Judit Balog
Leiden, ZH, Netherlands
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 34 publications
Fibro-adipogenic progenitors enhance functional and structural properties of human 3D tissue engineered skeletal muscles.
Journal: Journal of tissue engineering
Published: January 13, 2026
DUX4 activates common and context-specific intergenic transcripts and isoforms.
Journal: Science advances
Published: May 07, 2025
Lrif1 modulates Trim28-mediated repression of the Dux locus in mouse embryonic stem cells.
Journal: bioRxiv : the preprint server for biology
Published: November 28, 2024
Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophy.
Journal: Brain : a journal of neurology
Published: May 17, 2023
snRNA-seq analysis in multinucleated myogenic FSHD cells identifies heterogeneous FSHD transcriptome signatures associated with embryonic-like program activation and oxidative stress-induced apoptosis.
Journal: Human molecular genetics
Published: February 03, 2023
Facioscapulohumeral muscular dystrophy: the road to targeted therapies.
Journal: Nature reviews. Neurology
Published: December 07, 2022
Adenine base editing of the DUX4 polyadenylation signal for targeted genetic therapy in facioscapulohumeral muscular dystrophy.
Journal: Molecular therapy. Nucleic acids
Published: January 08, 2021
Hippocampal glucocorticoid target genes associated with enhancement of memory consolidation.
Journal: The European journal of neuroscience
Published: November 09, 2020
Premature termination codons in the DMD gene cause reduced local mRNA synthesis.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: July 04, 2020
Chromosome 10q-linked FSHD identifies DUX4 as principal disease gene.
Journal: Journal of medical genetics
Published: May 28, 2020
Last Updated: 09/26/2026