Evidence map›Paper›PMID 1454531›Full record

ArticleNucleic acids research1992

Oligonucleotide probes detect splicing variants in situ in Drosophila embryos.

R D Artero, M Akam, M Pérez-Alonso

Open access · bronzeAbstract read
In one paragraph

Article in Nucleic acids research, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. RNA molecules lighting up under the microscope.Histochemistry and cell biology · 1996
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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 2 institutions in 2 countries.

R D ArteroDepartment of Genetics, University of Valencia, Burjasot, Spain.
M Akam
M Pérez-Alonso
Universitat de València · ESWellcome/Cancer Research UK Gurdon Institute · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

We describe a method for the in situ detection of specific splicing variants. The method is based on the use of antisense oligonucleotides designed to span splice junctions labelled with digoxigenin by terminal transferase tailing. We find that the spatial patterns of Ubx splicing variants Ia and IIa are similar in early embryos, but differ in late embryos. Variant IVa is only detected in the CNS (ps6) at stages 16 and 17. We also present evidence indicating that the first splicing event is cotranscriptional.

Indexed as

Alternative SplicingOligonucleotide ProbesAnimalsBase SequenceDigoxigeninDrosophilaIn Situ HybridizationMolecular Sequence DataOligonucleotides, AntisenseTranscription, GeneticDigoxigeninOligonucleotide ProbesOligonucleotides, Antisense

Identifiers

PMID1454531
PMCPMC334403
OpenAlexW1984515917

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.