Evidence map›Paper›PMID 28236036›Full record

ReviewCurrent osteoporosis reports2017

Functional Diversity of Ciliary Proteins in Bone Development and Disease.

Masaru Kaku, Yoshihiro Komatsu

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current osteoporosis reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Ciliary-Mediated Mechanotransduction in Skeletal Development and Diseases.Results and problems in cell differentiation · 2026
    Review
  2. Article
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  4. Disruption of distal appendage protein CEP164 causes skeletal malformation in mice.Biochemical and biophysical research communications · 2024
    Article
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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

2 authors at 1 institution in 1 country.

Masaru KakuDivision of Bioprosthodontics, Niigata University Graduate School of Medical and Dental Sciences, Niigata, 951-8514, Japan. kakum@dent.niigata-u.ac.jp.
Yoshihiro KomatsuDepartment of Pediatrics, The University of Texas Medical School at Houston, Houston, TX, 77030, USA. Yoshihiro.Komatsu@uth.tmc.edu.
Niigata University · JP

Funding

The role of BMP signaling in craniofacial cartilage developmentR01DE025897 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KOMATSU, YOSHIHIRO · 2017 to 2021
$1.8M
Role of BMP signaling for chondrogenic fate determination in neural crest cellsR00DE021054 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KOMATSU, YOSHIHIRO · 2013 to 2015
$737k
NIDCR NIH HHS R00 DE021054NIDCR NIH HHS R01 DE025897
6 · The paper itself

Abstract

purpose of reviewThe primary cilium is a non-motile microtubule-based organelle that senses a diverse range of extracellular signals. While recent studies highlight the importance of ciliary-dependent developmental signals, including Hedgehog, Wnt, and platelet-derived growth factor, it is not well understood whether and how bone morphogenetic protein (BMP) signaling, a key regulator of skeletogenesis, is involved in cilia-related bone developmental aspects and in the etiology of skeletal disorders. RECENT

findingsIncreasing evidence suggests that osteoblast- or osteocyte-specific deletion of ciliary proteins leads to diverse skeletal malformations, reinforcing the idea that primary cilia are indispensable for regulating bone development and maintenance. Furthermore, it became evident that ciliary proteins not only contribute to ciliogenesis but also orchestrate cellular trafficking. This review summarizes the current understanding of ciliary proteins in bone development and discusses the potential role of BMP signaling in primary cilia, enabling us to unravel the potential pathogenesis of skeletal ciliopathies.

Indexed as

Bone DevelopmentWnt Signaling PathwayBone DiseasesBone Morphogenetic ProteinsCell MovementCiliaHedgehog ProteinsHumansOsteoblastsOsteocytesPlatelet-Derived Growth FactorSignal TransductionBone Morphogenetic ProteinsHedgehog ProteinsPlatelet-Derived Growth FactorBone diseaseBone morphogenetic proteinCiliaGrowth factor signaling

Identifiers

PMID28236036
OpenAlexW2591532262

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.