Evidence map›Paper›PMID 36478568›Full record

ArticleThe EMBO journal2023

Closing the autophagosome is easy-PC.

Devin M Fuller, Thomas J Melia

Open access · greenAbstract readComment
In one paragraph

Article in The EMBO journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Devin M FullerDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT, USA.
Thomas J MeliaDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0002-5798-4624
Yale University · US

Funding

Regulation of Autophagosome Membrane Dynamics by the AtgB Family of ProteinsR01GM100930 · NIGMS · YALE UNIVERSITY · PI MELIA, THOMAS JAMES · 2013 to 2024
$5.4M
ATG2 transfers lipids from ER exit site membranes to directly expand the growing autophagosomeF31AG079606 · NIA · YALE UNIVERSITY · PI FULLER, DEVIN · 2022 to 2024
$143k
NIA NIH HHS F31 AG079606NIGMS NIH HHS R01 GM100930
6 · The paper itself

Abstract

In their recent article, Polyansky et al identify phosphatidylcholine (PC) as the most abundant lipid in the autophagosome membrane and demonstrate that eliminating de novo PC synthesis sharply impairs autophagic processing. In the absence of PC synthesis, open cup-like structures accumulate, implicating PC as a key component in the closure of autophagosomes.

Indexed as

AutophagosomesPhosphatidylcholinesAutophagyPhosphatidylcholines

Identifiers

PMID36478568
PMCPMC9841321
OpenAlexW4310956252

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.