Erratum for Purviance et al., “In the Simian Virus 40 In Vitro Replication System, Start Site Selection by the Polymerase α-Primase Complex Is Not Significantly Altered by Changes...

Por Purviance, John D., Prack, Andrea E., Barbaro, Brett A., Bullock, Peter A.
Publicado no J Virol (2017)

CellPAINT: Interactive Illustration of Dynamic Mesoscale Cellular Environments

Por Gardner, Adam, Autin, Ludovic, Barbaro, Brett A., Olson, Arthur J., Goodsell, David S.
Publicado no IEEE Comput Graph Appl (2018)

The Simian Virus 40 Core Origin Contains Two Separate Sequence Modules That Support T-Antigen Double-Hexamer Assembly

Por Sreekumar, K. R., Prack, Andrea E., Winters, Danielle R., Barbaro, Brett A., Bullock, Peter A.
Publicado em 2000

Phosphorylation of Simian Virus 40 T Antigen on Thr 124 Selectively Promotes Double-Hexamer Formation on Subfragments of the Viral Core Origin

Por Barbaro, Brett A., Sreekumar, K. R., Winters, Danielle R., Prack, Andrea E., Bullock, Peter A.
Publicado em 2000

Sequence Requirements for the Assembly of Simian Virus 40 T Antigen and the T-Antigen Origin Binding Domain on the Viral Core Origin of Replication

Por Kim, Henry Y., Barbaro, Brett A., Joo, Woo S., Prack, Andrea E., Sreekumar, K. R., Bullock, Peter A.
Publicado em 1999

Disruption of the nuclear membrane by perinuclear inclusions of mutant huntingtin causes cell-cycle re-entry and striatal cell death in mouse and cell models of Huntington's diseas...

Por Liu, Kuan-Yu, Shyu, Yu-Chiau, Barbaro, Brett A., Lin, Yuan-Ta, Chern, Yijuang, Thompson, Leslie Michels, James Shen, Che-Kun, Marsh, J. Lawrence
Publicado no Hum Mol Genet (2015)

Effects of flanking sequences and cellular context on subcellular behavior and pathology of mutant HTT

Por Chongtham, Anjalika, Bornemann, Douglas J, Barbaro, Brett A, Lukacsovich, Tamas, Agrawal, Namita, Syed, Adeela, Worthge, Shane, Purcell, Judith, Burke, John, Chin, Theodore M, Marsh, J Lawrence
Publicado no Hum Mol Genet (2020)

Comparative study of naturally occurring huntingtin fragments in Drosophila points to exon 1 as the most pathogenic species in Huntington's disease

Por Barbaro, Brett A., Lukacsovich, Tamas, Agrawal, Namita, Burke, John, Bornemann, Doug J., Purcell, Judith M., Worthge, Shane A., Caricasole, Andrea, Weiss, Andreas, Song, Wan, Morozova, Olga A., Colby, David W., Marsh, J. Lawrence
Publicado no Hum Mol Genet (2015)

A potent and selective Sirtuin 1 inhibitor alleviates pathology in multiple animal and cell models of Huntington's disease

Por Smith, Marianne R., Syed, Adeela, Lukacsovich, Tamas, Purcell, Judy, Barbaro, Brett A., Worthge, Shane A., Wei, Stephen R., Pollio, Giuseppe, Magnoni, Letizia, Scali, Carla, Massai, Luisa, Franceschini, Davide, Camarri, Michela, Gianfriddo, Marco, Diodato, Enrica, Thomas, Russell, Gokce, Ozgun, Tabrizi, S.J., Caricasole, Andrea, Landwehrmeyer, Bernard, Menalled, Liliana, Murphy, Carol, Ramboz, Sylvie, Luthi-Carter, Ruth, Westerberg, Goran, Marsh, J. Lawrence
Publicado em 2014