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Results: 1-25 | 26-41
Results: 1-25/41
Identification of genetic loci associated with paralysis, inflammation andweight loss in mouse experimental autoimmune encephalomyelitis
Authors: Encinas, JA Lees, MB Sobel, RA Symonowicz, C Weiner, HL Seidman, CE Seidman, JG Kuchroo, VK
Citation: Ja. Encinas et al., Identification of genetic loci associated with paralysis, inflammation andweight loss in mouse experimental autoimmune encephalomyelitis, INT IMMUNOL, 13(3), 2001, pp. 257-264
Development of left ventricular hypertrophy in adults with hypertrophic cardiomyopathy caused by cardiac myosin-binding protein C gene mutations
Authors: Maron, BJ Niimura, H Casey, SA Soper, MK Wright, GB Seidman, JG Seidman, CE
Citation: Bj. Maron et al., Development of left ventricular hypertrophy in adults with hypertrophic cardiomyopathy caused by cardiac myosin-binding protein C gene mutations, J AM COL C, 38(2), 2001, pp. 315-321
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
A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease
Authors: Bruneau, BG Nemer, G Schmitt, JP Charron, F Robitaille, L Caron, S Conner, DA Gessler, M Nemer, M Seidman, CE Seidman, JG
Citation: Bg. Bruneau et al., A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease, CELL, 106(6), 2001, pp. 709-721
The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms
Authors: Seidman, JG Seidman, C
Citation: Jg. Seidman et C. Seidman, The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms, CELL, 104(4), 2001, pp. 557-567
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
Ventricular arrhythmia vulnerability in cardiomyopathic mice with homozygous mutant myosin-binding protein C gene
Authors: Berul, CI McConnell, RK Wakimoto, H Moskowitz, IPG Maguire, CT Semsarian, C Vargas, MM Gehrmann, J Seidman, CE Seidman, JG
Citation: Ci. Berul et al., Ventricular arrhythmia vulnerability in cardiomyopathic mice with homozygous mutant myosin-binding protein C gene, CIRCULATION, 104(22), 2001, pp. 2734-2739
A nonsense mutation in MSX1 causes Witkop syndrome
Authors: Jumlongras, D Bei, M Stimson, JM Wang, WF DePalma, SR Seidman, CE Felbor, U Maas, R Seidman, JG Olsen, BR
Citation: D. Jumlongras et al., A nonsense mutation in MSX1 causes Witkop syndrome, AM J HU GEN, 69(1), 2001, pp. 67-74
Mutations in COCH (formerly Coch5b2) cause DFNA9
Authors: Eavey, RD Manolis, EN Lubianca, J Merchant, S Seidman, JG Seidman, C
Citation: Rd. Eavey et al., Mutations in COCH (formerly Coch5b2) cause DFNA9, ADV OTO-RH, 56, 2000, pp. 101-102
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
Authors: Kamisago, M Sharma, SD DePalma, SR Solomon, S Sharma, P McDonough, B Smoot, L Mullen, MP Woolf, PK Wigle, ED Seidman, JG Seidman, CE
Citation: M. Kamisago et al., Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy, N ENG J MED, 343(23), 2000, pp. 1688-1696
Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease
Authors: Kasahara, H Lee, B Schott, JJ Benson, DW Seidman, JG Seidman, CE Izumo, S
Citation: H. Kasahara et al., Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease, J CLIN INV, 106(2), 2000, pp. 299-308
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
Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2-5 and dHand
Authors: Bruneau, BG Bao, ZZ Tanaka, M Schott, JJ Izumo, S Cepko, CL Seidman, JG Seidman, CE
Citation: Bg. Bruneau et al., Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2-5 and dHand, DEVELOP BIO, 217(2), 2000, pp. 266-277
Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophic cardiomyopathy
Authors: Tyska, MJ Hayes, E Giewat, M Seidman, CE Seidman, JG Warshaw, DM
Citation: Mj. Tyska et al., Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophic cardiomyopathy, CIRCUL RES, 86(7), 2000, pp. 737-744
Homozygous mutation in cardiac troponin T - Implications for hypertrophic cardiomyopathy
Authors: Ho, CY Lever, HM DeSanctis, R Farver, CF Seidman, JG Seidman, CE
Citation: Cy. Ho et al., Homozygous mutation in cardiac troponin T - Implications for hypertrophic cardiomyopathy, CIRCULATION, 102(16), 2000, pp. 1950-1955
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
Pyogenic arthritis, pyoderma gangrenosum, and acne syndrome maps to chromosome 15q
Authors: Yeon, HB Lindor, NM Seidman, JG Seidman, CE
Citation: Hb. Yeon et al., Pyogenic arthritis, pyoderma gangrenosum, and acne syndrome maps to chromosome 15q, AM J HU GEN, 66(4), 2000, pp. 1443-1448
The pathogenesis of familial hypertrophic cardiomyopathy: Early and evolving effects from an alpha-cardiac myosin heavy chain missense mutation
Authors: Georgakopoulos, D Christe, ME Giewat, M Seidman, CM Seidman, JG Kass, DA
Citation: D. Georgakopoulos et al., The pathogenesis of familial hypertrophic cardiomyopathy: Early and evolving effects from an alpha-cardiac myosin heavy chain missense mutation, NAT MED, 5(3), 1999, pp. 327-330
QTL influencing autoimmune diabetes and encephalomyelitis map to a 0.15-cMregion containing I/2
Authors: Encinas, JA Wicker, LS Peterson, LB Mukasa, A Teuscher, C Sobel, R Weiner, HL Seidman, CE Seidman, JG Kuchroo, VK
Citation: Ja. Encinas et al., QTL influencing autoimmune diabetes and encephalomyelitis map to a 0.15-cMregion containing I/2, NAT GENET, 21(2), 1999, pp. 158-160
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
An alpha-cardiac myosin heavy chain gene mutation impairs contraction and relaxation function of cardiac myocytes
Authors: Kim, SJ Iizuka, K Kelly, RA Geng, YJ Bishop, SP Yang, GP Kudej, A McConnell, BK Seidman, CE Seidman, JG Vatner, SF
Citation: Sj. Kim et al., An alpha-cardiac myosin heavy chain gene mutation impairs contraction and relaxation function of cardiac myocytes, AM J P-HEAR, 45(5), 1999, pp. H1780-H1787
Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21
Authors: Manolis, EN Eavey, RD Sangwatanaroj, S Halpin, C Rosenbaum, S Watkins, H Jarcho, J Seidman, CE Seidman, JG
Citation: En. Manolis et al., Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21, AM J OTOL, 20(5), 1999, pp. 621-626
Regulation of chamber-specific gene expression in the developing heart by Irx4
Authors: Bao, ZZ Bruneau, BG Seidman, JG Seidman, CE Cepko, CL
Citation: Zz. Bao et al., Regulation of chamber-specific gene expression in the developing heart by Irx4, SCIENCE, 283(5405), 1999, pp. 1161-1164
QT dispersion in alpha-myosin heavy-chain familial hypertrophic cardiomyopathy mice
Authors: Bevilacqua, LM Maguire, CT Seidman, JG Seidman, CE Berul, CI
Citation: Lm. Bevilacqua et al., QT dispersion in alpha-myosin heavy-chain familial hypertrophic cardiomyopathy mice, PEDIAT RES, 45(5), 1999, pp. 643-647
Risultati: 1-25 | 26-41