Degradation of IRS1 leads to impaired glucose uptake in adipose tissue of the type 2 diabetes mouse model TALLYHO/Jng

per Wang, Yun, Nishina, Patsy M., Naggert, Jürgen K.
Publicat 2009

A new mouse model of metabolic syndrome and associated complications

per Wang, Yun, Zheng, Yue, Nishina, Patsy M, Naggert, Jürgen K.
Publicat 2009

Molecular characterization of TUB, TULP1, and TULP2, members of the novel tubby gene family and their possible relation to ocular diseases

per North, Michael A., Naggert, Juergen K., Yan, Yingzhuo, Noben-Trauth, Konrad, Nishina, Patsy M.
Publicat 1997

New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene

per Sakamoto, Kenji, McCluskey, Michael, Wensel, Theodore G., Naggert, Jürgen K., Nishina, Patsy M.
Publicat 2009

Gene therapy provides long-term visual function in a pre-clinical model of retinitis pigmentosa

per Wert, Katherine J., Davis, Richard J., Sancho-Pelluz, Javier, Nishina, Patsy M., Tsang, Stephen H.
Publicat 2013

Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θ

per Ji, Xiaojie, Liu, Ye, Hurd, Ron, Wang, Jieping, Fitzmaurice, Bernie, Nishina, Patsy M., Chang, Bo
Publicat a Invest Ophthalmol Vis Sci (2016)

Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1(rd8) Allele

per Chang, Bo, FitzMaurice, Bernard, Wang, Jieping, Low, Benjamin E., Wiles, Michael V., Nishina, Patsy M.
Publicat a Invest Ophthalmol Vis Sci (2018)

Membrane Frizzled Related Protein is necessary for the normal development and maintenance of photoreceptor outer segments

per Won, Jungyeon, Smith, Richard S., Peachey, Neal S., Wu, Jiang, Hicks, Wanda L., Naggert, Jürgen K., Nishina, Patsy M.
Publicat 2008

Microtubule-associated protein 1A is a modifier of tubby hearing (moth1)

per Ikeda, Akihiro, Zheng, Qing Yin, Zuberi, Aamir R., Johnson, Kenneth R., Naggert, Jürgen K., Nishina, Patsy M.
Publicat 2002

A novel ENU-induced mutation, peewee, causes dwarfism in the mouse

per Bon-Ryon, Lee, Kano, Kiyoshi, Young, Jay, John, Simon, Nishina, Patsy M, Naggert, Jurgen K, Naito, Kunihiko
Publicat 2009

Meckelin Is Necessary for Photoreceptor Intraciliary Transport and Outer Segment Morphogenesis

per Collin, Gayle B., Won, Jungyeon, Hicks, Wanda L., Cook, Susan A., Nishina, Patsy M., Naggert, Jürgen K.
Publicat 2012

An ENU-Induced Mutation in the Mertk Gene (Mertk(nmf12)) Leads to a Slow Form of Retinal Degeneration

per Maddox, Dennis M., Hicks, Wanda L., Vollrath, Douglas, LaVail, Matthew M., Naggert, Jürgen K., Nishina, Patsy M.
Publicat 2011

An Allele of Microtubule-Associated Protein 1A (Mtap1a) Reduces Photoreceptor Degeneration in Tulp1 and Tub Mutant Mice

per Maddox, Dennis M., Ikeda, Sakae, Ikeda, Akihiro, Zhang, Weidong, Krebs, Mark P., Nishina, Patsy M., Naggert, Jürgen K.
Publicat 2012

Correction of the Crb1(rd8) Allele and Retinal Phenotype in C57BL/6N Mice Via TALEN-Mediated Homology-Directed Repair

per Low, Benjamin E., Krebs, Mark P., Joung, J. Keith, Tsai, Shengdar Q., Nishina, Patsy M., Wiles, Michael V.
Publicat 2014

An FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiency

per Kong, Yang, Zhao, Lihong, Charette, Jeremy R, Hicks, Wanda L, Stone, Lisa, Nishina, Patsy M, Naggert, Jürgen K
Publicat a Hum Mol Genet (2018)

A Novel Dwarfism with Gonadal Dysfunction Due to Loss-of-Function Allele of the Collagen Receptor Gene, Ddr2, in the Mouse

per Kano, Kiyoshi, Marín de Evsikova, C., Young, James, Wnek, Christopher, Maddatu, Terry P., Nishina, Patsy M., Naggert, Jürgen K.
Publicat 2008

Transcriptome analysis reveals an unexpected role of a collagen tyrosine kinase receptor gene, Ddr2, as a regulator of ovarian function

per Matsumura, Hirokazu, Kano, Kiyoshi, de Evsikova, Caralina Marín, Young, James A., Nishina, Patsy M., Naggert, Jürgen K., Naito, Kunihiko
Publicat 2009

Mouse Model Resources for Vision Research

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

Myosin 6 Is Required for Iris Development and Normal Function of the Outer Retina

per Samuels, Ivy S., Bell, Brent A., Sturgill-Short, Gwen, Ebke, Lindsey A., Rayborn, Mary, Shi, Lanying, Nishina, Patsy M., Peachey, Neal S
Publicat 2013

Carbonic anhydrase related protein 8 mutation results in aberrant synaptic morphology and excitatory synaptic function in the cerebellum

per Hirasawa, Michiru, Xu, Xinjie, Trask, Robert B., Maddatu, Terry P., Johnson, Britt A, Naggert, Jürgen K., Nishina, Patsy M., Ikeda, Akihiro
Publicat 2007