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A A Larson

Showing results (21-30 of 120) with videos related to

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Pain|October 1, 1996
Nitric oxide mediates long-term hyperalgesic and antinociceptive effects of the N-terminus of substance P in the formalin assay in miceV M Goettl, A A Larson
Neuroscience|May 1, 1994
Activity at phencyclidine and mu opioid sites mediates the hyperalgesic and antinociceptive properties of the N-terminus of substance P in a model of visceral painV M Goettl, A A Larson
Life Sciences|December 15, 1977
Effect of fluoxetine hydrochloride (Lilly 110140), a specific inhibitor of serotonin uptake, on morphine analgesia and the development of toleranceA A Larson, A E Takemori
Journal of Chromatography|February 14, 1986
Quantification of tryptamine in brain using high-performance liquid chromatographyA A Larson, N L Dalo
European Journal of Pharmacology|July 31, 1998
Up-regulation of [3H]DTG but not [3H](+)-pentazocine labeled sigma sites in mouse spinal cord by chronic morphine treatmentK J Kovács, A A Larson
Cryobiology|June 1, 1991
Spinal seizures evoked by sudden cooling of amphibian isolated spinal cords: involvement of excitatory amino acidsN L Daló, A A Larson
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 1, 1991
Behavioral sensitization to kainic acid and quisqualic acid in mice: comparison to NMDA and substance P responsesX F Sun, A A Larson
The Journal of Pharmacology and Experimental Therapeutics|December 1, 1989
Selective inhibition of excitatory amino acids by divalent cations. A novel means for distinguishing N-methyl-D-aspartic acid-, kainate- and quisqualate-mediated actions in the mouse spinal cordC S Hornfeldt, A A Larson
Brain Research|April 11, 1994
Antinociception induced by 3-((+-)-2-carboxypiperazin-4-yl)-propyl-1- phosphonic acid (CPP), an N-methyl-D-aspartate (NMDA) competitive antagonist, plus 6,7-dinitroquinoxaline-2,3-dione (DNQX), a non-NMDA antagonist, differs from that induced by MK-801 plus DNQXV M Goettl, A A Larson
Brain Research|February 25, 1998
An antagonist of substance P N-terminal fragments, D-substance P(1-7), reveals that both nociceptive and antinociceptive effects are induced by substance P N-terminal activity during noxious chemical stimulationV M Goettl, A A Larson
Pageof 12

Showing results (21-30 of 120) with videos related to

Sort By:
Pageof 12
Pain|October 1, 1996
Nitric oxide mediates long-term hyperalgesic and antinociceptive effects of the N-terminus of substance P in the formalin assay in miceV M Goettl, A A Larson
Neuroscience|May 1, 1994
Activity at phencyclidine and mu opioid sites mediates the hyperalgesic and antinociceptive properties of the N-terminus of substance P in a model of visceral painV M Goettl, A A Larson
Life Sciences|December 15, 1977
Effect of fluoxetine hydrochloride (Lilly 110140), a specific inhibitor of serotonin uptake, on morphine analgesia and the development of toleranceA A Larson, A E Takemori
Journal of Chromatography|February 14, 1986
Quantification of tryptamine in brain using high-performance liquid chromatographyA A Larson, N L Dalo
European Journal of Pharmacology|July 31, 1998
Up-regulation of [3H]DTG but not [3H](+)-pentazocine labeled sigma sites in mouse spinal cord by chronic morphine treatmentK J Kovács, A A Larson
Cryobiology|June 1, 1991
Spinal seizures evoked by sudden cooling of amphibian isolated spinal cords: involvement of excitatory amino acidsN L Daló, A A Larson
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 1, 1991
Behavioral sensitization to kainic acid and quisqualic acid in mice: comparison to NMDA and substance P responsesX F Sun, A A Larson
The Journal of Pharmacology and Experimental Therapeutics|December 1, 1989
Selective inhibition of excitatory amino acids by divalent cations. A novel means for distinguishing N-methyl-D-aspartic acid-, kainate- and quisqualate-mediated actions in the mouse spinal cordC S Hornfeldt, A A Larson
Brain Research|April 11, 1994
Antinociception induced by 3-((+-)-2-carboxypiperazin-4-yl)-propyl-1- phosphonic acid (CPP), an N-methyl-D-aspartate (NMDA) competitive antagonist, plus 6,7-dinitroquinoxaline-2,3-dione (DNQX), a non-NMDA antagonist, differs from that induced by MK-801 plus DNQXV M Goettl, A A Larson
Brain Research|February 25, 1998
An antagonist of substance P N-terminal fragments, D-substance P(1-7), reveals that both nociceptive and antinociceptive effects are induced by substance P N-terminal activity during noxious chemical stimulationV M Goettl, A A Larson
Pageof 12