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Drosophila TDP-43 dysfunction in glia and muscle cells cause cytological and behavioural phenotypes that characterize ALS and FTLD
Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) are neurodegenerative disorders that are characterized by cytoplasmic aggregates and nuclear clearance of TAR DNA-binding protein 43 (TDP-43). Studies in Drosophila, zebrafish and mouse demonstrate that the neuronal dys...
Autores principales: | Diaper, Danielle C., Adachi, Yoshitsugu, Lazarou, Luke, Greenstein, Max, Simoes, Fabio A., Di Domenico, Angelique, Solomon, Daniel A., Lowe, Simon, Alsubaie, Rawan, Cheng, Daryl, Buckley, Stephen, Humphrey, Dickon M., Shaw, Christopher E., Hirth, Frank |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3766182/ https://www.ncbi.nlm.nih.gov/pubmed/23727833 http://dx.doi.org/10.1093/hmg/ddt243 |
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