James Rosinski, Ph.D.
Affiliations: | Department of Genetics | North Carolina State University, Raleigh, NC |
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"James Rosinski"
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| Lu AT, Narayan P, Grant MJ, et al. (2020) DNA methylation study of Huntington's disease and motor progression in patients and in animal models. Nature Communications. 11: 4529 |
| Mégret L, Nair SS, Dancourt J, et al. (2020) Combining feature selection and shape analysis uncovers precise rules for miRNA regulation in Huntington’s disease mice Bmc Bioinformatics. 21: 75 |
| Bigan E, Sasidharan Nair S, Lejeune FX, et al. (2020) Genetic cooperativity in multi-layer networks implicates cell survival and senescence in the striatum of Huntington's disease mice synchronous to symptoms. Bioinformatics (Oxford, England). 36: 186-196 |
| Ament SA, Pearl JR, Cantle JP, et al. (2018) Transcriptional regulatory networks underlying gene expression changes in Huntington's disease. Molecular Systems Biology. 14: e7435 |
| Langfelder P, Gao F, Wang N, et al. (2018) MicroRNA signatures of endogenous Huntingtin CAG repeat expansion in mice. Plos One. 13: e0190550 |
| Mégret L, Nair SS, Aaronson J, et al. (2018) A10 Accurate data-driven approaches for modeling MIRNA regulation in the brain of huntington’s disease mice Journal of Neurology, Neurosurgery, and Psychiatry. 89 |
| Bondulich MK, Jolinon N, Osborne GF, et al. (2017) Myostatin inhibition prevents skeletal muscle pathophysiology in Huntington's disease mice. Scientific Reports. 7: 14275 |
| Beaumont V, Zhong S, Lin H, et al. (2016) Phosphodiesterase 10A Inhibition Improves Cortico-Basal Ganglia Function in Huntington's Disease Models. Neuron |
| Alexandrov V, Brunner D, Menalled LB, et al. (2016) Large-scale phenome analysis defines a behavioral signature for Huntington's disease genotype in mice. Nature Biotechnology |
| Langfelder P, Cantle JP, Chatzopoulou D, et al. (2016) Integrated genomics and proteomics define huntingtin CAG length-dependent networks in mice. Nature Neuroscience |