NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain

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NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain

Context-specific Polycomb mechanisms in development

Epigenomes, Free Full-Text

Genes, Free Full-Text

Edoardo Errichiello - SciTok

Cells, Free Full-Text

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Polycomb‐mediated gene regulation in human brain development and neurodevelopmental disorders - Bölicke - 2022 - Developmental Neurobiology - Wiley Online Library

Frontiers Comparing a Novel Malformation Syndrome Caused by Pathogenic Variants in FBRSL1 to AUTS2 Syndrome

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Rubinstein–Taybi syndrome - Wikipedia
Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf
A novel mutation c.4003 G>C in the CREBBP gene in an adult female with Rubinstein–Taybi syndrome presenting with subtle dysmorphic features - Li - 2010 - American Journal of Medical Genetics Part
Floating-Harbor syndrome: MedlinePlus Genetics

NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain

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