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Inhibitory effect of anti-diabetic agents on rat organic anion transporter rOAT1.
Uwai Y, Saito H, Hashimoto Y, Inui K. Uwai Y, et al. Eur J Pharmacol. 2000 Jun 16;398(2):193-7. doi: 10.1016/s0014-2999(00)00324-1. Eur J Pharmacol. 2000. PMID: 10854830
Dietary docosahexaenoic acid increases cerebral acetylcholine levels and improves passive avoidance performance in stroke-prone spontaneously hypertensive rats.
Minami M, Kimura S, Endo T, Hamaue N, Hirafuji M, Togashi H, Matsumoto M, Yoshioka M, Saito H, Watanabe S, Kobayashi T, Okuyama H. Minami M, et al. Pharmacol Biochem Behav. 1997 Dec;58(4):1123-9. doi: 10.1016/s0091-3057(97)00300-6. Pharmacol Biochem Behav. 1997. PMID: 9408223
Effect of docosahexaenoic acid on intracellular calcium dynamics in vascular smooth muscle cells from normotensive and genetically hypertensive rats.
Hirafuji M, Ebihara T, Kawahara F, Nezu A, Taminura A, Saito H, Minami M. Hirafuji M, et al. Res Commun Mol Pathol Pharmacol. 1998 Oct;102(1):29-42. Res Commun Mol Pathol Pharmacol. 1998. PMID: 9920344
Effects of idazoxan on dopamine release in the prefrontal cortex of freely moving rats.
Matsumoto M, Yoshioka M, Togashi H, Mori K, Ueno K, Saito H. Matsumoto M, et al. Eur J Pharmacol. 1998 Feb 19;343(2-3):165-70. doi: 10.1016/s0014-2999(97)01544-6. Eur J Pharmacol. 1998. PMID: 9570464
Changes in the regulation of 5-hydroxytryptamine release by alpha2-adrenoceptors in the rat hippocampus after long-term desipramine treatment.
Yoshioka M, Matsumoto M, Numazawa R, Togashi H, Smith CB, Saito H. Yoshioka M, et al. Eur J Pharmacol. 1995 Dec 29;294(2-3):565-70. doi: 10.1016/0014-2999(95)00582-x. Eur J Pharmacol. 1995. PMID: 8750719
., every 12 h for 14 days. When added to the perfusion solution, brimonidine, an alpha2-adrenoceptor agonist, significantly inhibited the K+-evoked release of 5-HT in the hippocampi of saline-treated, control rats. ...
., every 12 h for 14 days. When added to the perfusion solution, brimonidine, an alpha2-adrenoceptor agonist, significantly inhibited …
Recognition of beta-lactam antibiotics by rat peptide transporters, PEPT1 and PEPT2, in LLC-PK1 cells.
Terada T, Saito H, Mukai M, Inui K. Terada T, et al. Am J Physiol. 1997 Nov;273(5):F706-11. doi: 10.1152/ajprenal.1997.273.5.F706. Am J Physiol. 1997. PMID: 9374833
PEPT1 and PEPT2 are H(+)-coupled peptide transporters expressed preferentially in the intestine and kidney, respectively, which mediate uphill transport of oligopeptides and peptide-like drugs such as beta-lactam antibiotics. ...
PEPT1 and PEPT2 are H(+)-coupled peptide transporters expressed preferentially in the intestine and kidney, respectively, which media …
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