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Comparative Pharmacodynamics and Pharmacokinetics of Oral Direct Thrombin and Factor Xa Inhibitors in Development
Comparative Pharmacodynamics and Pharmacokinetics of Oral Direct Thrombin and Factor Xa Inhibitors in Development
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Comparative Pharmacodynamics and Pharmacokinetics of Oral Direct Thrombin and Factor Xa Inhibitors in Development

Eriksson, Bengt I. ; Quinlan, Daniel J. ; Weitz, Jeffrey I.

Clinical pharmacokinetics, 2009, Vol.48 (1), p.1-22 [Peer Reviewed Journal]

Cham: Springer International Publishing

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2
International Union of Basic and Clinical Pharmacology. XCI. structure, function, and pharmacology of acid-sensing ion channels and the epithelial Na+ channel
International Union of Basic and Clinical Pharmacology. XCI. structure, function, and pharmacology of acid-sensing ion channels and the epithelial Na+ channel
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International Union of Basic and Clinical Pharmacology. XCI. structure, function, and pharmacology of acid-sensing ion channels and the epithelial Na+ channel

Kellenberger, Stephan ; Schild, Laurent Ohlstein, Eliot H.

Pharmacological reviews, 2015-01, Vol.67 (1), p.1-35 [Peer Reviewed Journal]

United States

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3
Targeting apoptosis pathways by natural compounds in cancer: Marine compounds as lead structures and chemical tools for cancer therapy
Targeting apoptosis pathways by natural compounds in cancer: Marine compounds as lead structures and chemical tools for cancer therapy
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Targeting apoptosis pathways by natural compounds in cancer: Marine compounds as lead structures and chemical tools for cancer therapy

von Schwarzenberg, Karin ; Vollmar, Angelika M

Cancer letters, 2013-05, Vol.332 (2), p.295-303 [Peer Reviewed Journal]

Ireland: Elsevier Ireland Ltd

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4
Presynaptic α4β2 nicotinic acetylcholine receptors increase glutamate release and serotonin neuron excitability in the dorsal raphe nucleus
Presynaptic α4β2 nicotinic acetylcholine receptors increase glutamate release and serotonin neuron excitability in the dorsal raphe nucleus
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Presynaptic α4β2 nicotinic acetylcholine receptors increase glutamate release and serotonin neuron excitability in the dorsal raphe nucleus

Garduño, Julieta ; Galindo-Charles, Luis ; Jiménez-Rodríguez, Javier ; Galarraga, Elvira ; Tapia, Dagoberto ; Mihailescu, Stefan ; Hernandez-Lopez, Salvador

The Journal of neuroscience, 2012-10, Vol.32 (43), p.15148-15157 [Peer Reviewed Journal]

United States: Society for Neuroscience

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5
Pharmacology of Antisense Drugs
Pharmacology of Antisense Drugs
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Pharmacology of Antisense Drugs

Bennett, C. Frank ; Baker, Brenda F ; Pham, Nguyen ; Swayze, Eric ; Geary, Richard S

Annual review of pharmacology and toxicology, 2017-01, Vol.57 (1), p.81-105 [Peer Reviewed Journal]

United States: Annual Reviews

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6
Opioid pharmacology
Opioid pharmacology
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Opioid pharmacology

Trescot, Andrea M ; Datta, Sukdeb ; Lee, Marion ; Hansen, Hans

Pain physician, 2008-03, Vol.11 (2 Suppl), p.S133-S153 [Peer Reviewed Journal]

United States: American Society of Interventional Pain Physician

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7
Serotonin-1A receptor stimulation mediates effects of a metabotropic glutamate 2/3 receptor antagonist, 2S-2-amino-2-(1S,2S-2-carboxycycloprop-1-yl)-3-(xanth-9-yl)propanoic acid (LY341495), and an N-methyl-D-aspartate receptor antagonist, ketamine, in the novelty-suppressed feeding test
Serotonin-1A receptor stimulation mediates effects of a metabotropic glutamate 2/3 receptor antagonist, 2S-2-amino-2-(1S,2S-2-carboxycycloprop-1-yl)-3-(xanth-9-yl)propanoic acid (LY341495), and an N-methyl-D-aspartate receptor antagonist, ketamine, in the novelty-suppressed feeding test
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Serotonin-1A receptor stimulation mediates effects of a metabotropic glutamate 2/3 receptor antagonist, 2S-2-amino-2-(1S,2S-2-carboxycycloprop-1-yl)-3-(xanth-9-yl)propanoic acid (LY341495), and an N-methyl-D-aspartate receptor antagonist, ketamine, in the novelty-suppressed feeding test

Fukumoto, Kenichi ; Iijima, Michihiko ; Chaki, Shigeyuki

Psychopharmacology, 2014-06, Vol.231 (11), p.2291-2298 [Peer Reviewed Journal]

Berlin/Heidelberg: Springer Berlin Heidelberg

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8
Pharmacology of bisphosphonates
Pharmacology of bisphosphonates
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Pharmacology of bisphosphonates

Cremers, Serge ; Drake, Matthew T. ; Ebetino, F. Hal ; Bilezikian, John P. ; Russell, R. Graham G.

British journal of clinical pharmacology, 2019-06, Vol.85 (6), p.1052-1062 [Peer Reviewed Journal]

England: John Wiley and Sons Inc

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9
The Pharmacology and Clinical Pharmacology of 3,4-Methylenedioxymethamphetamine (MDMA, “Ecstasy”)
The Pharmacology and Clinical Pharmacology of 3,4-Methylenedioxymethamphetamine (MDMA, “Ecstasy”)
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The Pharmacology and Clinical Pharmacology of 3,4-Methylenedioxymethamphetamine (MDMA, “Ecstasy”)

Green, A Richard ; Mechan, Annis O ; Elliott, J Martin ; O'Shea, Esther ; Colado, M Isabel

Pharmacological reviews, 2003-09, Vol.55 (3), p.463-508 [Peer Reviewed Journal]

United States: American Society for Pharmacology and Experimental Therapeutics

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10
Antioxidant activity of caffeic acid (3,4-dihydroxycinnamic acid)
Antioxidant activity of caffeic acid (3,4-dihydroxycinnamic acid)
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Antioxidant activity of caffeic acid (3,4-dihydroxycinnamic acid)

GULCIN, I

Toxicology (Amsterdam), 2006-01, Vol.217 (2), p.213-220 [Peer Reviewed Journal]

Shannon: Elsevier Ireland Ltd

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