Evidence map›Paper›PMID 23776616›Full record

ArticlePloS one2013

Augmented BMPRIA-mediated BMP signaling in cranial neural crest lineage leads to cleft palate formation and delayed tooth differentiation.

Lu Li, Ying Wang, Minkui Lin, Guohua Yuan, Guobin Yang, Yuqian Zheng, Yiping Chen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

30 citing papers in PubMed, 40 citations in OpenAlex.

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  15. The Morphology of Cross-Beaks andAnimals : an open access journal from MDPI · 2019
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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 4 institutions in 2 countries.

Lu LiDepartment of Cell and Molecular Biology, Tulane University, New Orleans, Louisiana, United States of America.
Ying Wang
Minkui Lin
Guohua Yuan
Guobin Yang
Yuqian Zheng
Yiping Chen
Tulane University · USAir Force Medical University · CNFujian Medical University · CNWuhan University · CN

Funding

Growth Factor Signaling in Mouse PalatogensisR01DE014044 · NIDCR · TULANE UNIVERSITY OF LOUISIANA · PI CHEN, YIPING · 2002 to 2013
$3.4M
NIDCR NIH HHS R01 DE014044NIDCR NIH HHS R01DE14044
6 · The paper itself

Abstract

The importance of BMP receptor Ia (BMPRIa) mediated signaling in the development of craniofacial organs, including the tooth and palate, has been well illuminated in several mouse models of loss of function, and by its mutations associated with juvenile polyposis syndrome and facial defects in humans. In this study, we took a gain-of-function approach to further address the role of BMPR-IA-mediated signaling in the mesenchymal compartment during tooth and palate development. We generated transgenic mice expressing a constitutively active form of BmprIa (caBmprIa) in cranial neural crest (CNC) cells that contributes to the dental and palatal mesenchyme. Mice bearing enhanced BMPRIa-mediated signaling in CNC cells exhibit complete cleft palate and delayed odontogenic differentiation. We showed that the cleft palate defect in the transgenic animals is attributed to an altered cell proliferation rate in the anterior palatal mesenchyme and to the delayed palatal elevation in the posterior portion associated with ectopic cartilage formation. Despite enhanced activity of BMP signaling in the dental mesenchyme, tooth development and patterning in transgenic mice appeared normal except delayed odontogenic differentiation. These data support the hypothesis that a finely tuned level of BMPRIa-mediated signaling is essential for normal palate and tooth development.

Indexed as

AnimalsBone Morphogenetic Protein Receptors, Type IBone Morphogenetic ProteinsBromodeoxyuridineCell DifferentiationCleft PalateImmunohistochemistryIn Situ HybridizationMesodermMiceMice, TransgenicNeural CrestSignal TransductionToothBmpr1a protein, mouseBone Morphogenetic Protein Receptors, Type IBone Morphogenetic ProteinsBromodeoxyuridine

Identifiers

PMID23776616
PMCPMC3680418
OpenAlexW1997068004

What OpenQuestion holds

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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 OpenQuestion graph.