Deciphering cell-cell communication in the developing mammalian brain

Por Yuzwa, Scott A., Miller, Freda D.
Publicado no Neurogenesis (Austin) (2017)

The Emerging Link between O-GlcNAc and Alzheimer Disease

Por Zhu, Yanping, Shan, Xiaoyang, Yuzwa, Scott A., Vocadlo, David J.
Publicado no J Biol Chem (2014)

Insights into O-Linked N-Acetylglucosamine ([0-9]O-GlcNAc) Processing and Dynamics through Kinetic Analysis of O-GlcNAc Transferase and O-GlcNAcase Activity on Protein Substrates

Por Shen, David L., Gloster, Tracey M., Yuzwa, Scott A., Vocadlo, David J.
Publicado em 2012

Elevation of Global O-GlcNAc in Rodents Using a Selective O-GlcNAcase Inhibitor Does Not Cause Insulin Resistance or Perturb Glucohomeostasis

Por Macauley, Matthew S., Shan, Xiaoyang, Yuzwa, Scott A., Gloster, Tracey M., Vocadlo, David J.
Publicado em 2010

Post-translational O-GlcNAcylation is essential for nuclear pore integrity and maintenance of the pore selectivity filter

Por Zhu, Yanping, Liu, Ta-Wei, Madden, Zarina, Yuzwa, Scott A., Murray, Kelsey, Cecioni, Samy, Zachara, Natasha, Vocadlo, David J.
Publicado no J Mol Cell Biol (2016)

Identification of Drugs that Regulate Dermal Stem Cells and Enhance Skin Repair

Por Naska, Sibel, Yuzwa, Scott A., Johnston, Adam P.W., Paul, Smitha, Smith, Kristen M., Paris, Maryline, Sefton, Michael V., Datti, Alessandro, Miller, Freda D., Kaplan, David R.
Publicado no Stem Cell Reports (2015)

Metabolism of Vertebrate Amino Sugars with N-Glycolyl Groups: INTRACELLULAR β-O-LINKED N-GLYCOLYLGLUCOSAMINE (GlcNGc), UDP-GlcNGc, AND THE BIOCHEMICAL AND STRUCTURAL RATIONALE FOR...

Por Macauley, Matthew S., Chan, Jefferson, Zandberg, Wesley F., He, Yuan, Whitworth, Garrett E., Stubbs, Keith A., Yuzwa, Scott A., Bennet, Andrew J., Varki, Ajit, Davies, Gideon J., Vocadlo, David J.
Publicado em 2012

Pharmacological inhibition of O-GlcNAcase (OGA) prevents cognitive decline and amyloid plaque formation in bigenic tau/APP mutant mice

Por Yuzwa, Scott A, Shan, Xiaoyang, Jones, Bryan A, Zhao, Gang, Woodward, Melissa L, Li, Xiaojing, Zhu, Yanping, McEachern, Ernest J, Silverman, Michael A, Watson, Neil V, Gong, Cheng-Xin, Vocadlo, David J
Publicado no Mol Neurodegener (2014)

Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation

Por Ravindran, Ethiraj, Hu, Hao, Yuzwa, Scott A., Hernandez-Miranda, Luis R., Kraemer, Nadine, Ninnemann, Olaf, Musante, Luciana, Boltshauser, Eugen, Schindler, Detlev, Hübner, Angela, Reinecker, Hans-Christian, Ropers, Hans-Hilger, Birchmeier, Carmen, Miller, Freda D., Wienker, Thomas F., Hübner, Christoph, Kaindl, Angela M.
Publicado no PLoS Genet (2017)