Interference with the C-terminal structure of MARF1 causes defective oocyte meiotic division and female infertility in mice

Por Cao, Guang-Yi, Li, Ming-Zhe, Wang, Hao, Shi, Lan-Ying, Su, You-Qiang
Publicado no J Biomed Res (2018)

Mouse Model Resources for Vision Research

Por Won, Jungyeon, Shi, Lan Ying, Hicks, Wanda, Wang, Jieping, Hurd, Ronald, Naggert, Jürgen K., Chang, Bo, Nishina, Patsy M.
Publicado em 2011

L-carnitine ameliorated fasting-induced fatigue, hunger, and metabolic abnormalities in patients with metabolic syndrome: a randomized controlled study

Por Zhang, Jun-jie, Wu, Zhi-bing, Cai, You-jin, Ke, Bin, Huang, Ying-juan, Qiu, Chao-ping, Yang, Yu-bing, Shi, Lan-ying, Qin, Jian
Publicado no Nutr J (2014)

A Chemical Mutagenesis Screen Identifies Mouse Models with ERG Defects

Por Charette, Jeremy R., Samuels, Ivy S., Yu, Minzhong, Stone, Lisa, Hicks, Wanda, Shi, Lan Ying, Krebs, Mark P., Naggert, Jürgen K, Nishina, Patsy M., Peachey, Neal S.
Publicado no Adv Exp Med Biol (2016)

Mouse models of human ocular disease for translational research

Por Krebs, Mark P., Collin, Gayle B., Hicks, Wanda L., Yu, Minzhong, Charette, Jeremy R., Shi, Lan Ying, Wang, Jieping, Naggert, Jürgen K., Peachey, Neal S., Nishina, Patsy M.
Publicado no PLoS One (2017)

Elevation of 20-carbon long chain bases due to a mutation in serine palmitoyltransferase small subunit b results in neurodegeneration

Por Zhao, Lihong, Spassieva, Stefka, Gable, Kenneth, Gupta, Sita D., Shi, Lan-Ying, Wang, Jieping, Bielawski, Jacek, Hicks, Wanda L., Krebs, Mark P., Naggert, Juergen, Hannun, Yusuf A., Dunn, Teresa M., Nishina, Patsy M.
Publicado no Proc Natl Acad Sci U S A (2015)

A Murine Rp1 Missense Mutation Causes Protein Mislocalization and Slowly Progressive Photoreceptor Degeneration

Por Song, Delu, Grieco, Steve, Li, Yafeng, Hunter, Allan, Chu, Sally, Zhao, Liangliang, Song, Ying, DeAngelis, Robert A., Shi, Lan-Ying, Liu, Qin, Pierce, Eric A., Nishina, Patsy M., Lambris, John D., Dunaief, Joshua L.
Publicado em 2014

Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human Disease

Por Greenwald, Scott H., Charette, Jeremy R., Staniszewska, Magdalena, Shi, Lan Ying, Brown, Steve D.M., Stone, Lisa, Liu, Qin, Hicks, Wanda L., Collin, Gayle B., Bowl, Michael R., Krebs, Mark P., Nishina, Patsy M., Pierce, Eric A.
Publicado no Am J Pathol (2016)