Evidence map›Paper›PMID 37065628›Full record

ArticleJBMR plus2023

Augmentation of BMP Signaling in Cranial Neural Crest Cells Leads to Premature Cranial Sutures Fusion through Endochondral Ossification in Mice.

Hiroki Ueharu, Haichun Pan, Xia Liu, Mamoru Ishii, Jessica Pongetti, Anshul K Kulkarni, Folasade E Adegbenro, Jaden Wurn, Robert E Maxson, Hongchen Sun and 4 more

Open access · goldAbstract read
In one paragraph

Article in JBMR plus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 11 citations in OpenAlex.

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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

14 authors at 4 institutions in 2 countries.

Hiroki UeharuDepartment of Biologic and Materials Sciences & Prosthodontics University Michigan School of Dentistry Ann Arbor Michigan USA.
Haichun PanDepartment of Biologic and Materials Sciences & Prosthodontics University Michigan School of Dentistry Ann Arbor Michigan USA.
Xia LiuDepartment of Biologic and Materials Sciences & Prosthodontics University Michigan School of Dentistry Ann Arbor Michigan USA.
Mamoru IshiiDepartment of Biochemistry & Molecular Medicine Keck School of Medicine of University of Southern California Los Angeles California USA.
Jessica PongettiDepartment of Orthodontics and Pediatric Dentistry University Michigan School of Dentistry Ann Arbor Michigan USA.
Anshul K KulkarniDepartment of Biologic and Materials Sciences & Prosthodontics University Michigan School of Dentistry Ann Arbor Michigan USA.
Folasade E AdegbenroDepartment of Biologic and Materials Sciences & Prosthodontics University Michigan School of Dentistry Ann Arbor Michigan USA.
Jaden WurnDepartment of Biologic and Materials Sciences & Prosthodontics University Michigan School of Dentistry Ann Arbor Michigan USA.
Robert E MaxsonDepartment of Biochemistry & Molecular Medicine Keck School of Medicine of University of Southern California Los Angeles California USA.
Hongchen SunDepartment of Oral Pathology Hospital of Stomatology, Jilin University Changchun China.
Yoshihiro KomatsuDepartment of Pediatrics University of Texas Health Science Center Houston Texas USA.ORCID https://orcid.org/0000-0003-3115-1437
Honghao ZhangDepartment of Biologic and Materials Sciences & Prosthodontics University Michigan School of Dentistry Ann Arbor Michigan USA.ORCID https://orcid.org/0000-0002-2338-6992
Jingwen YangDepartment of Biologic and Materials Sciences & Prosthodontics University Michigan School of Dentistry Ann Arbor Michigan USA.ORCID https://orcid.org/0000-0001-8969-6486
Yuji MishinaDepartment of Biologic and Materials Sciences & Prosthodontics University Michigan School of Dentistry Ann Arbor Michigan USA.ORCID https://orcid.org/0000-0002-6268-4204
University of Michigan · USJilin University · CNUniversity of Southern California · USThe University of Texas Health Science Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Craniosynostosis is a congenital anomaly characterized by the premature fusion of cranial sutures. Sutures are a critical connective tissue that regulates bone growth; their aberrant fusion results in abnormal shapes of the head and face. The molecular and cellular mechanisms have been investigated for a long time, but knowledge gaps remain between genetic mutations and mechanisms of pathogenesis for craniosynostosis. We previously demonstrated that the augmentation of bone morphogenetic protein (BMP) signaling through constitutively active BMP type 1A receptor (caBmpr1a) in neural crest cells (NCCs) caused the development of premature fusion of the anterior frontal suture, leading to craniosynostosis in mice. In this study, we demonstrated that ectopic cartilage forms in sutures prior to premature fusion in

Indexed as

BMP SIGNALINGCELL FATECRANIOSYNOSTOSISP0‐CreWnt1‐Cre

Identifiers

PMID37065628
PMCPMC10097634
OpenAlexW4313357399

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.