| Year |
Citation |
Score |
| 2012 |
Yoshida H, Bao L, Kefaloyianni E, Taskin E, Okorie U, Hong M, Dhar-Chowdhury P, Kaneko M, Coetzee WA. AMP-activated protein kinase connects cellular energy metabolism to K ATP channel function Journal of Molecular and Cellular Cardiology. 52: 410-418. PMID 21888913 DOI: 10.1016/J.Yjmcc.2011.08.013 |
0.762 |
|
| 2009 |
Ohno S, Toyoda F, Zankov DP, Yoshida H, Makiyama T, Tsuji K, Honda T, Obayashi K, Ueyama H, Shimizu W, Miyamoto Y, Kamakura S, Matsuura H, Kita T, Horie M. Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome. Human Mutation. 30: 557-63. PMID 19306396 DOI: 10.1002/humu.20834 |
0.311 |
|
| 2007 |
Ohno S, Zankov DP, Yoshida H, Tsuji K, Makiyama T, Itoh H, Akao M, Hancox JC, Kita T, Horie M. N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 4: 332-40. PMID 17341399 DOI: 10.1016/j.hrthm.2006.11.004 |
0.387 |
|
| 2006 |
Tong X, Porter LM, Liu G, Dhar-Chowdhury P, Srivastava S, Pountney DJ, Yoshida H, Artman M, Fishman GI, Yu C, Iyer R, Morley GE, Gutstein DE, Coetzee WA. Consequences of cardiac myocyte-specific ablation of KATP channels in transgenic mice expressing dominant negative Kir6 subunits. American Journal of Physiology. Heart and Circulatory Physiology. 291: H543-51. PMID 16501027 DOI: 10.1152/Ajpheart.00051.2006 |
0.718 |
|
| 2005 |
Dhar-Chowdhury P, Harrell MD, Han SY, Jankowska D, Parachuru L, Morrissey A, Srivastava S, Liu W, Malester B, Yoshida H, Coetzee WA. The glycolytic enzymes, glyceraldehyde-3-phosphate dehydrogenase, triose-phosphate isomerase, and pyruvate kinase are components of the K(ATP) channel macromolecular complex and regulate its function. The Journal of Biological Chemistry. 280: 38464-70. PMID 16170200 DOI: 10.1074/Jbc.M508744200 |
0.758 |
|
| 2005 |
Morrissey A, Parachuru L, Leung M, Lopez G, Nakamura TY, Tong X, Yoshida H, Srivastiva S, Chowdhury PD, Artman M, Coetzee WA. Expression of ATP-sensitive K+ channel subunits during perinatal maturation in the mouse heart. Pediatric Research. 58: 185-92. PMID 16085792 DOI: 10.1203/01.Pdr.0000169967.83576.Cb |
0.715 |
|
| 2005 |
Morrissey A, Rosner E, Lanning J, Parachuru L, Dhar Chowdhury P, Han S, Lopez G, Tong X, Yoshida H, Nakamura TY, Artman M, Giblin JP, Tinker A, Coetzee WA. Immunolocalization of KATP channel subunits in mouse and rat cardiac myocytes and the coronary vasculature. Bmc Physiology. 5: 1. PMID 15647111 DOI: 10.1186/1472-6793-5-1 |
0.778 |
|
| 2004 |
Yoshida H, Feig JE, Morrissey A, Ghiu IA, Artman M, Coetzee WA. K ATP channels of primary human coronary artery endothelial cells consist of a heteromultimeric complex of Kir6.1, Kir6.2, and SUR2B subunits. Journal of Molecular and Cellular Cardiology. 37: 857-69. PMID 15380676 DOI: 10.1016/J.Yjmcc.2004.05.022 |
0.796 |
|
| 2002 |
Haruna T, Yoshida H, Nakamura TY, Xie LH, Otani H, Ninomiya T, Takano M, Coetzee WA, Horie M. Alpha1-adrenoceptor-mediated breakdown of phosphatidylinositol 4,5-bisphosphate inhibits pinacidil-activated ATP-sensitive K+ currents in rat ventricular myocytes. Circulation Research. 91: 232-9. PMID 12169649 DOI: 10.1161/01.Res.0000029971.60214.49 |
0.797 |
|
| 2002 |
Kubota T, Horie M, Takano M, Yoshida H, Otani H, Sasayama S. Role of KCNQ1 in the cell swelling-induced enhancement of the slowly activating delayed rectifier K(+) current. The Japanese Journal of Physiology. 52: 31-9. PMID 12047800 |
0.504 |
|
| 2002 |
Kubota T, Horie M, Takano M, Yoshida H, Takenaka K, Watanabe E, Tsuchiya T, Otani H, Sasayama S. Evidence for a single nucleotide polymorphism in the KCNQ1 potassium channel that underlies susceptibility to life-threatening arrhythmias. Journal of Cardiovascular Electrophysiology. 12: 1223-9. PMID 11761407 DOI: 10.1046/j.1540-8167.2001.01223.x |
0.33 |
|
| 2001 |
Yamashita F, Horie M, Kubota T, Yoshida H, Yumoto Y, Kobori A, Ninomiya T, Kono Y, Haruna T, Tsuji K, Washizuka T, Takano M, Otani H, Sasayama S, Aizawa Y. Characterization and subcellular localization of KCNQ1 with a heterozygous mutation in the C terminus. Journal of Molecular and Cellular Cardiology. 33: 197-207. PMID 11162126 DOI: 10.1006/jmcc.2000.1300 |
0.303 |
|
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