Evidence map›Paper›PMID 35114205›Full record

ArticleExperimental neurology2022

Mice lacking full length Adgrb1 (Bai1) exhibit social deficits, increased seizure susceptibility, and altered brain development.

Fu Hung Shiu, Jennifer C Wong, Takahiro Yamamoto, Trisha Lala, Ryan H Purcell, Sharon Owino, Dan Zhu, Erwin G Van Meir, Randy A Hall, Andrew Escayg

Open access · bronzeAbstract read
In one paragraph

Article in Experimental neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.3field-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

27 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  4. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
    Review
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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

10 authors at 2 institutions in 1 country.

Fu Hung ShiuDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA; Neuroscience Graduate Program, Graduate Division of Biological and Biomedical Sciences, Laney Graduate School, Emory University, Atlanta, GA, USA.
Jennifer C WongDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
Takahiro YamamotoDepartment of Neurosurgery, School of Medicine, University of Alabama at Birmingham (UAB), Birmingham, AL, USA.
Trisha LalaNeuroscience Graduate Program, Graduate Division of Biological and Biomedical Sciences, Laney Graduate School, Emory University, Atlanta, GA, USA; Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA.
Ryan H PurcellDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA, USA.
Sharon OwinoDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA.
Dan ZhuDepartment of Neurosurgery, Emory University School of Medicine, Atlanta, GA, USA.
Erwin G Van MeirDepartment of Neurosurgery, School of Medicine, University of Alabama at Birmingham (UAB), Birmingham, AL, USA; O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham (UAB), Birmingham, AL, USA.
Randy A HallDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA.
Andrew EscaygDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA. Electronic address: aescayg@emory.edu.
Emory University · USUniversity of Alabama at Birmingham · US

Funding

ENNCF - Viral Vector CoreP30NS055077 · NINDS · EMORY UNIVERSITY · PI LEVEY, ALLAN I · 2008 to 2018
$6.8M
Evaluating ADGRB3 as a tumor suppressor epigenetically silenced in WNT medulloblastomaR01CA235162 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI VAN MEIR, ERWIN G. · 2019 to 2024
$2.3M
Mechanisms underlying BAI1/ADGRB1 negative regulation of glioblastoma mesenchymal transition and invasion.R01NS117666 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ERWIN G. VAN MEIR · 2021 to 2026
$2.2M
Targeting Mechanisms of Medulloblastoma FormationR01NS096236 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI VAN MEIR, ERWIN G. · 2016 to 2020
$1.9M
NCI NIH HHS R01 CA235162NINDS NIH HHS P30 NS055077NINDS NIH HHS R01 NS096236NINDS NIH HHS R01 NS117666
6 · The paper itself

Abstract

The adhesion G protein-coupled receptor BAI1/ADGRB1 plays an important role in suppressing angiogenesis, mediating phagocytosis, and acting as a brain tumor suppressor. BAI1 is also a critical regulator of dendritic spine and excitatory synapse development and interacts with several autism-relevant proteins. However, little is known about the relationship between altered BAI1 function and clinically relevant phenotypes. Therefore, we studied the effect of reduced expression of full length Bai1 on behavior, seizure susceptibility, and brain morphology in Adgrb1 mutant mice. We compared homozygous (Adgrb1

Indexed as

Receptors, G-Protein-CoupledAngiogenic ProteinsAnimalsBrainHippocampusMiceSeizuresAdgrb1 protein, mouseAngiogenic ProteinsReceptors, G-Protein-CoupledAutismBAI1EpilepsyGPCRSeizures

Identifiers

PMID35114205
PMCPMC9817291
OpenAlexW4210572443

What Socratic 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 Socratic graph.