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Results: 1-15 |
Results: 15

Authors: Kurokawa, J Abriel, H Kass, RS
Citation: J. Kurokawa et al., Molecular basis of the delayed rectifier current I-Ks in heart, J MOL CEL C, 33(5), 2001, pp. 873-882

Authors: Kurokawa, J Motoike, HK Kass, RS
Citation: J. Kurokawa et al., TEA(+)-sensitive KCNQ1 constructs reveal pore-independent access to KCNE1 in assembled I-Ks channels, J GEN PHYSL, 117(1), 2001, pp. 43-52

Authors: Rivolta, I Abriel, H Tateyama, M Liu, HH Memmi, M Vardas, P Napolitano, C Priori, SG Kass, RS
Citation: I. Rivolta et al., Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes, J BIOL CHEM, 276(33), 2001, pp. 30623-30630

Authors: Abriel, H Cabo, C Wehrens, XHT Rivolta, I Motoike, HK Memmi, M Napolitano, C Priori, SG Kass, RS
Citation: H. Abriel et al., Novel arrhythmogenic mechanism revealed by a Long-QT syndrome mutation in the cardiac Na+ channel, CIRCUL RES, 88(7), 2001, pp. 740-745

Authors: Malhotra, JD Chen, CL Rivolta, I Abriel, H Malhotra, R Mattei, LN Brosius, FC Kass, RS Isom, LL
Citation: Jd. Malhotra et al., Characterization of sodium channel alpha- and beta-subunits in rat and mouse cardiac myocytes, CIRCULATION, 103(9), 2001, pp. 1303-1310

Authors: Heath, BM Wehrens, X Kass, RS
Citation: Bm. Heath et al., Overview: Molecular physiology of cardiac potassium channels, POTASSIUM CHANNELS IN CARDIOVASCULAR BIOLOGY, 2001, pp. 281-296

Authors: Abriel, H Motoike, H Kass, RS
Citation: H. Abriel et al., KChAP: a novel chaperone for specific K+ channels key to repolarization ofthe cardiac action potential. Focus on "KChAP as a chaperone for specific K+ channels", AM J P-CELL, 278(5), 2000, pp. C863-C864

Authors: Kass, RS Cabo, C
Citation: Rs. Kass et C. Cabo, Channel structure and drug-induced cardiac arrhythmias, P NAS US, 97(22), 2000, pp. 11683-11684

Authors: Doevendans, PA Kubalak, SW An, RH Becker, KD Chien, KR Kass, RS
Citation: Pa. Doevendans et al., Differentiation of cardiomyocytes in floating embryoid bodies is comparable to fetal cardiomyocytes, J MOL CEL C, 32(5), 2000, pp. 839-851

Authors: Abriel, H Wehrens, XHT Benhorin, J Kerem, B Kass, RS
Citation: H. Abriel et al., Molecular pharmacology of the sodium channel mutation D1790G linked to thelong-QT syndrome, CIRCULATION, 102(8), 2000, pp. 921-925

Authors: Wehrens, XHT Abriel, H Cabo, C Benhorin, J Kass, RS
Citation: Xht. Wehrens et al., Arrhythmogenic mechanism of an LQT-3 mutation of the human heart Na+ channel alpha-subunit - A computational analysis, CIRCULATION, 102(5), 2000, pp. 584-590

Authors: Benhorin, J Taub, R Goldmit, M Kerem, B Kass, RS Windman, I Medina, A
Citation: J. Benhorin et al., Effects of flecainide in patients with new SCN5A mutation - Mutation-specific therapy for long-QT syndrome?, CIRCULATION, 101(14), 2000, pp. 1698-1706

Authors: An, RH Heath, BM Higgins, JP Koch, WJ Lefkowitz, RJ Kass, RS
Citation: Rh. An et al., beta(2)-adrenergic receptor overexpression in the developing mouse heart: evidence for targeted modulation of ion channels, J PHYSL LON, 516(1), 1999, pp. 19-30

Authors: Lacinova, L An, RH Xia, J Ito, H Klugbauer, N Triggle, D Hofmann, F Kass, RS
Citation: L. Lacinova et al., Distinctions in the molecular determinants of charged and neutral dihydropyridine block of L-type calcium channels, J PHARM EXP, 289(3), 1999, pp. 1472-1479

Authors: Wang, WY Xia, J Kass, RS
Citation: Wy. Wang et al., MinK-KvLQT1 fusion proteins, evidence for multiple stoichiometries of the assembled I-sK channel, J BIOL CHEM, 273(51), 1998, pp. 34069-34074
Risultati: 1-15 |