A Human Pluripotent Stem Cell Model of Facioscapulohumeral Muscular Dystrophy-Affected Skeletal Muscles
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Title
A Human Pluripotent Stem Cell Model of Facioscapulohumeral Muscular Dystrophy-Affected Skeletal Muscles
Authors
Keywords
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Journal
Stem Cells Translational Medicine
Volume 5, Issue 9, Pages 1145-1161
Publisher
Wiley
Online
2016-05-24
DOI
10.5966/sctm.2015-0224
References
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Related references
Note: Only part of the references are listed.- Robust generation and expansion of skeletal muscle progenitors and myocytes from human pluripotent stem cells
- (2016) Michael Shelton et al. METHODS
- GSTT1 is upregulated by oxidative stress through p38-MK2 signaling pathway in human granulosa cells: possible association with mitochondrial activity
- (2016) Megumu Ito et al. Aging-US
- Pluripotent Stem Cells for Gene Therapy of Degenerative Muscle Diseases
- (2015) Mariana Loperfido et al. CURRENT GENE THERAPY
- Endogenous DUX4 expression in FSHD myotubes is sufficient to cause cell death and disrupts RNA splicing and cell migration pathways
- (2015) Amanda M. Rickard et al. HUMAN MOLECULAR GENETICS
- Differentiation of pluripotent stem cells to muscle fiber to model Duchenne muscular dystrophy
- (2015) Jérome Chal et al. NATURE BIOTECHNOLOGY
- Efficient derivation and inducible differentiation of expandable skeletal myogenic cells from human ES and patient-specific iPS cells
- (2015) Sara M Maffioletti et al. Nature Protocols
- Emerging preclinical animal models for FSHD
- (2015) Angela Lek et al. TRENDS IN MOLECULAR MEDICINE
- DUX4-induced gene expression is the major molecular signature in FSHD skeletal muscle
- (2014) Zizhen Yao et al. HUMAN MOLECULAR GENETICS
- -catenin is central to DUX4-driven network rewiring in facioscapulohumeral muscular dystrophy
- (2014) C. R. S. Banerji et al. Journal of the Royal Society Interface
- Abnormalities in human pluripotent cells due to reprogramming mechanisms
- (2014) Hong Ma et al. NATURE
- Population-based incidence and prevalence of facioscapulohumeral dystrophy
- (2014) J. C. W. Deenen et al. NEUROLOGY
- Dominant Lethal Pathologies in Male Mice Engineered to Contain an X-Linked DUX4 Transgene
- (2014) Abhijit Dandapat et al. Cell Reports
- Derivation of Myogenic Progenitors Directly From Human Pluripotent Stem Cells Using a Sphere-Based Culture
- (2014) Tohru Hosoyama et al. Stem Cells Translational Medicine
- Derivation and Expansion of PAX7-Positive Muscle Progenitors from Human and Mouse Embryonic Stem Cells
- (2014) Michael Shelton et al. Stem Cell Reports
- Facioscapulohumeral dystrophy: the path to consensus on pathophysiology
- (2014) Rabi Tawil et al. Skeletal Muscle
- Wnt/β-catenin signaling suppresses DUX4 expression and prevents apoptosis of FSHD muscle cells
- (2013) Gregory J. Block et al. HUMAN MOLECULAR GENETICS
- DUX4 and DUX4 downstream target genes are expressed in fetal FSHD muscles
- (2013) Maxime Ferreboeuf et al. HUMAN MOLECULAR GENETICS
- Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophy
- (2013) Natacha Broucqsault et al. HUMAN MOLECULAR GENETICS
- DUX4 Differentially Regulates Transcriptomes of Human Rhabdomyosarcoma and Mouse C2C12 Cells
- (2013) Vishakha Sharma et al. PLoS One
- Directed In Vitro Myogenesis of Human Embryonic Stem Cells and Their In Vivo Engraftment
- (2013) Yongsung Hwang et al. PLoS One
- Altered Expression of Cyclin A 1 In Muscle of Patients with Facioscapulohumeral Muscle Dystrophy (FSHD-1)
- (2013) Anna Pakula et al. PLoS One
- Intrinsic Epigenetic Regulation of the D4Z4 Macrosatellite Repeat in a Transgenic Mouse Model for FSHD
- (2013) Yvonne D. Krom et al. PLoS Genetics
- Derivation and FACS-Mediated Purification of PAX3+/PAX7+ Skeletal Muscle Precursors from Human Pluripotent Stem Cells
- (2013) Bianca Borchin et al. Stem Cell Reports
- Human ES- and iPS-Derived Myogenic Progenitors Restore DYSTROPHIN and Improve Contractility upon Transplantation in Dystrophic Mice
- (2012) Radbod Darabi et al. Cell Stem Cell
- Functional muscle impairment in facioscapulohumeral muscular dystrophy is correlated with oxidative stress and mitochondrial dysfunction
- (2012) Ahmed Turki et al. FREE RADICAL BIOLOGY AND MEDICINE
- DUX4 expression in FSHD muscle cells: how could such a rare protein cause a myopathy?
- (2012) Alexandra Tassin et al. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
- Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2
- (2012) Richard J L F Lemmers et al. NATURE GENETICS
- FSHD Myotubes with Different Phenotypes Exhibit Distinct Proteomes
- (2012) Alexandra Tassin et al. PLoS One
- Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers
- (2012) F. Rahimov et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Highly Efficient Derivation of Skeletal Myotubes from Human Embryonic Stem Cells
- (2012) Lingjun Rao et al. Stem Cell Reviews and Reports
- Conditional over-expression of PITX1 causes skeletal muscle dystrophy in mice
- (2012) S. N. Pandey et al. Biology Open
- Gene expression during normal and FSHD myogenesis
- (2011) Koji Tsumagari et al. BMC Medical Genomics
- Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?
- (2011) Mark Richards et al. HUMAN GENETICS
- Expression Profiling of FSHD-1 and FSHD-2 Cells during Myogenic Differentiation Evidences Common and Distinctive Gene Dysregulation Patterns
- (2011) Stefania Cheli et al. PLoS One
- The FSHD Atrophic Myotube Phenotype Is Caused by DUX4 Expression
- (2011) Céline Vanderplanck et al. PLoS One
- Retinoic Acid Enhances Skeletal Myogenesis in Human Embryonic Stem Cells by Expanding the Premyogenic Progenitor Population
- (2011) Tammy Ryan et al. Stem Cell Reviews and Reports
- FSHD: copy number variations on the theme of muscular dystrophy
- (2010) Daphne Selvaggia Cabianca et al. JOURNAL OF CELL BIOLOGY
- A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy
- (2010) R. J. L. F. Lemmers et al. SCIENCE
- In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy
- (2010) Maria V Neguembor et al. Epigenomics
- Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene
- (2010) Lauren Snider et al. PLoS Genetics
- Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation
- (2009) Beatrice Bodega et al. BMC BIOLOGY
- Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level
- (2009) Rinse Klooster et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies
- (2008) Darko Bosnakovski et al. EMBO JOURNAL
- Myoblasts from affected and non-affected FSHD muscles exhibit morphological differentiation defects
- (2008) Marietta Barro et al. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
- Facioscapulohumeral Dystrophy
- (2007) Shree Pandya et al. PHYSICAL THERAPY
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