Evidence map›Paper›PMID 8320169›Full record

ArticleJapanese journal of cancer research : Gann1993

The murine cot proto-oncogene: genome structure and tissue-specific expression.

R Ohara, J Miyoshi, M Aoki, K Toyoshima

Abstract readComparative Study
In one paragraph

Article in Japanese journal of cancer research : Gann, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Cot, a novel kinase of histone H3, induces cellular transformation through up-regulation of c-fos transcriptional activity.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2008
    Article
  3. Article
  4. Article
  5. 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

4 authors at 2 institutions in 2 countries.

R OharaDepartment of Oncogene Research, Osaka University.
J Miyoshi
M Aoki
K Toyoshima
The University of Osaka · JPOncoGenex Pharmaceuticals (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We cloned and analyzed the murine cot proto-oncogene and examined its tissue-specific expression in fetal, newborn and adult mice. Genomic cot DNA consists of eight exons, spanning more than 25 kb, and all intron-exon borders are well conserved as compared to the human homolog. Analysis of the full-length cot cDNA revealed that it contained an open reading frame of 1,401 nucleotides, like human cot proto-oncogene. The sequence identity between murine and human cot gene is 84.4% at the nucleotide level and 93.9% at the deduced amino acid level. On northern blot analysis of poly (A)+ RNA, the cot message was detected at 2.9 kb in size. Expression of the cot gene was observed in many tissues from fetal to adult mice, though the level of expression was low in all tissues examined.

Indexed as

MAP Kinase Kinase KinasesProto-OncogenesAmino Acid SequenceAnimalsBase SequenceChromosome MappingCloning, MolecularDNAHumansMiceMice, Inbred BALB CMolecular Sequence DataOrgan SpecificityProtein Serine-Threonine KinasesProto-Oncogene MasProto-Oncogene ProteinsDNAMAP3K8 protein, humanMap3k8 protein, mouseMAP Kinase Kinase KinasesMAS1 protein, humanProtein Serine-Threonine KinasesProto-Oncogene MasProto-Oncogene ProteinsRNA, Messenger

Identifiers

PMID8320169
PMCPMC5919168
OpenAlexW2070192901

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.