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Neurodevelopmental Disorders Caused by Defective Chromatin Remodeling: Phenotypic Complexity Is Highlighted by a Review of ATRX Function

Frontiers in genetics, 2020-08, Vol.11, p.885

2020

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ATRX ADD domain links an atypical histone methylation recognition mechanism to human mental-retardation syndrome

Nature structural & molecular biology, 2011-07, Vol.18 (7), p.769-776

2011

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Correction to: C3aR signaling and gliosis in response to neurodevelopmental damage in the cerebellum

Journal of neuroinflammation, 2020-01, Vol.17 (1), p.32-32, Article 32

2020

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Author Correction: Atrx inactivation drives disease-defining phenotypes in glioma cells of origin through global epigenomic remodeling

Nature communications, 2022-01, Vol.13 (1), p.190-190, Article 190

2022

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Impaired SNF2L Chromatin Remodeling Prolongs Accessibility at Promoters Enriched for Fos/Jun Binding Sites and Delays Granule Neuron Differentiation

Frontiers in molecular neuroscience, 2021-07, Vol.14, p.680280-680280

2021

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PHF6 Degrees of Separation: The Multifaceted Roles of a Chromatin Adaptor Protein

Genes, 2015-06, Vol.6 (2), p.325-352

2015

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Snf2h Drives Chromatin Remodeling to Prime Upper Layer Cortical Neuron Development

Frontiers in molecular neuroscience, 2019-10, Vol.12, p.243

2019

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A Novel Transcription Regulatory Complex Containing Death Domain-associated Protein and the ATR-X Syndrome Protein

The Journal of biological chemistry, 2004-05, Vol.279 (19), p.20369-20377

2004

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A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects

Human molecular genetics, 2023-07, Vol.32 (15), p.2485-2501

2023

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PHF6 Interacts with the Nucleosome Remodeling and Deacetylation (NuRD) Complex

Journal of proteome research, 2012-08, Vol.11 (8), p.4326-4337

2012

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Börjeson-Forssman-Lehmann Syndrome Due to a Novel Plant Homeodomain Zinc Finger Mutation in the PHF6 Gene

Journal of child neurology, 2009-05, Vol.24 (5), p.610-614

2009

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Patient mutations alter ATRX targeting to PML nuclear bodies

European journal of human genetics : EJHG, 2008-02, Vol.16 (2), p.192-201

2008

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The sub-nucleolar localization of PHF6 defines its role in rDNA transcription and early processing events

European journal of human genetics : EJHG, 2016-10, Vol.24 (10), p.1453-1459

2016

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Snf2I Regulates Foxg1-Dependent Progenitor Cell Expansion in the Developing Brain

Developmental cell, 2012-04, Vol.22 (4), p.871-878

2012

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Novel genetically engineered H3.3G34R model reveals cooperation with ATRX loss in upregulation of Hoxa cluster genes and promotion of neuronal lineage

Neuro-oncology advances, 2023-01, Vol.5 (1), p.vdad003-vdad003

2023

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Characterization of novel isoforms and evaluation of SNF2L/SMARCA1 as a candidate gene for X-linked mental retardation in 12 families linked to Xq25-26

BMC medical genetics, 2008-02, Vol.9 (1), p.11-11, Article 11

2008

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T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6

Pediatric blood & cancer, 2010-10, Vol.55 (4), p.722-724

2010

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Hedgehog regulates Norrie disease protein to drive neural progenitor self-renewal

Human molecular genetics, 2013-03, Vol.22 (5), p.1005-1016

2013

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Mutations in a putative global transcriptional regulator cause X-linked mental retardation with α-thalassemia (ATR-X syndrome)

Cell, 1995-03, Vol.80 (6), p.837-845

1995

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Further clinical delineation of the Börjeson–Forssman–Lehmann syndrome in patients with PHF6 mutations

American journal of medical genetics. Part A, 2009-02, Vol.149A (2), p.246-250

2009

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Matters of life and death: the role of chromatin remodeling proteins in retinal neuron survival

Journal of ocular biology, diseases, and informatics, 2011-09, Vol.4 (3), p.111-120

2011

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GENE-37. ATRX INACTIVATION DISRUPTS GLOBAL HETEROCHROMATIN LANDSCAPES AND ALTERS DISEASE-RELEVANT TRANSCRIPTIONAL ACTIVITY

Neuro-oncology (Charlottesville, Va.), 2018-11, Vol.20 (suppl_6), p.vi111-vi111

2018

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Abstract 912: A novel genetically engineered H3.3G34R model reveals cooperation with ATRX loss in upregulation of PRC2 target genes

Cancer research (Chicago, Ill.), 2022-06, Vol.82 (12_Supplement), p.912-912

2022

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Abstract 4322: Atrx inactivation drives motility and dysregulates differentiation in glioma cells of origin through global epigenomic remodeling

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.4322-4322

2018

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Genome-wide characterisation of Foxa1 binding sites reveals several mechanisms for regulating neuronal differentiation in midbrain dopamine cells

Journal of cell science, 2015-04, Vol.128 (8), p.e031-e031

2015

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Neurodevelopmental Disorders Caused by Defective Chromatin Remodeling: Phenotypic Complexity Is Highlighted by a Review of ATRX Function

ATRX ADD domain links an atypical histone methylation recognition mechanism to human mental-retardation syndrome

Correction to: C3aR signaling and gliosis in response to neurodevelopmental damage in the cerebellum

Author Correction: Atrx inactivation drives disease-defining phenotypes in glioma cells of origin through global epigenomic remodeling

Impaired SNF2L Chromatin Remodeling Prolongs Accessibility at Promoters Enriched for Fos/Jun Binding Sites and Delays Granule Neuron Differentiation

PHF6 Degrees of Separation: The Multifaceted Roles of a Chromatin Adaptor Protein

Snf2h Drives Chromatin Remodeling to Prime Upper Layer Cortical Neuron Development

A Novel Transcription Regulatory Complex Containing Death Domain-associated Protein and the ATR-X Syndrome Protein

A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects

PHF6 Interacts with the Nucleosome Remodeling and Deacetylation (NuRD) Complex

Börjeson-Forssman-Lehmann Syndrome Due to a Novel Plant Homeodomain Zinc Finger Mutation in the PHF6 Gene

Patient mutations alter ATRX targeting to PML nuclear bodies

The sub-nucleolar localization of PHF6 defines its role in rDNA transcription and early processing events

Snf2I Regulates Foxg1-Dependent Progenitor Cell Expansion in the Developing Brain

Novel genetically engineered H3.3G34R model reveals cooperation with ATRX loss in upregulation of Hoxa cluster genes and promotion of neuronal lineage

Characterization of novel isoforms and evaluation of SNF2L/SMARCA1 as a candidate gene for X-linked mental retardation in 12 families linked to Xq25-26

T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6

Hedgehog regulates Norrie disease protein to drive neural progenitor self-renewal

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with α-thalassemia (ATR-X syndrome)

Further clinical delineation of the Börjeson–Forssman–Lehmann syndrome in patients with PHF6 mutations

Matters of life and death: the role of chromatin remodeling proteins in retinal neuron survival

GENE-37. ATRX INACTIVATION DISRUPTS GLOBAL HETEROCHROMATIN LANDSCAPES AND ALTERS DISEASE-RELEVANT TRANSCRIPTIONAL ACTIVITY

Abstract 912: A novel genetically engineered H3.3G34R model reveals cooperation with ATRX loss in upregulation of PRC2 target genes

Abstract 4322: Atrx inactivation drives motility and dysregulates differentiation in glioma cells of origin through global epigenomic remodeling

Genome-wide characterisation of Foxa1 binding sites reveals several mechanisms for regulating neuronal differentiation in midbrain dopamine cells

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