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Ben A. Bahr

Affiliations: 
University of Connecticut, Storrs, CT, United States 
Area:
Neuroprotection in models of Alzheimer-type pathogenesis
Website:
https://web1.uits.uconn.edu/pharmacy/index.php?option=com_content&task=view&id=370&Itemid=
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"Ben Bahr"
Mean distance: 21373.2
 
Cross-listing: Alzheimer's Tree

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Publications

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Romine H, Rentschler KM, Smith K, et al. (2017) Potential Alzheimer's Disease Therapeutics Among Weak Cysteine Protease Inhibitors Exhibit Mechanistic Differences Regarding Extent of Cathepsin B Up-Regulation and Ability to Block Calpain. European Scientific Journal. 13: 38-59
Farizatto KLG, McEwan SA, Naidoo V, et al. (2017) Inhibitor of Endocannabinoid Deactivation Protects Against In Vitro and In Vivo Neurotoxic Effects of Paraoxon. Journal of Molecular Neuroscience : Mn
Carrasco DI, Bahr BA, Seburn KL, et al. (2016) Abnormal response of distal Schwann cells to denervation in a mouse model of motor neuron disease. Experimental Neurology
Maltecca F, Baseggio E, Consolato F, et al. (2015) Purkinje neuron Ca2+ influx reduction rescues ataxia in SCA28 model. The Journal of Clinical Investigation. 125: 263-74
Bahr BA. (2015) Meet the editorial board member Current Neuropharmacology. 13: 1
Bahr BA. (2014) A single pathway targets several health challenges of the elderly. Rejuvenation Research. 17: 382-4
Hoffmann DB, Williams SK, Bojcevski J, et al. (2013) Calcium influx and calpain activation mediate preclinical retinal neurodegeneration in autoimmune optic neuritis. Journal of Neuropathology and Experimental Neurology. 72: 745-57
Melo CV, Okumoto S, Gomes JR, et al. (2013) Spatiotemporal resolution of BDNF neuroprotection against glutamate excitotoxicity in cultured hippocampal neurons. Neuroscience. 237: 66-86
Bahr BA. (2013) Monitoring the activation of calpain i for sensitive assessment of pathogenesis and neuroprotectant action Enzymes and Enzyme Activity: Structure, Biology and Clinical Significance. 39-72
Viswanathan K, Hoover DJ, Hwang J, et al. (2012) Nonpeptidic lysosomal modulators derived from z-phe-ala-diazomethylketone for treating protein accumulation diseases. Acs Medicinal Chemistry Letters. 3: 920-4
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