Hauswirth WW - Search Results

1

Six Years and Counting: Restoration of Photopic Retinal Function and Visual Behavior Following Gene Augmentation Therapy in a Sheep Model of CNGA3 Achromatopsia.

Ofri R, Averbukh E, Ezra-Elia R, Ross M, Honig H, Obolensky A, Rosov A, Hauswirth WW, Gootwine E, Banin E. Ofri R, et al. Among authors: hauswirth ww. Hum Gene Ther. 2018 Dec;29(12):1376-1386. doi: 10.1089/hum.2018.076. Epub 2018 Jul 30. Hum Gene Ther. 2018. PMID: 29926749

2

Recombinant adeno-associated virus vector-based gene transfer for defects in oxidative metabolism.

Owen R IV, Lewin AP, Peel A, Wang J, Guy J, Hauswirth WW, Stacpoole PW, Flotte TR. Owen R IV, et al. Among authors: hauswirth ww. Hum Gene Ther. 2000 Oct 10;11(15):2067-78. doi: 10.1089/104303400750001381. Hum Gene Ther. 2000. PMID: 11044909

3

Adeno-associated virus-vectored gene therapy for retinal disease.

Dinculescu A, Glushakova L, Min SH, Hauswirth WW. Dinculescu A, et al. Among authors: hauswirth ww. Hum Gene Ther. 2005 Jun;16(6):649-63. doi: 10.1089/hum.2005.16.649. Hum Gene Ther. 2005. PMID: 15960597 Review.

4

Prolonged recovery of retinal structure/function after gene therapy in an Rs1h-deficient mouse model of x-linked juvenile retinoschisis.

Min SH, Molday LL, Seeliger MW, Dinculescu A, Timmers AM, Janssen A, Tonagel F, Tanimoto N, Weber BH, Molday RS, Hauswirth WW. Min SH, et al. Among authors: hauswirth ww. Mol Ther. 2005 Oct;12(4):644-51. doi: 10.1016/j.ymthe.2005.06.002. Mol Ther. 2005. PMID: 16027044 Free article.

5

Gene therapy restores vision-dependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosis.

Pang JJ, Chang B, Kumar A, Nusinowitz S, Noorwez SM, Li J, Rani A, Foster TC, Chiodo VA, Doyle T, Li H, Malhotra R, Teusner JT, McDowell JH, Min SH, Li Q, Kaushal S, Hauswirth WW. Pang JJ, et al. Among authors: hauswirth ww. Mol Ther. 2006 Mar;13(3):565-72. doi: 10.1016/j.ymthe.2005.09.001. Epub 2005 Oct 11. Mol Ther. 2006. PMID: 16223604 Free article.

6

Adeno-associated virus-mediated expression of vascular endothelial growth factor peptides inhibits retinal neovascularization in a mouse model of oxygen-induced retinopathy.

Deng WT, Yan Z, Dinculescu A, Pang J, Teusner JT, Cortez NG, Berns KI, Hauswirth WW. Deng WT, et al. Among authors: hauswirth ww. Hum Gene Ther. 2005 Nov;16(11):1247-54. doi: 10.1089/hum.2005.16.1247. Hum Gene Ther. 2005. PMID: 16259558

7

Increased sensitivity to light-induced damage in a mouse model of autosomal dominant retinal disease.

White DA, Fritz JJ, Hauswirth WW, Kaushal S, Lewin AS. White DA, et al. Among authors: hauswirth ww. Invest Ophthalmol Vis Sci. 2007 May;48(5):1942-51. doi: 10.1167/iovs.06-1131. Invest Ophthalmol Vis Sci. 2007. PMID: 17460245

8

Restoration of cone vision in a mouse model of achromatopsia.

Alexander JJ, Umino Y, Everhart D, Chang B, Min SH, Li Q, Timmers AM, Hawes NL, Pang JJ, Barlow RB, Hauswirth WW. Alexander JJ, et al. Among authors: hauswirth ww. Nat Med. 2007 Jun;13(6):685-7. doi: 10.1038/nm1596. Epub 2007 May 21. Nat Med. 2007. PMID: 17515894 Free PMC article.

9

Targeting gene expression to cones with human cone opsin promoters in recombinant AAV.

Komáromy AM, Alexander JJ, Cooper AE, Chiodo VA, Glushakova LG, Acland GM, Hauswirth WW, Aguirre GD. Komáromy AM, et al. Among authors: hauswirth ww. Gene Ther. 2008 Jul;15(14):1049-55. doi: 10.1038/gt.2008.32. Epub 2008 Mar 13. Gene Ther. 2008. PMID: 18337838 Free PMC article.

10

Prospects for retinal cone-targeted gene therapy.

Alexander JJ, Hauswirth WW. Alexander JJ, et al. Among authors: hauswirth ww. Drug News Perspect. 2008 Jun;21(5):267-71. doi: 10.1358/dnp.2008.21.5.1219012. Drug News Perspect. 2008. PMID: 18596991 Free article.

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