Found: 17
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Impaired Synaptic Vesicle Release and Immaturity of Neuromuscular Junctions in Spinal Muscular Atrophy Mice.
- Published in:
- Journal of Neuroscience, 2009, v. 29, n. 3, p. 842, doi. 10.1523/JNEUROSCI.4434-08.2009
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- Publication type:
- Article
Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamics.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 18, p. 4745, doi. 10.1093/hmg/ddu189
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- Publication type:
- Article
Histone deacetylase inhibition suppresses myogenin-dependent atrogene activation in spinal muscular atrophy mice.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 20, p. 4448, doi. 10.1093/hmg/dds286
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- Publication type:
- Article
Increasing expression and decreasing degradation of SMN ameliorate the spinal muscular atrophy phenotype in mice.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 18, p. 3667, doi. 10.1093/hmg/ddr288
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- Publication type:
- Article
Mitochondrial abnormalities in spinal and bulbar muscular atrophy.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 1, p. 27, doi. 10.1093/hmg/ddn310
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- Publication type:
- Article
Akt blocks ligand binding and protects against expanded polyglutamine androgen receptor toxicity.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 13, p. 1593, doi. 10.1093/hmg/ddm109
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- Publication type:
- Article
Neurogenic and Myogenic Contributions to Hereditary Motor Neuron Disease.
- Published in:
- Neurodegenerative Diseases, 2012, v. 9, n. 4, p. 199, doi. 10.1159/000335311
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- Publication type:
- Article
Mutations in TRPV4 cause Charcot-Marie-Tooth disease type 2C.
- Published in:
- Nature Genetics, 2010, v. 42, n. 2, p. 170, doi. 10.1038/ng.512
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- Publication type:
- Article
Survival motor neuron deficiency slows myoblast fusion through reduced myomaker and myomixer expression.
- Published in:
- Journal of Cachexia, Sarcopenia & Muscle, 2021, v. 12, n. 4, p. 1098, doi. 10.1002/jcsm.12740
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- Publication type:
- Article
Survival motor neuron protein deficiency alters microglia reactivity.
- Published in:
- Glia, 2022, v. 70, n. 7, p. 1337, doi. 10.1002/glia.24177
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- Publication type:
- Article
Viral mediated knockdown of GATA6 in SMA iPSC‐derived astrocytes prevents motor neuron loss and microglial activation.
- Published in:
- Glia, 2022, v. 70, n. 5, p. 989, doi. 10.1002/glia.24153
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- Publication type:
- Article
SMN-deficiency disrupts SERCA2 expression and intracellular Ca2+ signaling in cardiomyocytes from SMA mice and patient-derived iPSCs.
- Published in:
- Skeletal Muscle, 2020, v. 10, n. 1, p. 1, doi. 10.1186/s13395-020-00232-7
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- Publication type:
- Article
Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy.
- Published in:
- 2007
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- Publication type:
- journal article
combinatorial approach increases SMN level in SMA model mice.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 17, p. 2989, doi. 10.1093/hmg/ddac068
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- Publication type:
- Article
Sustained improvement of spinal muscular atrophy mice treated with trichostatin a plus nutrition.
- Published in:
- Annals of Neurology, 2008, v. 64, n. 4, p. 465, doi. 10.1002/ana.21449
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- Publication type:
- Article
Targeting splicing in spinal muscular atrophy.
- Published in:
- Annals of Neurology, 2008, v. 63, n. 1, p. 3, doi. 10.1002/ana.21305
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- Publication type:
- Article
Genetics and genomic medicine in Mali: challenges and future perspectives.
- Published in:
- Molecular Genetics & Genomic Medicine, 2016, v. 4, n. 2, p. 126, doi. 10.1002/mgg3.212
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- Publication type:
- Article