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N-Desmethylclozapine, an Allosteric Agonist at Muscarinic 1 Receptor, Potentiates N-Methyl-D-Aspartate Receptor Activity

Proceedings of the National Academy of Sciences - PNAS, 2003-11, Vol.100 (23), p.13674-13679

2003

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The Glycine Transporter Type 1 Inhibitor N-[3-(4'-Fluorophenyl)-3-(4'-Phenylphenoxy)Propyl]Sarcosine Potentiates NMDA Receptor-Mediated Responses In Vivo and Produces an Antipsychotic Profile in Rodent Behavior

The Journal of neuroscience, 2003-08, Vol.23 (20), p.7586-7591

2003

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Effects of muscarinic cholinergic receptor antagonists on postnatal eye growth of rhesus monkeys

Optometry and vision science, 1999-06, Vol.76 (6), p.397-407

1999

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New isomeric classes of topically active ocular hypotensive carbonic anhydrase inhibitors: 5-substituted thieno[2,3-b]thiophene-2-sulfonamides and 5-substituted thieno[3,2-b]thiophene-2-sulfonamides

Journal of medicinal chemistry, 1991-06, Vol.34 (6), p.1805-1818

1991

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Sulfonylmethanesulfonamide inhibitors of carbonic anhydrase

Journal of medicinal chemistry, 1993-07, Vol.36 (15), p.2134-2141

1993

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The effects of deleting the mouse neurotensin receptor NTR1 on central and peripheral responses to neurotensin

The Journal of pharmacology and experimental therapeutics, 2002-01, Vol.300 (1), p.305-313

2002

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Pharmacology and expression analysis of glycine transporter GlyT1 with [ 3H]-(N-[3-(4′-fluorophenyl)-3-(4′phenylphenoxy)propyl])sarcosine

Neuropharmacology, 2003-10, Vol.45 (5), p.585-593

2003

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Mepacrine Blocks β -Adrenergic Agonist-Induced Desensitization in Astrocytoma Cells

Proceedings of the National Academy of Sciences - PNAS, 1980-03, Vol.77 (3), p.1341-1345

1980

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Ocular penetration and intraocular pressure (IOP) lowering activity of the angiotensin II (AII) antagonists losartan and L-158,338

Vision research (Oxford), 1995-10, Vol.35 (1), p.S210

Mallorga, P

1995

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Effects of typical and atypical antipsychotics on human glycine transporters

Schizophrenia research, 2004-11, Vol.71 (1), p.103-112

2004

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4-Substituted thiophene- and furan-2-sulfonamides as topical carbonic anhydrase inhibitors

Journal of medicinal chemistry, 1992-10, Vol.35 (21), p.3822-3831

1992

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A comparison of L-671,152 and MK-927, two topically effective ocular hypotensive carbonic anhydrase inhibitors, in experimental animals

Current eye research, 1990, Vol.9 (6), p.607-615

1990

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L‐662,583 is a topically effective ocular hypotensive carbonic anhydrase inhibitor in experimental animals

British journal of pharmacology, 1990-01, Vol.99 (1), p.59-64

1990

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Development of a scintillation proximity assay for analysis of Na +/Cl −-dependent neurotransmitter transporter activity

Analytical biochemistry, 2003-10, Vol.321 (1), p.31-37

2003

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P 324 Ocular penetration and intraocular pressure (IOP) lowering activity of the angiotensin II (AII) antagonists losartan and L-158,338

Vision research (Oxford), 1995-10, Vol.35, p.S210-S210

1995

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Characterization of serotonin receptors in the iris + ciliary body of the albino rabbit

Current eye research, 1987, Vol.6 (3), p.527-532

1987

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Pharmacology and expression analysis of glycine transporter GlyT1 with [ super(3)H]-(N-[3-(4'-fluorophenyl)-3-(4'phenylphenoxy)propyl])sarc osine

Neuropharmacology, 2003-10, Vol.45 (5), p.585-593

2003

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Preclinical studies on L-671,152, a topically effective ocular hypotensive carbonic anhydrase inhibitor

British journal of pharmacology, 1989-12, Vol.98 Suppl, p.820P-820P

1989

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Catecholamine-induced desensitization of adenylate cyclase in rat glioma C6 cells. Evidence for a specific uncoupling of beta-adrenergic receptors from a functional regulatory component of adenylate cyclase

Molecular pharmacology, 1981-01, Vol.20 (2), p.310-318

1981

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Development of a scintillation proximity assay for analysis of Na super(+)/Cl super(-)-dependent neurotransmitter transporter activity

Analytical biochemistry, 2003-10, Vol.321 (1), p.31-37

2003

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Thienothiopyran-2-sulfonamides: novel topically active carbonic anhydrase inhibitors for the treatment of glaucoma

Journal of medicinal chemistry, 1989-12, Vol.32 (12), p.2510-2513

1989

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L-653,328: an ocular hypotensive agent with modest beta receptor blocking activity

Investigative ophthalmology & visual science, 1988-05, Vol.29 (5), p.776-784

1988

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Angiotensin II receptors labelled with 125I-[Sar1, Ile8]-AII in albino rabbit ocular tissues

Current eye research, 1989-08, Vol.8 (8), p.841-849

1989

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MK-927 : a topically active ocular hypotensive carbonic anhydrase inhibitor

Journal of ocular pharmacology, 1990, Vol.6 (1), p.9-22

1990

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Characterization of [ 3H]forskolin binding sites in the iris-ciliary body of the albino rabbit

Life sciences (1973), 1988, Vol.42 (13), p.1307-1314

1988

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N-Desmethylclozapine, an Allosteric Agonist at Muscarinic 1 Receptor, Potentiates N-Methyl-D-Aspartate Receptor Activity

The Glycine Transporter Type 1 Inhibitor N-[3-(4'-Fluorophenyl)-3-(4'-Phenylphenoxy)Propyl]Sarcosine Potentiates NMDA Receptor-Mediated Responses In Vivo and Produces an Antipsychotic Profile in Rodent Behavior

Effects of muscarinic cholinergic receptor antagonists on postnatal eye growth of rhesus monkeys

New isomeric classes of topically active ocular hypotensive carbonic anhydrase inhibitors: 5-substituted thieno[2,3-b]thiophene-2-sulfonamides and 5-substituted thieno[3,2-b]thiophene-2-sulfonamides

Sulfonylmethanesulfonamide inhibitors of carbonic anhydrase

The effects of deleting the mouse neurotensin receptor NTR1 on central and peripheral responses to neurotensin

Pharmacology and expression analysis of glycine transporter GlyT1 with [ 3H]-(N-[3-(4′-fluorophenyl)-3-(4′phenylphenoxy)propyl])sarcosine

Mepacrine Blocks β -Adrenergic Agonist-Induced Desensitization in Astrocytoma Cells

Ocular penetration and intraocular pressure (IOP) lowering activity of the angiotensin II (AII) antagonists losartan and L-158,338

Effects of typical and atypical antipsychotics on human glycine transporters

4-Substituted thiophene- and furan-2-sulfonamides as topical carbonic anhydrase inhibitors

A comparison of L-671,152 and MK-927, two topically effective ocular hypotensive carbonic anhydrase inhibitors, in experimental animals

L‐662,583 is a topically effective ocular hypotensive carbonic anhydrase inhibitor in experimental animals

Development of a scintillation proximity assay for analysis of Na +/Cl −-dependent neurotransmitter transporter activity

P 324 Ocular penetration and intraocular pressure (IOP) lowering activity of the angiotensin II (AII) antagonists losartan and L-158,338

Characterization of serotonin receptors in the iris + ciliary body of the albino rabbit

Pharmacology and expression analysis of glycine transporter GlyT1 with [ super(3)H]-(N-[3-(4'-fluorophenyl)-3-(4'phenylphenoxy)propyl])sarc osine

Preclinical studies on L-671,152, a topically effective ocular hypotensive carbonic anhydrase inhibitor

Catecholamine-induced desensitization of adenylate cyclase in rat glioma C6 cells. Evidence for a specific uncoupling of beta-adrenergic receptors from a functional regulatory component of adenylate cyclase

Development of a scintillation proximity assay for analysis of Na super(+)/Cl super(-)-dependent neurotransmitter transporter activity

Thienothiopyran-2-sulfonamides: novel topically active carbonic anhydrase inhibitors for the treatment of glaucoma

L-653,328: an ocular hypotensive agent with modest beta receptor blocking activity

Angiotensin II receptors labelled with 125I-[Sar1, Ile8]-AII in albino rabbit ocular tissues

MK-927 : a topically active ocular hypotensive carbonic anhydrase inhibitor

Characterization of [ 3H]forskolin binding sites in the iris-ciliary body of the albino rabbit

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