-
1
-
-
0010452459
-
Nitrendipine block of cardiac calcium channels: High-affinity binding to the inactivated state
-
Bean, B.P. 1984. Nitrendipine block of cardiac calcium channels: high-affinity binding to the inactivated state. Proc. Natl. Acad. Sci. USA. 81:6388-6392.
-
(1984)
Proc. Natl. Acad. Sci. USA
, vol.81
, pp. 6388-6392
-
-
Bean, B.P.1
-
2
-
-
0020624782
-
Lidocaine block of cardiac sodium channels
-
Bean, B.P., C.J. Cohen, and R.W. Tsien. 1983. Lidocaine block of cardiac sodium channels. J. Gen. Physiol. 81:613-642.
-
(1983)
J. Gen. Physiol
, vol.81
, pp. 613-642
-
-
Bean, B.P.1
Cohen, C.J.2
Tsien, R.W.3
-
3
-
-
0029946602
-
Adjacent porelining residues within sodium channels identified by paired cysteine mutagenesis
-
Béinitah, J.-P., G.F. Tomaselli, and E. Marban. 1996. Adjacent porelining residues within sodium channels identified by paired cysteine mutagenesis. Proc. Natl. Acad. Sci. USA. 93:7392-7396.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 7392-7396
-
-
Béinitah, J.-P.1
Tomaselli, G.F.2
Marban, E.3
-
4
-
-
0031972937
-
-
Benzinger, G.R., J.W. Kyle, K.M. Blumenthal, and D.A. Hanck. 1998. A specific interaction between the cardiac sodium channel and site-3 toxin anthopleurin B. J. Biol. Chem. 273:80-84.
-
Benzinger, G.R., J.W. Kyle, K.M. Blumenthal, and D.A. Hanck. 1998. A specific interaction between the cardiac sodium channel and site-3 toxin anthopleurin B. J. Biol. Chem. 273:80-84.
-
-
-
-
5
-
-
0025263891
-
Molecular mechanisms of local anesthesia: A review
-
Butterworth, J.F., and G.R. Strichartz. 1990. Molecular mechanisms of local anesthesia: a review. Anesthesiology. 72:711-734.
-
(1990)
Anesthesiology
, vol.72
, pp. 711-734
-
-
Butterworth, J.F.1
Strichartz, G.R.2
-
6
-
-
0021504608
-
The use of double mutants to detect structural changes in the active site of the tyrosyl-tRNA synthetase (Bacillus stearothermophilus)
-
Carter, P.J., G. Winter, A.J. Wilkinson, and A.R. Fersht. 1984. The use of double mutants to detect structural changes in the active site of the tyrosyl-tRNA synthetase (Bacillus stearothermophilus). Cell. 38:835-840.
-
(1984)
Cell
, vol.38
, pp. 835-840
-
-
Carter, P.J.1
Winter, G.2
Wilkinson, A.J.3
Fersht, A.R.4
-
7
-
-
0028326016
-
Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation
-
Chahine, M., A.L. George, M. Zhou, S.J.W. Sun, R.L. Barchi, and R. Horn. 1994. Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation. Neuron. 12:281-294.
-
(1994)
Neuron
, vol.12
, pp. 281-294
-
-
Chahine, M.1
George, A.L.2
Zhou, M.3
Sun, S.J.W.4
Barchi, R.L.5
Horn, R.6
-
8
-
-
0030453610
-
A unique role for the S4 segment of domain 4 in the inactivation of sodium channels
-
Chen, L.-Q., V. Santarelli, R. Horn, and R.G. Kallen. 1996. A unique role for the S4 segment of domain 4 in the inactivation of sodium channels. J. Gen. Physiol. 108:549-556.
-
(1996)
J. Gen. Physiol
, vol.108
, pp. 549-556
-
-
Chen, L.-Q.1
Santarelli, V.2
Horn, R.3
Kallen, R.G.4
-
9
-
-
35548983328
-
Design of a specific activator for skeletal muscle sodium channels uncovers channel architecture
-
Cohen, L., N. Ilan, M. Gur, W. Stühmer, D. Gordon, and M. Gurevitz. 2007. Design of a specific activator for skeletal muscle sodium channels uncovers channel architecture. J. Biol. Chem. 282:29424-29430.
-
(2007)
J. Biol. Chem
, vol.282
, pp. 29424-29430
-
-
Cohen, L.1
Ilan, N.2
Gur, M.3
Stühmer, W.4
Gordon, D.5
Gurevitz, M.6
-
10
-
-
0018245196
-
The rate of interaction of local anesthetics with sodium channels in nerve
-
Courtney, K.R., J.J. Kendig, and E.N. Cohen. 1978. The rate of interaction of local anesthetics with sodium channels in nerve. J. Pharmacol. Exp. Ther. 207:594-604.
-
(1978)
J. Pharmacol. Exp. Ther
, vol.207
, pp. 594-604
-
-
Courtney, K.R.1
Kendig, J.J.2
Cohen, E.N.3
-
11
-
-
0043202587
-
State-dependent access to the batrachotoxin receptor on the sodium channel
-
De Leon, L., and D.S. Ragsdale. 2003. State-dependent access to the batrachotoxin receptor on the sodium channel. Neuroreport. 14:1353-1356.
-
(2003)
Neuroreport
, vol.14
, pp. 1353-1356
-
-
De Leon, L.1
Ragsdale, D.S.2
-
14
-
-
13444262028
-
Recognition of transmembrane helices by the endoplasmic reticulum translocon
-
Hessa, T., H. Kim, K. Bihlmaier, C. Lundin, J. Boekel, H. Andersson, I. Nilsson, S.H. White, and G. von Heijne. 2005. Recognition of transmembrane helices by the endoplasmic reticulum translocon. Nature. 433:377-381.
-
(2005)
Nature
, vol.433
, pp. 377-381
-
-
Hessa, T.1
Kim, H.2
Bihlmaier, K.3
Lundin, C.4
Boekel, J.5
Andersson, H.6
Nilsson, I.7
White, S.H.8
von Heijne, G.9
-
15
-
-
0035958956
-
The selectivity filter of the voltage-gated sodium channel is involved in channel activation
-
Hilber, K., W. Sandtner, O. Kudlacek, I.W. Glaaser, E. Weisz, J.W. Kyle, R.J. French, H.A. Fozzard, S.C. Dudley, and H. Todt. 2001. The selectivity filter of the voltage-gated sodium channel is involved in channel activation. J. Biol. Chem. 276:27831-27839.
-
(2001)
J. Biol. Chem
, vol.276
, pp. 27831-27839
-
-
Hilber, K.1
Sandtner, W.2
Kudlacek, O.3
Glaaser, I.W.4
Weisz, E.5
Kyle, J.W.6
French, R.J.7
Fozzard, H.A.8
Dudley, S.C.9
Todt, H.10
-
16
-
-
0017332486
-
Local anesthetics: Hydrophilic and hydrophobic pathways for the drug-receptor reaction
-
Hille, B. 1977. Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction. J. Gen. Physiol. 69:497-515.
-
(1977)
J. Gen. Physiol
, vol.69
, pp. 497-515
-
-
Hille, B.1
-
17
-
-
34447135007
-
Role of aromatic side chains in the folding and thermodynamic stability of integral membrane proteins
-
Hong, H., S. Park, R.H.F. Jiménez, D. Rinehart, and L.K. Tamm. 2007. Role of aromatic side chains in the folding and thermodynamic stability of integral membrane proteins. J. Am. Chem. Soc. 129:8320-8327.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 8320-8327
-
-
Hong, H.1
Park, S.2
Jiménez, R.H.F.3
Rinehart, D.4
Tamm, L.K.5
-
18
-
-
0034284386
-
How proteins adapt to a membrane-water interface
-
Killian, J.A., and G. von Heijne. 2000. How proteins adapt to a membrane-water interface. Trends Biochem. Sci. 25:429-434.
-
(2000)
Trends Biochem. Sci
, vol.25
, pp. 429-434
-
-
Killian, J.A.1
von Heijne, G.2
-
19
-
-
0343152628
-
Movement of voltage sensor S4 in domain 4 is tightly coupled to sodium channel fast inactivation and gating charge immobilization
-
Kühn, F.J.P., and N.G. Greeff. 1999. Movement of voltage sensor S4 in domain 4 is tightly coupled to sodium channel fast inactivation and gating charge immobilization. J. Gen. Physiol. 114:167-183.
-
(1999)
J. Gen. Physiol
, vol.114
, pp. 167-183
-
-
Kühn, F.J.P.1
Greeff, N.G.2
-
20
-
-
0031754721
-
A common anticonvulsant binding site for phenytoin, carbamazepine, and lamotrigine in neuronal Na+ channels
-
Kuo, C.-C. 1998a. A common anticonvulsant binding site for phenytoin, carbamazepine, and lamotrigine in neuronal Na+ channels. Mol. Pharmacol. 54:712-721.
-
(1998)
Mol. Pharmacol
, vol.54
, pp. 712-721
-
-
Kuo, C.-C.1
-
21
-
-
0031738322
-
Imipramine inhibition of transient K+ current: An open-channel blocker preventing fast inactivation
-
Kuo, C.-C. 1998b. Imipramine inhibition of transient K+ current: an open-channel blocker preventing fast inactivation. Biophys. J. 75:2845-2857.
-
(1998)
Biophys. J
, vol.75
, pp. 2845-2857
-
-
Kuo, C.-C.1
-
22
-
-
0028072470
-
Slow binding of phenytoin to inactivated sodium channels in rat hippocampal neurons
-
Kuo, C.-C., and B.P. Bean. 1994. Slow binding of phenytoin to inactivated sodium channels in rat hippocampal neurons. Mol. Pharmacol. 46:716-725.
-
(1994)
Mol. Pharmacol
, vol.46
, pp. 716-725
-
-
Kuo, C.-C.1
Bean, B.P.2
-
23
-
-
0030787547
-
+ channels in rat hippocampal neurons
-
+ channels in rat hippocampal neurons. Br. J. Pharmacol. 121:1231-1238.
-
(1997)
Br. J. Pharmacol
, vol.121
, pp. 1231-1238
-
-
Kuo, C.-C.1
Lu, L.2
-
24
-
-
0030949912
-
+ currents: Quantitative distinction from phenytoin and possible therapeutic implications
-
+ currents: quantitative distinction from phenytoin and possible therapeutic implications. Mol. Pharmacol. 51:1077-1083.
-
(1997)
Mol. Pharmacol
, vol.51
, pp. 1077-1083
-
-
Kuo, C.-C.1
Chen, R.-S.2
Lu, L.3
Chen, R.-C.4
-
25
-
-
0033976628
-
Inhibition of Na+ current by diphenhydramine and other diphenyl compounds: Molecular determinants of selective binding to the inactivated channels
-
Kuo, C.-C., B.-S. Lou, and R.-C. Huang. 2000. Inhibition of Na+ current by diphenhydramine and other diphenyl compounds: molecular determinants of selective binding to the inactivated channels. Mol. Pharmacol. 57:135-143.
-
(2000)
Mol. Pharmacol
, vol.57
, pp. 135-143
-
-
Kuo, C.-C.1
Lou, B.-S.2
Huang, R.-C.3
-
27
-
-
0042697277
-
Atomic proximity between S4 segment and pore domain in Shaker potassium channels
-
Laine, M., M.-C.A. Lin, J.P.A. Bannister, W.R. Silverman, A.F. Mock, B. Roux, and D.M. Papazian. 2003. Atomic proximity between S4 segment and pore domain in Shaker potassium channels. Neuron. 39:467-481.
-
(2003)
Neuron
, vol.39
, pp. 467-481
-
-
Laine, M.1
Lin, M.-C.A.2
Bannister, J.P.A.3
Silverman, W.R.4
Mock, A.F.5
Roux, B.6
Papazian, D.M.7
-
28
-
-
0027507511
-
Lamotrigine, phenytoin and carbamazepine interactions on the sodium current present in N4TG1 mouse neuroblastoma cells
-
Lang, D.E., C.M. Wang, and B.R. Cooper. 1993. Lamotrigine, phenytoin and carbamazepine interactions on the sodium current present in N4TG1 mouse neuroblastoma cells. J. Pharmacol. Exp. Ther. 266:829-835.
-
(1993)
J. Pharmacol. Exp. Ther
, vol.266
, pp. 829-835
-
-
Lang, D.E.1
Wang, C.M.2
Cooper, B.R.3
-
29
-
-
0035941419
-
Cardiac-specific external paths for lidocaine, defined by isoform-specific residues, accelerate recovery from use-dependent block
-
Lee, P.J., A. Sunami, and H.A. Fozzard. 2001. Cardiac-specific external paths for lidocaine, defined by isoform-specific residues, accelerate recovery from use-dependent block. Circ. Res. 89:1014-1021.
-
(2001)
Circ. Res
, vol.89
, pp. 1014-1021
-
-
Lee, P.J.1
Sunami, A.2
Fozzard, H.A.3
-
30
-
-
0032506024
-
Interaction of batrachotoxin with the local anesthetic receptor site in transmembrane segment IVS6 of the voltage-gated sodium channel
-
Linford, N.J., A.R. Cantrell, Y. Qu, T. Scheuer, and W.A. Catterall. 1998. Interaction of batrachotoxin with the local anesthetic receptor site in transmembrane segment IVS6 of the voltage-gated sodium channel. Proc. Natl. Acad. Sci. USA. 95:13947-13952.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 13947-13952
-
-
Linford, N.J.1
Cantrell, A.R.2
Qu, Y.3
Scheuer, T.4
Catterall, W.A.5
-
31
-
-
0015374556
-
Diphenylhydantoin inhibition of sodium conductance in squid giant axon
-
Lipicky, R.J., D.J. Gilbert, and I.M. Stillman. 1972. Diphenylhydantoin inhibition of sodium conductance in squid giant axon. Proc. Natl. Acad. Sci. USA. 69:1758-1760.
-
(1972)
Proc. Natl. Acad. Sci. USA
, vol.69
, pp. 1758-1760
-
-
Lipicky, R.J.1
Gilbert, D.J.2
Stillman, I.M.3
-
34
-
-
23244441222
-
Voltage sensor of Kv1.2: Structural basis of electromechanical coupling
-
Long, S.B., E.B. Campbell, and R. MacKinnon. 2005b. Voltage sensor of Kv1.2: structural basis of electromechanical coupling. Science. 309:903-908.
-
(2005)
Science
, vol.309
, pp. 903-908
-
-
Long, S.B.1
Campbell, E.B.2
MacKinnon, R.3
-
35
-
-
0021325805
-
Characterization of the block of sodium channels by phenytoin in mouse neuroblastoma cells
-
Matsuki, N., F.N. Quandt, E.R.E. Ten, and J.Z. Yeh. 1984. Characterization of the block of sodium channels by phenytoin in mouse neuroblastoma cells. J. Pharmacol. Exp. Ther. 228:523-530.
-
(1984)
J. Pharmacol. Exp. Ther
, vol.228
, pp. 523-530
-
-
Matsuki, N.1
Quandt, F.N.2
Ten, E.R.E.3
Yeh, J.Z.4
-
36
-
-
34249674070
-
Charge at the lidocaine binding site residue Phe-1759 affects permeation in human cardiac voltage-gated sodium channels
-
McNulty, M.M., G.B. Edgerton, R.D. Shah, D.A. Hanck, H.A. Fozzard, and G.M. Lipkind. 2007. Charge at the lidocaine binding site residue Phe-1759 affects permeation in human cardiac voltage-gated sodium channels. J. Physiol. 581:741-755.
-
(2007)
J. Physiol
, vol.581
, pp. 741-755
-
-
McNulty, M.M.1
Edgerton, G.B.2
Shah, R.D.3
Hanck, D.A.4
Fozzard, H.A.5
Lipkind, G.M.6
-
37
-
-
0029044707
-
A critical role for transmembrane segment IVS6 of the sodium channel α-subunit in fast inactivation
-
McPhee, J.C., D.S. Ragsdale, T. Scheuer, and W.A. Catterall. 1995. A critical role for transmembrane segment IVS6 of the sodium channel α-subunit in fast inactivation. J. Biol. Chem. 270:12025-12034.
-
(1995)
J. Biol. Chem
, vol.270
, pp. 12025-12034
-
-
McPhee, J.C.1
Ragsdale, D.S.2
Scheuer, T.3
Catterall, W.A.4
-
38
-
-
0031975208
-
A critical role of the S4-S5 intracellular loop in domain IV of the sodium channel α-subunit in fast inactivation
-
McPhee, J.C., D.S. Ragsdale, T. Scheuer, and W.A. Catterall. 1998. A critical role of the S4-S5 intracellular loop in domain IV of the sodium channel α-subunit in fast inactivation. J. Biol. Chem. 273:1121-1129.
-
(1998)
J. Biol. Chem
, vol.273
, pp. 1121-1129
-
-
McPhee, J.C.1
Ragsdale, D.S.2
Scheuer, T.3
Catterall, W.A.4
-
44
-
-
30044445578
-
A novel drug binding site on voltage-gated sodium channels in rat brain
-
Riddall, D.R., M.J. Leach, and J. Garthwaite. 2006. A novel drug binding site on voltage-gated sodium channels in rat brain. Mol. Pharmacol. 69:278-287.
-
(2006)
Mol. Pharmacol
, vol.69
, pp. 278-287
-
-
Riddall, D.R.1
Leach, M.J.2
Garthwaite, J.3
-
46
-
-
0024372376
-
+ currents in mammalian myelinated nerve fibers
-
+ currents in mammalian myelinated nerve fibers. Epilepsia. 30:286-294.
-
(1989)
Epilepsia
, vol.30
, pp. 286-294
-
-
Schwartz, J.R.1
Grigat, G.2
-
47
-
-
0025756736
-
Aromatic-aromatic interactions and protein stability. Investigation by double-mutant cycles
-
Serrano, L., M. Bycroft, and A.R. Fersht. 1991. Aromatic-aromatic interactions and protein stability. Investigation by double-mutant cycles. J. Mol. Biol. 218:465-475.
-
(1991)
J. Mol. Biol
, vol.218
, pp. 465-475
-
-
Serrano, L.1
Bycroft, M.2
Fersht, A.R.3
-
48
-
-
0032805568
-
+ channel voltage sensor associated with inactivation is localized to the external charged residues of domain IV, S4
-
+ channel voltage sensor associated with inactivation is localized to the external charged residues of domain IV, S4. Biophys. J. 77:747-757.
-
(1999)
Biophys. J
, vol.77
, pp. 747-757
-
-
Sheets, M.F.1
Kyle, J.W.2
Kallen, R.G.3
Hanck, D.A.4
-
49
-
-
0028792105
-
Guidelines for protein design: The energetics of β sheet side chain interactions
-
Smith, C.K., and L. Regan. 1995. Guidelines for protein design: the energetics of β sheet side chain interactions. Science. 270:980-982.
-
(1995)
Science
, vol.270
, pp. 980-982
-
-
Smith, C.K.1
Regan, L.2
-
50
-
-
0024368695
-
Structural parts involved in activation and inactivation of the sodium channel
-
Stühmer, W., F. Conti, H. Suzuki, X.D. Wang, M. Noda, N. Yahagi, H. Kubo, and S. Numa. 1989. Structural parts involved in activation and inactivation of the sodium channel. Nature. 339:597-603.
-
(1989)
Nature
, vol.339
, pp. 597-603
-
-
Stühmer, W.1
Conti, F.2
Suzuki, H.3
Wang, X.D.4
Noda, M.5
Yahagi, N.6
Kubo, H.7
Numa, S.8
-
51
-
-
0035056966
-
Structural and gating changes of the sodium channel induced by mutation of a residue in the upper third of IVS6, creating an external access path for local anesthetics
-
Sunami, A., I.W. Glaaser, and H.A. Fozzard. 2001. Structural and gating changes of the sodium channel induced by mutation of a residue in the upper third of IVS6, creating an external access path for local anesthetics. Mol. Pharmacol. 59:684-691.
-
(2001)
Mol. Pharmacol
, vol.59
, pp. 684-691
-
-
Sunami, A.1
Glaaser, I.W.2
Fozzard, H.A.3
-
53
-
-
0029814358
-
Role of an S4-S5 linker in sodium channel inactivation probed by mutagenesis and a peptide blocker
-
Tang, L., R.G. Kallen, and R. Horn. 1996. Role of an S4-S5 linker in sodium channel inactivation probed by mutagenesis and a peptide blocker. J. Gen. Physiol. 108:89-104.
-
(1996)
J. Gen. Physiol
, vol.108
, pp. 89-104
-
-
Tang, L.1
Kallen, R.G.2
Horn, R.3
-
54
-
-
0037077578
-
Selective aromatic interactions in β-hairpin peptides
-
Tatko, C.D., and M.L. Waters. 2002. Selective aromatic interactions in β-hairpin peptides. J. Am. Chem. Soc. 124:9372-9373.
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 9372-9373
-
-
Tatko, C.D.1
Waters, M.L.2
-
55
-
-
0024240855
-
A site of covalent attachment of alpha-scorpion toxin derivativesin domain I of the sodium channel alpha subunit
-
Tejedor, F.J., and W.A. Catterall. 1988. A site of covalent attachment of alpha-scorpion toxin derivativesin domain I of the sodium channel alpha subunit. Proc. Natl. Acad. Sci. USA. 85:8742-8746.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 8742-8746
-
-
Tejedor, F.J.1
Catterall, W.A.2
-
56
-
-
0024811112
-
Localization of the receptor site for α-scorpion toxins by antibody mapping: Implications for sodium channel topology
-
Thomsen, W.J., and W.A. Catterall. 1989. Localization of the receptor site for α-scorpion toxins by antibody mapping: implications for sodium channel topology. Proc. Natl. Acad. Sci. USA. 86:10161-10165.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 10161-10165
-
-
Thomsen, W.J.1
Catterall, W.A.2
-
57
-
-
34548641160
-
Sodium channels: Ionic model of slow inactivation and state-dependent drug binding
-
Tikhonov, D.B., and B.S. Zhorov. 2007. Sodium channels: ionic model of slow inactivation and state-dependent drug binding. Biophys. J. 93:1557-1570.
-
(2007)
Biophys. J
, vol.93
, pp. 1557-1570
-
-
Tikhonov, D.B.1
Zhorov, B.S.2
-
58
-
-
0028927960
-
A mutation in the pore of the sodium channel alters gating
-
Tomaselli, G.F., N. Chiamvimonvat, H.B. Nuss, J.R. Balser, M.T. Perez-Garcia, R.H. Xu, D.W. Orias, P.H. Backx, and E. Marban. 1995. A mutation in the pore of the sodium channel alters gating. Biophys. J. 68:1814-1827.
-
(1995)
Biophys. J
, vol.68
, pp. 1814-1827
-
-
Tomaselli, G.F.1
Chiamvimonvat, N.2
Nuss, H.B.3
Balser, J.R.4
Perez-Garcia, M.T.5
Xu, R.H.6
Orias, D.W.7
Backx, P.H.8
Marban, E.9
-
59
-
-
0032920359
-
Interaction between the pore and a fast gate of the cardiac sodium channel
-
Townsend, C., and R. Horn. 1999. Interaction between the pore and a fast gate of the cardiac sodium channel. J. Gen. Physiol. 113:321-331.
-
(1999)
J. Gen. Physiol
, vol.113
, pp. 321-331
-
-
Townsend, C.1
Horn, R.2
-
61
-
-
0030894992
-
Altered ionic selectivity of the sodium channel revealed by cysteine mutations within the pore
-
Tsushima, R.G., R.A. Li, and P.H. Backx. 1997. Altered ionic selectivity of the sodium channel revealed by cysteine mutations within the pore. J. Gen. Physiol. 109:463-475.
-
(1997)
J. Gen. Physiol
, vol.109
, pp. 463-475
-
-
Tsushima, R.G.1
Li, R.A.2
Backx, P.H.3
-
64
-
-
0344171945
-
+ channels derived from point mutations in transmembrane segment D4-S6
-
+ channels derived from point mutations in transmembrane segment D4-S6. Biophys. J. 76:3141-3149.
-
(1999)
Biophys. J
, vol.76
, pp. 3141-3149
-
-
Wang, S.Y.1
Wang, G.K.2
-
66
-
-
0021913947
-
Voltage clamp analysis of the inhibitory actions of diphenylhydantoin and carbamazepine on voltage-sensitive sodium channels in neuroblastoma cells
-
Willow, M., T. Gonoi, and W.A. Catteral. 1985. Voltage clamp analysis of the inhibitory actions of diphenylhydantoin and carbamazepine on voltage-sensitive sodium channels in neuroblastoma cells. Mol. Pharmacol. 27:549-558.
-
(1985)
Mol. Pharmacol
, vol.27
, pp. 549-558
-
-
Willow, M.1
Gonoi, T.2
Catteral, W.A.3
-
67
-
-
0029738872
-
Experimentally determined hydrophobicity scale for proteins at membrane interfaces
-
Wimley, W.C., and S.H. White. 1996. Experimentally determined hydrophobicity scale for proteins at membrane interfaces. Nat. Struct. Biol. 3:842-848.
-
(1996)
Nat. Struct. Biol
, vol.3
, pp. 842-848
-
-
Wimley, W.C.1
White, S.H.2
-
69
-
-
0036841397
-
+ current by imipramine and related compounds: Different binding kinetics as an inactivation stabilizer and as an open channel blocker
-
+ current by imipramine and related compounds: different binding kinetics as an inactivation stabilizer and as an open channel blocker. Mol. Pharmacol. 62:1228-1237.
-
(2002)
Mol. Pharmacol
, vol.62
, pp. 1228-1237
-
-
Yang, Y.-C.1
Kuo, C.-C.2
-
71
-
-
18544371320
-
An inactivation stabilizer of the Na+ channel acts as an opportunistic pore blocker modulated by external Na+
-
Yang, Y.-C., and C.-C. Kuo. 2005. An inactivation stabilizer of the Na+ channel acts as an opportunistic pore blocker modulated by external Na+. J. Gen. Physiol. 125:465-481.
-
(2005)
J. Gen. Physiol
, vol.125
, pp. 465-481
-
-
Yang, Y.-C.1
Kuo, C.-C.2
-
74
-
-
0028059091
-
Transcainide causes two modes of open-channel block with different voltage sensitivities in batrachotoxin- activated sodium channels
-
Zamponi, G.W., and R.J. French. 1994. Transcainide causes two modes of open-channel block with different voltage sensitivities in batrachotoxin- activated sodium channels. Biophys. J. 67:1028-1039.
-
(1994)
Biophys. J
, vol.67
, pp. 1028-1039
-
-
Zamponi, G.W.1
French, R.J.2
-
75
-
-
34250343443
-
Tetracaine-membrane interactions: Effects of lipid composition and phase on drug partitioning, location, and ionization
-
Zhang, J., T. Hadlock, A. Gent, and G.R. Strichartz. 2007. Tetracaine-membrane interactions: effects of lipid composition and phase on drug partitioning, location, and ionization. Biophys. J. 92:3988-4001.
-
(2007)
Biophys. J
, vol.92
, pp. 3988-4001
-
-
Zhang, J.1
Hadlock, T.2
Gent, A.3
Strichartz, G.R.4
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