Evidence map›Paper›PMID 8587124›Full record

ArticleJournal of molecular evolution1995

Comparative analysis of Homo sapiens and Mus musculus cyclin-dependent kinase (CDK) inhibitor genes p16 (MTS1) and p15 (MTS2).

P Jiang, S Stone, R Wagner, S Wang, P Dayananth, C A Kozak, B Wold, A Kamb

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Journal of molecular evolution, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 20 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

P JiangMyriad Genetics, Inc., Salt Lake City, UT 84108, USA.
S Stone
R Wagner
S Wang
P Dayananth
C A Kozak
B Wold
A Kamb
Myriad Genetics · USCalifornia Institute of Technology · USNational Institute of Allergy and Infectious Diseases · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclin-dependent kinase inhibitors are a growing family of molecules that regulate important transitions in the cell cycle. At least one of these molecules, p16, has been implicated in human tumorigenesis while its close homolog, p15, is induced by cell contact and transforming growth factor-beta (TGF-beta). To investigate the evolutionary and functional features of p15 and p16, we have isolated mouse (Mus musculus) homologs of each gene. Comparative analysis of these sequences provides evidence that the genes have similar functions in mouse and human. In addition, the comparison suggests that a gene conversion event is part of the evolution of the human p15 and p16 genes.

Indexed as

Cell Cycle ProteinsSequence AlignmentTumor Suppressor ProteinsAmino Acid SequenceAnimalsBase SequenceCarrier ProteinsConserved SequenceCyclin-Dependent Kinase Inhibitor p15Cyclin-Dependent Kinase Inhibitor p16Enzyme InhibitorsEvolution, MolecularHominidaeHumansMiceMolecular Sequence DataCarrier ProteinsCDKN2B protein, humanCdkn2b protein, mouseCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor p15Cyclin-Dependent Kinase Inhibitor p16Enzyme InhibitorsProtein Kinase InhibitorsTumor Suppressor Proteins

Identifiers

PMID8587124
OpenAlexW2038015229

What OpenQuestion holds

Textmetadata
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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.