Explore how FANCF gene promoter hypermethylation disrupts DNA repair mechanisms and drives non-small cell lung cancer development through epigenetic silencing.
Explore the fascinating world of genomic imprinting in mouse development and its implications for human health and reproduction.
Explore the fascinating world of genomic imprinting and how DNA methylation creates parental memories in our chromosomes that shape development and health.
Explore how DNA methylation patterns guide precursor B-cell development in umbilical cord blood and their implications for understanding immunity and blood cancers.
Explore how cell-specific DNA methylation patterns in placental cells shape pregnancy health and influence lifelong outcomes.
Discover how a 330 kb CENP-A binding domain and altered replication timing at human neocentromeres challenge our understanding of chromosome biology and epigenetic inheritance.
Explore the fascinating world of genomic imprinting, an epigenetic phenomenon that causes genes to be expressed differently based on parental origin, and its role in development and disease.
Explore how CG dinucleotides act as molecular switches controlling gene expression through DNA methylation and their critical role in health and disease.
Explore the fascinating world of DNA methylation and how this epigenetic mechanism controls gene expression without altering the DNA sequence itself.
Discover how DNA methylation suppresses transcriptional noise to maintain cellular harmony and precision in gene expression.