Hypomorphic Smn knockdown C2C12 myoblasts reveal intrinsic defects in myoblast fusion and myotube morphology
- 1 November 2005
- journal article
- Published by Elsevier in Experimental Cell Research
- Vol. 311 (1) , 49-61
- https://doi.org/10.1016/j.yexcr.2005.08.019
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Defining and Assaying RNAi in Mammalian CellsMolecular Cell, 2005
- Reduced expression of nicotinic AChRs in myotubes from spinal muscular atrophy I patientsLaboratory Investigation, 2004
- Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfindingThe Journal of cell biology, 2003
- SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiensHuman Genetics, 2001
- Alternative Splicing, Expression, and Genomic Structure of the 3′ Region of the Gene Encoding the Sarcolemmal-associated Proteins (SLAPs) Defines a Novel Class of Coiled-coil Tail-anchored Membrane ProteinsJournal of Biological Chemistry, 2000
- The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn-/- mice and results in a mouse with spinal muscular atrophyHuman Molecular Genetics, 2000
- The domain encoded by exon 2 of the survival motor neuron protein mediates nucleic acid binding [published erratum appears in Hum Mol Genet 1998 Oct;7(11):1831]Human Molecular Genetics, 1998
- Correlation between severity and SMN protein level in spinal muscular atrophyNature Genetics, 1997
- Identification of Proximal Spinal Muscular Atrophy Carriers and Patients by Analysis of SMNT and SMNC Gene Copy NumberAmerican Journal of Human Genetics, 1997
- Identification and characterization of a spinal muscular atrophy-determining geneCell, 1995