Evidence map›Paper›PMID 18664640›Full record

ArticleAmerican journal of respiratory cell and molecular biology2009

Expression profiles of the mouse lung identify a molecular signature of time-to-birth.

Alvin T Kho, Soumyaroop Bhattacharya, Brigham H Mecham, Jungha Hong, Isaac S Kohane, Thomas J Mariani

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

31 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Proteomic Analysis of Human Lung Development.American journal of respiratory and critical care medicine · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Age, Sexual Dimorphism, and Disease Associations in the Developing Human Fetal Lung Transcriptome.American journal of respiratory cell and molecular biology · 2016
    Article
  10. Article
  11. Regulation of alveolar septation by microRNA-489.American journal of physiology. Lung cellular and molecular physiology · 2016
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. The genome-wide transcriptional response to neonatal hyperoxia identifies Ahr as a key regulator.American journal of physiology. Lung cellular and molecular physiology · 2014
    Article
  17. Dynamic expression of chymotrypsin-like elastase 1 over the course of murine lung development.American journal of physiology. Lung cellular and molecular physiology · 2014
    Article
  18. Review
  19. Article
  20. Article
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

6 authors at 2 institutions in 1 country.

Alvin T KhoChildrens Hospital Informatics Program, Children's Hospital Boston, Harvard-MIT Division of Health Sciences and Technology, Boston, Massachusetts, USA.
Soumyaroop Bhattacharya
Brigham H Mecham
Jungha Hong
Isaac S Kohane
Thomas J Mariani
Brigham and Women's Hospital · USBoston Children's Hospital · US

Funding

Progenitor Cells inHuman Skeletal MuscleP01NS040828 · NINDS · CHILDREN'S HOSPITAL BOSTON · PI KUNKEL, LOUIS M · 2001 to 2007
$8.6M
Progenitor Cells inHuman Skeletal MuscleP50NS040828 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI KOHANE, ISAAC S. · 2008 to 2011
$5.9M
Functional Genomics of AlveogenesisR01HL071885 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI MARIANI, THOMAS J · 2003 to 2006
$1.4M
Mechanisms of hedge-hog induced neuroproliferationR01NS047527 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROWITCH, DAVID H · 2004 to 2007
$1.4M
A Developmental Basis for Chronic Obstructive Lung DiseaseK25HL091124 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI KHO, ALVIN THONG-JUAK · 2008 to 2012
$743k
NHLBI NIH HHS HL71885NHLBI NIH HHS K25 HL091124NINDS NIH HHS NS040828NINDS NIH HHS NS047527
6 · The paper itself

Abstract

A greater understanding of the regulatory processes contributing to lung development could help ameliorate morbidity and mortality in premature infants and identify individuals at risk for congenital and/or chronic lung diseases. Genomics technologies have provided rich gene expression datasets for the developing lung that enable systems biology approaches for identifying large-scale molecular signatures within this complex phenomenon. Here, we applied unsupervised principal component analysis on two developing lung datasets and identified common dominant transcriptomic signatures. Of particular interest, we identify an overlying biological program we term "time-to-birth," which describes the distance in age from the day of birth. We identify groups of genes contributing to the time-to-birth molecular signature. Statistically overrepresented are genes involved in oxygen and gas transport activity, as expected for a transition to air breathing, as well as host defense function. In addition, we identify genes with expression patterns associated with the initiation of alveolar formation. Finally, we present validation of gene expression patterns across the two datasets, and independent validation of select genes by qPCR and immunohistochemistry. These data contribute to our understanding of genetic components contributing to large-scale biological processes and may be useful, particularly in animal models of abnormal lung development, to predict the state of organ development or preparation for birth.

Indexed as

Gene Expression ProfilingLungOligonucleotide Array Sequence AnalysisAnimalsBiomarkersFemaleHumansMicePregnancyPrincipal Component AnalysisReproducibility of ResultsBiomarkers

Identifiers

PMID18664640
PMCPMC2606946
OpenAlexW2040751641

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.