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Results: 1-5 |
Results: 5

Authors: Bianchi, L Priori, SG Napolitano, C Surewicz, KA Dennis, AT Memmi, M Schwartz, PJ Brown, AM
Citation: L. Bianchi et al., Mechanisms of I-Ks suppression in LQT1 mutants, AM J P-HEAR, 279(6), 2000, pp. H3003-H3011

Authors: Ficker, E Thomas, D Viswanathan, PC Dennis, AT Priori, SG Napolitano, C Memmi, M Wible, BA Kaufman, ES Iyengar, S Schwartz, PJ Rudy, Y Brown, AM
Citation: E. Ficker et al., Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome, AM J P-HEAR, 279(4), 2000, pp. H1748-H1756

Authors: Ficker, E Dennis, AT Obejero-Paz, CA Castaldo, P Taglialatela, M Brown, AM
Citation: E. Ficker et al., Retention in the endoplasmic reticulum as a mechanism of dominant-negativecurrent suppression in human long QT syndrome, J MOL CEL C, 32(12), 2000, pp. 2327-2337

Authors: Bianchi, L Shen, ZJ Dennis, AT Priori, SG Napolitano, C Ronchetti, E Bryskin, R Schwartz, PJ Brown, AM
Citation: L. Bianchi et al., Cellular dysfunction of LQT5-minK mutants: abnormalities of I-Ks, I-Kr andtrafficking in long QT syndrome, HUM MOL GEN, 8(8), 1999, pp. 1499-1507

Authors: Bianchi, L Shen, ZJ Dennis, AT Priori, SG Napolitano, C Ronchetti, E Bryskin, R Schwartz, PJ Brown, AM
Citation: L. Bianchi et al., Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome (vol 8, 1499, 1999), HUM MOL GEN, 8(12), 1999, pp. 2335-2335
Risultati: 1-5 |