Evidence map›Paper›PMID 18280462›Full record

ArticleDevelopmental biology2008

Expression and function of Dlx genes in the osteoblast lineage.

Haitao Li, Inga Marijanovic, Mark S Kronenberg, Ivana Erceg, Mary Louise Stover, Dimitrios Velonis, Mina Mina, Jelica Gluhak Heinrich, Stephen E Harris, William B Upholt and 2 more

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

40 citing papers in PubMed, 92 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Haitao LiDepartment of Genetics and Developmental Biology, University of Connecticut Health Center, 263 Farmington Avenue, CT 06030, USA.
Inga Marijanovic
Mark S Kronenberg
Ivana Erceg
Mary Louise Stover
Dimitrios Velonis
Mina Mina
Jelica Gluhak Heinrich
Stephen E Harris
William B Upholt
Ivo Kalajzic
Alexander C Lichtler
UConn Health · USThe University of Texas Health Science Center at San Antonio · US

Funding

Transgenic CoreP01AR046798 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI BONEWALD, LYNDA F · 2001 to 2010
$10.5M
MSX2 AND DLX-5 IN LIMB PATTERN FORMATION AND CARTILAGE DIFFERENTIATIONP01HD022610 · NICHD · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MUNEOKA, KEN · 1988 to 2009
$6.7M
Src tyrosine kinase in calcium signalingP30AR046026 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LORENZO, JOSEPH A · 2001 to 2005
$2.9M
DLX GENE REGULATION OF OSTEOBLAST DIFFERENTIATIONR01AR049341 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LICHTLER, ALEXANDER C · 2004 to 2008
$1.5M
GROWTH AND DEVELOPMENT OF THE MANDIBULAR ARCHR01DE008682 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MINA, MINA · 1988 to 2004
$1.1M
Strategy to assess the function of osteocyte restricted genesR03AR053275 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI KALAJZIC, IVO · 2007 to 2009
$219k
NIAMS NIH HHS AR46798NIAMS NIH HHS P01 AR046798NIAMS NIH HHS P01 AR46026NIAMS NIH HHS P30 AR046026NIAMS NIH HHS R01 AR049341NIAMS NIH HHS R03 AR053275NICHD NIH HHS P01 HD022610NICHD NIH HHS P01 HD22610NIDCR NIH HHS R01 DE008682NIDCR NIH HHS R01 DE08682
6 · The paper itself

Abstract

Our laboratory and others have shown that overexpression of Dlx5 stimulates osteoblast differentiation. Dlx5(-/-)/Dlx6(-/-) mice have more severe craniofacial and limb defects than Dlx5(-/-), some of which are potentially due to defects in osteoblast maturation. We wished to investigate the degree to which other Dlx genes compensate for the lack of Dlx5, thus allowing normal development of the majority of skeletal elements in Dlx5(-/-) mice. Dlx gene expression in cells from different stages of the osteoblast lineage isolated by FACS sorting showed that Dlx2, Dlx5 and Dlx6 are expressed most strongly in less mature osteoblasts, whereas Dlx3 is very highly expressed in differentiated osteoblasts and osteocytes. In situ hybridization and Northern blot analysis demonstrated the presence of endogenous Dlx3 mRNA within osteoblasts and osteocytes. Dlx3 strongly upregulates osteoblastic markers with a potency comparable to Dlx5. Cloned chick or mouse Dlx6 showed stimulatory effects on osteoblast differentiation. Our results suggest that Dlx2 and Dlx6 have the potential to stimulate osteoblastic differentiation and may compensate for the absence of Dlx5 to produce relatively normal osteoblastic differentiation in Dlx5 knockout mice, while Dlx3 may play a distinct role in late stage osteoblast differentiation and osteocyte function.

Indexed as

AnimalsAnimals, NewbornBone Marrow CellsCell DifferentiationCloning, MolecularGene Expression RegulationHomeodomain ProteinsMiceMice, Inbred StrainsMice, TransgenicOsteoblastsOsteocytesPolymerase Chain ReactionRNA, MessengerStromal CellsTranscription FactorsDistal-less homeobox proteinsHomeodomain ProteinsRNA, MessengerTranscription Factors

Identifiers

PMID18280462
PMCPMC2679944
OpenAlexW2034408332

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.