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Human primary osteoclasts: in vitro generation and applications as pharmacological and clinical assay

Journal of translational medicine, 2004-03, Vol.2 (1), p.6-6, Article 6

2004

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Potentiation of tachykinin-induced plasma protein extravasation by calcitonin gene-related peptide

European journal of pharmacology, 1985-08, Vol.114 (1), p.61-66

1985

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The Serotonin 5-HT4 Receptor. 2. Structure-Activity Studies of the Indole Carbazimidamide Class of Agonists

Journal of medicinal chemistry, 1995-06, Vol.38 (13), p.2331-2338

1995

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The Serotonin 5-HT4 Receptor. 1. Design of a New Class of Agonists and Receptor Map of the Agonist Recognition Site

Journal of medicinal chemistry, 1995-06, Vol.38 (13), p.2326-2330

1995

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ATF936, a novel oral calcilytic, increases bone mineral density in rats and transiently releases parathyroid hormone in humans

Bone (New York, N.Y.), 2011-08, Vol.49 (2), p.233-241

2011

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1-Alkyl-4-phenyl-6-alkoxy-1H-quinazolin-2-ones: A Novel Series of Potent Calcium-Sensing Receptor Antagonists

Journal of medicinal chemistry, 2010-03, Vol.53 (5), p.2250-2263

2010

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SDZ 205-557, a selective, surmountable antagonist for 5-HT4 receptors in the isolated guinea pig ileum

Naunyn-Schmiedeberg's archives of pharmacology, 1992-04, Vol.345 (4), p.387-393

1992

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Substance P release from spinal cord slices by capsaicin

Life sciences (1973), 1979-08, Vol.25 (7), p.629-636

1979

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Penta-substituted benzimidazoles as potent antagonists of the calcium-sensing receptor (CaSR-antagonists)

Bioorganic & medicinal chemistry letters, 2010-09, Vol.20 (17), p.5161-5164

2010

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Capsaicin applied to peripheral nerve inhibits axoplasmic transport of substance P and somatostatin

Brain research, 1982-05, Vol.239 (2), p.447-462

1982

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Differential effects of capsaicin on the content of somatostatin, substance P, and neurotensin in the nervous system of the rat

Naunyn-Schmiedeberg's archives of pharmacology, 1981-01, Vol.317 (2), p.140-148

1981

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Effect of capsaicin pretreatment on capsaicin-evoked release of immunoreactive somatostatin and substance P from primary sensory neurons

Naunyn-Schmiedeberg's archives of pharmacology, 1981-02, Vol.316 (1), p.38-41

1981

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1-Alkyl-4-phenyl-6-alkoxy-1 H -quinazolin-2-ones: A Novel Series of Potent Calcium-Sensing Receptor Antagonists

Journal of medicinal chemistry, 2010-03, Vol.53 (5), p.2250-2263

2010

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Endogenous 5-Hydroxytryptamine Modulates the Release of Tachykinins and Calcitonin Gene-related Peptide from the Rat Spinal Cord via 5-HT3 Receptors

Annals of the New York Academy of Sciences, 1991-01, Vol.632 (1), p.464-465

1991

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Capsaicin and nociception in the rat and mouse. Possible role of substance P

Naunyn-Schmiedeberg's archives of pharmacology, 1982-09, Vol.320 (3), p.205-216

Gamse, R

1982

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Release of multiple tachykinins from capsaicin-sensitive sensory nerves in the lung by bradykinin, histamine, dimethylphenyl piperazinium, and vagal nerve stimulation

The American review of respiratory disease, 1988-06, Vol.137 (6), p.1330-1335

1988

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SDZ 205-557, a selective antagonist at 5-HT4 receptors in the isolated guinea pig ileum

European journal of pharmacology, 1991-08, Vol.200 (2-3), p.373-374

1991

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N-terminal truncation of salmon calcitonin leads to calcitonin antagonists : structure activity relationship of N-terminally truncated salmon calcitonin fragments in vitro and in vivo

Biochemical and biophysical research communications, 1992-08, Vol.187 (1), p.8-13

1992

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Dipeptide mimetics can substitute for the receptor activation domain resulting in highly potent analogues of hPTH(1–36)

Bioorganic & medicinal chemistry letters, 1996-05, Vol.6 (10), p.1151-1156

1996

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Reduced neurogenic inflammation in streptozotocin-diabetic rats due to microvascular changes but not to substance P depletion

European journal of pharmacology, 1985-11, Vol.118 (1), p.175-180

1985

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Distribution of substance P in the rat gastrointestinal tract — Lack of effect of capsaicin pretreatment

European journal of pharmacology, 1980-02, Vol.61 (3), p.303-307

1980

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Endogenous 5‐Hydroxytryptamine Modulates the Release of Tachykinins and Calcitonin Gene—related Peptide from the Rat Spinal Cord via 5‐HT 3 Receptors

Annals of the New York Academy of Sciences, 1991-09, Vol.632 (1), p.464-465

1991

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Release of substance P- and substance K-like immunoreactivities from the isolated perfused guinea-pig lung

European journal of pharmacology, 1984-10, Vol.106 (1), p.207-208

1984

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Release of Immunoreactive Somatostatin from Hypothalamic Cells in Culture: Inhibition by γ -Aminobutyric Acid

Proceedings of the National Academy of Sciences - PNAS, 1980-09, Vol.77 (9), p.5552-5556

1980

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SDZ 205–557, a selective antagonist at 5-HT 4 receptors in the isolated guinea pig ileum

European journal of pharmacology, 1991, Vol.200 (2), p.373-374

1991

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Human primary osteoclasts: in vitro generation and applications as pharmacological and clinical assay

Potentiation of tachykinin-induced plasma protein extravasation by calcitonin gene-related peptide

The Serotonin 5-HT4 Receptor. 2. Structure-Activity Studies of the Indole Carbazimidamide Class of Agonists

The Serotonin 5-HT4 Receptor. 1. Design of a New Class of Agonists and Receptor Map of the Agonist Recognition Site

ATF936, a novel oral calcilytic, increases bone mineral density in rats and transiently releases parathyroid hormone in humans

1-Alkyl-4-phenyl-6-alkoxy-1H-quinazolin-2-ones: A Novel Series of Potent Calcium-Sensing Receptor Antagonists

SDZ 205-557, a selective, surmountable antagonist for 5-HT4 receptors in the isolated guinea pig ileum

Substance P release from spinal cord slices by capsaicin

Penta-substituted benzimidazoles as potent antagonists of the calcium-sensing receptor (CaSR-antagonists)

Capsaicin applied to peripheral nerve inhibits axoplasmic transport of substance P and somatostatin

Differential effects of capsaicin on the content of somatostatin, substance P, and neurotensin in the nervous system of the rat

Effect of capsaicin pretreatment on capsaicin-evoked release of immunoreactive somatostatin and substance P from primary sensory neurons

1-Alkyl-4-phenyl-6-alkoxy-1 H -quinazolin-2-ones: A Novel Series of Potent Calcium-Sensing Receptor Antagonists

Endogenous 5-Hydroxytryptamine Modulates the Release of Tachykinins and Calcitonin Gene-related Peptide from the Rat Spinal Cord via 5-HT3 Receptors

Capsaicin and nociception in the rat and mouse. Possible role of substance P

Release of multiple tachykinins from capsaicin-sensitive sensory nerves in the lung by bradykinin, histamine, dimethylphenyl piperazinium, and vagal nerve stimulation

SDZ 205-557, a selective antagonist at 5-HT4 receptors in the isolated guinea pig ileum

N-terminal truncation of salmon calcitonin leads to calcitonin antagonists : structure activity relationship of N-terminally truncated salmon calcitonin fragments in vitro and in vivo

Dipeptide mimetics can substitute for the receptor activation domain resulting in highly potent analogues of hPTH(1–36)

Reduced neurogenic inflammation in streptozotocin-diabetic rats due to microvascular changes but not to substance P depletion

Distribution of substance P in the rat gastrointestinal tract — Lack of effect of capsaicin pretreatment

Endogenous 5‐Hydroxytryptamine Modulates the Release of Tachykinins and Calcitonin Gene—related Peptide from the Rat Spinal Cord via 5‐HT 3 Receptors

Release of substance P- and substance K-like immunoreactivities from the isolated perfused guinea-pig lung

Release of Immunoreactive Somatostatin from Hypothalamic Cells in Culture: Inhibition by γ -Aminobutyric Acid

SDZ 205–557, a selective antagonist at 5-HT 4 receptors in the isolated guinea pig ileum

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