Evidence map›Paper›PMID 8632989›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1996

A rat genetic map constructed by representational difference analysis markers with suitability for large-scale typing.

M Toyota, F Canzian, T Ushijima, Y Hosoya, T Kuramoto, T Serikawa, K Imai, T Sugimura, M Nagao

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Linkage mapping of rat Rb1 gene on chromosome 15.Mammalian genome : official journal of the International Mammalian Genome Society · 1997
    Article
  6. Article
  7. Cloning of rat Brca2 and linkage mapping to chromosome 12.Mammalian genome : official journal of the International Mammalian Genome Society · 1997
    Article
  8. Linkage mapping of the rat Tp53 gene on chromosome 10.Mammalian genome : official journal of the International Mammalian Genome Society · 1996
    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

9 authors.

M ToyotaCarcinogenesis Division, National Cancer Center Research Institute, Tokyo, Japan.
F Canzian
T Ushijima
Y Hosoya
T Kuramoto
T Serikawa
K Imai
T Sugimura
M Nagao

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Representational difference analysis (RDA) was applied to isolate chromosomal markers in the rat. Four series of RDA [restriction enzymes, BamHI and HindIII; subtraction of ACI/N (ACI) amplicon from BUF/Nac (BUF) amplicon and vice versa] yielded 131 polymorphic markers; 125 of these markers were mapped to all chromosomes except for chromosome X. This was done by using a mapping panel of 105 ACI x BUF F2 rats. To complement the relative paucity of chromosomal markers in the rat, genetically directed RDA, which allows isolation of polymorphic markers in the specific chromosomal region, was performed. By changing the F2 driver-DNA allele frequency around the region, four markers were isolated from the D1Ncc1 locus. Twenty-five of 27 RDA markers were informative regarding the dot blot analysis of amplicons, hybridizing only with tester amplicons. Dot blot analysis at a high density per unit of area made it possible to process a large number of samples. Quantitative trait loci can now be mapped in the rat genome by processing a large number of samples with RDA markers and then by isolating markers close to the loci of interest by genetically directed RDA.

Indexed as

Chromosome MappingAllelesAnimalsBlotting, SouthernCrosses, GeneticDeoxyribonuclease BamHIDeoxyribonuclease HindIIIDNAElectrophoresis, Agar GelGenetic MarkersPolymerase Chain ReactionRatsRats, Inbred ACIRats, Inbred BUFRestriction MappingDeoxyribonuclease BamHIDeoxyribonuclease HindIIIDNAGenetic Markers

Identifiers

PMID8632989
PMCPMC39459

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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.