Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains.

Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains.

Podrobná bibliografie
Hlavní autoři:	Picketts, D, Tastan, A, Higgs, D, Gibbons, R
Médium:	Journal article
Jazyk:	English
Vydáno:	1998

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alpha-thalassaemia, X-linked mental retardation syndrome protein, ATRX, interacts with ribosomal genes.
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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 and the replication of structured DNA.
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Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes.
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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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ATRX dysfunction induces replication defects in primary mouse cells
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Conservation of position and sequence of a novel, widely expressed gene containing the major human alpha-globin regulatory element.
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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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How to tackle challenging ChIP-Seq, with long-range cross-linking, using ATRX as an example
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Acquired alpha-thalassaernia in association with myelodysplastic syndrome (ATMDS): Two further private ATRX mutations
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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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ATRX targets variable number tandem repeats and thereby influences allele-specific expression
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Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin.
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Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).
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Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin
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Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53.
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ATRX dysfunction induces replication defects in primary mouse cells.
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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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