Inherited cardiomyopathies are a major cause of mortality and morbidity worldwide and can
be caused by mutations in a wide range of proteins located in different cellular …

Background Dilated cardiomyopathy (DCM), characterized by progressive left ventricular
enlargement and systolic dysfunction, is the most common type of cardiomyopathy and a …

Dilated cardiomyopathy (DCM), characterized by left ventricular or biventricular enlargement
with systolic dysfunction, is the most common type of cardiac muscle disease. It is a major …

Endoplasmic reticulum (ER) stress has been implicated in the mechanisms underlying the
fibrotic process in dilated cardiomyopathy (DCM) and results in disease exacerbation; …

Background The mechanisms of the occurrence and progression of dilated cardiomyopathy
are still unclear and further exploration is needed. The upgrading of programming …

The relationship between autophagy and immunity has been well studied. However, little is
known about the role of autophagy in the immune microenvironment during the progression …

Objectives To assess the disease burden and changing trend of cardiomyopathy in children
aged 0–14 years in China from 1990 to 2019. Methods This study was based on the Global …

Objective This paper was performed to decipher the serum microRNA (miR)-125b-5p
expression in patients with dilated cardiomyopathy (DCM) combined with heart failure (HF) …

Background Synonymous variations have always been ignored while studying the
underlying genetic mechanisms for most of the human diseases. However, recent studies …

Aims Dilated cardiomyopathy (DCM) belongs to the common types of cardiomyopathies. The
pathogenesis remains unclear despite the fact that various genes have been found …