Evidence map›Paper›PMID 29950492›Full record

ArticleGenes & development2018

The C9orf72-interacting protein Smcr8 is a negative regulator of autoimmunity and lysosomal exocytosis.

Yingying Zhang, Aaron Burberry, Jin-Yuan Wang, Jackson Sandoe, Sulagna Ghosh, Namrata D Udeshi, Tanya Svinkina, Daniel A Mordes, Joanie Mok, Maura Charlton and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
–field-weighted citation impact
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

48 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Defective Lamtor5 Leads to Autoimmunity by Deregulating v-ATPase and Lysosomal Acidification.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  6. Endosomal Toll-Like Receptors as Therapeutic Targets for Autoimmune Diseases.Advances in experimental medicine and biology · 2024
    Article
  7. Review
  8. ALS-linked C9orf72-SMCR8 complex is a negative regulator of primary ciliogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. The progress inSmall GTPases · 2022
    Review
  18. Review
  19. Review
  20. 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

13 authors at 5 institutions in 1 country.

Yingying ZhangDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Aaron BurberryDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Jin-Yuan WangDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Jackson SandoeDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Sulagna GhoshDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Namrata D UdeshiProteomics Platform, Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Tanya SvinkinaProteomics Platform, Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Daniel A MordesDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Joanie MokDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Maura CharltonDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Quan-Zhen LiDepartment of Immunology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Steven A CarrProteomics Platform, Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Kevin EgganDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Broad Institute · USHarvard University · USMassachusetts Institute of Technology · USMassachusetts General Hospital · USThe University of Texas Southwestern Medical Center · US

Funding

C9ORF72 in Motor System Biology and ALSR01NS089742 · NINDS · HARVARD UNIVERSITY · PI EGGAN, KEVIN C · 2014 to 2018
$2.3M
NINDS NIH HHS R01 NS089742
6 · The paper itself

Abstract

While a mutation in

Indexed as

Amyotrophic Lateral SclerosisAnimalsAutoimmunityC9orf72 ProteinCarrier ProteinsExocytosisGene Expression RegulationHumansLymph NodesLysosomal-Associated Membrane Protein 1LysosomesMacrophagesMiceMice, KnockoutMutationProtein IsoformsC9orf72 ProteinCarrier ProteinsLysosomal-Associated Membrane Protein 1Protein IsoformsSMCR8 protein, mouseamyotrophic lateral sclerosis (ALS)autoimmunityautophagyC9ORF72lysosomeSMCR8

Identifiers

PMID29950492
PMCPMC6075033
OpenAlexW2810520726

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.