Evidence map›Paper›PMID 29540554›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2018

Major Vault Protein, a Candidate Gene in 16p11.2 Microdeletion Syndrome, Is Required for the Homeostatic Regulation of Visual Cortical Plasticity.

Jacque P K Ip, Ikue Nagakura, Jeremy Petravicz, Keji Li, Erik A C Wiemer, Mriganka Sur

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 47 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

6 authors at 2 institutions in 2 countries.

Jacque P K IpDepartment of Brain and Cognitive Sciences, Picower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 and.ORCID 0000-0003-4545-8261
Ikue NagakuraDepartment of Brain and Cognitive Sciences, Picower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 and.
Jeremy PetraviczDepartment of Brain and Cognitive Sciences, Picower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 and.ORCID 0000-0001-5161-4641
Keji LiDepartment of Brain and Cognitive Sciences, Picower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 and.ORCID 0000-0002-0737-2558
Erik A C WiemerDepartment of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, 3015 CN Rotterdam, The Netherlands.ORCID 0000-0002-0673-7236
Mriganka SurDepartment of Brain and Cognitive Sciences, Picower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 and msur@mit.edu.ORCID 0000-0003-2442-5671
McGovern Institute for Brain Research · USErasmus MC · NL

Funding

MicroRNA mechanisms of Rett SyndromeR01MH085802 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SUR, MRIGANKA · 2010 to 2025
$6.2M
STRUCTURE AND FUNCTION IN THE RETINOGENICULATE PATHWAYR01EY007023 · NEI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SUR, MRIGANKA · 1985 to 2018
$5.6M
NEUROTROPHIC REQUIREMENTS OF DEVELOPING OCULAR MOTONEUROF32EY007023 · NEI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI MACDONALD, MELANIE L · 1999 to 2000
$38k
NEI NIH HHS F32 EY007023NEI NIH HHS R01 EY007023NIMH NIH HHS R01 MH085802
6 · The paper itself

Abstract

Microdeletion of a region in chromosome 16p11.2 increases susceptibility to autism. Although this region contains exons of 29 genes, disrupting only a small segment of the region, which spans five genes, is sufficient to cause autistic traits. One candidate gene in this critical segment is

Indexed as

Neuronal PlasticityAnimalsAutistic DisorderChromosome DeletionChromosome DisordersChromosomes, Human, Pair 16Dominance, OcularExcitatory Postsynaptic PotentialsFemaleHomeostasisIntellectual DisabilityMajor Vault ProteinMaleMiceMice, Inbred C57BLMiniature Postsynaptic PotentialsMajor Vault ProteinMitogen-Activated Protein Kinase 3Receptors, AMPAStat1 protein, mouseSTAT1 Transcription FactorVault Ribonucleoprotein Particlesautism spectrum disorderglutamate receptorsocular dominance plasticitysignaling moleculessynapse developmentvisual cortex

Identifiers

PMID29540554
PMCPMC5907052
OpenAlexW2793983761

What OpenQuestion holds

Textmetadata
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.