Brett A. Barbaro

affective disorders, neurogenesis, imaging genetics

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Chongtham A, Bornemann DJ, Barbaro BA, et al. (2020) Effects of flanking sequences and cellular context on subcellular behavior and pathology of mutant HTT. Human Molecular Genetics
Chongtham A, Barbaro B, Filip T, et al. (2018) Nonmammalian Models of Huntington's Disease. Methods in Molecular Biology (Clifton, N.J.). 1780: 75-96
Liu KY, Shyu YC, Barbaro BA, et al. (2015) 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 disease. Human Molecular Genetics. 24: 1602-16
Barbaro BA, Lukacsovich T, Agrawal N, et al. (2015) Comparative study of naturally occurring huntingtin fragments in Drosophila points to exon 1 as the most pathogenic species in Huntington's disease. Human Molecular Genetics. 24: 913-25
Smith MR, Syed A, Lukacsovich T, et al. (2014) A potent and selective Sirtuin 1 inhibitor alleviates pathology in multiple animal and cell models of Huntington's disease. Human Molecular Genetics. 23: 2995-3007
Song W, Smith MR, Syed A, et al. (2013) Morphometric analysis of Huntington's disease neurodegeneration in Drosophila. Methods in Molecular Biology (Clifton, N.J.). 1017: 41-57