Dai X - Search Results

1

Gene therapy following subretinal AAV5 vector delivery is not affected by a previous intravitreal AAV5 vector administration in the partner eye.

Li W, Kong F, Li X, Dai X, Liu X, Zheng Q, Wu R, Zhou X, Lü F, Chang B, Li Q, Hauswirth WW, Qu J, Pang JJ. Li W, et al. Among authors: dai x. Mol Vis. 2009;15:267-75. Epub 2009 Feb 6. Mol Vis. 2009. PMID: 19190735 Free PMC article.

2

Self-complementary AAV5 vector facilitates quicker transgene expression in photoreceptor and retinal pigment epithelial cells of normal mouse.

Kong F, Li W, Li X, Zheng Q, Dai X, Zhou X, Boye SL, Hauswirth WW, Qu J, Pang JJ. Kong F, et al. Among authors: dai x. Exp Eye Res. 2010 May;90(5):546-54. doi: 10.1016/j.exer.2010.01.011. Epub 2010 Feb 4. Exp Eye Res. 2010. PMID: 20138034 Free PMC article.

3

Long-term retinal function and structure rescue using capsid mutant AAV8 vector in the rd10 mouse, a model of recessive retinitis pigmentosa.

Pang JJ, Dai X, Boye SE, Barone I, Boye SL, Mao S, Everhart D, Dinculescu A, Liu L, Umino Y, Lei B, Chang B, Barlow R, Strettoi E, Hauswirth WW. Pang JJ, et al. Among authors: dai x. Mol Ther. 2011 Feb;19(2):234-42. doi: 10.1038/mt.2010.273. Epub 2010 Dec 7. Mol Ther. 2011. PMID: 21139570 Free PMC article.

4

Gene therapy rescues cone structure and function in the 3-month-old rd12 mouse: a model for midcourse RPE65 leber congenital amaurosis.

Li X, Li W, Dai X, Kong F, Zheng Q, Zhou X, Lü F, Chang B, Rohrer B, Hauswirth WW, Qu J, Pang JJ. Li X, et al. Among authors: dai x. Invest Ophthalmol Vis Sci. 2011 Jan 5;52(1):7-15. doi: 10.1167/iovs.10-6138. Print 2011 Jan. Invest Ophthalmol Vis Sci. 2011. PMID: 21169527 Free PMC article.

5

Differential proteomics and functional research following gene therapy in a mouse model of Leber congenital amaurosis.

Zheng Q, Ren Y, Tzekov R, Zhang Y, Chen B, Hou J, Zhao C, Zhu J, Zhang Y, Dai X, Ma S, Li J, Pang J, Qu J, Li W. Zheng Q, et al. Among authors: dai x. PLoS One. 2012;7(8):e44855. doi: 10.1371/journal.pone.0044855. Epub 2012 Aug 31. PLoS One. 2012. PMID: 22953002 Free PMC article.

6

Review: the history and role of naturally occurring mouse models with Pde6b mutations.

Han J, Dinculescu A, Dai X, Du W, Smith WC, Pang J. Han J, et al. Among authors: dai x. Mol Vis. 2013 Dec 20;19:2579-89. Mol Vis. 2013. PMID: 24367157 Free PMC article. Review.

7

AAV-mediated lysophosphatidylcholine acyltransferase 1 (Lpcat1) gene replacement therapy rescues retinal degeneration in rd11 mice.

Dai X, Han J, Qi Y, Zhang H, Xiang L, Lv J, Li J, Deng WT, Chang B, Hauswirth WW, Pang JJ. Dai X, et al. Invest Ophthalmol Vis Sci. 2014 Mar 20;55(3):1724-34. doi: 10.1167/iovs.13-13654. Invest Ophthalmol Vis Sci. 2014. PMID: 24557352 Free PMC article.

8

[Progress on study of achromatopsia and targeted gene therapy].

Dai XF, Pang JJ. Dai XF, et al. Zhonghua Yan Ke Za Zhi. 2012 Aug;48(8):755-8. Zhonghua Yan Ke Za Zhi. 2012. PMID: 23141518 Review. Chinese.

9

[Effect of voltage-dependent calcium channel α1F subunit deficiency on the structure and function of the murine retina].

Dai XF, Pang JJ, Han JJ, Qi Y. Dai XF, et al. Zhonghua Yan Ke Za Zhi. 2013 Jun;49(6):521-5. Zhonghua Yan Ke Za Zhi. 2013. PMID: 24119965 Chinese.

10

Self-complementary AAV-mediated gene therapy restores cone function and prevents cone degeneration in two models of Rpe65 deficiency.

Pang J, Boye SE, Lei B, Boye SL, Everhart D, Ryals R, Umino Y, Rohrer B, Alexander J, Li J, Dai X, Li Q, Chang B, Barlow R, Hauswirth WW. Pang J, et al. Among authors: dai x. Gene Ther. 2010 Jul;17(7):815-26. doi: 10.1038/gt.2010.29. Epub 2010 Mar 18. Gene Ther. 2010. PMID: 20237510 Free PMC article.

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