Evidence map›Paper›PMID 20954177›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2011

Systems genetics analysis of mouse chondrocyte differentiation.

Jaijam Suwanwela, Charles R Farber, Bau-Lin Haung, Buer Song, Calvin Pan, Karen M Lyons, Aldons J Lusis

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  8. Review
  9. Genome-wide association of an integrated osteoporosis-related phenotype: is there evidence for pleiotropic genes?Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2012
    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

7 authors at 3 institutions in 2 countries.

Jaijam SuwanwelaDepartment of Oral Biology, School of Dentistry, UCLA, Los Angeles, CA 90095, USA. jaijam1220@gmail.com
Charles R Farber
Bau-Lin Haung
Buer Song
Calvin Pan
Karen M Lyons
Aldons J Lusis
University of California, Los Angeles · USChulalongkorn University · THOffice of Public Health Genomics · US

Funding

Systems genomics of metabolic syndrome traitsP01HL028481 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CANTOR, RITA M. · 1985 to 2019
$50.2M
CHARACTERIZATION OF A MAJOR OBESITY LOCUSF32DK074317 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI FARBER, CHARLES R · 2006 to 2008
$116k
NHLBI NIH HHS P01 HL028481NHLBI NIH HHS P01 HL28481NIDDK NIH HHS 5F32DK074317NIDDK NIH HHS F32 DK074317
6 · The paper itself

Abstract

One of the goals of systems genetics is the reconstruction of gene networks that underlie key processes in development and disease. To identify cartilage gene networks that play an important role in bone development, we used a systems genetics approach that integrated microarray gene expression profiles from cartilage and bone phenotypic data from two sets of recombinant inbred strains. Microarray profiles generated from isolated chondrocytes were used to generate weighted gene coexpression networks. This analysis resulted in the identification of subnetworks (modules) of coexpressed genes that then were examined for relationships with bone geometry and density. One module exhibited significant correlation with femur length (r = 0.416), anteroposterior diameter (r = 0.418), mediolateral diameter (r = 0.576), and bone mineral density (r = 0.475). Highly connected genes (n = 28) from this and other modules were tested in vitro using prechondrocyte ATDC5 cells and RNA interference. Five of the 28 genes were found to play a role in chondrocyte differentiation. Two of these, Hspd1 and Cdkn1a, were known previously to function in chondrocyte development, whereas the other three, Bhlhb9, Cugbp1, and Spcs3, are novel genes. Our integrative analysis provided a systems-level view of cartilage development and identified genes that may be involved in bone development.

Indexed as

AnimalsAnimals, NewbornBone and BonesBone DensityCartilageCELF1 ProteinCell DifferentiationCell LineChaperonin 60ChondrocytesChondrogenesisChromosomesCollagenCore Binding Factor Alpha 1 SubunitCyclin-Dependent Kinase Inhibitor p21Embryo, MammalianCdkn1a protein, mouseCELF1 ProteinCELF1 protein, mouseChaperonin 60CollagenCore Binding Factor Alpha 1 SubunitCyclin-Dependent Kinase Inhibitor p21GlycosaminoglycansHbegf protein, mouseHeparin-binding EGF-like Growth FactorHspd1 protein, mouseIntercellular Signaling Peptides and ProteinsMitochondrial ProteinsRNA-Binding ProteinsRNA, Small InterferingRunx2 protein, mouse

Identifiers

PMID20954177
PMCPMC3179327
OpenAlexW1970606350

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.