-
1
-
-
0029992905
-
Genomic organization of the human SCN5A gene encoding the cardiac sodium channel
-
Wang, Q., Li, Z., Shen, J., and Keating, M. T. (1996) Genomic organization of the human SCN5A gene encoding the cardiac sodium channel. Genomics 34, 9-16
-
(1996)
Genomics
, vol.34
, pp. 9-16
-
-
Wang, Q.1
Li, Z.2
Shen, J.3
Keating, M.T.4
-
2
-
-
0030981050
-
Molecular genetics of long QT syndrome from genes to patients
-
Wang, Q., Chen, Q., Li, H., and Towbin, J. A. (1997) Molecular genetics of long QT syndrome from genes to patients. Curr. Opin. Cardiol. 12, 310-320
-
(1997)
Curr. Opin. Cardiol.
, vol.12
, pp. 310-320
-
-
Wang, Q.1
Chen, Q.2
Li, H.3
Towbin, J.A.4
-
3
-
-
0031980283
-
Genetics, molecular mechanisms and management of long QT syndrome
-
Wang, Q., Chen, Q., and Towbin, J. A. (1998) Genetics, molecular mechanisms and management of long QT syndrome. Ann. Med. 30, 58-65
-
(1998)
Ann. Med.
, vol.30
, pp. 58-65
-
-
Wang, Q.1
Chen, Q.2
Towbin, J.A.3
-
4
-
-
84878064672
-
MOG1 rescues defective trafficking of Na( v)1.5 mutations in Brugada syndrome and sick sinus syndrome
-
Chakrabarti, S., Wu, X., Yang, Z., Wu, L., Yong, S. L., Zhang, C., Hu, K., Wang, Q. K., and Chen, Q. (2013) MOG1 rescues defective trafficking of Na( v)1.5 mutations in Brugada syndrome and sick sinus syndrome. Circ. Arrhythm. Electrophysiol. 6, 392-401
-
(2013)
Circ. Arrhythm. Electrophysiol
, vol.6
, pp. 392-401
-
-
Chakrabarti, S.1
Wu, X.2
Yang, Z.3
Wu, L.4
Yong, S.L.5
Zhang, C.6
Hu, K.7
Wang, Q.K.8
Chen, Q.9
-
5
-
-
15744372528
-
Regulation of the voltage-gated cardiac sodium channel Nav1.5 by interacting proteins
-
Abriel, H., and Kass, R. S. (2005) Regulation of the voltage-gated cardiac sodium channel Nav1.5 by interacting proteins. Trends Cardiovasc. Med. 15, 35-40
-
(2005)
Trends Cardiovasc. Med.
, vol.15
, pp. 35-40
-
-
Abriel, H.1
Kass, R.S.2
-
6
-
-
43749100705
-
Identification of a new co-factor, MOG1, required for the full function of cardiac sodium channel Nav1.5
-
Wu, L., Yong, S. L., Fan, C., Ni, Y., Yoo, S., Zhang, T., Zhang, X., Obejero-Paz, C. A., Rho, H. J., Ke, T., Szafranski, P., Jones, S. W., Chen, Q., and Wang, Q. K. (2008) Identification of a new co-factor, MOG1, required for the full function of cardiac sodium channel Nav1.5. J. Biol. Chem. 283, 6968-6978
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 6968-6978
-
-
Wu, L.1
Yong, S.L.2
Fan, C.3
Ni, Y.4
Yoo, S.5
Zhang, T.6
Zhang, X.7
Obejero-Paz, C.A.8
Rho, H.J.9
Ke, T.10
Szafranski, P.11
Jones, S.W.12
Chen, Q.13
Wang, Q.K.14
-
7
-
-
84939241268
-
The multi-faceted aspects of the complex cardiac Nav1.5 protein in membrane function and pathophysiology
-
Detta, N., Frisso, G., and Salvatore, F. (2015) The multi-faceted aspects of the complex cardiac Nav1.5 protein in membrane function and pathophysiology. Biochim. Biophys. Acta 1854, 1502-1509
-
(2015)
Biochim. Biophys. Acta
, vol.1854
, pp. 1502-1509
-
-
Detta, N.1
Frisso, G.2
Salvatore, F.3
-
8
-
-
4043059200
-
Cardiac voltage-gated sodium channel Nav1.5 is regulated by Nedd4-2 mediated ubiquitination
-
van Bemmelen, M. X., Rougier, J. S., Gavillet, B., Apothéloz, F., Daidié, D., Tateyama, M., Rivolta, I., Thomas, M. A., Kass, R. S., Staub, O., and Abriel, H. (2004) Cardiac voltage-gated sodium channel Nav1.5 is regulated by Nedd4-2 mediated ubiquitination. Circ. Res. 95, 284-291
-
(2004)
Circ. Res.
, vol.95
, pp. 284-291
-
-
Van Bemmelen, M.X.1
Rougier, J.S.2
Gavillet, B.3
Apothéloz, F.4
Daidié, D.5
Tateyama, M.6
Rivolta, I.7
Thomas, M.A.8
Kass, R.S.9
Staub, O.10
Abriel, H.11
-
9
-
-
61849122908
-
Genetics of crystallins: Cataract and beyond
-
Graw, J. (2009) Genetics of crystallins: cataract and beyond. Exp. Eye Res. 88, 173-189
-
(2009)
Exp. Eye Res.
, vol.88
, pp. 173-189
-
-
Graw, J.1
-
10
-
-
43049090044
-
Cataract mutation P20S of αB-crystallin impairs chaperone activity of αA-crystallin and induces apoptosis of human lens epithelial cells
-
Li, H., Li, C., Lu, Q., Su, T., Ke, T., Li, D. W., Yuan, M., Liu, J., Ren, X., Zhang, Z., Zeng, S., Wang, Q. K., and Liu, M. (2008) Cataract mutation P20S of αB-crystallin impairs chaperone activity of αA-crystallin and induces apoptosis of human lens epithelial cells. Biochim. Biophys. Acta 1782, 303-309
-
(2008)
Biochim. Biophys. Acta
, vol.1782
, pp. 303-309
-
-
Li, H.1
Li, C.2
Lu, Q.3
Su, T.4
Ke, T.5
Li, D.W.6
Yuan, M.7
Liu, J.8
Ren, X.9
Zhang, Z.10
Zeng, S.11
Wang, Q.K.12
Liu, M.13
-
11
-
-
22844445484
-
Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder
-
Du, W, Bautista, J. F., Yang, H., Diez-Sampedro, A., You, S. A., Wang, L., Kotagal, P., Luders, H. O., Shi, J., Cui, J., Richerson, G. B., and Wang, Q. K. (2005) Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder. Nat. Genet. 37, 733-738
-
(2005)
Nat. Genet.
, vol.37
, pp. 733-738
-
-
Du, W.1
Bautista, J.F.2
Yang, H.3
Diez-Sampedro, A.4
You, S.A.5
Wang, L.6
Kotagal, P.7
Luders, H.O.8
Shi, J.9
Cui, J.10
Richerson, G.B.11
Wang, Q.K.12
-
12
-
-
57349179985
-
Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death
-
Zhang, X., Chen, S., Yoo, S., Chakrabarti, S., Zhang, T., Ke, T., Oberti, C., Yong, S. L., Fang, F., Li, L., de la Fuente, R., Wang, L., Chen, Q., and Wang, Q. K. (2008) Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death. Cell 135, 1017-1027
-
(2008)
Cell
, vol.135
, pp. 1017-1027
-
-
Zhang, X.1
Chen, S.2
Yoo, S.3
Chakrabarti, S.4
Zhang, T.5
Ke, T.6
Oberti, C.7
Yong, S.L.8
Fang, F.9
Li, L.10
De La Fuente, R.11
Wang, L.12
Chen, Q.13
Wang, Q.K.14
-
13
-
-
0032546384
-
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
-
Chen, Q., Kirsch, G. E., Zhang, D., Brugada, R., Brugada, J., Brugada, P., Potenza, D., Moya, A., Borggrefe, M., Breithardt, G., Ortiz-Lopez, R., Wang, Z., Antzelevitch, C., O'Brien, R. E., Schulze-Bahr, E., et al. (1998) Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature 392, 293-296
-
(1998)
Nature
, vol.392
, pp. 293-296
-
-
Chen, Q.1
Kirsch, G.E.2
Zhang, D.3
Brugada, R.4
Brugada, J.5
Brugada, P.6
Potenza, D.7
Moya, A.8
Borggrefe, M.9
Breithardt, G.10
Ortiz-Lopez, R.11
Wang, Z.12
Antzelevitch, C.13
O'Brien, R.E.14
Schulze-Bahr, E.15
-
14
-
-
0033752765
-
1 -subunits as a molecular mechanism of idiopathic ventricular fibrillation
-
1 -subunits as a molecular mechanism of idiopathic ventricular fibrillation. J. Mol. Cell Cardiol. 32, 1873-1884
-
(2000)
J. Mol. Cell Cardiol.
, vol.32
, pp. 1873-1884
-
-
Wan, X.1
Wang, Q.2
Kirsch, G.E.3
-
16
-
-
70350025509
-
Functional role of transcriptional factor TBX5 in pre-mRNA splicing and Holt-Oram syndrome via association with SC35
-
Fan, C., Chen, Q., and Wang, Q. K. (2009) Functional role of transcriptional factor TBX5 in pre-mRNA splicing and Holt-Oram syndrome via association with SC35. J. Biol. Chem. 284, 25653-25663
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 25653-25663
-
-
Fan, C.1
Chen, Q.2
Wang, Q.K.3
-
17
-
-
10744223472
-
Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome
-
Tian, X. L., Kadaba, R., You, S. A., Liu, M., Timur, A. A., Yang, L., Chen, Q., Szafranski, P., Rao, S., Wu, L., Housman, D. E., DiCorleto, P. E., Driscoll, D. J., Borrow, J., and Wang, Q. (2004) Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome. Nature 427, 640-645
-
(2004)
Nature
, vol.427
, pp. 640-645
-
-
Tian, X.L.1
Kadaba, R.2
You, S.A.3
Liu, M.4
Timur, A.A.5
Yang, L.6
Chen, Q.7
Szafranski, P.8
Rao, S.9
Wu, L.10
Housman, D.E.11
DiCorleto, P.E.12
Driscoll, D.J.13
Borrow, J.14
Wang, Q.15
-
18
-
-
9144246925
-
Mechanisms by which SCN5A mutation N1325S causes cardiac arrhythmias and sudden death in vivo
-
Tian, X. L., Yong, S. L., Wan, X., Wu, L., Chung, M. K., Tchou, P. J., Rosenbaum, D. S., Van Wagoner, D. R., Kirsch, G. E., and Wang, Q. (2004) Mechanisms by which SCN5A mutation N1325S causes cardiac arrhythmias and sudden death in vivo. Cardiovasc. Res. 61, 256-267
-
(2004)
Cardiovasc. Res.
, vol.61
, pp. 256-267
-
-
Tian, X.L.1
Yong, S.L.2
Wan, X.3
Wu, L.4
Chung, M.K.5
Tchou, P.J.6
Rosenbaum, D.S.7
Van Wagoner, D.R.8
Kirsch, G.E.9
Wang, Q.10
-
19
-
-
33751540669
-
Characterization of the cardiac sodium channel SCN5A mutation, N1325S, in single murine ventricular myocytes
-
Yong, S. L., Ni, Y., Zhang, T., Tester, D. J., Ackerman, M. J., and Wang, Q. K. (2007) Characterization of the cardiac sodium channel SCN5A mutation, N1325S, in single murine ventricular myocytes. Biochem. Biophys. Res. Commun. 352, 378-383
-
(2007)
Biochem. Biophys. Res. Commun.
, vol.352
, pp. 378-383
-
-
Yong, S.L.1
Ni, Y.2
Zhang, T.3
Tester, D.J.4
Ackerman, M.J.5
Wang, Q.K.6
-
20
-
-
33847111638
-
Cardiac-specific overexpression of SCN5A gene leads to shorter P wave duration and PR interval in transgenic mice
-
Zhang, T., Yong, S. L., Tian, X. L., and Wang, Q. K. (2007) Cardiac-specific overexpression of SCN5A gene leads to shorter P wave duration and PR interval in transgenic mice. Biochem. Biophys. Res. Commun. 355, 444-450
-
(2007)
Biochem. Biophys. Res. Commun.
, vol.355
, pp. 444-450
-
-
Zhang, T.1
Yong, S.L.2
Tian, X.L.3
Wang, Q.K.4
-
21
-
-
79951946247
-
LQTS mutation N1325S in cardiac sodium channel gene SCN5A causes cardiomyocyte apoptosis, cardiac fibrosis and contractile dysfunction in mice
-
Zhang, T., Yong, S. L., Drinko, J. K., Popović, Z. B., Shryock, J. C., Belardinelli, L., and Wang, Q. K. (2011) LQTS mutation N1325S in cardiac sodium channel gene SCN5A causes cardiomyocyte apoptosis, cardiac fibrosis and contractile dysfunction in mice. Int. J. Cardiol. 147, 239-245
-
(2011)
Int. J. Cardiol.
, vol.147
, pp. 239-245
-
-
Zhang, T.1
Yong, S.L.2
Drinko, J.K.3
Popović, Z.B.4
Shryock, J.C.5
Belardinelli, L.6
Wang, Q.K.7
-
22
-
-
79953207296
-
Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population
-
Wang, F., Xu, C. Q., He, Q., Cai, J. P., Li, X. C., Wang, D., Xiong, X., Liao, Y. H., Zeng, Q. T., Yang, Y. Z., Cheng, X., Li, C., Yang, R., Wang, C. C., Wu, G., et al. (2011) Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population. Nat. Genet. 43, 345-349
-
(2011)
Nat. Genet.
, vol.43
, pp. 345-349
-
-
Wang, F.1
Xu, C.Q.2
He, Q.3
Cai, J.P.4
Li, X.C.5
Wang, D.6
Xiong, X.7
Liao, Y.H.8
Zeng, Q.T.9
Yang, Y.Z.10
Cheng, X.11
Li, C.12
Yang, R.13
Wang, C.C.14
Wu, G.15
-
23
-
-
84894528778
-
Role of microRNA-27a in down-regulation of angiogenic factor AGGF1 under hypoxia associated with high-grade bladder urothelial carcinoma
-
Xu, Y., Zhou, M., Wang, J., Zhao, Y., Li, S., Zhou, B., Su, Z., Xu, C., Xia, Y., Qian, H., Tu, X., Xiao, W., Chen, X., Chen, Q., and Wang, Q. K. (2014) Role of microRNA-27a in down-regulation of angiogenic factor AGGF1 under hypoxia associated with high-grade bladder urothelial carcinoma. Biochim. Biophys. Acta 1842, 712-725
-
(2014)
Biochim. Biophys. Acta
, vol.1842
, pp. 712-725
-
-
Xu, Y.1
Zhou, M.2
Wang, J.3
Zhao, Y.4
Li, S.5
Zhou, B.6
Su, Z.7
Xu, C.8
Xia, Y.9
Qian, H.10
Tu, X.11
Xiao, W.12
Chen, X.13
Chen, Q.14
Wang, Q.K.15
-
24
-
-
84875215586
-
Transcriptional activation of the Prox1 gene by HIF-1α and HIF-2α in response to hypoxia
-
Zhou, B., Si, W., Su, Z., Deng, W., Tu, X., and Wang, Q. (2013) Transcriptional activation of the Prox1 gene by HIF-1α and HIF-2α in response to hypoxia. FEBS Lett. 587, 724-731
-
(2013)
FEBS Lett.
, vol.587
, pp. 724-731
-
-
Zhou, B.1
Si, W.2
Su, Z.3
Deng, W.4
Tu, X.5
Wang, Q.6
-
25
-
-
84876737342
-
MicroRNA-503 targets FGF2 and VEGFA and inhibits tumor angiogenesis and growth
-
Zhou, B., Ma, R., Si, W., Li, S., Xu, Y., Tu, X., and Wang, Q. (2013) MicroRNA-503 targets FGF2 and VEGFA and inhibits tumor angiogenesis and growth. Cancer Lett. 333, 159-169
-
(2013)
Cancer Lett.
, vol.333
, pp. 159-169
-
-
Zhou, B.1
Ma, R.2
Si, W.3
Li, S.4
Xu, Y.5
Tu, X.6
Wang, Q.7
-
26
-
-
0029988774
-
+ channel-linked long-QT syndrome
-
+ channel-linked long-QT syndrome. Circ. Res. 78, 916-924
-
(1996)
Circ. Res.
, vol.78
, pp. 916-924
-
-
Dumaine, R.1
Wang, Q.2
Keating, M.T.3
Hartmann, H.A.4
Schwartz, P.J.5
Brown, A.M.6
Kirsch, G.E.7
-
27
-
-
34948863477
-
Small heat shock protein αA-crystallin regulates epithelial sodium channel expression
-
Kashlan, O. B., Mueller, G. M., Qamar, M. Z., Poland, P. A., Ahner, A., Rubenstein, R. C., Hughey, R. P., Brodsky, J. L., and Kleyman, T. R. (2007) Small heat shock protein αA-crystallin regulates epithelial sodium channel expression. J. Biol. Chem. 282, 28149-28156
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 28149-28156
-
-
Kashlan, O.B.1
Mueller, G.M.2
Qamar, M.Z.3
Poland, P.A.4
Ahner, A.5
Rubenstein, R.C.6
Hughey, R.P.7
Brodsky, J.L.8
Kleyman, T.R.9
-
28
-
-
33947134399
-
Small heat-shock proteins select δF508-CFTR for endoplasmic reticulum-associated degradation
-
Ahner, A., Nakatsukasa, K., Zhang, H., Frizzell, R. A., and Brodsky, J. L. (2007) Small heat-shock proteins select δF508-CFTR for endoplasmic reticulum-associated degradation. Mol. Biol. Cell 18, 806-814
-
(2007)
Mol. Biol. Cell
, vol.18
, pp. 806-814
-
-
Ahner, A.1
Nakatsukasa, K.2
Zhang, H.3
Frizzell, R.A.4
Brodsky, J.L.5
-
29
-
-
77951448229
-
αB-crystallin regulation of angiogenesis by modulation of VEGF
-
Kase, S., He, S., Sonoda, S., Kitamura, M., Spee, C., Wawrousek, E., Ryan, S. J., Kannan, R., and Hinton, D. R. (2010) αB-crystallin regulation of angiogenesis by modulation of VEGF. Blood 115, 3398-3406
-
(2010)
Blood
, vol.115
, pp. 3398-3406
-
-
Kase, S.1
He, S.2
Sonoda, S.3
Kitamura, M.4
Spee, C.5
Wawrousek, E.6
Ryan, S.J.7
Kannan, R.8
Hinton, D.R.9
-
30
-
-
33344474711
-
αB-crystallin mutation in dilated cardiomyopathy
-
Inagaki, N., Hayashi, T., Arimura, T., Koga, Y., Takahashi, M., Shibata, H., Teraoka, K., Chikamori, T., Yamashina, A., and Kimura, A. (2006) αB-crystallin mutation in dilated cardiomyopathy. Biochem. Biophys. Res. Commun. 342, 379-386
-
(2006)
Biochem. Biophys. Res. Commun.
, vol.342
, pp. 379-386
-
-
Inagaki, N.1
Hayashi, T.2
Arimura, T.3
Koga, Y.4
Takahashi, M.5
Shibata, H.6
Teraoka, K.7
Chikamori, T.8
Yamashina, A.9
Kimura, A.10
-
31
-
-
33745365549
-
αB-crystallin mutation in dilated cardiomyopathies: Low prevalence in a consecutive series of 200 unrelated probands
-
Pilotto, A., Marziliano, N., Pasotti, M., Grasso, M., Costante, A. M., and Arbustini, E. (2006) αB-crystallin mutation in dilated cardiomyopathies: low prevalence in a consecutive series of 200 unrelated probands. Biochem. Biophys. Res. Commun. 346, 1115-1117
-
(2006)
Biochem. Biophys. Res. Commun.
, vol.346
, pp. 1115-1117
-
-
Pilotto, A.1
Marziliano, N.2
Pasotti, M.3
Grasso, M.4
Costante, A.M.5
Arbustini, E.6
-
32
-
-
77950932697
-
The p.G154S mutation of the α-B crystallin gene (CRYAB) causes late-onset distal myopathy
-
Reilich, P., Schoser, B., Schramm, N., Krause, S., Schessl, J., Kress, W., Müller-Höcker, J., Walter, M. C., and Lochmuller, H. (2010) The p.G154S mutation of the α-B crystallin gene (CRYAB) causes late-onset distal myopathy. Neuromuscul. Disord. 20, 255-259
-
(2010)
Neuromuscul. Disord
, vol.20
, pp. 255-259
-
-
Reilich, P.1
Schoser, B.2
Schramm, N.3
Krause, S.4
Schessl, J.5
Kress, W.6
Müller-Höcker, J.7
Walter, M.C.8
Lochmuller, H.9
-
33
-
-
84941932690
-
The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology
-
Veerman, C. C., Wilde, A. A., and Lodder, E. M. (2015) The cardiac sodium channel gene SCN5A and its gene product NaV1.5: role in physiology and pathophysiology. Gene 573, 177-187
-
(2015)
Gene
, vol.573
, pp. 177-187
-
-
Veerman, C.C.1
Wilde, A.A.2
Lodder, E.M.3
|