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.

Manylion Llyfryddiaeth
Prif Awduron:	Picketts, D, Tastan, A, Higgs, D, Gibbons, R
Fformat:	Journal article
Iaith:	English
Cyhoeddwyd:	1998

Eitemau Tebyg

Identification of mutations in ATRX by RNase mismatch cleavage.
gan: Gibbons, R, et al.
Cyhoeddwyd: (1997)

Disruption of ATRX in mouse by conditional knockout.
gan: Gibbons, R, et al.
Cyhoeddwyd: (2002)

Functional significance of mutations in the Snf2 domain of ATRX.
gan: Mitson, M, et al.
Cyhoeddwyd: (2011)

ATRX: taming tandem repeats.
gan: Gibbons, R, et al.
Cyhoeddwyd: (2010)

Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain.
gan: Gibbons, R, et al.
Cyhoeddwyd: (1997)

The chromatin remodeller ATRX: A repeat offender in human disease
gan: Clynes, D, et al.
Cyhoeddwyd: (2013)

The chromatin remodeller ATRX: a repeat offender in human disease.
gan: Clynes, D, et al.
Cyhoeddwyd: (2013)

The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.
gan: Bérubé, N, et al.
Cyhoeddwyd: (2005)

ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.
gan: Picketts, D, et al.
Cyhoeddwyd: (1996)

Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX.
gan: Argentaro, A, et al.
Cyhoeddwyd: (2007)

Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndrome.
gan: Medina, C, et al.
Cyhoeddwyd: (2009)

XNP/ATRX at sites of nucleosome replacement.
gan: Garrick, D, et al.
Cyhoeddwyd: (2009)

Neurodevelopmental Disorders Caused by Defective Chromatin Remodeling: Phenotypic Complexity Is Highlighted by a Review of ATRX Function
gan: Sara Timpano, et al.
Cyhoeddwyd: (2020-08-01)

Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.
gan: Steensma, D, et al.
Cyhoeddwyd: (2004)

alpha-thalassaemia, X-linked mental retardation syndrome protein, ATRX, interacts with ribosomal genes.
gan: Law, M, et al.
Cyhoeddwyd: (2003)

A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy.
gan: Guerrini, R, et al.
Cyhoeddwyd: (2000)

Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genes.
gan: Qiao, Y, et al.
Cyhoeddwyd: (2014)

Mutations in the human ATRX gene, encoding a putative transcription regulator, cause diverse changes in the pattern of DNA methylation.
gan: Garrick, D, et al.
Cyhoeddwyd: (2000)

ATRX and the replication of structured DNA.
gan: Clynes, D, et al.
Cyhoeddwyd: (2013)

Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes.
gan: McDowell, T, et al.
Cyhoeddwyd: (1999)

Syndromal mental retardation due to mutations in a regulator of gene expression.
gan: Gibbons, R, et al.
Cyhoeddwyd: (1995)

DHPLC analysis of the ATRX gene in myelodysplastic syndrome (MDS) associated with acquired alpha thalassemia (AT-MDS): Novel mutation detection despite somatic mosaicism.
gan: Steensma, D, et al.
Cyhoeddwyd: (2003)

ATRX dysfunction induces replication defects in primary mouse cells
gan: Clynes, D, et al.
Cyhoeddwyd: (2014)

Conservation of position and sequence of a novel, widely expressed gene containing the major human alpha-globin regulatory element.
gan: Vyas, P, et al.
Cyhoeddwyd: (1995)

A novel splicing mutation in the gene encoding the chromatin-associated factor ATRX associated with acquired hemoglobin H disease in myelodysplastic syndrome (ATMDS)
gan: Steensma, D, et al.
Cyhoeddwyd: (2004)

How to tackle challenging ChIP-Seq, with long-range cross-linking, using ATRX as an example
gan: Truch, J, et al.
Cyhoeddwyd: (2018)

Two novel somatic mutations of the ATRX gene in female patients with acquired alpha thalassemia of myelodysplastic syndrome (ATMDS).
gan: Haas, P, et al.
Cyhoeddwyd: (2006)

Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.
gan: Garrick, D, et al.
Cyhoeddwyd: (2006)

Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.
gan: Garrick, D, et al.
Cyhoeddwyd: (2006)

A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndrome.
gan: Costa, D, et al.
Cyhoeddwyd: (2006)

Acquired alpha-thalassaernia in association with myelodysplastic syndrome (ATMDS): Two further private ATRX mutations
gan: Fisher, C, et al.
Cyhoeddwyd: (2007)

A nonsense mutation of the ATRX gene causing mild, moderate and profound mental retardation in members of a single family.
gan: Gibbons, R, et al.
Cyhoeddwyd: (1999)

ATRX targets variable number tandem repeats and thereby influences allele-specific expression
gan: Lower, K, et al.
Cyhoeddwyd: (2010)

Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin.
gan: Eustermann, S, et al.
Cyhoeddwyd: (2011)

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).
gan: Gibbons, R, et al.
Cyhoeddwyd: (2003)

Mutant ATRX: pathogenesis of ATRX syndrome and cancer
gan: Kejia Yuan, et al.
Cyhoeddwyd: (2024-10-01)

Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin
gan: Eustermann, S, et al.
Cyhoeddwyd: (2011)

Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53.
gan: Seah, C, et al.
Cyhoeddwyd: (2008)

ATRX dysfunction induces replication defects in primary mouse cells.
gan: David Clynes, et al.
Cyhoeddwyd: (2014-01-01)

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation.
gan: Gibbons, R, et al.
Cyhoeddwyd: (2000)