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

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Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Cornelia de Lange syndrome mutations in NIPBL can impair cohesin-mediated DNA loop extrusion
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
STAG2 promotes the myelination transcriptional program in oligodendrocytes
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Chung–Jansen syndrome can mimic Cornelia de Lange syndrome: Another player among chromatinopathies? - Conti - 2023 - American Journal of Medical Genetics Part A - Wiley Online Library
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Cornelia de Lange syndrome in diverse populations - Dowsett - 2019 - American Journal of Medical Genetics Part A - Wiley Online Library
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Cornelia de Lange syndrome: from molecular diagnosis to therapeutic approach
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Multiple Organ System Defects and Transcriptional Dysregulation in the Nipbl+/− Mouse, a Model of Cornelia de Lange Syndrome
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Frontiers Regulation of Carbohydrate-Responsive Metabolic Genes by Histone Acetylation and the Acetylated Histone Reader BRD4 in the Gene Body Region
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Emerging roles of BET proteins in transcription and co‐transcriptional RNA processing - Eischer - 2023 - WIREs RNA - Wiley Online Library
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
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin
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
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Functional coordination of BET family proteins underlies altered transcription associated with memory impairment in fragile X syndrome
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