Evidence map›Paper›PMID 24938228›Full record

ReviewMolecules and cells2014

Nuclease delivery: versatile functions of SLX4/FANCP in genome maintenance.

Yonghwan Kim

Open access · diamondAbstract readReview
In one paragraph

Review in Molecules and cells, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Rescue from replication stress during mitosis.Cell cycle (Georgetown, Tex.) · 2017
    Review
  10. The SMX DNA Repair Tri-nuclease.Molecular cell · 2017
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. SLX4 gains weight with SUMO in genome maintenance.Molecular & cellular oncology · 2016
    Article
  16. Article
  17. 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

1 author at 1 institution in 1 country.

Yonghwan KimDepartment of Life Systems, Sookmyung Women's University, Seoul 140-742, Korea.
Sookmyung Women's University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a scaffold, SLX4/FANCP interacts with multiple proteins involved in genome integrity. Although not having recognizable catalytic domains, SLX4 participates in diverse genome maintenance pathways by delivering nucleases where they are needed, and promoting their cooperative execution to prevent genomic instabilities. Physiological importance of SLX4 is emphasized by the identification of causative mutations of SLX4 genes in patients diagnosed with Fanconi anemia (FA), a rare recessive genetic disorder characterized by genomic instability and predisposition to cancers. Recent progress in understanding functional roles of SLX4 has greatly expanded our knowledge in the repair of DNA interstrand crosslinks (ICLs), Holliday junction (HJ) resolution, telomere homeostasis and regulation of DNA damage response induced by replication stress. Here, these diverse functions of SLX4 are reviewed in detail.

Indexed as

DNA RepairDNA ReplicationGenome, HumanAnimalsDNA, CruciformDNA DamageFanconi AnemiaGenomic InstabilityHumansMutationProtein BindingProtein Interaction MappingRecombinasesSaccharomyces cerevisiaeSchizosaccharomycesTelomere HomeostasisDNA, CruciformRecombinasesSLX4 protein, humanfanconi anemiaHolliday junctionICL repairSLX4/FANCPtelomere maintenance

Identifiers

PMID24938228
PMCPMC4145367
OpenAlexW1990468205

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.