Evidence map›Paper›PMID 23773569›Full record

ReviewCurrent opinion in cell biology2013

The balance of protein expression and degradation: an ESCRTs point of view.

Markus Babst, Greg Odorizzi

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 29 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

2 authors at 2 institutions in 1 country.

Markus BabstDepartment of Biology and Center for Cell and Genome Science, University of Utah, 257 South 1400 East, Salt Lake City, UT 84112, USA. babst@biology.utah.edu
Greg Odorizzi
University of Colorado Boulder · USUniversity of Utah · US

Funding

Vps4 and the MVB sorting pathway.R01GM074171 · NIGMS · UNIVERSITY OF UTAH · PI BABST, MARKUS · 2006 to 2014
$3.0M
Molecular Analysis of Multivesicular Body FormationR01GM065505 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI ODORIZZI, CHARLES G · 2003 to 2013
$2.8M
NIGMS NIH HHS R01 GM065505NIGMS NIH HHS R01 GM074171
6 · The paper itself

Abstract

Endosomal sorting complexes required for transport (ESCRTs) execute the biogenesis of late endosomal multivesicular bodies (MVBs). The ESCRT pathway has traditionally been viewed as a means by which transmembrane proteins are degraded in vacuoles/lysosomes. More recent studies aimed at understanding the broader functions of ESCRTs have uncovered unexpected links with pathways that control cellular metabolism. Central to this communication is TORC1, the kinase complex that controls many of the catabolic and anabolic systems. The connection between TORC1 activity and ESCRTs allows cells to quickly adapt to the stress of nutrient limitations until the longer-term autophagic pathway is activated. Increasing evidence also points to ESCRTs regulating RNA interference (RNAi) pathways that control translation.

Indexed as

AnimalsEndosomal Sorting Complexes Required for TransportEndosomesEukaryotic CellsHumansLysosomesMembrane ProteinsMultivesicular BodiesRNA InterferenceYeastsEndosomal Sorting Complexes Required for TransportMembrane Proteins

Identifiers

PMID23773569
PMCPMC3740199
OpenAlexW2141502554

What OpenQuestion holds

Textmetadata
LicenceTDM
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.