Genomic imprinting refers to the parent-of-origin expression of genes, which originates from
epigenetic events in the mammalian germ line. The evolution of imprinting may reflect a …

Genomic imprinting is illustrative of intergenerational epigenetic inheritance. The passage of
parental genomes into the embryo is accompanied by epigenetic modifications, resulting in …

X chromosome inactivation (XCI) generates clonal heterogeneity within XX individuals.
Combined with sequence variation between human X chromosomes, XCI gives rise to intra …

To investigate the paternal genetic effects of cadmium (Cd) exposure on hormone synthesis
disorders in the ovarian granulosa cells (GCs) of offspring. Here, male Sprague‒Dawley …

Genomic imprinting is an epigenetically mediated mechanism that regulates allelic
expression of genes based upon parent-of-origin and provides a paradigm for studying …

We tracked the consequences of in utero protein restriction in mice throughout their
development and life course using a luciferase-based allelic reporter of imprinted Cdkn1c …

Evidence for parental environments profoundly influencing the physiology, biology, and
neurobiology of future generations has been accumulating in the literature. Recent efforts to …

Growing evidence suggests that epigenetic changes through various parental
environmental factors alter the phenotypes of descendants in various organisms …

Duchenne muscular dystrophy (DMD) is an X-linked disorder caused by loss of function
mutations in the dystrophin gene (Dmd), resulting in progressive muscle weakening. Here …

Background/Objectives: Atherosclerosis is a chronic inflammatory disease developing and
progressing in the presence of risk factors including hyperlipidemia, hypercholesterolemia …