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Description
A glycine site associated with N-methyl-D-aspartic acid receptors: characterization and identification of a new class of antagonists
For patients with complex immune reactivity, Dr
This enzymatic reduction was performed using GR (SigmaAldrich) and the cofactor NADPH (SigmaAldrich)
According to our structural analysis, zinc binding to sites of types 1, 4 and 5 ( Table 3 ) results in this fragment localizing at the intermolecular interface of the resulting dimer/trimer, impeding its access to the receptor (Fig
