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Title
Splicing biomarkers of disease severity in myotonic dystrophy
Authors
Keywords
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Journal
ANNALS OF NEUROLOGY
Volume 74, Issue 6, Pages 862-872
Publisher
Wiley
Online
2013-08-08
DOI
10.1002/ana.23992
References
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Related references
Note: Only part of the references are listed.- Design of a Bioactive Small Molecule That Targets the Myotonic Dystrophy Type 1 RNA via an RNA Motif–Ligand Database and Chemical Similarity Searching
- (2012) Raman Parkesh et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- The myotonic dystrophies: molecular, clinical, and therapeutic challenges
- (2012) Bjarne Udd et al. LANCET NEUROLOGY
- Targeting nuclear RNA for in vivo correction of myotonic dystrophy
- (2012) Thurman M. Wheeler et al. NATURE
- If you build a rare disease registry, will they enroll and will they use it? Methods and data from the National Registry of Myotonic Dystrophy (DM) and Facioscapulohumeral Muscular Dystrophy (FSHD)
- (2011) James E. Hilbert et al. Contemporary Clinical Trials
- Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy
- (2011) Charlotte Fugier et al. NATURE MEDICINE
- Alternative splicing dysregulation secondary to skeletal muscle regeneration
- (2010) James P. Orengo et al. ANNALS OF NEUROLOGY
- Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues
- (2010) Arturo López Castel et al. HUMAN MOLECULAR GENETICS
- CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1
- (2010) Amanda J. Ward et al. HUMAN MOLECULAR GENETICS
- Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients
- (2010) Claudia Braida et al. HUMAN MOLECULAR GENETICS
- Repeat instability as the basis for human diseases and as a potential target for therapy
- (2010) Arturo López Castel et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Selective silencing of mutated mRNAs in DM1 by using modified hU7-snRNAs
- (2010) Virginie François et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy
- (2010) Hongqing Du et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Myotonic Dystrophy Transgenic Mice Exhibit Pathologic Abnormalities in Diaphragm Neuromuscular Junctions and Phrenic Nerves
- (2009) Petrica-Adrian Panaite et al. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
- Pentamidine reverses the splicing defects associated with myotonic dystrophy
- (2009) M. B. Warf et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Triplet-repeat oligonucleotide-mediated reversal of RNA toxicity in myotonic dystrophy
- (2009) S. A. M. Mulders et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Reversal of RNA Dominance by Displacement of Protein Sequestered on Triplet Repeat RNA
- (2009) T. M. Wheeler et al. SCIENCE
- Aberrantly spliced -dystrobrevin alters -syntrophin binding in myotonic dystrophy type 1
- (2008) M. Nakamori et al. NEUROLOGY
- 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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