Crossref
journal-article
Elsevier BV
Developmental Biology (78)
References
44
Referenced
58
10.1006/excr.2001.5191
/ Exp. Cell Res. / Purification of mouse primary myoblasts based on alpha 7 integrin expression by Blanco-Bose (2001)10.1016/S0140-6736(95)90869-2
/ Lancet / Constitutive muscular abnormalities in culture in spinal muscular atrophy by Braun (1995)10.1086/513886
/ Am. J. Hum. Genet. / Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotype by Campbell (1997)10.1016/j.cell.2008.05.049
/ Cell / Highly efficient, functional engraftment of skeletal muscle stem cells in dystrophic muscles by Cerletti (2008)10.1371/journal.pone.0003209
/ PLoS One / Modeling spinal muscular atrophy in Drosophila by Chang (2008)10.1083/jcb.152.5.1107
/ J. Cell Biol. / Deletion of murine SMN exon 7 directed to skeletal muscle leads to severe muscular dystrophy by Cifuentes-Diaz (2001)10.1093/hmg/11.12.1439
/ Hum. Mol. Genet. / Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model by Cifuentes-Diaz (2002)10.1016/j.cell.2005.05.010
/ Cell / Stem cell function, self-renewal, and behavioral heterogeneity of cells from the adult muscle satellite cell niche by Collins (2005)10.1126/science.1087573
/ Science / Notch-mediated restoration of regenerative potential to aged muscle by Conboy (2003)10.1093/hmg/6.8.1205
/ Hum. Mol. Genet. / The survival motor neuron protein in spinal muscular atrophy by Coovert (1997)10.1006/dbio.2001.0416
/ Dev. Biol. / Syndecan-3 and syndecan-4 specifically mark skeletal muscle satellite cells and are implicated in satellite cell maintenance and muscle regeneration by Cornelison (2001)10.1006/nbdi.1996.0010
/ Neurobiol. Dis. / The neurobiology of childhood spinal muscular atrophy by Crawford (1996)10.1101/gr.7.4.339
/ Genome Res. / Cloning, characterization, and copy number of the murine survival motor neuron gene: homolog of the spinal muscular atrophy-determining gene by DiDonato (1997)10.1086/338627
/ Am. J. Hum. Genet. / Quantitative analyses of SMN1 and SMN2 based on real-time lightCycler PCR: fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy by Feldkotter (2002)10.1093/hmg/ddm379
/ Hum. Mol. Genet. / Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect by Gavrilina (2008)10.1038/3030
/ Nat Genet / Differential SMN2 expression associated with SMA severity by Gavrilov (1998)10.1002/mus.10081
/ Muscle Nerve / Possible pathogenic role of muscle cell dysfunction in motor neuron death in spinal muscular atrophy by Guettier-Sigrist (2002)10.1152/jappl.2001.91.2.534
/ J. Appl. Physiol. / Myogenic satellite cells: physiology to molecular biology by Hawke (2001)10.1212/WNL.37.8.1361
/ Neurology / Extracts of muscle biopsies from patients with spinal muscular atrophies inhibit neurite outgrowth from spinal neurons by Henderson (1987)10.1038/ncb2015
/ Nat. Cell Biol. / Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis by Joe (2010)10.1093/hmg/ddn156
/ Hum. Mol. Genet. / Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy by Kariya (2008)10.1016/j.cell.2007.03.044
/ Cell / Asymmetric self-renewal and commitment of satellite stem cells in muscle by Kuang (2007)10.1093/hmg/ddi078
/ Hum. Mol. Genet. / SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN by Le (2005)10.1016/j.ydbio.2011.05.667
/ Dev. Biol / Muscles in a mouse model of spinal muscular atrophy show profound defects in neuromuscular development even in the absence of failure in neuromuscular transmission or loss of motor neurons by Lee (2011)10.1016/0092-8674(95)90460-3
/ Cell / Identification and characterization of a spinal muscular atrophy-determining gene by Lefebvre (1995)10.1073/pnas.96.11.6307
/ Proc. Natl. Acad. Sci. U S A / A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy by Lorson (1999)10.1093/hmg/ddn189
/ Hum. Mol. Genet. / Embryonic motor axon development in the severe SMA mouse by McGovern (2008)10.1083/jcb.200303168
/ J. Cell Biol. / Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding by McWhorter (2003)10.1093/hmg/9.3.333
/ Hum. Mol. Genet. / The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(−/−) mice and results in a mouse with spinal muscular atrophy by Monani (2000)10.1126/science.1114758
/ Science / Direct isolation of satellite cells for skeletal muscle regeneration by Montarras (2005)10.1093/hmg/ddm367
/ Hum. Mol. Genet. / Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy by Murray (2008)10.1083/jcb.200210117
/ J. Cell Biol. / Intact satellite cells lead to remarkable protection against Smn gene defect in differentiated skeletal muscle by Nicole (2003)10.1007/s11910-010-0095-5
/ Curr. Neurol. Neurosci. Rep. / Spinal muscular atrophy: new and emerging insights from model mice by Park (2010)10.1083/jcb.200610053
/ J. Cell Biol. / A Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle by Rajendra (2007)10.1083/jcb.200304128
/ J. Cell. Biol. / Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons by Rossoll (2003)10.1073/pnas.1010929108
/ Proc. Natl. Acad. Sci. U S A / Identification of inducible brown adipocyte progenitors residing in skeletal muscle and white fat by Schulz (2011)10.1016/S0092-8674(00)00066-0
/ Cell / Pax7 is required for the specification of myogenic satellite cells by Seale (2000)10.1016/j.yexcr.2005.08.019
/ Exp. Cell Res. / Hypomorphic Smn knockdown C2C12 myoblasts reveal intrinsic defects in myoblast fusion and myotube morphology by Shafey (2005)10.1002/jnr.21743
/ J. Neurosci. Res. / Neurodevelopmental abnormalities in neurosphere-derived neural stem cells from SMN-depleted mice by Shafey (2008)10.1016/j.cell.2004.10.021
/ Cell / Isolation of adult mouse myogenic progenitors: functional heterogeneity of cells within and engrafting skeletal muscle by Sherwood (2004)10.1038/ncb2014
/ Nat. Cell Biol. / Mesenchymal progenitors distinct from satellite cells contribute to ectopic fat cell formation in skeletal muscle by Uezumi (2010)10.1083/jcb.128.4.563
/ J. Cell Biol. / Myogenin is required for late but not early aspects of myogenesis during mouse development by Venuti (1995)10.1016/j.cell.2005.08.021
/ Cell / Cellular and molecular signatures of muscle regeneration: current concepts and controversies in adult myogenesis by Wagers (2005)10.1242/jcs.019661
/ J. Cell Sci. / All muscle satellite cells are equal, but are some more equal than others? by Zammit (2008)
Dates
Type | When |
---|---|
Created | 13 years, 2 months ago (June 15, 2012, 6:12 a.m.) |
Deposited | 2 years, 6 months ago (Feb. 21, 2023, 6:17 a.m.) |
Indexed | 1 month, 3 weeks ago (July 2, 2025, 1:54 p.m.) |
Issued | 13 years ago (Aug. 1, 2012) |
Published | 13 years ago (Aug. 1, 2012) |
Published Print | 13 years ago (Aug. 1, 2012) |
Funders
2
Flow Cytometry Core
Awards
1
- NIH P30 DK036836
the Spinal Muscular Atrophy Foundation, NINDS
10.13039/100000894
Spinal Muscular Atrophy FoundationRegion: Americas
gov (Trusts, charities, foundations (both public and private))
Labels
3
- SMA Foundation
- Spinal Muscular Atrophy (SMA) Foundation
- SMAF
Awards
1
- P01NS066888-01A1
@article{Hayhurst_2012, title={A cell-autonomous defect in skeletal muscle satellite cells expressing low levels of survival of motor neuron protein}, volume={368}, ISSN={0012-1606}, url={http://dx.doi.org/10.1016/j.ydbio.2012.05.037}, DOI={10.1016/j.ydbio.2012.05.037}, number={2}, journal={Developmental Biology}, publisher={Elsevier BV}, author={Hayhurst, Monica and Wagner, Amanda K. and Cerletti, Massimiliano and Wagers, Amy J. and Rubin, Lee L.}, year={2012}, month=aug, pages={323–334} }