Cargando…
The Role of the L-Type Ca(2+) Channel in Altered Metabolic Activity in a Murine Model of Hypertrophic Cardiomyopathy
Heterozygous mice (αMHC(403/+)) expressing the human disease-causing mutation Arg403Gln exhibit cardinal features of hypertrophic cardiomyopathy (HCM) including hypertrophy, myocyte disarray, and increased myocardial fibrosis. Treatment of αMHC(403/+)mice with the L-type calcium channel (I(Ca-L)) an...
Autores principales: | Viola, Helena M., Johnstone, Victoria P.A., Cserne Szappanos, Henrietta, Richman, Tara R., Tsoutsman, Tatiana, Filipovska, Aleksandra, Semsarian, Christopher, Seidman, Jonathan G., Seidman, Christine E., Hool, Livia C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113168/ https://www.ncbi.nlm.nih.gov/pubmed/30167506 http://dx.doi.org/10.1016/j.jacbts.2015.12.001 |
Ejemplares similares
-
Characterization and validation of a preventative therapy for hypertrophic cardiomyopathy in a murine model of the disease
por: Viola, Helena M., et al.
Publicado: (2020) -
Preventative therapeutic approaches for hypertrophic cardiomyopathy
por: Solomon, Tanya, et al.
Publicado: (2020) -
Cytoskeletal disarray increases arrhythmogenic vulnerability during sympathetic stimulation in a model of hypertrophic cardiomyopathy
por: Cserne Szappanos, Henrietta, et al.
Publicado: (2023) -
A maladaptive feedback mechanism between the extracellular matrix and cytoskeleton contributes to hypertrophic cardiomyopathy pathophysiology
por: Viola, Helena M., et al.
Publicado: (2023) -
Evidence for redox sensing by a human cardiac calcium channel
por: Muralidharan, Padmapriya, et al.
Publicado: (2016)