about
A cell cycle role for the epigenetic factor CTCF-L/BORISCTCF regulates the local epigenetic state of ribosomal DNA repeats.Mesenchymal-endothelial transition contributes to cardiac neovascularization.Structural considerations for chromatin state models with transcription as a functional readout.Reciprocal Regulation of the Cardiac Epigenome by Chromatin Structural Proteins Hmgb and Ctcf: IMPLICATIONS FOR TRANSCRIPTIONAL REGULATION.High Resolution Mapping of Chromatin Conformation in Cardiac Myocytes Reveals Structural Remodeling of the Epigenome in Heart FailureUndiscovered Physiology of Transcript and Protein Networks.Novel CTCF binding at a site in exon1A of BCL6 is associated with active histone marks and a transcriptionally active locus.Nuclear targeting of a bacterial integrase that mediates site-specific recombination between bacterial and human target sequencesThe male germ cell gene regulator CTCFL is functionally different from CTCF and binds CTCF-like consensus sites in a nucleosome composition-dependent manner.p73 plays a role in erythroid differentiation through GATA1 induction.The chromatin-binding protein Smyd1 restricts adult mammalian heart growth.PU.1 expression is restored upon treatment of chronic myeloid leukemia patients.Epigenomes in Cardiovascular Disease.Spatial Principles of Chromatin Architecture Associated With Organ-Specific Gene RegulationDirect visualization of cardiac transcription factories reveals regulatory principles of nuclear architecture during pathological remodelingDissecting Chromatin Architecture for Novel Cardiovascular Disease TargetsMitoBKCa channel is functionally associated with its regulatory β1 subunit in cardiac mitochondria
P50
Q27300849-D53EDF88-28EC-4063-A6E1-1B32A9C61606Q34360792-EFB41394-76FA-405E-8623-D726C288B628Q34429225-42CDC47F-A856-44C4-A61C-0F52988036F4Q36391402-C214AB7C-AEAC-4F57-9AC9-915C6690912CQ37117250-F82F4675-56B9-487B-8BC3-375285DBF689Q38643488-EC42353F-A340-4237-9091-21AE62AAE7C0Q38805134-1C35F224-403D-4651-B310-8A7C94D52217Q39041021-696A7598-7E12-419E-8469-5BF105015E52Q39822300-9781A57A-ADF2-41D3-AE48-2F18BB871281Q42121580-86306F40-1B80-4FBA-B679-60B37427DA9EQ42575247-F1932685-1739-4650-828A-3198C2898DBCQ42784088-D383864C-76EE-4982-B417-B094088CBB15Q46477940-43D7F196-282B-4EB0-9BD5-8288E3206A94Q55098768-3A4B69FB-906A-4654-AB4D-16456BBCA818Q61448069-6C635B98-28C5-42CC-9B0F-2EEDD7205D23Q91454853-645E9644-ADE5-4100-AB2F-9EEB2D377E54Q92415764-9D84DC52-6EA4-4A99-9BDF-1A836E739095Q92583197-D680FBAA-B227-45D3-8CDD-9ED53026A4F0
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Manuel Rosa-Garrido
@ast
Manuel Rosa-Garrido
@en
Manuel Rosa-Garrido
@es
Manuel Rosa-Garrido
@nl
Manuel Rosa-Garrido
@sl
type
label
Manuel Rosa-Garrido
@ast
Manuel Rosa-Garrido
@en
Manuel Rosa-Garrido
@es
Manuel Rosa-Garrido
@nl
Manuel Rosa-Garrido
@sl
prefLabel
Manuel Rosa-Garrido
@ast
Manuel Rosa-Garrido
@en
Manuel Rosa-Garrido
@es
Manuel Rosa-Garrido
@nl
Manuel Rosa-Garrido
@sl
P106
P21
P31
P496
0000-0002-2169-3972