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ATR-X Syndrome Protein Targets Tandem Repeats and Influences Allele-Specific Expression in a Size-Dependent Manner
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ATRX Partners with Cohesin and MeCP2 and Contributes to Developmental Silencing of Imprinted Genes in the Brain
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ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cells
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GENOME RESEARCH (2010)
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Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that includes locus for X-linked recessive type of chondrodysplasia punctata (CDPX1)
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An age-related sprouting transcriptome provides molecular control of axonal sprouting after stroke
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Daxx is an H3.3-specific histone chaperone and cooperates with ATRX in replication-independent chromatin assembly at telomeres
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Loss of Maternal ATRX Results in Centromere Instability and Aneuploidy in the Mammalian Oocyte and Pre-Implantation Embryo
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ATRX marks the inactive X chromosome (Xi) in somatic cells and during imprinted X chromosome inactivation in trophoblast stem cells
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Nonallelic transvection of multiple imprinted loci is organized by the H19 imprinting control region during germline development
Kuljeet Singh Sandhu et al.
GENES & DEVELOPMENT (2009)
Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndrome
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HUMAN MOLECULAR GENETICS (2009)
Loss of ATRX in Chondrocytes Has Minimal Effects on Skeletal Development
Lauren A. Solomon et al.
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The XNP remodeler targets dynamic chromatin in Drosophila
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The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome
Michael A. Levy et al.
BMC GENOMICS (2008)
Association of ATRX with pericentric heterochromatin and the Y chromosome of neonatal mouse spermatogonia
Claudia Baumann et al.
BMC MOLECULAR BIOLOGY (2008)
ATP-dependent chromatin remodeling by the Saccharomyces cerevisiae homologous recombination factor Rdh54
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JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Loss of ATRX leads to chromosome cohesion and congression defects
Kieran Ritchie et al.
JOURNAL OF CELL BIOLOGY (2008)
Neuronal Death Resulting from Targeted Disruption of the Snf2 Protein ATRX Is Mediated by p53
Claudia Seah et al.
JOURNAL OF NEUROSCIENCE (2008)
Cohesin mediates transcriptional insulation by CCCTC-binding factor
Kerstin S. Wendt et al.
NATURE (2008)
The Chromatin Remodelling Factor dATRX Is Involved in Heterochromatin Formation
Andrew R. Bassett et al.
PLOS ONE (2008)
Patient mutations alter ATRX targeting to PML nuclear bodies
Nathalie G. Berube et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX
Anthony Argentaro et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia
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MOLECULAR PSYCHIATRY (2007)
Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation
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Heterochromatin revisited
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Circular chromosome conformation capture (4C) uncovers extensive networks of epigenetically regulated intra- and interchromosomal interactions
Zhihu Zhao et al.
NATURE GENETICS (2006)
Visualization of Rad54, a chromatin remodeling protein, translocating on single DNA molecules
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MOLECULAR CELL (2006)
Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues
David Garrick et al.
PLOS GENETICS (2006)
Acute myeloid leukemia subgroups identified by pathway - Restricted gene expression signatures
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ACTA HAEMATOLOGICA (2006)
Epigenetic regulation of mammalian pericentric heterochromatin in vivo by HP1
N Kourmouli et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)
RNA polymerase II is required for RNAi-dependent heterochromatin assembly
H Kato et al.
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The mammalian heterochromatin protein 1 binds diverse nuclear proteins through a common motif that targets the chromoshadow domain
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The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis
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JOURNAL OF CLINICAL INVESTIGATION (2005)
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)
A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain
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Separase-mediated cleavage of cohesin at interphase is required for DNA repair
K Nagao et al.
NATURE (2004)
Postreplicative recruitment of cohesin to double-strand breaks is required for DNA repair
L Ström et al.
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ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes
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A novel transcription regulatory complex containing death domain-associated protein and the ATR-X syndrome protein
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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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Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)
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HUMAN MOLECULAR GENETICS (2002)
ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein
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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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Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22.3, related to the cytosine-5-methyltransferase 3 gene family
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