Search Results - "Fur, G L"
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SR 144528, the first potent and selective antagonist of the CB2 cannabinoid receptor
Published in The Journal of pharmacology and experimental therapeutics (01-02-1998)“…Based on both binding and functional data, this study introduces SR 144528 as the first, highly potent, selective and orally active antagonist for the CB2…”
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2
Modulation and functional involvement of CB2 peripheral cannabinoid receptors during B-cell differentiation
Published in Blood (15-11-1998)“…Two subtypes of G-protein-coupled cannabinoid receptors have been identified to date: the CB1 central receptor subtype, which is mainly expressed in the brain,…”
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3
Cloning and characterization of PRAX-1. A new protein that specifically interacts with the peripheral benzodiazepine receptor
Published in The Journal of biological chemistry (29-01-1999)“…Using a cytoplasmic domain of the peripheral benzodiazepine receptor (PBR) as a bait in the yeast two-hybrid system, we have isolated a cDNA encoding a new…”
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4
Blockade of cannabinoid CB1 receptors improves renal function, metabolic profile, and increased survival of obese Zucker rats
Published in Kidney international (01-12-2007)“…Obesity is a major risk factor in the development of chronic renal failure. Rimonabant, a cannabinoid CB1 receptor antagonist, improves body weight and…”
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5
Blockade of CRF1 or V1b receptors reverses stress-induced suppression of neurogenesis in a mouse model of depression
Published in Molecular psychiatry (01-03-2004)“…Repeated exposure to stress is known to induce structural remodelling and reduction of neurogenesis in the dentate gyrus. Corticotrophin-releasing factor (CRF)…”
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6
Sub-Band Time Reversal Efficiency Measurement: An Enhanced Method for Efficiency Characterization of UWB Antennas
Published in IEEE transactions on antennas and propagation (01-03-2012)“…Antenna efficiency is a critical parameter if one wishes to characterize the performance of an antenna. It is a measure of the radiation quality of an antenna…”
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7
Improvement of memory in rodents by the selective CB1 cannabinoid receptor antagonist, SR 141716
Published in Psychopharmacologia (01-07-1996)“…Social short-term memory in rodents is based on the recognition of a juvenile by an adult conspecific when the juvenile is presented on two successive…”
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Involvement of Peripheral Benzodiazepine Receptors in the Protection of Hematopoietic Cells Against Oxygen Radical Damage
Published in Blood (15-04-1996)“…Several putative functions have been attributed to the peripheral benzodiazepine receptor (PBR), but its precise physiologic role has not been elucidated. In…”
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Blockade of cannabinoid receptors by SR141716 selectively increases fos expression in rat mesocorticolimbic areas via reduced dopamine D sub(2) function
Published in Neuroscience (01-04-1999)“…The present study investigated, in rats, whether blockade of cannabinoid CB sub(1) receptors may alter Fos protein expression in a manner comparable to that…”
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10
In vitro and in vivo biological activities of SR140333, a novel potent non-peptide tachykinin NK1 receptor antagonist
Published in European journal of pharmacology (21-12-1993)“…(S)1-(2-[3-(3,4-dichlorophenyl)-1-(3-isopropoxyphenylacetyl)pip eridin-3- yl]ethyl)-4-phenyl-1-azoniabicyclo[2.2.2]octane chloride (SR140333) is a new…”
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11
Primary structure and functional expression of mouse pituitary and human brain corticotrophin releasing factor receptors
Published in FEBS letters (29-11-1993)“…Corticotrophin-releasing factor (CRF) is the principal hypothalamic factor governing the pituitary-adrenal axis, but the wide extra-pituitary distribution of…”
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12
Blockade of cannabinoid receptors by SR141716 selectively increases fos expression in rat mesocorticolimbic areas via reduced dopamine D2 function
Published in Neuroscience (01-06-1999)“…The present study investigated, in rats, whether blockade of cannabinoid CB1 receptors may alter Fos protein expression in a manner comparable to that observed…”
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13
Biochemical and Pharmacological Profile of a Potent and Selective Nonpeptide Antagonist of the Neurotensin Receptor
Published in Proceedings of the National Academy of Sciences - PNAS (01-01-1993)“…We describe the characteristics of SR 48692, a selective, nonpeptide antagonist of the neurotensin receptor. In vitro, this compound competitively…”
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In vitro functional evidence of different neurotensin‐receptors modulating the motor response of human colonic muscle strips
Published in British journal of pharmacology (01-08-1999)“…The newly developed non‐peptide neurotensin (NT)‐receptor antagonists SR 48692 and SR 142948 were used to challenge NT responses of human colonic circular…”
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15
In vitro functional evidence of neuronal cannabinoid CB sub(1) receptors in human ileum
Published in British journal of pharmacology (01-12-1998)“…We investigated the effect of the cannabinoid agonist (+)WIN-55212-2 on human ileum longitudinal smooth muscle preparations, either electrically stimulated or…”
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16
Poster abstracts
Published in Sleep and biological rhythms (01-08-2007)Get full text
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17
Role of tachykinins in castor oil diarrhoea in rats
Published in British journal of pharmacology (01-06-1997)“…We set out to ascertain the role of tachykinins, neurokinin A and substance P, in castor oil‐induced diarrhoea in rats as disclosed by the inhibitory effect of…”
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Functional identification of rat atypical β‐adrenoceptors by the first β3‐selective antagonists, aryloxypropanolaminotetralins
Published in British journal of pharmacology (01-02-1996)“…1 We have assessed the relative abilities of compounds belonging to the new aryloxypropanolaminotetralin (APAT) class and of the reference…”
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19
Cloning and expression of a complementary DNA encoding a high affinity human neurotensin receptor
Published in FEBS letters (08-02-1993)“…A human neurotensin receptor (hNTR) cDNA was cloned from the colonic adenocarcinoma cell line HT29. The cloned cDNA encodes a putative peptide of 418 amino…”
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Pharmacological characterization of SR 47436, a new nonpeptide AT1 subtype angiotensin II receptor antagonist
Published in The Journal of pharmacology and experimental therapeutics (01-05-1993)“…SR 47436, 2-n-butyl-3-[(2'-(1H-tetrazol-5-yl)-biphenyl-4-yl) methyl]-1,3-diaza-spiro[4,4]non-1-en-4-one, is a new potent and selective AT1 angiotensin II (AII)…”
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