Evidence map›Paper›PMID 24616662›Full record

ReviewFrontiers in cellular neuroscience2014

Non-coding RNAs in chromatin disease involving neurological defects.

Floriana Della Ragione, Miriam Gagliardi, Maurizio D'Esposito, Maria R Matarazzo

Abstract readReview
In one paragraph

Review in Frontiers in cellular neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Editorial for "Regulatory RNAs in the nervous system".Frontiers in cellular neuroscience · 2015
    Article
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

4 authors.

Floriana Della RagioneFunctional Genomics and Epigenomics Laboratory, Institute of Genetics and Biophysics "ABT," Consiglio Nazionale delle Ricerche Naples, Italy ; Laboratorio di Genomica e di Epigenomica, Istituto di Ricovero e Cura a Carattere Scientifico Neuromed Pozzilli, Italy.
Miriam GagliardiFunctional Genomics and Epigenomics Laboratory, Institute of Genetics and Biophysics "ABT," Consiglio Nazionale delle Ricerche Naples, Italy ; Laboratorio di Genomica e di Epigenomica, Istituto di Ricovero e Cura a Carattere Scientifico Neuromed Pozzilli, Italy.
Maurizio D'EspositoFunctional Genomics and Epigenomics Laboratory, Institute of Genetics and Biophysics "ABT," Consiglio Nazionale delle Ricerche Naples, Italy ; Laboratorio di Genomica e di Epigenomica, Istituto di Ricovero e Cura a Carattere Scientifico Neuromed Pozzilli, Italy.
Maria R MatarazzoFunctional Genomics and Epigenomics Laboratory, Institute of Genetics and Biophysics "ABT," Consiglio Nazionale delle Ricerche Naples, Italy ; Laboratorio di Genomica e di Epigenomica, Istituto di Ricovero e Cura a Carattere Scientifico Neuromed Pozzilli, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Novel classes of small and long non-coding RNAs (ncRNAs) are increasingly becoming apparent, being engaged in diverse structural, functional and regulatory activities. They take part in target gene silencing, play roles in transcriptional, post-transcriptional and epigenetic processes, such as chromatin remodeling, nuclear reorganization with the formation of silent compartments and fine-tuning of gene recruitment into them. Among their functions, non-coding RNAs are thought to act either as guide or scaffold for epigenetic modifiers that write, erase, and read the epigenetic signature over the genome. Studies on human disorders caused by defects in epigenetic modifiers and involving neurological phenotypes highlight the disruption of diverse classes of non-coding RNAs. Noteworthy, these molecules mediate a wide spectrum of neuronal functions, including brain development, and synaptic plasticity. These findings imply a significant contribution of ncRNAs in pathophysiology of the aforesaid diseases and provide new concepts for potential therapeutic applications.

Indexed as

chromatinICF syndromeimprintingneurological deseasenon-coding RNARett syndrome

Identifiers

PMID24616662
PMCPMC3933927

What OpenQuestion holds

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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.