Correction of GSK3β at young age prevents muscle pathology in mice with myotonic dystrophy type 1

Neonatal cardiac dysfunction and transcriptome changes caused by the absence of Celf1

(2016) Jimena Giudice et al.   Scientific Reports

A critical and previously unsuspected role for doublecortin at the neuromuscular junction in mouse and human

(2015) F. Bourgeois et al.   NEUROMUSCULAR DISORDERS

Reduction of toxic RNAs in myotonic dystrophies type 1 and type 2 by the RNA helicase p68/DDX5

(2015) Karlie Jones et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Doublecortin marks a new population of transiently amplifying muscle progenitor cells and is required for myofiber maturation during skeletal muscle regeneration

(2014) R. Ogawa et al.   DEVELOPMENT

DDX6 regulates sequestered nuclear CUG-expanded DMPK-mRNA in dystrophia myotonica type 1

(2014) O. J. Pettersson et al.   NUCLEIC ACIDS RESEARCH

Vitamin D Signaling in Myogenesis: Potential for Treatment of Sarcopenia

(2014) Akira Wagatsuma et al.   Biomed Research International

Evaluating the effects of CELF1 deficiency in a mouse model of RNA toxicity

(2013) Yun Kyoung Kim et al.   HUMAN MOLECULAR GENETICS

Molecular mechanisms of muscle atrophy in myotonic dystrophies

(2013) Lubov Timchenko   INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY

X-linked microtubule-associated protein, Mid1, regulates axon development

(2013) T. Lu et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The RNA-binding protein Staufen1 is increased in DM1 skeletal muscle and promotes alternative pre-mRNA splicing

(2012) Aymeric Ravel-Chapuis et al.   JOURNAL OF CELL BIOLOGY

GSK3β mediates muscle pathology in myotonic dystrophy

(2012) Karlie Jones et al.   JOURNAL OF CLINICAL INVESTIGATION

New function for the RNA helicase p68/DDX5 as a modifier of MBNL1 activity on expanded CUG repeats

(2011) François-Xavier Laurent et al.   NUCLEIC ACIDS RESEARCH

Expression of a Dominant Negative CELF Protein In Vivo Leads to Altered Muscle Organization, Fiber Size, and Subtype

(2011) Dara S. Berger et al.   PLoS One

Myotonic Dystrophies 1 and 2: Complex Diseases with Complex Mechanisms

(2010) Benedikt Schoser et al.   CURRENT GENOMICS

Expansion of CUG RNA repeats causes stress and inhibition of translation in myotonic dystrophy 1 (DM1) cells

(2010) Claudia Huichalaf et al.   FASEB JOURNAL

CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1

(2010) Amanda J. Ward et al.   HUMAN MOLECULAR GENETICS

Heart-specific overexpression of CUGBP1 reproduces functional and molecular abnormalities of myotonic dystrophy type 1

(2010) Misha Koshelev et al.   HUMAN MOLECULAR GENETICS

Muscle-Derived Collagen XIII Regulates Maturation of the Skeletal Neuromuscular Junction

(2010) A. Latvanlehto et al.   JOURNAL OF NEUROSCIENCE

Systematic Analysis of Cis-Elements in Unstable mRNAs Demonstrates that CUGBP1 Is a Key Regulator of mRNA Decay in Muscle Cells

(2010) Jerome E. Lee et al.   PLoS One

Developmental and Pathogenic Mechanisms of Basement Membrane Assembly

(2009) Peter Yurchenco et al.   CURRENT PHARMACEUTICAL DESIGN

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