An Oak Ridge legacy: the specific locus test and its role in mouse mutagenesis.

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.

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.

Who cites it

15 citing papers in PubMed.

1. Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor loci.Proceedings of the National Academy of Sciences of the United States of America · 2017
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2. Alkylator-Induced and Patient-Derived Xenograft Mouse Models of Therapy-Related Myeloid Neoplasms Model Clinical Disease and Suggest the Presence of Multiple Cell Subpopulations with Leukemia Stem Cell Activity.PloS one · 2016
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3. Estimation of the frequency of inherited germline mutations by whole exome sequencing in ethyl nitrosourea-treated and untreated gpt delta mice.Genes and environment : the official journal of the Japanese Environmental Mutagen Society · 2016
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4. Spontaneous 8bp Deletion in Nbeal2 Recapitulates the Gray Platelet Syndrome in Mice.PloS one · 2016
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5. Neurobehavioral mutants identified in an ENU-mutagenesis project.Mammalian genome : official journal of the International Mammalian Genome Society · 2007
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6. Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2007
   Review
7. Genomic anatomy of the Tyrp1 (brown) deletion complex.Proceedings of the National Academy of Sciences of the United States of America · 2006
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8. Overlapping deletions spanning the proximal two-thirds of the mouse t complex.Mammalian genome : official journal of the International Mammalian Genome Society · 2003
   Article
9. Development of an enhanced GFP-based dual-color reporter to facilitate genetic screens for the recovery of mutations in mice.Proceedings of the National Academy of Sciences of the United States of America · 2003
   Article
10. One hundred years of mouse genetics: an intellectual history. II. The molecular revolution (1981-2002).Genetics · 2003
    Article
11. C. C. Little, cancer and inbred mice.Genetics · 2002
    Article
12. Molecular and functional mapping of the piebald deletion complex on mouse chromosome 14.Genetics · 2001
    Article
13. The ascendency of developmental genetics, or how the T complex educated a generation of developmental biologists.Genetics · 1999
    Article
14. A phenotype-based screen for embryonic lethal mutations in the mouse.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
15. Meeting report: 11th International Mouse Genome Conference.Mammalian genome : official journal of the International Mammalian Genome Society · 1998
    Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

2 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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