Zobrazeno 1 - 10
of 77
pro vyhledávání: '"M J, Millan"'
Autor:
M. Jacoupy, E. Hamon-Keromen, A. Ordureau, Z. Erpapazoglou, F. Coge, J.-C. Corvol, O. Nosjean, C. Mannoury la Cour, M. J. Millan, J. A. Boutin, J. W. Harper, A. Brice, D. Guedin, C. A. Gautier, O. Corti
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-15 (2019)
Abstract Most of over a thousand mitochondrial proteins are encoded by nuclear genes and must be imported from the cytosol. Little is known about the cytosolic events regulating mitochondrial protein import, partly due to the lack of appropriate tool
Externí odkaz:
https://doaj.org/article/e3de579c73004127a500e989a78a21a9
Autor:
M. J. Millan
Publikováno v:
Current Drug Target -CNS & Neurological Disorders. 1:191-213
Glutamatergic pathways, metabotropic receptors, and ionotropic alpha-amino-3-hydroxy-5-methylisoxazole-4-proprionic acid (AMPA), kainate and N-methyl-D-aspartate (NMDA) receptors are all implicated in the etiology and management of schizophrenia. As
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c82e800f3065e1bd6058ceda1219f82
https://doi.org/10.2174/1568007024606258
https://doi.org/10.2174/1568007024606258
Autor:
M. J. Millan, F. Lejeune
Publikováno v:
European Journal of Neuroscience. 12:3265-3275
Pindolol accelerates the clinical actions of selective serotonin reuptake inhibitors (SSRIs) in man, and modulates extracellular levels of monoamines in corticolimbic structures in rats. Herein, we examined its influence upon electrical activity of s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c3126ab0e31da6e466990d047b55934
https://doi.org/10.1046/j.1460-9568.2000.00222.x
https://doi.org/10.1046/j.1460-9568.2000.00222.x
Publikováno v:
British journal of pharmacology. 171(15)
Agomelatine behaves both as a potent agonist at melatonin MT1 and MT2 receptors and as a neutral antagonist at 5-HT2C receptors. Accumulating evidence in a broad range of experimental procedures supports the notion that the psychotropic effects of ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3af74d998f9688072825b1fb61371c94
https://pubmed.ncbi.nlm.nih.gov/24724693
https://pubmed.ncbi.nlm.nih.gov/24724693
Autor:
A, Dekeyne, M J, Millan
Publikováno v:
Behavioural pharmacology. 14(5-6)
Though drug discrimination techniques have proven invaluable in characterizing the interoceptive properties of drugs of abuse, antipsychotics and anxiolytics, with the exception of some fragmentary data with tricyclic agents, surprisingly few studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ccc5530f9d5b323eb17d02db125859b7
https://pubmed.ncbi.nlm.nih.gov/14501253
https://pubmed.ncbi.nlm.nih.gov/14501253
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 305(1)
In a dialysis procedure not requiring perfusate addition of acetylcholinesterase inhibitors to "boost" basal levels of acetylcholine (ACh), the influence of the antiparkinson agent piribedil upon levels of ACh in frontal cortex and dorsal hippocampus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa1756389c89d74f8842016ac01a5b2e
https://pubmed.ncbi.nlm.nih.gov/12649387
https://pubmed.ncbi.nlm.nih.gov/12649387
Publikováno v:
Pharmacology, biochemistry, and behavior. 71(4)
Although several tritiated agonists have been used for radiolabelling serotonin (5-hydroxytryptamine, 5-HT)(1B) receptors in rats, data with a selective, radiolabelled antagonist have not been presented. Inasmuch as [3H]GR125,743 specifically labels
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5f87e475979175d1a0b79c5af363a033
https://pubmed.ncbi.nlm.nih.gov/11888550
https://pubmed.ncbi.nlm.nih.gov/11888550
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 298(2)
S33005 displayed marked affinity for native, rat, and cloned human serotonin (5-HT) transporters (SERT) and less pronounced affinity for norepinephrine (NE) transporters (NET), while its affinity at dopamine (DA) transporters and50 other sites was ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::75091214929e8c61231b00a7646d9c87
https://pubmed.ncbi.nlm.nih.gov/11454918
https://pubmed.ncbi.nlm.nih.gov/11454918
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 298(2)
Reflecting its potent inhibition of serotonin (5-HT) reuptake (accompanying paper), S33005 blocked spontaneous tail-flicks induced by parachloroamphetamine in rats. This action was mimicked by the 5-HT reuptake inhibitor, citalopram, and the 5-HT/nor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c14b7318df192019c5eafea9b012560c
https://pubmed.ncbi.nlm.nih.gov/11454919
https://pubmed.ncbi.nlm.nih.gov/11454919