Memory impairment
|
0.500 |
Biomarker
|
phenotype |
HPO |
|
|
|
Memory impairment
|
0.500 |
AlteredExpression
|
phenotype |
BEFREE |
129S6 mice are resistant to the lethal effects of APP overexpression, allowing sufficient levels of Abeta expression for the development of amyloid plaques and age-dependent memory deficits.
|
15254013 |
2004 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
APP/PS1 mice exhibited significant memory deficits from 5 months old, which were aggravated at the later stage of life.
|
28191738 |
2017 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
APP mice exhibited spatial memory deficits in the MWM.
|
28513774 |
2017 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
APP/PS1 mice and KCa3.1<sup>-/-</sup>/APP/PS1 mice were subjected to Morris water maze test to evaluate the spatial memory deficits.
|
30442153 |
2018 |
Memory impairment
|
0.500 |
GeneticVariation
|
phenotype |
BEFREE |
A recently described mouse line, Tg(HuAPP695.K670N/M671L)2576, expressing human amyloid precursor protein with a familial AD gene mutation, age-related amyloid deposits, and memory deficits, was found to develop a significant microglial response using Griffonia simplicifolia lectin or phosphotyrosine probe to identify microglia Both Griffonia simplicifolia lectin and phosphotyrosine staining showed increased numbers of intensely labeled, often enlarged microglia clustered in and around plaques, consistent with microglial activation related to beta-amyloid formation.
|
9422548 |
1998 |
Memory impairment
|
0.500 |
AlteredExpression
|
phenotype |
BEFREE |
Accumulations increased with age, and this was paralleled by decreased brain sizes on volumetric MRI, compared to age-matched and similar transgene-expressing APP wild-type mice, although, with these levels of transgenic expression we did not detect neuronal loss or significant memory impairment.
|
17112635 |
2008 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
CTD_human |
Adenosine A2A receptor blockade prevents memory dysfunction caused by beta-amyloid peptides but not by scopolamine or MK-801.
|
18191838 |
2008 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
Administration of PPARA agonists decreases amyloid pathology and reverses memory deficits and anxiety symptoms in APP-PSEN1ΔE9 mice.
|
30898012 |
2020 |
Memory impairment
|
0.500 |
GeneticVariation
|
phenotype |
BEFREE |
After three months treatment with CBZ in the APP(swe)/PS1(deltaE9) mice, we demonstrated that the spatial learning and memory deficits in these mice are significantly alleviated.
|
23305067 |
2013 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
Aged APP/PS1 mice had reference memory deficits as well as anxiety, hyperactivity, and social interaction impairment.
|
27439903 |
2016 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
Although Abeta derived from the Abeta precursor protein (beta-APP) is believed to play a central etiological role in AD, it is not clear whether soluble and/or fibrillar forms are responsible for the memory deficit.
|
11724968 |
2001 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
Although the primary causes of these disturbances are still under investigation, a growing body of evidence suggests that the amyloid precursor protein (APP) intracellular C-terminal fragment β (C99), generated by cleavage of APP by β-site APP cleaving enzyme 1 (BACE-1), is the primary cause of the endosome enlargement in AD and the earliest initiator of synaptic plasticity and long-term memory impairment.
|
28254759 |
2017 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
Amyloid-β peptide 42 (Aβ42) is produced through the sequential proteolytic cleavage of APP by β- and γ-secretase and causes the synaptic dysfunction associated with memory impairment in Alzheimer's disease.
|
24373902 |
2014 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
An efficacy test carried out in APP/PS1 transgenic mice showed a reduction of memory deficit in mice chronically treated with PGZ-NPs.
|
30271148 |
2018 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
Antioxidative and Anti-Apoptotic Roles of Silibinin in Reversing Learning and Memory Deficits in APP/PS1 Mice.
|
28852940 |
2017 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
At completion of the treatment, we found that the MSX-3 treatment prevented the development of memory deficits in APP/PS1dE9 mice, without significantly altering hippocampal and cortical gene expressions.
|
30050407 |
2018 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
CTD_human |
Atorvastatin prevents hippocampal cell death, neuroinflammation and oxidative stress following amyloid-β(1-40) administration in mice: evidence for dissociation between cognitive deficits and neuronal damage.
|
20816828 |
2010 |
Memory impairment
|
0.500 |
GeneticVariation
|
phenotype |
BEFREE |
BACE1 gene deletion prevents neuron loss and memory deficits in 5XFAD APP/PS1 transgenic mice.
|
17258906 |
2007 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
BBR improved learning and memory deficits of APP/PS1 mice.
|
29962345 |
2018 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
Behavioral assessment using Barnes maze showed that APP + PS1 rats exhibited a larger learning and memory deficit than APP21 rats.
|
27388605 |
2016 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
Behavioral tests further confirmed PTS' potential of overcoming memory deficits in APP/PS1 mice (AD model).
|
31737188 |
2019 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
CTD_human |
Beta-amyloid (1-42)-induced learning and memory deficits in mice: involvement of oxidative burdens in the hippocampus and cerebral cortex.
|
15364477 |
2004 |
Memory impairment
|
0.500 |
Biomarker
|
phenotype |
BEFREE |
CART modulates beta-amyloid metabolism-associated enzymes and attenuates memory deficits in APP/PS1 mice.
|
28743230 |
2017 |
Memory impairment
|
0.500 |
GeneticVariation
|
phenotype |
BEFREE |
Chronic treatments with two γ-secretase modulators, ibuprofen and CHF5074, disclosed higher activity of CHF5074 in ameliorating brain plaque deposition and spatial memory deficits in transgenic mice expressing human amyloid precursor protein (hAPP) with Swedish and London mutations (APP(SL) mice).
|
21181298 |
2011 |