AAAAAA

   
Results: 1-20 |
Results: 20
Molecular and cellular mechanisms of cardiac arrhythmias
Authors: Keating, MT Sanguinetti, MC
Citation: Mt. Keating et Mc. Sanguinetti, Molecular and cellular mechanisms of cardiac arrhythmias, CELL, 104(4), 2001, pp. 569-580
Mammalian myotube dedifferentiation induced by newt regeneration extract
Authors: McGann, CJ Odelberg, SJ Keating, MT
Citation: Cj. Mcgann et al., Mammalian myotube dedifferentiation induced by newt regeneration extract, P NAS US, 98(24), 2001, pp. 13699-13704
ETL, a novel seven-transmembrane receptor that is Developmentally regulated in the heart - ETL is a member of the secretin family and belongs to the epidermal growth factor seven-transmembrane subfamily
Authors: Nechiporuk, T Urness, LD Keating, MT
Citation: T. Nechiporuk et al., ETL, a novel seven-transmembrane receptor that is Developmentally regulated in the heart - ETL is a member of the secretin family and belongs to the epidermal growth factor seven-transmembrane subfamily, J BIOL CHEM, 276(6), 2001, pp. 4150-4157
Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channel
Authors: Huang, FD Chen, J Lin, M Keating, MT Sanguinetti, MC
Citation: Fd. Huang et al., Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channel, CIRCULATION, 104(9), 2001, pp. 1071-1075
Genotype-phenotype correlation in the long-QT syndrome - Gene-specific triggers for life-threatening arrhythmias
Authors: Schwartz, PJ Priori, SG Spazzolini, C Moss, AJ Vincent, GM Napolitano, C Denjoy, I Guicheney, P Breithardt, G Keating, MT Towbin, JA Beggs, AH Brink, P Wilde, AAM Toivonen, L Zareba, W Robinson, JL Timothy, KW Corfield, V Wattanasirichaigoon, D Corbett, C Haverkamp, W Schulze-Bahr, E Lehmann, MH Schwartz, K Coumel, P Bloise, R
Citation: Pj. Schwartz et al., Genotype-phenotype correlation in the long-QT syndrome - Gene-specific triggers for life-threatening arrhythmias, CIRCULATION, 103(1), 2001, pp. 89-95
Induction of lef1 during zebrafish fin regeneration
Authors: Poss, KD Shen, JX Keating, MT
Citation: Kd. Poss et al., Induction of lef1 during zebrafish fin regeneration, DEV DYNAM, 219(2), 2000, pp. 282-286
Impaired distal airway development in mice lacking elastin
Authors: Wendel, DP Taylor, DG Albertine, KH Keating, MT Li, DY
Citation: Dp. Wendel et al., Impaired distal airway development in mice lacking elastin, AM J RESP C, 23(3), 2000, pp. 320-326
Dedifferentiation of mammalian myotubes induced by msx1
Authors: Odelberg, SJ Kollhoff, A Keating, MT
Citation: Sj. Odelberg et al., Dedifferentiation of mammalian myotubes induced by msx1, CELL, 103(7), 2000, pp. 1099-1109
Roles for Fgf signaling during zebrafish fin regeneration
Authors: Poss, FD Shen, JX Nechiporuk, A McMahon, G Thisse, B Thisse, C Keating, MT
Citation: Fd. Poss et al., Roles for Fgf signaling during zebrafish fin regeneration, DEVELOP BIO, 222(2), 2000, pp. 347-358
Spectrum of ST-T-wave patterns and repolarization parameters in congenitallong-QT syndrome - ECG findings identify genotypes
Authors: Zhang, L Timothy, KW Vincent, GM Lehmann, MH Fox, J Giuli, LC Shen, JX Splawski, I Priori, SG Compton, SJ Yanowitz, F Benhorin, J Moss, AJ Schwartz, PJ Robinson, JL Wang, Q Zareba, W Keating, MT Towbin, JA Napolitano, C Medina, A
Citation: L. Zhang et al., Spectrum of ST-T-wave patterns and repolarization parameters in congenitallong-QT syndrome - ECG findings identify genotypes, CIRCULATION, 102(23), 2000, pp. 2849-2855
Spectrum of mutations in long-QT syndrome genes KVLQT1, HERG, SCN5A, KCNE1, and KCNE2
Authors: Splawski, I Shen, JX Timothy, KW Lehmann, MH Priori, S Robinson, JL Moss, AJ Schwartz, PJ Towbin, JA Vincent, GM Keating, MT
Citation: I. Splawski et al., Spectrum of mutations in long-QT syndrome genes KVLQT1, HERG, SCN5A, KCNE1, and KCNE2, CIRCULATION, 102(10), 2000, pp. 1178-1185
Assessment of polymorphism in zebrafish mapping strains
Authors: Nechiporuk, A Finney, JE Keating, MT Johnson, SL
Citation: A. Nechiporuk et al., Assessment of polymorphism in zebrafish mapping strains, GENOME RES, 9(12), 1999, pp. 1231-1238
Functional effects of mutations in KvLQT1 that cause long QT syndrome
Authors: Wang, Z Tristani-Firouzi, M Xu, Q Lin, M Keating, MT Sanguinetti, MC
Citation: Z. Wang et al., Functional effects of mutations in KvLQT1 that cause long QT syndrome, J CARD ELEC, 10(6), 1999, pp. 817-826
Relation between outer and luminal diameter in cannulated arteries
Authors: Faury, G Maher, GM Li, DY Keating, MT Mecham, RP Boyle, WA
Citation: G. Faury et al., Relation between outer and luminal diameter in cannulated arteries, AM J P-HEAR, 277(5), 1999, pp. H1745-H1753
MiRP1 forms I-Kr potassium channels with HERG and is associated with cardiac arrhythmia
Authors: Abbott, GW Sesti, F Splawski, I Buck, ME Lehmann, WH Timothy, KW Keating, MT Goldstein, SAN
Citation: Gw. Abbott et al., MiRP1 forms I-Kr potassium channels with HERG and is associated with cardiac arrhythmia, CELL, 97(2), 1999, pp. 175-187
Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits. (vol 274, pg21063, 1999)
Authors: Franqueza, L Lin, M Shen, JX Keating, MT Sanguinetti, MC
Citation: L. Franqueza et al., Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits. (vol 274, pg21063, 1999), J BIOL CHEM, 274(35), 1999, pp. 25188-25188
Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits
Authors: Franqueza, L Lin, M Splawski, I Keating, MT Sanguinetti, MC
Citation: L. Franqueza et al., Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits, J BIOL CHEM, 274(30), 1999, pp. 21063-21070
Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation
Authors: Chen, J Zou, AR Splawski, I Keating, MT Sanguinetti, MC
Citation: J. Chen et al., Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation, J BIOL CHEM, 274(15), 1999, pp. 10113-10118
A novel human gene, WSTF, is deleted in Williams syndrome
Authors: Lu, XJ Meng, X Morris, CA Keating, MT
Citation: Xj. Lu et al., A novel human gene, WSTF, is deleted in Williams syndrome, GENOMICS, 54(2), 1998, pp. 241-249
Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes
Authors: Meng, X Lu, XJ Li, ZZ Green, ED Massa, H Trask, BJ Morris, CA Keating, MT
Citation: X. Meng et al., Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes, HUM GENET, 103(5), 1998, pp. 590-599
Risultati: 1-20 |