Evidence map›Paper›PMID 29804746›Full record

ArticleTrends in genetics : TIG2018

Long-Distance Relationships: Suppression of Repeat-Mediated Deletions.

Maria E Morales, Tiffany Kaul, Prescott Deininger

Abstract readComment
In one paragraph

Article in Trends in genetics : TIG, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Maria E MoralesTulane Cancer Center, Tulane University, New Orleans, LA 70122, USA.
Tiffany KaulTulane Cancer Center, Tulane University, New Orleans, LA 70122, USA.
Prescott DeiningerTulane Cancer Center, Tulane University, New Orleans, LA 70122, USA. Electronic address: pdeinin@tulane.edu.

Funding

The diverse influences of Alu elements on human genetic instabilityR01GM121812 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI DEININGER, PRESCOTT L. · 2017 to 2020
$1.3M
NIGMS NIH HHS R01 GM121812
6 · The paper itself

Abstract

The high proportion of repetitive DNA sequences in the human genome provides tremendous opportunities for DNA rearrangements between non-allelic repetitive elements. The genome must use multiple competing and collaborating repair mechanisms to minimize these types of DNA rearrangements, some of which fail in cancer cells where DNA repair pathways are suppressed.

Indexed as

Chromosome BreakageRepetitive Sequences, Nucleic AcidDNA RepairGenome, HumanHumansSequence Deletion

Identifiers

PMID29804746
PMCPMC6054550

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.