Evidence map›Paper›PMID 28348230›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Deficiency of transcription factor RelB perturbs myeloid and DC development by hematopoietic-extrinsic mechanisms.

Carlos G Briseño, Marco Gargaro, Vivek Durai, Jesse T Davidson, Derek J Theisen, David A Anderson, Deborah V Novack, Theresa L Murphy, Kenneth M Murphy

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

22 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. New insights into the Lck-NF-κB signaling pathway.Frontiers in cell and developmental biology · 2023
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Epidermal resident γδ T cell development and function in skin.Cellular and molecular life sciences : CMLS · 2021
    Review
  14. Article
  15. TAO-kinase 3 governs the terminal differentiation of NOTCH2-dependent splenic conventional dendritic cells.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Development, Diversity, and Function of Dendritic Cells in Mouse and Human.Cold Spring Harbor perspectives in biology · 2018
    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

9 authors at 1 institution in 1 country.

Carlos G BriseñoDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110.
Marco GargaroDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110.
Vivek DuraiDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110.
Jesse T DavidsonDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110.
Derek J TheisenDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110.
David A AndersonDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110.
Deborah V NovackDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110.
Theresa L MurphyDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110.
Kenneth M MurphyDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110; kmurphy@wustl.edu.
Washington University in St. Louis · US

Funding

TRAINING PROGRAM IN IMMUNOLOGY AND IMMUNOGENETICST32AI007163 · NIAID · WASHINGTON UNIVERSITY · PI Kenneth M Murphy, Kodi S Ravichandran · 1985 to 2026
$14.8M
SURGICAL ONCOLOGY TRAINING GRANTT32CA009621 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN, William E. Gillanders · 1988 to 2026
$12.9M
NF-kB SUBUNITS p65 AND RelB IN OSTEOCLASTSR01AR052705 · NIAMS · WASHINGTON UNIVERSITY · PI VEIS, DEBORAH J · 2006 to 2015
$3.0M
The role of cross-presentation of self-antigens by dendritic cells in type 1 diabetesF30DK108498 · NIDDK · WASHINGTON UNIVERSITY · PI DURAI, VIVEK · 2015 to 2017
$109k
Howard Hughes Medical InstituteNCI NIH HHS T32 CA009621NIAID NIH HHS T32 AI007163NIAMS NIH HHS R01 AR052705NIDDK NIH HHS F30 DK108498
6 · The paper itself

Abstract

RelB is an NF-κB family transcription factor activated in the noncanonical pathway downstream of NF-κB-inducing kinase (NIK) and TNF receptor family members including lymphotoxin-β receptor (LTβR) and CD40. Early analysis suggested that RelB is required for classical dendritic cell (cDC) development based on a severe reduction of cDCs in

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDendritic CellsHematopoietic SystemLymphotoxin-betaLymphotoxin beta ReceptorMice, Inbred C57BLMice, Mutant StrainsMyeloid CellsNF-kappaB-Inducing KinaseProtein Serine-Threonine KinasesSpleenTranscription Factor RelBLtbr protein, mouseLymphotoxin-betaLymphotoxin beta ReceptorNF-kappaB-Inducing KinaseProtein Serine-Threonine KinasesRelb protein, mouseTranscription Factor RelBdendritic cellshematopoiesishematopoietic nichetranscription factors

Identifiers

PMID28348230
PMCPMC5393217
OpenAlexW2597588685

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.