Evidence map›Paper›PMID 35899604›Full record

ArticleDevelopment (Cambridge, England)2022

Rapid and robust directed differentiation of mouse epiblast stem cells into definitive endoderm and forebrain organoids.

Daniel Medina-Cano, Emily K Corrigan, Rachel A Glenn, Mohammed T Islam, Yuan Lin, Juliet Kim, Hyunwoo Cho, Thomas Vierbuchen

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 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

8 authors at 2 institutions in 1 country.

Daniel Medina-CanoDevelopmental Biology Program, Sloan Kettering Institute for Cancer Research, New York, NY 10065, USA.ORCID 0000-0003-4545-7664
Emily K CorriganDevelopmental Biology Program, Sloan Kettering Institute for Cancer Research, New York, NY 10065, USA.
Rachel A GlennDevelopmental Biology Program, Sloan Kettering Institute for Cancer Research, New York, NY 10065, USA.
Mohammed T IslamDevelopmental Biology Program, Sloan Kettering Institute for Cancer Research, New York, NY 10065, USA.
Yuan LinDevelopmental Biology Program, Sloan Kettering Institute for Cancer Research, New York, NY 10065, USA.
Juliet KimDevelopmental Biology Program, Sloan Kettering Institute for Cancer Research, New York, NY 10065, USA.
Hyunwoo ChoDevelopmental Biology Program, Sloan Kettering Institute for Cancer Research, New York, NY 10065, USA.ORCID 0000-0003-3166-585X
Thomas VierbuchenDevelopmental Biology Program, Sloan Kettering Institute for Cancer Research, New York, NY 10065, USA.ORCID 0000-0002-5690-5680
Kettering University · USCornell University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Directed differentiation of pluripotent stem cells (PSCs) is a powerful model system for deconstructing embryonic development. Although mice are the most advanced mammalian model system for genetic studies of embryonic development, state-of-the-art protocols for directed differentiation of mouse PSCs into defined lineages require additional steps and generates target cell types with lower purity than analogous protocols for human PSCs, limiting their application as models for mechanistic studies of development. Here, we examine the potential of mouse epiblast stem cells cultured in media containing Wnt pathway inhibitors as a starting point for directed differentiation. As a proof of concept, we focused our efforts on two specific cell/tissue types that have proven difficult to generate efficiently and reproducibly from mouse embryonic stem cells: definitive endoderm and neural organoids. We present new protocols for rapid generation of nearly pure definitive endoderm and forebrain-patterned neural organoids that model the development of prethalamic and hippocampal neurons. These differentiation models present new possibilities for combining mouse genetic tools with in vitro differentiation to characterize molecular and cellular mechanisms of embryonic development.

Indexed as

EndodermPluripotent Stem CellsAnimalsCell DifferentiationFemaleGerm LayersHumansMammalsMiceOrganoidsPregnancyProsencephalonDefinitive endodermDirected differentiationNeural developmentOrganoidsPluripotent stem cells

Identifiers

PMID35899604
PMCPMC10655922
OpenAlexW4288080896

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.