Zobrazeno 1 - 10
of 61
pro vyhledávání: '"V, Fardin"'
Autor:
Romeu Moreira dos Santos, G. D. A. HARAGUCHI, G. R. S. SLIUZAS, M. C. MENEZES, E. LEGA, B. PALUDETO, V. FARDIN
Publikováno v:
Nucleus Animalium. 4:7-10
Publikováno v:
Equine Veterinary Journal. 46:5-6
Introduction Swimming can be used for conditioning and rehabilitation of horses. Its main advantage is minimal musculoskeletal stress. The purpose of this study was to evaluate the influence of swimming on athletic performance of Mangalarga Marchador
Publikováno v:
ChemInform. 29
Autor:
L, Pradier, E, Habert-Ortoli, L, Emile, J, Le Guern, I, Loquet, M D, Bock, J, Clot, L, Mercken, V, Fardin, C, Garret
Publikováno v:
Molecular pharmacology. 47(2)
Most nonpeptide neurokinin (NK)1 antagonists display a marked difference in affinity for rat versus human NK1 receptors. The molecular basis for the species selectivity of RP67580 and CP96,345 has been previously addressed [J. Biol. Chem. 267:25668-2
Autor:
L, Pradier, J, Ménager, J, Le Guern, M D, Bock, E, Heuillet, V, Fardin, C, Garret, A, Doble, J F, Mayaux
Publikováno v:
Molecular pharmacology. 45(2)
The hexapeptide [pGlu6,Pro9]substance P (SP)6-11, septide, has been shown to be an agonist as potent as SP in eliciting smooth muscle contraction in several in vitro preparations, while being a poor competitor of labeled SP binding. These results, as
Autor:
C, Garret, A, Carruette, V, Fardin, S, Moussaoui, J F, Peyronel, J C, Blanchard, P M, Laduron
Publikováno v:
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie. 314(5)
The pharmacological properties of 7,7-Diphenyl-2 [1-imino-2 (2-methoxy-phenyl)-ethyl] perhydroisoindol-4-one (3 aR, 7 aR) or RP67580 are described. This compound, derived from a novel chemical family, is a potent and selective substance P (SP) antago
Autor:
V. Fardin, A. Carruette, J. Menager, M. Bock, O. Flamand, F. Foucault, E. Heuillet, S.M. Moussaoui, M. Tabart, J.F. Peyronel, C. Garret
Publikováno v:
Neuropeptides. 26:34
Publikováno v:
Neuropeptides. 22:14
Publikováno v:
Pain. 41:S192
Publikováno v:
Journal de physiologie. 77(2-3)
Numerous studies in the rat have shown that powerful analgesia can be induced by electrical stimulation of the periaqueductal grey matter (PGM). From an extensive mapping (300 sites of stimulation) performed on unrestrained cats, we have demonstrated