Evidence map›Paper›PMID 28367114›Full record

ArticleFrontiers in molecular neuroscience2017

Whole Genome Expression Analysis in a Mouse Model of Tauopathy Identifies MECP2 as a Possible Regulator of Tau Pathology.

Nicole M Maphis, Shanya Jiang, Jessica Binder, Carrie Wright, Banu Gopalan, Bruce T Lamb, Kiran Bhaskar

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Review
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  10. [Tau Protein Induces Aberrant Alternative Splicing Changes in PS19 Transgenic Mice].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2023
    Article
  11. Review
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  18. Tau Is Truncated in Five Regions of the Normal Adult Human Brain.International journal of molecular sciences · 2021
    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

7 authors at 4 institutions in 1 country.

Nicole M MaphisDepartment of Molecular Genetics and Microbiology, University of New Mexico, Albuquerque NM, USA.
Shanya JiangDepartment of Molecular Genetics and Microbiology, University of New Mexico, Albuquerque NM, USA.
Jessica BinderDepartment of Molecular Genetics and Microbiology, University of New Mexico, Albuquerque NM, USA.
Carrie WrightLieber Institute for Brain Development, Baltimore MD, USA.
Banu GopalanDepartment of Biostatistics, Cleveland Clinic Foundation Cleveland OH, USA.
Bruce T LambStark Neurosciences Research Institute, Indiana University, Indianapolis IN, USA.
Kiran BhaskarDepartment of Molecular Genetics and Microbiology, University of New Mexico, Albuquerque NM, USA.
University of New Mexico · USCleveland Clinic · USIndiana University – Purdue University Indianapolis · USLieber Institute for Brain Development · US

Funding

Modifiers of Beta-Amyloid Metabolism and DepositionR01AG023012 · NIA · CLEVELAND CLINIC LERNER COM-CWRU · PI LAMB, BRUCE T · 2004 to 2013
$2.9M
The Role of Inflammasome Signaling in TauopathiesRF1NS083704 · NINDS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI BHASKAR, KIRAN · 2020 to 2020
$2.7M
The role of fractalkine signaling in neurodegenerative diseaseR01NS074804 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI LAMB, BRUCE T, RANSOHOFF, RICHARD M. · 2011 to 2015
$1.7M
The role of inflammasome signaling in tauopathiesR01NS083704 · NINDS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI BHASKAR, KIRAN · 2014 to 2018
$1.4M
The role of microglial-and neuron-specific MyD88 signaling in tauopathiesR21NS077089 · NINDS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI BHASKAR, KIRAN · 2012 to 2013
$418k
Light-based regulation of autophagy processing to target pathological forms of tauR21NS093442 · NINDS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI BHASKAR, KIRAN, WEICK, JASON P · 2016 to 2017
$417k
NIA NIH HHS R01 AG023012NINDS NIH HHS R01 NS074804NINDS NIH HHS R01 NS083704NINDS NIH HHS R21 NS077089NINDS NIH HHS R21 NS093442NINDS NIH HHS RF1 NS083704
6 · The paper itself

Abstract

Increasing evidence suggests that hyperphosphorylation and aggregation of microtubule-associated protein tau (MAPT or tau) correlates with the development of cognitive impairment in Alzheimer's disease (AD) and related tauopathies. While numerous attempts have been made to model AD-relevant tau pathology in various animal models, there has been very limited success for these models to fully recapitulate the progression of disease as seen in human tauopathies. Here, we performed whole genome gene expression in a genomic mouse model of tauopathy that expressed human

Indexed as

Alzheimer’s diseaseMECP2methyl-CpG-binding protein-2microarraytauopathiestau proteintau transgenic mice

Identifiers

PMID28367114
PMCPMC5355442
OpenAlexW2595038576

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.