Genomic imprinting affects a subset of genes in mammals and results in a monoallelic,
parental-specific expression pattern. Most of these genes are located in clusters that are …

X chromosome inactivation and genomic imprinting are classic epigenetic processes that
cause disease when not appropriately regulated in mammals. Whereas X chromosome …

ABSTRACT Enterovirus 71 (EV71) has emerged as a major cause of neurological disease
following the near eradication of poliovirus. Accumulating evidence suggests that …

Genomic imprinting is a parent-of-origin dependent phenomenon that restricts transcription
to predominantly one parental allele. Since the discovery of the first long noncoding RNA …

Parathyroid carcinoma (PC) is an extremely rare malignancy, accounting less than 1% of all
parathyroid neoplasms, and an uncommon cause of primary hyperparathyroidism (PHPT) …

In mammals, the expression of a subset of microRNA (miRNA) genes is governed by
genomic imprinting, an epigenetic mechanism that confers monoallelic expression in a …

Imprinted genes play diverse roles in mammalian development, homeostasis, and disease.
Most imprinted chromosomal domains express one or more long non-coding RNAs …

Inflammasomes are a group of cytosolic multi-protein signaling complexes that regulate
maturation of the interleukin (IL)-1 family cytokines IL-1β and IL-18 through activation of …

Abstract Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is a new
member of the Betacoronaviridae family, responsible for the recent pandemic outbreak of …

Esophageal cancer (EC) is the most invasive disease associated with inclusive poor
prognosis. EC usually is found as either adenocarcinoma (EAC) or squamous cell …