Benjamin R. Miller
Affiliations: | Indiana University, Bloomington, Bloomington, IN, United States |
Area:
Basa ganglia, striatum, cortex, Huntington's disease, glutamate, ascorbate, dopamineWebsite:
http://mypage.iu.edu/~benmille/Google:
"Benjamin Miller"Mean distance: 16.26 (cluster 19) | S | N | B | C | P |
Parents
Sign in to add mentor| George V. Rebec | grad student | 2009 | Indiana University | |
| (The role of glutamate uptake on neuronal activity patterns and ascorbate release in striatum of Huntington's disease mice.) | ||||
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Publications
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| Ponzi A, Barton SJ, Bunner KD, et al. (2020) Striatal network modeling in Huntington's Disease. Plos Computational Biology. 16: e1007648 |
| Miller BR, Dorner JL, Bunner KD, et al. (2012) Up-regulation of GLT1 reverses the deficit in cortically evoked striatal ascorbate efflux in the R6/2 mouse model of Huntington's disease. Journal of Neurochemistry. 121: 629-38 |
| Miller BR, Walker AG, Barton SJ, et al. (2011) Dysregulated Neuronal Activity Patterns Implicate Corticostriatal Circuit Dysfunction in Multiple Rodent Models of Huntington's Disease. Frontiers in Systems Neuroscience. 5: 26 |
| Miller BR, Bezprozvanny I. (2010) Corticostriatal circuit dysfunction in Huntington's disease: intersection of glutamate, dopamine and calcium. Future Neurology. 5: 735-756 |
| Ball KT, Wellman CL, Miller BR, et al. (2010) Electrophysiological and structural alterations in striatum associated with behavioral sensitization to (±)3,4-methylenedioxymethamphetamine (Ecstasy) in rats: role of drug context. Neuroscience. 171: 794-811 |
| Sari Y, Prieto AL, Barton SJ, et al. (2010) Ceftriaxone-induced up-regulation of cortical and striatal GLT1 in the R6/2 model of Huntington's disease. Journal of Biomedical Science. 17: 62 |
| Miller BR, Walker AG, Fowler SC, et al. (2010) Dysregulation of coordinated neuronal firing patterns in striatum of freely behaving transgenic rats that model Huntington's disease. Neurobiology of Disease. 37: 106-13 |
| Dorner JL, Miller BR, Klein EL, et al. (2009) Corticostriatal dysfunction underlies diminished striatal ascorbate release in the R6/2 mouse model of Huntington's disease. Brain Research. 1290: 111-20 |
| Fowler SC, Miller BR, Gaither TW, et al. (2009) Force-plate quantification of progressive behavioral deficits in the R6/2 mouse model of Huntington's disease. Behavioural Brain Research. 202: 130-7 |
| Walker AG, Miller BR, Fritsch JN, et al. (2008) Altered information processing in the prefrontal cortex of Huntington's disease mouse models. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 8973-82 |