Evidence map›Paper›PMID 30305734›Full record

ArticleNature2018

Neural blastocyst complementation enables mouse forebrain organogenesis.

Amelia N Chang, Zhuoyi Liang, Hai-Qiang Dai, Aimee M Chapdelaine-Williams, Nick Andrews, Roderick T Bronson, Bjoern Schwer, Frederick W Alt

Abstract read
In one paragraph

Article in Nature, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

34 citing papers in PubMed, 66 citations in OpenAlex.

  1. The making of cells and organs in xenogeneic animal bioreactor.Signal transduction and targeted therapy · 2026
    Review
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  7. Article
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  10. Parathyroid Gland Generation from Pluripotent Stem Cells.Endocrinology and metabolism (Seoul, Korea) · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Amelia N Chang *Howard Hughes Medical Institute, Program in Cellular and Molecular Medicine, Boston Children's Hospital, Department of Genetics and Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Zhuoyi Liang *Howard Hughes Medical Institute, Program in Cellular and Molecular Medicine, Boston Children's Hospital, Department of Genetics and Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Hai-Qiang Dai *Howard Hughes Medical Institute, Program in Cellular and Molecular Medicine, Boston Children's Hospital, Department of Genetics and Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Aimee M Chapdelaine-WilliamsHoward Hughes Medical Institute, Program in Cellular and Molecular Medicine, Boston Children's Hospital, Department of Genetics and Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Nick AndrewsDivision of Neurology, Kirby Center for Neurobiology, Boston Children's Hospital, Boston, MA, USA.
Roderick T BronsonRodent Histopathology Core, Harvard Medical School, Boston, MA, USA.
Bjoern Schwer *Department of Neurological Surgery and Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA, USA. bjoern.schwer@ucsf.edu.
Frederick W Alt *Howard Hughes Medical Institute, Program in Cellular and Molecular Medicine, Boston Children's Hospital, Department of Genetics and Department of Pediatrics, Harvard Medical School, Boston, MA, USA. alt@enders.tch.harvard.edu.
Boston Children's Hospital · USHarvard University · USBroad Center · US

Funding

Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI CHEN, CHINFEI · 2016 to 2020
$5.2M
Elucidation of The Role Of SIRT6 In Neural Function, Aging, And NeurodegenerationK01AG043630 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SCHWER, BJOERN · 2012 to 2016
$647k
NIA NIH HHS K01 AG043630NICHD NIH HHS 1U54HD090255NICHD NIH HHS U54 HD090255
6 · The paper itself

Abstract

Genetically modified mice are commonly generated by the microinjection of pluripotent embryonic stem (ES) cells into wild-type host blastocysts

Indexed as

OrganogenesisAnimalsBlastocystChimeraDNA-Binding ProteinsDoublecortin Domain ProteinsFemaleGenetic Complementation TestGerm CellsHippocampusMaleMiceMice, TransgenicMicrotubule-Associated ProteinsMouse Embryonic Stem CellsNeocortexDNA-Binding ProteinsDoublecortin Domain ProteinsMicrotubule-Associated ProteinsNeuropeptidesRag2 protein, mouse

Identifiers

PMID30305734
PMCPMC6588192
OpenAlexW2897095895

What OpenQuestion holds

Textmetadata
LicenceTDM
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.