Evidence map›Paper›PMID 31130512›Full record

ArticleCell stem cell2019

OLIG2 Drives Abnormal Neurodevelopmental Phenotypes in Human iPSC-Based Organoid and Chimeric Mouse Models of Down Syndrome.

Ranjie Xu, Andrew T Brawner, Shenglan Li, Jing-Jing Liu, Hyosung Kim, Haipeng Xue, Zhiping P Pang, Woo-Yang Kim, Ronald P Hart, Ying Liu and 1 more

Abstract read
In one paragraph

Article in Cell stem cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed, 2 pooled it
24.2field-weighted citation impact, top 1% 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

119 citing papers in PubMed, 2 syntheses or guidelines pooled it, 198 citations in OpenAlex.

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  19. Accelerated Tempo of Cortical Neurogenesis in Down Syndrome.bioRxiv : the preprint server for biology · 2025
    Article
  20. Article

59 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Ranjie XuDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA; Department of Developmental Neuroscience, Munroe-Meyer Institute and Mary & Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Andrew T BrawnerDepartment of Developmental Neuroscience, Munroe-Meyer Institute and Mary & Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Shenglan LiDepartment of Neurosurgery and Center for Stem Cell and Regenerative Medicine, University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Jing-Jing LiuDepartment of Neuroscience and Cell Biology and Child Health Institute of New Jersey, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ 08901, USA.
Hyosung KimDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.
Haipeng XueDepartment of Neurosurgery and Center for Stem Cell and Regenerative Medicine, University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Zhiping P PangDepartment of Neuroscience and Cell Biology and Child Health Institute of New Jersey, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ 08901, USA.
Woo-Yang KimDepartment of Biological Sciences, Kent State University, Kent, OH 44242, USA.
Ronald P HartDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.
Ying LiuDepartment of Neurosurgery and Center for Stem Cell and Regenerative Medicine, University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Peng JiangDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA; Department of Developmental Neuroscience, Munroe-Meyer Institute and Mary & Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, NE 68198, USA. Electronic address: peng.jiang@rutgers.edu.
Rutgers, The State University of New Jersey · USThe University of Texas Health Science Center at Houston · USKent State University · USNebraska Medical Center · US

Funding

UNMC Histology/Imaging and Creighton University Imaging Core FacilityP30GM110768 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WALSH, EDWARD J · 2014 to 2018
$5.1M
Deciphering the neural basis of alcohol use disorders using human and mouse neuronsR01AA023797 · NIAAA · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI ZHIPING P. PANG · 2016 to 2026
$4.8M
Epigenetic mechanisms of indole-3-carbinol/diindolylemthane and triterpenoids in prevention of prostate inflammation and related diseaseR01AT009152 · NCCIH · RUTGERS, THE STATE UNIV OF N.J. · PI KONG, AH-NG TONY · 2015 to 2019
$3.3M
Mechanism of Gene Environment Interactions in Alzheimer's DiseaseR01ES026057 · NIEHS · NORTHEAST OHIO MEDICAL UNIVERSITY · PI RICHARDSON, JASON R · 2016 to 2020
$2.4M
Reconnecting the injured cervical spinal cord by transplanted human iPSC-derived neural progenitorsR01NS110707 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LIU, YING · 2019 to 2023
$1.7M
Novel Functions of OLIG2 in Regulating Human Interneuron Production in Health and DiseaseR01NS102382 · NINDS · RUTGERS, THE STATE UNIV OF N.J. · PI JIANG, PENG · 2018 to 2022
$1.6M
Post-transcriptional gene regulation in normal and diseased neuronsR21NS097992 · NINDS · RBHS-NEW JERSEY MEDICAL SCHOOL · PI PANG, ZHIPING P., TIAN, BIN · 2017 to 2018
$437k
Developing an Astroglial Model for Down SyndromeR21HD091512 · NICHD · RUTGERS, THE STATE UNIV OF N.J. · PI JIANG, PENG · 2017 to 2018
$426k
High throughput multicompartment culture chambers to develop neurocircuit models of addiction riskR21DA039686 · NIDA · RUTGERS, THE STATE UNIV OF N.J. · PI HART, RONALD P, PANG, ZHIPING P. · 2015 to 2016
$382k
NCCIH NIH HHS R01 AT009152NIAAA NIH HHS R01 AA023797NICHD NIH HHS R21 HD091512NIDA NIH HHS R21 DA039686NIEHS NIH HHS R01 ES026057NIGMS NIH HHS P30 GM110768NINDS NIH HHS R01 NS102382NINDS NIH HHS R01 NS110707NINDS NIH HHS R21 NS097992
6 · The paper itself

Abstract

Down syndrome (DS) is a common neurodevelopmental disorder, and cognitive defects in DS patients may arise from imbalances in excitatory and inhibitory neurotransmission. Understanding the mechanisms underlying such imbalances may provide opportunities for therapeutic intervention. Here, we show that human induced pluripotent stem cells (hiPSCs) derived from DS patients overproduce OLIG2

Indexed as

AnimalsCell DifferentiationCell LineageCells, CulturedDisease Models, AnimalDown SyndromeHumansInduced Pluripotent Stem CellsInterneuronsMiceMice, Inbred C57BLNeural Stem CellsNeurodevelopmental DisordersNeurogenesisOligodendrocyte Transcription Factor 2OrganoidsOLIG2 protein, humanOligodendrocyte Transcription Factor 2RNA, Small Interferingbrain organoidchimeric mouse brainDown syndromehuman induced pluripotent stem cellinterneuronneurodevelopmental disorderOLIG1OLIG2

Identifiers

PMID31130512
PMCPMC6944064
OpenAlexW2945934042

What OpenQuestion holds

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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.