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.

Chi tiết về thư mục
Những tác giả chính:	Picketts, D, Tastan, A, Higgs, D, Gibbons, R
Định dạng:	Journal article
Ngôn ngữ:	English
Được phát hành:	1998

Những quyển sách tương tự

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Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain.
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The chromatin remodeller ATRX: a repeat offender in human disease.
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The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.
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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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Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX.
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Neurodevelopmental Disorders Caused by Defective Chromatin Remodeling: Phenotypic Complexity Is Highlighted by a Review of ATRX Function
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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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alpha-thalassaemia, X-linked mental retardation syndrome protein, ATRX, interacts with ribosomal genes.
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Variant ATRX syndrome with dysfunction of ATRX and MAGT1 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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Syndromal mental retardation due to mutations in a regulator of gene expression.
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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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Two novel somatic mutations of the ATRX gene in female patients with acquired alpha thalassemia of myelodysplastic syndrome (ATMDS).
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Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.
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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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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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Được phát hành: (2011)

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).
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Mutant ATRX: pathogenesis of ATRX syndrome and cancer
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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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