Evidence map›Paper›PMID 24252615›Full record

ReviewBiochimica et biophysica acta2014

Ribosome biogenesis in skeletal development and the pathogenesis of skeletal disorders.

Paul A Trainor, Amy E Merrill

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 107 citations in OpenAlex.

  1. A novel homozygous variant in the POLR1A gene: a complicated hereditary spastic paraplegia (c-HSP) or a hypomyelinating leukodystrophy type-27 (HLD27) phenotype?Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Pooled it
  2. Trial
  3. Article
  4. Article
  5. Lysophosphatidic Acid Synergizes With 1,25-Dihydroxyvitamin D to Promote Fibroblast Growth Factor-23 Synthesis via MAPK Signaling and Induction of the IL12A Gene.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  6. Article
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  8. International journal of molecular sciences · 2025
    Article
  9. NBS1 facilitates preribosomal RNA biogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  20. RNA Polymerases I and III in development and disease.Seminars in cell & developmental biology · 2023
    Review

12 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

2 authors at 2 institutions in 1 country.

Paul A TrainorStowers Institute for Medical Research, Kansas City, MO, USA; Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, KS, USA. Electronic address: pat@stowers.org.
Amy E MerrillCenter for Craniofacial Molecular Biology, Ostrow School of Dentistry, University of Southern California, Los Angeles, CA, USA; Department of Biochemistry and Molecular Biology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA. Electronic address: amerrill@usc.edu.
Stowers Institute for Medical Research · USUniversity of Southern California · US

Funding

Intrinsic and extrinsic regulation of cranial mesodermR01DE016082 · NIDCR · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI TRAINOR, PAUL · 2004 to 2014
$3.9M
Interdisciplinary New Faculty Recruitment in Craniofacial DevelopmentP30DE020750 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHAI, YANG · 2009 to 2010
$1.6M
NIDCR NIH HHS 50P30DE020750-02NIDCR NIH HHS DE016082NIDCR NIH HHS P30 DE020750NIDCR NIH HHS R01 DE016082
6 · The paper itself

Abstract

The skeleton affords a framework and structural support for vertebrates, while also facilitating movement, protecting vital organs, and providing a reservoir of minerals and cells for immune system and vascular homeostasis. The mechanical and biological functions of the skeleton are inextricably linked to the size and shape of individual bones, the diversity of which is dependent in part upon differential growth and proliferation. Perturbation of bone development, growth and proliferation, can result in congenital skeletal anomalies, which affect approximately 1 in 3000 live births [1]. Ribosome biogenesis is integral to all cell growth and proliferation through its roles in translating mRNAs and building proteins. Disruption of any steps in the process of ribosome biogenesis can lead to congenital disorders termed ribosomopathies. In this review, we discuss the role of ribosome biogenesis in skeletal development and in the pathogenesis of congenital skeletal anomalies. This article is part of a Special Issue entitled: Role of the Nucleolus in Human Disease.

Indexed as

SkeletonAnemia, Diamond-BlackfanBone DevelopmentBone Diseases, DevelopmentalBone Marrow DiseasesExocrine Pancreatic InsufficiencyHairHirschsprung DiseaseHumansImmunologic Deficiency SyndromesLipomatosisMandibulofacial DysostosisOsteochondrodysplasiasPrimary Immunodeficiency DiseasesRibosomesRNA, MessengerRNA, MessengerCartilage hair hypoplasiaRibosome biogenesisRoberts syndromeShwachman–Diamond syndromeSkeletal developmentTreacher Collins syndrome

Identifiers

PMID24252615
PMCPMC4020712
OpenAlexW1965184827

What Socratic 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 Socratic graph.