Evidence map›Paper›PMID 35852018›Full record

ArticleGlia2022

Microglia deficiency accelerates prion disease but does not enhance prion accumulation in the brain.

Barry M Bradford, Lynne I McGuire, David A Hume, Clare Pridans, Neil A Mabbott

Open access · hybridAbstract read
In one paragraph

Article in Glia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 40 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

5 authors at 3 institutions in 2 countries.

Barry M BradfordThe Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush Campus, Midlothian, UK.
Lynne I McGuireThe Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush Campus, Midlothian, UK.
David A HumeMater Research Institute-University of Queensland, Translational Research Institute, Woolloongabba, Queensland, Australia.
Clare PridansSimons Initiative for the Developing Brain, Centre for Discovery Brain Sciences, University of Edinburgh, Hugh Robson Building, Edinburgh, UK.
Neil A MabbottThe Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush Campus, Midlothian, UK.ORCID 0000-0001-7395-1796
Roslin Institute · GBCentre for Inflammation Research · GBTranslational Research Institute · AU

Funding

Biotechnology and Biological Sciences Research Council BB/S005471/1Biotechnology and Biological Sciences Research Council BBS/E/D/10002071Biotechnology and Biological Sciences Research Council BBS/E/D/20002173Medical Research Council MR/M019969/1
6 · The paper itself

Abstract

Prion diseases are transmissible, neurodegenerative disorders associated with misfolding of the prion protein. Previous studies show that reduction of microglia accelerates central nervous system (CNS) prion disease and increases the accumulation of prions in the brain, suggesting that microglia provide neuroprotection by phagocytosing and destroying prions. In Csf1r

Indexed as

Prion DiseasesPrionsAnimalsAstrocytesBrainMiceMicrogliaPrionscentral nervous systemmicroglianeurodegenerationprion diseasereactive astrocyte

Identifiers

PMID35852018
PMCPMC9544114
OpenAlexW4285794295

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.