Evidence map›Paper›PMID 20947703›Full record

ReviewAmerican journal of physiology. Gastrointestinal and liver physiology2011

Random mutagenesis of the mouse genome: a strategy for discovering gene function and the molecular basis of disease.

Nhung Nguyen, Louise M Judd, Anastasia Kalantzis, Belinda Whittle, Andrew S Giraud, Ian R van Driel

Abstract readReview
In one paragraph

Review in American journal of physiology. Gastrointestinal and liver physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Controlling complexity: the clinical relevance of mouse complex genetics.European journal of human genetics : EJHG · 2013
    Review
  7. Article
  8. Review
  9. Article
  10. Functional annotation and ENU.BMC research notes · 2012
    Article
  11. Article
  12. Review
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.

Nhung NguyenDepartment of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Australia.
Louise M Judd
Anastasia Kalantzis
Belinda Whittle
Andrew S Giraud
Ian R van Driel

Funding

Novel models for gastrointestinal disease, physiology and developmentR21DK078946 · NIDDK · UNIVERSITY OF MELBOURNE · PI VAN DRIEL, IAN R · 2008 to 2009
$297k
NIDDK NIH HHS 1R21DK078946-01A1
6 · The paper itself

Abstract

Mutagenesis of mice with N-ethyl-N-nitrosourea (ENU) is a phenotype-driven approach to unravel gene function and discover new biological pathways. Phenotype-driven approaches have the advantage of making no assumptions about the function of genes and their products and have been successfully applied to the discovery of novel gene-phenotype relationships in many physiological systems. ENU mutagenesis of mice is used in many large-scale and more focused projects to generate and identify novel mouse models for the study of gene functions and human disease. This review examines the strategies and tools used in ENU mutagenesis screens to efficiently generate and identify functional mutations.

Indexed as

EthylnitrosoureaMutagenesisAnimalsBreedingDisease Models, AnimalFemaleGenesGenomeGenome-Wide Association StudyInflammatory Bowel DiseasesMaleMicePhenotypeEthylnitrosourea

Identifiers

PMID20947703
PMCPMC3774088

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.