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Filters: Keyword is Mice, Transgenic  [Clear All Filters]
2023
Hardwiring tissue-specific AAV transduction in mice through engineered receptor expression., Zengel, James, Wang Yu Xin, Seo Jai Woong, Ning Ke, Hamilton James N., Wu Bo, Raie Marina, Holbrook Colin, Su Shiqi, Clements Derek R., et al. , Nat Methods, 2023 Jul, Volume 20, Issue 7, p.1070-1081, (2023)
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)
2012
Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome., McIntyre, Rebecca E., Chavali Pavithra Lakshminar, Ismail Ozama, Carragher Damian M., Sanchez-Andrade Gabriela, Forment Josep V., Fu Beiyuan, Velasco-Herrera Martin Del Castil, Edwards Andrew, van der Weyden Louise, et al. , PLoS Genet, 2012, Volume 8, Issue 11, p.e1003022, (2012)
2011
Mouse eye enucleation for remote high-throughput phenotyping., Mahajan, Vinit B., Skeie Jessica M., Assefnia Amir H., Mahajan Maryann, and Tsang Stephen H. , Journal of visualized experiments : JoVE, 2011, Issue 57, (2011)
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)