Evidence map›Paper›PMID 37596357›Full record

ReviewNature protocols2023

Efficient generation of functional neurons from mouse embryonic stem cells via neurogenin-2 expression.

Yingfei Liu, Jinzhao Wang, Thomas C Südhof, Marius Wernig

Open access · greenAbstract readReview
In one paragraph

Review in Nature protocols, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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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

4 authors at 3 institutions in 3 countries.

Yingfei LiuInstitute for Stem Cell Biology and Regenerative Medicine, Departments of Pathology and Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0003-2303-576X
Jinzhao WangInstitute for Stem Cell Biology and Regenerative Medicine, Departments of Pathology and Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA.
Thomas C SüdhofDepartment of Molecular & Cellular Physiology, Stanford University School of Medicine, Stanford, CA, USA.
Marius WernigInstitute for Stem Cell Biology and Regenerative Medicine, Departments of Pathology and Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA. wernig@stanford.edu.
Stanford University · USCalifornia Institute for Regenerative Medicine · USShaanxi Provincial People's Hospital · CN

Funding

Multimodal analysis of high-risk psychosis mutations in induced neuronal cellsU19MH104172 · NIMH · STANFORD UNIVERSITY · PI WERNIG, MARIUS · 2014 to 2018
$9.7M
Induced neuronal cells: A novel tool to study neuropsychiatric diseasesR01MH092931 · NIMH · STANFORD UNIVERSITY · PI Thomas C. Sudhof, Marius Wernig · 2010 to 2026
$9.7M
NIMH NIH HHS R01 MH092931NIMH NIH HHS U19 MH104172
6 · The paper itself

Abstract

The production of induced neuronal (iN) cells from human embryonic stem cells (ESCs) and induced pluripotent stem cells by the forced expression of proneural transcription factors is rapid, efficient and reproducible. The ability to generate large numbers of human neurons in such a robust manner enables large-scale studies of human neural differentiation and neuropsychiatric diseases. Surprisingly, similar transcription factor-based approaches for converting mouse ESCs into iN cells have been challenging, primarily because of low cell survival. Here, we provide a detailed approach for the efficient and reproducible generation of functional iN cells from mouse ESC cultures by the genetically induced expression of neurogenin-2. The resulting iN cells display mature pre- and postsynaptic specializations and form synaptic networks. Our method provides the basis for studying neuronal development and enables the direct comparison of cellular phenotypes in mouse and human neurons generated in an equivalent way. The procedure requires 14 d and can be carried out by users with expertise in stem cell culture.

Indexed as

Basic Helix-Loop-Helix ProteinsCell DifferentiationMouse Embryonic Stem CellsNerve Tissue ProteinsNeuronsAnimalsCell Culture TechniquesHumansMiceBasic Helix-Loop-Helix ProteinsNerve Tissue ProteinsNeurog2 protein, mouse

Identifiers

PMID37596357
PMCPMC11349042
OpenAlexW4385987225

What OpenQuestion holds

Textmetadata
LicenceTDM
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.