Evidence map›Paper›PMID 32573436›Full record

ArticleeLife2020

A new genetic strategy for targeting microglia in development and disease.

Gabriel L McKinsey, Carlos O Lizama, Amber E Keown-Lang, Abraham Niu, Nicolas Santander, Amara Larpthaveesarp, Elin Chee, Fernando F Gonzalez, Thomas D Arnold

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed
9.8field-weighted citation impact, top 1% 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

117 citing papers in PubMed, 173 citations in OpenAlex.

  1. Review
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  7. Immune dysfunction in Alzheimer disease.Nature reviews. Neuroscience · 2026
    Review
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57 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

Gabriel L McKinseyDepartment of Pediatrics, University of California San Francisco, San Francisco, United States.ORCID 0000-0002-5503-2830
Carlos O LizamaCardiovascular Research Institute, University of California San Francisco, San Francisco, United States.
Amber E Keown-LangDepartment of Pediatrics, University of California San Francisco, San Francisco, United States.
Abraham NiuDepartment of Pediatrics, University of California San Francisco, San Francisco, United States.
Nicolas SantanderDepartment of Pediatrics, University of California San Francisco, San Francisco, United States.ORCID 0000-0001-8919-833X
Amara LarpthaveesarpDepartment of Pediatrics, University of California San Francisco, San Francisco, United States.
Elin CheeDepartment of Pediatrics, University of California San Francisco, San Francisco, United States.
Fernando F GonzalezDepartment of Pediatrics, University of California San Francisco, San Francisco, United States.
Thomas D ArnoldDepartment of Pediatrics, University of California San Francisco, San Francisco, United States.
University of California, San Francisco · US

Funding

Translational InformaticsP30CA082103 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jennifer Leigh Clarke · 1999 to 2026
$209.7M
Enhanced cellular therapy for neonatal strokeR01NS107039 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Fernando Francisco Gonzalez · 2018 to 2026
$3.8M
Smad3-Sox17 Angiogenic Signaling Underlies Vascular Instability and Germinal Matrix HemorrhageK08NS096192 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ARNOLD, THOMAS DARMODY · 2016 to 2019
$815k
American Heart Association 20POST35120371NCI NIH HHS P30 CA082103NINDS NIH HHS K08 NS096192NINDS NIH HHS R01 NS107039
6 · The paper itself

Abstract

As the resident macrophages of the brain and spinal cord, microglia are crucial for the phagocytosis of infectious agents, apoptotic cells and synapses. During brain injury or infection, bone-marrow derived macrophages invade neural tissue, making it difficult to distinguish between invading macrophages and resident microglia. In addition to circulation-derived monocytes, other non-microglial central nervous system (CNS) macrophage subtypes include border-associated meningeal, perivascular and choroid plexus macrophages. Using immunofluorescent labeling, flow cytometry and Cre-dependent ribosomal immunoprecipitations, we describe

Indexed as

AnimalsBrain IschemiaEmbryo, MammalianFlow CytometryFluorescent Antibody TechniqueGene Knock-In TechniquesImmunoprecipitationInflammationMiceMicrogliaReceptors, Purinergic P2Y12Recombinant ProteinsP2ry12 protein, mouseReceptors, Purinergic P2Y12Recombinant Proteinsfate mappingimmunologyinflammationmicrogliamousemultiple sclerosisneuroinflammationneuroscienceribosomal profilingstroke

Identifiers

PMID32573436
PMCPMC7375817
OpenAlexW3036521963

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.