Cargando…
MiR-1-3p that correlates with left ventricular function of HCM can serve as a potential target and differentiate HCM from DCM
BACKGROUND: MicroRNAs (miRNAs) are non-coding RNAs that function as regulators of gene expression and thereby contribute to the complex disease phenotypes. Hypertrophic cardiomyopathy (HCM) and Dilated cardiomyopathy (DCM) can cause sudden cardiac death and eventually develop into heart failure. How...
Autores principales: | Li, Mengmeng, Chen, Xiao, Chen, Liang, Chen, Kai, Zhou, Jianye, Song, Jiangping |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994246/ https://www.ncbi.nlm.nih.gov/pubmed/29885652 http://dx.doi.org/10.1186/s12967-018-1534-3 |
Ejemplares similares
-
Value of MRI derived parameters in the discrimination of familial left ventricular noncompaction (LVNC), DCM and HCM in comparison to healthy volunteers
por: Gutberlet, Matthias, et al.
Publicado: (2011) -
Histopathology in HCM
por: Tejado, Beatriz San Millán, et al.
Publicado: (2018) -
Cardiac MRI findings to differentiate athlete's heart from hypertrophic (HCM), arrhythmogenic right ventricular (ARVC) and dilated (DCM) cardiomyopathy
por: Kübler, J., et al.
Publicado: (2021) -
Follow-up and prognosis of HCM
por: Dominguez, Fernando, et al.
Publicado: (2018) -
Foreword to the Special Issue: HCM in 2018
por: Elliott, Perry
Publicado: (2018)