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Extensive phenotypic characterisation of a human TDP-43(Q331K) transgenic mouse model of amyotrophic lateral sclerosis (ALS)

The majority of preclinical studies in ALS have relied on transgenic models with overexpression of mutant human superoxide dismutase 1 (SOD1), widely regarded to have failed in terms of translation of therapeutic effects. However, there are still no widely accepted models of other genetic subtypes o...

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Detalles Bibliográficos
Autores principales: Watkins, Jodie A., Alix, James J. P., Shaw, Pamela J., Mead, Richard J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370970/
https://www.ncbi.nlm.nih.gov/pubmed/34404845
http://dx.doi.org/10.1038/s41598-021-96122-z

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