Evidence map›Paper›PMID 22538718›Full record

ArticleNature genetics2012

Photosensitivity syndrome brings to light a new transcription-coupled DNA repair cofactor.

James E Cleaver

Abstract readComment
PubMed Publisher
In one paragraph

Article in Nature genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 24 citations in OpenAlex.

  1. Cancer and stem cells.Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Hypomorphic PCNA mutation underlies a human DNA repair disorder.The Journal of clinical investigation · 2014
    Article
  7. Article
  8. Review
  9. Genome stability pathways in head and neck cancers.International journal of genomics · 2013
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

James E CleaverDepartment of Dermatology, University of California, San Francisco, California, USA. jcleaver@cc.ucsf.edu
University of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Three teams have applied whole-exome and proteome methods to identify a new cofactor of human RNA polymerase II that is required for the recovery of transcription on damaged templates. The identification of this new factor raises questions about the causal relationships between molecular mechanisms of transcription regulation and excision repair and developmental and neurological disease and nonmalignant skin photosensitivity.

Indexed as

Transcription, GeneticUltraviolet RaysCarrier ProteinsCockayne SyndromeDNA DamageDNA HelicasesDNA RepairDNA Repair EnzymesHumansMutationPoly-ADP-Ribose Binding ProteinsProtein StabilityRNA Polymerase IIUbiquitinUbiquitin-Specific Peptidase 7Ubiquitin ThiolesteraseCarrier ProteinsDNA HelicasesDNA Repair EnzymesERCC6 protein, humanPoly-ADP-Ribose Binding ProteinsRNA Polymerase IIUbiquitinUbiquitin-Specific Peptidase 7Ubiquitin ThiolesteraseUSP7 protein, humanUVSSA protein, human

Identifiers

PMID22538718
OpenAlexW2021565974

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.