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 em 2009

A new mouse model of metabolic syndrome and associated complications

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

Alström Syndrome: Genetics and Clinical Overview

Por Marshall, Jan D, Maffei, Pietro, Collin, Gayle B, Naggert, Jürgen K
Publicado em 2011

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 em 2009

Clinical utility gene card for: Alström Syndrome - update 2013

Por Marshall, Jan D, Maffei, Pietro, Beck, Sebastian, Barrett, Timothy G, Paisey, Richard, Naggert, Jürgen K
Publicado em 2013

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 em 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 em 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 em 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 em 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 em 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 em 2012

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 em 2008

A Mouse Model for Meckel Syndrome Type 3

Por Cook, Susan A., Collin, Gayle B., Bronson, Roderick T., Naggert, Jürgen K., Liu, Dong P., Akeson, Ellen C., Davisson, Muriel T.
Publicado em 2009

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 em 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 em 2011

Novel Alu Retrotransposon Insertion Leading to Alström Syndrome

Por Taşkesen, Mustafa, Collin, Gayle B., Evsikov, Alexei V., Güzel, Ayşegül, Özgül, R. Köksal, Marshall, Jan D., Naggert, Jürgen K.
Publicado em 2011

The Alström Syndrome Protein, ALMS1, Interacts with α-Actinin and Components of the Endosome Recycling Pathway

Por Collin, Gayle B., Marshall, Jan D., King, Benjamin L., Milan, Gabriella, Maffei, Pietro, Jagger, Daniel J., Naggert, Jürgen K.
Publicado em 2012

GLUT4 Defects in Adipose Tissue Are Early Signs of Metabolic Alterations in Alms1(GT/GT), a Mouse Model for Obesity and Insulin Resistance

Por Favaretto, Francesca, Milan, Gabriella, Collin, Gayle B., Marshall, Jan D., Stasi, Fabio, Maffei, Pietro, Vettor, Roberto, Naggert, Jürgen K.
Publicado em 2014

Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader–Willi and Alström syndromes

Por Butler, Merlin G, Wang, Kun, Marshall, Jan D, Naggert, Jürgen K, Rethmeyer, Jasmine A, Gunewardena, Sumedha S, Manzardo, Ann M
Publicado no Adv Genomics Genet (2015)

Diminished gallbladder motility in rotund leptin-resistant obese mice

Por Graewin, Shannon J., Tran, Khoi Q., Naggert, Jurgen K., Lee, Keun-Ho, Swartz-Basile, Debbie, Nakeeb, Attila, Pitt, Henry A.
Publicado em 2005