Evidence map›Paper›PMID 19828212›Full record

ArticleNeurobiology of aging2011

Abnormal neuronal networks and seizure susceptibility in mice overexpressing the APP intracellular domain.

D L Vogt, D Thomas, V Galvan, D E Bredesen, B T Lamb, S W Pimplikar

Abstract read
In one paragraph

Article in Neurobiology of aging, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
4.9field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

67 citing papers in PubMed, 112 citations in OpenAlex.

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  20. Review

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

D L VogtDepartment of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA. daniel.vogt@ucsf.edu
D Thomas
V Galvan
D E Bredesen
B T Lamb
S W Pimplikar
Cleveland Clinic · USBuck Institute for Research on Aging · USThe University of Texas Health Science Center at San Antonio · US

Funding

TRAINING IN NORMAL AND ABNORMAL DEVELOPMENTT32HD007104 · NICHD · CASE WESTERN RESERVE UNIVERSITY · PI HARTE, PETER J. · 1985 to 2010
$3.5M
The In Vivo Role of AICD in Neuronal DysfunctionR01AG026146 · NIA · CLEVELAND CLINIC LERNER COM-CWRU · PI PIMPLIKAR, SANJAY W · 2006 to 2010
$1.2M
NIA NIH HHS R01 AG026146NIA NIH HHS R01AG026146NICHD NIH HHS 5T32HD007104-31NICHD NIH HHS T32 HD007104
6 · The paper itself

Abstract

Alterations in the processing of the amyloid precursor protein (APP) lead to familial Alzheimer's disease (AD). AD patients exhibit increased seizure susceptibility and alterations in their EEGs, which suggests that APP and its metabolites may modulate neuronal networks. Here we demonstrate that transgenic mice overexpressing APP intracellular domain (AICD) and its binding partner Fe65 exhibit abnormal spiking events and a susceptibility to induced seizures. These abnormalities are not observed in PDAPP(D664A) mice, which express high Aβ levels but harbor a mutation in the APP intracellular domain. These data suggest that alterations in the levels of AICD contribute to network dysfunction in AD.

Indexed as

Alzheimer DiseaseAmyloid beta-Protein PrecursorAnimalsDisease Models, AnimalEpilepsyFemaleGenetic Predisposition to DiseaseHumansMiceMice, Inbred C57BLMice, TransgenicNerve NetProtein Structure, TertiaryAmyloid beta-Protein Precursor

Identifiers

PMID19828212
PMCPMC2889215
OpenAlexW2097623950

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.