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.

Номзүйн дэлгэрэнгүй
Үндсэн зохиолчид:	Picketts, D, Tastan, A, Higgs, D, Gibbons, R
Формат:	Journal article
Хэл сонгох:	English
Хэвлэсэн:	1998

Ижил төстэй зүйлс

Identification of mutations in ATRX by RNase mismatch cleavage.
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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: taming tandem repeats.
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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
-н: Clynes, D, зэрэг
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The chromatin remodeller ATRX: a repeat offender in human disease.
-н: Clynes, D, зэрэг
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The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.
-н: Bérubé, N, зэрэг
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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.
-н: Picketts, D, зэрэг
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Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX.
-н: Argentaro, A, зэрэг
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Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndrome.
-н: Medina, C, зэрэг
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XNP/ATRX at sites of nucleosome replacement.
-н: Garrick, D, зэрэг
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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.
-н: Steensma, D, зэрэг
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alpha-thalassaemia, X-linked mental retardation syndrome protein, ATRX, interacts with ribosomal genes.
-н: Law, M, зэрэг
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A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy.
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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.
-н: Garrick, D, зэрэг
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ATRX and the replication of structured DNA.
-н: Clynes, D, зэрэг
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Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes.
-н: McDowell, T, зэрэг
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Syndromal mental retardation due to mutations in a regulator of gene expression.
-н: Gibbons, R, зэрэг
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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.
-н: Steensma, D, зэрэг
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ATRX dysfunction induces replication defects in primary mouse cells
-н: Clynes, D, зэрэг
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Conservation of position and sequence of a novel, widely expressed gene containing the major human alpha-globin regulatory element.
-н: Vyas, P, зэрэг
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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)
-н: Steensma, D, зэрэг
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How to tackle challenging ChIP-Seq, with long-range cross-linking, using ATRX as an example
-н: Truch, J, зэрэг
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Two novel somatic mutations of the ATRX gene in female patients with acquired alpha thalassemia of myelodysplastic syndrome (ATMDS).
-н: Haas, P, зэрэг
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Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.
-н: Garrick, D, зэрэг
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Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.
-н: Garrick, D, зэрэг
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A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndrome.
-н: Costa, D, зэрэг
Хэвлэсэн: (2006)

Acquired alpha-thalassaernia in association with myelodysplastic syndrome (ATMDS): Two further private ATRX mutations
-н: Fisher, C, зэрэг
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A nonsense mutation of the ATRX gene causing mild, moderate and profound mental retardation in members of a single family.
-н: Gibbons, R, зэрэг
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ATRX targets variable number tandem repeats and thereby influences allele-specific expression
-н: Lower, K, зэрэг
Хэвлэсэн: (2010)

Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin.
-н: Eustermann, S, зэрэг
Хэвлэсэн: (2011)

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).
-н: Gibbons, R, зэрэг
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Mutant ATRX: pathogenesis of ATRX syndrome and cancer
-н: Kejia Yuan, зэрэг
Хэвлэсэн: (2024-10-01)

Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin
-н: Eustermann, S, зэрэг
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Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53.
-н: Seah, C, зэрэг
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ATRX dysfunction induces replication defects in primary mouse cells.
-н: David Clynes, зэрэг
Хэвлэсэн: (2014-01-01)

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation.
-н: Gibbons, R, зэрэг
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