Evidence map›Paper›PMID 24158334›Full record

ReviewJournal of dental research2013

Genetic networks in osseointegration.

I Nishimura

Abstract readReview
In one paragraph

Review in Journal of dental research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
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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

1 author.

I NishimuraWeintraub Center for Reconstructive Biotechnology, Divisions of Advanced Prosthodontics and Oral Medicine & Biology, UCLA School of Dentistry, Los Angeles, CA 90095-1668.

Funding

The Role of P4H in Tissue-Titanium IntegrationR21EB004379 · NIBIB · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI OGAWA, TAKAHIRO · 2005 to 2006
$420k
EXTRAMURAL RESEARCH FACILITIES CONSTRUCTION PROJECTSC06RR014529 · NCRR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PARK, NO-HEE · 1999 to 1999
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NCRR NIH HHS C06 RR014529NIBIB NIH HHS R21 EB004379NIBIB NIH HHS R21EB004379
6 · The paper itself

Abstract

Osseointegration-based dental implants have become a well-accepted treatment modality for complete and partial edentulism. The success of this treatment largely depends on the stable integration and maintenance of implant fixtures in alveolar bone; however, the molecular and cellular mechanisms regulating this unique tissue reaction have not yet been fully uncovered. Radiographic and histologic observations suggest the sustained retention of peri-implant bone without an apparent susceptibility to catabolic bone remodeling; therefore, implant-induced bone formation continues to be intensively investigated. Increasing numbers of whole-genome transcriptome studies suggest complex molecular pathways that may play putative roles in osseointegration. This review highlights genetic networks related to bone quality, the transient chondrogenic phase, the vitamin D axis, and the peripheral circadian rhythm to elute the regulatory mechanisms underlying the establishment and maintenance of osseointegration.

Indexed as

Bone DensityBone RemodelingChondrogenesisCircadian RhythmDental ImplantsGene Regulatory NetworksHumansOsseointegrationOsteogenesisTranscriptomeVitamin DDental ImplantsVitamin Dbone remodelingcartilage matrix proteincircadian rhythmdental implantsgene expressionmicroarray analysis

Identifiers

PMID24158334
PMCPMC3827622

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.