Evidence map›Paper›PMID 23053848›Full record

ArticleJournal of dental research2012

Chemerin-ChemR23 signaling in tooth development.

T Ohira, D Spear, N Azimi, V Andreeva, P C Yelick

Abstract read
In one paragraph

Article in Journal of dental research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.1field-weighted citation impact, top 47% 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

6 citing papers in PubMed, 23 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

5 authors at 1 institution in 1 country.

T OhiraDepartment of Oral and Maxillofacial Pathology, Tufts University, Boston, MA 02111, USA.
D Spear
N Azimi
V Andreeva
P C Yelick
Tufts University · US

Funding

Dental Stem Cells and Tooth Tissue EngineeringR01DE016132 · NIDCR · TUFTS UNIVERSITY BOSTON · PI YELICK, PAMELA C · 2005 to 2014
$5.5M
NIDCR NIH HHS R01 DE016132NIDCR NIH HHS R01DE016132
6 · The paper itself

Abstract

Our long-term goal is to identify and characterize molecular mechanisms regulating tooth development, including those mediating the critical dental epithelial-dental mesenchymal (DE-DM) cell interactions required for normal tooth development. The goal of this study was to investigate Chemerin (Rarres2)/ChemR23(Cmklr1) signaling in DE-DM cell interactions in normal tooth development. Here we present, for the first time, tissue-specific expression patterns of Chemerin and ChemR23 in mouse tooth development. We show that Chemerin is expressed in cultured DE progenitor cells, while ChemR23 is expressed in cultured DM cells. Moreover, we demonstrate that ribosomal protein S6 (rS6) and Akt, downstream targets of Chemerin/ChemR23 signaling, are phosphorylated in response to Chemerin/ChemR23 signaling in vitro and are expressed in mouse tooth development. Together, these results suggest roles for Chemerin/ChemR23-mediated DE-DM cell signaling during tooth morphogenesis.

Indexed as

AnimalsCell CommunicationCell DifferentiationCells, CulturedChemokinesChemotactic FactorsEpithelial CellsEpithelial-Mesenchymal TransitionIntercellular Signaling Peptides and ProteinsMesenchymal Stem CellsMiceMice, Inbred C57BLOdontogenesisReceptors, ChemokineReceptors, G-Protein-CoupledSignal Transductionchemerin protein, mouseChemokinesChemotactic FactorsCMKLR1 protein, mouseIntercellular Signaling Peptides and ProteinsReceptors, ChemokineReceptors, G-Protein-Coupled

Identifiers

PMID23053848
PMCPMC3497907
OpenAlexW2096682750

What OpenQuestion holds

Textmetadata
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.