Evidence map›Paper›PMID 30720798›Full record

ArticleScientific data2019

RNA-Seq profiling in peripheral blood mononuclear cells of amyotrophic lateral sclerosis patients and controls.

Susanna Zucca, Stella Gagliardi, Cecilia Pandini, Luca Diamanti, Matteo Bordoni, Daisy Sproviero, Maddalena Arigoni, Martina Olivero, Orietta Pansarasa, Mauro Ceroni and 2 more

Open access · goldAbstract readDataset
In one paragraph

Article in Scientific data, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 39 citations in OpenAlex.

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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

12 authors at 3 institutions in 3 countries.

Susanna ZuccaGenomic and post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Stella GagliardiGenomic and post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.ORCID 0000-0002-6589-6907
Cecilia PandiniGenomic and post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Luca DiamantiDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Matteo BordoniGenomic and post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Daisy SprovieroGenomic and post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Maddalena ArigoniDepartment of Molecular Biotechnology and Health Sciences, Bioinformatics and Genomics Unit, University of Turin, Torino, Italy.
Martina OliveroDepartment of Molecular Biotechnology and Health Sciences, Bioinformatics and Genomics Unit, University of Turin, Torino, Italy.
Orietta PansarasaGenomic and post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Mauro CeroniDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Raffaele CalogeroDepartment of Molecular Biotechnology and Health Sciences, Bioinformatics and Genomics Unit, University of Turin, Torino, Italy.
Cristina CeredaGenomic and post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Center for Genomic Science · ITUniversity of Pavia · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coding and long non-coding RNA (lncRNA) metabolism is now revealing its crucial role in Amyotrophic Lateral Sclerosis (ALS) pathogenesis. In this work, we present a dataset obtained via Illumina RNA-seq analysis on Peripheral Blood Mononuclear Cells (PBMCs) from sporadic and mutated ALS patients (mutations in FUS, TARDBP, SOD1 and VCP genes) and healthy controls. This dataset allows the whole-transcriptome characterization of PBMCs content, both in terms of coding and non-coding RNAs, in order to compare the disease state to the healthy controls, both for sporadic patients and for mutated patients. Our dataset is a starting point for the omni-comprehensive analysis of coding and lncRNAs, from an easy to withdraw, manage and store tissue that shows to be a suitable model for RNA profiling in ALS.

Indexed as

Gene Expression ProfilingAmyotrophic Lateral SclerosisDNA-Binding ProteinsHumansLeukocytes, MononuclearMutationRNA-Binding Protein FUSRNA, Long NoncodingSuperoxide Dismutase-1Valosin Containing ProteinDNA-Binding ProteinsFUS protein, humanRNA-Binding Protein FUSRNA, Long NoncodingSOD1 protein, humanSuperoxide Dismutase-1TARDBP protein, humanValosin Containing ProteinVCP protein, human

Identifiers

PMID30720798
PMCPMC6362931
OpenAlexW2914760194

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.