Evidence map›Paper›PMID 32747436›Full record

ArticleDevelopment (Cambridge, England)2020

Temporal-specific roles of fragile X mental retardation protein in the development of the hindbrain auditory circuit.

Xiaoyu Wang, Ayelet Kohl, Xiaoyan Yu, Diego A R Zorio, Avihu Klar, Dalit Sela-Donenfeld, Yuan Wang

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
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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 2 institutions in 3 countries.

Xiaoyu WangDepartment of Biomedical Sciences, Program in Neuroscience, Florida State University College of Medicine, Tallahassee, FL 32306, USA.ORCID 0000-0003-2104-7089
Ayelet KohlKoret School of Veterinary Medicine, Robert H. Smith Faculty of Agriculture, Food and Environment, The Hebrew University of Jerusalem, Rehovot 76100, Israel.
Xiaoyan YuDepartment of Biomedical Sciences, Program in Neuroscience, Florida State University College of Medicine, Tallahassee, FL 32306, USA.ORCID 0000-0002-4877-0114
Diego A R ZorioDepartment of Biomedical Sciences, Program in Neuroscience, Florida State University College of Medicine, Tallahassee, FL 32306, USA.
Avihu KlarDepartment of Medical Neurobiology IMRIC, Hebrew University Medical School, Jerusalem 91120, Israel.
Dalit Sela-DonenfeldKoret School of Veterinary Medicine, Robert H. Smith Faculty of Agriculture, Food and Environment, The Hebrew University of Jerusalem, Rehovot 76100, Israel yuan.wang@med.fsu.edu dalit.seladon@mail.huji.ac.il.ORCID 0000-0001-7498-061X
Yuan WangDepartment of Biomedical Sciences, Program in Neuroscience, Florida State University College of Medicine, Tallahassee, FL 32306, USA yuan.wang@med.fsu.edu dalit.seladon@mail.huji.ac.il.ORCID 0000-0003-4347-7063
Florida State University · USHebrew University of Jerusalem · IL

Funding

Development and afferent regulation of auditory neuronsR01DC013074 · NIDCD · UNIVERSITY OF WASHINGTON · PI WANG, YUAN · 2014 to 2018
$1.9M
Development of a Fragile X Syndrome model in the gerbil to study auditory dysfunctionR21DC017267 · NIDCD · FLORIDA STATE UNIVERSITY · PI WANG, YUAN · 2019 to 2020
$463k
NIDCD NIH HHS R01 DC013074NIDCD NIH HHS R21 DC017267
6 · The paper itself

Abstract

Fragile X mental retardation protein (FMRP) is an RNA-binding protein abundant in the nervous system. Functional loss of FMRP leads to sensory dysfunction and severe intellectual disabilities. In the auditory system, FMRP deficiency alters neuronal function and synaptic connectivity and results in perturbed processing of sound information. Nevertheless, roles of FMRP in embryonic development of the auditory hindbrain have not been identified. Here, we developed high-specificity approaches to genetically track and manipulate throughout development of the Atoh1

Indexed as

AnimalsAuditory PathwaysAxonsBase SequenceChick EmbryoChickensCRISPR-Cas SystemsDendritesFragile X Messenger Ribonucleoprotein 1Neural Stem CellsPresynaptic TerminalsRhombencephalonRNA, Small InterferingSynapsesTime FactorsFragile X Messenger Ribonucleoprotein 1RNA, Small InterferingAuditory circuitAutism spectrum disorderAxon developmentAxon fasciculationAxon targetingCRISPR-Cas9Fragile X syndromeRNA-binding proteins

Identifiers

PMID32747436
PMCPMC7473654
OpenAlexW3047569120

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.