Evidence map›Paper›PMID 30787436›Full record

ArticleNature2019

A single-cell molecular map of mouse gastrulation and early organogenesis.

Blanca Pijuan-Sala, Jonathan A Griffiths, Carolina Guibentif, Tom W Hiscock, Wajid Jawaid, Fernando J Calero-Nieto, Carla Mulas, Ximena Ibarra-Soria, Richard C V Tyser, Debbie Lee Lian Ho and 6 more

Abstract read
In one paragraph

Article in Nature, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 606 papers.

0numbers the graph read from it
0cells of the map it votes in
606citing papers in PubMed
45.7field-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

606 citing papers in PubMed, 1,114 citations in OpenAlex.

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

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

16 authors at 5 institutions in 1 country.

Blanca Pijuan-Sala *Department of Haematology, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.
Jonathan A Griffiths *Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Carolina Guibentif *Department of Haematology, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.
Tom W HiscockCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Wajid JawaidDepartment of Haematology, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.
Fernando J Calero-NietoDepartment of Haematology, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.
Carla MulasWellcome-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.
Ximena Ibarra-SoriaCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Richard C V TyserDepartment of Physiology Anatomy and Genetics, University of Oxford, Oxford, UK.
Debbie Lee Lian HoWellcome-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.
Wolf ReikEpigenetics Programme, Babraham Institute, Cambridge, UK.
Shankar SrinivasDepartment of Physiology Anatomy and Genetics, University of Oxford, Oxford, UK.
Benjamin D SimonsWellcome-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.
Jennifer NicholsWellcome-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.
John C MarioniCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK. john.marioni@cruk.cam.ac.uk.
Berthold GöttgensDepartment of Haematology, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK. bg200@cam.ac.uk.
University of Cambridge · GBMedical Research Council · GBUniversity of Oxford · GBWellcome/MRC Cambridge Stem Cell Institute · GBWellcome Sanger Institute · GB

Funding

VISION: ValIdated Systematic IntegratiON of epigenomic dataR24DK106766 · NIDDK · PENNSYLVANIA STATE UNIVERSITY, THE · PI BLOBEL, GERD A, BODINE, DAVID M. · 2016 to 2020
$6.2M
British Heart Foundation FS/18/24/33424Cancer Research UK 21762Cancer Research UK A21762Medical Research Council MC_PC_12009Medical Research Council MR/M008975/1NIDDK NIH HHS R24 DK106766Wellcome Trust 079895Wellcome Trust 097922Wellcome Trust 105031Wellcome Trust 109081Wellcome Trust 203151Wellcome Trust 206328Wellcome Trust 206328/Z/17/Z
6 · The paper itself

Abstract

Across the animal kingdom, gastrulation represents a key developmental event during which embryonic pluripotent cells diversify into lineage-specific precursors that will generate the adult organism. Here we report the transcriptional profiles of 116,312 single cells from mouse embryos collected at nine sequential time points ranging from 6.5 to 8.5 days post-fertilization. We construct a molecular map of cellular differentiation from pluripotency towards all major embryonic lineages, and explore the complex events involved in the convergence of visceral and primitive streak-derived endoderm. Furthermore, we use single-cell profiling to show that Tal1

Indexed as

GastrulationOrganogenesisSingle-Cell AnalysisAnimalsCell DifferentiationCell LineageChimeraEmbryo, MammalianEndodermEndotheliumFemaleGene Expression ProfilingGene Expression Regulation, DevelopmentalHematopoiesisMaleMesodermTal1 protein, mouseT-Cell Acute Lymphocytic Leukemia Protein 1

Identifiers

PMID30787436
PMCPMC6522369
OpenAlexW2912272542

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.