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A cre-inducible DUX4 transgenic mouse model for investigating facioscapulohumeral muscular dystrophy

PloS one, 2018-02, Vol.13 (2), p.e0192657-e0192657

2018

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CRISPR/dCas9-mediated Transcriptional Inhibition Ameliorates the Epigenetic Dysregulation at D4Z4 and Represses DUX4-fl in FSH Muscular Dystrophy

Molecular therapy, 2016-03, Vol.24 (3), p.527-535

2016

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The Genetics and Epigenetics of Facioscapulohumeral Muscular Dystrophy

Annual review of genomics and human genetics, 2019-08, Vol.20 (1), p.265-291

2019

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Transient high glucose causes persistent epigenetic changes and altered gene expression during subsequent normoglycemia

The Journal of experimental medicine, 2008-09, Vol.205 (10), p.2409-2417

2008

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Identification of candidate miRNA biomarkers for facioscapulohumeral muscular dystrophy using DUX4-based mouse models

Disease models & mechanisms, 2021-08, Vol.14 (8)

2021

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Targeted epigenetic repression by CRISPR/dSaCas9 suppresses pathogenic DUX4-fl expression in FSHD

Molecular therapy. Methods & clinical development, 2021-03, Vol.20, p.298-311

2021

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Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

Human molecular genetics, 2012-10, Vol.21 (20), p.4419-4430

2012

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Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD)

PloS one, 2016-03, Vol.11 (3), p.e0150938-e0150938

2016

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Myogenic Enhancers Regulate Expression of the Facioscapulohumeral Muscular Dystrophy-Associated DUX4 Gene

Molecular and cellular biology, 2014-06, Vol.34 (11), p.1942-1955

2014

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Emerging preclinical animal models for FSHD

Trends in molecular medicine, 2015-05, Vol.21 (5), p.295-306

2015

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Transgenic mice expressing tunable levels of DUX4 develop characteristic facioscapulohumeral muscular dystrophy-like pathophysiology ranging in severity

Skeletal muscle, 2020-04, Vol.10 (1), p.8-28, Article 8

2020

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Precise Epigenetic Analysis Using Targeted Bisulfite Genomic Sequencing Distinguishes FSHD1, FSHD2, and Healthy Subjects

Diagnostics (Basel), 2021-08, Vol.11 (8), p.1469

2021

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Functional CpG Methylation System in a Social Insect

Science (American Association for the Advancement of Science), 2006-10, Vol.314 (5799), p.645-647

2006

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FSHD Therapeutic Strategies: What Will It Take to Get to Clinic?

Journal of personalized medicine, 2022-05, Vol.12 (6), p.865

2022

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mTOR is required for pulmonary arterial vascular smooth muscle cell proliferation under chronic hypoxia

The FASEB journal, 2011-06, Vol.25 (6), p.1922-1933

2011

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Temporal uncoupling of the DNA methylome and transcriptional repression during embryogenesis

Genome research, 2011-08, Vol.21 (8), p.1313-1327

2011

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Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing

Clinical epigenetics, 2014-10, Vol.6 (1), p.23-23, Article 23

2014

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A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing

Bioscience reports, 2011-10, Vol.31 (5), p.333-343

2011

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Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

Nature genetics, 1998-06, Vol.19 (2), p.187-191

1998

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Have a Little Heart (or Not): Highly Minimized Skeletal Muscle Regulatory Cassettes with Low or No Activity in the Heart

Human gene therapy, 2024-08, Vol.35 (15-16), p.543-554

2024

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Human DUX4 and porcine DUXC activate similar early embryonic programs in pig muscle cells: implications for preclinical models of FSHD

Human molecular genetics, 2023-05, Vol.32 (11), p.1864-1874

2023

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Muscle eosinophilia is a hallmark of chronic disease in facioscapulohumeral muscular dystrophy

Human molecular genetics, 2024-05, Vol.33 (10), p.872-883

2024

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Muscular dystrophy candidate gene FRG1 is critical for muscle development

Developmental dynamics, 2009-06, Vol.238 (6), p.1502-1512

2009

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Gene delivery from a DNA controlled-release stent in porcine coronary arteries

Nature biotechnology, 2000-11, Vol.18 (11), p.1181-1184

2000

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A cre-inducible DUX4 transgenic mouse model for investigating facioscapulohumeral muscular dystrophy

CRISPR/dCas9-mediated Transcriptional Inhibition Ameliorates the Epigenetic Dysregulation at D4Z4 and Represses DUX4-fl in FSH Muscular Dystrophy

The Genetics and Epigenetics of Facioscapulohumeral Muscular Dystrophy

Transient high glucose causes persistent epigenetic changes and altered gene expression during subsequent normoglycemia

Identification of candidate miRNA biomarkers for facioscapulohumeral muscular dystrophy using DUX4-based mouse models

Targeted epigenetic repression by CRISPR/dSaCas9 suppresses pathogenic DUX4-fl expression in FSHD

Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD)

Myogenic Enhancers Regulate Expression of the Facioscapulohumeral Muscular Dystrophy-Associated DUX4 Gene

Emerging preclinical animal models for FSHD

Transgenic mice expressing tunable levels of DUX4 develop characteristic facioscapulohumeral muscular dystrophy-like pathophysiology ranging in severity

Precise Epigenetic Analysis Using Targeted Bisulfite Genomic Sequencing Distinguishes FSHD1, FSHD2, and Healthy Subjects

Functional CpG Methylation System in a Social Insect

Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies

FSHD Therapeutic Strategies: What Will It Take to Get to Clinic?

mTOR is required for pulmonary arterial vascular smooth muscle cell proliferation under chronic hypoxia

Temporal uncoupling of the DNA methylome and transcriptional repression during embryogenesis

Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing

A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

Have a Little Heart (or Not): Highly Minimized Skeletal Muscle Regulatory Cassettes with Low or No Activity in the Heart

Human DUX4 and porcine DUXC activate similar early embryonic programs in pig muscle cells: implications for preclinical models of FSHD

Muscle eosinophilia is a hallmark of chronic disease in facioscapulohumeral muscular dystrophy

Muscular dystrophy candidate gene FRG1 is critical for muscle development

Gene delivery from a DNA controlled-release stent in porcine coronary arteries

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