Evidence map›Paper›PMID 14557804›Full record

ReviewOncogene2003

Mouse models for induced genetic instability at endogenous loci.

Ramune Reliene, Robert H Schiestl

Abstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

2 authors at 1 institution in 1 country.

Ramune RelieneDepartment of Pathology, David Geffen School of Medicine and School of Public Health, UCLA, 650 Charles E Young Drive South, Los Angeles, CA 90024, USA.
Robert H Schiestl
University of California, Los Angeles · US

Funding

ATM, P53, GADD45 AND P21 EFFECTS ON RECOMBINATIONR01ES009519 · NIEHS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SCHIESTL, ROBERT H · 1999 to 2009
$2.7M
CARCINOGEN INDUCED DELETIONS IN VIVO AND IN VITROK02ES000299 · NIEHS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SCHIESTL, ROBERT H · 1996 to 2000
$69k
NIEHS NIH HHS KO2 ES00299NIEHS NIH HHS R01 ES09519
6 · The paper itself

Abstract

Exposure to environmental factors and genetic predisposition of an individual may lead individually or in combination to various genetic diseases including cancer. These diseases may be a consequence of genetic instability resulting in large-scale genomic rearrangements, such as DNA deletions, duplications, and translocations. This review focuses on mouse assays detecting genetic instability at endogenous loci. The frequency of DNA deletions by homologous recombination at the pink-eyed unstable (p(un)) locus is elevated in mice with mutations in ATM, Trp53, Gadd45, and WRN genes and after exposure to carcinogens. Other quantitative in vivo assays detecting loss of heterozygosity events, such as the mammalian spot assay, Dlb-1 mouse and Aprt mouse assays, are also reviewed. These in vivo test systems may predict hazardous effects of an environmental agent and/or genetic predisposition to cancer.

Indexed as

Carrier ProteinsDNA DamageGenomic InstabilityAnimalsMembrane ProteinsMiceModels, AnimalOxidative StressRecombination, GeneticSequence DeletionCarrier ProteinsMembrane ProteinsP protein, mouse

Identifiers

PMID14557804
OpenAlexW2047870217

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.