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Christopher K. Daniels

Researcher at Idaho State University

Publications -  22
Citations -  791

Christopher K. Daniels is an academic researcher from Idaho State University. The author has contributed to research in topics: Apoptosis & Signal transduction. The author has an hindex of 11, co-authored 22 publications receiving 725 citations.

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Comprehensive review on the HSC70 functions, interactions with related molecules and involvement in clinical diseases and therapeutic potential.

TL;DR: A comprehensive review on HSC70 from the literatures including the basic general information such as classification, structure and cellular location, genetics and function, as well as its protein association and interaction with other proteins.
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Exposure to titanium dioxide and other metallic oxide nanoparticles induces cytotoxicity on human neural cells and fibroblasts.

TL;DR: It is found that TiO2 micro- and nanoparticles induced cell death on both human cell types in a concentration-related manner and it was noted that zinc oxide (ZnO) nanoparticles were the most effective,TiO2 nanoparticles the secondmost effective, and magnesium oxide (MgO), the least effective in inducing cell death in U87 cells.
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Manganese-induced neurotoxicity is differentially enhanced by glutathione depletion in astrocytoma and neuroblastoma cells.

TL;DR: Because BSO treatment accentuated Mn toxicity in both cell lines, GSH may act to combat Mn toxicity, and further investigation in oxidative stress mediated by glutathione depletion will unravel new Mn toxicity mechanism(s).
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Differential lowering by manganese treatment of activities of glycolytic and tricarboxylic acid (TCA) cycle enzymes investigated in neuroblastoma and astrocytoma cells is associated with manganese-induced cell death.

TL;DR: The hypothesis that Mn induces alterations in energy metabolism in neural cells by interfering with the activities of various glycolytic and TCA cycle enzymes is investigated using human neuroblastoma and astrocytoma cells and the results suggest the two cell types exhibited differential susceptibility toward the Mn-induced effects.
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Biochanin A reduces pancreatic cancer survival and progression.

TL;DR: The results suggest that biochanin A is effective in reducing pancreatic cancer cell survival by inhibiting their proliferation and inducing apoptosis, which may lead to novel approaches to treat pancreatic cancers using isoflavones in combination with other therapeutic drugs.