Evidence map›Paper›PMID 9278247›Full record

ArticleMolecular and cellular biochemistry1997

Potent and selective gene inhibition using antisense oligodeoxynucleotides.

W M Flanagan, R W Wagner

Abstract read
PubMed
In one paragraph

Article in Molecular and cellular biochemistry, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. A cytosine analog that confers enhanced potency to antisense oligonucleotides.Proceedings of the National Academy of Sciences of the United States of America · 1999
    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

2 authors.

W M FlanaganGilead Sciences, Foster City, CA 94404, USA.
R W Wagner

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of antisense technology as a generally useful tool relies on the use of potent agents and the utilization of many controls in experiments. Here we describe our experience using oligodeoxynucleotides (ODNs) containing C-5 propynyl pyrimidine and phosphorothioate modifications as broadly applicable gene inhibition agents in cell culture. Methods include selection of antisense sequences, synthesis and purification of ODNs, choice of controls, delivery methods (microinjection, cationic lipid transfection, and electroporation), and analysis of gene inhibition.

Indexed as

AnimalsBlotting, NorthernBlotting, WesternCationsCDC2 Protein KinaseCell LineChlorocebus aethiopsElectroporationGene Expression RegulationLipid MetabolismMicroinjectionsOligonucleotides, AntisenseRibonucleasesRNAThionucleotidesCationsCDC2 Protein KinaseOligonucleotides, AntisenseRibonucleasesRNAThionucleotides

Identifiers

PMID9278247

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.