Expression of the Human FSHD-Linked DUX4 Gene Induces Neurogenesis During Differentiation of Murine Embryonic Stem Cells
Author:
Affiliation:
1. Department of Pediatrics, Lillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota.
Publisher
Mary Ann Liebert Inc
Subject
Cell Biology,Developmental Biology,Hematology
Link
https://www.liebertpub.com/doi/pdf/10.1089/scd.2012.0643
Reference34 articles.
1. Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element
2. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy
3. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit
4. DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1
5. A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy
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1. The FSHD muscle–blood biomarker: a circulating transcriptomic biomarker for clinical severity in facioscapulohumeral muscular dystrophy;Brain Communications;2023
2. A circulating biomarker of facioscapulohumeral muscular dystrophy clinical severity, valid in skeletal muscle and blood;2022-09-03
3. Canine DUXC: implications for DUX4 retrotransposition and preclinical models of FSHD;Human Molecular Genetics;2021-12-09
4. A SARS-CoV-2 host infection model network based on genomic human Transcription Factors (TFs) depletion;Heliyon;2020-10
5. DUX4 regulates oocyte to embryo transition in human;2019-08-12
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