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.

ग्रंथसूची विवरण
मुख्य लेखकों:	Picketts, D, Tastan, A, Higgs, D, Gibbons, R
स्वरूप:	Journal article
भाषा:	English
प्रकाशित:	1998

समान संसाधन

Identification of mutations in ATRX by RNase mismatch cleavage.
द्वारा: Gibbons, R, और अन्य
प्रकाशित: (1997)

Disruption of ATRX in mouse by conditional knockout.
द्वारा: Gibbons, R, और अन्य
प्रकाशित: (2002)

Functional significance of mutations in the Snf2 domain of ATRX.
द्वारा: Mitson, M, और अन्य
प्रकाशित: (2011)

ATRX: taming tandem repeats.
द्वारा: Gibbons, R, और अन्य
प्रकाशित: (2010)

Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain.
द्वारा: Gibbons, R, और अन्य
प्रकाशित: (1997)

The chromatin remodeller ATRX: A repeat offender in human disease
द्वारा: Clynes, D, और अन्य
प्रकाशित: (2013)

The chromatin remodeller ATRX: a repeat offender in human disease.
द्वारा: Clynes, D, और अन्य
प्रकाशित: (2013)

The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.
द्वारा: Bérubé, N, और अन्य
प्रकाशित: (2005)

ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.
द्वारा: Picketts, D, और अन्य
प्रकाशित: (1996)

Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX.
द्वारा: Argentaro, A, और अन्य
प्रकाशित: (2007)

Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndrome.
द्वारा: Medina, C, और अन्य
प्रकाशित: (2009)

XNP/ATRX at sites of nucleosome replacement.
द्वारा: Garrick, D, और अन्य
प्रकाशित: (2009)

Neurodevelopmental Disorders Caused by Defective Chromatin Remodeling: Phenotypic Complexity Is Highlighted by a Review of ATRX Function
द्वारा: Sara Timpano, और अन्य
प्रकाशित: (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.
द्वारा: Steensma, D, और अन्य
प्रकाशित: (2004)

alpha-thalassaemia, X-linked mental retardation syndrome protein, ATRX, interacts with ribosomal genes.
द्वारा: Law, M, और अन्य
प्रकाशित: (2003)

A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy.
द्वारा: Guerrini, R, और अन्य
प्रकाशित: (2000)

Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genes.
द्वारा: Qiao, Y, और अन्य
प्रकाशित: (2014)

Mutations in the human ATRX gene, encoding a putative transcription regulator, cause diverse changes in the pattern of DNA methylation.
द्वारा: Garrick, D, और अन्य
प्रकाशित: (2000)

ATRX and the replication of structured DNA.
द्वारा: Clynes, D, और अन्य
प्रकाशित: (2013)

Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes.
द्वारा: McDowell, T, और अन्य
प्रकाशित: (1999)

Syndromal mental retardation due to mutations in a regulator of gene expression.
द्वारा: Gibbons, R, और अन्य
प्रकाशित: (1995)

DHPLC analysis of the ATRX gene in myelodysplastic syndrome (MDS) associated with acquired alpha thalassemia (AT-MDS): Novel mutation detection despite somatic mosaicism.
द्वारा: Steensma, D, और अन्य
प्रकाशित: (2003)

ATRX dysfunction induces replication defects in primary mouse cells
द्वारा: Clynes, D, और अन्य
प्रकाशित: (2014)

Conservation of position and sequence of a novel, widely expressed gene containing the major human alpha-globin regulatory element.
द्वारा: Vyas, P, और अन्य
प्रकाशित: (1995)

A novel splicing mutation in the gene encoding the chromatin-associated factor ATRX associated with acquired hemoglobin H disease in myelodysplastic syndrome (ATMDS)
द्वारा: Steensma, D, और अन्य
प्रकाशित: (2004)

How to tackle challenging ChIP-Seq, with long-range cross-linking, using ATRX as an example
द्वारा: Truch, J, और अन्य
प्रकाशित: (2018)

Two novel somatic mutations of the ATRX gene in female patients with acquired alpha thalassemia of myelodysplastic syndrome (ATMDS).
द्वारा: Haas, P, और अन्य
प्रकाशित: (2006)

Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.
द्वारा: Garrick, D, और अन्य
प्रकाशित: (2006)

Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.
द्वारा: Garrick, D, और अन्य
प्रकाशित: (2006)

A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndrome.
द्वारा: Costa, D, और अन्य
प्रकाशित: (2006)

Acquired alpha-thalassaernia in association with myelodysplastic syndrome (ATMDS): Two further private ATRX mutations
द्वारा: Fisher, C, और अन्य
प्रकाशित: (2007)

A nonsense mutation of the ATRX gene causing mild, moderate and profound mental retardation in members of a single family.
द्वारा: Gibbons, R, और अन्य
प्रकाशित: (1999)

ATRX targets variable number tandem repeats and thereby influences allele-specific expression
द्वारा: Lower, K, और अन्य
प्रकाशित: (2010)

Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin.
द्वारा: Eustermann, S, और अन्य
प्रकाशित: (2011)

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).
द्वारा: Gibbons, R, और अन्य
प्रकाशित: (2003)

Mutant ATRX: pathogenesis of ATRX syndrome and cancer
द्वारा: Kejia Yuan, और अन्य
प्रकाशित: (2024-10-01)

Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin
द्वारा: Eustermann, S, और अन्य
प्रकाशित: (2011)

Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53.
द्वारा: Seah, C, और अन्य
प्रकाशित: (2008)

ATRX dysfunction induces replication defects in primary mouse cells.
द्वारा: David Clynes, और अन्य
प्रकाशित: (2014-01-01)

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation.
द्वारा: Gibbons, R, और अन्य
प्रकाशित: (2000)