Evidence map›Paper›PMID 23047063›Full record

ArticleRNA biology2012

A novel molecular mechanism in human genetic disease: a DNA repeat-derived lncRNA.

Daphne S Cabianca, Valentina Casa, Davide Gabellini

Open access · bronzeAbstract read
In one paragraph

Article in RNA biology, 2012. 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
1.0field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Focus on PD-1/PD-L1 as a Therapeutic Target in Ovarian Cancer.International journal of molecular sciences · 2022
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Functional role of lncRNA DB327252 in lung cancer.Journal of thoracic disease · 2016
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. 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

3 authors at 2 institutions in 1 country.

Daphne S CabiancaDulbecco Telethon Institute and Division of Regenerative Medicine, Stem cells, and Gene therapy, San Raffaele Scientific Institute, Milan, Italy.
Valentina Casa
Davide Gabellini
San Raffaele University of Rome · ITThe San Raffaele Telethon Institute for Gene Therapy · IT

Funding

European Research Council 204279Telethon TCR11003
6 · The paper itself

Abstract

Two thirds of the human genome is composed of repetitive sequences. Despite their prevalence, DNA repeats are largely ignored. The vast majority of our genome is transcribed to produce non protein-coding RNAs. Among these, long non protein-coding RNAs represent the most prevalent and functionally diverse class. The relevance of the non protein-coding genome to human disease has mainly been studied regarding the altered microRNA expression and function in human cancer. On the contrary, the elucidation of the involvement of long non-coding RNAs in disease is only in its infancy. We have recently found that a chromatin associated, long non protein-coding RNA regulates a Polycomb/Trithorax epigenetic switch at the basis of the repeat associated facioscapulohumeral muscular dystrophy, a common muscle disorder. Based on this, we propose that long non-coding RNAs produced by repetitive sequences contribute in shaping the epigenetic landscape in normal human physiology and in disease.

Indexed as

Epigenesis, GeneticChromatinDNAGenome, HumanHistone-Lysine N-MethyltransferaseHumansMuscle, SkeletalMuscular Dystrophy, FacioscapulohumeralMyeloid-Lymphoid Leukemia ProteinPolycomb-Group ProteinsRepetitive Sequences, Nucleic AcidRNA, Long NoncodingChromatinDNAHistone-Lysine N-MethyltransferaseKMT2A protein, humanMyeloid-Lymphoid Leukemia ProteinPolycomb-Group ProteinsRNA, Long Noncodingchromatinmuscular dystrophynon protein-coding RNApolycombrepetitive elementtrithorax

Identifiers

PMID23047063
PMCPMC3583850
OpenAlexW2610499739

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.