Sarah E. Dougherty

Affiliations: 
University of Alabama, Birmingham, Birmingham, AL, United States 
Area:
Huntington's Disease
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"Sarah Dougherty"
Mean distance: 21.18 (cluster 6)
 
SNBCP

Parents

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Rita M. Cowell grad student UAB
John J. Hablitz grad student 2008-2013 UAB
David J. Linden post-doc 2013- Johns Hopkins
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Publications

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Dougherty SE, Kajstura TJ, Jin Y, et al. (2019) Catecholaminergic axons in the neocortex of adult mice regrow following brain injury. Experimental Neurology. 113089
Akassoglou K, Merlini M, Rafalski VA, et al. (2017) In Vivo Imaging of CNS Injury and Disease. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 37: 10808-10816
Kajstura TJ, Dougherty SE, Linden DJ. (2017) Serotonin axons in the neocortex of the adult female mouse regrow after traumatic brain injury. Journal of Neuroscience Research
Cudmore RH, Dougherty SE, Linden DJ. (2016) Cerebral vascular structure in the motor cortex of adult mice is stable and is not altered by voluntary exercise. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 271678X16682508
Jin Y, Dougherty SE, Wood K, et al. (2016) Regrowth of Serotonin Axons in the Adult Mouse Brain Following Injury. Neuron
Lucas EK, Reid CS, McMeekin LJ, et al. (2014) Cerebellar transcriptional alterations with Purkinje cell dysfunction and loss in mice lacking PGC-1α. Frontiers in Cellular Neuroscience. 8: 441
Lucas EK, Dougherty SE, McMeekin LJ, et al. (2014) PGC-1α provides a transcriptional framework for synchronous neurotransmitter release from parvalbumin-positive interneurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 14375-87
Dougherty SE, Bartley AF, Lucas EK, et al. (2014) Mice lacking the transcriptional coactivator PGC-1α exhibit alterations in inhibitory synaptic transmission in the motor cortex. Neuroscience. 271: 137-48
Dougherty SE, Hollimon JJ, McMeekin LJ, et al. (2014) Hyperactivity and cortical disinhibition in mice with restricted expression of mutant huntingtin to parvalbumin-positive cells. Neurobiology of Disease. 62: 160-71
Dougherty SE, Reeves JL, Lesort M, et al. (2013) Purkinje cell dysfunction and loss in a knock-in mouse model of Huntington disease. Experimental Neurology. 240: 96-102
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