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The histamine H 3 receptor: an attractive target for the treatment of cognitive disorders

British journal of pharmacology, 2008-07, Vol.154 (6), p.1166-1181

2008

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Blockade of mGluR1 receptor results in analgesia and disruption of motor and cognitive performances: effects of A‐841720, a novel non‐competitive mGluR1 receptor antagonist

British journal of pharmacology, 2006-11, Vol.149 (6), p.761-774

2006

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Nitric oxide independent activation of guanylate cyclase by YC-1 causes erectile responses in the rat

The Journal of urology, 2002-05, Vol.167 (5), p.2276

2002

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Characterization of a novel ATP‐sensitive K+ channel opener, A‐251179, on urinary bladder relaxation and cystometric parameters

British journal of pharmacology, 2007-06, Vol.151 (4), p.467-475

2007

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Activators of soluble guanylate cyclase for the treatment of male erectile dysfunction

International journal of impotence research, 2002-02, Vol.14 (1), p.8-14

2002

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(+/-)-Epibatidine elicits a diversity of in vitro and in vivo effects mediated by nicotinic acetylcholine receptors

The Journal of pharmacology and experimental therapeutics, 1994-11, Vol.271 (2), p.624

1994

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Activation of soluble guanylate cyclase causes relaxation of corpus cavernosum tissue: Synergism of nitric oxide and YC-1

International journal of impotence research, 2002-04, Vol.14 (2), p.121-127

2002

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In vivo evaluation of the potency and bladder‐vascular selectivity of the ATP‐sensitive potassium channel openers (–)‐cromakalim, ZD6169 and WAY‐133537 in rats

BJU international, 2003-02, Vol.91 (3), p.284-290

2003

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The histamine H3 receptor: an attractive target for the treatment of cognitive disorders

British journal of pharmacology, 2008-07, Vol.154 (6), p.1166-1181

2008

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Pharmacological and molecular analysis of ATP-sensitive K + channels in the pig and human detrusor

European journal of pharmacology, 2000-07, Vol.400 (2), p.287-295

2000

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Nicotinic receptor agonists exhibit anxiolytic-like effects on the elevated plus-maze test

European journal of pharmacology, 1993-07, Vol.238 (1), p.1-8

1993

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Use of the H3 receptor antagonist radioligand [3H]‐A‐349821 to reveal in vivo receptor occupancy of cognition enhancing H3 receptor antagonists

British journal of pharmacology, 2009-05, Vol.157 (1), p.139-149

2009

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(S)-3-methyl-5-(1-methyl-2-pyrrolidinyl)isoxazole (ABT 418): a novel cholinergic ligand with cognition-enhancing and anxiolytic activities: II. In vivo characterization

The Journal of pharmacology and experimental therapeutics, 1994-07, Vol.270 (1), p.319

1994

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Anxiolytic-like effects of the novel cholinergic channel activator ABT-418

The Journal of pharmacology and experimental therapeutics, 1994-10, Vol.271 (1), p.353

1994

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Dual mechanism of action of nicorandil on rabbit corpus cavernosal smooth muscle tone

International journal of impotence research, 2001-08, Vol.13 (4), p.240-246

2001

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Influence of Separate and Combined Septal and Amygdala Lesions on Memory, Acoustic Startle, Anxiety, and Locomotor Activity in Rats

Neurobiology of learning and memory, 1995-09, Vol.64 (2), p.156-168

1995

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In vitro and in vivo characterization of A‐940894: a potent histamine H 4 receptor antagonist with anti‐inflammatory properties

British journal of pharmacology, 2009-05, Vol.157 (1), p.44-54

2009

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The biochemical and neurologic basis for the treatment of male erectile dysfunction

The Journal of pharmacology and experimental therapeutics, 2001-02, Vol.296 (2), p.225

2001

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Pharmacology of human sulphonylurea receptor SUR1 and inward rectifier K+ channel Kir6.2 combination expressed in HEK‐293 cells

British journal of pharmacology, 2000-04, Vol.129 (7), p.1323-1332

2000

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Novel Isoxazoles which Interact with Brain Cholinergic Channel Receptors Have Intrinsic Cognitive Enhancing and Anxiolytic Activities

Journal of medicinal chemistry, 1994-04, Vol.37 (8), p.1055-1059

1994

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Involvement of the amygdala GABAergic system in the modulation of memory storage

Brain research, 1989-05, Vol.487 (1), p.105-112

1989

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Use of the H 3 receptor antagonist radioligand [ 3 H]‐A‐349821 to reveal in vivo receptor occupancy of cognition enhancing H 3 receptor antagonists

British journal of pharmacology, 2009-05, Vol.157 (1), p.139-149

2009

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Erysodine, a competitive antagonist at neuronal nicotinic acetylcholine receptors

European journal of pharmacology, 1995-06, Vol.280 (1), p.79-89

1995

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Pharmacological and molecular characterization of ATP-sensitive K + channels in the TE671 human medulloblastoma cell line

European journal of pharmacology, 1999-04, Vol.370 (2), p.179-185

1999

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Post-training administration of GABAergic antagonists enhances retention of aversively motivated tasks

Psychopharmacologia, 1988-12, Vol.96 (4), p.505-510

1988

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The histamine H 3 receptor: an attractive target for the treatment of cognitive disorders

Blockade of mGluR1 receptor results in analgesia and disruption of motor and cognitive performances: effects of A‐841720, a novel non‐competitive mGluR1 receptor antagonist

Nitric oxide independent activation of guanylate cyclase by YC-1 causes erectile responses in the rat

Characterization of a novel ATP‐sensitive K+ channel opener, A‐251179, on urinary bladder relaxation and cystometric parameters

Activators of soluble guanylate cyclase for the treatment of male erectile dysfunction

(+/-)-Epibatidine elicits a diversity of in vitro and in vivo effects mediated by nicotinic acetylcholine receptors

Activation of soluble guanylate cyclase causes relaxation of corpus cavernosum tissue: Synergism of nitric oxide and YC-1

In vivo evaluation of the potency and bladder‐vascular selectivity of the ATP‐sensitive potassium channel openers (–)‐cromakalim, ZD6169 and WAY‐133537 in rats

The histamine H3 receptor: an attractive target for the treatment of cognitive disorders

Pharmacological and molecular analysis of ATP-sensitive K + channels in the pig and human detrusor

Nicotinic receptor agonists exhibit anxiolytic-like effects on the elevated plus-maze test

Use of the H3 receptor antagonist radioligand [3H]‐A‐349821 to reveal in vivo receptor occupancy of cognition enhancing H3 receptor antagonists

(S)-3-methyl-5-(1-methyl-2-pyrrolidinyl)isoxazole (ABT 418): a novel cholinergic ligand with cognition-enhancing and anxiolytic activities: II. In vivo characterization

Anxiolytic-like effects of the novel cholinergic channel activator ABT-418

Dual mechanism of action of nicorandil on rabbit corpus cavernosal smooth muscle tone

Influence of Separate and Combined Septal and Amygdala Lesions on Memory, Acoustic Startle, Anxiety, and Locomotor Activity in Rats

In vitro and in vivo characterization of A‐940894: a potent histamine H 4 receptor antagonist with anti‐inflammatory properties

The biochemical and neurologic basis for the treatment of male erectile dysfunction

Pharmacology of human sulphonylurea receptor SUR1 and inward rectifier K+ channel Kir6.2 combination expressed in HEK‐293 cells

Novel Isoxazoles which Interact with Brain Cholinergic Channel Receptors Have Intrinsic Cognitive Enhancing and Anxiolytic Activities

Involvement of the amygdala GABAergic system in the modulation of memory storage

Use of the H 3 receptor antagonist radioligand [ 3 H]‐A‐349821 to reveal in vivo receptor occupancy of cognition enhancing H 3 receptor antagonists

Erysodine, a competitive antagonist at neuronal nicotinic acetylcholine receptors

Pharmacological and molecular characterization of ATP-sensitive K + channels in the TE671 human medulloblastoma cell line

Post-training administration of GABAergic antagonists enhances retention of aversively motivated tasks

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