List of works - Jessica C de Greef

Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei.

scientific article

Collagen VI deficiency reduces muscle pathology, but does not improve muscle function, in the γ-sarcoglycan-null mouse

scientific article published on 24 January 2016

Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD.

scientific article

Correlation analysis of clinical parameters with epigenetic modifications in the DUX4 promoter in FSHD.

scientific article

Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome

scientific article

Cytoskeletal disorganization underlies PABPN1-mediated myogenic disability

scientific article published on 19 October 2020

Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

scientific article (publication date: 11 November 2012)

Dnmt3b regulates DUX4 expression in a tissue-dependent manner in transgenic D4Z4 mice

scientific article published on 01 October 2020

Epigenetic mechanisms of facioscapulohumeral muscular dystrophy

scientific article published on 03 August 2008

Generation of genetically matched hiPSC lines from two mosaic facioscapulohumeral dystrophy type 1 patients

scientific article published on 28 August 2019

Mouse models for muscular dystrophies: an overview

scientific article published on 21 February 2020

Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome

scientific article published on 28 July 2015

Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2.

scientific article

Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity.

scientific article published on 7 October 2011

Protective role for the N-terminal domain of α-dystroglycan in Influenza A virus proliferation.

scientific article

Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model

scientific article

Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).

scientific article

The prospects of targeting DUX4 in facioscapulohumeral muscular dystrophy

scientific article published on 10 August 2020

List of works by Jessica C de Greef

Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei.

Collagen VI deficiency reduces muscle pathology, but does not improve muscle function, in the γ-sarcoglycan-null mouse

Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD.

Correlation analysis of clinical parameters with epigenetic modifications in the DUX4 promoter in FSHD.

Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome

Cytoskeletal disorganization underlies PABPN1-mediated myogenic disability

Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

Dnmt3b regulates DUX4 expression in a tissue-dependent manner in transgenic D4Z4 mice

Epigenetic mechanisms of facioscapulohumeral muscular dystrophy

Generation of genetically matched hiPSC lines from two mosaic facioscapulohumeral dystrophy type 1 patients

Mouse models for muscular dystrophies: an overview

Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome

Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2.

Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity.

Protective role for the N-terminal domain of α-dystroglycan in Influenza A virus proliferation.

Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model

Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).

The prospects of targeting DUX4 in facioscapulohumeral muscular dystrophy