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Results: 1-13 |
Results: 13
Cardiomyopathy in Irx4-deficient mice is preceded by abnormal ventricular gene expression
Authors: Bruneau, BG Bao, ZZ Fatkin, D Xavier-Neto, J Georgakopoulos, D Maguire, CT Berul, CI Kass, DA Kuroski-de Bold, ML de Bold, AJ Conner, DA Rosenthal, N Cepko, CL Seidman, CE Seidman, JG
Citation: Bg. Bruneau et al., Cardiomyopathy in Irx4-deficient mice is preceded by abnormal ventricular gene expression, MOL CELL B, 21(5), 2001, pp. 1730-1736
Prognostic value of left ventricular hypertrophy in hypertrophic cardiomyopathy.
Authors: Fatkin, D Graham, RM
Citation: D. Fatkin et Rm. Graham, Prognostic value of left ventricular hypertrophy in hypertrophic cardiomyopathy., N ENG J MED, 344(1), 2001, pp. 63-64
A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy
Authors: Semsarian, C Healey, MJ Fatkin, D Giewat, M Duffy, C Seidman, CE Seidman, JG
Citation: C. Semsarian et al., A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy, J MOL CEL C, 33(11), 2001, pp. 2055-2060
Comparison of two murine models of familial hypertrophic cardiomyopathy
Authors: McConnell, BK Fatkin, D Semsarian, C Jones, KA Georgakopoulos, D Maguire, CT Healey, MJ Mudd, JO Moskowitz, IPG Conner, DA Giewat, M Wakimoto, H Berul, CI Schoen, FJ Kass, DA Seidman, CE Seidman, JG
Citation: Bk. Mcconnell et al., Comparison of two murine models of familial hypertrophic cardiomyopathy, CIRCUL RES, 88(4), 2001, pp. 383-389
An abnormal Ca2+ response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy
Authors: Fatkin, D McConnell, BK Mudd, JO Semsarian, C Moskowitz, IGP Schoen, FJ Giewat, M Seidman, CE Seidman, JG
Citation: D. Fatkin et al., An abnormal Ca2+ response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy, J CLIN INV, 106(11), 2000, pp. 1351-1359
Dilated cardiomyopathy and sensorineural hearing loss - A heritable syndrome that maps to 6q23-24
Authors: Schonberger, J Levy, H Grunig, E Sangwatanaroj, S Fatkin, D MacRae, C Stacker, H Halpin, C Eavey, R Philbin, EF Katus, H Seidman, JG Seidman, CE
Citation: J. Schonberger et al., Dilated cardiomyopathy and sensorineural hearing loss - A heritable syndrome that maps to 6q23-24, CIRCULATION, 101(15), 2000, pp. 1812-1818
Electrophysiologic characteristics of accessory atrioventricular connections in an inherited form of Wolff-Parkinson-White syndrome
Authors: Mehdirad, AA Fatkin, D DiMarco, JP MacRae, CA Wase, A Seidman, JG Seidman, CE Benson, DW
Citation: Aa. Mehdirad et al., Electrophysiologic characteristics of accessory atrioventricular connections in an inherited form of Wolff-Parkinson-White syndrome, J CARD ELEC, 10(5), 1999, pp. 629-635
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.
Authors: Fatkin, D MacRae, C Sasaki, T Wolff, MR Porcu, M Frenneaux, M Atherton, J Vidaillet, HJ Spudich, S De Girolami, U Seidman, JG Seidman, CE Muntoni, F Muehle, G Johnson, W McDonough, B
Citation: D. Fatkin et al., Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease., N ENG J MED, 341(23), 1999, pp. 1715-1724
Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice
Authors: McConnell, BK Jones, KA Fatkin, D Arroyo, LH Lee, RT Aristizabal, O Turnbull, DH Georgakopoulos, D Kass, D Bond, M Niimura, H Schoen, FJ Conner, D Fischman, DH Seidman, CE Seidman, JG
Citation: Bk. Mcconnell et al., Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice, J CLIN INV, 104(9), 1999, pp. 1235-1244
Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice (vol 104, pg 1235, 1999)
Authors: McConnell, BK Jones, KA Fatkin, D Arroyo, LH Lee, RT Aristizabal, O Turnbull, DH Georgakopoulos, D Kass, D Bond, M Niimura, H Schoen, FJ Conner, D Fischman, DA Seidman, CE Seidman, JG
Citation: Bk. Mcconnell et al., Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice (vol 104, pg 1235, 1999), J CLIN INV, 104(12), 1999, pp. 1771-1771
Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene
Authors: Fatkin, D Christe, ME Aristizabal, O McConnell, BK Srinivasan, S Schoen, FJ Seidman, CE Turnbull, DH Seidman, JG
Citation: D. Fatkin et al., Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene, J CLIN INV, 103(1), 1999, pp. 147-153
Familial dilated cardiomyopathy locus maps to chromosome 2q31
Authors: Siu, BL Niimura, H Osborne, JA Fatkin, D MacRae, C Solomon, S Benson, W Seidman, JG Seidman, CE
Citation: Bl. Siu et al., Familial dilated cardiomyopathy locus maps to chromosome 2q31, CIRCULATION, 99(8), 1999, pp. 1022-1026
Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation
Authors: Gruver, EJ Fatkin, D Dodds, GA Kisslo, J Maron, BJ Seidman, JG Seidman, CE
Citation: Ej. Gruver et al., Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation, AM J CARD, 83(12A), 1999, pp. 13H-18H
Risultati: 1-13 |