Evidence map›Paper›PMID 16352715›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

Two types of precursor cells in a multipotential hematopoietic cell line.

Zhi-jia Ye, Yuval Kluger, Zheng Lian, Sherman M Weissman

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. An integrated global regulatory network of hematopoietic precursor cell self-renewal and differentiation.Integrative biology : quantitative biosciences from nano to macro · 2018
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. A CO-FISH assay to assess sister chromatid segregation patterns in mitosis of mouse embryonic stem cells.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2013
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Complex interactions in EML cell stimulation by stem cell factor and IL-3.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  17. Article
  18. Modeling the clonal heterogeneity of stem cells.Theoretical biology & medical modelling · 2010
    Article
  19. Identification of markers for newly formed beta-cells in the perinatal period: a time of recognized beta-cell immaturity.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2010
    Article
  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

4 authors at 2 institutions in 1 country.

Zhi-jia YeDepartment of Genetics, Yale University School of Medicine, New Haven, CT 06519, USA.
Yuval Kluger
Zheng Lian
Sherman M Weissman
New York University · USYale University · US

Funding

Global Analysis of Chromatin during Lineage DevelopmentR01AG023111 · NIA · YALE UNIVERSITY · PI WEISSMAN, SHERMAN MORTON · 2004 to 2009
$2.9M
NHLBI PROTEOMICS INITIATIVE-N01HV28186N01HV028186 · HV · YALE UNIVERSITY · PI WILLIAMS, KENNETH · 2002 to 2006
–
NHLBI NIH HHS N01 HV028186NHLBI NIH HHS N01-HV-28186NIA NIH HHS 1R01 AG23111-02NIA NIH HHS R01 AG023111
6 · The paper itself

Abstract

The biochemistry of early stages of hematopoietic differentiation is difficult to study because only relatively small numbers of precursor cells are available. The murine EML cell line is a multipotential cell line that can be used to model some of these steps. We found that the lineage- EML precursor cells can be separated into two populations based on cell surface markers including CD34. Both populations contain similar levels of stem cell factor (SCF) receptor (c-Kit) but only the CD34+ population shows a growth response when treated with SCF. Conversely, the CD34- population will grow in the presence of the cytokine IL-3. The human beta-globin locus control region hypersensitive site 2 plays different roles on beta-globin transcription in the CD34+ and CD34- populations. The two populations are present in about equal amounts in culture, and the CD34+ population rapidly regenerates the mixed population when grown in the presence of SCF. We suggest that this system may mimic a normal developmental transition in hematopoiesis.

Indexed as

Cell DifferentiationAnimalsAntigens, CD34Cell LineGene Expression ProfilingGene Expression RegulationGlobinsHematopoietic Stem CellsMiceMultipotent Stem CellsOligonucleotide Array Sequence AnalysisPhosphorylationProtein BindingProto-Oncogene Proteins c-kitReceptors, Interleukin-3Transcription FactorsAntigens, CD34GlobinsProto-Oncogene Proteins c-kitReceptors, Interleukin-3Transcription Factors

Identifiers

PMID16352715
PMCPMC1317970
OpenAlexW2049849095

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.