Utility of Survival Motor Neuron ELISA for Spinal Muscular Atrophy Clinical and Preclinical Analyses
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Title
Utility of Survival Motor Neuron ELISA for Spinal Muscular Atrophy Clinical and Preclinical Analyses
Authors
Keywords
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Journal
PLoS One
Volume 6, Issue 8, Pages e24269
Publisher
Public Library of Science (PLoS)
Online
2011-09-01
DOI
10.1371/journal.pone.0024269
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Related references
Note: Only part of the references are listed.- Spinal Muscular Atrophy: New and Emerging Insights from Model Mice
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- A degron created by SMN2 exon 7 skipping is a principal contributor to spinal muscular atrophy severity
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- SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy
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- SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy
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- Muscle Volume Estimation by Magnetic Resonance Imaging in Spinal Muscular Atrophy
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- (2010) Kevin D Foust et al. NATURE BIOTECHNOLOGY
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- LBH589 induces up to 10-fold SMN protein levels by several independent mechanisms and is effective even in cells from SMA patients non-responsive to valproate
- (2009) Lutz Garbes et al. HUMAN MOLECULAR GENETICS
- Differences in SMN1 allele frequencies among ethnic groups within North America
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- Vascular Perfusion Abnormalities in Infants with Spinal Muscular Atrophy
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- Tetracyclines That Promote SMN2 Exon 7 Splicing as Therapeutics for Spinal Muscular Atrophy
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- DcpS as a Therapeutic Target for Spinal Muscular Atrophy
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- Identification and characterization of the porcine (Sus scrofa) survival motor neuron (SMN1) gene: An animal model for therapeutic studies
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- Identification of a battery of tests for drug candidate evaluation in the SMNΔ7 neonate model of spinal muscular atrophy
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- A two-site ELISA can quantify upregulation of SMN protein by drugs for spinal muscular atrophy
- (2008) N. thi Man et al. NEUROLOGY
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- (2005) Susanna M. Grzeschik et al. ANNALS OF NEUROLOGY
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