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.

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Picketts, D, Tastan, A, Higgs, D, Gibbons, R
التنسيق:	Journal article
اللغة:	English
منشور في:	1998

مواد مشابهة

Identification of mutations in ATRX by RNase mismatch cleavage.
حسب: Gibbons, R, وآخرون
منشور في: (1997)

Disruption of ATRX in mouse by conditional knockout.
حسب: Gibbons, R, وآخرون
منشور في: (2002)

Functional significance of mutations in the Snf2 domain of ATRX.
حسب: Mitson, M, وآخرون
منشور في: (2011)

ATRX: taming tandem repeats.
حسب: Gibbons, R, وآخرون
منشور في: (2010)

Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain.
حسب: Gibbons, R, وآخرون
منشور في: (1997)

The chromatin remodeller ATRX: A repeat offender in human disease
حسب: Clynes, D, وآخرون
منشور في: (2013)

The chromatin remodeller ATRX: a repeat offender in human disease.
حسب: Clynes, D, وآخرون
منشور في: (2013)

The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.
حسب: Bérubé, N, وآخرون
منشور في: (2005)

ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.
حسب: Picketts, D, وآخرون
منشور في: (1996)

Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX.
حسب: Argentaro, A, وآخرون
منشور في: (2007)

Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndrome.
حسب: Medina, C, وآخرون
منشور في: (2009)

XNP/ATRX at sites of nucleosome replacement.
حسب: Garrick, D, وآخرون
منشور في: (2009)

Neurodevelopmental Disorders Caused by Defective Chromatin Remodeling: Phenotypic Complexity Is Highlighted by a Review of ATRX Function
حسب: Sara Timpano, وآخرون
منشور في: (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.
حسب: Steensma, D, وآخرون
منشور في: (2004)

alpha-thalassaemia, X-linked mental retardation syndrome protein, ATRX, interacts with ribosomal genes.
حسب: Law, M, وآخرون
منشور في: (2003)

A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy.
حسب: Guerrini, R, وآخرون
منشور في: (2000)

Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genes.
حسب: Qiao, Y, وآخرون
منشور في: (2014)

Mutations in the human ATRX gene, encoding a putative transcription regulator, cause diverse changes in the pattern of DNA methylation.
حسب: Garrick, D, وآخرون
منشور في: (2000)

ATRX and the replication of structured DNA.
حسب: Clynes, D, وآخرون
منشور في: (2013)

Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes.
حسب: McDowell, T, وآخرون
منشور في: (1999)

Syndromal mental retardation due to mutations in a regulator of gene expression.
حسب: Gibbons, R, وآخرون
منشور في: (1995)

DHPLC analysis of the ATRX gene in myelodysplastic syndrome (MDS) associated with acquired alpha thalassemia (AT-MDS): Novel mutation detection despite somatic mosaicism.
حسب: Steensma, D, وآخرون
منشور في: (2003)

ATRX dysfunction induces replication defects in primary mouse cells
حسب: Clynes, D, وآخرون
منشور في: (2014)

Conservation of position and sequence of a novel, widely expressed gene containing the major human alpha-globin regulatory element.
حسب: Vyas, P, وآخرون
منشور في: (1995)

A novel splicing mutation in the gene encoding the chromatin-associated factor ATRX associated with acquired hemoglobin H disease in myelodysplastic syndrome (ATMDS)
حسب: Steensma, D, وآخرون
منشور في: (2004)

How to tackle challenging ChIP-Seq, with long-range cross-linking, using ATRX as an example
حسب: Truch, J, وآخرون
منشور في: (2018)

Two novel somatic mutations of the ATRX gene in female patients with acquired alpha thalassemia of myelodysplastic syndrome (ATMDS).
حسب: Haas, P, وآخرون
منشور في: (2006)

Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.
حسب: Garrick, D, وآخرون
منشور في: (2006)

Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.
حسب: Garrick, D, وآخرون
منشور في: (2006)

A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndrome.
حسب: Costa, D, وآخرون
منشور في: (2006)

Acquired alpha-thalassaernia in association with myelodysplastic syndrome (ATMDS): Two further private ATRX mutations
حسب: Fisher, C, وآخرون
منشور في: (2007)

A nonsense mutation of the ATRX gene causing mild, moderate and profound mental retardation in members of a single family.
حسب: Gibbons, R, وآخرون
منشور في: (1999)

ATRX targets variable number tandem repeats and thereby influences allele-specific expression
حسب: Lower, K, وآخرون
منشور في: (2010)

Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin.
حسب: Eustermann, S, وآخرون
منشور في: (2011)

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).
حسب: Gibbons, R, وآخرون
منشور في: (2003)

Mutant ATRX: pathogenesis of ATRX syndrome and cancer
حسب: Kejia Yuan, وآخرون
منشور في: (2024-10-01)

Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin
حسب: Eustermann, S, وآخرون
منشور في: (2011)

Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53.
حسب: Seah, C, وآخرون
منشور في: (2008)

ATRX dysfunction induces replication defects in primary mouse cells.
حسب: David Clynes, وآخرون
منشور في: (2014-01-01)

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation.
حسب: Gibbons, R, وآخرون
منشور في: (2000)