Evidence map›Paper›PMID 24091626›Full record

ArticleCell cycle (Georgetown, Tex.)2013

Nature vs nurture: interplay between the genetic control of telomere length and environmental factors.

Yaniv Harari, Gal-Hagit Romano, Lior Ungar, Martin Kupiec

Open access · bronzeAbstract readComment
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

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  10. Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Yaniv HarariDepartment of Molecular Microbiology and Biotechnology; Tel Aviv University; Ramat Aviv, Israel.
Gal-Hagit Romano
Lior Ungar
Martin Kupiec
Alzheimer's Association of Israel · ILTel Aviv University · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telomeres are nucleoprotein structures that cap the ends of the linear eukaryotic chromosomes, thus protecting their stability and integrity. They play important roles in DNA replication and repair and are central to our understanding of aging and cancer development. In rapidly dividing cells, telomere length is maintained by the activity of telomerase. About 400 TLM (telomere length maintenance) genes have been identified in yeast, as participants of an intricate homeostasis network that keeps telomere length constant. Two papers have recently shown that despite this extremely complex control, telomere length can be manipulated by external stimuli. These results have profound implications for our understanding of cellular homeostatic systems in general and of telomere length maintenance in particular. In addition, they point to the possibility of developing aging and cancer therapies based on telomere length manipulation.

Indexed as

Stress, PhysiologicalTelomere ShorteningDNA-Binding ProteinsHumansSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSirolimusTelomereTelomere-Binding ProteinsTelomere HomeostasisTranscription FactorsDNA-Binding ProteinsSaccharomyces cerevisiae ProteinsSirolimusTelomere-Binding ProteinsTranscription Factorsagingcancergenome stabilityhomeostasistelomeresyeast

Identifiers

PMID24091626
PMCPMC3906331
OpenAlexW1967918395

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.