Evidence map›Paper›PMID 24765528›Full record

ReviewF1000prime reports2014

Fanconi anemia and the cell cycle: new perspectives on aneuploidy.

Grzegorz Nalepa, D Wade Clapp

Open access · bronzeAbstract readReview
In one paragraph

Review in F1000prime reports, 2014. 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
2.0field-weighted citation impact, top 14% 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, 30 citations in OpenAlex.

  1. Review
  2. bioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Article
  5. Focal Point of Fanconi Anemia Signaling.International journal of molecular sciences · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Impact of DNA repair and stability defects on cortical development.Cellular and molecular life sciences : CMLS · 2018
    Review
  11. Lipidomic Profiling Links the Fanconi Anemia Pathway to Glycosphingolipid Metabolism in Head and Neck Cancer Cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  12. DNA helix: the importance of being AT-rich.Mammalian genome : official journal of the International Mammalian Genome Society · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. What is wrong with Fanconi anemia cells?Cell cycle (Georgetown, Tex.) · 2014
    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

2 authors at 1 institution in 1 country.

Grzegorz NalepaDepartment of Pediatrics, Indiana University School of Medicine, Riley Hospital for Children 705 Riley Hospital Drive, Indianapolis, IN 46202 USA ; Division of Pediatric Hematology-Oncology, Indiana University School of Medicine, Riley Hospital for Children 705 Riley Hospital Drive, Indianapolis, IN 46202 USA ; Department of Medical and Molecular Genetics, Wells Center for Pediatric Research 1044 W. Walnut Street, Indiana University School of Medicine, Indianapolis, IN 46202 USA.
D Wade ClappDepartment of Pediatrics, Indiana University School of Medicine, Riley Hospital for Children 705 Riley Hospital Drive, Indianapolis, IN 46202 USA ; Department of Medical and Molecular Genetics, Wells Center for Pediatric Research 1044 W. Walnut Street, Indiana University School of Medicine, Indianapolis, IN 46202 USA ; Department of Microbiology and Immunology, Wells Center for Pediatric Research 1044 W. Walnut Street, Indiana University School of Medicine, Indianapolis, IN 46202 USA ; Department of Biochemistry and Molecular Biology, Wells Center for Pediatric Research 1044 W. Walnut Street, Indiana University School of Medicine, Indianapolis, IN 46202 USA.
Indiana University Bloomington · US

Funding

Fanconi Anemia stem cells allow molecular characterization of acute leukemiaR01CA138237 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI BAGBY, GROVER CARLTON, CLAPP, DAVID W · 2008 to 2012
$1.9M
Indiana Pediatric Scientist Award(IPSA)K12HD068371 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI CLAPP, DAVID W · 2013 to 2017
$1.9M
Genetic Therapy for Fanconi AnemiaR01CA155294 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI CLAPP, DAVID W, HANENBERG, HELMUT · 2011 to 2015
$1.6M
NCI NIH HHS R01 CA138237NCI NIH HHS R01 CA155294NICHD NIH HHS K12 HD068371
6 · The paper itself

Abstract

Fanconi anemia (FA) is a complex heterogenic disorder of genomic instability, bone marrow failure, cancer predisposition, and congenital malformations. The FA signaling network orchestrates the DNA damage recognition and repair in interphase as well as proper execution of mitosis. Loss of FA signaling causes chromosome instability by weakening the spindle assembly checkpoint, disrupting centrosome maintenance, disturbing resolution of ultrafine anaphase bridges, and dysregulating cytokinesis. Thus, the FA genes function as guardians of genome stability throughout the cell cycle. This review discusses recent advances in diagnosis and clinical management of Fanconi anemia and presents the new insights into the origins of genomic instability in FA. These new discoveries may facilitate the development of rational therapeutic strategies for FA and for FA-deficient malignancies in the general population.

Identifiers

PMID24765528
PMCPMC3974572
OpenAlexW2008881929

What OpenQuestion holds

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LicenceCC BY-NC
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.