Evidence map›Paper›PMID 26339479›Full record

ReviewF1000Research2015

Membrane manipulations by the ESCRT machinery.

Greg Odorizzi

Open access · goldAbstract readReview
In one paragraph

Review in F1000Research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Reverse-topology membrane scission by the ESCRT proteins.Nature reviews. Molecular cell biology · 2017
    Review
  6. The role of CHMP2BBrain research · 2016
    Review
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

1 author at 1 institution in 1 country.

Greg OdorizziMolecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO, USA.
University of Colorado Boulder · US

Funding

Regulation of ESCRT-III Activity in YeastR01GM111335 · NIGMS · UNIVERSITY OF COLORADO · PI ODORIZZI, CHARLES G · 2014 to 2022
$2.6M
NIGMS NIH HHS R01 GM111335
6 · The paper itself

Abstract

The endosomal sorting complexes required for transport (ESCRTs) collectively comprise a machinery that was first known for its function in the degradation of transmembrane proteins in the endocytic pathway of eukaryotic cells. Since their discovery, however, ESCRTs have been recognized as playing important roles at the plasma membrane, which appears to be the original site of function for the ESCRT machinery. This article reviews some of the major research findings that have shaped our current understanding of how the ESCRT machinery controls membrane dynamics and considers new roles for the ESCRT machinery that might be driven by these mechanisms.

Indexed as

cytokinesisendosomal sorting complexes required for transportESCRTESCRT machineryintralumenal vesicle budding pathwaymembrane dynamicsretrovirus budding

Identifiers

PMID26339479
PMCPMC4544380
OpenAlexW1612512763

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.