-
4
-
-
66349089328
-
Genetic deficit of SK3 and IK1 channels disrupts the endothelium-derived hyperpolarizing factor vasodilator pathway and causes hypertension
-
Brähler S, Kaistha A, Schmidt VJ, Wölfle SE, Busch C, Kaistha BP, Kacik M, Hasenau AL, Grgic I, and Si H et al. (2009) Genetic deficit of SK3 and IK1 channels disrupts the endothelium-derived hyperpolarizing factor vasodilator pathway and causes hypertension. Circulation 119:2323-2332.
-
(2009)
Circulation
, vol.119
, pp. 2323-2332
-
-
Brähler, S.1
Kaistha, A.2
Schmidt, V.J.3
Wölfle, S.E.4
Busch, C.5
Kaistha, B.P.6
Kacik, M.7
Hasenau, A.L.8
Grgic, I.9
Si, H.10
-
5
-
-
84906317786
-
Positive KCa channel gating modulators with selectivity for KCa3.1
-
Brown BM, Coleman N, Oliván-Viguera A, Köhler R, Wulff H (2014) Positive KCa channel gating modulators with selectivity for KCa3.1. FASEB J 28:1057.6.
-
(2014)
FASEB J
, vol.28
-
-
Brown, B.M.1
Coleman, N.2
Oliván-Viguera, A.3
Köhler, R.4
Wulff, H.5
-
8
-
-
77954812252
-
Calcium-activated potassium channels - A therapeutic target for modulating nitric oxide in cardiovascular disease?
-
Dalsgaard T, Kroigaard C, and Simonsen U (2010) Calcium-activated potassium channels - a therapeutic target for modulating nitric oxide in cardiovascular disease? Expert Opin Ther Targets 14:825-837.
-
(2010)
Expert Opin Ther Targets
, vol.14
, pp. 825-837
-
-
Dalsgaard, T.1
Kroigaard, C.2
Simonsen, U.3
-
9
-
-
81555229242
-
Pharmacological activation of KCa3.1/KCa2.3 channels produces endothelial hyperpolarization and lowers blood pressure in conscious dogs
-
Damkjaer M, Nielsen G, Bodendiek S, Staehr M, Gramsbergen JB, de Wit C, Jensen BL, Simonsen U, Bie P, and Wulff H et al. (2012) Pharmacological activation of KCa3.1/KCa2.3 channels produces endothelial hyperpolarization and lowers blood pressure in conscious dogs. Br J Pharmacol 165:223-234.
-
(2012)
Br J Pharmacol
, vol.165
, pp. 223-234
-
-
Damkjaer, M.1
Nielsen, G.2
Bodendiek, S.3
Staehr, M.4
Gramsbergen, J.B.5
De Wit, C.6
Jensen, B.L.7
Simonsen, U.8
Bie, P.9
Wulff, H.10
-
10
-
-
0027213025
-
Inhibition by riluzole of electrophysiological responses mediated by rat kainate and NMDA receptors expressed in Xenpus oocytes
-
Debono MW, Le Guern J, Canton T, Doble A, and Pradier L (1993) Inhibition by riluzole of electrophysiological responses mediated by rat kainate and NMDA receptors expressed in Xenopus oocytes. Eur J Pharmacol 235:283-289. (Pubitemid 23130445)
-
(1993)
European Journal of Pharmacology
, vol.235
, Issue.2-3
, pp. 283-289
-
-
Debono, M.-W.1
Le, G.J.2
Canton, T.3
Doble, A.4
Pradier, L.5
-
13
-
-
77955292086
-
Endothelium-derived hyperpolarising factors and associated pathways: A synopsis
-
Edwards G, Félétou M, and Weston AH (2010) Endothelium-derived hyperpolarising factors and associated pathways: a synopsis. Pflugers Arch 459:863 -879.
-
(2010)
Pflugers Arch
, vol.459
, pp. 863-879
-
-
Edwards, G.1
Félétou, M.2
Weston, A.H.3
-
14
-
-
0033605385
-
Calmodulin mediates calcium-dependent activation of the intermediate conductance K(Ca) channel, IKCa1
-
DOI 10.1074/jbc.274.9.5746
-
Fanger CM, Ghanshani S, Logsdon NJ, Rauer H, Kalman K, Zhou J, Beckingham K, Chandy KG, Cahalan MD, and Aiyar J (1999) Calmodulin mediates calcium-dependent activation of the intermediate conductance KCa channel, IKCa1. J Biol Chem 274:5746-5754. (Pubitemid 29109229)
-
(1999)
Journal of Biological Chemistry
, vol.274
, Issue.9
, pp. 5746-5754
-
-
Fanger, C.M.1
Ghanshani, S.2
Logsdon, N.J.3
Rauer, H.4
Kalman, K.5
Zhou, J.6
Beckingham, K.7
Chandy, K.G.8
Cahalan, M.D.9
Aiyar, J.10
-
16
-
-
84893123362
-
Aromatic-aromatic interactions between residues in KCa3.1 pore helix and S5 transmembrane segment control the channel gating process
-
Garneau L, Klein H, Lavoie MF, Brochiero E, Parent L, and Sauvé R (2014) Aromatic-aromatic interactions between residues in KCa3.1 pore helix and S5 transmembrane segment control the channel gating process. J Gen Physiol 143:289-307.
-
(2014)
J Gen Physiol
, vol.143
, pp. 289-307
-
-
Garneau, L.1
Klein, H.2
Lavoie, M.F.3
Brochiero, E.4
Parent, L.5
Sauvé, R.6
-
17
-
-
0035815729
-
+ channel, hIK1, is conferred by a C-terminal domain
-
+ channel, hIK1, is conferred by a C-terminal domain. J Biol Chem 276:10963-10970.
-
(2001)
J Biol Chem
, vol.276
, pp. 10963-10970
-
-
Gerlach, A.C.1
Syme, C.A.2
Giltinan, L.3
Adelman, J.P.4
Devor, D.C.5
-
18
-
-
13844310156
-
Synthesis and biological evaluation of 2-aminothiazoles and their amide derivatives on human adenosine receptors. Lack of effect of 2-aminothiazoles as allosteric enhancers
-
DOI 10.1016/j.bmc.2005.01.006
-
Göblyös A, Santiago SN, Pietra D, Mulder-Krieger T, von Frijtag Drabbe Künzel J, Brussee J, and Ijzerman AP (2005) Synthesis and biological evaluation of 2-aminothiazoles and their amide derivatives on human adenosine receptors. Lack of effect of 2-aminothiazoles as allosteric enhancers. Bioorg Med Chem 13:2079-2087. (Pubitemid 40261128)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.6
, pp. 2079-2087
-
-
Goblyos, A.1
Santiago, S.N.2
Pietra, D.3
Mulder-Krieger, T.4
Kunzel, J.V.F.D.5
Brussee, J.6
Ijzerman, A.P.7
-
19
-
-
70349895458
-
Endothelial Ca+-activated K+ channels in normal and impaired EDHF-dilator responses: Relevance to cardiovascular pathologies and drug discovery
-
Grgic I, Kaistha BP, Hoyer J, and Köhler R (2009) Endothelial Ca+-activated K+ channels in normal and impaired EDHF-dilator responses: relevance to cardiovascular pathologies and drug discovery. Br J Pharmacol 157:509-526.
-
(2009)
Br J Pharmacol
, vol.157
, pp. 509-526
-
-
Grgic, I.1
Kaistha, B.P.2
Hoyer, J.3
Köhler, R.4
-
20
-
-
0028228251
-
+ channels, types Kv1.1, 1.2, 1.3, 1.5, and 3.1, stably expressed in mammalian cell lines
-
+ channels, types Kv1.1, 1.2, 1.3, 1.5, and 3.1, stably expressed in mammalian cell lines. Mol Pharmacol 45:1227-1234.
-
(1994)
Mol Pharmacol
, vol.45
, pp. 1227-1234
-
-
Grissmer, S.1
Nguyen, A.N.2
Aiyar, J.3
Hanson, D.C.4
Mather, R.J.5
Gutman, G.A.6
Karmilowicz, M.J.7
Auperin, D.D.8
Chandy, K.G.9
-
21
-
-
0034982903
-
Pharmacological modulation of SK3 channels
-
DOI 10.1016/S0028-3908(01)00028-4, PII S0028390801000284
-
Grunnet M, Jespersen T, Angelo K, Frøkjaer-Jensen C, Klaerke DA, Olesen SP, and Jensen BS (2001) Pharmacological modulation of SK3 channels. Neuropharmacology 40:879-887. (Pubitemid 32510801)
-
(2001)
Neuropharmacology
, vol.40
, Issue.7
, pp. 879-887
-
-
Grunnet, M.1
Jespersen, T.2
Angelo, K.3
Frokjaer-Jensen, C.4
Klaerke, D.A.5
Olesen, S.-P.6
Jensen, B.S.7
-
22
-
-
34347330165
-
+ channels
-
+ channels. Br J Pharmacol 151:655-665.
-
(2007)
Br J Pharmacol
, vol.151
, pp. 655-665
-
-
Hougaard, C.1
Eriksen, B.L.2
Jørgensen, S.3
Johansen, T.H.4
Dyhring, T.5
Madsen, L.S.6
Strøbaek, D.7
Christophersen, P.8
-
23
-
-
84856068484
-
Evidence for a common pharmacological interaction site on K(Ca)2 channels providing both selective activation and selective inhibition of the human K(Ca)2.1 subtype
-
Hougaard C, Hammami S, Eriksen BL, Sørensen US, Jensen ML, Strøbæk D, and Christophersen P (2012) Evidence for a common pharmacological interaction site on K(Ca)2 channels providing both selective activation and selective inhibition of the human K(Ca)2.1 subtype. Mol Pharmacol 81:210-219.
-
(2012)
Mol Pharmacol
, vol.81
, pp. 210-219
-
-
Hougaard, C.1
Hammami, S.2
Eriksen, B.L.3
Sørensen, U.S.4
Jensen, M.L.5
Strøbæk, D.6
Christophersen, P.7
-
24
-
-
69649091600
-
+ channels by 4-(2- methoxyphenylcarbamoyloxymethyl)- piperidine-1-carboxylic acid tert-butyl ester (GW542573X) is dependent on serine 293 in the S5 segment
-
+ channels by 4-(2-methoxyphenylcarbamoyloxymethyl)- piperidine-1-carboxylic acid tert-butyl ester (GW542573X) is dependent on serine 293 in the S5 segment. Mol Pharmacol 76:569-578.
-
(2009)
Mol Pharmacol
, vol.76
, pp. 569-578
-
-
Hougaard, C.1
Jensen, M.L.2
Dale, T.J.3
Miller, D.D.4
Davies, D.J.5
Eriksen, B.L.6
Strøbaek, D.7
Trezise, D.J.8
Christophersen, P.9
-
25
-
-
84890903984
-
Development of a QPatch automated electrophysiology assay for identifying KCa3.1 inhibitors and activators
-
Jenkins DP, Yu W, Brown BM, Løjkner LD, and Wulff H (2013) Development of a QPatch automated electrophysiology assay for identifying KCa3.1 inhibitors and activators. Assay Drug Dev Technol 11:551-560.
-
(2013)
Assay Drug Dev Technol
, vol.11
, pp. 551-560
-
-
Jenkins, D.P.1
Yu, W.2
Brown, B.M.3
Løjkner, L.D.4
Wulff, H.5
-
26
-
-
0030987549
-
hSK4, a member of a novel subfamily of calcium-activated potassium channels
-
DOI 10.1073/pnas.94.20.11013
-
Joiner WJ, Wang LY, Tang MD, and Kaczmarek LK (1997) hSK4, a member of a novel subfamily of calcium-activated potassium channels. Proc Natl Acad Sci USA 94:11013-11018. (Pubitemid 27430852)
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, Issue.20
, pp. 11013-11018
-
-
Joiner, W.J.1
Wang, L.U.-Y.2
Tang, M.D.3
Kaczmarek, L.K.4
-
28
-
-
0142227938
-
Efficient Conversion of Substituted Aryl Thioureas to 2-Aminobenzothiazoles Using Benzyltrimethylammonium Tribromide
-
DOI 10.1021/jo0349431
-
Jordan AD, Luo C, and Reitz AB (2003) Efficient conversion of substituted aryl thioureas to 2-aminobenzothiazoles using benzyltrimethylammonium tribromide. J Org Chem 68:8693-8696. (Pubitemid 37329133)
-
(2003)
Journal of Organic Chemistry
, vol.68
, Issue.22
, pp. 8693-8696
-
-
Jordan, A.D.1
Luo, C.2
Reitz, A.B.3
-
29
-
-
84868015420
-
Selective positive modulator of calcium-activated potassium channels exerts beneficial effects in a mouse model of spinocerebellar ataxia type 2
-
Kasumu AW, Hougaard C, Rode F, Jacobsen TA, Sabatier JM, Eriksen BL, Strøbæk D, Liang X, Egorova P, and Vorontsova D et al. (2012) Selective positive modulator of calcium-activated potassium channels exerts beneficial effects in a mouse model of spinocerebellar ataxia type 2. Chem Biol 19:1340-1353.
-
(2012)
Chem Biol
, vol.19
, pp. 1340-1353
-
-
Kasumu, A.W.1
Hougaard, C.2
Rode, F.3
Jacobsen, T.A.4
Sabatier, J.M.5
Eriksen, B.L.6
Strøbæk, D.7
Liang, X.8
Egorova, P.9
Vorontsova, D.10
-
30
-
-
33947714200
-
Structural determinants of the closed KCa3.1 channel pore in relation to channel gating: Results from a substituted cysteine accessibility analysis
-
DOI 10.1085/jgp.200609726
-
Klein H, Garneau L, Banderali U, Simoes M, Parent L, and Sauvé R (2007) Structural determinants of the closed KCa3.1 channel pore in relation to channel gating: results from a substituted cysteine accessibility analysis. J Gen Physiol 129:299-315. (Pubitemid 46506981)
-
(2007)
Journal of General Physiology
, vol.129
, Issue.4
, pp. 299-315
-
-
Klein, H.1
Garneau, L.2
Banderali, U.3
Simoes, M.4
Parent, L.5
Sauve, R.6
-
31
-
-
0029796983
-
Small-conductance, calcium-activated potassium channels from mammalian brain
-
Köhler M, Hirschberg B, Bond CT, Kinzie JM, Marrion NV, Maylie J, and Adelman JP (1996) Small-conductance, calcium-activated potassium channels from mammalian brain. Science 273:1709-1714. (Pubitemid 26317786)
-
(1996)
Science
, vol.273
, Issue.5282
, pp. 1709-1714
-
-
Kohler, M.1
Hirschberg, B.2
Bond, C.T.3
Kinzie, J.M.4
Marrion, N.V.5
Maylie, J.6
Adelman, J.P.7
-
32
-
-
84906315551
-
Cardiovascular alterations in KCa3.1/KCa2.3-deficient mice and after acute treatment with KCa3.1/KCa2.3 activators
-
Feletou M, Vanhoutte PM (eds) Vaux-de-Cernay, France
-
Köhler R (2012) Cardiovascular alterations in KCa3.1/KCa2.3- deficient mice and after acute treatment with KCa3.1/KCa2.3 activators. EDHF 2012: 10th Anniversary Meeting June 27th-30th, 2012; Feletou M, Vanhoutte PM (eds) vol. 49, pp 1-54 Vaux-de-Cernay, France.
-
(2012)
EDHF 2012: 10th Anniversary Meeting June 27th-30th, 2012
, vol.49
, pp. 1-54
-
-
Köhler, R.1
-
33
-
-
74949130493
-
Vascular KCa-channels as therapeutic targets in hypertension and restenosis disease
-
Köhler R, Kaistha BP, and Wulff H (2010) Vascular KCa-channels as therapeutic targets in hypertension and restenosis disease. Expert Opin Ther Targets 14:143-155.
-
(2010)
Expert Opin Ther Targets
, vol.14
, pp. 143-155
-
-
Köhler, R.1
Kaistha, B.P.2
Wulff, H.3
-
34
-
-
70349641039
-
EF hands at the N-lobe of calmodulin are required for both SK channel gating and stable SK-calmodulin interaction
-
Li W, Halling DB, Hall AW, and Aldrich RW (2009) EF hands at the N-lobe of calmodulin are required for both SK channel gating and stable SK-calmodulin interaction. J Gen Physiol 134:281-293.
-
(2009)
J Gen Physiol
, vol.134
, pp. 281-293
-
-
Li, W.1
Halling, D.B.2
Hall, A.W.3
Aldrich, R.W.4
-
35
-
-
64549097688
-
Endothelium-derived hyperpolarizing factor mediated relaxations in pig coronary arteries do not involve Gi/o proteins
-
Ng KF, Leung SW, Man RY, and Vanhoutte PM (2008) Endothelium-derived hyperpolarizing factor mediated relaxations in pig coronary arteries do not involve Gi/o proteins. Acta Pharmacol Sin 29:1419-1424.
-
(2008)
Acta Pharmacol Sin
, vol.29
, pp. 1419-1424
-
-
Ng, K.F.1
Leung, S.W.2
Man, R.Y.3
Vanhoutte, P.M.4
-
36
-
-
0035971096
-
+ channels
-
+ channels. J Biol Chem 276:9762-9769.
-
(2001)
J Biol Chem
, vol.276
, pp. 9762-9769
-
-
Pedarzani, P.1
Mosbacher, J.2
Rivard, A.3
Cingolani, L.A.4
Oliver, D.5
Stocker, M.6
Adelman, J.P.7
Fakler, B.8
-
37
-
-
84883260008
-
Activation of KCa3.1 by SKA-31 induces arteriolar dilatation and lowers blood pressure in normo- and hypertensive connexin40-deficient mice
-
Radtke J, Schmidt K, Wulff H, Köhler R, and de Wit C (2013) Activation of KCa3.1 by SKA-31 induces arteriolar dilatation and lowers blood pressure in normo- and hypertensive connexin40-deficient mice. Br J Pharmacol 170:293-303.
-
(2013)
Br J Pharmacol
, vol.170
, pp. 293-303
-
-
Radtke, J.1
Schmidt, K.2
Wulff, H.3
Köhler, R.4
De Wit, C.5
-
38
-
-
0031603012
-
+ channel
-
Rosa JC, Galanakis D, Ganellin CR, Dunn PM, and Jenkinson DH (1998) Bis-quinolinium cyclophanes: 6,10-diaza-3(1,3),8(1,4)-dibenzena-1,5(1,4)- diquinolinacyclodecaphane (UCL 1684), the first nanomolar, non-peptidic blocker of the apamin-sensitive Ca(2+)-activated K+ channel. J Med Chem 41:2-5. (Pubitemid 128719272)
-
(1998)
Journal of Medicinal Chemistry
, vol.41
, Issue.1
, pp. 2-5
-
-
Rosa, J.C.1
Galanakis, D.2
Ganellin, C.R.3
Dunn, P.M.4
Jenkinson, D.H.5
-
39
-
-
59449098672
-
Naphtho[1,2-d]thiazol-2-ylamine (SKA-31), a new activator of KCa2 and KCa3.1 potassium channels, potentiates the endothelium-derived hyperpolarizing factor response and lowers blood pressure
-
Sankaranarayanan A, Raman G, Busch C, Schultz T, Zimin PI, Hoyer J, Köhler R, and Wulff H (2009) Naphtho[1,2-d]thiazol-2-ylamine (SKA-31), a new activator of KCa2 and KCa3.1 potassium channels, potentiates the endothelium-derived hyperpolarizing factor response and lowers blood pressure. Mol Pharmacol 75:281-295.
-
(2009)
Mol Pharmacol
, vol.75
, pp. 281-295
-
-
Sankaranarayanan, A.1
Raman, G.2
Busch, C.3
Schultz, T.4
Zimin, P.I.5
Hoyer, J.6
Köhler, R.7
Wulff, H.8
-
40
-
-
27544454783
-
Design of PAP-1, a selective small molecule Kv1.3 blocker, for the suppression of effector memory t cells in autoimmune diseases
-
DOI 10.1124/mol.105.015669
-
Schmitz A, Sankaranarayanan A, Azam P, Schmidt-Lassen K, Homerick D, Hänsel W, and Wulff H (2005) Design of PAP-1, a selective small molecule Kv1.3 blocker, for the suppression of effector memory T cells in autoimmune diseases. Mol Pharmacol 68:1254-1270. (Pubitemid 41539982)
-
(2005)
Molecular Pharmacology
, vol.68
, Issue.5
, pp. 1254-1270
-
-
Schmitz, A.1
Sankaranarayanan, A.2
Azam, P.3
Schmidt-Lassen, K.4
Homerick, D.5
Hansel, W.6
Wulff, H.7
-
41
-
-
0015882117
-
[2-Aminooxazoles and 2-iminooxazolines. 1: Reaction of racemic alpha-methylaminopropiophenone using cyanobromide]
-
Schuart J and Müller HK (1973) [2-Aminooxazoles and 2-iminooxazolines. 1: reaction of racemic alpha-methylaminopropiophenone using cyanobromide]. Pharmazie 28:438-439.
-
(1973)
Pharmazie
, vol.28
, pp. 438-439
-
-
Schuart, J.1
Müller, H.K.2
-
42
-
-
37549039510
-
A short history of SHELX
-
Sheldrick GM (2008) A short history of SHELX. Acta Crystallogr A 64:112-122.
-
(2008)
Acta Crystallogr A
, vol.64
, pp. 112-122
-
-
Sheldrick, G.M.1
-
43
-
-
0035146762
-
Benzimidazolone activators of chloride secretion: Potentialtherapeutics for cystic fibrosis and chronic obstructive pulmonarydisease
-
Singh S, Syme CA, Singh AK, Devor DC, and Bridges RJ (2001) Benzimidazolone activators of chloride secretion: potential therapeutics for cystic fibrosis and chronic obstructive pulmonary disease. J Pharmacol Exp Ther 296:600-611. (Pubitemid 32112491)
-
(2001)
Journal of Pharmacology and Experimental Therapeutics
, vol.296
, Issue.2
, pp. 600-611
-
-
Singh, S.1
Syme, C.A.2
Singh, A.K.3
Devor, D.C.4
Bridges, R.J.5
-
44
-
-
4644325419
-
+ channels by NS309 (6,7-dichloro-1H-indole-2,3-dione 3-oxime)
-
+ channels by NS309 (6,7-dichloro-1H-indole-2,3-dione 3-oxime). Biochim Biophys Acta 1665:1-5.
-
(2004)
Biochim Biophys Acta
, vol.1665
, pp. 1-5
-
-
Strøbaek, D.1
Teuber, L.2
Jørgensen, T.D.3
Ahring, P.K.4
Kjaer, K.5
Hansen, R.S.6
Olesen, S.P.7
Christophersen, P.8
Skaaning-Jensen, B.9
-
45
-
-
29844439979
-
International Union of Pharmacology. LII. Nomenclature and molecular relationships of calcium-activated potassium channels
-
DOI 10.1124/pr.57.4.9
-
Wei AD, Gutman GA, Aldrich R, Chandy KG, Grissmer S, and Wulff H (2005) International Union of Pharmacology. LII. Nomenclature and molecular relationships of calcium-activated potassium channels. Pharmacol Rev 57:463-472. (Pubitemid 43036436)
-
(2005)
Pharmacological Reviews
, vol.57
, Issue.4
, pp. 463-472
-
-
Wei, A.D.1
Gutman, G.A.2
Aldrich, R.3
Chandy, K.G.4
Grissmer, S.5
Wulff, H.6
-
46
-
-
84873414518
-
Endothelial small-conductance and intermediate-conductance KCa channels: An update on their pharmacology and usefulness as cardiovascular targets
-
Wulff H and Köhler R (2013) Endothelial small-conductance and intermediate-conductance KCa channels: an update on their pharmacology and usefulness as cardiovascular targets. J Cardiovasc Pharmacol 61:102-112.
-
(2013)
J Cardiovasc Pharmacol
, vol.61
, pp. 102-112
-
-
Wulff, H.1
Köhler, R.2
-
47
-
-
0034608869
-
+ channel, IKCa1: A potential immunosuppressant
-
+ channel, IKCa1: a potential immunosuppressant. Proc Natl Acad Sci USA 97:8151-8156.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 8151-8156
-
-
Wulff, H.1
Miller, M.J.2
Hansel, W.3
Grissmer, S.4
Cahalan, M.D.5
Chandy, K.G.6
-
48
-
-
44849093511
-
+ channel modulators for the treatment of neurological disorders and autoimmune diseases
-
+ channel modulators for the treatment of neurological disorders and autoimmune diseases. Chem Rev 108:1744-1773.
-
(2008)
Chem Rev
, vol.108
, pp. 1744-1773
-
-
Wulff, H.1
Zhorov, B.S.2
-
49
-
-
0032189766
-
Mechanism of calcium gating in small-conductance calcium-activated potassium channels
-
DOI 10.1038/26758
-
Xia XM, Fakler B, Rivard A, Wayman G, Johnson-Pais T, Keen JE, Ishii T, Hirschberg B, Bond CT, and Lutsenko S et al. (1998) Mechanism of calcium gating in small-conductance calcium-activated potassium channels. Nature 395:503-507. (Pubitemid 28462445)
-
(1998)
Nature
, vol.395
, Issue.6701
, pp. 503-507
-
-
Xia, X.-M.1
Fakler, B.2
Rivard, A.3
Wayman, G.4
Johnson-Pais, T.5
Keen, J.E.6
Ishii, T.7
Hirschberg, B.8
Bond, C.T.9
Lutsenko, S.10
Maylie, J.11
Adelman, J.P.12
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