Evidence map›Paper›PMID 37481904›Full record

ReviewDifferentiation; research in biological diversity

Sonic hedgehog signaling in craniofacial development.

Jingyue Xu, Paul P R Iyyanar, Yu Lan, Rulang Jiang

Open access · greenAbstract readReview
In one paragraph

Review in Differentiation; research in biological diversity. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
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  11. Clinical and Molecular Study of a Gorlin Syndrome Type 1 Case.Advances in experimental medicine and biology · 2026
    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

4 authors at 1 institution in 1 country.

Jingyue XuDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA. Electronic address: Jingyue.Xu@cchmc.org.
Paul P R IyyanarDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.
Yu LanDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA; Division of Plastic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA; Departments of Pediatrics and Surgery, University of Cincinnati College of Medicine, Cincinnati, OH, 45267, USA.
Rulang JiangDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA; Division of Plastic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA; Departments of Pediatrics and Surgery, University of Cincinnati College of Medicine, Cincinnati, OH, 45267, USA. Electronic address: Rulang.Jiang@cchmc.org.
Cincinnati Children's Hospital Medical Center · US

Funding

MOLECULAR GENETIC ANALYSIS OF CRANIOFACIAL DEVELOPMENTR01DE013681 · NIDCR · UNIVERSITY OF ROCHESTER · PI JIANG, RULANG · 2000 to 2014
$6.3M
Regulation of Craniofacial Development by ALX Transcription FactorsR01DE029417 · NIDCR · CINCINNATI CHILDRENS HOSP MED CTR · PI JIANG, RULANG · 2020 to 2024
$3.3M
Mandible DevelopmentR01DE027046 · NIDCR · CINCINNATI CHILDRENS HOSP MED CTR · PI JIANG, RULANG · 2017 to 2021
$3.2M
NIDCR NIH HHS R01 DE013681NIDCR NIH HHS R01 DE027046NIDCR NIH HHS R01 DE029417
6 · The paper itself

Abstract

Mutations in SHH and several other genes encoding components of the Hedgehog signaling pathway have been associated with holoprosencephaly syndromes, with craniofacial anomalies ranging in severity from cyclopia to facial cleft to midfacial and mandibular hypoplasia. Studies in animal models have revealed that SHH signaling plays crucial roles at multiple stages of craniofacial morphogenesis, from cranial neural crest cell survival to growth and patterning of the facial primordia to organogenesis of the palate, mandible, tongue, tooth, and taste bud formation and homeostasis. This article provides a summary of the major findings in studies of the roles of SHH signaling in craniofacial development, with emphasis on recent advances in the understanding of the molecular and cellular mechanisms regulating the SHH signaling pathway activity and those involving SHH signaling in the formation and patterning of craniofacial structures.

Indexed as

Hedgehog ProteinsHoloprosencephalyAnimalsMorphogenesisNeural CrestSignal TransductionHedgehog ProteinscholesterolMandibleNeural crestPalatePrimary ciliumShhTongue

Identifiers

PMID37481904
PMCPMC10529669
OpenAlexW4384156522

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.