Canonical histone H3 and histone variant H3. 3 are posttranslationally modified with the
genomic distribution of these marks denoting different features and these modifications may …

H3. 3 is a histone variant that marks transcription start sites as well as telomeres and
heterochromatic sites on the genome. The presence of H3. 3 is thought to positively …

Histone variants can replace canonical histones in the nucleosome and modify chromatin
structure and gene expression. The histone variant H3. 3 preferentially associates with …

H3. 3 is a highly conserved nonreplicative histone variant. H3. 3 is enriched in promoters
and enhancers of active genes, but it is also found within suppressed heterochromatin …

H1 linker histones facilitate higher-order chromatin folding and are essential for mammalian
development. To achieve high-resolution mapping of H1 variants H1d and H1c in embryonic …

The histone variant H3. 3 is enriched at enhancers and active genes, as well as repeat
regions such as telomeres and retroelements, in mouse embryonic stem cells (mESCs) …

During metazoan development, the marked change in developmental potential from the
parental germline to the embryo raises an important question regarding how the next life …

There are seven linker histone variants in human somatic cells (H1. 0 to H1. 5 and H1X),
and their prevalence varies as a function of cell type and differentiation stage, suggesting …

Histone H3. 3 is a highly conserved histone H3 replacement variant in metazoans and has
been implicated in many important biological processes, including cell differentiation and …

H1 linker histones are key chromatin architectural proteins facilitating the formation of higher
order chromatin structures. The H1 family constitutes the most heterogeneous group of …