Modulation of cytoskeleton in cardiomyopathy caused by mutations in LMNA gene

M Chatzifrangkeskou, C Le Dour… - American Journal of …, 2023 - journals.physiology.org
Dilated cardiomyopathy caused by mutations in LMNA, encoding A-type lamins (ie, LMNA
cardiomyopathy), is characterized by a left ventricle enlargement and ultimately results in …

Metabolic alterations in inherited cardiomyopathies

C Sacchetto, V Sequeira, E Bertero, J Dudek… - Journal of Clinical …, 2019 - mdpi.com
The normal function of the heart relies on a series of complex metabolic processes
orchestrating the proper generation and use of energy. In this context, mitochondria serve a …

Liver T1 mapping derived from cardiac magnetic resonance imaging: A potential prognostic marker in idiopathic dilated cardiomyopathy

J Wang, Y Diao, Y Xu, J Guo, W Li, Y Li… - Journal of Magnetic …, 2024 - Wiley Online Library
Background Hepatic alterations are common aftereffects of heart failure (HF) and ventricular
dysfunction. The prognostic value of liver injury markers derived from cardiac MRI studies in …

A comprehensive guide to genetic variants and post-translational modifications of cardiac troponin C

TR Reinoso, M Landim-Vieira, Y Shi… - Journal of muscle …, 2021 - Springer
Familial cardiomyopathy is an inherited disease that affects the structure and function of
heart muscle and has an extreme range of phenotypes. Among the millions of affected …

Diagnostic biomarkers of dilated cardiomyopathy

A Moeinafshar, N Yazdanpanah, N Rezaei - Immunobiology, 2021 - Elsevier
Background Dilated cardiomyopathy (DCM) is a condition involving dilation of cardiac
chambers, which results in contraction impairment. Besides invasive and non-invasive …

The genetic pathways underlying immunotherapy in dilated cardiomyopathy

A Kadhi, F Mohammed, G Nemer - Frontiers in Cardiovascular …, 2021 - frontiersin.org
Heart failure (HF) is a global public health threat affecting 26 million individuals worldwide
with an estimated prevalence increase of 46% by 2030. One of the main causes of HF and …

Young and early‐onset dilated cardiomyopathy with malignant ventricular arrhythmia and sudden cardiac death induced by the heterozygous LDB3, MYH6, and …

T Zhao, Y Ma, Z Zhang, J Xian, X Geng… - Annals of …, 2021 - Wiley Online Library
Background The whole exome sequencing (WES) with targeted gene analysis is an effective
diagnostic tool for cardiomyopathy. The early‐onset sudden cardiac death (SCD) was …

A novel compound, tanshinol borneol ester, ameliorates pressure overload-induced cardiac hypertrophy by inhibiting oxidative stress via the mTOR/β-TrCP/NRF2 …

D Han, F Wang, B Wang, Z Qiao, X Cui… - Frontiers in …, 2022 - frontiersin.org
Tanshinol borneol ester (DBZ) exerts anti-atherosclerotic and anti-inflammatory effects.
However, its effects on cardiac hypertrophy are not well understood. In this work, we …

Multimodal characterization of dilated cardiomyopathy: Geno‐And Phenotyping of PrImary Cardiomyopathy (GrAPHIC)

L Keil, F Berisha, S Ritter, J Skibowski… - ESC Heart …, 2024 - Wiley Online Library
Abstract Aims Cardiomyopathies (CMPs) are a heterogeneous group of diseases that are
defined by structural and functional abnormalities of the cardiac muscle. Dilated …

Three-dimensional microCT imaging of mouse heart development from early post-implantation to late fetal stages

N Li-Villarreal, TL Rasmussen, AE Christiansen… - Mammalian …, 2023 - Springer
Comprehensive detailed characterization of new mouse models can be challenging due to
the individual focus involved in developing these models. Often models are engineered to …