Characterization of human cardiac Na(+) channel mutations in the congenital long QT syndrome

Por Wang, Dao W., Yazawa, Kazuto, George, Alfred L., Bennett, Paul B.
Publicado em 1996

The transient outward current in mice lacking the potassium channel gene Kv1.4

Por London, Barry, Wang, Dao W, Hill, Joseph A, Bennett, Paul B
Publicado em 1998

Nadolol block of Nav1.5 does not explain its efficacy in the long QT syndrome

Por Besana, Alessandra, Wang, Dao W., George, Alfred L., Schwartz, Peter J.
Publicado em 2012

Prolonged action potential duration in cardiac ablation of PDK1 mice

Por Han, Zhonglin, Jiang, Yu, Yang, Zhongzhou, Cao, Kejiang, Wang, Dao W
Publicado no Int J Clin Exp Med (2015)

The ER Stress-Mediated Mitochondrial Apoptotic Pathway and MAPKs Modulate Tachypacing-Induced Apoptosis in HL-1 Atrial Myocytes

Por Shi, Jiaojiao, Jiang, Qi, Ding, Xiangwei, Xu, Wenhua, Wang, Dao W., Chen, Minglong
Publicado no PLoS One (2015)

Decreased Peripheral Mitochondrial DNA Copy Number is Associated with the Risk of Heart Failure and Long-term Outcomes

Por Huang, Jin, Tan, Lun, Shen, Rufei, Zhang, Lina, Zuo, Houjuan, Wang, Dao W.
Publicado no Medicine (Baltimore) (2016)

Noninactivating voltage-gated sodium channels in severe myoclonic epilepsy of infancy

Por Rhodes, Thomas H., Lossin, Christoph, Vanoye, Carlos G., Wang, Dao W., George, Alfred L.
Publicado em 2004

Deletion of PDK1 Causes Cardiac Sodium Current Reduction in Mice

Por Han, Zhonglin, Jiang, Yu, Yang, Yuqing, Li, Xuehan, Yang, Zhongzhou, Cao, Kejiang, Wang, Dao W.
Publicado no PLoS One (2015)

Activation of protein kinase C alters the intracellular distribution and mobility of cardiac Na(+) channels

Por Hallaq, Haifa, Wang, Dao W., Kunic, Jennifer D., George, Alfred L., Wells, K. Sam, Murray, Katherine T.
Publicado em 2012

Propranolol Blocks Cardiac and Neuronal Voltage-Gated Sodium Channels

Por Wang, Dao W., Mistry, Akshitkumar M., Kahlig, Kristopher M., Kearney, Jennifer A., Xiang, Jizhou, George, Alfred L.
Publicado em 2010

Novel Deletion Mutation in the Cardiac Sodium Channel Inactivation Gate Causes Long QT Syndrome

Por Detta, Nicola, Frisso, Giulia, Zullo, Alberto, Sarubbi, Berardo, Cozzolino, Carla, Romeo, Emanuele, Wang, Dao W., Calabrò, Raffaele, Salvatore, Francesco, George, Alfred L.
Publicado em 2012

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

Por Benson, D. Woodrow, Wang, Dao W., Dyment, Macaira, Knilans, Timothy K., Fish, Frank A., Strieper, Margaret J., Rhodes, Thomas H., George, Alfred L.
Publicado em 2003

Malignant Perinatal Variant of Long-QT Syndrome Caused by a Profoundly Dysfunctional Cardiac Sodium Channel

Por Wang, Dao W., Crotti, Lia, Shimizu, Wataru, Pedrazzini, Matteo, Cantu', Francesco, De Filippo, Paolo, Kishiki, Kanako, Miyazaki, Aya, Ikeda, Tomoaki, Schwartz, Peter J., George, Alfred L.
Publicado em 2008

Conditional Mutation of Pkd2 Causes Cystogenesis and Upregulates β-Catenin

Por Kim, Ingyu, Ding, Tianbing, Fu, Yulong, Li, Cunxi, Cui, Lan, Li, Ao, Lian, Peiwen, Liang, Dan, Wang, Dao W., Guo, Caiying, Ma, Jie, Zhao, Ping, Coffey, Robert J., Zhan, Qimin, Wu, Guanqing
Publicado em 2009

Striking in Vivo Phenotype of a Disease-Associated Human SCN5A Mutation Producing Minimal Changes in Vitro

Por Watanabe, Hiroshi, Yang, Tao, Stroud, Dina M., Lowe, John S., Harris, Louise, Atack, Thomas C., Wang, Dao W., Hipkens, Susan B., Leake, Brenda, Hall, Lynn, Kupershmidt, Sabina, Chopra, Nagesh, Magnuson, Mark A., Tanabe, Naohito, Knollmann, Björn C., George, Alfred L., Roden, Dan M.
Publicado em 2011