Analysis of homozygous and heterozygous Csf1r knockout in the rat as a model for understanding microglial function in brain development and the impacts of human CSF1R mutations

Mutations in the human CSF1R gene have been associated with dominant and recessive forms of neurodegenerative disease. Here we describe the impacts of Csf1r mutation in the rat on development of the brain. Diffusion imaging indicated small reductions in major fiber tracts that may be associated in p...

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Detalles Bibliográficos
Autores principales: Patkar, Omkar L., Caruso, Melanie, Teakle, Ngari, Keshvari, Sahar, Bush, Stephen J., Pridans, Clare, Belmer, Arnauld, Summers, Kim M., Irvine, Katharine M., Hume, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941205/
https://www.ncbi.nlm.nih.gov/pubmed/33450391
http://dx.doi.org/10.1016/j.nbd.2021.105268

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941205/
https://www.ncbi.nlm.nih.gov/pubmed/33450391
http://dx.doi.org/10.1016/j.nbd.2021.105268

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