Evidence map›Paper›PMID 23619198›Full record

ReviewBiochimica et biophysica acta2013

Transgenic models of Alzheimer's disease: better utilization of existing models through viral transgenesis.

Thomas L Platt, Valerie L Reeves, M Paul Murphy

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Intranasal AβJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
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  15. cAMP-PKA phosphorylation of tau confers risk for degeneration in aging association cortex.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
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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

3 authors.

Thomas L PlattDepartment of Cellular and Molecular Biochemistry, University of Kentucky, Lexington, KY 40536, USA.
Valerie L Reeves
M Paul Murphy

Funding

Cellular Nucleic Acid Binding Protein (CNBP) in Aging and DiseaseR01NS058382 · NINDS · UNIVERSITY OF KENTUCKY · PI MURPHY, MICHAEL PAUL · 2007 to 2011
$1.5M
NINDS NIH HHS NS058382NINDS NIH HHS R01 NS058382
6 · The paper itself

Abstract

Animal models have been used for decades in the Alzheimer's disease (AD) research field and have been crucial for the advancement of our understanding of the disease. Most models are based on familial AD mutations of genes involved in the amyloidogenic process, such as the amyloid precursor protein (APP) and presenilin 1 (PS1). Some models also incorporate mutations in tau (MAPT) known to cause frontotemporal dementia, a neurodegenerative disease that shares some elements of neuropathology with AD. While these models are complex, they fail to display pathology that perfectly recapitulates that of the human disease. Unfortunately, this level of pre-existing complexity creates a barrier to the further modification and improvement of these models. However, as the efficacy and safety of viral vectors improves, their use as an alternative to germline genetic modification is becoming a widely used research tool. In this review we discuss how this approach can be used to better utilize common mouse models in AD research. This article is part of a Special Issue entitled: Animal Models of Disease.

Indexed as

Disease Models, AnimalGene Transfer TechniquesAlzheimer DiseaseAnimalsGenetic VectorsHumansMiceMice, TransgenicTransgenesViruses

Identifiers

PMID23619198
PMCPMC3690778

What OpenQuestion holds

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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.