Evidence map›Paper›PMID 24782713›Full record

ReviewFrontiers in cellular neuroscience2014

Optimizing neuronal differentiation from induced pluripotent stem cells to model ASD.

Dae-Sung Kim, P Joel Ross, Kirill Zaslavsky, James Ellis

Abstract readReview
In one paragraph

Review in Frontiers in cellular neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
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

37 citing papers in PubMed.

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  20. Stem cell therapy in autism: recent insights.Stem cells and cloning : advances and applications · 2018
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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.

Dae-Sung KimProgram in Developmental and Stem Cell Biology, The Hospital for Sick Children Toronto, ON, Canada.
P Joel RossProgram in Developmental and Stem Cell Biology, The Hospital for Sick Children Toronto, ON, Canada.
Kirill ZaslavskyProgram in Developmental and Stem Cell Biology, The Hospital for Sick Children Toronto, ON, Canada ; Department of Molecular Genetics, University of Toronto Toronto, ON, Canada.
James EllisProgram in Developmental and Stem Cell Biology, The Hospital for Sick Children Toronto, ON, Canada ; Department of Molecular Genetics, University of Toronto Toronto, ON, Canada.

Funding

Patient iPS cells with Copy Number Variations to Model Nuropsychiatric DsordersR33MH087908 · NIMH · HOSPITAL FOR SICK CHLDRN (TORONTO) · PI ELLIS, JAMES RYALL · 2011 to 2012
$685k
NIMH NIH HHS R33 MH087908
6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is an early-onset neurodevelopmental disorder characterized by deficits in social communication, and restricted and repetitive patterns of behavior. Despite its high prevalence, discovery of pathophysiological mechanisms underlying ASD has lagged due to a lack of appropriate model systems. Recent advances in induced pluripotent stem cell (iPSC) technology and neural differentiation techniques allow for detailed functional analyses of neurons generated from living individuals with ASD. Refinement of cortical neuron differentiation methods from iPSCs will enable mechanistic studies of specific neuronal subpopulations that may be preferentially impaired in ASD. In this review, we summarize recent accomplishments in differentiation of cortical neurons from human pluripotent stems cells and efforts to establish in vitro model systems to study ASD using personalized neurons.

Indexed as

autism spectrum disorders (ASD)cellular phenotypedisease modelinghuman pluripotent stem cellsneocortical neuronsneural differentiation

Identifiers

PMID24782713
PMCPMC3990101

What OpenQuestion holds

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Registered trials

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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.