Found: 11
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The inner nuclear membrane protein Emerin regulates β-catenin activity by restricting its accumulation in the nucleus.
- Published in:
- EMBO Journal, 2006, v. 25, n. 14, p. 3275, doi. 10.1038/sj.emboj.7601230
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- Article
Novel and recurrent EMD mutations in patients with Emery-Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spot.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 589, doi. 10.1038/jhg.2011.65
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- Article
Uncoordinated Transcription and Compromised Muscle Function in the Lmna-Null Mouse Model of Emery-Dreifuss Muscular Dystrophy.
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- PLoS ONE, 2011, v. 6, n. 2, p. 1, doi. 10.1371/journal.pone.0016651
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- Article
Further Characterisation of the Molecular Signature of Quiescent and Activated Mouse Muscle Satellite Cells.
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- PLoS ONE, 2009, v. 4, n. 4, p. 1, doi. 10.1371/journal.pone.0005205
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- Article
Mapping disease-related missense mutations in the immunoglobulin-like fold domain of lamin A/C reveals novel genotype-phenotype associations for laminopathies.
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- Proteins, 2014, v. 82, n. 6, p. 904, doi. 10.1002/prot.24465
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- Article
The Emery–Dreifuss muscular dystrophy associated-protein emerin is phosphorylated on serine 49 by protein kinase A.
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- FEBS Journal, 2006, v. 273, n. 19, p. 4562, doi. 10.1111/j.1742-4658.2006.05464.x
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- Article
Cell biology: Patches for wounded muscle.
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- Nature, 2003, v. 423, n. 6936, p. 129, doi. 10.1038/423129a
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- Article
Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.
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- Human Molecular Genetics, 2013, v. 22, n. 14, p. 2852, doi. 10.1093/hmg/ddt135
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- Article
Identification of an emerin–β-catenin complex in the heart important for intercalated disc architecture and β-catenin localisation.
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- Cellular & Molecular Life Sciences, 2010, v. 67, n. 5, p. 781, doi. 10.1007/s00018-009-0219-8
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- Article
Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations.
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- Human Mutation, 2011, v. 32, n. 2, p. 152, doi. 10.1002/humu.21361
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- Article
Nesprin-1 and -2 are involved in the pathogenesis of Emery–Dreifuss muscular dystrophy and are critical for nuclear envelope integrity.
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- Human Molecular Genetics, 2007, v. 16, n. 23, p. 2816, doi. 10.1093/hmg/ddm238
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- Article