4.5 Article

Targeted loss of the ATR-X syndrome protein in the limb mesenchyme of mice causes brachydactyly

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。
Article Medicine, Research & Experimental

Atrx deficiency induces telomere dysfunction, endocrine defects, and reduced life span

L. Ashley Watson et al.

JOURNAL OF CLINICAL INVESTIGATION (2013)

Article Biochemistry & Molecular Biology

Inner Nuclear Envelope Proteins SUN1 and SUN2 Play a Prominent Role in the DNA Damage Response

Kai Lei et al.

CURRENT BIOLOGY (2012)

Article Medicine, Research & Experimental

Compromised genomic integrity impedes muscle growth after Atrx inactivation

Michael S. Huh et al.

JOURNAL OF CLINICAL INVESTIGATION (2012)

Article Medicine, Research & Experimental

A misplaced IncRNA causes brachydactyly in humans

Philipp G. Maass et al.

JOURNAL OF CLINICAL INVESTIGATION (2012)

Article Multidisciplinary Sciences

Persistent DNA Damage after High Dose In Vivo Gamma Exposure of Minipig Skin

Emad A. Ahmed et al.

PLOS ONE (2012)

Article Multidisciplinary Sciences

Loss of Atrx Sensitizes Cells to DNA Damaging Agents through p53-Mediated Death Pathways

Damiano Conte et al.

PLOS ONE (2012)

Article Biochemistry & Molecular Biology

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)

Article Biochemistry & Molecular Biology

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)

Article Biochemistry & Molecular Biology

ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cells

Lee H. Wong et al.

GENOME RESEARCH (2010)

Article Multidisciplinary Sciences

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)

Article Multidisciplinary Sciences

Loss of ATRX in Chondrocytes Has Minimal Effects on Skeletal Development

Lauren A. Solomon et al.

PLOS ONE (2009)

Article Cell Biology

Loss of ATRX leads to chromosome cohesion and congression defects

Kieran Ritchie et al.

JOURNAL OF CELL BIOLOGY (2008)

Article Developmental Biology

Genetic ablation of Rac1 in cartilage results in chondrodysplasia

Guoyan Wang et al.

DEVELOPMENTAL BIOLOGY (2007)

Article Cell Biology

Positional stability of single double-strand breaks in mammalian cells

Evi Soutoglou et al.

NATURE CELL BIOLOGY (2007)

Review Genetics & Heredity

Alpha thalassaemia-mental retardation, X linked

Richard Gibbons

ORPHANET JOURNAL OF RARE DISEASES (2006)

Article Biochemistry & Molecular Biology

Co-localization of PARP-1 and lamin B in the nuclear architecture: A halo-fluorescence- and confocal-microscopy study

M Vidakovic et al.

JOURNAL OF CELLULAR BIOCHEMISTRY (2005)

Article Medicine, Research & Experimental

The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis

NG Bérubé et al.

JOURNAL OF CLINICAL INVESTIGATION (2005)

Article Biochemistry & Molecular Biology

p38 MAP kinase signaling is necessary for rat chondrosarcoma cell proliferation

D Halawani et al.

ONCOGENE (2004)

Article Multidisciplinary Sciences

A-type lamins regulate retinoblastoma protein function by promoting subnuclear localization and preventing proteasomal degradation

BR Johnson et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)

Article Multidisciplinary Sciences

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)