Overexpression of CUGBP1 in Skeletal Muscle from Adult Classic Myotonic Dystrophy Type 1 but Not from Myotonic Dystrophy Type 2
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Title
Overexpression of CUGBP1 in Skeletal Muscle from Adult Classic Myotonic Dystrophy Type 1 but Not from Myotonic Dystrophy Type 2
Authors
Keywords
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Journal
PLoS One
Volume 8, Issue 12, Pages e83777
Publisher
Public Library of Science (PLoS)
Online
2013-12-21
DOI
10.1371/journal.pone.0083777
References
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Note: Only part of the references are listed.- Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy
- (2015) R Cardani et al. EUROPEAN JOURNAL OF HISTOCHEMISTRY
- Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2
- (2012) Rosanna Cardani et al. JOURNAL OF NEUROLOGY
- Autoregulated Splicing ofmuscleblind-like 1 (MBNL1) Pre-mRNA
- (2011) Devika P. Gates et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Mutant (CCTG)n Expansion Causes Abnormal Expression of Zinc Finger Protein 9 (ZNF9) in Myotonic Dystrophy Type 2
- (2010) Olayinka Raheem et al. AMERICAN JOURNAL OF PATHOLOGY
- Alternative splicing dysregulation secondary to skeletal muscle regeneration
- (2010) James P. Orengo et al. ANNALS OF NEUROLOGY
- CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1
- (2010) Amanda J. Ward et al. HUMAN MOLECULAR GENETICS
- Muscleblind-like 1 (Mbnl1) Promotes Insulin Receptor Exon 11 Inclusion via Binding to a Downstream Evolutionarily Conserved Intronic Enhancer
- (2010) Supriya Sen et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' muscles
- (2010) R. Massa et al. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
- Expression of RNA CCUG Repeats Dysregulates Translation and Degradation of Proteins in Myotonic Dystrophy 2 Patients
- (2009) Elizabeth Salisbury et al. AMERICAN JOURNAL OF PATHOLOGY
- Type 2 Myotonic Dystrophy Can Be Predicted by the Combination of Type 2 Muscle Fiber Central Nucleation and Scattered Atrophy
- (2009) Guillaume Bassez et al. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
- Reduction of the Rate of Protein Translation in Patients with Myotonic Dystrophy 2
- (2009) C. Huichalaf et al. JOURNAL OF NEUROSCIENCE
- Absence of a differentiation defect in muscle satellite cells from DM2 patients
- (2009) Richard Pelletier et al. NEUROBIOLOGY OF DISEASE
- MBNL and CELF proteins regulate alternative splicing of the skeletal muscle chloride channel CLCN1
- (2009) Yoshihiro Kino et al. NUCLEIC ACIDS RESEARCH
- Ectopic expression of cyclin D3 corrects differentiation of DM1 myoblasts through activation of RNA CUG-binding protein, CUGBP1
- (2008) Elizabeth Salisbury et al. EXPERIMENTAL CELL RESEARCH
- SRp20 and CUG-BP1 Modulate Insulin Receptor Exon 11 Alternative Splicing
- (2008) S. Sen et al. MOLECULAR AND CELLULAR BIOLOGY
- Preferential central nucleation of type 2 myofibers is an invariable feature of myotonic dystrophy type 2
- (2008) Valerio Pisani et al. MUSCLE & NERVE
- Premutation allele pool in myotonic dystrophy type 2
- (2008) L. L. Bachinski et al. NEUROLOGY
- Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy
- (2008) J. P. Orengo et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- A postnatal switch of CELF and MBNL proteins reprograms alternative splicing in the developing heart
- (2008) A. Kalsotra et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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