Evidence map›Paper›PMID 29114037›Full record

ArticleScience signaling2017

Reducing eIF4E-eIF4G interactions restores the balance between protein synthesis and actin dynamics in fragile X syndrome model mice.

Emanuela Santini, Thu N Huynh, Francesco Longo, So Yeon Koo, Edward Mojica, Laura D'Andrea, Claudia Bagni, Eric Klann

Abstract read
In one paragraph

Article in Science signaling, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
9.7field-weighted citation impact, top 2% 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

59 citing papers in PubMed, 99 citations in OpenAlex.

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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

8 authors at 2 institutions in 4 countries.

Emanuela SantiniCenter for Neural Science, New York University, New York, NY 10003, USA.ORCID http://orcid.org/0000-0002-8948-9652
Thu N HuynhCenter for Neural Science, New York University, New York, NY 10003, USA.ORCID http://orcid.org/0000-0002-7625-5101
Francesco LongoCenter for Neural Science, New York University, New York, NY 10003, USA.ORCID http://orcid.org/0000-0002-1183-0101
So Yeon KooCenter for Neural Science, New York University, New York, NY 10003, USA.ORCID http://orcid.org/0000-0001-8634-7643
Edward MojicaCenter for Neural Science, New York University, New York, NY 10003, USA.ORCID http://orcid.org/0000-0002-6054-3096
Laura D'AndreaDepartment of Biomedicine and Prevention, University of Rome "Tor Vergata," 00133 Rome, Italy.
Claudia BagniDepartment of Biomedicine and Prevention, University of Rome "Tor Vergata," 00133 Rome, Italy.
Eric KlannCenter for Neural Science, New York University, New York, NY 10003, USA. eklann@cns.nyu.edu.ORCID http://orcid.org/0000-0001-7379-6802
New York University · USUniversity of Rome Tor Vergata · IT

Funding

Strategies to rescue PI3K dysregulation in Fragile X SyndromeU54HD082013 · NICHD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI RICHTER, JOEL D · 2014 to 2019
$10.2M
Translation Regulation in Hippocampal LTP and LTDR01NS047384 · NINDS · NEW YORK UNIVERSITY · PI KLANN, ERIC · 2005 to 2020
$5.2M
Reactive Oxygen Species Signaling in the HippocampusR01NS034007 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KLANN, ERIC · 2000 to 2012
$4.2M
eIF2alpha Phosphorylation in Synaptic Plasticity, Memory, and Brain DisordersR37NS034007 · NINDS · NEW YORK UNIVERSITY · PI KLANN, ERIC · 2014 to 2020
$3.3M
STRIATAL SPECIFIC ALTERATIONS IN TRANSLATION, SYNAPTIC FUNCTION, AND BEHAVIOR INR00NS087112 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SANTINI, EMANUELA · 2017 to 2018
$498k
Striatal Specific Alterations in Translation, Synaptic Function, and Behavior inK99NS087112 · NINDS · NEW YORK UNIVERSITY · PI SANTINI, EMANUELA · 2014 to 2015
$163k
OXIDATIVE ACTIVATION OF PKC DURING INDUCTION OF LTPR29NS034007 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KLANN, ERIC · 1995 to 1999
–
NICHD NIH HHS U54 HD082013NINDS NIH HHS K99 NS087112NINDS NIH HHS R00 NS087112NINDS NIH HHS R01 NS034007NINDS NIH HHS R01 NS047384NINDS NIH HHS R29 NS034007NINDS NIH HHS R37 NS034007
6 · The paper itself

Abstract

Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and autism spectrum disorder. FXS is caused by silencing of the

Indexed as

ActinsAdaptor Proteins, Signal TransducingAnimalsDendritic SpinesDisease Models, AnimalEukaryotic Initiation Factor-4EEukaryotic Initiation Factor-4GFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeHippocampusHydrazonesMaleMemory DisordersMiceMice, Inbred C57BLNerve Tissue Proteins4EGI-1 compoundActinsAdaptor Proteins, Signal TransducingCyfip1 protein, mouseeIF4E protein, mouseEukaryotic Initiation Factor-4EEukaryotic Initiation Factor-4GFmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1HydrazonesNerve Tissue ProteinsThiazoles

Identifiers

PMID29114037
PMCPMC5858943
OpenAlexW2767324723

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.