Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
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The Cornelia de Lange Syndrome-associated factor NIPBL interacts with BRD4 ET domain for transcription control of a common set of genes
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
PDF) BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
STAG2 promotes the myelination transcriptional program in oligodendrocytes
Functional coordination of BET family proteins underlies altered transcription associated with memory impairment in fragile X syndrome
STAG2 promotes the myelination transcriptional program in oligodendrocytes
STAG2 promotes the myelination transcriptional program in oligodendrocytes
What causes Cornelia de Lange Syndrome - CdLS Foundation UK and Ireland
Chromatinopathies: A focus on Cornelia de Lange syndrome - Avagliano - 2020 - Clinical Genetics - Wiley Online Library
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PDF) BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome