Molecular mechanism of the E99K mutation in cardiac actin (ACTC Gene) that causes apical hypertrophy in man and mouse.
We generated a transgenic mouse model expressing the apical hypertrophic cardiomyopathy-causing mutation ACTC E99K at 50% of total heart actin and compared it with actin from patients carrying the same mutation. The actin mutation caused a higher Ca(2+) sensitivity in reconstituted thin filaments me...
المؤلفون الرئيسيون: | Song, W, Dyer, E, Stuckey, D, Copeland, O, Leung, M, Bayliss, C, Messer, A, Wilkinson, R, Tremoleda, J, Schneider, MD, Harding, SE, Redwood, C, Clarke, K, Nowak, K, Monserrat, L, Wells, D, Marston, S |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2011
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مواد مشابهة
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PHENOTYPE OF THE ACTC E99K TRANSGENIC MOUSE REPRODUCES HYPERTROPHIC CARDIOMYOPATHY IN PATIENTS
حسب: Song, W, وآخرون
منشور في: (2010) -
Mouse HCM Model Expression E99K ACTC Mutation Reproduces the Clinical HCM Phenotype
حسب: Song, W, وآخرون
منشور في: (2009) -
Mouse Model of Familial Hypertrophic Cardiomyopathy with E99K ACTC Mutation Recapitulates Many Features of Hypertrophic Cardiomyopathy in Patients
حسب: Song, W, وآخرون
منشور في: (2008) -
Investigation of a mouse model of familial DCM with ACTC E361G mutation
حسب: Song, W, وآخرون
منشور في: (2008) -
Age and strain related aberrant Ca(2+) release is associated with sudden cardiac death in the ACTC E99K mouse model of hypertrophic cardiomyopathy
حسب: Rowlands, C, وآخرون
منشور في: (2017)