相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Defective survival of proliferating Sertoli cells and androgen receptor function in a mouse model of the ATR-X syndrome
Stefan Bagheri-Fam et al.
HUMAN MOLECULAR GENETICS (2011)
The ATRX-ADD domain binds to H3 tail peptides and reads the combined methylation state of K4 and K9
Arunkumar Dhayalan et al.
HUMAN MOLECULAR GENETICS (2011)
Aberrant Calcium/Calmodulin-Dependent Protein Kinase II (CaMKII) Activity Is Associated with Abnormal Dendritic Spine Morphology in the ATRX Mutant Mouse Brain
Norifumi Shioda et al.
JOURNAL OF NEUROSCIENCE (2011)
The H19 locus: Role of an imprinted non-coding RNA in growth and development
Anne Gabory et al.
BIOESSAYS (2010)
Distinct Factors Control Histone Variant H3.3 Localization at Specific Genomic Regions
Aaron D. Goldberg et al.
CELL (2010)
ATR-X Syndrome Protein Targets Tandem Repeats and Influences Allele-Specific Expression in a Size-Dependent Manner
Martin J. Law et al.
CELL (2010)
ATRX Taming tandem repeats
Richard J. Gibbons et al.
CELL CYCLE (2010)
ATRX Partners with Cohesin and MeCP2 and Contributes to Developmental Silencing of Imprinted Genes in the Brain
Kristin D. Kernohan et al.
DEVELOPMENTAL CELL (2010)
The death-associated protein DAXX is a novel histone chaperone involved in the replication-independent deposition of H3.3
Pascal Drane et al.
GENES & DEVELOPMENT (2010)
ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cells
Lee H. Wong et al.
GENOME RESEARCH (2010)
SMARCA2 and other genome-wide supported schizophrenia-associated genes: regulation by REST/NRSF, network organization and primate-specific evolution
Yann Loe-Mie et al.
HUMAN MOLECULAR GENETICS (2010)
Protein Complex of Drosophila ATRX/XNP and HP1a Is Required for the Formation of Pericentric Beta-heterochromatin in Vivo
Alexander V. Emelyanov et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that includes locus for X-linked recessive type of chondrodysplasia punctata (CDPX1)
Tsuguhiro Horikoshi et al.
JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH (2010)
An age-related sprouting transcriptome provides molecular control of axonal sprouting after stroke
Songlin Li et al.
NATURE NEUROSCIENCE (2010)
Daxx is an H3.3-specific histone chaperone and cooperates with ATRX in replication-independent chromatin assembly at telomeres
Peter W. Lewis et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Loss of Maternal ATRX Results in Centromere Instability and Aneuploidy in the Mammalian Oocyte and Pre-Implantation Embryo
Claudia Baumann et al.
PLOS GENETICS (2010)
On the Molecular Etiology of Cornelia de Lange Syndrome
Dale Dorsett et al.
YEAR IN HUMAN AND MEDICAL GENETICS 2009 (2009)
A family-based study of the IL3RA gene on susceptibility to schizophrenia in a Chinese Han population
Shilong Sun et al.
BRAIN RESEARCH (2009)
ATRX marks the inactive X chromosome (Xi) in somatic cells and during imprinted X chromosome inactivation in trophoblast stem cells
Claudia Baumann et al.
CHROMOSOMA (2009)
Nonallelic transvection of multiple imprinted loci is organized by the H19 imprinting control region during germline development
Kuljeet Singh Sandhu et al.
GENES & DEVELOPMENT (2009)
Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndrome
Chantal F. Medina et al.
HUMAN MOLECULAR GENETICS (2009)
Loss of ATRX in Chondrocytes Has Minimal Effects on Skeletal Development
Lauren A. Solomon et al.
PLOS ONE (2009)
The XNP remodeler targets dynamic chromatin in Drosophila
Jonathan I. Schneiderman et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome
Michael A. Levy et al.
BMC GENOMICS (2008)
Association of ATRX with pericentric heterochromatin and the Y chromosome of neonatal mouse spermatogonia
Claudia Baumann et al.
BMC MOLECULAR BIOLOGY (2008)
ATP-dependent chromatin remodeling by the Saccharomyces cerevisiae homologous recombination factor Rdh54
YoungHo Kwon et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Loss of ATRX leads to chromosome cohesion and congression defects
Kieran Ritchie et al.
JOURNAL OF CELL BIOLOGY (2008)
Neuronal Death Resulting from Targeted Disruption of the Snf2 Protein ATRX Is Mediated by p53
Claudia Seah et al.
JOURNAL OF NEUROSCIENCE (2008)
Cohesin mediates transcriptional insulation by CCCTC-binding factor
Kerstin S. Wendt et al.
NATURE (2008)
The Chromatin Remodelling Factor dATRX Is Involved in Heterochromatin Formation
Andrew R. Bassett et al.
PLOS ONE (2008)
Patient mutations alter ATRX targeting to PML nuclear bodies
Nathalie G. Berube et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX
Anthony Argentaro et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia
T. Lencz et al.
MOLECULAR PSYCHIATRY (2007)
Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation
Xinsheng Nan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Heterochromatin revisited
Shiv I. S. Grewal et al.
NATURE REVIEWS GENETICS (2007)
Circular chromosome conformation capture (4C) uncovers extensive networks of epigenetically regulated intra- and interchromosomal interactions
Zhihu Zhao et al.
NATURE GENETICS (2006)
Visualization of Rad54, a chromatin remodeling protein, translocating on single DNA molecules
Ichiro Amitani et al.
MOLECULAR CELL (2006)
Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues
David Garrick et al.
PLOS GENETICS (2006)
Acute myeloid leukemia subgroups identified by pathway - Restricted gene expression signatures
Elena Serrano et al.
ACTA HAEMATOLOGICA (2006)
Epigenetic regulation of mammalian pericentric heterochromatin in vivo by HP1
N Kourmouli et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)
RNA polymerase II is required for RNAi-dependent heterochromatin assembly
H Kato et al.
SCIENCE (2005)
The mammalian heterochromatin protein 1 binds diverse nuclear proteins through a common motif that targets the chromoshadow domain
MS Lechner et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)
The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis
NG Bérubé et al.
JOURNAL OF CLINICAL INVESTIGATION (2005)
Acquired somatic ATRX mutations in myelodysplastic syndrome associated with α thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations
DP Steensma et al.
BLOOD (2004)
A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain
D Garrick et al.
GENE (2004)
Separase-mediated cleavage of cohesin at interphase is required for DNA repair
K Nagao et al.
NATURE (2004)
Postreplicative recruitment of cohesin to double-strand breaks is required for DNA repair
L Ström et al.
MOLECULAR CELL (2004)
ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes
R De La Fuente et al.
DEVELOPMENTAL BIOLOGY (2004)
A novel transcription regulatory complex containing death domain-associated protein and the ATR-X syndrome protein
J Tang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD
KM Boycott et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2003)
The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies
YT Xue et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)
RJ Gibbons et al.
NATURE GENETICS (2003)
Neurodevelopmental defects resulting from ATRX overexpression in transgenic mice
NG Bérubé et al.
HUMAN MOLECULAR GENETICS (2002)
ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein
C Cardoso et al.
JOURNAL OF MEDICAL GENETICS (2000)
Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association
NG Bérubé et al.
HUMAN MOLECULAR GENETICS (2000)
Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation
RJ Gibbons et al.
NATURE GENETICS (2000)
Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22.3, related to the cytosine-5-methyltransferase 3 gene family
U Aapola et al.
GENOMICS (2000)
分享论文
