Evidence map›Paper›PMID 27771363›Full record

ReviewSeminars in cell & developmental biology2017

Articular cartilage and joint development from embryogenesis to adulthood.

Rebekah S Decker

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

64 citing papers in PubMed, 106 citations in OpenAlex.

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4 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

1 author at 1 institution in 1 country.

Rebekah S DeckerTranslational Research Program in Pediatric Orthopaedics, Division of Orthopaedic Surgery, The Children's Hospital of Philadelphia, PA 19104, United States. Electronic address: RDecker@gnf.org.
Children's Hospital of Philadelphia · US

Funding

Mechanisms of Synovial Joint FormationR01AR062908 · NIAMS · CHILDREN'S HOSP OF PHILADELPHIA · PI ENOMOTO-IWAMOTO, MOTOMI, PACIFICI, MAURIZIO · 2011 to 2020
$4.5M
Mechansisms directing synovial joint morphogenesisF32AR064071 · NIAMS · CHILDREN'S HOSP OF PHILADELPHIA · PI DECKER, REBEKAH STACEY · 2013 to 2015
$179k
NIAMS NIH HHS F32 AR064071NIAMS NIH HHS R01 AR062908
6 · The paper itself

Abstract

Within each synovial joint, the articular cartilage is uniquely adapted to bear dynamic compressive loads and shear forces throughout the joint's range of motion. Injury and age-related degeneration of the articular cartilage often lead to significant pain and disability, as the intrinsic repair capability of the tissue is extremely limited. Current surgical and biological treatment options have been unable to restore cartilage de novo. Before successful clinical cartilage restoration strategies can be developed, a better understanding of how the cartilage forms during normal development is essential. This review focuses on recent progress made towards addressing key questions about articular cartilage morphogenesis, including the origin of synovial joint progenitor cells, postnatal development and growth of the tissue. These advances have provided novel insight into fundamental questions about the developmental biology of articular cartilage, as well as potential cell sources that may participate in joint response to injury.

Indexed as

Embryonic DevelopmentAgingAnimalsCartilage, ArticularHumansJointsMorphogenesisStem CellsArticular cartilageCartilage developmentJoint formationLineage tracingProgenitor cells

Identifiers

PMID27771363
PMCPMC6041433
OpenAlexW2533905132

What OpenQuestion holds

Textmetadata
LicenceTDM
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.