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

por Wang, Yun, Nishina, Patsy M., Naggert, Jürgen K.
Publicado 2009

A new mouse model of metabolic syndrome and associated complications

por Wang, Yun, Zheng, Yue, Nishina, Patsy M, Naggert, Jürgen K.
Publicado 2009

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Meckelin Is Necessary for Photoreceptor Intraciliary Transport and Outer Segment Morphogenesis

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

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

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

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

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

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

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

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

por Kong, Yang, Zhao, Lihong, Charette, Jeremy R, Hicks, Wanda L, Stone, Lisa, Nishina, Patsy M, Naggert, Jürgen K
Publicado en 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

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

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

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

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 2011

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

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

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

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