Neurovascular dysfunction and neuroinflammation in a Cockayne syndrome mouse model

Cockayne syndrome (CS) is a rare, autosomal genetic disorder characterized by premature aging-like features, such as cachectic dwarfism, retinal atrophy, and progressive neurodegeneration. The molecular defect in CS lies in genes associated with the transcription-coupled branch of the nucleotide exc...

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Detalles Bibliográficos
Autores principales: Kajitani, Gustavo Satoru, Brace, Lear, Trevino-Villarreal, Jose Humberto, Trocha, Kaspar, MacArthur, Michael Robert, Vose, Sarah, Vargas, Dorathy, Bronson, Roderick, Mitchell, Sarah Jayne, Menck, Carlos Frederico Martins, Mitchell, James Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8544306/
https://www.ncbi.nlm.nih.gov/pubmed/34628368
http://dx.doi.org/10.18632/aging.203617

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8544306/
https://www.ncbi.nlm.nih.gov/pubmed/34628368
http://dx.doi.org/10.18632/aging.203617

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