ATRX: taming tandem repeats.

ATRX: taming tandem repeats.

Bibliographische Detailangaben
Hauptverfasser:	Gibbons, R, Higgs, D
Format:	Journal article
Sprache:	English
Veröffentlicht:	2010

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The chromatin remodeller ATRX: a repeat offender in human disease.
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XNP/ATRX at sites of nucleosome replacement.
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Identification of mutations in ATRX by RNase mismatch cleavage.
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Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.
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The chromatin remodelling factor ATRX suppresses R-loops in transcribed telomeric repeats
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Disruption of ATRX in mouse by conditional knockout.
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Functional significance of mutations in the Snf2 domain of ATRX.
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ATRX and the replication of structured DNA.
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Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX.
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alpha-thalassaemia, X-linked mental retardation syndrome protein, ATRX, interacts with ribosomal genes.
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A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy.
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ATRX dysfunction induces replication defects in primary mouse cells
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How to tackle challenging ChIP-Seq, with long-range cross-linking, using ATRX as an example
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Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genes.
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The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.
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Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.
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A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndrome.
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ATRX dysfunction induces replication defects in primary mouse cells.
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Mutant ATRX: pathogenesis of ATRX syndrome and cancer
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DHPLC analysis of the ATRX gene in myelodysplastic syndrome (MDS) associated with acquired alpha thalassemia (AT-MDS): Novel mutation detection despite somatic mosaicism.
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Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53.
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Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin.
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Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin
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Mutations in the chromatin-associated protein ATRX.
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A novel splicing mutation in the gene encoding the chromatin-associated factor ATRX associated with acquired hemoglobin H disease in myelodysplastic syndrome (ATMDS)
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The loss of ATRX increases susceptibility to pancreatic injury and oncogenic KRAS in female but not male mice
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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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Two novel somatic mutations of the ATRX gene in female patients with acquired alpha thalassemia of myelodysplastic syndrome (ATMDS).
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A nonsense mutation of the ATRX gene causing mild, moderate and profound mental retardation in members of a single family.
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Mutations in the human ATRX gene, encoding a putative transcription regulator, cause diverse changes in the pattern of DNA methylation.
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ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.
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Identification of acquired somatic mutations in the chromatin remodelling factor ATRX in the a thalassaemia myelodysplasia syndrome (ATMDS)
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Identification of acquired somatic mutations in the chromatin remodelling factor ATRX in the alpha thalassemia myelodysplasia syndrome (ATMDS).
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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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