[HTML][HTML] Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia

D Xia, S Lianoglou, T Sandmann, M Calvert… - Molecular …, 2022 - Springer
Background Genetic mutations underlying familial Alzheimer's disease (AD) were identified
decades ago, but the field is still in search of transformative therapies for patients. While …

[HTML][HTML] Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia

D Xia, S Lianoglou, T Sandmann… - Molecular …, 2022 - ncbi.nlm.nih.gov
Background Genetic mutations underlying familial Alzheimer's disease (AD) were identified
decades ago, but the field is still in search of transformative therapies for patients. While …

Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia

D Xia, S Lianoglou, T Sandmann… - Molecular …, 2022 - search.proquest.com
Background Genetic mutations underlying familial Alzheimer's disease (AD) were identified
decades ago, but the field is still in search of transformative therapies for patients. While …

Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia.

D Xia, S Lianoglou, T Sandmann, M Calvert… - Mol …, 2022 - mouseion.jax.org
BACKGROUND: Genetic mutations underlying familial Alzheimer's disease (AD) were
identified decades ago, but the field is still in search of transformative therapies for patients …

[HTML][HTML] Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia.

D Xia, S Lianoglou, T Sandmann… - Molecular …, 2022 - escholarship.org
BackgroundGenetic mutations underlying familial Alzheimer's disease (AD) were identified
decades ago, but the field is still in search of transformative therapies for patients. While …

Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia.

D Xia, S Lianoglou, T Sandmann… - Molecular …, 2022 - search.ebscohost.com
Background: Genetic mutations underlying familial Alzheimer's disease (AD) were identified
decades ago, but the field is still in search of transformative therapies for patients. While …

[HTML][HTML] Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia

D Xia, S Lianoglou… - Molecular …, 2022 - molecularneurodegeneration …
Genetic mutations underlying familial Alzheimer's disease (AD) were identified decades
ago, but the field is still in search of transformative therapies for patients. While mouse …

Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia.

D Xia, S Lianoglou, T Sandmann, M Calvert… - Molecular …, 2022 - europepmc.org
Background Genetic mutations underlying familial Alzheimer's disease (AD) were identified
decades ago, but the field is still in search of transformative therapies for patients. While …

[引用][C] Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia

D Xia, S Lianoglou, T Sandmann… - Molecular …, 2022 - espace.library.uq.edu.au
Background: Genetic mutations underlying familial Alzheimer's disease (AD) were identified
decades ago, but the field is still in search of transformative therapies for patients. While …

Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia

D Xia, S Lianoglou, T Sandmann… - Molecular …, 2022 - epub.ub.uni-muenchen.de
Background Genetic mutations underlying familial Alzheimer's disease (AD) were identified
decades ago, but the field is still in search of transformative therapies for patients. While …