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Increased Insoluble Amyloid-β Induces Negligible Cognitive Deficits in Old App(NL/NL) Knock-In Mice
Commonly used Alzheimer’s disease mouse models are based on the ectopic overexpression of the human amyloid precursor protein (APP) gene, together with a mutant presenilin gene. Surprisingly, humanized APP knock-in mouse models carrying a single APP Swedish mutation (App(NL)), failed to develop amyl...
Autores principales: | Salas, Isabel H., Callaerts-Vegh, Zsuzsanna, D’Hooge, Rudi, Saido, Takaomi C., Dotti, Carlos G., De Strooper, Bart |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218137/ https://www.ncbi.nlm.nih.gov/pubmed/30320577 http://dx.doi.org/10.3233/JAD-180410 |
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