Evidence map›Paper›PMID 33498186›Full record

ReviewInternational journal of molecular sciences2021

Little Helpers or Mean Rogue-Role of Microglia in Animal Models of Amyotrophic Lateral Sclerosis.

Hilal Cihankaya, Carsten Theiss, Veronika Matschke

Open access · goldAbstract readReview
In one paragraph

Review 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 14 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

3 authors at 1 institution in 1 country.

Hilal CihankayaDepartment of Cytology, Institute of Anatomy, Ruhr-University Bochum, D-44801 Bochum, Germany.
Carsten TheissDepartment of Cytology, Institute of Anatomy, Ruhr-University Bochum, D-44801 Bochum, Germany.ORCID 0000-0001-7983-0143
Veronika MatschkeDepartment of Cytology, Institute of Anatomy, Ruhr-University Bochum, D-44801 Bochum, Germany.ORCID 0000-0001-9717-4485
Ruhr University Bochum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is one of the most common neurodegenerative diseases, causing degeneration of both upper and lower motor neurons in the central nervous system (CNS). ALS patients suffer from hyperreflexia, spasticity, paralysis and muscle atrophy and typically die due to respiratory failure 1-5 years after disease onset. In addition to the degeneration of motor neurons on the cellular level, ALS has been associated with neuroinflammation, such as microgliosis. Microglial activation in ALS can either be protective or degenerative to the neurons. Among others, mutations in superoxide dismutase 1 (SOD1), chromosome 9 open reading frame 72 (C9Orf72), transactive response DNA binding protein (TDP) 43 and vacuolar protein sorting-associated protein 54 (VPS54) genes have been associated with ALS. Here, we describe the dual role and functionality of microglia in four different in vivo ALS models and search for the lowest common denominator with respect to the role of microglia in the highly heterogeneous disease of ALS.

Indexed as

Disease Models, AnimalAmyotrophic Lateral SclerosisAnimalsC9orf72 ProteinDNA-Binding ProteinsMiceMicrogliaSuperoxide Dismutase-1Vesicular Transport ProteinsC9orf72 ProteinDNA-Binding ProteinsSuperoxide Dismutase-1Tardbp protein, mouseVesicular Transport ProteinsVps54 protein, mouseALSchromosome 9 open reading frame 72microglial activationneuroinflammationsuperoxide dismutase 1transactive response DNA binding protein 43wobbler mouse

Identifiers

PMID33498186
PMCPMC7863915
OpenAlexW3121984570

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.