Published in Pharma Investments, Ventures and Law Weekly, November 19th, 2006
"Selective antagonism of NMDA 2B subunit containing receptors has been suggested to have potential therapeutic application for multiple CNS disorders. The amino terminal NR2B residues 1 to 282 were found to be both necessary and sufficient for the binding and function of highly NR2B subunit specific antagonists like ifenprodil and CP-101,606," wrote T.W. Rosahl and colleagues, Merck & Co.
"Using a genetic approach in mice, we successfully replaced the murine NR2B gene...
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