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Remethylation disorders may result from genetic mutations causing a lack of functional Met synthase, a lack of functional coenzyme (methylcobalamin), or a lack of synthesis of the cosubstrate (N 5 -methyl-THF)

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It was possible to use the physicochemical properties which were already identified for particles and fibres for defining NP toxicity

The 13-amino-acid N-terminal extension (sequence MFPAMPLLSLFVN) shifts the three-dimensional conformation of the binding interface, while the Arg 3 Glu 3 substitution disrupts a key contact residue with IGFBPs

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