Evidence map›Paper›PMID 29802403›Full record

ArticleNature cell biology2018

Single-cell analysis identifies a CD33

David J H F Knapp, Colin A Hammond, Tony Hui, Marijn T J van Loenhout, Fangwu Wang, Nima Aghaeepour, Paul H Miller, Michelle Moksa, Gabrielle M Rabu, Philip A Beer and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Cell Lineage Affiliation During Hematopoiesis.International journal of molecular sciences · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Hematopoietic Stem Cells and the Immune System in Development and Aging.International journal of molecular sciences · 2023
    Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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

15 authors.

David J H F KnappTerry Fox Laboratory, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
Colin A HammondTerry Fox Laboratory, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
Tony HuiMichael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada.
Marijn T J van LoenhoutMichael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada.
Fangwu WangTerry Fox Laboratory, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
Nima AghaeepourBaxter Laboratory for Stem Cell Biology Department of Microbiology & Immunology, Stanford University, Palo Alto, CA, USA.
Paul H MillerTerry Fox Laboratory, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
Michelle MoksaMichael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada.
Gabrielle M RabuTerry Fox Laboratory, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
Philip A BeerTerry Fox Laboratory, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
Davide PellacaniTerry Fox Laboratory, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
R Keith HumphriesTerry Fox Laboratory, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
Carl HansenMichael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada.
Martin HirstMichael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada.ORCID http://orcid.org/0000-0001-9136-9054
Connie J EavesTerry Fox Laboratory, British Columbia Cancer Agency, Vancouver, British Columbia, Canada. ceaves@bccrc.ca.ORCID http://orcid.org/0000-0002-3452-1926

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elucidation of the identity and diversity of mechanisms that sustain long-term human blood cell production remains an important challenge. Previous studies indicate that, in adult mice, this property is vested in cells identified uniquely by their ability to clonally regenerate detectable, albeit highly variable levels and types, of mature blood cells in serially transplanted recipients. From a multi-parameter analysis of the molecular features of very primitive human cord blood cells that display long-term cell outputs in vitro and in immunodeficient mice, we identified a prospectively separable CD33

Indexed as

Cell ProliferationMitosisAnimalsBiomarkersCell SeparationCord Blood Stem Cell TransplantationDNA MethylationFemaleFetal BloodFlow CytometryGene Expression ProfilingGene Expression Regulation, DevelopmentalGenotypeHumansMaleMice, TransgenicBiomarkersCD33 protein, humanSialic Acid Binding Ig-like Lectin 3

Identifiers

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.