Pages that link to "Q47689534"
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The following pages link to Immaturity of muscle fibers in the congenital form of myotonic dystrophy: its consequences and its origin (Q47689534):
Displaying 29 items.
- Six and Eya expression during human somitogenesis and MyoD gene family activation (Q28219080) (← links)
- Targeting DMPK with Antisense Oligonucleotide Improves Muscle Strength in Myotonic Dystrophy Type 1 Mice (Q33752585) (← links)
- Arrest is a regulator of fiber-specific alternative splicing in the indirect flight muscles of Drosophila (Q34262628) (← links)
- A novel function of heparan sulfate in the regulation of cell-cell fusion (Q35000955) (← links)
- The Change of Grip Strength in a Patient with Congenital Myotonic Dystrophy Over a 4-year Period (Q35047171) (← links)
- Overexpression of CUGBP1 in skeletal muscle from adult classic myotonic dystrophy type 1 but not from myotonic dystrophy type 2. (Q35078193) (← links)
- Skeletal muscle characterization of Japanese quail line selectively bred for lower body weight as an avian model of delayed muscle growth with hypoplasia (Q35157246) (← links)
- Genetic risks for children of women with myotonic dystrophy (Q35196691) (← links)
- Myogenic defects in myotonic dystrophy (Q35633172) (← links)
- Changes in myotonic dystrophy protein kinase levels and muscle development in congenital myotonic dystrophy (Q35791378) (← links)
- Regulation of the growth of multinucleated muscle cells by an NFATC2-dependent pathway (Q36316579) (← links)
- Mutant DMPK 3'-UTR transcripts disrupt C2C12 myogenic differentiation by compromising MyoD. (Q36323744) (← links)
- New Insights into the Mechanisms and Roles of Cell–Cell Fusion (Q37900409) (← links)
- Over-expression of stomatin causes syncytium formation in nonfusogenic JEG-3 choriocarcinoma placental cells (Q38764290) (← links)
- Overexpression of 3′-Untranslated Region of the Myotonic Dystrophy Kinase cDNA Inhibits Myoblast Differentiation in Vitro (Q41075540) (← links)
- Aberrant Myokine Signaling in Congenital Myotonic Dystrophy (Q44925270) (← links)
- Myotubular myopathy: arrest of morphogenesis of myofibres associated with persistence of fetal vimentin and desmin. Four cases compared with fetal and neonatal muscle. (Q46101159) (← links)
- CTG repeat size and histologic findings of skeletal muscle from patients with congenital myotonic dystrophy (Q47321814) (← links)
- Did giant mitochondria delay muscle maturation? An uncommon congenital myopathy. (Q53163047) (← links)
- Abnormalities in Skeletal Muscle Myogenesis, Growth, and Regeneration in Myotonic Dystrophy. (Q54982478) (← links)
- Reply to Poulton. (Q55400008) (← links)
- Potassium currents in human myogenic cells from healthy and congenital myotonic dystrophy foetuses (Q57268499) (← links)
- Amphiphilic random copolymer vesicle induces differentiation of mouse C2C12 myoblasts (Q57464955) (← links)
- Desmin myopathy: a multisystem disorder involving skeletal, cardiac, and smooth muscle (Q72054052) (← links)
- Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene (Q72896182) (← links)
- Overexpression of myotonic dystrophy protein kinase in C2C12 myogenic culture involved in the expression of ferritin heavy chain and interleukin-1alpha mRNAs (Q73026520) (← links)
- Opinion: the origin of the cancer stem cell: current controversies and new insights (Q81573645) (← links)
- Myotonic Dystrophy and Developmental Regulation of RNA Processing (Q88453318) (← links)
- Human iPSC Models to Study Orphan Diseases: Muscular Dystrophies (Q90327070) (← links)