Evidence map›Paper›PMID 18245837›Full record

ArticleGenetics2008

The impact of dissociation on transposon-mediated disease control strategies.

John M Marshall

Abstract read
In one paragraph

Article in Genetics, 2008. 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
–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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
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  9. Review
  10. 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

1 author.

John M MarshallDepartment of Biomathematics, University of California School of Medicine, Los Angeles, California 90095-1766, USA. johnmm@ucla.edu

Funding

Niono Irrigation Project and Malaria: A Computer ModelR01AI051633 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TAYLOR, CHARLES E · 2002 to 2006
$1.8M
Dynamics of Transposable Elements in Mosquito VectorsR56AI072549 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TAYLOR, CHARLES E · 2007 to 2007
$150k
NIAID NIH HHS 1R56AI072549NIAID NIH HHS R01 AI051633NIAID NIH HHS R01 AI51633NIAID NIH HHS R56 AI072549
6 · The paper itself

Abstract

Vector-borne diseases such as malaria and dengue fever continue to be a major health concern through much of the world. The emergence of chloroquine-resistant strains of malaria and insecticide-resistant mosquitoes emphasize the need for novel methods of disease control. Recently, there has been much interest in the use of transposable elements to drive resistance genes into vector populations as a means of disease control. One concern that must be addressed before a release is performed is the potential loss of linkage between a transposable element and a resistance gene. Transposable elements such as P and hobo have been shown to produce internal deletion derivatives at a significant rate, and there is concern that a similar process could lead to loss of the resistance gene from the drive system following a transgenic release. Additionally, transposable elements such as Himar1 have been shown to transpose significantly more frequently when free of exogenous DNA. Here, we show that any transposon-mediated gene drive strategy must have an exceptionally low rate of dissociation if it is to be effective. Additionally, the resistance gene must confer a large selective advantage to the vector to surmount the effects of a moderate dissociation rate and transpositional handicap.

Indexed as

DiseaseAnimalsDNA Transposable ElementsImmunity, InnateInsect VectorsSequence DeletionDNA Transposable Elements

Identifiers

PMID18245837
PMCPMC2278053

What OpenQuestion holds

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Registered trials

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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.