-
1
-
-
23044441734
-
Voltage-gated sodium channel expression and potentiation of human breast cancer metastasis
-
Fraser S.P., Diss J.K., Chioni A.M., Mycielska M.E., Pan H., Yamaci R.F., Pani F., Siwy Z., Krasowska M., Grzywna Z., Brackenbury W.J., Theodorou D., Koyuturk M., Kaya H., Battaloglu E., De Bella M.T., Slade M.J., Tolhurst R., Palmieri C., Jiang J., Latchman D.S., Coombes R.C., and Djamgoz M.B. Voltage-gated sodium channel expression and potentiation of human breast cancer metastasis. Clin. Cancer Res. 11 (2005) 5381-5389
-
(2005)
Clin. Cancer Res.
, vol.11
, pp. 5381-5389
-
-
Fraser, S.P.1
Diss, J.K.2
Chioni, A.M.3
Mycielska, M.E.4
Pan, H.5
Yamaci, R.F.6
Pani, F.7
Siwy, Z.8
Krasowska, M.9
Grzywna, Z.10
Brackenbury, W.J.11
Theodorou, D.12
Koyuturk, M.13
Kaya, H.14
Battaloglu, E.15
De Bella, M.T.16
Slade, M.J.17
Tolhurst, R.18
Palmieri, C.19
Jiang, J.20
Latchman, D.S.21
Coombes, R.C.22
Djamgoz, M.B.23
more..
-
2
-
-
0015856482
-
Voltage dependent charge movement in skeletal muscle: a possible step in excitation-contraction coupling
-
Schneider M.F., and Chandler W.K. Voltage dependent charge movement in skeletal muscle: a possible step in excitation-contraction coupling. Nature 242 (1973) 244-246
-
(1973)
Nature
, vol.242
, pp. 244-246
-
-
Schneider, M.F.1
Chandler, W.K.2
-
3
-
-
0033222872
-
Modular assembly of voltage-gated channel proteins: a sequence analysis and phylogenetic study
-
Nelson R.D., Kauan G., Saier Jr. M.H., and Montal M. Modular assembly of voltage-gated channel proteins: a sequence analysis and phylogenetic study. J. Mol. Microbiol. Biotechnol. 1 (1999) 281-287
-
(1999)
J. Mol. Microbiol. Biotechnol.
, vol.1
, pp. 281-287
-
-
Nelson, R.D.1
Kauan, G.2
Saier Jr., M.H.3
Montal, M.4
-
4
-
-
0032478818
-
+ conduction and selectivity
-
+ conduction and selectivity. Science 280 (1998) 69-77
-
(1998)
Science
, vol.280
, pp. 69-77
-
-
Doyle, D.A.1
Cabral, J.M.2
Pfuetzner, R.A.3
Kuo, A.4
Gulbis, J.M.5
Cohen, S.L.6
Chait, B.T.7
MacKinnon, R.8
-
5
-
-
23244456428
-
Crystal structure of a mammalian voltage-dependent Shaker family K+ channel
-
Long S.B., Campbell E.B., and Mackinnon R. Crystal structure of a mammalian voltage-dependent Shaker family K+ channel. Science 309 (2005) 897-903
-
(2005)
Science
, vol.309
, pp. 897-903
-
-
Long, S.B.1
Campbell, E.B.2
Mackinnon, R.3
-
7
-
-
13444273448
-
The Universal Protein Resource (UniProt)
-
Bairoch A., Apweiler R., Wu C.H., Barker W.C., Boeckmann B., Ferro S., Gasteiger E., Huang H., Lopez R., Magrane M., Martin M.J., Natale D.A., O'Donovan C., Redaschi N., and Yeh L.S. The Universal Protein Resource (UniProt). Nucleic Acids Res. 33 (2005) D154-D159
-
(2005)
Nucleic Acids Res.
, vol.33
-
-
Bairoch, A.1
Apweiler, R.2
Wu, C.H.3
Barker, W.C.4
Boeckmann, B.5
Ferro, S.6
Gasteiger, E.7
Huang, H.8
Lopez, R.9
Magrane, M.10
Martin, M.J.11
Natale, D.A.12
O'Donovan, C.13
Redaschi, N.14
Yeh, L.S.15
-
8
-
-
0036169928
-
Tolerating some redundancy significantly speeds up clustering of large protein databases
-
Li W., Jaroszewski L., and Godzik A. Tolerating some redundancy significantly speeds up clustering of large protein databases. Bioinformatics 18 (2002) 77-82
-
(2002)
Bioinformatics
, vol.18
, pp. 77-82
-
-
Li, W.1
Jaroszewski, L.2
Godzik, A.3
-
9
-
-
0027968068
-
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
-
Thompson J.D., Higgins D.G., and Gibson T.J. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 22 (1994) 4673-4680
-
(1994)
Nucleic Acids Res.
, vol.22
, pp. 4673-4680
-
-
Thompson, J.D.1
Higgins, D.G.2
Gibson, T.J.3
-
10
-
-
0030784438
-
An artificial intelligence approach to motif discovery in protein sequences: application to steroid dehydrogenases
-
Bailey T.L., Baker M.E., and Elkan C.P. An artificial intelligence approach to motif discovery in protein sequences: application to steroid dehydrogenases. J. Steroid Biochem. Mol. Biol. 62 (1997) 29-44
-
(1997)
J. Steroid Biochem. Mol. Biol.
, vol.62
, pp. 29-44
-
-
Bailey, T.L.1
Baker, M.E.2
Elkan, C.P.3
-
12
-
-
0001290045
-
PROSITE: a documented database using patterns and profiles as motif descriptors
-
Sigrist C.J., Cerutti L., Hulo N., Gattiker A., Falquet L., Pagni M., Bairoch A., and Bucher P. PROSITE: a documented database using patterns and profiles as motif descriptors. Brief Bioinform. 3 (2002) 265-274
-
(2002)
Brief Bioinform.
, vol.3
, pp. 265-274
-
-
Sigrist, C.J.1
Cerutti, L.2
Hulo, N.3
Gattiker, A.4
Falquet, L.5
Pagni, M.6
Bairoch, A.7
Bucher, P.8
-
16
-
-
0036715180
-
Movement and crevices around a sodium channel S3 segment
-
Nguyen T.P., and Horn R. Movement and crevices around a sodium channel S3 segment. J. Gen. Physiol. 120 (2002) 419-436
-
(2002)
J. Gen. Physiol.
, vol.120
, pp. 419-436
-
-
Nguyen, T.P.1
Horn, R.2
-
18
-
-
0347479237
-
Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A
-
Lossin C., Rhodes T.H., Desai R.R., Vanoye C.G., Wang D., Carniciu S., Devinsky O., and George Jr. A.L. Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A. J. Neurosci. 23 (2003) 11289-11295
-
(2003)
J. Neurosci.
, vol.23
, pp. 11289-11295
-
-
Lossin, C.1
Rhodes, T.H.2
Desai, R.R.3
Vanoye, C.G.4
Wang, D.5
Carniciu, S.6
Devinsky, O.7
George Jr., A.L.8
-
19
-
-
0034069675
-
Local movement in the S2 region of the voltage-gated potassium channel hKv2.1 studied using cysteine mutagenesis
-
J Milligan C., and Wary D. Local movement in the S2 region of the voltage-gated potassium channel hKv2.1 studied using cysteine mutagenesis. Biophys. J. 78 (2000) 1852-1861
-
(2000)
Biophys. J.
, vol.78
, pp. 1852-1861
-
-
J Milligan, C.1
Wary, D.2
-
20
-
-
33751539566
-
Molecular basis of charge movement in voltage-gated sodium channels
-
Yang N., George A.L., and Horn R. Molecular basis of charge movement in voltage-gated sodium channels. Neuron 14 (1996) 1047-1054
-
(1996)
Neuron
, vol.14
, pp. 1047-1054
-
-
Yang, N.1
George, A.L.2
Horn, R.3
-
21
-
-
0030963793
-
Sodium channel activation gating is affected by substitutions of voltage sensor positive charges in all four domains
-
Knotis K.J., Rounaghi A., and Goldin A.L. Sodium channel activation gating is affected by substitutions of voltage sensor positive charges in all four domains. J. Gen. Physiol. 110 (1997) 391-401
-
(1997)
J. Gen. Physiol.
, vol.110
, pp. 391-401
-
-
Knotis, K.J.1
Rounaghi, A.2
Goldin, A.L.3
-
23
-
-
0032407663
-
Voltage-dependent gating of single wild type and S4 mutant KAT1 inward rectifier potassium channels
-
Zei P.C., and Aldrich R.W. Voltage-dependent gating of single wild type and S4 mutant KAT1 inward rectifier potassium channels. J. Gen. Physiol 112 (1998) 670-713
-
(1998)
J. Gen. Physiol
, vol.112
, pp. 670-713
-
-
Zei, P.C.1
Aldrich, R.W.2
-
26
-
-
0027430335
-
Molecular localization of ion selectivity sites within the pore of a human L-type cardiac calcium channel
-
Tang S., Mikala G., Bahinski A., Yatani A., Varadi G., and Schwartz A. Molecular localization of ion selectivity sites within the pore of a human L-type cardiac calcium channel. J. Biol. Chem. 268 (1993) 13026-13029
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 13026-13029
-
-
Tang, S.1
Mikala, G.2
Bahinski, A.3
Yatani, A.4
Varadi, G.5
Schwartz, A.6
-
27
-
-
0033103648
-
Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine
-
Hans M., Luvisetto S., Williams M.E., Spagnolo M., Urrutia A., Tottene A., Brust P.F., Johnson E.C., Harpold M.M., Stauderman K.A., and Pietrobon D. Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine. J. Neurosci. 19 (1999) 610-1619
-
(1999)
J. Neurosci.
, vol.19
, pp. 610-1619
-
-
Hans, M.1
Luvisetto, S.2
Williams, M.E.3
Spagnolo, M.4
Urrutia, A.5
Tottene, A.6
Brust, P.F.7
Johnson, E.C.8
Harpold, M.M.9
Stauderman, K.A.10
Pietrobon, D.11
-
28
-
-
0026517122
-
Calcium channel characteristics conferred on the sodium channel by single mutations
-
Heinemann S.H., Terlau H., Stuhmer W., Imoto K., and Numa S. Calcium channel characteristics conferred on the sodium channel by single mutations. Nature 356 (1992) 441-443
-
(1992)
Nature
, vol.356
, pp. 441-443
-
-
Heinemann, S.H.1
Terlau, H.2
Stuhmer, W.3
Imoto, K.4
Numa, S.5
-
31
-
-
11144221751
-
Reversed voltage-dependent gating of a bacterial sodium channel with proline substitutions in the S6 transmembrane segment
-
Zhao Y., Scheuer T., and Catterall W.A. Reversed voltage-dependent gating of a bacterial sodium channel with proline substitutions in the S6 transmembrane segment. Proc. Natl. Acad. Sci. USA 101 (2004) 17873-17878
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 17873-17878
-
-
Zhao, Y.1
Scheuer, T.2
Catterall, W.A.3
-
32
-
-
0346118860
-
Gating of shaker-type channels requires the flexibility of S6 caused by pralines
-
Labro A.J., Raes A.L., Bellens I., Ottschytsch N., and Snyders D.J. Gating of shaker-type channels requires the flexibility of S6 caused by pralines. J. Biol. Chem. 278 (2003) 50724-50731
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 50724-50731
-
-
Labro, A.J.1
Raes, A.L.2
Bellens, I.3
Ottschytsch, N.4
Snyders, D.J.5
-
33
-
-
0032053452
-
A mutation affecting dihydropyridine-sensitive current levels and activation kinetics in Drosophila muscle and mammalian heart calcium channels
-
Ren D., Xu H., Eberl D.F., Chopra M., and Hall L.M. A mutation affecting dihydropyridine-sensitive current levels and activation kinetics in Drosophila muscle and mammalian heart calcium channels. J. Neurosci. 18 (1998) 2335-2341
-
(1998)
J. Neurosci.
, vol.18
, pp. 2335-2341
-
-
Ren, D.1
Xu, H.2
Eberl, D.F.3
Chopra, M.4
Hall, L.M.5
-
34
-
-
10344235279
-
Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia
-
Imbrici P., Jaffe S.L., Eunson L.H., Davies N.P., Herd C., Robertson R., Kullmann D.M., and Hanna M.G. Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia. Brain 127 (2004) 2682-2692
-
(2004)
Brain
, vol.127
, pp. 2682-2692
-
-
Imbrici, P.1
Jaffe, S.L.2
Eunson, L.H.3
Davies, N.P.4
Herd, C.5
Robertson, R.6
Kullmann, D.M.7
Hanna, M.G.8
-
35
-
-
14844299777
-
A Korean family of hypokalemic periodic paralysis with mutation in a voltage-gated calcium channel (R1239G)
-
Kim J.B., Lee K.Y., and Hur J.K. A Korean family of hypokalemic periodic paralysis with mutation in a voltage-gated calcium channel (R1239G). J. Korean Med. Sci. 20 (2005) 62-165
-
(2005)
J. Korean Med. Sci.
, vol.20
, pp. 62-165
-
-
Kim, J.B.1
Lee, K.Y.2
Hur, J.K.3
-
36
-
-
33644684859
-
Structural determinants of L-type channel activation in segment IIS6 revealed by a retinal disorder
-
Hohaus A., Beyl S., Kudrnac M., Berjukow S., Timin E.N., Marksteiner R., Maw M.A., and Hering S. Structural determinants of L-type channel activation in segment IIS6 revealed by a retinal disorder. J. Biol. Chem. 280 (2005) 38471-38477
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 38471-38477
-
-
Hohaus, A.1
Beyl, S.2
Kudrnac, M.3
Berjukow, S.4
Timin, E.N.5
Marksteiner, R.6
Maw, M.A.7
Hering, S.8
-
37
-
-
23644433670
-
Inherited disorders of voltage-gated sodium channels
-
George Jr. A.L. Inherited disorders of voltage-gated sodium channels. J. Clin. Invest. 115 (2005) 1990-1999
-
(2005)
J. Clin. Invest.
, vol.115
, pp. 1990-1999
-
-
George Jr., A.L.1
-
38
-
-
0035956488
-
Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation
-
Abou-Khalil B., Ge Q., Desai R., Ryther R., Bazyk A., Bailey R., Haines J.L., Sutcliffe J.S., and George Jr. A.L. Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation. Neurology 57 (2001) 2265-2272
-
(2001)
Neurology
, vol.57
, pp. 2265-2272
-
-
Abou-Khalil, B.1
Ge, Q.2
Desai, R.3
Ryther, R.4
Bazyk, A.5
Bailey, R.6
Haines, J.L.7
Sutcliffe, J.S.8
George Jr., A.L.9
-
39
-
-
8644232427
-
Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndrome
-
Shin D.J., Jang Y., Park H.Y., Lee J.E., Yang K., Kim E., Bae Y., Kim J., Kim S.S., Lee M.H., Chahine M., and Yoon S.K. Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndrome. J. Hum. Genet. 49 (2004) 573-578
-
(2004)
J. Hum. Genet.
, vol.49
, pp. 573-578
-
-
Shin, D.J.1
Jang, Y.2
Park, H.Y.3
Lee, J.E.4
Yang, K.5
Kim, E.6
Bae, Y.7
Kim, J.8
Kim, S.S.9
Lee, M.H.10
Chahine, M.11
Yoon, S.K.12
-
40
-
-
5644229494
-
-
W.P. McNair, L. Ku, M.R. Taylor, P.R. Fain, D. Dao, E. Wolfel, L. Mestroni, Familial Cardiomyopathy Registry Research Group, SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia, Circulation 110 (2004) 2163-2167.
-
-
-
-
43
-
-
0038726473
-
Functional characterization of an episodic ataxia type-1 mutation occurring in the S1 segment of hKv1.1 channels
-
Imbrici P., Cusimano A., D'Adamo M.C., De Curtis A., and Pessia M. Functional characterization of an episodic ataxia type-1 mutation occurring in the S1 segment of hKv1.1 channels. Pflugers Arch. 446 (2003) 373-379
-
(2003)
Pflugers Arch.
, vol.446
, pp. 373-379
-
-
Imbrici, P.1
Cusimano, A.2
D'Adamo, M.C.3
De Curtis, A.4
Pessia, M.5
-
45
-
-
10744231816
-
-
W. Zareba, A.J. Moss, G. Sheu, E.S. Kaufman, S. Priori, G.M. Vincent, J.A. Towbin, J. Benhorin, P.J. Schwartz, C. Napolitano, W.J. Hall, M.T. Keating, M. Qi, J.L. Robinson, M.L. Andrews, International LQTS Registry, University of Rochester, Rochester, New York, Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome, J. Cardiovasc. Electrophysiol. 14 (2003) 1149-1153.
-
-
-
-
46
-
-
0038059165
-
Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2
-
Dedek K., Fusco L., Teloy N., and Steinlein O.K. Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2. Epilepsy Res. 54 (2003) 21-27
-
(2003)
Epilepsy Res.
, vol.54
, pp. 21-27
-
-
Dedek, K.1
Fusco, L.2
Teloy, N.3
Steinlein, O.K.4
-
47
-
-
0030799943
-
Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias
-
Chouabe C., Neyroud N., Guicheney P., Lazdunski M., Romey G., and Barhanin J. Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias. EMBO J. 16 (1997) 5472-5479
-
(1997)
EMBO J.
, vol.16
, pp. 5472-5479
-
-
Chouabe, C.1
Neyroud, N.2
Guicheney, P.3
Lazdunski, M.4
Romey, G.5
Barhanin, J.6
-
48
-
-
7044246176
-
Identification and characterisation of a novel KCNQ1 mutation in a family with Romano-Ward syndrome
-
Zehelein J., Thomas D., Khalil M., Wimmer A.B., Koenen M., Licka M., Wu K., Kiehn J., Brockmeier K., Kreye V.A., Karle C.A., Katus H.A., Ulmer H.E., and Schoels W. Identification and characterisation of a novel KCNQ1 mutation in a family with Romano-Ward syndrome. Biochim. Biophys. Acta 1690 (2004) 185-192
-
(2004)
Biochim. Biophys. Acta
, vol.1690
, pp. 185-192
-
-
Zehelein, J.1
Thomas, D.2
Khalil, M.3
Wimmer, A.B.4
Koenen, M.5
Licka, M.6
Wu, K.7
Kiehn, J.8
Brockmeier, K.9
Kreye, V.A.10
Karle, C.A.11
Katus, H.A.12
Ulmer, H.E.13
Schoels, W.14
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