Mouse Models for Drug Discovery. Can New Tools and Technology Improve Translational Power?

por Zuberi, Aamir, Lutz, Cathleen
Publicado 2016

Loss of Pex1 in Inner Ear Hair Cells Contributes to Cochlear Synaptopathy and Hearing Loss

por Mauriac, Stephanie A., Peineau, Thibault, Zuberi, Aamir, Lutz, Cathleen, Géléoc, Gwénaëlle S. G.
Publicado 2022

Neurobehavioral deficits of mice expressing a low level of G127V mutant frataxin

por Fil, Daniel, Conley, Robbie L., Zuberi, Aamir R., Lutz, Cathleen M., Gemelli, Terry, Napierala, Marek, Napierala, Jill S.
Publicado 2023

Molecular Mechanisms for Activation of the Agouti-Related Protein and Stimulation of Appetite

por Ilnytska, Olha, Stütz, Adrian M., Park-York, MieJung, York, David A., Ribnicky, David M., Zuberi, Aamir, Cefalu, William T., Argyropoulos, George
Publicado 2011

Mitochondrial damage and senescence phenotype of cells derived from a novel frataxin G127V point mutation mouse model of Friedreich's ataxia

por Fil, Daniel, Chacko, Balu K., Conley, Robbie, Ouyang, Xiaosen, Zhang, Jianhua, Darley-Usmar, Victor M., Zuberi, Aamir R., Lutz, Cathleen M., Napierala, Marek, Napierala, Jill S.
Publicado 2020

Regulation of BMP4/Dpp retrotranslocation and signaling by deglycosylation

por Galeone, Antonio, Adams, Joshua M, Matsuda, Shinya, Presa, Maximiliano F, Pandey, Ashutosh, Han, Seung Yeop, Tachida, Yuriko, Hirayama, Hiroto, Vaccari, Thomas, Suzuki, Tadashi, Lutz, Cathleen M, Affolter, Markus, Zuberi, Aamir, Jafar-Nejad, Hamed
Publicado 2020

A Drosophila screen identifies NKCC1 as a modifier of NGLY1 deficiency

por Talsness, Dana M, Owings, Katie G, Coelho, Emily, Mercenne, Gaelle, Pleinis, John M, Partha, Raghavendran, Hope, Kevin A, Zuberi, Aamir R, Clark, Nathan L, Lutz, Cathleen M, Rodan, Aylin R, Chow, Clement Y
Publicado 2020