-
1
-
-
27644518764
-
Pathways modulating neural KCNQ/M (Kv7) potassium channels
-
Delmas P, Brown DA. Pathways modulating neural KCNQ/M (Kv7) potassium channels. Nat Rev Neurosci 2005; 6(11): 850-62.
-
(2005)
Nat Rev Neurosci
, vol.6
, Issue.11
, pp. 850-862
-
-
Delmas, P.1
Brown, D.A.2
-
2
-
-
0034929557
-
KCNQ potassium channels: Physiology, pathophysiology, and pharmacology
-
Robbins J. KCNQ potassium channels: Physiology, pathophysiology, and pharmacology. Pharmacol Ther 2001; 90(1): 1-19.
-
(2001)
Pharmacol Ther
, vol.90
, Issue.1
, pp. 1-19
-
-
Robbins, J.1
-
3
-
-
0034303612
-
Neuronal KCNQ potassium channels: Physiology and role in disease
-
Jentsch TJ. Neuronal KCNQ potassium channels: Physiology and role in disease. Nat Rev Neurosci 2000; 1(1): 21-30.
-
(2000)
Nat Rev Neurosci
, vol.1
, Issue.1
, pp. 21-30
-
-
Jentsch, T.J.1
-
4
-
-
0034636056
-
KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway
-
Kharkovets T, Hardelin JP, Safieddine S, Schweizer M, El-Amraoui A, Petit C, et al. KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway. Proc Natl Acad Sci USA 2000; 97(8): 4333-8.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, Issue.8
, pp. 4333-4338
-
-
Kharkovets, T.1
Hardelin, J.P.2
Safieddine, S.3
Schweizer, M.4
El-Amraoui, A.5
Petit, C.6
-
5
-
-
0032536030
-
A potassium channel mutation in neonatal human epilepsy
-
Biervert C, Schroeder BC, Kubisch C, Berkovic SF, Propping P, Jentsch TJ, et al. A potassium channel mutation in neonatal human epilepsy. Science 1998; 279(5349): 403-6.
-
(1998)
Science
, vol.279
, Issue.5349
, pp. 403-406
-
-
Biervert, C.1
Schroeder, B.C.2
Kubisch, C.3
Berkovic, S.F.4
Propping, P.5
Jentsch, T.J.6
-
6
-
-
0031974209
-
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
-
Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, et al. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family. Nat Genet 1998; 18(1): 53-5.
-
(1998)
Nat Genet
, vol.18
, Issue.1
, pp. 53-55
-
-
Charlier, C.1
Singh, N.A.2
Ryan, S.G.3
Lewis, T.B.4
Reus, B.E.5
Leach, R.J.6
-
7
-
-
17344372328
-
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
-
Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, et al. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns. Nat Genet 1998; 18(1): 25-9.
-
(1998)
Nat Genet
, vol.18
, Issue.1
, pp. 25-29
-
-
Singh, N.A.1
Charlier, C.2
Stauffer, D.3
DuPont, B.R.4
Leach, R.J.5
Melis, R.6
-
8
-
-
0034283908
-
KCNQ2/KCNQ3 K+ channels and the molecular pathogenesis of epilepsy: Implications for therapy
-
Rogawski MA. KCNQ2/KCNQ3 K+ channels and the molecular pathogenesis of epilepsy: Implications for therapy. Trends Neurosci 2000; 23(9): 393-8.
-
(2000)
Trends Neurosci
, vol.23
, Issue.9
, pp. 393-398
-
-
Rogawski, M.A.1
-
10
-
-
0029088690
-
Reduction of spike frequency adaptation and blockade of M-current in rat CA1 pyramidal neurones by linopirdine (DuP 996), a neurotransmitter release enhancer
-
Aiken SP, Lampe BJ, Murphy PA, Brown BS. Reduction of spike frequency adaptation and blockade of M-current in rat CA1 pyramidal neurones by linopirdine (DuP 996), a neurotransmitter release enhancer. Br J Pharmacol 1995; 115(7): 1163-8.
-
(1995)
Br J Pharmacol
, vol.115
, Issue.7
, pp. 1163-1168
-
-
Aiken, S.P.1
Lampe, B.J.2
Murphy, P.A.3
Brown, B.S.4
-
11
-
-
0030959835
-
Effects of a cognition-enhancer, linopirdine (DuP 996), on M-type potassium currents (IK(M)) and some other voltage- and ligand-gated membrane currents in rat sympathetic neurons
-
Lamas JA, Selyanko AA, Brown DA. Effects of a cognition-enhancer, linopirdine (DuP 996), on M-type potassium currents (IK(M)) and some other voltage- and ligand-gated membrane currents in rat sympathetic neurons. Eur J Neurosci 1997; 9(3): 605-16.
-
(1997)
Eur J Neurosci
, vol.9
, Issue.3
, pp. 605-616
-
-
Lamas, J.A.1
Selyanko, A.A.2
Brown, D.A.3
-
12
-
-
0032442105
-
Selectivity of linopirdine (DuP 996), a neurotransmitter release enhancer, in blocking voltage-dependent and calcium-activated potassium currents in hippocampal neurons
-
Schnee ME, Brown BS. Selectivity of linopirdine (DuP 996), a neurotransmitter release enhancer, in blocking voltage-dependent and calcium-activated potassium currents in hippocampal neurons. J Pharmacol Exp Ther 1998; 286(2): 709-17.
-
(1998)
J Pharmacol Exp Ther
, vol.286
, Issue.2
, pp. 709-717
-
-
Schnee, M.E.1
Brown, B.S.2
-
13
-
-
0032483972
-
KCNQ2 and KCNQ3 potassium channel subunits: Molecular correlates of the M-channel
-
Wang HS, Pan Z, Shi W, Brown BS, Wymore RS, Cohen IS, et al. KCNQ2 and KCNQ3 potassium channel subunits: Molecular correlates of the M-channel. Science 1998; 282(5395): 1890-3.
-
(1998)
Science
, vol.282
, Issue.5395
, pp. 1890-1893
-
-
Wang, H.S.1
Pan, Z.2
Shi, W.3
Brown, B.S.4
Wymore, R.S.5
Cohen, I.S.6
-
14
-
-
0035122602
-
Characterization of KCNQ5/Q3 potassium channels expressed in mammalian cells
-
Wickenden AD, Zou A, Wagoner PK, Jegla T. Characterization of KCNQ5/Q3 potassium channels expressed in mammalian cells. Br J Pharmacol 2001; 132(2): 381-4.
-
(2001)
Br J Pharmacol
, vol.132
, Issue.2
, pp. 381-384
-
-
Wickenden, A.D.1
Zou, A.2
Wagoner, P.K.3
Jegla, T.4
-
15
-
-
0031809240
-
Two new potent neurotransmitter release enhancers, 10,10-bis(4-pyridinylmethyl)-9(10H)-anthracenone and 10,10-bis(2-fluoro-4-pyridinylmethyl)-9(10H)-anthracenone: Comparison to linopirdine
-
Zaczek R, Chorvat RJ, Saye JA, Pierdomenico ME, Maciag CM, Logue AR, et al. Two new potent neurotransmitter release enhancers, 10,10-bis(4-pyridinylmethyl)-9(10H)-anthracenone and 10,10-bis(2-fluoro-4-pyridinylmethyl)-9(10H)-anthracenone: Comparison to linopirdine. J Pharmacol Exp Ther 1998; 285(2): 724-30.
-
(1998)
J Pharmacol Exp Ther
, vol.285
, Issue.2
, pp. 724-730
-
-
Zaczek, R.1
Chorvat, R.J.2
Saye, J.A.3
Pierdomenico, M.E.4
Maciag, C.M.5
Logue, A.R.6
-
16
-
-
15444350005
-
2-Fluoro-4-pyridinylmethyl analogues of linopirdine as orally active acetylcholine release-enhancing agents with good efficacy and duration of action
-
Earl RA, Zaczek R, Teleha CA, Fisher BN, Maciag CM, Marynowski ME, et al. 2-Fluoro-4-pyridinylmethyl analogues of linopirdine as orally active acetylcholine release-enhancing agents with good efficacy and duration of action. J Med Chem 1998; 41(23): 4615-22.
-
(1998)
J Med Chem
, vol.41
, Issue.23
, pp. 4615-4622
-
-
Earl, R.A.1
Zaczek, R.2
Teleha, C.A.3
Fisher, B.N.4
Maciag, C.M.5
Marynowski, M.E.6
-
17
-
-
0030668611
-
The new anticonvulsant retigabine (D-23129) acts as an opener of K+ channels in neuronal cells
-
Rundfeldt C. The new anticonvulsant retigabine (D-23129) acts as an opener of K+ channels in neuronal cells. Eur J Pharmacol 1997; 336(2-3): 243-9.
-
(1997)
Eur J Pharmacol
, vol.336
, Issue.2-3
, pp. 243-249
-
-
Rundfeldt, C.1
-
18
-
-
0033011118
-
Characterization of the K+ channel opening effect of the anticonvulsant retigabine in PC12 cells
-
Rundfeldt C. Characterization of the K+ channel opening effect of the anticonvulsant retigabine in PC12 cells. Epilepsy Res 1999; 35(2): 99-107.
-
(1999)
Epilepsy Res
, vol.35
, Issue.2
, pp. 99-107
-
-
Rundfeldt, C.1
-
19
-
-
0034677733
-
The novel anticonvulsant retigabine activates M-currents in Chinese hamster ovary-cells tranfected with human KCNQ2/3 subunits
-
Rundfeldt C, Netzer R. The novel anticonvulsant retigabine activates M-currents in Chinese hamster ovary-cells tranfected with human KCNQ2/3 subunits. Neurosci Lett 2000; 282(1-2): 73-6.
-
(2000)
Neurosci Lett
, vol.282
, Issue.1-2
, pp. 73-76
-
-
Rundfeldt, C.1
Netzer, R.2
-
20
-
-
0033862433
-
-
Wickenden AD, Yu W, Zou A, Jegla T, Wagoner PK. Retigabine, a novel anti-convulsant, enhances activation of KCNQ2/Q3 potassium channels. Mol Pharmacol 2000; 58(3): 591-600.
-
Wickenden AD, Yu W, Zou A, Jegla T, Wagoner PK. Retigabine, a novel anti-convulsant, enhances activation of KCNQ2/Q3 potassium channels. Mol Pharmacol 2000; 58(3): 591-600.
-
-
-
-
21
-
-
0033916576
-
Modulation of KCNQ2/3 potassium channels by the novel anticonvulsant retigabine
-
Main MJ, Cryan JE, Dupere JR, Cox B, Clare JJ, Burbidge SA. Modulation of KCNQ2/3 potassium channels by the novel anticonvulsant retigabine. Mol Pharmacol 2000; 58(2): 253-62.
-
(2000)
Mol Pharmacol
, vol.58
, Issue.2
, pp. 253-262
-
-
Main, M.J.1
Cryan, J.E.2
Dupere, J.R.3
Cox, B.4
Clare, J.J.5
Burbidge, S.A.6
-
22
-
-
0035425653
-
Activation of expressed KCNQ potassium currents and native neuronal M-type potassium currents by the anti-convulsant drug retigabine
-
Tatulian L, Delmas P, Abogadie FC, Brown DA. Activation of expressed KCNQ potassium currents and native neuronal M-type potassium currents by the anti-convulsant drug retigabine. J Neurosci 2001; 21(15): 5535-45.
-
(2001)
J Neurosci
, vol.21
, Issue.15
, pp. 5535-5545
-
-
Tatulian, L.1
Delmas, P.2
Abogadie, F.C.3
Brown, D.A.4
-
23
-
-
0043127363
-
KCNQ/M currents in sensory neurons: Significance for pain therapy
-
Passmore GM, Selyanko AA, Mistry M, Al-Qatari M, Marsh SJ, Matthews EA, et al. KCNQ/M currents in sensory neurons: Significance for pain therapy. J Neurosci 2003; 23(18): 7227-36.
-
(2003)
J Neurosci
, vol.23
, Issue.18
, pp. 7227-7236
-
-
Passmore, G.M.1
Selyanko, A.A.2
Mistry, M.3
Al-Qatari, M.4
Marsh, S.J.5
Matthews, E.A.6
-
24
-
-
0028806375
-
The effects of D-23129, a new experimental anticonvulsant drug, on neurotransmitter amino acids in the rat hippocampus in vitro
-
Kapetanovic IM, Yonekawa WD, Kupferberg HJ. The effects of D-23129, a new experimental anticonvulsant drug, on neurotransmitter amino acids in the rat hippocampus in vitro. Epilepsy Res 1995; 22(3): 167-73
-
(1995)
Epilepsy Res
, vol.22
, Issue.3
, pp. 167-173
-
-
Kapetanovic, I.M.1
Yonekawa, W.D.2
Kupferberg, H.J.3
-
25
-
-
0000130273
-
Multiple actions of the new anticonvulsant D-23129 on voltage-gated inward currents and GABA-induced currents in cultured neuronal cells
-
Rundfeldt C AV, Heinnemann U. Multiple actions of the new anticonvulsant D-23129 on voltage-gated inward currents and GABA-induced currents in cultured neuronal cells.. Naunyn-Schmiedeberg's Arch Pharmacol 1995; 351(Suppl): R160.
-
(1995)
Naunyn-Schmiedeberg's Arch Pharmacol
, vol.351
, Issue.SUPPL.
-
-
Rundfeldt, C.A.1
Heinnemann, U.2
-
26
-
-
0027456560
-
Flupirtine. A review of its pharmacological properties, and therapeutic efficacy in pain states
-
Friedel HA, Fitton A. Flupirtine. A review of its pharmacological properties, and therapeutic efficacy in pain states. Drugs 1993; 45(4): 548-69.
-
(1993)
Drugs
, vol.45
, Issue.4
, pp. 548-569
-
-
Friedel, H.A.1
Fitton, A.2
-
27
-
-
40849085408
-
N-(6-chloro-pyridin-3-yl)-3,4-difluoro-benzamide (ICA-27243): A novel, selective KCNQ2/Q3 potassium channel activator
-
Wickenden AD, Krajewski JL, London B, Wagoner PK, Wilson WA, Clark S, et al. N-(6-chloro-pyridin-3-yl)-3,4-difluoro-benzamide (ICA-27243): A novel, selective KCNQ2/Q3 potassium channel activator. Mol Pharmacol 2008; 73(3): 977-86.
-
(2008)
Mol Pharmacol
, vol.73
, Issue.3
, pp. 977-986
-
-
Wickenden, A.D.1
Krajewski, J.L.2
London, B.3
Wagoner, P.K.4
Wilson, W.A.5
Clark, S.6
-
28
-
-
53849148633
-
In vivo profile of ICA-27243, a potent and selective KCNQ2/Q3 activator in rodent anticonvulsant models
-
Roeloffs R, Wickenden AD, Crean C, Werness S, McNaughton-Smith G, Stables J, et al. In vivo profile of ICA-27243, a potent and selective KCNQ2/Q3 activator in rodent anticonvulsant models. J Pharmacol Exp Ther 2008; 326(3): 818-28.
-
(2008)
J Pharmacol Exp Ther
, vol.326
, Issue.3
, pp. 818-828
-
-
Roeloffs, R.1
Wickenden, A.D.2
Crean, C.3
Werness, S.4
McNaughton-Smith, G.5
Stables, J.6
-
29
-
-
0842305796
-
M channels containing KCNQ2 subunits modulate norepinephrine, aspartate, and GABA release from hippocampal nerve terminals
-
Martire M, Castaldo P, D'Amico M, Preziosi P, Annunziato L, Taglialatela M. M channels containing KCNQ2 subunits modulate norepinephrine, aspartate, and GABA release from hippocampal nerve terminals. J Neurosci 2004; 24(3): 592-7.
-
(2004)
J Neurosci
, vol.24
, Issue.3
, pp. 592-597
-
-
Martire, M.1
Castaldo, P.2
D'Amico, M.3
Preziosi, P.4
Annunziato, L.5
Taglialatela, M.6
-
30
-
-
38849088576
-
The KCNQ/ M-current modulates arterial baroreceptor function at the sensory terminal in rats
-
Wladyka CL, Feng B, Glazebrook PA, Schild JH, Kunze DL. The KCNQ/ M-current modulates arterial baroreceptor function at the sensory terminal in rats. J Physiol 2008; 586(3): 795-802.
-
(2008)
J Physiol
, vol.586
, Issue.3
, pp. 795-802
-
-
Wladyka, C.L.1
Feng, B.2
Glazebrook, P.A.3
Schild, J.H.4
Kunze, D.L.5
-
31
-
-
43949142503
-
Effects of M-channel modulators on peripheral excitability in rat hairy skin
-
Passmore G, and Brown, DA. Effects of M-channel modulators on peripheral excitability in rat hairy skin. Soc Neurosci Abstr 2007; 681: 8.
-
(2007)
Soc Neurosci Abstr
, vol.681
, pp. 8
-
-
Passmore, G.1
Brown, D.A.2
-
32
-
-
68449100645
-
-
Wickenden A, Ye F, Liu Y, McNaugton-Smith G, Roeloffs R, Rigdon GC. KCNQ Channel expression in rat DRG following nerve ligation. Soc Neurosci Abstr 2002; 454: 7.
-
Wickenden A, Ye F, Liu Y, McNaugton-Smith G, Roeloffs R, Rigdon GC. KCNQ Channel expression in rat DRG following nerve ligation. Soc Neurosci Abstr 2002; 454: 7.
-
-
-
-
33
-
-
33746782064
-
KCNQ/M-currents contribute to the resting membrane potential in rat visceral sensory neurons
-
Wladyka CL, Kunze DL. KCNQ/M-currents contribute to the resting membrane potential in rat visceral sensory neurons. J Physiol 2006; 575(Pt 1): 175-89.
-
(2006)
J Physiol
, vol.575
, Issue.PART 1
, pp. 175-189
-
-
Wladyka, C.L.1
Kunze, D.L.2
-
34
-
-
68449083348
-
Sub-type selective activation of KCNQ2/ 3 channels modulates the excitability of nociceptive dorsal root ganglion neurons
-
Gerlach A, Stoehr SJ, Rigdon GC. Sub-type selective activation of KCNQ2/ 3 channels modulates the excitability of nociceptive dorsal root ganglion neurons. Soc Neurosci Abstr 2007; 509: 7.
-
(2007)
Soc Neurosci Abstr
, vol.509
, pp. 7
-
-
Gerlach, A.1
Stoehr, S.J.2
Rigdon, G.C.3
-
35
-
-
68449085792
-
-
Rose K, Dalle C, Mucha M, Robertson B, Gamper N. M-channel expression and activity as a possible mechanism controlling excitability of DRG neurons. Soc Neurosci Abstr 2007: 285.16.
-
Rose K, Dalle C, Mucha M, Robertson B, Gamper N. M-channel expression and activity as a possible mechanism controlling excitability of DRG neurons. Soc Neurosci Abstr 2007: 285.16.
-
-
-
-
36
-
-
0842346580
-
KCNQ2 is a nodal K+ channel
-
Devaux JJ, Kleopa KA, Cooper EC, Scherer SS. KCNQ2 is a nodal K+ channel. J Neurosci 2004; 24(5): 1236-44.
-
(2004)
J Neurosci
, vol.24
, Issue.5
, pp. 1236-1244
-
-
Devaux, J.J.1
Kleopa, K.A.2
Cooper, E.C.3
Scherer, S.S.4
-
37
-
-
33646378890
-
KCNQ channels mediate IKs, a slow K+ current regulating excitability in the rat node of Ranvier
-
Schwarz JR, Glassmeier G, Cooper EC, Kao TC, Nodera H, Tabuena D, et al. KCNQ channels mediate IKs, a slow K+ current regulating excitability in the rat node of Ranvier. J Physiol 2006; 573(Pt 1): 17-34.
-
(2006)
J Physiol
, vol.573
, Issue.PART 1
, pp. 17-34
-
-
Schwarz, J.R.1
Glassmeier, G.2
Cooper, E.C.3
Kao, T.C.4
Nodera, H.5
Tabuena, D.6
-
38
-
-
43949085016
-
Retigabine reduces the excitability of unmyelinated peripheral human axons
-
Lang PM, Fleckenstein J, Passmore GM, Brown DA, Grafe P. Retigabine reduces the excitability of unmyelinated peripheral human axons. Neuropharmacology 2008; 54(8): 1271-8.
-
(2008)
Neuropharmacology
, vol.54
, Issue.8
, pp. 1271-1278
-
-
Lang, P.M.1
Fleckenstein, J.2
Passmore, G.M.3
Brown, D.A.4
Grafe, P.5
-
39
-
-
0035834007
-
Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel
-
Dedek K, Kunath B, Kananura C, Reuner U, Jentsch TJ, Steinlein OK. Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel. Proc Natl Acad Sci USA 2001; 98(21): 12272-7.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, Issue.21
, pp. 12272-12277
-
-
Dedek, K.1
Kunath, B.2
Kananura, C.3
Reuner, U.4
Jentsch, T.J.5
Steinlein, O.K.6
-
40
-
-
29344437462
-
Effects of M-current modulators on the excitability of immature rat spinal sensory and motor neurones
-
Rivera-Arconada I, Lopez-Garcia JA. Effects of M-current modulators on the excitability of immature rat spinal sensory and motor neurones. Eur J Neurosci 2005; 22(12): 3091-8.
-
(2005)
Eur J Neurosci
, vol.22
, Issue.12
, pp. 3091-3098
-
-
Rivera-Arconada, I.1
Lopez-Garcia, J.A.2
-
41
-
-
33748175036
-
Retigabine-induced population primary afferent hyperpolarisation in vitro
-
Rivera-Arconada I, Lopez-Garcia JA. Retigabine-induced population primary afferent hyperpolarisation in vitro. Neuropharmacology 2006; 51(4): 756-63.
-
(2006)
Neuropharmacology
, vol.51
, Issue.4
, pp. 756-763
-
-
Rivera-Arconada, I.1
Lopez-Garcia, J.A.2
-
42
-
-
0031768841
-
The KCNQ2 potassium channel: Splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3
-
Tinel N, Lauritzen I, Chouabe C, Lazdunski M, Borsotto M. The KCNQ2 potassium channel: Splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3. FEBS Lett 1998; 438(3): 171-6.
-
(1998)
FEBS Lett
, vol.438
, Issue.3
, pp. 171-176
-
-
Tinel, N.1
Lauritzen, I.2
Chouabe, C.3
Lazdunski, M.4
Borsotto, M.5
-
43
-
-
0035399872
-
Differential expression of genes encoding subthreshold-operating voltage-gated K+ channels in brain
-
Saganich MJ, Machado E, Rudy B. Differential expression of genes encoding subthreshold-operating voltage-gated K+ channels in brain. J Neurosci 2001; 21(13): 4609-24.
-
(2001)
J Neurosci
, vol.21
, Issue.13
, pp. 4609-4624
-
-
Saganich, M.J.1
Machado, E.2
Rudy, B.3
-
44
-
-
0035894853
-
M channel KCNQ2 subunits are localized to key sites for control of neuronal network oscillations and synchronization in mouse brain
-
Cooper EC, Harrington E, Jan YN, Jan LY. M channel KCNQ2 subunits are localized to key sites for control of neuronal network oscillations and synchronization in mouse brain. J Neurosci 2001; 21(24): 9529-40.
-
(2001)
J Neurosci
, vol.21
, Issue.24
, pp. 9529-9540
-
-
Cooper, E.C.1
Harrington, E.2
Jan, Y.N.3
Jan, L.Y.4
-
45
-
-
0141923490
-
Localization of KCNQ5 in the normal and epileptic human temporal neocortex and hippocampal formation
-
Yus-Najera E, Munoz A, Salvador N, Jensen BS, Rasmussen HB, Defelipe J, et al. Localization of KCNQ5 in the normal and epileptic human temporal neocortex and hippocampal formation. Neuroscience 2003; 120(2): 353-64.
-
(2003)
Neuroscience
, vol.120
, Issue.2
, pp. 353-364
-
-
Yus-Najera, E.1
Munoz, A.2
Salvador, N.3
Jensen, B.S.4
Rasmussen, H.B.5
Defelipe, J.6
-
46
-
-
33646135533
-
Immunohistochemical analysis of KCNQ3 potassium channels in mouse brain
-
Geiger J, Weber YG, Landwehrmeyer B, Sommer C, Lerche H. Immunohistochemical analysis of KCNQ3 potassium channels in mouse brain. Neurosci Lett 2006; 400(1-2): 101-4.
-
(2006)
Neurosci Lett
, vol.400
, Issue.1-2
, pp. 101-104
-
-
Geiger, J.1
Weber, Y.G.2
Landwehrmeyer, B.3
Sommer, C.4
Lerche, H.5
-
47
-
-
33644942847
-
Immunohistochemical analysis of KCNQ2 potassium channels in adult and developing mouse brain
-
Weber YG, Geiger J, Kampchen K, Landwehrmeyer B, Sommer C, Lerche H. Immunohistochemical analysis of KCNQ2 potassium channels in adult and developing mouse brain. Brain Res 2006; 1077(1): 1-6.
-
(2006)
Brain Res
, vol.1077
, Issue.1
, pp. 1-6
-
-
Weber, Y.G.1
Geiger, J.2
Kampchen, K.3
Landwehrmeyer, B.4
Sommer, C.5
Lerche, H.6
-
48
-
-
0022559280
-
Mechanisms of action of acetylcholine in the guinea-pig cerebral cortex in vitro
-
McCormick DA, Prince DA. Mechanisms of action of acetylcholine in the guinea-pig cerebral cortex in vitro. J Physiol 1986; 375: 169-94.
-
(1986)
J Physiol
, vol.375
, pp. 169-194
-
-
McCormick, D.A.1
Prince, D.A.2
-
49
-
-
0034712923
-
Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy
-
Cooper EC, Aldape KD, Abosch A, Barbaro NM, Berger MS, Peacock WS, et al. Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy. Proc Natl Acad Sci USA 2000; 97(9): 4914-9.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, Issue.9
, pp. 4914-4919
-
-
Cooper, E.C.1
Aldape, K.D.2
Abosch, A.3
Barbaro, N.M.4
Berger, M.S.5
Peacock, W.S.6
-
50
-
-
33847179784
-
M-channels (Kv7/KCNQ channels) that regulate synaptic integration, excitability, and spike pattern of CA1 pyramidal cells are located in the perisomatic region
-
Hu H, Vervaeke K, Storm JF. M-channels (Kv7/KCNQ channels) that regulate synaptic integration, excitability, and spike pattern of CA1 pyramidal cells are located in the perisomatic region. J Neurosci 2007; 27(8): 1853-67.
-
(2007)
J Neurosci
, vol.27
, Issue.8
, pp. 1853-1867
-
-
Hu, H.1
Vervaeke, K.2
Storm, J.F.3
-
51
-
-
34247372307
-
Requirement of subunit co-assembly and ankyrin-G for M-channel localization at the axon initial segment
-
Rasmussen HB, Frokjaer-Jensen C, Jensen CS, Jensen HS, Jorgensen NK, Misonou H, et al. Requirement of subunit co-assembly and ankyrin-G for M-channel localization at the axon initial segment. J Cell Sci 2007; 120(Pt 6): 953-63.
-
(2007)
J Cell Sci
, vol.120
, Issue.PART 6
, pp. 953-963
-
-
Rasmussen, H.B.1
Frokjaer-Jensen, C.2
Jensen, C.S.3
Jensen, H.S.4
Jorgensen, N.K.5
Misonou, H.6
-
52
-
-
1242283867
-
Mcurrent modulators alter rat spinal nociceptive transmission: An electrophysiological study in vitro
-
Rivera-Arconada I, Martinez-Gomez J, Lopez-Garcia JA. Mcurrent modulators alter rat spinal nociceptive transmission: An electrophysiological study in vitro. Neuropharmacology 2004; 46(4): 598-606.
-
(2004)
Neuropharmacology
, vol.46
, Issue.4
, pp. 598-606
-
-
Rivera-Arconada, I.1
Martinez-Gomez, J.2
Lopez-Garcia, J.A.3
-
53
-
-
50549100189
-
-
Roza C, Lopez-Garcia JA. Retigabine, the specific KCNQ channel opener, blocks ectopic discharges in axotomized sensory fibres. Pain 2008.
-
Roza C, Lopez-Garcia JA. Retigabine, the specific KCNQ channel opener, blocks ectopic discharges in axotomized sensory fibres. Pain 2008.
-
-
-
-
54
-
-
0037462422
-
The anticonvulsant retigabine attenuates nociceptive behaviours in rat models of persistent and neuropathic pain
-
Blackburn-Munro G, Jensen BS. The anticonvulsant retigabine attenuates nociceptive behaviours in rat models of persistent and neuropathic pain. Eur J Pharmacol 2003; 460(2-3): 109-16.
-
(2003)
Eur J Pharmacol
, vol.460
, Issue.2-3
, pp. 109-116
-
-
Blackburn-Munro, G.1
Jensen, B.S.2
-
55
-
-
34250209086
-
Kv7 (KCNQ) channel modulators and neuropathic pain
-
Munro G, Dalby-Brown W. Kv7 (KCNQ) channel modulators and neuropathic pain. J Med Chem 2007; 50(11): 2576-82.
-
(2007)
J Med Chem
, vol.50
, Issue.11
, pp. 2576-2582
-
-
Munro, G.1
Dalby-Brown, W.2
-
56
-
-
2142701447
-
The anti-hyperalgesic activity of retigabine is mediated by KCNQ potassium channel activation
-
Dost R, Rostock A, Rundfeldt C. The anti-hyperalgesic activity of retigabine is mediated by KCNQ potassium channel activation. Naunyn Schmiedebergs Arch Pharmacol 2004; 369(4): 382-90.
-
(2004)
Naunyn Schmiedebergs Arch Pharmacol
, vol.369
, Issue.4
, pp. 382-390
-
-
Dost, R.1
Rostock, A.2
Rundfeldt, C.3
-
57
-
-
1642285193
-
Pharmacological characterisation of acid-induced muscle allodynia in rats
-
Nielsen AN, Mathiesen C, Blackburn-Munro G. Pharmacological characterisation of acid-induced muscle allodynia in rats. Eur J Pharmacol 2004; 487(1-3): 93-103.
-
(2004)
Eur J Pharmacol
, vol.487
, Issue.1-3
, pp. 93-103
-
-
Nielsen, A.N.1
Mathiesen, C.2
Blackburn-Munro, G.3
-
58
-
-
33846675852
-
Kv7.2-7.5 voltage-gated potassium channel (KCNQ2-5) opener, retigabine, reduces capsaicin-induced visceral pain in mice
-
Hirano K, Kuratani K, Fujiyoshi M, Tashiro N, Hayashi E, Kinoshita M. Kv7.2-7.5 voltage-gated potassium channel (KCNQ2-5) opener, retigabine, reduces capsaicin-induced visceral pain in mice. Neurosci Lett 2007; 413(2): 159-62.
-
(2007)
Neurosci Lett
, vol.413
, Issue.2
, pp. 159-162
-
-
Hirano, K.1
Kuratani, K.2
Fujiyoshi, M.3
Tashiro, N.4
Hayashi, E.5
Kinoshita, M.6
-
59
-
-
68449095671
-
-
Ilyin V, Carlin KP, Hodges DD, Robledo S, Woodward RM. Flupirtine A positive modulator of heteromeric KCNQ2/Q3 channels. Socr Neurosci Abstr 2002: 758.10.
-
Ilyin V, Carlin KP, Hodges DD, Robledo S, Woodward RM. Flupirtine A positive modulator of heteromeric KCNQ2/Q3 channels. Socr Neurosci Abstr 2002: 758.10.
-
-
-
-
60
-
-
0023276485
-
The antinociceptive activity of flupirtine: A structurally new analgesic
-
Nickel B. The antinociceptive activity of flupirtine: A structurally new analgesic. Postgrad Med J 1987; 63(Suppl 3): 19-28.
-
(1987)
Postgrad Med J
, vol.63
, Issue.SUPPL. 3
, pp. 19-28
-
-
Nickel, B.1
-
61
-
-
0023639729
-
Effect of flupirtine maleate on the nociceptive pathway, EEG, evoked potentials and polysynaptic reflexes in laboratory animals
-
Gordon R, Sofia RD, Diamantis W. Effect of flupirtine maleate on the nociceptive pathway, EEG, evoked potentials and polysynaptic reflexes in laboratory animals. Postgrad Med J 1987; 63(Suppl 3): 49-55.
-
(1987)
Postgrad Med J
, vol.63
, Issue.SUPPL. 3
, pp. 49-55
-
-
Gordon, R.1
Sofia, R.D.2
Diamantis, W.3
-
62
-
-
0023552033
-
Depression by flupirtine, a novel analgesic agent, of motor and sensory responses of the nociceptive system in the rat spinal cord
-
Carlsson KH, Jurna I. Depression by flupirtine, a novel analgesic agent, of motor and sensory responses of the nociceptive system in the rat spinal cord. Eur J Pharmacol 1987; 143(1): 89-99.
-
(1987)
Eur J Pharmacol
, vol.143
, Issue.1
, pp. 89-99
-
-
Carlsson, K.H.1
Jurna, I.2
-
63
-
-
0024382495
-
Mode of antinociceptive action of flupirtine in the rat
-
Szelenyi I, Nickel B, Borbe HO, Brune K. Mode of antinociceptive action of flupirtine in the rat. Br J Pharmacol 1989; 97(3): 835-42.
-
(1989)
Br J Pharmacol
, vol.97
, Issue.3
, pp. 835-842
-
-
Szelenyi, I.1
Nickel, B.2
Borbe, H.O.3
Brune, K.4
-
64
-
-
0028285945
-
The mouse grid-shock analgesia test: Pharmacological characterization of latency to vocalization threshold as an index of antinociception
-
Swedberg MD. The mouse grid-shock analgesia test: Pharmacological characterization of latency to vocalization threshold as an index of antinociception. J Pharmacol Exp Ther 1994; 269(3): 1021-8.
-
(1994)
J Pharmacol Exp Ther
, vol.269
, Issue.3
, pp. 1021-1028
-
-
Swedberg, M.D.1
-
65
-
-
0023232593
-
Analgesic activity following combined oral administration of flupirtine maleate and peripherally acting analgesics in mice and rats
-
Diamantis W, Gordon R, Sofia RD. Analgesic activity following combined oral administration of flupirtine maleate and peripherally acting analgesics in mice and rats. Postgrad Med J 1987; 63(Suppl 3): 29-34.
-
(1987)
Postgrad Med J
, vol.63
, Issue.SUPPL. 3
, pp. 29-34
-
-
Diamantis, W.1
Gordon, R.2
Sofia, R.D.3
-
66
-
-
0025301724
-
The effect of flupirtine, various analgesics and muscle relaxants on skeletal muscle tone in the conscious rat]
-
Nickel B, Jakovlev V, Szelenyi I. [The effect of flupirtine, various analgesics and muscle relaxants on skeletal muscle tone in the conscious rat]. Arzneimittelforschung 1990; 40(8): 909-11.
-
(1990)
Arzneimittelforschung
, vol.40
, Issue.8
, pp. 909-911
-
-
Nickel, B.1
Jakovlev, V.2
Szelenyi, I.3
-
67
-
-
68449088926
-
In vivo profile of ICA-27243, a potent and selective KCNQ2/3 activator in rodent models of pain
-
Roeloffs R, Wickenden AD, McNaughton-Smith G, Jones LD, Harrison W, Porreca F, et al. In vivo profile of ICA-27243, a potent and selective KCNQ2/3 activator in rodent models of pain. Socr Neurosci Abstr 2005; 153: 14.
-
(2005)
Socr Neurosci Abstr
, vol.153
, pp. 14
-
-
Roeloffs, R.1
Wickenden, A.D.2
McNaughton-Smith, G.3
Jones, L.D.4
Harrison, W.5
Porreca, F.6
-
68
-
-
68449102491
-
Activity of a KCNQ2/3 opener in rat models of neuropathic pain
-
Mark L, Harrison, JE, Cummons T, Strassle BW, Smith V, Childers W, et al. Activity of a KCNQ2/3 opener in rat models of neuropathic pain. Soc Neurosci Abstr 2007; 509: 3.
-
(2007)
Soc Neurosci Abstr
, vol.509
, pp. 3
-
-
Mark, L.1
Harrison, J.E.2
Cummons, T.3
Strassle, B.W.4
Smith, V.5
Childers, W.6
-
69
-
-
68449090764
-
Activity of a KCNQ2/3 opener in rat models of inflammatory pain
-
Leventhal L, Lu P, Piesla MJ, Harrison J, McDevitt R, Childers W, et al. Activity of a KCNQ2/3 opener in rat models of inflammatory pain. Socr Neurosci Abstr 2007; 509: 17.
-
(2007)
Socr Neurosci Abstr
, vol.509
, pp. 17
-
-
Leventhal, L.1
Lu, P.2
Piesla, M.J.3
Harrison, J.4
McDevitt, R.5
Childers, W.6
-
70
-
-
85044686852
-
Treatment of tumor pain with flupirtine. Results of a double-blind study versus tramadol
-
Luben V, Muller H, Lobisch M, Worz R. Treatment of tumor pain with flupirtine. Results of a double-blind study versus tramadol. Fortschr Med 1994; 112(19): 282-6.
-
(1994)
Fortschr Med
, vol.112
, Issue.19
, pp. 282-286
-
-
Luben, V.1
Muller, H.2
Lobisch, M.3
Worz, R.4
-
71
-
-
0023203562
-
Analgesic efficacy and safety of oral flupirtine in the treatment of cancer pain
-
Scheef W. Analgesic efficacy and safety of oral flupirtine in the treatment of cancer pain. Postgrad Med J 1987; 63(Suppl 3): 67-70.
-
(1987)
Postgrad Med J
, vol.63
, Issue.SUPPL. 3
, pp. 67-70
-
-
Scheef, W.1
-
72
-
-
0021933356
-
Flupirtine in patients with cancer pain]
-
Scheef W, Wolf-Gruber D. [Flupirtine in patients with cancer pain]. Arzneimittelforschung 1985; 35(1): 75-7.
-
(1985)
Arzneimittelforschung
, vol.35
, Issue.1
, pp. 75-77
-
-
Scheef, W.1
Wolf-Gruber, D.2
-
73
-
-
0023689142
-
Analgesic activity of flupirtine maleate: A controlled double-blind study with diclofenac sodium in orthopaedics
-
Mastronardi P, D'Onofrio M, Scanni E, Pinto M, Frontespezi S, Ceccarelli MG, et al. Analgesic activity of flupirtine maleate: A controlled double-blind study with diclofenac sodium in orthopaedics. J Int Med Res 1988; 16(5): 338-48.
-
(1988)
J Int Med Res
, vol.16
, Issue.5
, pp. 338-348
-
-
Mastronardi, P.1
D'Onofrio, M.2
Scanni, E.3
Pinto, M.4
Frontespezi, S.5
Ceccarelli, M.G.6
-
75
-
-
0023206019
-
Flupirtine in the treatment of postoperative pain
-
Riethmuller-Winzen H. Flupirtine in the treatment of postoperative pain. Postgrad Med J 1987; 63(Suppl 3): 61-5.
-
(1987)
Postgrad Med J
, vol.63
, Issue.SUPPL. 3
, pp. 61-65
-
-
Riethmuller-Winzen, H.1
-
76
-
-
0020549862
-
Comparison of flupirtine maleate and dihydrocodeine in patients following surgery
-
Moore RA, Bullingham RE, Simpson S, O'Sullivan G, Evans PJ, McQuay HJ, et al. Comparison of flupirtine maleate and dihydrocodeine in patients following surgery. Br J Anaesth 1983; 55(5): 429-32.
-
(1983)
Br J Anaesth
, vol.55
, Issue.5
, pp. 429-432
-
-
Moore, R.A.1
Bullingham, R.E.2
Simpson, S.3
O'Sullivan, G.4
Evans, P.J.5
McQuay, H.J.6
-
77
-
-
0030466360
-
Flupirtine in comparison with chlormezanone in chronic musculoskeletal back pain. Results of a multicenter randomized double-blind study]
-
Worz R, Bolten W, Heller B, Krainick JU, Pergande G. [Flupirtine in comparison with chlormezanone in chronic musculoskeletal back pain. Results of a multicenter randomized double-blind study]. Fortschr Med 1996; 114(35-36): 500-4.
-
(1996)
Fortschr Med
, vol.114
, Issue.35-36
, pp. 500-504
-
-
Worz, R.1
Bolten, W.2
Heller, B.3
Krainick, J.U.4
Pergande, G.5
-
78
-
-
0021182990
-
Clinical trial of flupirtine maleate in patients with migraine
-
Million R, Finlay BR, Whittington JR. Clinical trial of flupirtine maleate in patients with migraine. Curr Med Res Opin 1984; 9(3): 204-12.
-
(1984)
Curr Med Res Opin
, vol.9
, Issue.3
, pp. 204-212
-
-
Million, R.1
Finlay, B.R.2
Whittington, J.R.3
-
79
-
-
0033948454
-
Fibromyalgia symptoms relieved by flupirtine: An openlabel case series
-
Stoll AL. Fibromyalgia symptoms relieved by flupirtine: An openlabel case series. Psychosomatics 2000; 41(4): 371-2.
-
(2000)
Psychosomatics
, vol.41
, Issue.4
, pp. 371-372
-
-
Stoll, A.L.1
-
80
-
-
0023280897
-
On the adverse reactions and efficacy of long-term treatment with flupirtine: Preliminary results of an ongoing twelve-month study with 200 patients suffering from chronic pain states in arthrosis or arthritis
-
Herrmann WM, Kern U, Aigner M. On the adverse reactions and efficacy of long-term treatment with flupirtine: Preliminary results of an ongoing twelve-month study with 200 patients suffering from chronic pain states in arthrosis or arthritis. Postgrad Med J 1987; 63(Suppl 3): 87-103.
-
(1987)
Postgrad Med J
, vol.63
, Issue.SUPPL. 3
, pp. 87-103
-
-
Herrmann, W.M.1
Kern, U.2
Aigner, M.3
-
81
-
-
0023243071
-
-
McMahon FG, Arndt WF Jr, Newton JJ, Montgomery PA, Perhach JL. Clinical experience with flupirtine in the U.S. Postgrad Med J 1987; 63(Suppl 3): 81-5.
-
McMahon FG, Arndt WF Jr, Newton JJ, Montgomery PA, Perhach JL. Clinical experience with flupirtine in the U.S. Postgrad Med J 1987; 63(Suppl 3): 81-5.
-
-
-
-
82
-
-
68449092033
-
-
Carter-Wallace submitting additional Flupirtine efficacy study, firm tells shareholders; Hoyt family gains voting strength with antitakeover measure. Pink Sheet 1987; 49(Number 030): Page 16
-
Carter-Wallace submitting additional Flupirtine efficacy study, firm tells shareholders; Hoyt family gains voting strength with antitakeover measure. Pink Sheet 1987; 49(Number 030): Page 16
-
-
-
-
83
-
-
68449097501
-
Carter-Wallace notes at annual meeting; McNeil submitting further angina data this year
-
Bepridil anti-arrhythmia indication under development
-
Bepridil anti-arrhythmia indication under development, Carter-Wallace notes at annual meeting; McNeil submitting further angina data this year. Pink Sheet 1988; 50(030): 8-9.
-
(1988)
Pink Sheet
, vol.50
, Issue.30
, pp. 8-9
-
-
-
84
-
-
68449092652
-
-
Khanzhin N, Rottländer M, Watson WP; H Lundbeck A/S. Substituted indoline and indole derivatives. United States patent application WO2004/ 096767. November 11, 2004
-
Khanzhin N, Rottländer M, Watson WP; H Lundbeck A/S. Substituted indoline and indole derivatives. United States patent application WO2004/ 096767. November 11, 2004
-
-
-
-
85
-
-
68449103083
-
-
Rottlander M, Ritzen A, Norgaard MB, Khanzhin N, Tornoe CW; H Lundbeck A/ S. 1,2,4-Triaminobenzene derivatives useful for the treating disorders of the central nervous system. United States patent US20087368472. May 6, 2008.
-
Rottlander M, Ritzen A, Norgaard MB, Khanzhin N, Tornoe CW; H Lundbeck A/ S. 1,2,4-Triaminobenzene derivatives useful for the treating disorders of the central nervous system. United States patent US20087368472. May 6, 2008.
-
-
-
-
86
-
-
68449101214
-
-
Vernier J-M, De La Rosa MA, Chen H, Wu, JZ, Larson GL Cheney IW; Valeant pharmaceuticals. Derivatives of 4-(Nazacycloalkyl) anilides as potassium channel modulators. United States patent application WO2008/024398. February 28, 2008.
-
Vernier J-M, De La Rosa MA, Chen H, Wu, JZ, Larson GL Cheney IW; Valeant pharmaceuticals. Derivatives of 4-(Nazacycloalkyl) anilides as potassium channel modulators. United States patent application WO2008/024398. February 28, 2008.
-
-
-
-
87
-
-
68449091405
-
-
Vernier J-M, Ouk S, De La Rosa MA, Paisner DA; Valeant pharmaceuticals. Derivatives of 1,3-diamino benzene as potassium channel modulators. United States patent application WO2008/0045534. February 21, 2008
-
Vernier J-M, Ouk S, De La Rosa MA, Paisner DA; Valeant pharmaceuticals. Derivatives of 1,3-diamino benzene as potassium channel modulators. United States patent application WO2008/0045534. February 21, 2008
-
-
-
-
88
-
-
68449092032
-
-
McNaughton-Smith GA, Gross MF, Wickenden AD; Icagen Inc. Benzanilides as potassium channel openers. United States patent US20026372767. April 16, 2002
-
McNaughton-Smith GA, Gross MF, Wickenden AD; Icagen Inc. Benzanilides as potassium channel openers. United States patent US20026372767. April 16, 2002
-
-
-
-
89
-
-
68449087642
-
-
McNaughton-Smith G, Fritch PC, Amato GS; Icagen Inc. Pyridine substituted benzanilides as potassium channel openers. United States patent US20026495550. December 17, 2002.
-
McNaughton-Smith G, Fritch PC, Amato GS; Icagen Inc. Pyridine substituted benzanilides as potassium channel openers. United States patent US20026495550. December 17, 2002.
-
-
-
-
90
-
-
68449085791
-
-
McNaughton-Smith GA, Gross MF, Wickenden AD; Icagen Inc. Benzanilides as potassium channel openers. United States patent US20036605725. August 12, 2003.
-
McNaughton-Smith GA, Gross MF, Wickenden AD; Icagen Inc. Benzanilides as potassium channel openers. United States patent US20036605725. August 12, 2003.
-
-
-
-
91
-
-
68449104306
-
-
McNaughton-Smith G. The identification of KCNQ channel modulators and their potential use in disorders associated with excessive neuronal excitability. American Chemical Society meeting abstract, August 28th 2005, Washington DC: USA 2005.
-
McNaughton-Smith G. The identification of KCNQ channel modulators and their potential use in disorders associated with excessive neuronal excitability. American Chemical Society meeting abstract, August 28th 2005, Washington DC: USA 2005.
-
-
-
-
92
-
-
68449099455
-
-
McNaughton-Smith GA, Amato GS Icagen Inc. Bisarylamines as potassium channel openers. United States patent US20036593349. July 15, 2003.
-
McNaughton-Smith GA, Amato GS Icagen Inc. Bisarylamines as potassium channel openers. United States patent US20036593349. July 15, 2003.
-
-
-
-
93
-
-
18344363352
-
Activation of KCNQ5 channels stably expressed in HEK293 cells by BMS-204352
-
Dupuis DS, Schroder RL, Jespersen T, Christensen JK, Christophersen P, Jensen BS, et al. Activation of KCNQ5 channels stably expressed in HEK293 cells by BMS-204352. Eur J Pharmacol 2002; 437(3): 129-37.
-
(2002)
Eur J Pharmacol
, vol.437
, Issue.3
, pp. 129-137
-
-
Dupuis, D.S.1
Schroder, R.L.2
Jespersen, T.3
Christensen, J.K.4
Christophersen, P.5
Jensen, B.S.6
-
94
-
-
17144444950
-
KCNQ4 channel activation by BMS-204352 and retigabine
-
Schroder RL, Jespersen T, Christophersen P, Strobaek D, Jensen BS, Olesen SP. KCNQ4 channel activation by BMS-204352 and retigabine. Neuropharmacology 2001; 40(7): 888-98.
-
(2001)
Neuropharmacology
, vol.40
, Issue.7
, pp. 888-898
-
-
Schroder, R.L.1
Jespersen, T.2
Christophersen, P.3
Strobaek, D.4
Jensen, B.S.5
Olesen, S.P.6
-
95
-
-
0041828391
-
Voltage-independent KCNQ4 currents induced by (+/-)BMS-204352
-
Schroder RL, Strobaek D, Olesen SP, Christophersen P. Voltage-independent KCNQ4 currents induced by (+/-)BMS-204352. Pflugers Arch 2003; 446(5): 607-16.
-
(2003)
Pflugers Arch
, vol.446
, Issue.5
, pp. 607-616
-
-
Schroder, R.L.1
Strobaek, D.2
Olesen, S.P.3
Christophersen, P.4
-
96
-
-
68449096289
-
-
Jensen BS, SchrØder RL, StrØbæk D, Olesen, SP; Neuro-search A/S. Use of 3-oxindole derivatives as KCNQ potassium channel modulators. United States patent application WO2002/000217. January 3, 2002
-
Jensen BS, SchrØder RL, StrØbæk D, Olesen, SP; Neuro-search A/S. Use of 3-oxindole derivatives as KCNQ potassium channel modulators. United States patent application WO2002/000217. January 3, 2002
-
-
-
-
97
-
-
68449090765
-
-
Hewawasam P, Dextraze P, Gribkoff VK, Kinney GG, Dworetzky SI; Bristol-Myers Squibb Company. Fluoro-oxindole derivatives as modulators of KCNQ potassium channels. United States patent US20026469042. October 22, 2002
-
Hewawasam P, Dextraze P, Gribkoff VK, Kinney GG, Dworetzky SI; Bristol-Myers Squibb Company. Fluoro-oxindole derivatives as modulators of KCNQ potassium channels. United States patent US20026469042. October 22, 2002
-
-
-
-
98
-
-
1542613876
-
The synthesis and structure-activity relationships of 3-amino-4-benzylquinolin-2-ones; discovery of novel KCNQ2 channel openers
-
Hewawasam P, Chen N, Ding M, Natale JT, Boissard CG, Yeola S, et al. The synthesis and structure-activity relationships of 3-amino-4-benzylquinolin-2-ones; discovery of novel KCNQ2 channel openers. Bioorg Med Chem Lett 2004; 14(7): 1615-8.
-
(2004)
Bioorg Med Chem Lett
, vol.14
, Issue.7
, pp. 1615-1618
-
-
Hewawasam, P.1
Chen, N.2
Ding, M.3
Natale, J.T.4
Boissard, C.G.5
Yeola, S.6
-
99
-
-
68449095109
-
-
Hewawasam P, Dodd, DS, Weaver, CD, Dextraze P, Gribkoff VK, Kinney GG, Dworetzky SI; Bristol-Myers Squibb Company. 2,4-Disubstituted pyrimidine-5-carboxamides as KCNQ potassium channel modulators. United States patent application WO2002/066036. August 29, 2002
-
Hewawasam P, Dodd, DS, Weaver, CD, Dextraze P, Gribkoff VK, Kinney GG, Dworetzky SI; Bristol-Myers Squibb Company. 2,4-Disubstituted pyrimidine-5-carboxamides as KCNQ potassium channel modulators. United States patent application WO2002/066036. August 29, 2002
-
-
-
-
100
-
-
68449085163
-
-
Khanzhin N, Greve DR, Rottlander M; Lundbeck Research USA. Substituted pyrimidine derivatives. United States patent application WO2007/0066612. March 22, 2007
-
Khanzhin N, Greve DR, Rottlander M; Lundbeck Research USA. Substituted pyrimidine derivatives. United States patent application WO2007/0066612. March 22, 2007
-
-
-
-
101
-
-
68449095672
-
-
TornrØe CW, Khanzhin N, Rottländer M, Watson, WP, Greve DR; H. Lundbeck A/S Substituted pyridine derivatives. United States patent application WO2006/092143. September 8, 2006
-
TornrØe CW, Khanzhin N, Rottländer M, Watson, WP, Greve DR; H. Lundbeck A/S Substituted pyridine derivatives. United States patent application WO2006/092143. September 8, 2006
-
-
-
-
102
-
-
68449087643
-
-
Wu Y-J, Sun L-Q, Chen J, He H, L'Heureux A, Dextraze P, Daris J-P, Kinney GG, Dworetzky SI, Hewawasam, P; Bristol-Myers Squibb Company. Cinnamides as KCNQ potassium channel modulators. United States patent application WO2002/096858. December 5, 2002
-
Wu Y-J, Sun L-Q, Chen J, He H, L'Heureux A, Dextraze P, Daris J-P, Kinney GG, Dworetzky SI, Hewawasam, P; Bristol-Myers Squibb Company. Cinnamides as KCNQ potassium channel modulators. United States patent application WO2002/096858. December 5, 2002
-
-
-
-
103
-
-
0042921620
-
Fluorine substitution can block CYP3A4 metabolism-dependent inhibition: Identification of (S)-N-[1-(4-fluoro-3- morpholin-4-ylphenyl)ethyl]-3- (4-fluorophenyl)acrylamide as an orally bioavailable KCNQ2 opener devoid of CYP3A4 metabolism-dependent inhibition
-
Wu YJ, Davis CD, Dworetzky S, Fitzpatrick WC, Harden D, He H, et al. Fluorine substitution can block CYP3A4 metabolism-dependent inhibition: Identification of (S)-N-[1-(4-fluoro-3- morpholin-4-ylphenyl)ethyl]-3- (4-fluorophenyl)acrylamide as an orally bioavailable KCNQ2 opener devoid of CYP3A4 metabolism-dependent inhibition. J Med Chem 2003; 46(18): 3778-81.
-
(2003)
J Med Chem
, vol.46
, Issue.18
, pp. 3778-3781
-
-
Wu, Y.J.1
Davis, C.D.2
Dworetzky, S.3
Fitzpatrick, W.C.4
Harden, D.5
He, H.6
-
104
-
-
68449101856
-
-
Wu Y-J, Sun L-Q, He H, L'Heureux, A; Bristol-Myers Squibb Company. 1-Aryl-2-hydroxethyl amides as potassium channel openers. United States patent application WO2004/047743. June 10, 2004
-
Wu Y-J, Sun L-Q, He H, L'Heureux, A; Bristol-Myers Squibb Company. 1-Aryl-2-hydroxethyl amides as potassium channel openers. United States patent application WO2004/047743. June 10, 2004
-
-
-
-
105
-
-
68449087015
-
-
Wu Y-J, L'Heureux, A, He H; Bristol-Myers Squibb Company. 3-Heterocyclic benzylamide derivatives as potassium channel openers. United States patent application WO2004/047744. June 10, 2004
-
Wu Y-J, L'Heureux, A, He H; Bristol-Myers Squibb Company. 3-Heterocyclic benzylamide derivatives as potassium channel openers. United States patent application WO2004/047744. June 10, 2004
-
-
-
-
106
-
-
10644255478
-
(S,E)-N-[1-(3-heteroarylphenyl)ethyl]-3-(2-fluorophenyl)acrylamides: Synthesis and KCNQ2 potassium channel opener activity
-
L'Heureux A, Martel A, He H, Chen J, Sun LQ, Starrett JE, et al. (S,E)-N-[1-(3-heteroarylphenyl)ethyl]-3-(2-fluorophenyl)acrylamides: synthesis and KCNQ2 potassium channel opener activity. Bioorg Med Chem Lett 2005; 15(2): 363-6.
-
(2005)
Bioorg Med Chem Lett
, vol.15
, Issue.2
, pp. 363-366
-
-
L'Heureux, A.1
Martel, A.2
He, H.3
Chen, J.4
Sun, L.Q.5
Starrett, J.E.6
-
107
-
-
68449098205
-
-
Wu Y-J, Sun L-Q, Chen J; Bristol-Myers Squibb Company. 3-(Pyridyl-piperazin-1-yl)-phenethyl amides as potassium channel openers. United States patent application WO2004/047745. June 10, 2004
-
Wu Y-J, Sun L-Q, Chen J; Bristol-Myers Squibb Company. 3-(Pyridyl-piperazin-1-yl)-phenethyl amides as potassium channel openers. United States patent application WO2004/047745. June 10, 2004
-
-
-
-
108
-
-
68449103707
-
-
Wu Y-J, Sun L-Q, L'Heureux, A; Bristol-Myers Squibb Company. Arylcyclopropylcarboxylic amides as potassium channel openers. United States patent application WO2004/047738. June 10, 2004
-
Wu Y-J, Sun L-Q, L'Heureux, A; Bristol-Myers Squibb Company. Arylcyclopropylcarboxylic amides as potassium channel openers. United States patent application WO2004/047738. June 10, 2004
-
-
-
-
109
-
-
0038493792
-
(S)-N-[1-(3-morpholin-4-ylphenyl)ethyl]- 3-phenylacrylamide: An orally bioavailable KCNQ2 opener with significant activity in a cortical spreading depression model of migraine
-
Wu YJ, Boissard CG, Greco C, Gribkoff VK, Harden DG, He H, et al. (S)-N-[1-(3-morpholin-4-ylphenyl)ethyl]- 3-phenylacrylamide: An orally bioavailable KCNQ2 opener with significant activity in a cortical spreading depression model of migraine. J Med Chem 2003; 46(15): 3197-200.
-
(2003)
J Med Chem
, vol.46
, Issue.15
, pp. 3197-3200
-
-
Wu, Y.J.1
Boissard, C.G.2
Greco, C.3
Gribkoff, V.K.4
Harden, D.G.5
He, H.6
-
110
-
-
33750614291
-
The acrylamide (S)-1 differentially affects Kv7 (KCNQ) potassium channels
-
Bentzen BH, Schmitt N, Calloe K, Dalby Brown W, Grunnet M, Olesen SP. The acrylamide (S)-1 differentially affects Kv7 (KCNQ) potassium channels. Neuropharmacology 2006; 51(6): 1068-77.
-
(2006)
Neuropharmacology
, vol.51
, Issue.6
, pp. 1068-1077
-
-
Bentzen, B.H.1
Schmitt, N.2
Calloe, K.3
Dalby Brown, W.4
Grunnet, M.5
Olesen, S.P.6
-
111
-
-
2442700343
-
Synthesis and structure-activity relationship of acrylamides as KCNQ2 potassium channel openers
-
Wu YJ, He H, Sun LQ, L'Heureux A, Chen J, Dextraze P, et al. Synthesis and structure-activity relationship of acrylamides as KCNQ2 potassium channel openers. J Med Chem 2004; 47(11): 2887-96.
-
(2004)
J Med Chem
, vol.47
, Issue.11
, pp. 2887-2896
-
-
Wu, Y.J.1
He, H.2
Sun, L.Q.3
L'Heureux, A.4
Chen, J.5
Dextraze, P.6
-
112
-
-
68449099456
-
-
Boy K, Wu Y-J, Guernon JM; Bristol-Myers Squibb Company. 2-Aryl thiazole derivatives KCNQ modulators. United States patent application WO2004/ 060281. July 22, 2004
-
Boy K, Wu Y-J, Guernon JM; Bristol-Myers Squibb Company. 2-Aryl thiazole derivatives KCNQ modulators. United States patent application WO2004/ 060281. July 22, 2004
-
-
-
-
113
-
-
68449099457
-
-
Boy K, Wu Y-J; Bristol-Myers Squibb Company. Aminoalkyl thiazole derivatives KCNQ modulators. United States patent application WO2004/ 0138268. July 15, 2004
-
Boy K, Wu Y-J; Bristol-Myers Squibb Company. Aminoalkyl thiazole derivatives KCNQ modulators. United States patent application WO2004/ 0138268. July 15, 2004
-
-
-
-
114
-
-
68449100079
-
-
Boy K, Wu Y-J; Bristol-Myers Squibb Company. Aminoalkyl thiazole derivatives KCNQ modulators. United States patent application WO2004/ 0138268. July 15, 2004
-
Boy K, Wu Y-J; Bristol-Myers Squibb Company. Aminoalkyl thiazole derivatives KCNQ modulators. United States patent application WO2004/ 0138268. July 15, 2004
-
-
-
-
115
-
-
68449088929
-
-
McNaughton-Smith G. Novel KCNQ agonists as potential new therapeutics. SERMACS: Atlanta 2003.
-
McNaughton-Smith G. Novel KCNQ agonists as potential new therapeutics. SERMACS: Atlanta 2003.
-
-
-
-
116
-
-
68449092650
-
-
McNaughton-Smith GA, Thomas JB, Amato, G; Icagen, Inc. Quinazolinones as potassium channel modulators. United States patent application WO2004/ 058704. July 15, 2004
-
McNaughton-Smith GA, Thomas JB, Amato, G; Icagen, Inc. Quinazolinones as potassium channel modulators. United States patent application WO2004/ 058704. July 15, 2004
-
-
-
-
117
-
-
68449099454
-
-
McNaughton-Smith GA, Amato GS, Thomas JB; Icagen, Inc. Fused ring heterocycles as potassium channel modulators. United States patent US7223768. May 29, 2007.
-
McNaughton-Smith GA, Amato GS, Thomas JB; Icagen, Inc. Fused ring heterocycles as potassium channel modulators. United States patent US7223768. May 29, 2007.
-
-
-
-
118
-
-
68449089571
-
-
McNaughton-Smith GA, Amato GS, Thomas JB; Icagen, Inc. Fused ring heterocycles as potassium channel modulators. United States patent application WO2008/0058319. March 6, 2008.
-
McNaughton-Smith GA, Amato GS, Thomas JB; Icagen, Inc. Fused ring heterocycles as potassium channel modulators. United States patent application WO2008/0058319. March 6, 2008.
-
-
-
-
119
-
-
68449104307
-
-
Brown WD, Jessen, C, Demnitz J, Dyhring T, StrØbæk D; Neurosearch A/S. Quniazolinones and their use as potassium channel activators. United States patent application WO2007/104717. September 20, 2007
-
Brown WD, Jessen, C, Demnitz J, Dyhring T, StrØbæk D; Neurosearch A/S. Quniazolinones and their use as potassium channel activators. United States patent application WO2007/104717. September 20, 2007
-
-
-
-
120
-
-
68449103706
-
-
Brown WD, Teuber, L, Dyhring T, StrØbæÆk D, Jessen, C; Neurosearch A/S. Novel quinazoline derivatives and their medical use. United States patent application WO2007/057447. May 24, 2007
-
Brown WD, Teuber, L, Dyhring T, StrØbæÆk D, Jessen, C; Neurosearch A/S. Novel quinazoline derivatives and their medical use. United States patent application WO2007/057447. May 24, 2007
-
-
-
-
121
-
-
68449096896
-
-
Brown WD, Teuber, L, Dahl B. Neurosearch A/S. Novel KCNQ channel modulating compounds and their use. United States patent application WO2004/080377. September 23, 2004
-
Brown WD, Teuber, L, Dahl B. Neurosearch A/S. Novel KCNQ channel modulating compounds and their use. United States patent application WO2004/080377. September 23, 2004
-
-
-
-
122
-
-
68449088928
-
-
Attali B, Peretz, A. Ramot AT Tel Aviv University Ltd. Derivatives of N-phenylanthranilic acid and 2-benzimidazolon as potassium channel and/ or cortical neuron activity modulators. United States patent application WO2004/035037. April 29, 2004
-
Attali B, Peretz, A. Ramot AT Tel Aviv University Ltd. Derivatives of N-phenylanthranilic acid and 2-benzimidazolon as potassium channel and/ or cortical neuron activity modulators. United States patent application WO2004/035037. April 29, 2004
-
-
-
-
123
-
-
15744362456
-
Meclofenamic acid and diclofenac, novel templates of KCNQ2/Q3 potassium channel openers, depress cortical neuron activity and exhibit anticonvulsant properties
-
Peretz A, Degani N, Nachman R, Uziyel Y, Gibor G, Shabat D, et al. Meclofenamic acid and diclofenac, novel templates of KCNQ2/Q3 potassium channel openers, depress cortical neuron activity and exhibit anticonvulsant properties. Mol Pharmacol 2005; 67(4): 1053-66.
-
(2005)
Mol Pharmacol
, vol.67
, Issue.4
, pp. 1053-1066
-
-
Peretz, A.1
Degani, N.2
Nachman, R.3
Uziyel, Y.4
Gibor, G.5
Shabat, D.6
-
124
-
-
33846418401
-
Pre- and postsynaptic activation of M-channels by a novel opener dampens neuronal firing and transmitter release
-
Peretz A, Sheinin A, Yue C, Degani-Katzav N, Gibor G, Nachman R, et al. Pre- and postsynaptic activation of M-channels by a novel opener dampens neuronal firing and transmitter release. J Neurophysiol 2007; 97(1): 283-95.
-
(2007)
J Neurophysiol
, vol.97
, Issue.1
, pp. 283-295
-
-
Peretz, A.1
Sheinin, A.2
Yue, C.3
Degani-Katzav, N.4
Gibor, G.5
Nachman, R.6
-
125
-
-
68449098825
-
-
Welmaker GS, Wilson MA, McFarlane GR, Sabalski JE, Butera JA, Trybulski; EJ, Herbst DR;. Wyeth. Benzofurans as potassium channel modulators. United States patent application WO2008/0027049. January 31, 2008
-
Welmaker GS, Wilson MA, McFarlane GR, Sabalski JE, Butera JA, Trybulski; EJ, Herbst DR;. Wyeth. Benzofurans as potassium channel modulators. United States patent application WO2008/0027049. January 31, 2008
-
-
-
-
126
-
-
68449092651
-
-
Wilson MA, Welmaker GS, Trybulski EJ, Butera JA, Magolda RL; Wyeth. Tetracyclic indoles as potassium channel modulators. United States patent application WO2008/0027090. January 31, 2008.
-
Wilson MA, Welmaker GS, Trybulski EJ, Butera JA, Magolda RL; Wyeth. Tetracyclic indoles as potassium channel modulators. United States patent application WO2008/0027090. January 31, 2008.
-
-
-
-
127
-
-
68449101215
-
-
Li, M, Sun H, Xiong Q; The John Hopkins University. Method of treating KCNQ related disorders using organozinc compounds. United States patent application WO2007/087424. August 2, 2007
-
Li, M, Sun H, Xiong Q; The John Hopkins University. Method of treating KCNQ related disorders using organozinc compounds. United States patent application WO2007/087424. August 2, 2007
-
-
-
-
128
-
-
34247202495
-
Zinc pyrithione-mediated activation of voltage-gated KCNQ potassium channels rescues epileptogenic mutants
-
Xiong Q, Sun H, Li M. Zinc pyrithione-mediated activation of voltage-gated KCNQ potassium channels rescues epileptogenic mutants. Nat Chem Biol 2007; 3(5): 287-96.
-
(2007)
Nat Chem Biol
, vol.3
, Issue.5
, pp. 287-296
-
-
Xiong, Q.1
Sun, H.2
Li, M.3
-
129
-
-
32544435803
-
Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness
-
Kharkovets T, Dedek K, Maier H, Schweizer M, Khimich D, Nouvian R, et al. Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness. Embo J 2006; 25(3): 642-52.
-
(2006)
Embo J
, vol.25
, Issue.3
, pp. 642-652
-
-
Kharkovets, T.1
Dedek, K.2
Maier, H.3
Schweizer, M.4
Khimich, D.5
Nouvian, R.6
-
130
-
-
0018886033
-
Muscarinic suppression of a novel voltage-sensitive K+ current in a vertebrate neurone
-
Brown DA, Adams PR. Muscarinic suppression of a novel voltage-sensitive K+ current in a vertebrate neurone. Nature 1980; 283(5748): 673-6.
-
(1980)
Nature
, vol.283
, Issue.5748
, pp. 673-676
-
-
Brown, D.A.1
Adams, P.R.2
-
131
-
-
0035881421
-
Bradykinin activates airway parasympathetic ganglion neurons by inhibiting M-currents
-
Mochidome T, Ishibashi H, Takahama K. Bradykinin activates airway parasympathetic ganglion neurons by inhibiting M-currents. Neuroscience 2001; 105(3): 785-91.
-
(2001)
Neuroscience
, vol.105
, Issue.3
, pp. 785-791
-
-
Mochidome, T.1
Ishibashi, H.2
Takahama, K.3
-
132
-
-
50249146243
-
Bimodal effects of the Kv7 channel activator retigabine on vascular K+ currents
-
Yeung S, Schwake M, Pucovsky V, Greenwood I. Bimodal effects of the Kv7 channel activator retigabine on vascular K+ currents. Br J Pharmacol 2008; 155(1): 62-72.
-
(2008)
Br J Pharmacol
, vol.155
, Issue.1
, pp. 62-72
-
-
Yeung, S.1
Schwake, M.2
Pucovsky, V.3
Greenwood, I.4
-
133
-
-
44149085128
-
Expression profile and characterisation of a truncated KCNQ5 splice variant
-
Yeung SY, Lange W, Schwake M, Greenwood IA. Expression profile and characterisation of a truncated KCNQ5 splice variant. Biochem Biophys Res Commun 2008; 371(4): 741-6.
-
(2008)
Biochem Biophys Res Commun
, vol.371
, Issue.4
, pp. 741-746
-
-
Yeung, S.Y.1
Lange, W.2
Schwake, M.3
Greenwood, I.A.4
-
134
-
-
34447567309
-
Molecular expression and pharmacological identification of a role for K(v)7 channels in murine vascular reactivity
-
Yeung SY, Pucovsky V, Moffatt JD, Saldanha L, Schwake M, Ohya S, et al. Molecular expression and pharmacological identification of a role for K(v)7 channels in murine vascular reactivity. Br J Pharmacol 2007; 151(6): 758-70.
-
(2007)
Br J Pharmacol
, vol.151
, Issue.6
, pp. 758-770
-
-
Yeung, S.Y.1
Pucovsky, V.2
Moffatt, J.D.3
Saldanha, L.4
Schwake, M.5
Ohya, S.6
-
135
-
-
54349090357
-
Cardiovascular KCNQ (Kv7) Potassium Channels: Physiological Regulators and New Targets for Therapeutic Intervention
-
Mackie AR, Byron KL. Cardiovascular KCNQ (Kv7) Potassium Channels: Physiological Regulators and New Targets for Therapeutic Intervention. Mol Pharmacol 2008.
-
(2008)
Mol Pharmacol
-
-
Mackie, A.R.1
Byron, K.L.2
-
136
-
-
68449096288
-
-
Argentieri TM, Sheldon JH; Wyeth. Methods of selecting compounds for modulation of bladder function. United States patent US20077160684. January 9, 2007.
-
Argentieri TM, Sheldon JH; Wyeth. Methods of selecting compounds for modulation of bladder function. United States patent US20077160684. January 9, 2007.
-
-
-
-
137
-
-
27644446584
-
The KCNQ5 potassium channel from mouse: A broadly expressed Mcurrent like potassium channel modulated by zinc, pH, and volume changes
-
Jensen HS, Callo K, Jespersen T, Jensen BS, Olesen SP. The KCNQ5 potassium channel from mouse: A broadly expressed Mcurrent like potassium channel modulated by zinc, pH, and volume changes. Brain Res Mol Brain Res 2005; 139(1): 52-62.
-
(2005)
Brain Res Mol Brain Res
, vol.139
, Issue.1
, pp. 52-62
-
-
Jensen, H.S.1
Callo, K.2
Jespersen, T.3
Jensen, B.S.4
Olesen, S.P.5
-
138
-
-
4644244821
-
Potassium channel subtypes as molecular targets for overactive bladder and other urological disorders
-
Gopalakrishnan M, Shieh CC. Potassium channel subtypes as molecular targets for overactive bladder and other urological disorders. Expert Opin Ther Targets 2004; 8(5): 437-58.
-
(2004)
Expert Opin Ther Targets
, vol.8
, Issue.5
, pp. 437-458
-
-
Gopalakrishnan, M.1
Shieh, C.C.2
-
139
-
-
5444225675
-
Urodynamic effects of the K+ channel (KCNQ) opener retigabine in freely moving, conscious rats
-
Streng T, Christoph T, Andersson KE. Urodynamic effects of the K+ channel (KCNQ) opener retigabine in freely moving, conscious rats. J Urol 2004; 172(5 Pt 1): 2054-8.
-
(2004)
J Urol
, vol.172
, Issue.5 PART 1
, pp. 2054-2058
-
-
Streng, T.1
Christoph, T.2
Andersson, K.E.3
-
140
-
-
48749121762
-
The molecular epidemiology of pain: A new discipline for drug discovery
-
Max MB, Stewart WF. The molecular epidemiology of pain: A new discipline for drug discovery. Nat Rev Drug Discov 2008; 7(8): 647-58.
-
(2008)
Nat Rev Drug Discov
, vol.7
, Issue.8
, pp. 647-658
-
-
Max, M.B.1
Stewart, W.F.2
-
141
-
-
39449097036
-
TRPV1 receptors in the central nervous system: Potential for previously unforeseen therapeutic applications
-
Starowicz K, Cristino L, Di Marzo V. TRPV1 receptors in the central nervous system: Potential for previously unforeseen therapeutic applications. Curr Pharm Des 2008; 14(1): 42-54.
-
(2008)
Curr Pharm Des
, vol.14
, Issue.1
, pp. 42-54
-
-
Starowicz, K.1
Cristino, L.2
Di Marzo, V.3
-
142
-
-
48949117566
-
Chronic inflammatory pain and the neurovascular unit: A central role for glia in maintaining BBB integrity?
-
Willis CL, Davis TP. Chronic inflammatory pain and the neurovascular unit: A central role for glia in maintaining BBB integrity? Curr Pharm Des 2008; 14(16): 1625-43.
-
(2008)
Curr Pharm Des
, vol.14
, Issue.16
, pp. 1625-1643
-
-
Willis, C.L.1
Davis, T.P.2
|