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Results of search for 'au:"Takemori, A E"', page 8 of 12
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Authors
Ahlijanian, M K
Bowen, W D
Caruso, T P
Chang, A C
Contreras, P C
Fujimoto, J M
Hayashi, G
Ho, B Y
Larson, D L
Lipkowski, A W
Maruyama, Y
Mosberg, H I
Portoghese, P S
Sayre, L M
Sofuoglu, M
Sultana, M
TAKEMORI, A E
Takemori, A E
Tulunay, F C
Ward, S J
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Topics
Analgesics
Animals
Brain
Drug Tolerance
Guinea Pigs
In Vitro Techniques
Male
Mice
Morphine
Naloxone
Naltrexone
Narcotic Antagonists
Rats
Receptors, Opioid
Receptors, Opioid, delta
analogs & derivatives
antagonists & inhibitors
drug effects
metabolism
pharmacology
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141.
The potentiation of spinal analgesia by leucine enkephalin.
[electronic resource]
by
Larson, A A
Vaught, J L
Takemori, A E
Producer:
19800712
In:
European journal of pharmacology
vol. 61
Online resources:
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142.
Suppression by dynorphin A and [des-Tyr1]dynorphin A peptides of the expression of opiate withdrawal and tolerance in morphine-dependent mice.
[electronic resource]
by
Takemori, A E
Loh, H H
Lee, N M
Producer:
19930819
In:
The Journal of pharmacology and experimental therapeutics
vol. 266
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143.
A selective delta 1 opioid receptor agonist derived from oxymorphone. Evidence for separate recognition sites for delta 1 opioid receptor agonists and antagonists.
[electronic resource]
by
Portoghese, P S
Moe, S T
Takemori, A E
Producer:
19930923
In:
Journal of medicinal chemistry
vol. 36
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144.
A remarkable change of opioid receptor selectivity on the attachment of a peptidomimetic kappa address element to the delta antagonist, natrindole: 5'-[N2-alkylamidino)methyl]naltrindole derivatives as a novel class of kappa opioid receptor antagonists.
[electronic resource]
by
Olmsted, S L
Takemori, A E
Portoghese, P S
Producer:
19930216
In:
Journal of medicinal chemistry
vol. 36
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145.
Role of the spinal cord in the development of opiate tolerance and dependence.
[electronic resource]
by
Takemori, A E
DeLander, G E
Portoghese, P S
Producer:
19880329
In:
NIDA research monograph
vol. 76
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146.
Suppression by nor-binaltorphimine of kappa opioid-mediated diuresis in rats.
[electronic resource]
by
Takemori, A E
Schwartz, M M
Portoghese, P S
Producer:
19890131
In:
The Journal of pharmacology and experimental therapeutics
vol. 247
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147.
The irreversible narcotic antagonistic and reversible agonistic properties of the fumaramate methyl ester derivative of naltrexone.
[electronic resource]
by
Takemori, A E
Larson, D L
Portoghese, P S
Producer:
19810820
In:
European journal of pharmacology
vol. 70
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148.
Difference between mu-receptors in the guinea pig ileum and the mouse vas deferens.
[electronic resource]
by
Sayre, L M
Portoghese, P S
Takemori, A E
Producer:
19830923
In:
European journal of pharmacology
vol. 90
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149.
Electrophilic N-benzylnaltrindoles as delta opioid receptor-selective antagonists.
[electronic resource]
by
Korlipara, V L
Takemori, A E
Portoghese, P S
Producer:
19950531
In:
Journal of medicinal chemistry
vol. 38
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150.
Irreversible blockage of opioid receptor types by ester homologues of beta-funaltrexamine.
[electronic resource]
by
Schoenecker, J W
Takemori, A E
Portoghese, P S
Producer:
19861119
In:
Journal of medicinal chemistry
vol. 29
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151.
Alkylation of opioid receptor subtypes by alpha-chlornaltrexamine produces concurrent irreversible agonistic and irreversible antagonistic activities.
[electronic resource]
by
Sayre, L M
Takemori, A E
Portoghese, P S
Producer:
19830527
In:
Journal of medicinal chemistry
vol. 26
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152.
Pharmacological characterization in vivo of the novel opiate, beta-funaltrexamine.
[electronic resource]
by
Ward, S J
Portoghese, P S
Takemori, A E
Producer:
19820527
In:
The Journal of pharmacology and experimental therapeutics
vol. 220
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153.
Kinetics of microsomal metabolism and binding of enantiomerically related substrates.
[electronic resource]
by
Anders, M W
Cooper, M J
Takemori, A E
Producer:
19740404
In:
Drug metabolism and disposition: the biological fate of chemicals
vol. 1
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154.
A single-dose suppression test in morphine-dependent mice.
[electronic resource]
by
Takemori, A E
Stesin, A J
Tulunay, F C
Producer:
19740712
In:
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)
vol. 145
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155.
2-(3,4-Dichlorophenyl)-N-methyl-N-[(1S)-1-(3-isothiocyanatophenyl)-2-(1-pyrrolidinyl)ethyl]acetamide: an opioid receptor affinity label that produces selective and long-lasting kappa antagonism in mice.
[electronic resource]
by
Chang, A C
Takemori, A E
Portoghese, P S
Producer:
19940707
In:
Journal of medicinal chemistry
vol. 37
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156.
A highly selective delta 1-opioid receptor antagonist: 7-benzylidenenaltrexone.
[electronic resource]
by
Portoghese, P S
Sultana, M
Nagase, H
Takemori, A E
Producer:
19921120
In:
European journal of pharmacology
vol. 218
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157.
Differential antagonism by naltrindole-5'-isothiocyanate on [3H]DSLET and [3H]DPDPE binding to striatal slices of mice.
[electronic resource]
by
Chakrabarti, S
Sultana, M
Portoghese, P S
Takemori, A E
Producer:
19931229
In:
Life sciences
vol. 53
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158.
Studies on the relationship between 5-hydroxytryptamine turnover in brain and tolerance and physical dependence in mice.
[electronic resource]
by
Maruyama, Y
Hayashi, G
Smits, S E
Takemori, A E
Producer:
19710803
In:
The Journal of pharmacology and experimental therapeutics
vol. 178
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159.
Application of the message-address concept in the design of highly potent and selective non-peptide delta opioid receptor antagonists.
[electronic resource]
by
Portoghese, P S
Sultana, M
Nagase, H
Takemori, A E
Producer:
19880316
In:
Journal of medicinal chemistry
vol. 31
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160.
Agonist and antagonist activities of ligands derived from naltrexone and oxymorphone.
[electronic resource]
by
Takemori, A E
Sultana, M
Nagase, H
Portoghese, P S
Producer:
19920609
In:
Life sciences
vol. 50
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