ATRX: taming tandem repeats.

ATRX: taming tandem repeats.

Dettagli Bibliografici
Autori principali:	Gibbons, R, Higgs, D
Natura:	Journal article
Lingua:	English
Pubblicazione:	2010

Documenti analoghi

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

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

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

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

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

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

The chromatin remodelling factor ATRX suppresses R-loops in transcribed telomeric repeats
di: Nguyen, D, et al.
Pubblicazione: (2017)

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

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

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

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

Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains.
di: Picketts, D, et al.
Pubblicazione: (1998)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Mutations in the chromatin-associated protein ATRX.
di: Gibbons, R, et al.
Pubblicazione: (2008)

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

The loss of ATRX increases susceptibility to pancreatic injury and oncogenic KRAS in female but not male mice
di: Young, C, et al.
Pubblicazione: (2018)

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

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

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

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

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

Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.
di: David Garrick, et al.
Pubblicazione: (2006-04-01)

Identification of acquired somatic mutations in the chromatin remodelling factor ATRX in the a thalassaemia myelodysplasia syndrome (ATMDS)
di: Gibbons, R, et al.
Pubblicazione: (2003)

Identification of acquired somatic mutations in the chromatin remodelling factor ATRX in the alpha thalassemia myelodysplasia syndrome (ATMDS).
di: Gibbons, R, et al.
Pubblicazione: (2003)

The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies.
di: Xue, Y, et al.
Pubblicazione: (2003)