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Itamar Harel et al.
DEVELOPMENTAL CELL (2009)
Age-related muscle dysfunction
LaDora V. Thompson
EXPERIMENTAL GERONTOLOGY (2009)
microRNAs and muscle disorders
Jian-Fu Chen et al.
JOURNAL OF CELL SCIENCE (2009)
Reduction of the Rate of Protein Translation in Patients with Myotonic Dystrophy 2
Claudia Huichalaf et al.
JOURNAL OF NEUROSCIENCE (2009)
DMPK PROTEIN ISOFORMS ARE DIFFERENTIALLY EXPRESSED IN MYOGENIC AND NEURAL CELL LINEAGES
Ralph J. A. Oude Ophuis et al.
MUSCLE & NERVE (2009)
Absence of a differentiation defect in muscle satellite cells from DM2 patients
Richard Pelletier et al.
NEUROBIOLOGY OF DISEASE (2009)
Ribonuclear inclusions and MBNL1 nuclear sequestration do not affect myoblast differentiation but alter gene splicing in myotonic dystrophy type 2
Rosanna Cardani et al.
NEUROMUSCULAR DISORDERS (2009)
Satellite cell dysfunction contributes to the progressive muscle atrophy in myotonic dystrophy type 1
L. -E. Thornell et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2009)
Skeletal Muscle Differentiation of Embryonic Mesoangioblasts Requires Pax3 Activity
Graziella Messina et al.
STEM CELLS (2009)
Molecular Effects of the CTG Repeats in Mutant Dystrophia Myotonica Protein Kinase Gene
Beatriz Llamusi et al.
CURRENT GENOMICS (2008)
Hijacking of the mismatch repair system to cause CAG expansion and cell death in neurodegenerative disease
Cynthia T. McMurray
DNA REPAIR (2008)
Ectopic expression of cyclin D3 corrects differentiation of DM1 myoblasts through activation of RNA CUG-binding protein, CUGBP1
Elizabeth Salisbury et al.
EXPERIMENTAL CELL RESEARCH (2008)
All muscle satellite cells are equal, but are some more equal than others?
Peter S. Zammit
JOURNAL OF CELL SCIENCE (2008)
Type 2 myotonic dystrophy can be predicted by the combination of Type 2 muscle fiber central nucleation and scattered atrophy
Guillaume Bassez et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2008)
PREFERENTIAL CENTRAL NUCLEATION OF TYPE 2 MYOFIBERS IS AN INVARIABLE FEATURE OF MYOTONIC DYSTROPHY TYPE 2
Valerio Pisani et al.
MUSCLE & NERVE (2008)
Self-renewal and expansion of single transplanted muscle stem cells
Alessandra Sacco et al.
NATURE (2008)
MicroRNAs flex their muscles
Eva van Rooij et al.
TRENDS IN GENETICS (2008)
MEF2: a central regulator of diverse developmental programs
Matthew J. Potthoff et al.
DEVELOPMENT (2007)
Molecular mechanisms responsible for aberrant splicing of SERCA1 in myotonic dystrophy type 1
Shin-ichiro Hino et al.
HUMAN MOLECULAR GENETICS (2007)
Factors contributing to neuromuscular impairment and sarcopenia during aging
Erik Edstrom et al.
PHYSIOLOGY & BEHAVIOR (2007)
OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells
Irina V. Kovtun et al.
NATURE (2007)
Haploinsuffciency for Znf9 in Znf9+/- mice is associated with multiorgan abnormalities resembling myotonic dystrophy
Wei Chen et al.
JOURNAL OF MOLECULAR BIOLOGY (2007)
Chloride channelopathy in myotonic dystrophy resulting from loss of posttranscriptional regulation for CLCN1
John D. Lueck et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2007)
Ribonuclear foci at the neuromuscular junction in myotonic dystrophy type 1
T. M. Wheeler et al.
NEUROMUSCULAR DISORDERS (2007)
Pericytes of human skeletal muscle are myogenic precursors distinct from satellite cells
Arianna Dellavalle et al.
NATURE CELL BIOLOGY (2007)
Zebrafish miR-214 modulates Hedgehog signaling to specify muscle cell fate
Alex S. Flynt et al.
NATURE GENETICS (2007)
Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs
Maurilio Sampaolesi et al.
NATURE (2006)
Muscle stem cells in development, regeneration, and disease
Xiaozhong Shi et al.
GENES & DEVELOPMENT (2006)
Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy
Xiaoyan Lin et al.
HUMAN MOLECULAR GENETICS (2006)
Chemical modifiers of unstable expanded simple sequence repeats: What goes up, could come down
Mario Gomes-Pereira et al.
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2006)
Smooth muscle of the dorsal aorta shares a common clonal origin with skeletal muscle of the myotome
M Esner et al.
DEVELOPMENT (2006)
DNA structures, repeat expansions and human hereditary disorders
Sergei M. Mirkin
CURRENT OPINION IN STRUCTURAL BIOLOGY (2006)
Direct isolation of satellite cells for skeletal muscle regeneration
D Montarras et al.
SCIENCE (2005)
MyoD and the transcriptional control of myogenesis
CA Berkes et al.
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2005)
Pax3/Pax7 mark a novel population of primitive myogenic cells during development
L Kassar-Duchossoy et al.
GENES & DEVELOPMENT (2005)
Transgenic mice expressing CUG-BP1 reproduce splicing mis-regulation observed in myotonic dystrophy
TH Ho et al.
HUMAN MOLECULAR GENETICS (2005)
Six1 and Six4 homeoproteins are required for Pax3 and Mrf expression during myogenesis in the mouse embryo
R Grifone et al.
DEVELOPMENT (2005)
Transcriptional regulation of myotube fate specification and intrafusal muscle fiber morphogenesis
Y Albert et al.
JOURNAL OF CELL BIOLOGY (2005)
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy
G Vattemi et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2005)
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)
R Sallinen et al.
NEUROMUSCULAR DISORDERS (2004)
Overexpression of CUG triplet repeat-binding protein, CUGBP1, in mice inhibits myogenesis
NA Timchenko et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Intra-coronary arterial injection of mesenchymal stromal cells and microinfarction in dogs
PR Vulliet et al.
LANCET (2004)
Muscle pathology in 57 patients with myotonic dystrophy type 2
BGH Schoser et al.
MUSCLE & NERVE (2004)
Muscle building: mechanisms of myotube guidance and attachment site selection
F Schnorrer et al.
DEVELOPMENTAL CELL (2004)
Pax-7 up-regulation inhibits myogenesis and cell cycle progression in satellite cells: a potential mechanism for self-renewal
HC Olguin et al.
DEVELOPMENTAL BIOLOGY (2004)
Insulin receptor splicing alteration in myotonic dystrophy type 2
RS Savkur et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Cellular and molecular regulation of muscle regeneration
SBP Charge et al.
PHYSIOLOGICAL REVIEWS (2004)
A muscleblind knockout model for myotonic dystrophy
RN Kanadia et al.
SCIENCE (2003)
Contribution of hematopoietic stem cells to skeletal muscle
SY Corbel et al.
NATURE MEDICINE (2003)
Single hematopoietic stem cells generate skeletal muscle through myeloid intermediates
FD Camargo et al.
NATURE MEDICINE (2003)
Myotonic dystrophy type 2: Human founder haplotype and evolutionary conservation of the repeat tract
CL Liquori et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins:: A single shared haplotype indicates an ancestral founder effect
LL Bachinski et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Resetting the problem of cell death following muscle-derived cell transplantation: Detection, dynamics and mechanisms
D Skuk et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2003)
Alternative splicing controls myotonic dystrophy protein kinase structure, enzymatic activity, and subcellular localization
DG Wansink et al.
MOLECULAR AND CELLULAR BIOLOGY (2003)
Gene expression profile of aging in human muscle
S Welle et al.
PHYSIOLOGICAL GENOMICS (2003)
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2
A Vihola et al.
NEUROLOGY (2003)
The DMWD protein from the myotonic dystrophy (DM1) gene region is developmentally regulated and is present most prominently in synapse-dense brain areas
JHAM Westerlaken et al.
BRAIN RESEARCH (2003)
Skeletal muscle repair by adult human mesenchymal stem cells from synovial membrane
C De Bari et al.
JOURNAL OF CELL BIOLOGY (2003)
A uniform system for microRNA annotation
V Ambros et al.
RNA (2003)
Myotonic dystrophy type 2 - Molecular, diagnostic and clinical spectrum
JW Day et al.
NEUROLOGY (2003)
p21 is essential for normal myogenic progenitor cell function in regenerating skeletal muscle
TJ Hawke et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2003)
The formation of skeletal muscle: from somite to limb
M Buckingham et al.
JOURNAL OF ANATOMY (2003)
Transgenic mouse models for myotonic dystrophy type 1 (DM1)
DG Wansink et al.
CYTOGENETIC AND GENOME RESEARCH (2003)
Biological progression from adult bone marrow to mononucleate muscle stem cell to multinucleate muscle fiber in response to injury
MA LaBarge et al.
CELL (2002)
Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells
A Buj-Bello et al.
HUMAN MOLECULAR GENETICS (2002)
Myotonic dystrophy type 2
J Finsterer
EUROPEAN JOURNAL OF NEUROLOGY (2002)
The regulation of notch signaling controls satellite cell activation and cell fate determination in postnatal myogenesis
IM Conboy et al.
DEVELOPMENTAL CELL (2002)
ErbB2 is required for muscle spindle and myoblast cell survival
ER Andrechek et al.
MOLECULAR AND CELLULAR BIOLOGY (2002)
Identification of myogenic-endothelial progenitor cells in the interstitial spaces of skeletal muscle
T Tamaki et al.
JOURNAL OF CELL BIOLOGY (2002)
Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells
M Fardaei et al.
HUMAN MOLECULAR GENETICS (2002)
Human skeletal muscle fiber type classifications
W Scott et al.
PHYSICAL THERAPY (2001)
Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblasts
D Furling et al.
NEUROMUSCULAR DISORDERS (2001)
Molecular basis for impaired muscle differentiation in myotonic dystrophy
NA Timchenko et al.
MOLECULAR AND CELLULAR BIOLOGY (2001)
Decreased DMPK transcript levels in myotonic dystrophy 1 type IIA muscle fibers
M Eriksson et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2001)
Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy
RS Savkur et al.
NATURE GENETICS (2001)
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9
CL Liquori et al.
SCIENCE (2001)
CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus
GN Filippova et al.
NATURE GENETICS (2001)
Drosophila homolog of the myotonic dystrophy-associated gene, SIX5, is required for muscle and gonad development
RJ Kirby et al.
CURRENT BIOLOGY (2001)
The transcription factor Egr3 modulates sensory axon-myotube interactions during muscle spindle morphogenesis
WG Tourtellotte et al.
DEVELOPMENTAL BIOLOGY (2001)
Multilineage cells from human adipose tissue: Implications for cell-based therapies
PA Zuk et al.
TISSUE ENGINEERING (2001)
RNA CUG repeats sequester CUGBP1 and alter protein levels and activity of CUGBP1
NA Timchenko et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Expression of CD34 and Myf5 defines the majority of quiescent adult skeletal muscle satellite cells
JR Beauchamp et al.
JOURNAL OF CELL BIOLOGY (2000)
Skeletal myogenic potential of human and mouse neural stem cells
R Galli et al.
NATURE NEUROSCIENCE (2000)
Pax7 is required for the specification of myogenic satellite cells
P Seale et al.
CELL (2000)
Proximal myotonic myopathy - Evidence for anticipation in families with linkage to chromosome 3q
C Schneider et al.
NEUROLOGY (2000)
Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts
PS Sarkar et al.
NATURE GENETICS (2000)
Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy
TR Klesert et al.
NATURE GENETICS (2000)
Constitutive and regulated modes of splicing produce six major myotonic dystrophy protein kinase (DMPK) isoforms with distinct properties
PJTA Groenen et al.
HUMAN MOLECULAR GENETICS (2000)
The molecular regulation of myogenesis
LA Sabourin et al.
CLINICAL GENETICS (2000)
Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy
JW Miller et al.
EMBO JOURNAL (2000)
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