Presenilin-1 familial Alzheimer鈥檚 disease mutation alters hippocampal neurogenesis and memory function in CCL2 null mice
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文摘

Generation of a novel mouse containing the presenilin 1 FAD mutation in a CCL2 knock out background.

The murine model is associated with abnormal hippocampal neurogenesis and synaptic plasticity.

Significant aging-dependent impairments in learning and memory are operative.

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