Evidence map›Paper›PMID 8524838›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1995

Specific activation in jun-transformed avian fibroblasts of a gene (bkj) related to the avian beta-keratin gene family.

M Hartl, K Bister

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. JAC, a direct target of oncogenic transcription factor Jun, is involved in cell transformation and tumorigenesis.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
  12. Article
  13. Review
  14. Jun, the oncoprotein.Oncogene · 2001
    Review
  15. Article
  16. Article
  17. Heparin-binding epidermal growth factor-like growth factor, a v-Jun target gene, induces oncogenic transformation.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  18. Hormone-regulatable neoplastic transformation induced by a Jun-estrogen receptor chimera.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
  19. 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 at 1 institution in 1 country.

M HartlInstitute of Biochemistry, University of Innsbruck, Austria.
K Bister
Universität Innsbruck · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have analyzed differential gene expression in normal versus jun-transformed avian fibroblasts by using subtracted nucleic acid probes and differential nucleic acid hybridization techniques for the isolation of cDNA clones. One clone corresponded to a gene that was strongly expressed in a previously established quail (Coturnix japonica) embryo fibroblast line (VCD) transformed by a chimeric jun oncogene but whose expression was undetectable in normal quail embryo fibroblasts. Furthermore, the gene was expressed in quail or chicken fibroblast cultures that were freshly transformed by retroviral constructs carrying various viral or cellular jun alleles and in chicken fibroblasts transformed by the avian retrovirus ASV17 carrying the original viral v-jun allele. However, its expression was undetectable in a variety of established avian cell lines or freshly prepared avian fibroblast cultures transformed by other oncogenes or a chemical carcinogen. The nucleotide and deduced amino acid sequences of the cDNA clone were not identical to any sequence entries in the data bases but revealed significant similarities to avian beta-keratin genes; the highest degree of amino acid sequence identity was 63%. The gene, which we termed bkj, may represent a direct or indirect target for jun function.

Indexed as

Gene Expression Regulation, NeoplasticGenes, junAmino Acid SequenceAnimalsBase SequenceCell Line, TransformedCell Transformation, NeoplasticChickensCloning, MolecularCoturnixDNA, ComplementaryFibroblastsKeratinsMolecular Sequence DataMultigene FamilyNucleic Acid Hybridizationbkj protein, Coturnix japonicaDNA, ComplementaryKeratins

Identifiers

PMID8524838
PMCPMC40476
OpenAlexW2093673282

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.