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SMCHD1 activates the expression of genes required for the expansion of human myoblasts.
- Published in:
- Nucleic Acids Research, 2024, v. 52, n. 16, p. 9450, doi. 10.1093/nar/gkae600
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- Article
DUX4 Role in Normal Physiology and in FSHD Muscular Dystrophy.
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- Cells (2073-4409), 2021, v. 10, n. 12, p. 3322, doi. 10.3390/cells10123322
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- Article
Amino acid deprivation triggers a novel GCN2-independent response leading to the transcriptional reactivation of non-native DNA sequences.
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- PLoS ONE, 2018, v. 13, n. 7, p. 1, doi. 10.1371/journal.pone.0200783
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- Article
Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1.
- Published in:
- Nature, 2006, v. 439, n. 7079, p. 973, doi. 10.1038/nature04422
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- Article
FSHD: copy number variations on the theme of muscular dystrophy.
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- Journal of Cell Biology, 2010, v. 191, n. 6, p. 1049, doi. 10.1083/jcb.201007028
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- Article
Direct interplay between two candidate genes in FSHD muscular dystrophy.
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- Human Molecular Genetics, 2015, v. 24, n. 5, p. 1256, doi. 10.1093/hmg/ddu536
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- Article
WDR5 is required for DUX4 expression and its pathological effects in FSHD muscular dystrophy.
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- Nucleic Acids Research, 2023, v. 51, n. 10, p. 5144, doi. 10.1093/nar/gkad230
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- Article
The SUV4-20H Histone Methyltransferases in Health and Disease.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 9, p. 4736, doi. 10.3390/ijms23094736
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- Article
Rbfox1 Downregulation and Altered Calpain 3 Splicing by FRG1 in a Mouse Model of Facioscapulohumeral Muscular Dystrophy (FSHD).
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- PLoS Genetics, 2013, v. 9, n. 1, p. 1, doi. 10.1371/journal.pgen.1003186
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- Article
AAV6-mediated Systemic shRNA Delivery Reverses Disease in a Mouse Model of Facioscapulohumeral Muscular Dystrophy.
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- Molecular Therapy, 2011, v. 19, n. 11, p. 2055, doi. 10.1038/mt.2011.153
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- Article
The Trithorax protein Ash1L promotes myoblast fusion by activating Cdon expression.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07313-8
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- Article
Meeting report: the 2021 FSHD International Research Congress.
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- Skeletal Muscle, 2022, v. 12, n. 1, p. 1, doi. 10.1186/s13395-022-00287-8
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- Article
DNA Methylation Analysis of the Macrosatellite Repeat Associated with FSHD Muscular Dystrophy at Single Nucleotide Level.
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- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0115278
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- Article
Hmgb3 Is Regulated by MicroRNA-206 during Muscle Regeneration.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043464
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- Article
Diversification of the muscle proteome through alternative splicing.
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- Skeletal Muscle, 2018, v. 8, p. 1, doi. 10.1186/s13395-018-0152-3
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- Article
Report and Abstracts of the 17th Meeting of IIM, the Interuniversity Institute of Myology: Virtual meeting, October 16-18, 2020.
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- European Journal of Translational Myology, 2020, v. 30, n. 4, p. 1, doi. 10.4081/ejtm.2020.9485
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- Article
16th Meeting of the Interuniversity Institute of Myology (IIM) - Assisi (Italy), October 17-20, 2019: Foreword, Program and Abstracts.
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- European Journal of Translational Myology, 2020, v. 30, n. 3, p. 1, doi. 10.4081/ejtm.2020.9345
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- Article
A Human Pluripotent Stem Cell Model of Facioscapulohumeral Muscular Dystrophy-Affected Skeletal Muscles.
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- Stem Cells Translational Medicine, 2016, v. 5, n. 9, p. 1145, doi. 10.5966/sctm.2015-0224
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- Article
Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophy.
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- Human Molecular Genetics, 2017, v. 26, n. 4, p. 753, doi. 10.1093/hmg/ddw426
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- Article
FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis.
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- Journal of Molecular Cell Biology, 2013, v. 5, n. 5, p. 294, doi. 10.1093/jmcb/mjt018
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- Article