Evidence map›Paper›PMID 33116259›Full record

ArticleScientific reports2020

Enhanced FGFR3 activity in postmitotic principal neurons during brain development results in cortical dysplasia and axonal tract abnormality.

Jui-Yen Huang, Bruna Baumgarten Krebs, Marisha Lynn Miskus, May Lin Russell, Eamonn Patrick Duffy, Jason Michael Graf, Hui-Chen Lu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  7. Review
  8. Cerebral cortex maldevelopment in syndromic craniosynostosis.Developmental medicine and child neurology · 2022
    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 1 institution in 1 country.

Jui-Yen HuangDepartment of Psychological and Brain Sciences, the Linda and Jack Gill Center for Biomolecular Sciences, Indiana University, 1101 E. 10th Street, Bloomington, IN, 47405, USA. juiyhuan@indiana.edu.
Bruna Baumgarten KrebsDepartment of Psychological and Brain Sciences, the Linda and Jack Gill Center for Biomolecular Sciences, Indiana University, 1101 E. 10th Street, Bloomington, IN, 47405, USA.
Marisha Lynn MiskusDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, IN, 47405, USA.
May Lin RussellDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, IN, 47405, USA.
Eamonn Patrick DuffyDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, IN, 47405, USA.
Jason Michael GrafDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, IN, 47405, USA.
Hui-Chen LuDepartment of Psychological and Brain Sciences, the Linda and Jack Gill Center for Biomolecular Sciences, Indiana University, 1101 E. 10th Street, Bloomington, IN, 47405, USA. hclu@indiana.edu.
Indiana University Bloomington · US

Funding

Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
Molecular and genetic studies of NMNAT2 in neuroprotectionR01NS086794 · NINDS · TRUSTEES OF INDIANA UNIVERSITY · PI LU, HUI-CHEN · 2014 to 2025
$5.0M
Signaling Cascades in Sensory Map DevelopmentR01NS048884 · NINDS · TRUSTEES OF INDIANA UNIVERSITY · PI LU, HUI-CHEN · 2005 to 2015
$3.0M
NCATS NIH HHS UL1 TR001108NIH HHS NS048884NINDS NIH HHS R01 NS048884
6 · The paper itself

Abstract

Abnormal levels of fibroblast growth factors (FGFs) and FGF receptors (FGFRs) have been detected in various neurological disorders. The potent impact of FGF-FGFR in multiple embryonic developmental processes makes it challenging to elucidate their roles in postmitotic neurons. Taking an alternative approach to examine the impact of aberrant FGFR function on glutamatergic neurons, we generated a FGFR gain-of-function (GOF) transgenic mouse, which expresses constitutively activated FGFR3 (FGFR3

Indexed as

AnimalsAxonsBrainCell DifferentiationExcitatory Amino AcidsFemaleFibroblast Growth FactorsGain of Function MutationGlutamic AcidMaleMalformations of Cortical DevelopmentMiceMice, TransgenicMitosisNeurogenesisNeuronsExcitatory Amino AcidsFgfr3 protein, mouseFibroblast Growth FactorsGlutamic AcidReceptor, Fibroblast Growth Factor, Type 3Receptors, Fibroblast Growth Factor

Identifiers

PMID33116259
PMCPMC7595096
OpenAlexW3097225938

What Socratic 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 Socratic graph.