Liu X - Search Results

1

Mutation analysis of pre-mRNA splicing genes in Chinese families with retinitis pigmentosa.

Pan X, Chen X, Liu X, Gao X, Kang X, Xu Q, Chen X, Zhao K, Zhang X, Chu Q, Wang X, Zhao C. Pan X, et al. Among authors: liu x. Mol Vis. 2014 Jun 2;20:770-9. eCollection 2014. Mol Vis. 2014. PMID: 24940031 Free PMC article.

2

PRPF4 mutations cause autosomal dominant retinitis pigmentosa.

Chen X, Liu Y, Sheng X, Tam PO, Zhao K, Chen X, Rong W, Liu Y, Liu X, Pan X, Chen LJ, Zhao Q, Vollrath D, Pang CP, Zhao C. Chen X, et al. Among authors: liu y, liu x. Hum Mol Genet. 2014 Jun 1;23(11):2926-39. doi: 10.1093/hmg/ddu005. Epub 2014 Jan 12. Hum Mol Genet. 2014. PMID: 24419317

3

Targeted next-generation sequencing reveals novel USH2A mutations associated with diverse disease phenotypes: implications for clinical and molecular diagnosis.

Chen X, Sheng X, Liu X, Li H, Liu Y, Rong W, Ha S, Liu W, Kang X, Zhao K, Zhao C. Chen X, et al. Among authors: liu y, liu x, liu w. PLoS One. 2014 Aug 18;9(8):e105439. doi: 10.1371/journal.pone.0105439. eCollection 2014. PLoS One. 2014. PMID: 25133613 Free PMC article.

4

Targeted next-generation sequencing reveals novel EYS mutations in Chinese families with autosomal recessive retinitis pigmentosa.

Chen X, Liu X, Sheng X, Gao X, Zhang X, Li Z, Li H, Liu Y, Rong W, Zhao K, Zhao C. Chen X, et al. Among authors: liu y, liu x. Sci Rep. 2015 Mar 10;5:8927. doi: 10.1038/srep08927. Sci Rep. 2015. PMID: 25753737 Free PMC article.

5

Targeted next-generation sequencing extends the mutational spectrums for OPA1 mutations in Chinese families with optic atrophy.

Wang Y, Xu M, Liu X, Huang Y, Zhou Y, Liu Q, Chen X, Zhao C, Wang M. Wang Y, et al. Among authors: liu x, liu q. Mol Vis. 2019 Dec 31;25:912-920. eCollection 2019. Mol Vis. 2019. PMID: 32025183 Free PMC article.

6

Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2.

Rong W, Chen X, Zhao K, Liu Y, Liu X, Ha S, Liu W, Kang X, Sheng X, Zhao C. Rong W, et al. Among authors: liu y, liu x, liu w. PLoS One. 2014 May 15;9(5):e97808. doi: 10.1371/journal.pone.0097808. eCollection 2014. PLoS One. 2014. PMID: 24831256 Free PMC article.

7

Molecular genetic testing in clinical diagnostic assessments that demonstrate correlations in patients with autosomal recessive inherited retinal dystrophy.

Liu X, Xiao J, Huang H, Guan L, Zhao K, Xu Q, Zhang X, Pan X, Gu S, Chen Y, Zhang J, Shen Y, Jiang H, Gao X, Kang X, Sheng X, Chen X, Zhao C. Liu X, et al. JAMA Ophthalmol. 2015 Apr;133(4):427-36. doi: 10.1001/jamaophthalmol.2014.5831. JAMA Ophthalmol. 2015. PMID: 25611614

8

Relationship between High Expression of Kaiso Protein and Poor Prognosis of Lung Cancer and the Regulation Mechanism of Malignant Phenotype of Lung Cancer Cells.

Zhu S, Zhou N, Ding N, Li S, Liu X, Ren G, Li Q, Zhou M. Zhu S, et al. Among authors: liu x. J Oncol. 2021 Dec 22;2021:7388368. doi: 10.1155/2021/7388368. eCollection 2021. J Oncol. 2021. PMID: 34976058 Free PMC article.

9

In vivo assessment of human corneal epithelial cells in orthokeratology lens wearers: A pilot study.

Pattan HF, Liu X, Tankam P. Pattan HF, et al. Among authors: liu x. Optom Vis Sci. 2024 Apr 25. doi: 10.1097/OPX.0000000000002130. Online ahead of print. Optom Vis Sci. 2024. PMID: 38683973

10

Consistency-Aware Anchor Pyramid Network for Crowd Localization.

Liu X, Li G, Qi Y, Han Z, Hengel AVD, Sebe N, Yang MH, Huang Q. Liu X, et al. IEEE Trans Pattern Anal Mach Intell. 2024 Apr 29;PP. doi: 10.1109/TPAMI.2024.3392013. Online ahead of print. IEEE Trans Pattern Anal Mach Intell. 2024. PMID: 38683713

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