Evidence map›Paper›PMID 28361918›Full record

ArticleScientific reports2017

Single-cell RNA sequencing identifies distinct mouse medial ganglionic eminence cell types.

Ying-Jiun J Chen, Brad A Friedman, Connie Ha, Steffen Durinck, Jinfeng Liu, John L Rubenstein, Somasekar Seshagiri, Zora Modrusan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

55 citing papers in PubMed, 97 citations in OpenAlex.

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  8. Deletion of Slc9a1 in Cx3cr1Journal of neuroinflammation · 2024
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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

8 authors at 1 institution in 1 country.

Ying-Jiun J ChenDepartment of Molecular Biology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.
Brad A FriedmanDepartment of Bioinformatics and Computational Biology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.
Connie HaDepartment of Molecular Biology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.
Steffen DurinckDepartment of Molecular Biology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.
Jinfeng LiuDepartment of Bioinformatics and Computational Biology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.
John L RubensteinDepartment of Psychiatry, University of California San Francisco, CA 94158, USA.
Somasekar SeshagiriDepartment of Molecular Biology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.
Zora ModrusanDepartment of Molecular Biology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.
University of California, San Francisco · US

Funding

Genetic Control of Basal Telencephalic DevelopmentR01MH081880 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RUBENSTEIN, JOHN L. R. · 2009 to 2023
$8.1M
Genetic Regulation of Telencephalon DevelopmentR37MH049428 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RUBENSTEIN, JOHN L. R. · 2008 to 2017
$5.9M
NIMH NIH HHS R01 MH081880NIMH NIH HHS R37 MH049428
6 · The paper itself

Abstract

Many subtypes of cortical interneurons (CINs) are found in adult mouse cortices, but the mechanism generating their diversity remains elusive. We performed single-cell RNA sequencing on the mouse embryonic medial ganglionic eminence (MGE), the major birthplace for CINs, and on MGE-like cells differentiated from embryonic stem cells. Two distinct cell types were identified as proliferating neural progenitors and immature neurons, both of which comprised sub-populations. Although lineage development of MGE progenitors was reconstructed and immature neurons were characterized as GABAergic, cells that might correspond to precursors of different CINs were not identified. A few non-neuronal cell types were detected, including microglia. In vitro MGE-like cells resembled bona fide MGE cells but expressed lower levels of Foxg1 and Epha4. Together, our data provide detailed understanding of the embryonic MGE developmental program and suggest how CINs are specified.

Indexed as

Sequence Analysis, RNASingle-Cell AnalysisAnimalsCell LineGene Expression ProfilingInterneuronsMedian EminenceMiceNeural Stem Cells

Identifiers

PMID28361918
PMCPMC5374502
OpenAlexW2600207590

What OpenQuestion holds

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LicenceCC BY
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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.