Evidence map›Paper›PMID 10871381›Full record

ArticleNucleic acids research2000

PCR-generated padlock probes detect single nucleotide variation in genomic DNA.

D O Antson, A Isaksson, U Landegren, M Nilsson

Abstract read
In one paragraph

Article in Nucleic acids research, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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  11. Review
  12. Circle-to-circle amplification for precise and sensitive DNA analysis.Proceedings of the National Academy of Sciences of the United States of America · 2004
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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

4 authors.

D O AntsonRudbeck Laboratory, Department of Genetics and Pathology, SE-751 85, Uppsala, Sweden and Department of Molecular Cell Biology, Leiden University Medical Center, Wassenaarseweg 72, 2333 AL Leiden, The Netherlands.
A Isaksson
U Landegren
M Nilsson

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circularizing oligonucleotide probes, so-called padlock probes, have properties that should prove valuable in a wide range of genetic investigations, including in situ analyses, genotyping and measurement of gene expression. However, padlock probes can be difficult to obtain by standard oligonucleotide synthesis because they are relatively long and require intact 5'- and 3'-end sequences to function. We describe a PCR-based protocol for flexible small-scale enzymatic synthesis of such probes. The protocol also offers the advantage over chemical synthesis that longer probes can be made that are densely labeled with detectable functions, resulting in an increased detection signal. The utility of probes synthesized according to this protocol is demonstrated for the analysis of single nucleotide variations in human genomic DNA both in situ and in solution.

Indexed as

Cation Transport ProteinsGenetic VariationAdenosine TriphosphatasesCarrier ProteinsCells, CulturedCopper-Transporting ATPasesDNA, CircularDNA Mutational AnalysisHumansMetaphaseOligonucleotide ProbesPoint MutationPolymerase Chain ReactionAdenosine TriphosphatasesCarrier ProteinsCation Transport ProteinsCopper-Transporting ATPasesDNA, CircularOligonucleotide Probes

Identifiers

PMID10871381
PMCPMC102743

What OpenQuestion holds

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Read underepoch 390

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.