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Inhibition of NMDA receptors using non-competitive antagonist MK801, competitive antagonist D-CPP, or conditional deletion of the NR1 subunit of NMDA receptors in the dorsal horn of the spinal cord effectively reverses the hyperexcitability in nociceptive neurons, thereby abolishing activity-dependent central sensitization (Woolf and Thompson, 1991

Preparation and characterization of Sorafenib nano-emulsion: impact on pharmacokinetics and toxicity

This natural compound comes from three amino acids: glycine, cysteine, and glutamic acid

demonstrated that a new chemical entity termed ANG1005 developed by conjugation between targeting peptide angiopep-2 (19-amino acid peptide obtained from Kunitz domain of LRP1 ligands having affinity to LRP1 and efficiently bypasses the BBB through LRP-1 mediated transcytosis) to high molecular weight anti-HER2 mAb to amplify their uptake through BBB (i.e

A consensus statement from clinical toxicologists consulting to the Australasian poisons information centres"