Evidence map›Paper›PMID 33809456›Full record

ArticleInternational journal of molecular sciences2021

Molecular Alterations in Sporadic and

Isabel Lastres-Becker, Gracia Porras, Marina Arribas-Blázquez, Inés Maestro, Daniel Borrego-Hernández, Patricia Boya, Sebastián Cerdán, Alberto García-Redondo, Ana Martínez, Ángeles Martin-Requero

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  6. Impact of NQO1 dysregulation in CNS disorders.Journal of translational medicine · 2024
    Review
  7. New Pharmacological Approaches for Rare Diseases.International journal of molecular sciences · 2023
    Article
  8. Functional Characterization of a Familial ALS-Associated MissenseInternational journal of molecular sciences · 2023
    Article
  9. Review
  10. Article
  11. Article
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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

10 authors at 4 institutions in 1 country.

Isabel Lastres-BeckerInstituto de Investigaciones Biomédicas "Alberto Sols" UAM-CSIC, Arturo Duperier 4, 28029 Madrid, Spain.ORCID 0000-0002-4968-2175
Gracia PorrasCentro de Investigaciones Biológicas-CSIC, Avd, Ramiro Maetzu 9, 28031 Madrid, Spain.
Marina Arribas-BlázquezInstituto de Investigaciones Biomédicas "Alberto Sols" UAM-CSIC, Arturo Duperier 4, 28029 Madrid, Spain.
Inés MaestroCentro de Investigaciones Biológicas-CSIC, Avd, Ramiro Maetzu 9, 28031 Madrid, Spain.
Daniel Borrego-HernándezALS Unit, Hospital 12 de Octubre Research Institute (i+12), 28041 Madrid, Spain.
Patricia BoyaCentro de Investigaciones Biológicas-CSIC, Avd, Ramiro Maetzu 9, 28031 Madrid, Spain.ORCID 0000-0003-3045-951X
Sebastián CerdánInstituto de Investigaciones Biomédicas "Alberto Sols" UAM-CSIC, Arturo Duperier 4, 28029 Madrid, Spain.
Alberto García-RedondoALS Unit, Hospital 12 de Octubre Research Institute (i+12), 28041 Madrid, Spain.ORCID 0000-0001-7646-386X
Ana MartínezCentro de Investigación Biomédica en Red Sobre Enfermedades Neurodegenerativas (CIBERNED), Instituto de Salud Carlos III, 28031 Madrid, Spain.ORCID 0000-0002-2707-8110
Ángeles Martin-RequeroCentro de Investigación Biomédica en Red Sobre Enfermedades Neurodegenerativas (CIBERNED), Instituto de Salud Carlos III, 28031 Madrid, Spain.ORCID 0000-0002-3416-9440
Instituto de Salud Carlos III · ESCentro de Investigaciones Biológicas Margarita Salas · ESInstituto de Investigaciones Biomédicas Sols-Morreale · ESResearch Institute Hospital 12 de Octubre · ES

Funding

Agencia Estatal de Investigación PID2019-105600RB-I00Comunidad de Madrid B2017/BMD-3813Fundela 2019/00325/001H2020 Marie Skłodowska-Curie Actions MSCA-ITN-ETN (grant DRIVE GA: 765912
6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurological condition where motor neurons (MNs) degenerate. Most of the ALS cases are sporadic (sALS), whereas 10% are hereditarily transmitted (fALS), among which mutations are found in the gene that codes for the enzyme superoxide dismutase 1 (SOD1). A central question in ALS field is whether causative mutations display selective alterations not found in sALS patients, or they converge on shared molecular pathways. To identify specific and common mechanisms for designing appropriate therapeutic interventions, we focused on the

Indexed as

Precision MedicineAcidsAgedAged, 80 and overAmyotrophic Lateral SclerosisAutophagyCell Line, TransformedEnergy MetabolismFemaleHeterozygoteHumansLymphocytesMagnetic Resonance SpectroscopyMaleMetabolomicsMiddle AgedAcidsNFE2L2 protein, humanNF-E2-Related Factor 2Reactive Oxygen SpeciesRNA, MessengerSuperoxide Dismutase-1Thiobarbituric Acid Reactive Substancesamyotrophic lateral sclerosisautophagybioenergetic metabolisminflammationlymphoblastNRF2oxidative stress

Identifiers

PMID33809456
PMCPMC8000750
OpenAlexW3136115014

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.