Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL052768-03
Application #
2230364
Study Section
Pharmacology A Study Section (PHRA)
Project Start
1994-08-01
Project End
1999-07-31
Budget Start
1996-08-01
Budget End
1997-07-31
Support Year
3
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Yamagishi, Toshio; Xiong, Wei; Kondratiev, Andre et al. (2009) Novel molecular determinants in the pore region of sodium channels regulate local anesthetic binding. Mol Pharmacol 76:861-71
Azene, Ezana M; Sang, Dongpei; Tsang, Suk-Ying et al. (2005) Pore-to-gate coupling of HCN channels revealed by a pore variant that contributes to gating but not permeation. Biochem Biophys Res Commun 327:1131-42
Azene, Ezana M; Xue, Tian; Marban, Eduardo et al. (2005) Non-equilibrium behavior of HCN channels: insights into the role of HCN channels in native and engineered pacemakers. Cardiovasc Res 67:263-73
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Moore, Jennifer C; van Laake, Linda W; Braam, Stefan R et al. (2005) Human embryonic stem cells: genetic manipulation on the way to cardiac cell therapies. Reprod Toxicol 20:377-91
Wang, Kai; Xue, Tian; Tsang, Suk-Ying et al. (2005) Electrophysiological properties of pluripotent human and mouse embryonic stem cells. Stem Cells 23:1526-34
Xue, Tian; Cho, Hee Cheol; Akar, Fadi G et al. (2005) Functional integration of electrically active cardiac derivatives from genetically engineered human embryonic stem cells with quiescent recipient ventricular cardiomyocytes: insights into the development of cell-based pacemakers. Circulation 111:11-20
Li, Ronald A; Tomaselli, Gordon F (2004) Using the deadly mu-conotoxins as probes of voltage-gated sodium channels. Toxicon 44:117-22
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