Evidence map›Paper›PMID 8307327›Full record

ArticleGenetics1993

Deletion mapping of four loci defined by N-ethyl-N-nitrosourea-induced postimplantation-lethal mutations within the pid-Hbb region of mouse chromosome 7.

E M Rinchik, D A Carpenter, C L Long

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Chromatin regulators of genomic imprinting.Biochimica et biophysica acta · 2014
    Review
  2. Article
  3. Overlapping deletions spanning the proximal two-thirds of the mouse t complex.Mammalian genome : official journal of the International Mammalian Genome Society · 2003
    Article
  4. Article
  5. Article
  6. X-ray-induced mutations in mouse embryonic stem cells.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  7. The role of the laboratory mouse in the human genome project.American journal of human genetics · 1996
    Review
  8. Article
  9. Article
  10. Genetic and physical mapping of the fitness 1 (fit1) locus within the Fes-Hbb region of mouse chromosome 7.Mammalian genome : official journal of the International Mammalian Genome Society · 1995
    Article
  11. Article
  12. Article
  13. 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

3 authors at 1 institution in 1 country.

E M RinchikBiology Division, Oak Ridge National Laboratory, Tennessee 37831-8077.
D A Carpenter
C L Long
Oak Ridge National Laboratory · US

Funding

SATURATION MUTAGENESIS OF MOUSE GENOMIC REGIONSR01HG000370 · NHGRI · LOCKHEED MARTIN ENERGY SYSTEMS, INC. · PI RINCHIK, EUGENE M · 1990 to 1992
–
NHGRI NIH HHS HG 00370
6 · The paper itself

Abstract

As part of a long-term effort to refine the physical and functional maps of the Fes-Hbb region of mouse chromosome 7, four loci [l(7)1Rn, l(7)2Rn, l(7)3Rn, l(7)4Rn] defined by N-ethyl-N-nitrosourea (ENU)-induced, prenatally lethal mutations were mapped by means of trans complementation crosses to mice carrying lethal deletions of the mouse chromosome-7 albino (c) locus. Each locus was assigned to a defined subregion of the deletion map at the distal end of the Fes-Hbb interval. Of particular use for this mapping were preimplantation-lethal deletions having distal breakpoints localized between pid and Omp. Hemizygosity or homozygosity for each of the ENU-induced lethals was found to arrest development after uterine implantation; the specific time of postimplantation death varied, and depended on both the mutation itself and on whether it was hemizygous or homozygous. Based on their map positions outside of and distal to deletions that cause death at preimplantation stages, these ENU-induced mutations identify loci, necessary for postimplantation development, that could not have been discovered by phenotypic analyses of mice homozygous for any albino deletion. The mapping of these loci to specific genetic intervals defined by deletion breakpoints suggests a number of positional-cloning strategies for the molecular isolation of these genes. Phenotypic and genetic analyses of these mutations should provide useful information on the functional composition of the corresponding segment of the human genome (perhaps human 11q13.5).

Indexed as

Chromosome MappingGenes, LethalMutationAnimalsEmbryonic DevelopmentEthylnitrosoureaFemaleFetal DeathHomozygoteMaleMicePregnancySequence DeletionEthylnitrosourea

Identifiers

PMID8307327
PMCPMC1205743
OpenAlexW2101013701

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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.