Evidence map›Paper›PMID 21615334›Full record

ReviewThe Biochemical journal2011

ATR signalling: more than meeting at the fork.

Edward A Nam, David Cortez

Abstract readReview
In one paragraph

Review in The Biochemical journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 185 papers.

0numbers the graph read from it
0cells of the map it votes in
185citing papers in PubMed
12.9field-weighted citation impact, top 1% 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

185 citing papers in PubMed, 302 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. DNA damage and repair in cardiomyopathy: mechanisms and therapeutic opportunities.American journal of physiology. Heart and circulatory physiology · 2026
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

125 more citing papers are in PubMed but not listed here.

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.

Edward A NamDepartment of Biochemistry, Vanderbilt University School of Medicine, 613 Light Hall, 2215 Garland Avenue, Nashville, TN 37232, USA.
David Cortez
Vanderbilt University · US

Funding

Function of the ATR-ATRIP ComplexR01CA102729 · NCI · VANDERBILT UNIVERSITY · PI CORTEZ, DAVID K · 2003 to 2018
$4.2M
NCI NIH HHS CA102729NCI NIH HHS R01 CA102729
6 · The paper itself

Abstract

Preservation of genome integrity via the DNA-damage response is critical to prevent disease. ATR (ataxia telangiectasia mutated- and Rad3-related) is essential for life and functions as a master regulator of the DNA-damage response, especially during DNA replication. ATR controls and co-ordinates DNA replication origin firing, replication fork stability, cell cycle checkpoints and DNA repair. Since its identification 15 years ago, a model of ATR activation and signalling has emerged that involves localization to sites of DNA damage and activation through protein-protein interactions. Recent research has added an increasingly detailed understanding of the canonical ATR pathway, and an appreciation that the canonical model does not fully capture the complexity of ATR regulation. In the present article, we review the ATR signalling process, focusing on mechanistic findings garnered from the identification of new ATR-interacting proteins and substrates. We discuss how to incorporate these new insights into a model of ATR regulation and point out the significant gaps in our understanding of this essential genome-maintenance pathway.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAtaxia TelangiectasiaAtaxia Telangiectasia Mutated ProteinsBH3 Interacting Domain Death Agonist ProteinCarrier ProteinsCell Cycle ProteinsDNA-Binding ProteinsDNA DamageDNA HelicasesDNA RepairFanconi Anemia Complementation Group ProteinsHumansMutL Protein Homolog 1MutS DNA Mismatch-Binding ProteinNuclear ProteinsAdaptor Proteins, Signal TransducingAtaxia Telangiectasia Mutated ProteinsATRIP protein, humanATR protein, humanBH3 Interacting Domain Death Agonist ProteinBID protein, humanCarrier ProteinsCDC6 protein, humanCell Cycle ProteinsDNA-Binding ProteinsDNA HelicasesETV7 protein, humanFAAP24 protein, humanFANCM protein, humanFanconi Anemia Complementation Group ProteinsMLH1 protein, humanMutL Protein Homolog 1MutS DNA Mismatch-Binding ProteinNuclear ProteinsProtein Serine-Threonine KinasesProto-Oncogene Proteins c-etsTOPBP1 protein, human

Identifiers

PMID21615334
PMCPMC3678388
OpenAlexW2155650828

What OpenQuestion holds

Textmetadata
LicenceTDM
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.