Evidence map›Paper›PMID 31173710›Full record

ArticleCell stem cell2019

Dosage Counts: Correcting Trisomy-21-Related Phenotypes in Human Organoids and Xenografts.

William F Manley, Stewart A Anderson

Open access · bronzeAbstract readComment
PubMed Publisher
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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Down syndrome: A curative prospect?AIMS neuroscience · 2020
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

William F ManleyDepartment of Psychiatry, The Children's Hospital of Philadelphia and The University of Pennsylvania Perelman School of Medicine, ARC 517, 3615 Civic Center Blvd., Philadelphia, PA 19104, USA.
Stewart A AndersonDepartment of Psychiatry, The Children's Hospital of Philadelphia and The University of Pennsylvania Perelman School of Medicine, ARC 517, 3615 Civic Center Blvd., Philadelphia, PA 19104, USA. Electronic address: sande@pennmedicine.upenn.edu.
Children's Hospital of Philadelphia · US

Funding

TRANSGENIC MOUSE MODELS OF MENTAL RETARDATIONP30HD026979 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI YUDKOFF, MARC · 1990 to 2015
$15.3M
NICHD NIH HHS P30 HD026979
6 · The paper itself

Abstract

Studies in mice suggest that Olig2 gene dosage alters cerebral cortical interneuron development and contributes to trisomy-21/Down-syndrome-related intellectual disability. Xu et al. (2019) extend these studies through the remarkable use of cerebral organoid and human iPSC/mouse brain chimera experimental systems that provide an opportunity for the development of novel therapeutics.

Indexed as

Down SyndromeTrisomyAnimalsChimeraHeterograftsHumansMiceOligodendrocyte Transcription Factor 2OrganoidsPhenotypeOLIG2 protein, humanOlig2 protein, mouseOligodendrocyte Transcription Factor 2

Identifiers

PMID31173710
OpenAlexW2948569814

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.