Evidence map›Paper›PMID 30374414›Full record

ArticleCell death discovery2018

Lon protease inactivation in

Gautam Pareek, Ruth E Thomas, Evelyn S Vincow, David R Morris, Leo J Pallanck

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.4field-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

25 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Embedded CRISPRi Enhances Gene-Silencing Efficiency in Drosophila.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Gautam Pareek1Department of Genome Sciences, University of Washington, 3720 15th Avenue NE, Seattle, WA 98195 USA.
Ruth E Thomas1Department of Genome Sciences, University of Washington, 3720 15th Avenue NE, Seattle, WA 98195 USA.
Evelyn S Vincow1Department of Genome Sciences, University of Washington, 3720 15th Avenue NE, Seattle, WA 98195 USA.
David R Morris2Department of Biochemistry, University of Washington, 1705 NE Pacific St., Seattle, WA 98195 USA.
Leo J Pallanck1Department of Genome Sciences, University of Washington, 3720 15th Avenue NE, Seattle, WA 98195 USA.
University of Washington · USSeattle Pacific University · US

Funding

A proteomic approach to identify substrates of the AAA+ mitochondrial proteasesR21NS094901 · NINDS · UNIVERSITY OF WASHINGTON · PI PALLANCK, LEO J · 2015 to 2016
$425k
NINDS NIH HHS R21 NS094901
6 · The paper itself

Abstract

Mitochondrial dysfunction is a frequent participant in common diseases and a principal suspect in aging. To combat mitochondrial dysfunction, eukaryotes have evolved a large repertoire of quality control mechanisms. One such mechanism involves the selective degradation of damaged or misfolded mitochondrial proteins by mitochondrial resident proteases, including proteases of the ATPase Associated with diverse cellular Activities (AAA

Identifiers

PMID30374414
PMCPMC6197249
OpenAlexW2897721725

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.