Evidence map›Paper›PMID 29991556›Full record

ArticleBlood2018

Single-cell approaches identify the molecular network driving malignant hematopoietic stem cell self-renewal.

Mairi S Shepherd, Juan Li, Nicola K Wilson, Caroline A Oedekoven, Jiangbing Li, Miriam Belmonte, Juergen Fink, Janine C M Prick, Dean C Pask, Tina L Hamilton and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Single-cell Technology in Stem Cell Research.Current stem cell research & therapy · 2025
    Review
  6. Article
  7. Article
  8. PBX1: a TALE of two seasons-key roles during development and in cancer.Frontiers in cell and developmental biology · 2024
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Epigenetic Dysregulation of Myeloproliferative Neoplasms.Hematology/oncology clinics of North America · 2021
    Review
  16. Review
  17. Review
  18. Extensive exploration of T cell heterogeneity in cancers by single cell sequencing.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2019
    Article
  19. Article
  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

16 authors at 3 institutions in 4 countries.

Mairi S ShepherdWellcome MRC Cambridge Stem Cell Institute and.ORCID 0000-0002-4328-9882
Juan LiWellcome MRC Cambridge Stem Cell Institute and.
Nicola K WilsonWellcome MRC Cambridge Stem Cell Institute and.ORCID 0000-0003-0865-7333
Caroline A OedekovenWellcome MRC Cambridge Stem Cell Institute and.ORCID 0000-0002-2309-2097
Jiangbing LiWellcome MRC Cambridge Stem Cell Institute and.
Miriam BelmonteWellcome MRC Cambridge Stem Cell Institute and.
Juergen FinkWellcome MRC Cambridge Stem Cell Institute and.
Janine C M PrickWellcome MRC Cambridge Stem Cell Institute and.
Dean C PaskWellcome MRC Cambridge Stem Cell Institute and.
Tina L HamiltonWellcome MRC Cambridge Stem Cell Institute and.
Dirk LoefflerDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland; and.
Anjana RaoLa Jolla Institute and Department of Pharmacology, University of California, San Diego, La Jolla, CA.
Timm SchröderDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland; and.ORCID 0000-0001-9320-0252
Berthold GöttgensWellcome MRC Cambridge Stem Cell Institute and.ORCID 0000-0001-6302-5705
Anthony R GreenWellcome MRC Cambridge Stem Cell Institute and.ORCID 0000-0002-9795-0218
David G KentWellcome MRC Cambridge Stem Cell Institute and.ORCID 0000-0001-7871-8811
Wellcome/MRC Cambridge Stem Cell Institute · GBETH Zurich · CHLa Jolla Institute for Immunology · US

Funding

Biotechnology and Biological Sciences Research CouncilCancer Research UK 21762Medical Research Council MC_PC_12009Medical Research Council MR/M008975/1Medical Research Council MR/S036113/1Wellcome Trust
6 · The paper itself

Abstract

Recent advances in single-cell technologies have permitted the investigation of heterogeneous cell populations at previously unattainable resolution. Here we apply such approaches to resolve the molecular mechanisms driving disease in mouse hematopoietic stem cells (HSCs), using JAK2V617F mutant myeloproliferative neoplasms (MPNs) as a model. Single-cell gene expression and functional assays identified a subset of JAK2V617F mutant HSCs that display defective self-renewal. This defect is rescued at the single HSC level by crossing JAK2V617F mice with mice lacking TET2, the most commonly comutated gene in patients with MPN. Single-cell gene expression profiling of JAK2V617F-mutant HSCs revealed a loss of specific regulator genes, some of which were restored to normal levels in single TET2/JAK2 mutant HSCs. Of these,

Indexed as

Cell Self RenewalGene Expression Regulation, NeoplasticMutation, MissenseAmino Acid SubstitutionAnimalsHematologic NeoplasmsHematopoietic Stem CellsJanus Kinase 2MiceMice, TransgenicMyeloproliferative DisordersNeoplasm ProteinsNeoplastic Stem CellsJak2 protein, mouseJanus Kinase 2Neoplasm Proteins

Identifiers

PMID29991556
PMCPMC6107881
OpenAlexW2831177253

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.