Pathogenic variants in genes that cause dilated cardiomyopathy (DCM) and arrhythmogenic
cardiomyopathy (ACM) convey high risks for the development of heart failure through …

Atherosclerosis and its clinical manifestations, coronary and cerebral artery diseases, are
the most common cause of death worldwide. The main pathophysiological mechanism for …

Gene expression provides valuable insight into cell function. As such, vision researchers
have frequently employed gene expression studies to better understand retinal physiology …

During neocortical development, neural stem cells (NSCs) divide symmetrically to self‐
renew at the early stage and then divide asymmetrically to generate post‐mitotic neurons …

Diclofenac effectively reduces pain and inflammation; however, its use is associated with
hepato-and nephrotoxicity. To delineate mechanisms of injury, we investigated a clinically …

Sarcoidosis is a systemic granulomatous disease of unknown etiology.
Hypergammaglobulinemia and the presence of autoantibodies in sarcoidosis suggest active …

Growing data have recognized the significance of Response Gene to Complement (RGC)‐
32 in numerous tumour developments. Notwithstanding, the functional role and underlying …

Background Systemic sclerosis represents a persistent autoimmune disorder marked with
fibrosis affecting both skin and other organs, which leads to a diminished quality of life and …

Age-related macular degeneration (AMD) is a common cause of irreversible blindness
globally. The disease results in loss of light-sensing photoreceptor cells in the center of the …

Background RGCC (regulator of cell cycle) is a protein-coding gene, also known as RGC-32
(response gene to complement 32 protein), which is an important regulatory gene of cell …