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Results:
1-12
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Results: 12
Authors:
LAPALU S
MOISAND C
BUTOUR JL
MOLLEREAU C
MEUNIER JC
Citation: S. Lapalu et al., DIFFERENT DOMAINS OF THE ORL1 AND KAPPA-OPIOID RECEPTORS ARE INVOLVEDIN RECOGNITION OF NOCICEPTIN AND DYNORPHIN-A, FEBS letters, 427(2), 1998, pp. 296-300
Authors:
BUTOUR JL
MOISAND C
MOLLEREAU C
MEUNIER JC
Citation: Jl. Butour et al., [PHE(1)PSI(CH2-NH)GLY(2)]NOCICEPTIN-(1-13)-NH2 IS AN AGONIST OF THE NOCICEPTIN (ORL1) RECEPTOR, European journal of pharmacology, 349(1), 1998, pp. 5-6
Authors:
SAMSON M
EDINGER AL
STORDEUR P
RUCKER J
VERHASSELT V
SHARRON M
GOVAERTS C
MOLLEREAU C
VASSART G
DOMS RW
PARMENTIER M
Citation: M. Samson et al., CHEMR23, A PUTATIVE CHEMOATTRACTANT RECEPTOR, IS EXPRESSED IN MONOCYTE-DERIVED DENDRITIC CELLS AND MACROPHAGES AND IS A CORECEPTOR FOR SIV AND SOME PRIMARY HIV-1 STRAINS, European Journal of Immunology, 28(5), 1998, pp. 1689-1700
Authors:
GODART M
MOLLEREAU C
GOVAERTS C
DETHEUX M
VANDERHAEGHEN P
LIBERT F
LEDENT C
COSTENTIN J
MEUNIER JC
VASSART G
PARMENTIER M
Citation: M. Godart et al., ORPHAN RECEPTORS - HOW MANY UNKNOWN MESSENGERS, British Journal of Pharmacology, 123, 1998, pp. 364-364
Authors:
LAPALU S
MOISAND C
MAZARGUIL H
CAMBOIS G
MOLLEREAU C
MEUNIER JC
Citation: S. Lapalu et al., COMPARISON OF THE STRUCTURE-ACTIVITY-RELATIONSHIPS OF NOCICEPTIN AND DYNORPHIN-A USING CHIMERIC PEPTIDES, FEBS letters, 417(3), 1997, pp. 333-336
Authors:
BUTOUR JL
MOISAND C
MAZARGUIL H
MOLLEREAU C
MEUNIER JC
Citation: Jl. Butour et al., RECOGNITION AND ACTIVATION OF THE OPIOID RECEPTOR-LIKE ORL1 RECEPTOR BY NOCICEPTIN, NOCICEPTIN ANALOGS AND OPIOIDS, European journal of pharmacology, 321(1), 1997, pp. 97-103
Authors:
MEUNIER JC
MOLLEREAU C
COSTENTIN J
PARMENTIER M
VASSART G
Citation: Jc. Meunier et al., NOCICEPTIN AND ITS RECEPTOR, MS. Medecine sciences, 12(3), 1996, pp. 373-376
Authors:
MOLLEREAU C
SIMONS MJ
SOULARUE P
LINERS F
VASSART G
MEUNIER JC
PARMENTIER M
Citation: C. Mollereau et al., STRUCTURE, TISSUE DISTRIBUTION, AND CHROMOSOMAL LOCALIZATION OF THE PREPRONOCICEPTIN GENE, Proceedings of the National Academy of Sciences of the United Statesof America, 93(16), 1996, pp. 8666-8670
Authors:
MOLLEREAU C
MOISAND C
BUTOUR JL
PARMENTIER M
MEUNIER JC
Citation: C. Mollereau et al., REPLACEMENT OF GLN(280) BY HIS IN TM6 OF THE HUMAN ORL1 RECEPTOR INCREASES AFFINITY BUT REDUCES INTRINSIC ACTIVITY OF OPIOIDS, FEBS letters, 395(1), 1996, pp. 17-21
Authors:
SAMSON M
LABBE O
MOLLEREAU C
VASSART G
PARMENTIER M
Citation: M. Samson et al., MOLECULAR-CLONING AND FUNCTIONAL EXPRESSION OF A NEW HUMAN CC-CHEMOKINE RECEPTOR GENE, Biochemistry, 35(11), 1996, pp. 3362-3367
Authors:
MEUNIER JC
MOLLEREAU C
TOLL L
SUAUDEAU C
MOISAND C
ALVINERIE P
BUTOUR JL
GUILLEMOT JC
FERRARA P
MONSARRAT B
MAZARGUIL H
VASSART G
PARMENTIER M
COSTENTIN J
Citation: Jc. Meunier et al., ISOLATION AND STRUCTURE OF THE ENDOGENOUS AGONIST OF OPIOID RECEPTOR-LIKE ORL(1) RECEPTOR, Nature, 377(6549), 1995, pp. 532-535
ORL1, A NOVEL MEMBER OF THE OPIOID RECEPTOR FAMILY - CLONING, FUNCTIONAL EXPRESSION AND LOCALIZATION
Authors:
MOLLEREAU C
PARMENTIER M
MAILLEUX P
BUTOUR JL
MOISAND C
CHALON P
CAPUT D
VASSART G
MEUNIER JC
Citation: C. Mollereau et al., ORL1, A NOVEL MEMBER OF THE OPIOID RECEPTOR FAMILY - CLONING, FUNCTIONAL EXPRESSION AND LOCALIZATION, FEBS letters, 341(1), 1994, pp. 33-38
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