Evidence map›Paper›PMID 31504503›Full record

ArticleHuman molecular genetics2019

Amyotrophic lateral sclerosis-associated TDP-43 mutation Q331K prevents nuclear translocation of XRCC4-DNA ligase 4 complex and is linked to genome damage-mediated neuronal apoptosis.

Erika N Guerrero, Joy Mitra, Haibo Wang, Suganya Rangaswamy, Pavana M Hegde, Priyadarshini Basu, K S Rao, Muralidhar L Hegde

Abstract readPublished Erratum
In one paragraph

Article in Human molecular genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Trends in Understanding the Pathological Roles of TDP-43 and FUS Proteins.Advances in experimental medicine and biology · 2021
    Article
  9. Review
  10. DNA double-strand breaks: a potential therapeutic target for neurodegenerative diseases.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2019
    Review
  11. Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Erika N GuerreroDepartment of Radiation Oncology, Houston Methodist Research Institute, Houston, TX 77030, USA.
Joy MitraDepartment of Radiation Oncology, Houston Methodist Research Institute, Houston, TX 77030, USA.
Haibo WangDepartment of Radiation Oncology, Houston Methodist Research Institute, Houston, TX 77030, USA.
Suganya RangaswamyDepartment of Radiation Oncology, Houston Methodist Research Institute, Houston, TX 77030, USA.
Pavana M HegdeDepartment of Radiation Oncology, Houston Methodist Research Institute, Houston, TX 77030, USA.
Priyadarshini BasuDepartment of Radiation Oncology, Houston Methodist Research Institute, Houston, TX 77030, USA.
K S RaoCenter for Neuroscience, Instituto de Investigaciones Científicas y Servicios de Alta Tecnología (INDICASAT AIP), City of Knowledge, Republic of Panama.
Muralidhar L HegdeDepartment of Radiation Oncology, Houston Methodist Research Institute, Houston, TX 77030, USA.

Funding

Etiological Linkage of DNA Damage/Repair Deficiency in Neurodegenerative DiseasesR01NS088645 · NINDS · METHODIST HOSPITAL RESEARCH INSTITUTE · PI HEGDE, MURALIDHAR L · 2015 to 2019
$1.8M
NINDS NIH HHS R01 NS088645
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID31504503
PMCPMC6867871

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.