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1
Radiolabelling of the human 5-HT2A receptor with an agonist, a partial agonist and an antagonist : effects of apparent agonist affinities
Radiolabelling of the human 5-HT2A receptor with an agonist, a partial agonist and an antagonist : effects of apparent agonist affinities
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Radiolabelling of the human 5-HT2A receptor with an agonist, a partial agonist and an antagonist : effects of apparent agonist affinities

SLEIGHT, A. J ; STAM, N. J ; MUTEL, V ; VANDERHEYDEN, P. M. L

Biochemical pharmacology, 1996-01, Vol.51 (1), p.71-76 [Periódico revisado por pares]

New York, NY: Elsevier Science

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2
Agonist-induced muscarinic cholinergic receptor internalization, recycling and degradation in cultured neuronal cells: Cellular mechanisms and role in desensitization
Agonist-induced muscarinic cholinergic receptor internalization, recycling and degradation in cultured neuronal cells: Cellular mechanisms and role in desensitization
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Agonist-induced muscarinic cholinergic receptor internalization, recycling and degradation in cultured neuronal cells: Cellular mechanisms and role in desensitization

Maloteaux, J.M. ; Hermans, E.

Biochemical pharmacology, 1994-01, Vol.47 (1), p.77-88 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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3
Constitutive activation of chimeric m2/m5 muscarinic receptors and delineation of G-protein coupling selectivity domains
Constitutive activation of chimeric m2/m5 muscarinic receptors and delineation of G-protein coupling selectivity domains
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Constitutive activation of chimeric m2/m5 muscarinic receptors and delineation of G-protein coupling selectivity domains

Burstein, Ethan S. ; Spalding, Tracy A. ; Brann, Mark R.

Biochemical pharmacology, 1996-02, Vol.51 (4), p.539-544 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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4
5-Isothiocyanonicotine: A high-affinity irreversible ligand for brain nicotinic receptors
5-Isothiocyanonicotine: A high-affinity irreversible ligand for brain nicotinic receptors
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5-Isothiocyanonicotine: A high-affinity irreversible ligand for brain nicotinic receptors

Kim, Kee D. ; Lerner-Marmarosh, Nicole ; Saraswati, Manda ; Kende, Andrew S. ; Abood, Leo G.

Biochemical pharmacology, 1994-06, Vol.47 (11), p.1965-1967 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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5
Characterization of the catecholamine extraneuronal uptake2 carrier in human glioma cell lines SK-MG-1 and SKI-1 in relation to (2-chloroethyl)-3-sarcosinamide-1-nitrosourea (SarCNU) selective cytotoxicity
Characterization of the catecholamine extraneuronal uptake2 carrier in human glioma cell lines SK-MG-1 and SKI-1 in relation to (2-chloroethyl)-3-sarcosinamide-1-nitrosourea (SarCNU) selective cytotoxicity
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Characterization of the catecholamine extraneuronal uptake2 carrier in human glioma cell lines SK-MG-1 and SKI-1 in relation to (2-chloroethyl)-3-sarcosinamide-1-nitrosourea (SarCNU) selective cytotoxicity

NOË, A. J ; MARCANTONIO, D ; BARTON, J ; MALAPETSA, A ; PANASCI, L. C

Biochemical pharmacology, 1996-06, Vol.51 (12), p.1639-1648 [Periódico revisado por pares]

New York, NY: Elsevier Science

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6
Inhibition by ethaverine of catecholamine secretion through blocking L-type Ca2+ channels in PC12 cells
Inhibition by ethaverine of catecholamine secretion through blocking L-type Ca2+ channels in PC12 cells
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Inhibition by ethaverine of catecholamine secretion through blocking L-type Ca2+ channels in PC12 cells

Suh, B C ; Kim, K T

Biochemical pharmacology, 1994-03, Vol.47 (7), p.1262-1266 [Periódico revisado por pares]

New York, NY: Elsevier Science

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7
A2a/D2 receptor interactions are not observed in COS-7 cells transiently transfected with dopamine D2 and adenosine A2a receptor cDNA
A2a/D2 receptor interactions are not observed in COS-7 cells transiently transfected with dopamine D2 and adenosine A2a receptor cDNA
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A2a/D2 receptor interactions are not observed in COS-7 cells transiently transfected with dopamine D2 and adenosine A2a receptor cDNA

SNAPRUD, P ; GERWINS, P ; CARON, M. G ; LIBERT, F ; PERSSON, H ; FREDHOLM, B. B ; FUXE, K

Biochemical pharmacology, 1994-11, Vol.48 (11), p.2043-2047 [Periódico revisado por pares]

New York, NY: Elsevier Science

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8
Labeling of rat heart muscarinic receptors using the new M2 selective antagonist [3H]AF-DX 384
Labeling of rat heart muscarinic receptors using the new M2 selective antagonist [3H]AF-DX 384
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Labeling of rat heart muscarinic receptors using the new M2 selective antagonist [3H]AF-DX 384

ENTZEROTH, M ; MAYER, N

Biochemical pharmacology, 1990-10, Vol.40 (7), p.1674-1676 [Periódico revisado por pares]

New York, NY: Elsevier Science

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9
Serotonin inhibition of adenylate cyclase in human platelet membranes; relation to 5-HT-1A receptor-mediated activity
Serotonin inhibition of adenylate cyclase in human platelet membranes; relation to 5-HT-1A receptor-mediated activity
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Serotonin inhibition of adenylate cyclase in human platelet membranes; relation to 5-HT-1A receptor-mediated activity

Newman, Michael E.

Biochemical pharmacology, 1994-11, Vol.48 (9), p.1677-1682 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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10
Idebenone, an agent improving cerebral metabolism, stimulates [ 14C]tyrosine uptake and [ 14C]catecholamine formation by cultured bovine adrenal chromaffin cells
Idebenone, an agent improving cerebral metabolism, stimulates [ 14C]tyrosine uptake and [ 14C]catecholamine formation by cultured bovine adrenal chromaffin cells
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Idebenone, an agent improving cerebral metabolism, stimulates [ 14C]tyrosine uptake and [ 14C]catecholamine formation by cultured bovine adrenal chromaffin cells

Houchi, Hitoshi ; Yoshizumi, Masanori ; Minakuchi, Kazuo ; Azuma, Mami ; Morita, Kyoji ; Oka, Motoo

Biochemical pharmacology, 1991-07, Vol.42 (4), p.951-954 [Periódico revisado por pares]

England: Elsevier Inc

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