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601 Comparative tissue distribution of the HDAC inhibitor JNJ-26481585

European journal of cancer supplements, 2010, Vol.8 (7), p.189-189

2010

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5-Hydroxytryptamine1A receptor synthetic peptides. Mechanisms of adenylyl cyclase inhibition

The Journal of biological chemistry, 1994-06, Vol.269 (24), p.16720-16725

1994

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In vitro and In vivo Pharmacokinetic-Pharmacodynamic Relationships for the Trisubstituted Aminopurine Cyclin-Dependent Kinase Inhibitors Olomoucine, Bohemine and CYC202

Clinical cancer research, 2005-07, Vol.11 (13), p.4875-4888

2005

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Alpha 2-C10 adrenergic receptors expressed in rat 1 fibroblasts can regulate both adenylylcyclase and phospholipase D-mediated hydrolysis of phosphatidylcholine by interacting with pertussis toxin-sensitive guanine nucleotide-binding proteins

The Journal of biological chemistry, 1992-02, Vol.267 (4), p.2149-2156

1992

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Molecular interaction of the human alpha 2-C10-adrenergic receptor, when expressed in Rat-1 fibroblasts, with multiple pertussis toxin-sensitive guanine nucleotide-binding proteins: studies with site-directed antisera

Molecular pharmacology, 1991-11, Vol.40 (5), p.627-632

1991

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Subacute and Chronic In Vivo Lithium Treatment Inhibits Agonist‐ and Sodium Fluoride‐Stimulated Inositol Phosphate Production in Rat Cortex

Journal of neurochemistry, 1989-02, Vol.52 (2), p.498-506

1989

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In vitro and in vivo antitumor properties of the cyclin dependent kinase inhibitor CYC202 (R‐roscovitine)

International journal of cancer, 2002-12, Vol.102 (5), p.463-468

2002

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5‐Hydroxytryptamine‐Stimulated Inositol Phospholipid Hydrolysis in the Mouse Cortex Has Pharmacological Characteristics Compatible with Mediation via 5‐HT2 Receptors but This Response Does Not Reflect Altered 5‐HT2 Function After 5,7‐Dihydroxytryptamine Lesioning or Repeated Antidepressant Treatments

Journal of neurochemistry, 1988-03, Vol.50 (3), p.730-738

1988

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Abstract 1361: Fragment based drug discovery of selective inhibitors of Fibroblast Growth Factor Receptor (FGFR)

Cancer research (Chicago, Ill.), 2011-04, Vol.71 (8_Supplement), p.1361-1361

2011

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Hallucinogenic drugs are partial agonists of the human platelet shape change response: a physiological model of the 5-HT2 receptor

Biological psychiatry (1969), 1989-07, Vol.26 (3), p.297-302

1989

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Gi3 does not contribute to the inhibition of adenylate cyclase when stimulation of an α2-adrenergic receptor causes activation of both Gi2 and Gi3

Biochemical journal, 1992-06, Vol.284 (2), p.565-568

1992

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Gi3 does not contribute to the inhibition of adenylate cyclase when stimulation of an alpha 2-adrenergic receptor causes activation of both Gi2 and Gi3

Biochemical journal, 1992-06, Vol.284 ( Pt 2) (Pt 2), p.565-568

1992

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Inhibition of aggregation in Dictyostelium by EGTA-induced depletion of calcium

FEMS microbiology letters, 1984, Vol.21 (1), p.21-25

1984

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Serotonergic agonists stimulate inositol lipid metabolism in rabbit platelets

Life sciences (1973), 1985-10, Vol.37 (17), p.1641-1647

1985

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Discovery of a Novel Family of CDK Inhibitors with the Program LIDAEUS: Structural Basis for Ligand-Induced Disordering of the Activation Loop

Structure (London), 2003-04, Vol.11 (4), p.399-410

2003

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Relationship of increased food intake and plasma ACTH levels to 5-HT1A receptor activation in rats

Psychoneuroendocrinology, 1988, Vol.13 (6), p.471-478

1988

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Metabolism and pharmacokinetics of the cyclin-dependent kinase inhibitor R-roscovitine in the mouse

Molecular cancer therapeutics, 2005-01, Vol.4 (1), p.125-139

2005

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Expression of Human M2 Muscarinic Receptors in SF9 Cells: Characterisation and Reconstitution with G-Proteins

Journal of receptors and signal transduction, 1995, Vol.15 (1-4), p.55-70

1995

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5-Hydroxytryptamine (5-HT)-induced shape change in human platelets determined by computerized data acquisition: correlation with [125I]-iodoLSD binding at 5-HT2 receptors

Blood coagulation & fibrinolysis, 1991-02, Vol.2 (1), p.17

1991

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Signal transduction in Rat-1 fibroblasts expressing high levels of the α2-C10 adrenergic receptor

Biochemical Society transactions, 1991-04, Vol.19 (2), p.102-102S

1991

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5-Hydroxytryptamine (5-HT)-induced shape change in human platelets determined by computerized data acquisition: correlation with [125I]-iodo LSD binding at 5-HT2 receptors

Blood coagulation & fibrinolysis, 1991-02, Vol.2 (1), p.17-24

1991

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Characterisation of the neuropeptide Y receptor that mediates feeding in the rat: a role for the Y5 receptor?

Regulatory peptides, 1998-09, Vol.75, p.355-361

1998

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Synthesis and configuration of the cyclin-dependent kinase inhibitor roscovitine and its enantiomer

Tetrahedron: asymmetry, 2001-11, Vol.12 (20), p.2891-2894

2001

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Molecular interaction of the human α2-C10-adrenergic receptor, when expressed in rat-1 fibroblasts, with multiple pertussis toxin-sensitive guanine nucleotide-binding proteins : studies with site-directed antisera

Molecular pharmacology, 1991, Vol.40 (5), p.627-632

1991

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Molecular interaction of the human alpha sub(2)-C10-adrenergic receptor, when expressed in rat-1 fibroblasts, with multiple pertussis toxin-sensitive guanine nucleotide-binding proteins: Studies with site-directed antisera

Molecular pharmacology, 1991-01, Vol.40 (5), p.627-632

1991

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601 Comparative tissue distribution of the HDAC inhibitor JNJ-26481585

5-Hydroxytryptamine1A receptor synthetic peptides. Mechanisms of adenylyl cyclase inhibition

In vitro and In vivo Pharmacokinetic-Pharmacodynamic Relationships for the Trisubstituted Aminopurine Cyclin-Dependent Kinase Inhibitors Olomoucine, Bohemine and CYC202

Alpha 2-C10 adrenergic receptors expressed in rat 1 fibroblasts can regulate both adenylylcyclase and phospholipase D-mediated hydrolysis of phosphatidylcholine by interacting with pertussis toxin-sensitive guanine nucleotide-binding proteins

Molecular interaction of the human alpha 2-C10-adrenergic receptor, when expressed in Rat-1 fibroblasts, with multiple pertussis toxin-sensitive guanine nucleotide-binding proteins: studies with site-directed antisera

Subacute and Chronic In Vivo Lithium Treatment Inhibits Agonist‐ and Sodium Fluoride‐Stimulated Inositol Phosphate Production in Rat Cortex

In vitro and in vivo antitumor properties of the cyclin dependent kinase inhibitor CYC202 (R‐roscovitine)

Abstract 1361: Fragment based drug discovery of selective inhibitors of Fibroblast Growth Factor Receptor (FGFR)

Hallucinogenic drugs are partial agonists of the human platelet shape change response: a physiological model of the 5-HT2 receptor

Gi3 does not contribute to the inhibition of adenylate cyclase when stimulation of an α2-adrenergic receptor causes activation of both Gi2 and Gi3

Gi3 does not contribute to the inhibition of adenylate cyclase when stimulation of an alpha 2-adrenergic receptor causes activation of both Gi2 and Gi3

Inhibition of aggregation in Dictyostelium by EGTA-induced depletion of calcium

Serotonergic agonists stimulate inositol lipid metabolism in rabbit platelets

Discovery of a Novel Family of CDK Inhibitors with the Program LIDAEUS: Structural Basis for Ligand-Induced Disordering of the Activation Loop

Relationship of increased food intake and plasma ACTH levels to 5-HT1A receptor activation in rats

Metabolism and pharmacokinetics of the cyclin-dependent kinase inhibitor R-roscovitine in the mouse

Expression of Human M2 Muscarinic Receptors in SF9 Cells: Characterisation and Reconstitution with G-Proteins

5-Hydroxytryptamine (5-HT)-induced shape change in human platelets determined by computerized data acquisition: correlation with [125I]-iodoLSD binding at 5-HT2 receptors

Signal transduction in Rat-1 fibroblasts expressing high levels of the α2-C10 adrenergic receptor

5-Hydroxytryptamine (5-HT)-induced shape change in human platelets determined by computerized data acquisition: correlation with [125I]-iodo LSD binding at 5-HT2 receptors

Characterisation of the neuropeptide Y receptor that mediates feeding in the rat: a role for the Y5 receptor?

Synthesis and configuration of the cyclin-dependent kinase inhibitor roscovitine and its enantiomer

Molecular interaction of the human α2-C10-adrenergic receptor, when expressed in rat-1 fibroblasts, with multiple pertussis toxin-sensitive guanine nucleotide-binding proteins : studies with site-directed antisera

Molecular interaction of the human alpha sub(2)-C10-adrenergic receptor, when expressed in rat-1 fibroblasts, with multiple pertussis toxin-sensitive guanine nucleotide-binding proteins: Studies with site-directed antisera

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