Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome

The Cornelia de Lange Syndrome-associated factor NIPBL interacts with BRD4 ET domain for transcription control of a common set of genes

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The Drosophila melanogaster model for Cornelia de Lange syndrome: Implications for etiology and therapeutics - Dorsett - 2016 - American Journal of Medical Genetics Part C: Seminars in Medical Genetics - Wiley Online Library

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Functional coordination of BET family proteins underlies altered transcription associated with memory impairment in fragile X syndrome

Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome

PDF) BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome

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Frontiers A Chinese Case of Cornelia de Lange Syndrome Caused by a Pathogenic Variant in SMC3 and a Literature Review

Lyar-Mediated Recruitment of Brd2 to the Chromatin Attenuates Nanog Downregulation Following Induction of Differentiation - ScienceDirect

STAG2 promotes the myelination transcriptional program in oligodendrocytes

Chromatinopathies: A focus on Cornelia de Lange syndrome - Avagliano - 2020 - Clinical Genetics - Wiley Online Library