Evidence map›Paper›PMID 32095531›Full record

ArticleScience advances2020

Broadly conserved roles of TMEM131 family proteins in intracellular collagen assembly and secretory cargo trafficking.

Zhe Zhang, Meirong Bai, Guilherme Oliveira Barbosa, Andrew Chen, Yuehua Wei, Shuo Luo, Xin Wang, Bingying Wang, Tatsuya Tsukui, Hao Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
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  5. Core microRNAs regulate neural crest delamination and condensation in the developing trigeminal ganglion.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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

13 authors at 1 institution in 1 country.

Zhe ZhangCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0003-3616-6224
Meirong BaiCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0002-5919-7464
Guilherme Oliveira BarbosaCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0002-5881-0896
Andrew ChenCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0002-9818-8667
Yuehua WeiCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
Shuo LuoCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
Xin WangCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0003-1576-7127
Bingying WangCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
Tatsuya TsukuiCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0003-3100-6934
Hao LiDepartment of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA 94158, USA.
Dean SheppardCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0002-6277-2036
Thomas B KornbergCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0002-6879-7066
Dengke K MaCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0002-5619-7485
University of California, San Francisco · US

Funding

Molecular Mechanisms in DevelopmentR35GM122548 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI THOMAS B. KORNBERG · 2017 to 2026
$8.8M
Signals from the reproductive system that regulate aging in C. elegansR01AG032435 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LI, HAO · 2009 to 2018
$3.3M
Cellular Aging and Rejuvenation: A Comprehensive Picture from a Dynamic and Network Perspective - Administrative SupplementR01AG058742 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KENNEDY, BRIAN K, LI, HAO · 2018 to 2022
$3.0M
Dissecting a Novel Genetic Pathway for Fatty Acid Desaturation and Temperature AdaptationR01GM117461 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MA, DENGKE · 2016 to 2020
$1.6M
NIA NIH HHS R01 AG032435NIA NIH HHS R01 AG058742NIGMS NIH HHS R01 GM117461NIGMS NIH HHS R35 GM122548
6 · The paper itself

Abstract

Collagen is the most abundant protein in animals. Its dysregulation contributes to aging and many human disorders, including pathological tissue fibrosis in major organs. How premature collagen proteins in the endoplasmic reticulum (ER) assemble and route for secretion remains molecularly undefined. From an RNA interference screen, we identified an uncharacterized

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCollagenDrosophilaEndoplasmic Reticulum StressEvolution, MolecularGenomeGreen Fluorescent ProteinsHumansIntracellular SpaceMembrane ProteinsPhylogenyProtein BindingProtein DomainsProtein TransportCaenorhabditis elegans ProteinsCollagenGreen Fluorescent ProteinsMembrane Proteinstmem-131 protein, C elegansTRAPPC8 protein, humanVesicular Transport Proteins

Identifiers

PMID32095531
PMCPMC7015688
OpenAlexW3005874143

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.