Evidence map›Paper›PMID 18550849›Full record

ArticleBlood2008

HES1 is a novel interactor of the Fanconi anemia core complex.

Cédric S Tremblay, Feng F Huang, Ouassila Habi, Caroline C Huard, Chantal Godin, Georges Lévesque, Madeleine Carreau

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Blood, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

34 citing papers in PubMed, 60 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. The Fanconi anemia pathway has a dual function in Dickkopf-1 transcriptional repression.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Cédric S TremblayUnité de recherche en Pédiatrie, Centre de recherche du Centre Hospitalier de l'Université Laval, Québec, Canada.
Feng F Huang
Ouassila Habi
Caroline C Huard
Chantal Godin
Georges Lévesque
Madeleine Carreau
Centre hospitalier de l'Université Laval · CATechnologie Médicale (France) · FRUniversité Laval · CA

Funding

CIHR 64309
6 · The paper itself

Abstract

Fanconi anemia (FA) proteins are thought to play a role in chromosome stability and repair of DNA cross-links; however, these functions may not fully explain the developmental abnormalities and bone marrow failure that are characteristic of FA individuals. Here we associate the FA proteins with the Notch1 developmental pathway through a direct protein-protein interaction between the FA core complex and the hairy enhancer of split 1 (HES1). HES1 interaction with FA core complex members is dependent on a functional FA pathway. Cells depleted of HES1 exhibit an FA-like phenotype that includes cellular hypersensitivity to mitomycin C (MMC) and lack of FANCD2 monoubiquitination and foci formation. HES1 is also required for proper nuclear localization or stability of some members of the core complex. Our results suggest that HES1 is a novel interacting protein of the FA core complex.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCell LineCell Line, TransformedDrug ResistanceFanconi AnemiaFanconi Anemia Complementation Group C ProteinFanconi Anemia Complementation Group ProteinsHeLa CellsHomeodomain ProteinsHumansMiceMice, KnockoutMitomycinMultiprotein ComplexesProtein BindingBasic Helix-Loop-Helix ProteinsFancc protein, mouseFanconi Anemia Complementation Group C ProteinFanconi Anemia Complementation Group ProteinsHES1 protein, humanHes1 protein, mouseHomeodomain ProteinsMitomycinMultiprotein ComplexesNOTCH1 protein, humanReceptor, Notch1Recombinant ProteinsRNA, Small InterferingTranscription Factor HES-1

Identifiers

PMID18550849
PMCPMC5154739
OpenAlexW1985479322

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.