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Publications

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Filters: Keyword is Disease Models, Animal  [Clear All Filters]
2016
CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa., Wu, Wen-Hsuan, Tsai Yi-Ting, Justus Sally, Lee Ting-Ting, Zhang Lijuan, Lin Chyuan-Sheng, Bassuk Alexander G., Mahajan Vinit B., and Tsang Stephen H. , Mol Ther, 2016 08, Volume 24, Issue 8, p.1388-94, (2016)
Reprogramming metabolism by targeting sirtuin 6 attenuates retinal degeneration., Zhang, Lijuan, Du Jianhai, Justus Sally, Hsu Chun-Wei, Bonet-Ponce Luis, Wu Wen-Hsuan, Tsai Yi-Ting, Wu Wei-Pu, Jia Yading, Duong Jimmy K., et al. , J Clin Invest, 2016 Dec 01, Volume 126, Issue 12, p.4659-4673, (2016)
Reprogramming towards anabolism impedes degeneration in a preclinical model of retinitis pigmentosa., Zhang, Lijuan, Justus Sally, Xu Yu, Pluchenik Tamara, Hsu Chun-Wei, Yang Jin, Duong Jimmy K., Lin Chyuan-Sheng, Jia Yading, Bassuk Alexander G., et al. , Hum Mol Genet, 2016 10 01, Volume 25, Issue 19, p.4244-4255, (2016)
2014
Silencing of tuberin enhances photoreceptor survival and function in a preclinical model of retinitis pigmentosa (an american ophthalmological society thesis)., Tsang, Stephen H., Chan Lawrence, Tsai Yi-Ting, Wu Wen-Hsuan, Hsu Chun-Wei, Yang Jin, Tosi Joaquin, Wert Katherine J., Davis Richard J., and Mahajan Vinit B. , Trans Am Ophthalmol Soc, 2014 Jul, Volume 112, p.103-15, (2014)
2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes., White, Jacqueline K., Gerdin Anna-Karin, Karp Natasha A., Ryder Ed, Buljan Marija, Bussell James N., Salisbury Jennifer, Clare Simon, Ingham Neil J., Podrini Christine, et al. , Cell, 2013 Jul 18, Volume 154, Issue 2, p.452-64, (2013)
2007
Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness., Tsang, Stephen H., Woodruff Michael L., Jun Lin, Mahajan Vinit, Yamashita Clyde K., Pedersen Robert, Lin Chyuan-Sheng, Goff Stephen P., Rosenberg Thomas, Larsen Michael, et al. , Human mutation, 2007 Mar, Volume 28, Issue 3, p.243-54, (2007)