL, Liu X. Li X, et al. Among authors: liu x. PLoS One. 2016 Mar 24;11(3):e0151644. doi: 10.1371/journal.pone.0151644. eCollection 2016. PLoS One. 2016. PMID: 27011234 Free PMC article.

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