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List of works by Peter L. Jones

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

scientific article published on October 1, 2011

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

scientific article published on 7 February 2018

A multiple subunit Mi-2 histone deacetylase from Xenopus laevis cofractionates with an associated Snf2 superfamily ATPase ⬇️

scientific article (publication date: 2 July 1998)

Association of modified cytosines and the methylated DNA-binding protein MeCP2 with distinctive structural domains of lampbrush chromatin

scientific article

Association of modified cytosines and the methylated DNA-binding protein MeCP2 with distinctive structural domains of lampbrush chromatin.

scientific article

Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing

scientific article

C. elegans PAT-9 is a nuclear zinc finger protein critical for the assembly of muscle attachments ⬇️

scientific article published on May 22, 2012

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

scientific article published on 3 November 2015

Cloning and characterization of the murine manganous superoxide dismutase-encoding gene

scientific article published on February 1995

DNMT1 forms a complex with Rb, E2F1 and HDAC1 and represses transcription from E2F-responsive promoters

scientific article (publication date: July 2000)

Demethylated HSATII DNA and HSATII RNA Foci Sequester PRC1 and MeCP2 into Cancer-Specific Nuclear Bodies

scientific article published on March 2017

Dual functions of thyroid hormone receptors during Xenopus development

scientific article

Emerging preclinical animal models for FSHD.

scientific article published on 20 March 2015

Engineered telomeres in transgenic Xenopus laevis

scientific article

Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2.

scientific article

FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy

scientific article published on 21 April 2009

Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein

scientific article

Facioscapulohumeral muscular dystrophy as a model for epigenetic regulation and disease

scientific article published on 4 December 2014

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

scientific article

Facioscapulohumeral muscular dystrophy region gene 1 is a dynamic RNA-associated and actin-bundling protein

scientific article

Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites

scientific article

Functional CpG methylation system in a social insect

scientific article

Functional analysis of the SIN3-histone deacetylase RPD3-RbAp48-histone H4 connection in the Xenopus oocyte

scientific article

Histone deacetylase directs the dominant silencing of transcription in chromatin: association with MeCP2 and the Mi-2 chromodomain SWI/SNF ATPase

scientific article

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

scientific article

Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy

scientific article published on 29 March 2015

Large family cohorts of lymphoblastoid cells provide a new cellular model for investigating facioscapulohumeral muscular dystrophy

scientific article

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription ⬇️

scientific article (publication date: June 1998)

Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation

scientific article (publication date: September 1999)

Multiple N-CoR complexes contain distinct histone deacetylases

scientific article published on 19 January 2001

Muscular dystrophy candidate gene FRG1 is critical for muscle development

scientific article

Myogenic enhancers regulate expression of the facioscapulohumeral muscular dystrophy-associated DUX4 gene

scientific article

N-CoR-HDAC corepressor complexes: roles in transcriptional regulation by nuclear hormone receptors

scientific article

Nuclear receptor corepressor recruitment by unliganded thyroid hormone receptor in gene repression during Xenopus laevis development

scientific article

Programming the transcriptional state of replicating methylated dna.

scientific article published on 06 March 2001

Purification of MeCP2-containing deacetylase from Xenopus laevis

scientific article

Purification of a histone deacetylase complex from Xenopus laevis: preparation of substrates and assay procedures

scientific article published in January 1999

Purification of the MeCP2/histone deacetylase complex from Xenopus laevis

scientific article published on January 2001

Relationships between chromatin organization and DNA methylation in determining gene expression

scientific article

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

scientific article

Scalpel or Straitjacket: CRISPR/Cas9 Approaches for Muscular Dystrophies

scientific article

TNF regulates the in vivo occupancy of both distal and proximal regulatory regions of the MCP-1/JE gene

scientific article published on May 1996

Temporal uncoupling of the DNA methylome and transcriptional repression during embryogenesis

scientific article

Testing the effects of FSHD candidate gene expression in vertebrate muscle development

scientific article

The tripartite motif of nuclear factor 7 is required for its association with transcriptional units

scientific article published on 29 January 2007

Thyroid hormone regulation of Xenopus laevis metamorphosis: functions of thyroid hormone receptors and roles of extracellular matrix remodeling

scientific article published in July 1998

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

scientific article

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

scientific article published on 22 September 2008

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

scientific article published in October 2008

Tumor Necrosis Factor Alpha and Interleukin-1β Regulate the Murine Manganese Superoxide Dismutase Gene Through a Complex Intronic Enhancer Involving C/EBP-β and NF-κB ⬇️

scientific article published on December 1, 1997

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