-
1
-
-
0029887551
-
Activation of voltage dependent sodium channels in cultured cerebellar granule cells induces neurotoxicity that is not mediated by glutamate release
-
Dargent B., Arsac C., Tricaud N., Couraud F. Activation of voltage dependent sodium channels in cultured cerebellar granule cells induces neurotoxicity that is not mediated by glutamate release. Neuroscience. 73:1996;209-216.
-
(1996)
Neuroscience
, vol.73
, pp. 209-216
-
-
Dargent, B.1
Arsac, C.2
Tricaud, N.3
Couraud, F.4
-
2
-
-
0026079797
-
The marine toxin okadaic acid is a potent neurotoxin for cultured cerebellar neurons
-
Fernández M.T., Zitko V., Gascón S., Novelli A. The marine toxin okadaic acid is a potent neurotoxin for cultured cerebellar neurons. Life Sci. 49:1991;PL157-PL162.
-
(1991)
Life Sci.
, vol.49
-
-
Fernández, M.T.1
Zitko, V.2
Gascón, S.3
Novelli, A.4
-
3
-
-
0027441743
-
Basic fibroblast growth factor protects cerebellar neurons in primary culture from NMDA and non-NMDA receptor mediated neurotoxicity
-
Fernández-Sánchez M.T., Novelli A. Basic fibroblast growth factor protects cerebellar neurons in primary culture from NMDA and non-NMDA receptor mediated neurotoxicity. FEBS Lett. 335:1993;124-131.
-
(1993)
FEBS Lett.
, vol.335
, pp. 124-131
-
-
Fernández-Sánchez, M.T.1
Novelli, A.2
-
4
-
-
0025932157
-
Development of voltage-dependent ionic currents in rat cerebellar granule cells grown in primary culture
-
Galdzicki Z., Lin F., Moran O., Novelli A., Puia G., Sciancalepore M. Development of voltage-dependent ionic currents in rat cerebellar granule cells grown in primary culture. Int. J. Neurosci. 56:1991;193-200.
-
(1991)
Int. J. Neurosci.
, vol.56
, pp. 193-200
-
-
Galdzicki, Z.1
Lin, F.2
Moran, O.3
Novelli, A.4
Puia, G.5
Sciancalepore, M.6
-
5
-
-
0027340019
-
Cultured hippocampal neurons from trisomy 16 mouse, a model for Down's syndrome, have an abnormal action potential due to a reduced inward sodium current
-
Galdzicki Z., Coan E., Rapoport S.I. Cultured hippocampal neurons from trisomy 16 mouse, a model for Down's syndrome, have an abnormal action potential due to a reduced inward sodium current. Brain Res. 604:1993;69-78.
-
(1993)
Brain Res.
, vol.604
, pp. 69-78
-
-
Galdzicki, Z.1
Coan, E.2
Rapoport, S.I.3
-
6
-
-
0005982327
-
Selective release of glutamate from cerebellar granule cells differentiating in culture
-
Gallo V., Ciotti M.T., Aloisi F., Levi G. Selective release of glutamate from cerebellar granule cells differentiating in culture. Proc. Natl. Acad. Sci. U.S.A. 79:1982;7919-7923.
-
(1982)
Proc. Natl. Acad. Sci. U.S.A.
, vol.79
, pp. 7919-7923
-
-
Gallo, V.1
Ciotti, M.T.2
Aloisi, F.3
Levi, G.4
-
7
-
-
0030772640
-
International union of pharmacology: XIII. Classification of histamine receptors
-
Hill S.J., Ganellin C.R., Timmerman H., Schwartz J.C., Shankley N.P., Young J.M., Schunack W., Levi R., Haas H.L. International union of pharmacology: XIII. Classification of histamine receptors. Pharmacol. Rev. 49:1997;253-278.
-
(1997)
Pharmacol. Rev.
, vol.49
, pp. 253-278
-
-
Hill, S.J.1
Ganellin, C.R.2
Timmerman, H.3
Schwartz, J.C.4
Shankley, N.P.5
Young, J.M.6
Schunack, W.7
Levi, R.8
Haas, H.L.9
-
8
-
-
0030760793
-
2+ channel current in rat ventricular myocytes by terfenadine
-
2+ channel current in rat ventricular myocytes by terfenadine. Circ. Res. 81:1997;202-210.
-
(1997)
Circ. Res.
, vol.81
, pp. 202-210
-
-
Liu, S.1
Melchert, R.B.2
Kennedy, R.H.3
-
9
-
-
0025216725
-
Terfenadine. An updated review of its pharmacological properties and therapeutic efficacy
-
McTavish D., Goa K.L., Ferrill M. Terfenadine. An updated review of its pharmacological properties and therapeutic efficacy. Drugs. 39:1990;552-574.
-
(1990)
Drugs
, vol.39
, pp. 552-574
-
-
McTavish, D.1
Goa, K.L.2
Ferrill, M.3
-
10
-
-
0023895734
-
Glutamate becomes neurotoxic via the NMDA receptor when intracellular energy levels are reduced
-
Novelli A., Reilly J.A., Lysko P.G., Henneberry R.C. Glutamate becomes neurotoxic via the NMDA receptor when intracellular energy levels are reduced. Brain Res. 451:1988;205-212.
-
(1988)
Brain Res.
, vol.451
, pp. 205-212
-
-
Novelli, A.1
Reilly, J.A.2
Lysko, P.G.3
Henneberry, R.C.4
-
12
-
-
0029994611
-
Blockade of HERG channels expressed in Xenopus oocytes by the histamine receptor antagonists terfenadine and astemizole
-
Suessbrich H., Waldegger S., Lang F., Busch A.E. Blockade of HERG channels expressed in Xenopus oocytes by the histamine receptor antagonists terfenadine and astemizole. FEBS Lett. 385:1996;77-80.
-
(1996)
FEBS Lett.
, vol.385
, pp. 77-80
-
-
Suessbrich, H.1
Waldegger, S.2
Lang, F.3
Busch, A.E.4
-
13
-
-
0026072218
-
Mapping the site of block by tetrodotoxin and saxitoxin of sodium channel II
-
Terlau H., Heinemann S.H., Stühmer W., Pusch M., Conti F., Imoto K., Numa S. Mapping the site of block by tetrodotoxin and saxitoxin of sodium channel II. FEBS Lett. 293:1991;93-96.
-
(1991)
FEBS Lett.
, vol.293
, pp. 93-96
-
-
Terlau, H.1
Heinemann, S.H.2
Stühmer, W.3
Pusch, M.4
Conti, F.5
Imoto, K.6
Numa, S.7
-
14
-
-
0030974081
-
Comparative effects of nonsedating histamine H1 receptor antagonists, ebastine and terfenadine, on human Kv1.5 channels
-
Valenzuela C., Delpón E., Franqueza L., Gay P., Vicente J., Tamargo J. Comparative effects of nonsedating histamine H1 receptor antagonists, ebastine and terfenadine, on human Kv1.5 channels. Eur. J. Pharmacol. 326:1997;257-263.
-
(1997)
Eur. J. Pharmacol.
, vol.326
, pp. 257-263
-
-
Valenzuela, C.1
Delpón, E.2
Franqueza, L.3
Gay, P.4
Vicente, J.5
Tamargo, J.6
-
16
-
-
0028063849
-
Characteristics of P388/VMDRC.04, a simple, sensitive model for studying P-glycoprotein antagonists
-
Yang J.-M., Goldenberg S., Gottesman M.M., Hait W.N. Characteristics of P388/VMDRC.04, a simple, sensitive model for studying P-glycoprotein antagonists. Cancer Res. 54:1994;730-737.
-
(1994)
Cancer Res.
, vol.54
, pp. 730-737
-
-
Yang, J.-M.1
Goldenberg, S.2
Gottesman, M.M.3
Hait, W.N.4
-
17
-
-
0027534193
-
Calcium antagonism and structure-affinity relationships of terfenadine, a histamine H1 antagonist, and some related compounds
-
Zhang M.Q., Caldirola P., Timmerman H. Calcium antagonism and structure-affinity relationships of terfenadine, a histamine H1 antagonist, and some related compounds. J. Pharm. Pharmacol. 45:1993;63-66.
-
(1993)
J. Pharm. Pharmacol.
, vol.45
, pp. 63-66
-
-
Zhang, M.Q.1
Caldirola, P.2
Timmerman, H.3
|