Evidence map›Paper›PMID 29789608›Full record

ArticleScientific reports2018

Downregulation of Endothelin Receptor B Contributes to Defective B Cell Lymphopoiesis in Trisomy 21 Pluripotent Stem Cells.

Glenn A MacLean, Jennifer McEldoon, Jialiang Huang, Jeremy Allred, Matthew C Canver, Stuart H Orkin

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

18 citing papers in PubMed, 19 citations in OpenAlex.

  1. Modeling human B cell development with pluripotent stem cells.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Leukemogenesis in infants and young children with trisomy 21.Hematology. American Society of Hematology. Education Program · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. 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

6 authors at 4 institutions in 1 country.

Glenn A MacLeanDivision of Hematology/Oncology, Boston Children's Hospital and Dana Farber Cancer Institute, Harvard Medical School Boston, MA, 02115, Boston, USA.
Jennifer McEldoonDivision of Hematology/Oncology, Boston Children's Hospital and Dana Farber Cancer Institute, Harvard Medical School Boston, MA, 02115, Boston, USA.
Jialiang HuangDivision of Hematology/Oncology, Boston Children's Hospital and Dana Farber Cancer Institute, Harvard Medical School Boston, MA, 02115, Boston, USA.
Jeremy AllredDivision of Hematology/Oncology, Boston Children's Hospital and Dana Farber Cancer Institute, Harvard Medical School Boston, MA, 02115, Boston, USA.
Matthew C CanverDivision of Hematology/Oncology, Boston Children's Hospital and Dana Farber Cancer Institute, Harvard Medical School Boston, MA, 02115, Boston, USA.
Stuart H OrkinDivision of Hematology/Oncology, Boston Children's Hospital and Dana Farber Cancer Institute, Harvard Medical School Boston, MA, 02115, Boston, USA. stuart_orkin@dfci.harvard.edu.
Boston University · USDana-Farber Cancer Institute · USBoston Children's Hospital · USHarvard University · US

Funding

Human Pluripotent Stem Cell and Progenitor Models of Cardiac and Blood DiseasesU01HL100001 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI DALEY, GEORGE Q, ORKIN, STUART H · 2009 to 2015
$8.9M
NHLBI NIH HHS U01 HL100001
6 · The paper itself

Abstract

Individuals with Trisomy 21 (T21) exhibit numerous hematological abnormalities, including reductions in numbers of circulating B and T lymphocytes. To elucidate molecular mechanisms underlying these phenotypes, we differentiated human isogenic disomic and trisomic pluripotent cells, and observed that trisomic cells showed defects in B cell, but not T cell differentiation. Global gene expression of differentiated, trisomic B cells revealed reduced expression of genes encoding endothelin signaling components, namely the Endothelin Receptor B (EDNRB), and its ligand Endothelin1 (EDN1). Depletion of EDNRB mRNA in cord blood-derived CD34

Indexed as

B-LymphocytesCell DifferentiationCells, CulturedDown-RegulationDown SyndromeEndothelin-1Gene Expression ProfilingHEK293 CellsHematopoiesisHumansInduced Pluripotent Stem CellsLymphopoiesisMicroarray AnalysisReceptor, Endothelin BEDNRB protein, humanEndothelin-1Receptor, Endothelin B

Identifiers

PMID29789608
PMCPMC5964225
OpenAlexW2803569299

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.