Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Samer J. Nuwayhid"'
Publikováno v:
Journal of Lipid Research, Vol 47, Iss 7, Pp 1449-1456 (2006)
Mechanisms that function to regulate the rate of de novo phosphatidylinositol (PtdIns) synthesis in mammalian cells have not been elucidated. In this study, we characterize the effect of phorbol ester treatment on de novo PtdIns synthesis in C3A huma
Externí odkaz:
https://doaj.org/article/41d11756d72c41a68be62bca9ce071c0
Publikováno v:
Experimental Neurology. 207:248-257
We compared the binding profiles of medications potentially useful in the treatment of involuntary emotional expression disorder at twenty-six binding sites in rat brain tissue membranes. Sites were chosen based on likelihood of being target sites fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8213fcaaa281a1381549dabc250679e
https://doi.org/10.1016/j.expneurol.2007.06.013
https://doi.org/10.1016/j.expneurol.2007.06.013
Publikováno v:
Journal of Lipid Research, Vol 47, Iss 7, Pp 1449-1456 (2006)
Mechanisms that function to regulate the rate of de novo phosphatidylinositol (PtdIns) synthesis in mammalian cells have not been elucidated. In this study, we characterize the effect of phorbol ester treatment on de novo PtdIns synthesis in C3A huma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65852edbad641aa39d3a3f31f0e40864
http://www.sciencedirect.com/science/article/pii/S0022227520331898
http://www.sciencedirect.com/science/article/pii/S0022227520331898
Publikováno v:
Synapse. 54:102-110
In this study we investigated the effects of sigma receptor ligands and neurosteroids on bradykinin-induced intracellular calcium concentration ([Ca2+]i) changes in SH-SY5Y neuroblastoma cells. [Ca2+]i levels in cells loaded with fura-2 were monitore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::830267ca4acd5a80c475aefa79ae9ede
https://doi.org/10.1002/syn.20069
https://doi.org/10.1002/syn.20069
Autor:
Samer J. Nuwayhid, Linda L. Werling
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 306:934-940
Steroids have been proposed as endogenous ligands at sigma receptors. In the current study, we examined the ability of steroids to regulate N-methyl-d-aspartate (NMDA)-stimulated [3H]dopamine release from slices of rat striatal tissue. We found that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57465de6bbd828b3f40c1c3623676c9f
https://doi.org/10.1124/jpet.103.052324
https://doi.org/10.1124/jpet.103.052324
Publikováno v:
Sigma Receptors ISBN: 9780387365121
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75f31191f78ff4e9e527505ed5594633
https://doi.org/10.1007/978-0-387-36514-5_10
https://doi.org/10.1007/978-0-387-36514-5_10
Autor:
Samer J. Nuwayhid, Linda L. Werling
Publikováno v:
European journal of pharmacology. 535(1-3)
Studies from our laboratory have shown that agonists at sigma1 and sigma2 receptors inhibit N-methyl-D-aspartate (NMDA)-stimulated dopamine release from motor and limbic areas of rat brain. In the current study, we examined the effects of cocaine on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5962ebc88502b09d5d36922cd5e1a987
https://pubmed.ncbi.nlm.nih.gov/16480713
https://pubmed.ncbi.nlm.nih.gov/16480713
Autor:
Samer J. Nuwayhid, Linda L. Werling
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 304(1)
We have previously shown that ς1 receptor agonists inhibit N- methyl-d-aspartate (NMDA)-stimulated [3H]dopamine from slices of rat striatum in a concentration-related manner and that the inhibition is reversed by ς1 receptor-selective and nonsubtyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69c8c460ef6aed75ac6a43d43c67bdd2
https://pubmed.ncbi.nlm.nih.gov/12490613
https://pubmed.ncbi.nlm.nih.gov/12490613
Publikováno v:
European journal of pharmacology. 422(1-3)
Several trishomocubane analogues of the type 4-azahexacyclo [5.4.1.0(2,6).0(3,10).0(5,9).0(8,11)]dodecane exhibited moderate to high affinity at sigma-receptor subtypes and low or negligible affinity at dopamine and serotonin transporters (SERT). Sel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08b963644b7ab69b379f7b3d7e8b43ae
https://pubmed.ncbi.nlm.nih.gov/11430911
https://pubmed.ncbi.nlm.nih.gov/11430911