Evidence map›Paper›PMID 30370699›Full record

ReviewJournal of orthopaedic research : official publication of the Orthopaedic Research Society2019

Cellular biology of fracture healing.

Chelsea S Bahney, Robert L Zondervan, Patrick Allison, Alekos Theologis, Jason W Ashley, Jaimo Ahn, Theodore Miclau, Ralph S Marcucio, Kurt D Hankenson

Abstract readReview
In one paragraph

Review in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 327 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
327citing papers in PubMed, 3 pooled it
–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

327 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
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  8. ABCB5⁺ mesenchymal stem cells enable high-ratio cellular augmentation of bone grafts without loss of osteogenic function.European journal of trauma and emergency surgery : official publication of the European Trauma Society · 2026
    Article
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  13. COJournal of molecular histology · 2026
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267 more citing papers are in PubMed but not listed here.

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

9 authors.

Chelsea S BahneyDepartment of Orthopaedic Surgery, University of California at San Francisco, San Francisco, California.
Robert L ZondervanDepartment of Physiology, College of Osteopathic Medicine, Michigan State University, East Lansing, Michigan.
Patrick AllisonDepartment of Physiology, College of Osteopathic Medicine, Michigan State University, East Lansing, Michigan.
Alekos TheologisDepartment of Orthopaedic Surgery, University of California at San Francisco, San Francisco, California.
Jason W AshleyDepartment of Biology, Eastern Washington University, Cheney, Washington.
Jaimo AhnDepartment of Biology, Eastern Washington University, Cheney, Washington.
Theodore MiclauDepartment of Orthopaedic Surgery, University of California at San Francisco, San Francisco, California.
Ralph S MarcucioDepartment of Orthopaedic Surgery, University of California at San Francisco, San Francisco, California.
Kurt D HankensonDepartment of Orthopaedic Surgery, University of Michigan, Ann Arbor, Michigan.

Funding

Regulators of Ischemic Fracture HealingR01AR066028 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HANKENSON, KURT DAVID · 2015 to 2020
$2.7M
Disruption of CD47 signaling promotes healing in ischemic fractures and bone allograftsF30AR071201 · NIAMS · MICHIGAN STATE UNIVERSITY · PI ZONDERVAN, ROBERT LOUIS · 2017 to 2019
$126k
NIAMS NIH HHS F30 AR071201NIAMS NIH HHS R01 AR066028
6 · The paper itself

Abstract

The biology of bone healing is a rapidly developing science. Advances in transgenic and gene-targeted mice have enabled tissue and cell-specific investigations of skeletal regeneration. As an example, only recently has it been recognized that chondrocytes convert to osteoblasts during healing bone, and only several years prior, seminal publications reported definitively that the primary tissues contributing bone forming cells during regeneration were the periosteum and endosteum. While genetically modified animals offer incredible insights into the temporal and spatial importance of various gene products, the complexity and rapidity of healing-coupled with the heterogeneity of animal models-renders studies of regenerative biology challenging. Herein, cells that play a key role in bone healing will be reviewed and extracellular mediators regulating their behavior discussed. We will focus on recent studies that explore novel roles of inflammation in bone healing, and the origins and fates of various cells in the fracture environment. © 2018 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res.

Indexed as

OsteogenesisSignal TransductionAnimalsBony CallusChondrocytesEndothelial Progenitor CellsFracture HealingHumansMesenchymal Stem CellsNeovascularization, PhysiologicOsteoblastsOsteoclastsbone regenerationbone repairfracture healing

Identifiers

PMID30370699
PMCPMC6542569

What OpenQuestion holds

Textmetadata
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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.