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The ATRX-ADD domain binds to H3 tail peptides and reads the combined methylation state of K4 and K9
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Loss of ATRX in Chondrocytes Has Minimal Effects on Skeletal Development
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Loss of ATRX leads to chromosome cohesion and congression defects
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Neuronal Death Resulting from Targeted Disruption of the Snf2 Protein ATRX Is Mediated by p53
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Patient mutations alter ATRX targeting to PML nuclear bodies
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Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation
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Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues
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Inhibitor of apoptosis protein cIAP2 is essential for lipopolysaccharide-induced macrophage survival
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The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis
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Acquired somatic ATRX mutations in myelodysplastic syndrome associated with α thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations
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BLOOD (2004)
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A novel transcription regulatory complex containing death domain-associated protein and the ATR-X syndrome protein
J Tang et al.
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The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies
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Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association
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Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation
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