Zobrazeno 1 - 10
of 40
pro vyhledávání: '"P M, Laduron"'
Publikováno v:
Annals of the New York Academy of Sciences. 668:311-313
Publikováno v:
Biochemical pharmacology. 47(1)
Biochemical and anatomical data are reported which demonstrate for the first time the existence of a retrograde axonal transport process for a neuropeptide, neurotensin, in rat brain. Neurotensin receptors are mainly located in the striatum on nerve
Autor:
P M, Laduron
Publikováno v:
Biochemical pharmacology. 47(1)
Receptors involved in intercellular communication at the cell surface share the capacity to desensitize through molecular and cellular mechanisms. Cellular desensitization is a rapid and dynamic process whereby membrane receptors internalize in respo
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
Publikováno v:
Journal of neurochemistry. 54(3)
The effect of cycloheximide, a protein synthesis inhibitor, was studied on the axonal transport of noradrenergic synaptic vesicles and presynaptic muscarinic receptors, identified by in vitro binding of [3H]dihydrotetrabenazine and [3H]quinuclidinylb
Publikováno v:
Neuropsychopharmacology ISBN: 9783642740367
Our modern way of life with its high levels of stress and anxiety has increased the salience of problems associated with insomnia and consequently also the search for drugs to alleviate this symptom. This review presents the most recent pharmacologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d61c52754b660312efa28dedbcd0e39
https://doi.org/10.1007/978-3-642-74034-3_64
https://doi.org/10.1007/978-3-642-74034-3_64
Publikováno v:
Pain. 41:S192
Publikováno v:
Molecular pharmacology. 21(2)
Binding characteristics of astemizole were studied in vitro in various receptor binding models and in vivo by determining the occupancy of histamine H1 receptors in guinea pig lung and cerebellum. In vitro, astemizole was found to have a high affinit
Publikováno v:
Psychopharmacology series. 3
Publikováno v:
Molecular pharmacology. 22(2)
[3H]Spiperone binding sites were solubilized from rat frontal cortex and striatum by means of the mild detergent, lysolecithin. In the frontal cortex, the binding sites were extracted from a microsomal membrane fraction which was found to be enriched