Altered expression and splicing of Ca2+metabolism genes in myotonic dystrophies DM1 and DM2

Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of CaV1.1 calcium channel

(2011) Zhen Zhi Tang et al.   HUMAN MOLECULAR GENETICS

Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2

(2010) Anna Vihola et al.   ACTA NEUROPATHOLOGICA

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

MicroRNAs Involved in Molecular Circuitries Relevant for the Duchenne Muscular Dystrophy Pathogenesis Are Controlled by the Dystrophin/nNOS Pathway

(2010) Davide Cacchiarelli et al.   Cell Metabolism

Neuronal NOS is dislocated during muscle atrophy in amyotrophic lateral sclerosis

(2010) Naoki Suzuki et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Altered MEF2 isoforms in myotonic dystrophy and other neuromuscular disorders

(2010) Linda L. Bachinski et al.   MUSCLE & NERVE

Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy

(2010) Hongqing Du et al.   NATURE STRUCTURAL & MOLECULAR BIOLOGY

ZNF9 Activation of IRES-Mediated Translation of the Human ODC mRNA Is Decreased in Myotonic Dystrophy Type 2

(2010) Morgan A. Sammons et al.   PLoS One

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

Pathogenic mechanisms of myotonic dystrophy

(2009) Johanna E. Lee et al.   BIOCHEMICAL SOCIETY TRANSACTIONS

Alternative splicing of RyR1 alters the efficacy of skeletal EC coupling

(2009) Takashi Kimura et al.   CELL CALCIUM

Ca2+ signaling in striated muscle: the elusive roles of triadin, junctin, and calsequestrin

(2009) Nicole A. Beard et al.   EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS

Transcriptional and post-transcriptional impact of toxic RNA in myotonic dystrophy

(2009) Robert J. Osborne et al.   HUMAN MOLECULAR GENETICS

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

Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2)

(2009) Sergio Salvatori et al.   NEUROLOGICAL SCIENCES

Molecular evolution of the junctophilin gene family

(2009) Alejandro Garbino et al.   PHYSIOLOGICAL GENOMICS

NFAT isoforms control activity-dependent muscle fiber type specification

(2009) E. Calabria et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Myotonic dystrophy type 2 found in two of sixty-three persons diagnosed as having fibromyalgia

(2008) Satu Auvinen et al.   ARTHRITIS AND RHEUMATISM

Conserved GU-Rich Elements Mediate mRNA Decay by Binding to CUG-Binding Protein 1

(2008) Irina A. Vlasova et al.   MOLECULAR CELL

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