Evidence map›Paper›PMID 22016722›Full record

ArticleFrontiers in molecular neuroscience2011

Pluripotent stem cells for the study of CNS development.

Timothy J Petros, Jennifer A Tyson, Stewart A Anderson

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.3field-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

26 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Neuronal Replacement in Stem Cell Therapy for Stroke: Filling the Gap.Frontiers in cell and developmental biology · 2021
    Review
  7. Article
  8. Review
  9. Article
  10. Organs to Cells and Cells to Organoids: The Evolution ofFrontiers in cellular neuroscience · 2019
    Review
  11. Article
  12. Generation of defined neural populations from pluripotent stem cells.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Review
  13. Article
  14. Article
  15. Article
  16. Engineering Stem Cell Organoids.Cell stem cell · 2016
    Review
  17. Article
  18. Article
  19. Review
  20. Article
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

3 authors at 1 institution in 1 country.

Timothy J PetrosDepartment of Psychiatry, Weill Cornell Medical College New York, NY, USA.
Jennifer A Tyson
Stewart A Anderson
Cornell University · US

Funding

Specification of Interneurons of the Cerebral CortexR01MH066912 · NIMH · WEILL MEDICAL COLL OF CORNELL UNIV · PI ANDERSON, STEWART A · 2003 to 2020
$5.7M
Training Program in Developmental BiologyT32HD060600 · NICHD · WEILL MEDICAL COLL OF CORNELL UNIV · PI BAO, ZHIRONG, STUHLMANN, HEIDI · 2010 to 2024
$3.5M
Derivation of cerebral cortical GABAergic interneurons from human iPS cellsRC1MH089690 · NIMH · WEILL MEDICAL COLL OF CORNELL UNIV · PI ANDERSON, STEWART A, STUDER, LORENZ P. · 2009 to 2010
$999k
NICHD NIH HHS T32 HD060600NIMH NIH HHS R01 MH066912NIMH NIH HHS RC1 MH089690
6 · The paper itself

Abstract

The mammalian central nervous system is a complex neuronal network consisting of a diverse array of cellular subtypes generated in a precise spatial and temporal pattern throughout development. Achieving a greater understanding of the molecular and genetic mechanisms that direct a relatively uniform population of neuroepithelial progenitors into diverse neuronal subtypes remains a significant challenge. The advent of pluripotent stem cell (PSC) technology allows researchers to generate diverse neural populations in vitro. Although the primary focus of PSC-derived neural cells has been their therapeutic potential, utilizing PSCs to study neurodevelopment is another frequently overlooked and equally important application. In this review, we explore the potential for utilizing PSCs to study neural development. We introduce the types of neurodevelopmental questions that PSCs can help to address, and we discuss the different strategies and technologies that researchers use to generate diverse subtypes of PSC-derived neurons. Additionally, we highlight the derivation of several thoroughly characterized neural subtypes; spinal motoneurons, midbrain dopaminergic neurons and cortical neurons. We hope that this review encourages researchers to develop innovative strategies for using PSCs for the study of mammalian, and specifically human, neurodevelopment.

Indexed as

derivationdevelopmentembryonicnervous systemneuronspluripotentstem cells

Identifiers

PMID22016722
PMCPMC3191505
OpenAlexW2081714908

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.