Evidence map›Paper›PMID 38693682›Full record

ArticleClinical genetics2024

Abnormalities in pharyngeal arch-derived structures in SATB2-associated syndrome.

Yuri A Zarate, Katherine Bosanko, Nada Derar, Jennifer L Fish

Open access · hybridAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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

4 authors at 4 institutions in 1 country.

Yuri A ZarateDivision of Genetics and Metabolism, University of Kentucky, Lexington, Kentucky, USA.
Katherine BosankoDepartment of Pediatrics, Section of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Nada DerarDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.ORCID 0000-0002-7886-4939
Jennifer L FishDepartment of Biological Sciences, University of Massachusetts Lowell, Lowell, Massachusetts, USA.
University of Arkansas for Medical Sciences · USUniversity of Kentucky · USUniversity of Massachusetts Lowell · USYale University · US

Funding

Molecular mechanisms underlying variation in severity of craniofacial diseaseR15DE026611 · NIDCR · UNIVERSITY OF MASSACHUSETTS LOWELL · PI FISH, JENNIFER LESLIE · 2017 to 2020
$823k
NIDCR NIH HHS R15 DE026611NIH HHS R15 DE026611
6 · The paper itself

Abstract

SATB2-associated syndrome (SAS, glass syndrome, OMIM#612313) is a neurodevelopmental autosomal dominant disorder with frequent craniofacial abnormalities including palatal and dental anomalies. To assess the role of Satb2 in craniofacial development, we analyzed mutant mice at different stages of development. Here, we show that Satb2 is broadly expressed in early embryonic mouse development including the mesenchyme of the second and third arches. Satb2

Indexed as

Branchial RegionMatrix Attachment Region Binding ProteinsPhenotypeTranscription FactorsAnimalsCraniofacial AbnormalitiesFemaleHumansMaleMandibleMiceMice, KnockoutSyndromeMatrix Attachment Region Binding ProteinsSATB2 protein, humanSATB2 protein, mouseTranscription Factorscraniofacial anomaliespharyngeal archesSATB2SATB2‐associated syndrome

Identifiers

PMID38693682
PMCPMC11216868
OpenAlexW4396588494

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.