Evidence map›Paper›PMID 17339382›Full record

ArticleThe Journal of cell biology2007

To die or not to die--a role for Fork head.

Carl S Thummel

Open access · bronzeAbstract readComment
In one paragraph

Article in The Journal of cell biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. The Journal of biological chemistry · 2019
    Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Carl S ThummelDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT 84112, USA. carl.thummel@genetics.utah.edu
University of Utah · US

Funding

Mechanisms of Steroid-Triggered Programmed Cell DeathR01GM073670 · NIGMS · UNIVERSITY OF UTAH · PI THUMMEL, CARL S. · 2005 to 2009
$1.2M
NIGMS NIH HHS R01 GM073670
6 · The paper itself

Abstract

The precise determination of when and where cells undergo programmed cell death is critical for normal development and tissue homeostasis. Cao et al. (2007; see p. 843 of this issue) report that the Fork head (Fkh) transcription factor, which is essential for the early development and function of the larval salivary glands in Drosophila melanogaster, also contributes to its demise. These authors show that fkh expression in the salivary glands is normally lost at puparium formation, which is approximately 12 h before they undergo massive cell death triggered by the steroid hormone ecdysone, making room for their developing adult counterparts. The loss of Fkh eliminates its role in blocking cell death, allowing for subsequent ecdysone-induced reaper and head involution defective death activator expression and tissue destruction. This study provides new insights into the transcriptional regulation of programmed cell death and the mechanisms that underlie the precise spatial and temporal control of hormone responses during development.

Indexed as

AnimalsApoptosisDrosophila melanogasterEcdysoneForkhead Transcription FactorsLarvaModels, BiologicalNuclear ProteinsSalivary GlandsSignal TransductionTranscription FactorsEcdysonefkh protein, DrosophilaForkhead Transcription FactorsNuclear ProteinsTranscription Factors

Identifiers

PMID17339382
PMCPMC1976266
OpenAlexW2086893740

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.