Evidence map›Paper›PMID 9081236›Full record

ArticleInternational journal of legal medicine1997

Sequence variation of allele 27 at the D1S80 locus.

N Harashima, C Liu, Y Katsuyama, M Ota, H Fukushima

Abstract read
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Article in International journal of legal medicine, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

N HarashimaDepartment of Legal Medicine, Shinshu University School of Medicine, Nagano, Japan.
C Liu
Y Katsuyama
M Ota
H Fukushima

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In 180 unrelated Japanese individuals 18 examples of allele 27 were detected at the locus D1S80 (MCT118). On 6% polylacrylamide gels 5 out of these 18 alleles were found to migrate between allele 26 and allele 27, but closer to allele 27, and thus were labelled variants of allele 27. All 18 examples of allele 27 were sequenced and the results were compared. Although all had the same number of base pairs (578 bp) the five variants could be subdivided into three types. V1, V2 and V3. The variants and the standard allele were composed of the same kinds of repeat units, but the order of arrangement was different. We investigated whether it was possible to distinguish the standard allele 27, and the variants V1, V2, and V3 by PCR-RFLP. EcoRII and MspI which have restriction sites within the repeat units were adopted as restriction enzymes. The variants could be discriminated from each other after treatment of the PCR fragments with EcoRII or MspI, followed by PAG electrophoresis.

Indexed as

Chromosome MappingGenetic VariationBase SequenceEthnicityGene FrequencyGenetic MarkersGenetics, PopulationGenotypeHumansJapanMolecular Sequence DataPolymerase Chain ReactionPolymorphism, Restriction Fragment LengthRepetitive Sequences, Nucleic AcidGenetic Markers

Identifiers

PMID9081236

What OpenQuestion holds

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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.