Related references
Note: Only part of the references are listed.The Genetics and Epigenetics of Facioscapulohumeral Muscular Dystrophy
Charis L. Himeda et al.
Annual Review of Genomics and Human Genetics (2019)
Dynamic transcriptomic analysis reveals suppression of PGC1α/ERRα drives perturbed myogenesis in facioscapulohumeral muscular dystrophy
Christopher R. S. Banerji et al.
HUMAN MOLECULAR GENETICS (2019)
Chemistry, mechanism and clinical status of antisense oligonucleotides and duplex RNAs
Xiulong Shen et al.
NUCLEIC ACIDS RESEARCH (2018)
A cre-inducible DUX4 transgenic mouse model for investigating facioscapulohumeral muscular dystrophy
Takako Jones et al.
PLOS ONE (2018)
Cellular uptake and trafficking of antisense oligonucleotides
Stanley T. Crooke et al.
NATURE BIOTECHNOLOGY (2017)
Antisense Oligonucleotides Used to Target the DUX4 mRNA as Therapeutic Approaches in FaciosScapuloHumeral Muscular Dystrophy (FSHD)
Eugenie Ansseau et al.
GENES (2017)
Facioscapulohumeral Dystrophy
Leo H. Wang et al.
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2016)
Antisense targeting of 3′ end elements involved in DUX4 mRNA processing is an efficient therapeutic strategy for facioscapulohumeral dystrophy: a new gene-silencing approach
Anne-Charlotte Marsollier et al.
HUMAN MOLECULAR GENETICS (2016)
DUX4 induces a transcriptome more characteristic of a less-differentiated cell state and inhibits myogenesis
Paul Knopp et al.
JOURNAL OF CELL SCIENCE (2016)
Morpholino-mediated Knockdown of DUX4 Toward Facioscapulohumeral Muscular Dystrophy Therapeutics
Jennifer C. J. Chen et al.
MOLECULAR THERAPY (2016)
Loss of epigenetic silencing of the DUX4 transcription factor gene in facioscapulohumeral muscular dystrophy
Jane E. Hewitt
HUMAN MOLECULAR GENETICS (2015)
Endogenous DUX4 expression in FSHD myotubes is sufficient to cause cell death and disrupts RNA splicing and cell migration pathways
Amanda M. Rickard et al.
HUMAN MOLECULAR GENETICS (2015)
Culture Conditions Affect Expression of DUX4 in FSHD Myoblasts
Sachchida Nand Pandey et al.
MOLECULES (2015)
Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2
Richard J. L. F. Lemmers et al.
HUMAN MOLECULAR GENETICS (2015)
In Silico Screening Based on Predictive Algorithms as a Design Tool for Exon Skipping Oligonucleotides in Duchenne Muscular Dystrophy
Yusuke Echigoya et al.
PLOS ONE (2015)
Dominant Lethal Pathologies in Male Mice Engineered to Contain an X-Linked DUX4 Transgene
Abhijit Dandapat et al.
CELL REPORTS (2014)
Therapeutic antisense oligonucleotides against cancer: hurdling to the clinic
Pedro M. D. Moreno et al.
FRONTIERS IN CHEMISTRY (2014)
Mipomersen Sodium: First Global Approval
Philip Hair et al.
DRUGS (2013)
DUX4 expression in FSHD muscle cells: how could such a rare protein cause a myopathy?
Alexandra Tassin et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2013)
Antisense Therapy in Neurology
Joshua J. A. Lee et al.
JOURNAL OF PERSONALIZED MEDICINE (2013)
DUX4 Activates Germ line Genes, Retroelements, and Immune Mediators: Implications for Facioscapulohumeral Dystrophy
Linda N. Geng et al.
DEVELOPMENTAL CELL (2012)
The FSHD Atrophic Myotube Phenotype Is Caused by DUX4 Expression
Celine Vanderplanck et al.
PLOS ONE (2011)
Comprehensive Polyadenylation Site Maps in Yeast and Human Reveal Pervasive Alternative Polyadenylation
Fatih Ozsolak et al.
CELL (2010)
Myoblasts from affected and non-affected FSHD muscles exhibit morphological differentiation defects
Marietta Barro et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2010)
Clinical features of facioscapulohumeral muscular dystrophy 2
J. C. de Greef et al.
NEUROLOGY (2010)
A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy
Richard J. L. F. Lemmers et al.
SCIENCE (2010)
Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene
Lauren Snider et al.
PLOS GENETICS (2010)
An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies
Darko Bosnakovski et al.
EMBO JOURNAL (2008)
The DUX4 gene at the FSHDIA locus encodes a pro-apoptotic protein
Valeria Kowaljow et al.
NEUROMUSCULAR DISORDERS (2007)
Pharmacokinetics, biodistribution, stability and toxicity of a cell-penetrating peptide-morpholino oligomer conjugate
Adams Amantana et al.
BIOCONJUGATE CHEMISTRY (2007)
Severe phenotype in infantile facioscapulohumeral muscular dystrophy
Lars Klinge et al.
NEUROMUSCULAR DISORDERS (2006)
Increasing D4Z4 repeat copy number compromises C2C12 myoblast differentiation
DJ Yip et al.
FEBS LETTERS (2003)
Design of antisense oligonucleotides stabilized by locked nucleic acids
J Kurreck et al.
NUCLEIC ACIDS RESEARCH (2002)
Share Paper
