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ICF syndrome
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(1 - 24 of 26)
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SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in disease
The inactive X chromosome accumulates widespread epigenetic variability with age
SMCHD1 and LRIF1 converge at the FSHD-associated D4Z4 repeat and LRIF1 promoter yet display different modes of action
GRHL2-controlled gene expression networks in luminal breast cancer
GRHL2-controlled gene expression networks in luminal breast cancer
Inability to switch from ARID1A-BAF to ARID1B-BAF impairs exit from pluripotency and commitment towards neural crest formation in ARID1B-related neurodevelopmental disorders
The role of MORC3 in silencing transposable elements in mouse embryonic stem cells
Identical twins carry a persistent epigenetic signature of early genome programming
The route of early T cell development: crosstalk between epigenetic and transcription factors
A CSB-PAF1C axis restores processive transcription elongation after DNA damage repair
Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency
Genome-wide identification of genes regulating DNA methylation using genetic anchors for causal inference
Functional definition of a transcription factor hierarchy regulating T cell lineage commitment
Functional definition of a transcription factor hierarchy regulating T cell lineage commitment
A functional assay to classify ZBTB24 missense variants of unknown significance
Making headway towards understanding how epigenetic mechanisms contribute to early-life effects
DNA methylation in disease: Immunodeficiency, Centromeric instability, Facial anomalies syndrome
Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation
A Restricted Role for Fc gamma R in the Regulation of Adaptive Immunity
Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation
Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2
Converging disease genes in ICF syndrome: ZBTB24 controls expression of CDCA7 in mammals
Mouse MORC3 is a GHKL ATPase that localizes to H3K4me3 marked chromatin
Wiz binds active promoters and CTCF-binding sites and is required for normal behaviour in the mouse
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