Progranulin deficiency results in sex-dependent alterations in microglia in response to demyelination
Author:
Funder
NINDS/NIA
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00401-023-02578-w.pdf
Reference95 articles.
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2. Almeida MR, Macario MC, Ramos L, Baldeiras I, Ribeiro MH, Santana I (2016) Portuguese family with the co-occurrence of frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis phenotypes due to progranulin gene mutation. Neurobiol Aging 41(200):e201–e205. https://doi.org/10.1016/j.neurobiolaging.2016.02.019
3. Arambula SE, Reinl EL, El Demerdash N, McCarthy MM, Robertson CL (2019) Sex differences in pediatric traumatic brain injury. Exp Neurol 317:168–179. https://doi.org/10.1016/j.expneurol.2019.02.016
4. Babicki S, Arndt D, Marcu A, Liang Y, Grant JR, Maciejewski A et al (2016) Heatmapper: web-enabled heat mapping for all. Nucleic Acids Res 44:W147-153. https://doi.org/10.1093/nar/gkw419
5. Baker M, Mackenzie IR, Pickering-Brown SM, Gass J, Rademakers R, Lindholm C et al (2006) Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 442:916–919. https://doi.org/10.1038/nature05016
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