-
1
-
-
0242468060
-
Stable expression and characterization of human PN1 and PN3 sodium channels
-
Akiba I., Seki T., Mori M., Iizuka M., Nishimura S., Sasaki S., Imoto K., and Barsoumian E.L. Stable expression and characterization of human PN1 and PN3 sodium channels. Receptors Channels 9 5 (2003) 291-299
-
(2003)
Receptors Channels
, vol.9
, Issue.5
, pp. 291-299
-
-
Akiba, I.1
Seki, T.2
Mori, M.3
Iizuka, M.4
Nishimura, S.5
Sasaki, S.6
Imoto, K.7
Barsoumian, E.L.8
-
3
-
-
0023884915
-
Veratridine modifies open sodium channels
-
Barnes S., and Hille B. Veratridine modifies open sodium channels. J. Gen. Physiol. 91 3 (1988) 421-443
-
(1988)
J. Gen. Physiol.
, vol.91
, Issue.3
, pp. 421-443
-
-
Barnes, S.1
Hille, B.2
-
4
-
-
18344372371
-
A novel membrane potential-sensitive fluorescent dye improves cell-based assays for ion channels
-
Baxter D.F., Kirk M., Garcia A.F., Raimondi A., Holmqvist M.H., Flint K.K., Bojanic D., Distefano P.S., Curtis R., and Xie Y. A novel membrane potential-sensitive fluorescent dye improves cell-based assays for ion channels. J. Biomol. Screen. 7 1 (2002) 79-85
-
(2002)
J. Biomol. Screen.
, vol.7
, Issue.1
, pp. 79-85
-
-
Baxter, D.F.1
Kirk, M.2
Garcia, A.F.3
Raimondi, A.4
Holmqvist, M.H.5
Flint, K.K.6
Bojanic, D.7
Distefano, P.S.8
Curtis, R.9
Xie, Y.10
-
5
-
-
32844466512
-
m dye: on-target and off-target effects of diverse pharmacological agents
-
m dye: on-target and off-target effects of diverse pharmacological agents. J. Biomol. Screen. 11 1 (2006) 29-39
-
(2006)
J. Biomol. Screen.
, vol.11
, Issue.1
, pp. 29-39
-
-
Benjamin, E.R.1
Pruthi, F.2
Olanrewaju, S.3
Ilyin, V.I.4
Crumley, G.5
Kutlina, E.6
Valenzano, K.J.7
Woodward, R.M.8
-
6
-
-
0037008388
-
Investigation of the modulation of glutamate release by sodium channels using neurotoxins
-
Bicalho A.F.X., Guatimosim C., Prado M.A.M., Gomez M.V., and Romano-Silva M.A. Investigation of the modulation of glutamate release by sodium channels using neurotoxins. Neuroscience 113 1 (2002) 115-123
-
(2002)
Neuroscience
, vol.113
, Issue.1
, pp. 115-123
-
-
Bicalho, A.F.X.1
Guatimosim, C.2
Prado, M.A.M.3
Gomez, M.V.4
Romano-Silva, M.A.5
-
7
-
-
0022556533
-
3H-batrachotoxinin-A benzoate binding to voltage-sensitive sodium channels: inhibition by the channel blockers tetrodotoxin and saxitoxin
-
3H-batrachotoxinin-A benzoate binding to voltage-sensitive sodium channels: inhibition by the channel blockers tetrodotoxin and saxitoxin. J. Neurosci. 6 7 (1986) 2064-2070
-
(1986)
J. Neurosci.
, vol.6
, Issue.7
, pp. 2064-2070
-
-
Brown, G.B.1
-
8
-
-
0034712740
-
Potent blockade of sodium channels and protection of brain tissue from ischemia by BIII 890 CL
-
Carter A.J., Grauert M., Pschorn U., Bechtel W.D., Bartmann-Lindholm C., Qu Y., Scheuer T., Catterall W.A., and Weiser T. Potent blockade of sodium channels and protection of brain tissue from ischemia by BIII 890 CL. Proc. Natl. Acad. Sci. U. S. A. 97 9 (2000) 4944-4949
-
(2000)
Proc. Natl. Acad. Sci. U. S. A.
, vol.97
, Issue.9
, pp. 4944-4949
-
-
Carter, A.J.1
Grauert, M.2
Pschorn, U.3
Bechtel, W.D.4
Bartmann-Lindholm, C.5
Qu, Y.6
Scheuer, T.7
Catterall, W.A.8
Weiser, T.9
-
9
-
-
0017661782
-
+ ionophore by neurotoxins. An allosteric model
-
+ ionophore by neurotoxins. An allosteric model. J. Biol. Chem. 252 23 (1977) 8669-8676
-
(1977)
J. Biol. Chem.
, vol.252
, Issue.23
, pp. 8669-8676
-
-
Catterall, W.A.1
-
10
-
-
0019409782
-
Inhibition of voltage-sensitive sodium channels in neuroblastoma cells by antiarrhythmic drugs
-
Catterall W.A. Inhibition of voltage-sensitive sodium channels in neuroblastoma cells by antiarrhythmic drugs. Mol. Pharmacol. 20 2 (1981) 356-362
-
(1981)
Mol. Pharmacol.
, vol.20
, Issue.2
, pp. 356-362
-
-
Catterall, W.A.1
-
11
-
-
0026490286
-
Cellular and molecular biology of voltage-gated sodium channels
-
Catterall W.A. Cellular and molecular biology of voltage-gated sodium channels. Physiol. Rev. 72 4 Suppl. (1992) 15S-48S
-
(1992)
Physiol. Rev.
, vol.72
, Issue.4 SUPPL
-
-
Catterall, W.A.1
-
12
-
-
29844438166
-
International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels
-
Catterall W.A., Goldin A.L., and Waxman S.G. International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels. Pharmacol. Rev. 57 4 (2005) 397-409
-
(2005)
Pharmacol. Rev.
, vol.57
, Issue.4
, pp. 397-409
-
-
Catterall, W.A.1
Goldin, A.L.2
Waxman, S.G.3
-
13
-
-
29844439240
-
International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels
-
Catterall W.A., Perez-Reyes E., Snutch T.P., and Striessnig J. International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels. Pharmacol. Rev. 57 4 (2005) 411-425
-
(2005)
Pharmacol. Rev.
, vol.57
, Issue.4
, pp. 411-425
-
-
Catterall, W.A.1
Perez-Reyes, E.2
Snutch, T.P.3
Striessnig, J.4
-
14
-
-
0032732550
-
The assessment of antagonist potency under conditions of transient response kinetics
-
Christopoulos A., Parsons A.M., Lew M.J., and El Fakahany E.E. The assessment of antagonist potency under conditions of transient response kinetics. Eur. J. Pharmacol. 382 3 (1999) 217-227
-
(1999)
Eur. J. Pharmacol.
, vol.382
, Issue.3
, pp. 217-227
-
-
Christopoulos, A.1
Parsons, A.M.2
Lew, M.J.3
El Fakahany, E.E.4
-
15
-
-
0034327493
-
Voltage-gated sodium channels as therapeutic targets
-
Clare J.J., Tate S.N., Nobbs M., and Romanos M.A. Voltage-gated sodium channels as therapeutic targets. Drug Discov. Today 5 11 (2000) 506-520
-
(2000)
Drug Discov. Today
, vol.5
, Issue.11
, pp. 506-520
-
-
Clare, J.J.1
Tate, S.N.2
Nobbs, M.3
Romanos, M.A.4
-
16
-
-
0020628057
-
3H]batrachotoxinin-a 20 alpha-benzoate binding in a vesicular preparation from guinea pig cerebral cortex
-
3H]batrachotoxinin-a 20 alpha-benzoate binding in a vesicular preparation from guinea pig cerebral cortex. Mol. Pharmacol. 23 2 (1983) 350-358
-
(1983)
Mol. Pharmacol.
, vol.23
, Issue.2
, pp. 350-358
-
-
Creveling, C.R.1
McNeal, E.T.2
Daly, J.W.3
Brown, G.B.4
-
17
-
-
0035882277
-
v1.3 sodium channels: rapid repriming and slow closed-state inactivation display quantitative differences after expression in a mammalian cell line and in spinal sensory neurons
-
v1.3 sodium channels: rapid repriming and slow closed-state inactivation display quantitative differences after expression in a mammalian cell line and in spinal sensory neurons. J. Neurosci. 21 16 (2001) 5952-5961
-
(2001)
J. Neurosci.
, vol.21
, Issue.16
, pp. 5952-5961
-
-
Cummins, T.R.1
Aglieco, F.2
Renganathan, M.3
Herzog, R.I.4
Dib-Hajj, S.D.5
Waxman, S.G.6
-
18
-
-
0030582763
-
Inhibition of synaptosomal veratridine-induced sodium influx by antidepressants and neuroleptics used in chronic pain
-
Deffois A., Fage D., and Carter C. Inhibition of synaptosomal veratridine-induced sodium influx by antidepressants and neuroleptics used in chronic pain. Neurosci. Lett. 220 2 (1996) 117-120
-
(1996)
Neurosci. Lett.
, vol.220
, Issue.2
, pp. 117-120
-
-
Deffois, A.1
Fage, D.2
Carter, C.3
-
19
-
-
4043083603
-
Functional assay of voltage-gated sodium channels using membrane potential-sensitive dyes
-
Felix J.P., Williams B.S., Priest B.T., Brochu R.M., Dick I.E., Warren V.A., Yan L., Slaughter R.S., Kaczorowski G.J., Smith, et al. Functional assay of voltage-gated sodium channels using membrane potential-sensitive dyes. Assay Drug Dev. Technol. 2 3 (2004) 260-268
-
(2004)
Assay Drug Dev. Technol.
, vol.2
, Issue.3
, pp. 260-268
-
-
Felix, J.P.1
Williams, B.S.2
Priest, B.T.3
Brochu, R.M.4
Dick, I.E.5
Warren, V.A.6
Yan, L.7
Slaughter, R.S.8
Kaczorowski, G.J.9
Smith10
-
20
-
-
0032853255
-
2-Methyl-6-(phenylethynyl)-pyridine (MPEP), a potent, selective and systemically active mGlu5 receptor antagonist
-
Gasparini F., Lingenhohl K., Stoehr N., Flor P.J., Heinrich M., Vranesic I., Biollaz M., Allgeier H., Heckendorn R., and Urwyler S. 2-Methyl-6-(phenylethynyl)-pyridine (MPEP), a potent, selective and systemically active mGlu5 receptor antagonist. Neuropharmacology 38 10 (1999) 1493-1503
-
(1999)
Neuropharmacology
, vol.38
, Issue.10
, pp. 1493-1503
-
-
Gasparini, F.1
Lingenhohl, K.2
Stoehr, N.3
Flor, P.J.4
Heinrich, M.5
Vranesic, I.6
Biollaz, M.7
Allgeier, H.8
Heckendorn, R.9
Urwyler, S.10
-
21
-
-
0035859245
-
3H]noradrenaline in rat hippocampal slices
-
3H]noradrenaline in rat hippocampal slices. Neuroscience 104 3 (2001) 761-768
-
(2001)
Neuroscience
, vol.104
, Issue.3
, pp. 761-768
-
-
Gerevich, Z.1
Tretter, L.2
Adam-Vizi, V.3
Baranyi, M.4
Kiss, J.P.5
Zelles, T.6
Vizi, E.S.7
-
22
-
-
0031127384
-
Improved indicators of cell membrane potential that use fluorescence resonance energy transfer
-
Gonzalez J.E., and Tsien R.Y. Improved indicators of cell membrane potential that use fluorescence resonance energy transfer. Chem. Biol. 4 4 (1997) 269-277
-
(1997)
Chem. Biol.
, vol.4
, Issue.4
, pp. 269-277
-
-
Gonzalez, J.E.1
Tsien, R.Y.2
-
23
-
-
14844306307
-
Sodium channel blockers and activators
-
Handbook of Experimental Pharmacology. Endo M., Kurachi Y., and Mishina M. (Eds), Springer-Verlag, Berlin
-
Grant A.O. Sodium channel blockers and activators. In: Endo M., Kurachi Y., and Mishina M. (Eds). Handbook of Experimental Pharmacology. Pharmacology of Ionic Channel Function vol. 147 (2000), Springer-Verlag, Berlin 27-54
-
(2000)
Pharmacology of Ionic Channel Function
, vol.147
, pp. 27-54
-
-
Grant, A.O.1
-
24
-
-
0021127531
-
Behavioral properties of GBR 12909, GBR 13069 and GBR 13098: specific inhibitors of dopamine uptake
-
Heikkila R.E., and Manzino L. Behavioral properties of GBR 12909, GBR 13069 and GBR 13098: specific inhibitors of dopamine uptake. Eur. J. Pharmacol. 103 3-4 (1984) 241-248
-
(1984)
Eur. J. Pharmacol.
, vol.103
, Issue.3-4
, pp. 241-248
-
-
Heikkila, R.E.1
Manzino, L.2
-
25
-
-
33749536246
-
Development of FLIPR-based optical assays to characterize neuronal sodium channel function and synaptic activity
-
Hicks C.D., Rutherford-Root K.L., McKinley D.D., Gotow L.F., Hein N.D., Wolfe M.L., Dinh D.M., Hurst R.S., Roberds S.L., and Groppi V.E. Development of FLIPR-based optical assays to characterize neuronal sodium channel function and synaptic activity. Society for Neuroscience 33th Annual Meeting, Abstract 579.7 (2003)
-
(2003)
Society for Neuroscience 33th Annual Meeting, Abstract 579.7
-
-
Hicks, C.D.1
Rutherford-Root, K.L.2
McKinley, D.D.3
Gotow, L.F.4
Hein, N.D.5
Wolfe, M.L.6
Dinh, D.M.7
Hurst, R.S.8
Roberds, S.L.9
Groppi, V.E.10
-
26
-
-
0017332486
-
Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction
-
Hille B. Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction. J. Gen. Physiol. 69 4 (1977) 497-515
-
(1977)
J. Gen. Physiol.
, vol.69
, Issue.4
, pp. 497-515
-
-
Hille, B.1
-
27
-
-
0023471953
-
The properties of batrachotoxin-modified cardiac Na channels, including state-dependent block by tetrodotoxin
-
Huang L.Y., Yatani A., and Brown A.M. The properties of batrachotoxin-modified cardiac Na channels, including state-dependent block by tetrodotoxin. J. Gen. Physiol. 90 3 (1987) 341-360
-
(1987)
J. Gen. Physiol.
, vol.90
, Issue.3
, pp. 341-360
-
-
Huang, L.Y.1
Yatani, A.2
Brown, A.M.3
-
28
-
-
0035139342
-
Sodium channel beta subunits: anything but auxiliary
-
Isom L.L. Sodium channel beta subunits: anything but auxiliary. Neuroscientist 7 1 (2001) 42-54
-
(2001)
Neuroscientist
, vol.7
, Issue.1
, pp. 42-54
-
-
Isom, L.L.1
-
29
-
-
3042579803
-
2+ exchange by SN-6 [2-[4-(4-nitrobenzyloxy)benzyl]thiazolidine-4-carboxylic acid ethyl ester], a novel benzyloxyphenyl derivative
-
2+ exchange by SN-6 [2-[4-(4-nitrobenzyloxy)benzyl]thiazolidine-4-carboxylic acid ethyl ester], a novel benzyloxyphenyl derivative. Mol. Pharmacol. 66 1 (2004) 45-55
-
(2004)
Mol. Pharmacol.
, vol.66
, Issue.1
, pp. 45-55
-
-
Iwamoto, T.1
Inoue, Y.2
Ito, K.3
Sakaue, T.4
Kita, S.5
Katsuragi, T.6
-
30
-
-
0042895988
-
High throughput ion-channel pharmacology: planar-array-based voltage clamp
-
Kiss L., Bennett P.B., Uebele V.N., Koblan K.S., Kane S.A., Neagle B., and Schroeder K. High throughput ion-channel pharmacology: planar-array-based voltage clamp. Assay Drug Dev. Technol. 1 1, Part 2 (2003) 127-135
-
(2003)
Assay Drug Dev. Technol.
, vol.1
, Issue.1 PART 2
, pp. 127-135
-
-
Kiss, L.1
Bennett, P.B.2
Uebele, V.N.3
Koblan, K.S.4
Kane, S.A.5
Neagle, B.6
Schroeder, K.7
-
31
-
-
27744596064
-
Tolperisone-type drugs inhibit spinal reflexes via blockade of voltage-gated sodium and calcium channels
-
Kocsis P., Farkas S., Fodor L., Bielik N., Than M., Kolok S., Gere A., Csejtei M., and Tarnawa I. Tolperisone-type drugs inhibit spinal reflexes via blockade of voltage-gated sodium and calcium channels. J. Pharmacol. Exp. Ther. 315 3 (2005) 1237-1246
-
(2005)
J. Pharmacol. Exp. Ther.
, vol.315
, Issue.3
, pp. 1237-1246
-
-
Kocsis, P.1
Farkas, S.2
Fodor, L.3
Bielik, N.4
Than, M.5
Kolok, S.6
Gere, A.7
Csejtei, M.8
Tarnawa, I.9
-
32
-
-
0030787547
-
+ channels in rat hippocampal neurones
-
+ channels in rat hippocampal neurones. Br. J. Pharmacol. 121 6 (1997) 1231-1238
-
(1997)
Br. J. Pharmacol.
, vol.121
, Issue.6
, pp. 1231-1238
-
-
Kuo, C.C.1
Lu, L.2
-
33
-
-
0030949912
-
+ currents: quantitative distinction from phenytoin and possible therapeutic implications
-
+ currents: quantitative distinction from phenytoin and possible therapeutic implications. Mol. Pharmacol. 51 6 (1997) 1077-1083
-
(1997)
Mol. Pharmacol.
, vol.51
, Issue.6
, pp. 1077-1083
-
-
Kuo, C.C.1
Chen, R.S.2
Lu, L.3
Chen, R.C.4
-
34
-
-
0037731410
-
3H]R214127: a novel high-affinity radioligand for the mGlu1 receptor reveals a common binding site shared by multiple allosteric antagonists
-
3H]R214127: a novel high-affinity radioligand for the mGlu1 receptor reveals a common binding site shared by multiple allosteric antagonists. Mol. Pharmacol. 63 5 (2003) 1082-1093
-
(2003)
Mol. Pharmacol.
, vol.63
, Issue.5
, pp. 1082-1093
-
-
Lavreysen, H.1
Janssen, C.2
Bischoff, F.3
Langlois, X.4
Leysen, J.E.5
Lesage, A.S.J.6
-
35
-
-
0032506024
-
Interaction of batrachotoxin with the local anesthetic receptor site in transmembrane segment IVS6 of the voltage-gated sodium channel
-
Linford N.J., Cantrell A.R., Qu Y., Scheuer T., and Catterall W.A. Interaction of batrachotoxin with the local anesthetic receptor site in transmembrane segment IVS6 of the voltage-gated sodium channel. Proc. Natl. Acad. Sci. U. S. A. 95 23 (1998) 13947-13952
-
(1998)
Proc. Natl. Acad. Sci. U. S. A.
, vol.95
, Issue.23
, pp. 13947-13952
-
-
Linford, N.J.1
Cantrell, A.R.2
Qu, Y.3
Scheuer, T.4
Catterall, W.A.5
-
37
-
-
0032810560
-
+- and veratridine-induced increase of cytosolic calcium concentration in human cerebral cortical synaptosomes
-
+- and veratridine-induced increase of cytosolic calcium concentration in human cerebral cortical synaptosomes. J. Pharmacol. Exp. Ther. 290 3 (1999) 1126-1131
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.290
, Issue.3
, pp. 1126-1131
-
-
Meder, W.1
Fink, K.2
Zentner, J.3
Gothert, M.4
-
38
-
-
2142643648
-
A novel modulatory mechanism of sodium currents: frequency-dependence without state-dependent binding
-
Mike A., Karoly R., Vizi E.S., and Kiss J.P. A novel modulatory mechanism of sodium currents: frequency-dependence without state-dependent binding. Neuroscience 125 4 (2004) 1019-1028
-
(2004)
Neuroscience
, vol.125
, Issue.4
, pp. 1019-1028
-
-
Mike, A.1
Karoly, R.2
Vizi, E.S.3
Kiss, J.P.4
-
39
-
-
0642369910
-
Inhibitory effect of the DA uptake blocker GBR 12909 on sodium channels of hippocampal neurons
-
Mike A., Karoly R., Vizi E.S., and Kiss J.P. Inhibitory effect of the DA uptake blocker GBR 12909 on sodium channels of hippocampal neurons. Neuroreport 14 15 (2003) 1945-1949
-
(2003)
Neuroreport
, vol.14
, Issue.15
, pp. 1945-1949
-
-
Mike, A.1
Karoly, R.2
Vizi, E.S.3
Kiss, J.P.4
-
41
-
-
0028854770
-
+ channels in rat cortical neurons
-
+ channels in rat cortical neurons. Eur. J. Pharmacol. 273 3 (1995) 303-306
-
(1995)
Eur. J. Pharmacol.
, vol.273
, Issue.3
, pp. 303-306
-
-
Molnar, P.1
Erdo, S.L.2
-
42
-
-
0031912995
-
Glutamate receptors in the mammalian central nervous system
-
Ozawa S., Kamiya H., and Tsuzuki K. Glutamate receptors in the mammalian central nervous system. Prog. Neurobiol. 54 5 (1998) 581-618
-
(1998)
Prog. Neurobiol.
, vol.54
, Issue.5
, pp. 581-618
-
-
Ozawa, S.1
Kamiya, H.2
Tsuzuki, K.3
-
43
-
-
0031740691
-
A tetrodotoxin-resistant voltage-gated sodium channel from human dorsal root ganglia, hPN3/SCN10A
-
Rabert D.K., Koch B.D., Ilnicka M., Obernolte R.A., Naylor S.L., Herman R.C., Eglen R.M., Hunter J.C., and Sangameswaran L. A tetrodotoxin-resistant voltage-gated sodium channel from human dorsal root ganglia, hPN3/SCN10A. Pain 78 2 (1998) 107-114
-
(1998)
Pain
, vol.78
, Issue.2
, pp. 107-114
-
-
Rabert, D.K.1
Koch, B.D.2
Ilnicka, M.3
Obernolte, R.A.4
Naylor, S.L.5
Herman, R.C.6
Eglen, R.M.7
Hunter, J.C.8
Sangameswaran, L.9
-
44
-
-
0025827588
-
+ channels, expressed in a mammalian cell line, by local anesthetic, antiarrhythmic, and anticonvulsant drugs
-
+ channels, expressed in a mammalian cell line, by local anesthetic, antiarrhythmic, and anticonvulsant drugs. Mol. Pharmacol. 40 5 (1991) 756-765
-
(1991)
Mol. Pharmacol.
, vol.40
, Issue.5
, pp. 756-765
-
-
Ragsdale, D.S.1
Scheuer, T.2
Catterall, W.A.3
-
45
-
-
0022499323
-
The interaction between the activator agents batrachotoxin and veratridine and the gating processes of neuronal sodium channels
-
Rando T.A., Wang G.K., and Strichartz G.R. The interaction between the activator agents batrachotoxin and veratridine and the gating processes of neuronal sodium channels. Mol. Pharmacol. 29 5 (1986) 467-477
-
(1986)
Mol. Pharmacol.
, vol.29
, Issue.5
, pp. 467-477
-
-
Rando, T.A.1
Wang, G.K.2
Strichartz, G.R.3
-
46
-
-
0025136883
-
+ channel preparations from mouse cerebral cortex
-
+ channel preparations from mouse cerebral cortex. Eur. J. Pharmacol. 188 1 (1990) 33-41
-
(1990)
Eur. J. Pharmacol.
, vol.188
, Issue.1
, pp. 33-41
-
-
Reith, M.E.1
-
47
-
-
30044445578
-
A novel drug binding site on voltage-gated sodium channels in rat brain
-
Riddall D.R., Leach M.J., and Garthwaite J. A novel drug binding site on voltage-gated sodium channels in rat brain. Mol. Pharmacol. 69 1 (2006) 278-287
-
(2006)
Mol. Pharmacol.
, vol.69
, Issue.1
, pp. 278-287
-
-
Riddall, D.R.1
Leach, M.J.2
Garthwaite, J.3
-
49
-
-
0033054347
-
Biochemical and electrophysiological studies on the mechanism of action of PNU-151774E, a novel antiepileptic compound
-
Salvati P., Maj R., Caccia C., Cervini M.A., Fornaretto M.G., Lamberti E., Pevarello P., Skeen G.A., White H.S., Wolf, et al. Biochemical and electrophysiological studies on the mechanism of action of PNU-151774E, a novel antiepileptic compound. J. Pharmacol. Exp. Ther. 288 3 (1999) 1151-1159
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.288
, Issue.3
, pp. 1151-1159
-
-
Salvati, P.1
Maj, R.2
Caccia, C.3
Cervini, M.A.4
Fornaretto, M.G.5
Lamberti, E.6
Pevarello, P.7
Skeen, G.A.8
White, H.S.9
Wolf10
-
50
-
-
0042663013
-
Expression and distribution of voltage-gated sodium channels in the cerebellum
-
Schaller K.L., and Caldwell J.H. Expression and distribution of voltage-gated sodium channels in the cerebellum. Cerebellum 2 1 (2003) 2-9
-
(2003)
Cerebellum
, vol.2
, Issue.1
, pp. 2-9
-
-
Schaller, K.L.1
Caldwell, J.H.2
-
51
-
-
17444415714
-
Vinpocetine blockade of sodium channels inhibits the rise in sodium and calcium induced by 4-aminopyridine in synaptosomes
-
Sitges M., Galvan E., and Nekrassov V. Vinpocetine blockade of sodium channels inhibits the rise in sodium and calcium induced by 4-aminopyridine in synaptosomes. Neurochem. Int. 46 7 (2005) 533-540
-
(2005)
Neurochem. Int.
, vol.46
, Issue.7
, pp. 533-540
-
-
Sitges, M.1
Galvan, E.2
Nekrassov, V.3
-
54
-
-
0036847010
-
+ load and oxidative stress in nerve terminals: relevance to ischemia/reperfusion
-
+ load and oxidative stress in nerve terminals: relevance to ischemia/reperfusion. J. Neurochem. 83 4 (2002) 855-862
-
(2002)
J. Neurochem.
, vol.83
, Issue.4
, pp. 855-862
-
-
Tretter, L.1
Adam-Vizi, V.2
-
55
-
-
0021685359
-
Distinctly different rates of benzocaine action on sodium channels of Ranvier nodes kept open by chloramine-T and veratridine
-
Ulbricht W., and Stoye-Herzog M. Distinctly different rates of benzocaine action on sodium channels of Ranvier nodes kept open by chloramine-T and veratridine. Pflugers Archiv: Eur. J. Physiol. 402 4 (1984) 439-445
-
(1984)
Pflugers Archiv: Eur. J. Physiol.
, vol.402
, Issue.4
, pp. 439-445
-
-
Ulbricht, W.1
Stoye-Herzog, M.2
-
56
-
-
0031639628
-
Effects of veratridine on sodium currents and fluxes
-
Ulbricht W. Effects of veratridine on sodium currents and fluxes. Rev. Physiol. Biochem. Pharmacol. 133 (1998) 1-54
-
(1998)
Rev. Physiol. Biochem. Pharmacol.
, vol.133
, pp. 1-54
-
-
Ulbricht, W.1
-
57
-
-
0029971412
-
+ channels: a rational and effective strategy against ischemic brain damage
-
+ channels: a rational and effective strategy against ischemic brain damage. Pharmacol. Rev. 48 1 (1996) 21-67
-
(1996)
Pharmacol. Rev.
, vol.48
, Issue.1
, pp. 21-67
-
-
Urenjak, J.1
Obrenovitch, T.P.2
-
58
-
-
12144288319
-
V1. 5 voltage-gated sodium channel subtypes using a membrane potential sensitive dye and FLIPR
-
V1. 5 voltage-gated sodium channel subtypes using a membrane potential sensitive dye and FLIPR. Receptors Channels 10 1 (2004) 11-23
-
(2004)
Receptors Channels
, vol.10
, Issue.1
, pp. 11-23
-
-
Vickery, R.G.1
Amagasu, S.M.2
Chang, R.3
Mai, N.4
Kaufman, E.5
Martin, J.6
Hembrador, J.7
O'Keefe, M.D.8
Gee, C.9
Marquess, D.10
Smith, J.A.M.11
-
59
-
-
85012350978
-
+ channels in GH3 cells. Characterization and pharmacological modification
-
+ channels in GH3 cells. Characterization and pharmacological modification. J. Gen. Physiol. 99 1 (1992) 1-20
-
(1992)
J. Gen. Physiol.
, vol.99
, Issue.1
, pp. 1-20
-
-
Wang, G.K.1
Wang, S.Y.2
-
60
-
-
0037648783
-
v1.4 sodium channels in the inner vestibule
-
v1.4 sodium channels in the inner vestibule. J. Physiol. 548 Part 3 (2003) 667-675
-
(2003)
J. Physiol.
, vol.548
, Issue.PART 3
, pp. 667-675
-
-
Wang, G.K.1
Wang, S.Y.2
-
61
-
-
10344264994
-
+ channels by local anesthetics in stably transfected mammalian cells: evidence for drug binding along the activation pathway
-
+ channels by local anesthetics in stably transfected mammalian cells: evidence for drug binding along the activation pathway. J. Gen. Physiol. 124 6 (2004) 691-701
-
(2004)
J. Gen. Physiol.
, vol.124
, Issue.6
, pp. 691-701
-
-
Wang, S.Y.1
Mitchell, J.2
Moczydlowski, E.3
Wang, G.K.4
-
62
-
-
0033600578
-
WIN 17317-3, a new high-affinity probe for voltage-gated sodium channels
-
Wanner S.G., Glossmann H., Knaus H.G., Baker R., Parsons W., Rupprecht K.M., Brochu R., Cohen C.J., Schmalhofer W., Smith, et al. WIN 17317-3, a new high-affinity probe for voltage-gated sodium channels. Biochemistry 38 34 (1999) 11137-11146
-
(1999)
Biochemistry
, vol.38
, Issue.34
, pp. 11137-11146
-
-
Wanner, S.G.1
Glossmann, H.2
Knaus, H.G.3
Baker, R.4
Parsons, W.5
Rupprecht, K.M.6
Brochu, R.7
Cohen, C.J.8
Schmalhofer, W.9
Smith10
-
64
-
-
0020334077
-
3H]batrachotoxinin A 20-alpha-benzoate to sodium channels by the anticonvulsant drugs diphenylhydantoin and carbamazepine
-
3H]batrachotoxinin A 20-alpha-benzoate to sodium channels by the anticonvulsant drugs diphenylhydantoin and carbamazepine. Mol. Pharmacol. 22 3 (1982) 627-635
-
(1982)
Mol. Pharmacol.
, vol.22
, Issue.3
, pp. 627-635
-
-
Willow, M.1
Catterall, W.A.2
|