Evidence map›Paper›PMID 12529440›Full record

ArticleMolecular biology of the cell2003

Deregulation of the Egfr/Ras signaling pathway induces age-related brain degeneration in the Drosophila mutant vap.

José A Botella, Doris Kretzschmar, Claudia Kiermayer, Pascale Feldmann, David A Hughes, Stephan Schneuwly

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2003. 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
1.1field-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, 33 citations in OpenAlex.

  1. Article
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  6. Toxins · 2019
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  7. Review
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  12. Neurofibromin mediates FAK signaling in confining synapse growth at Drosophila neuromuscular junctions.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
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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

6 authors at 2 institutions in 2 countries.

José A BotellaLehrstuhl für Entwicklungsbiologie, Universität Regensburg, 93040 Regensburg, Germany. jose.botella-munoz@biologie.uni-regensburg.de
Doris Kretzschmar
Claudia Kiermayer
Pascale Feldmann
David A Hughes
Stephan Schneuwly
University of Regensburg · DEInstitute of Cancer Research · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Ras signaling has been shown to play an important role in promoting cell survival in many different tissues. Here we show that upregulation of Ras activity in adult Drosophila neurons induces neuronal cell death, as evident from the phenotype of vacuolar peduncle (vap) mutants defective in the Drosophila RasGAP gene, which encodes a Ras GTPase-activating protein. These mutants show age-related brain degeneration that is dependent on activation of the EGF receptor signaling pathway in adult neurons, leading to autophagic cell death (cell death type 2). These results provide the first evidence for a requirement of Egf receptor activity in differentiated adult Drosophila neurons and show that a delicate balance of Ras activity is essential for the survival of adult neurons.

Indexed as

AgingAnimalsBrainCell DeathDrosophilaErbB ReceptorsMutationras GTPase-Activating ProteinsSignal TransductionUp-RegulationVacuolesErbB Receptorsras GTPase-Activating Proteins

Identifiers

PMID12529440
PMCPMC140241
OpenAlexW2163983604

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.