Background Nonalcoholic fatty liver disease (NAFLD) is the main cause for hepatocellular
carcinoma (HCC). This study was intended to identify the function of long non-coding RNA …

Diabetes mellitus, characterized by hyperglycemia and insulin resistance, is a disorder of
the endocrine metabolic system which has emerged as a common chronic disease …

The human solute carrier 22A (SLC22A) family consists of 23 members, representing one of
the largest families in the human SLC superfamily. Despite their pharmacological and …

Background Androgen deprivation therapy (ADT) is the main clinical treatment for patients
with advanced prostate cancer (PCa). However, PCa eventually progresses to castration …

Genomic imprinting is a process that involves one gene copy turned-off in a parent-of-origin-
dependent manner. The regulation of imprinted genes is broadly dependent on promoter …

Background High-throughput sequencing experiments, which can determine allele origins,
have been used to assess genome-wide allele-specific expression. Despite the amount of …

Alternative splicing (AS), a crucial mechanism in post‐transcriptional regulation, has been
implicated in diverse cancer processes. Several splicing variants of solute carrier (SLC) …

Steroid production varies widely among species, with these differences becoming more
pronounced during pregnancy. As a result, each species has its own distinct pattern of …

We previously reported that solute carrier family 22 member 18 (Slc22a18) regulates lipid
accumulation in 3T3-L1 adipocytes. Here, we provide additional evidence derived from …

Background Wilson's disease is a genetic disorder inherited in a recessive manner, caused
by mutations in the copper-transporter ATP7B. Although it is a well-known disease, currently …