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In addition to the cell-dependent effects of arsenic to induce insulin resistance, another possibility can be expected by the fact that arsenic compounds can bind proteins through different chemical and electrostatic bonds, altering protein function

In animal or ex vivo experimental models for mechanistic investigation of peptidemetal interactions, copper bioavailability, and metal-mediated tissue signalling processes

They have been identified to date over 8000 phenolics with a very diverse range of chemical structures [27]

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