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Deep Proteomic Evaluation of Primary and Cell Line Motoneuron Disease Models Delineates Major Differences in Neuronal Characteristics

The fatal neurodegenerative disorders amyotrophic lateral sclerosis and spinal muscular atrophy are, respectively, the most common motoneuron disease and genetic cause of infant death. Various in vitro model systems have been established to investigate motoneuron disease mechanisms, in particular im...

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Detalles Bibliográficos
Publicado en:Mol Cell Proteomics
Main Authors: Hornburg, Daniel, Drepper, Carsten, Butter, Falk, Meissner, Felix, Sendtner, Michael, Mann, Matthias
Formato: Artigo
Idioma:Inglês
Publicado: The American Society for Biochemistry and Molecular Biology 2014
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4256493/
https://ncbi.nlm.nih.gov/pubmed/25193168
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/mcp.M113.037291
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