Rita Kumar, Ph.D.

Affiliations: 
2001 Wayne State University, Detroit, MI, United States 
Area:
Neuroscience Biology, Molecular Biology
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"Rita Kumar"
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Blaine C. White grad student 2001 Wayne State
 (Causal mechanisms of eIF2alpha phosphorylation during brain reperfusion.)
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Publications

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Kumar R, Bukowski MJ, Wider JM, et al. (2016) Mitochondrial dynamics following global cerebral ischemia. Molecular and Cellular Neurosciences
Sanderson TH, Raghunayakula S, Kumar R. (2015) Neuronal hypoxia disrupts mitochondrial fusion. Neuroscience. 301: 71-8
Sanderson TH, Gallaway M, Kumar R. (2015) Unfolding the unfolded protein response: unique insights into brain ischemia. International Journal of Molecular Sciences. 16: 7133-42
Sanderson TH, Raghunayakula S, Kumar R. (2015) Release of mitochondrial Opa1 following oxidative stress in HT22 cells. Molecular and Cellular Neurosciences. 64: 116-22
Sanderson TH, Mahapatra G, Pecina P, et al. (2013) Cytochrome C is tyrosine 97 phosphorylated by neuroprotective insulin treatment. Plos One. 8: e78627
Lagina AT, Calo L, Deogracias M, et al. (2013) Combination therapy with insulin-like growth factor-1 and hypothermia synergistically improves outcome after transient global brain ischemia in the rat. Academic Emergency Medicine : Official Journal of the Society For Academic Emergency Medicine. 20: 344-51
Calo L, Dong Y, Kumar R, et al. (2013) Mitochondrial dynamics: an emerging paradigm in ischemia-reperfusion injury. Current Pharmaceutical Design. 19: 6848-57
Sanderson TH, Reynolds CA, Kumar R, et al. (2013) Molecular mechanisms of ischemia-reperfusion injury in brain: pivotal role of the mitochondrial membrane potential in reactive oxygen species generation. Molecular Neurobiology. 47: 9-23
Sanderson TH, Deogracias MP, Nangia KK, et al. (2010) PKR-like endoplasmic reticulum kinase (PERK) activation following brain ischemia is independent of unfolded nascent proteins. Neuroscience. 169: 1307-14
Sanderson TH, Kumar R, Murariu-Dobrin AC, et al. (2009) Insulin activates the PI3K-Akt survival pathway in vulnerable neurons following global brain ischemia. Neurological Research. 31: 947-58
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