Evidence map›Paper›PMID 37524711›Full record

ArticleNature communications2023

Three-dimensional molecular architecture of mouse organogenesis.

Fangfang Qu, Wenjia Li, Jian Xu, Ruifang Zhang, Jincan Ke, Xiaodie Ren, Xiaogao Meng, Lexin Qin, Jingna Zhang, Fangru Lu and 10 more

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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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

20 authors.

Fangfang Qu *Center for Cell Lineage and Atlas, Bioland Laboratory, Guangzhou, China.
Wenjia Li *Center for Cell Lineage and Atlas, Bioland Laboratory, Guangzhou, China.
Jian Xu *Center for Cell Lineage and Atlas, Bioland Laboratory, Guangzhou, China.
Ruifang ZhangCenter for Cell Lineage and Atlas, Bioland Laboratory, Guangzhou, China.ORCID 0000-0003-2843-6976
Jincan KeCenter for Cell Lineage and Development, CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, GIBH-HKU Guangdong-Hong Kong Stem Cell and Regenerative Medicine Research Centre, Guangzhou Institutes of Biomedicine and Health, University of the Chinese Academy of Sciences, Chinese Academy of Sciences, 510530, Guangzhou, China.
Xiaodie RenCenter for Cell Lineage and Atlas, Bioland Laboratory, Guangzhou, China.
Xiaogao MengCenter for Cell Lineage and Development, CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, GIBH-HKU Guangdong-Hong Kong Stem Cell and Regenerative Medicine Research Centre, Guangzhou Institutes of Biomedicine and Health, University of the Chinese Academy of Sciences, Chinese Academy of Sciences, 510530, Guangzhou, China.
Lexin QinCenter for Cell Lineage and Development, CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, GIBH-HKU Guangdong-Hong Kong Stem Cell and Regenerative Medicine Research Centre, Guangzhou Institutes of Biomedicine and Health, University of the Chinese Academy of Sciences, Chinese Academy of Sciences, 510530, Guangzhou, China.
Jingna ZhangCenter for Cell Lineage and Atlas, Bioland Laboratory, Guangzhou, China.
Fangru LuCenter for Cell Lineage and Atlas, Bioland Laboratory, Guangzhou, China.
Xin ZhouCenter for Cell Lineage and Atlas, Bioland Laboratory, Guangzhou, China.
Xi LuoCenter for Cell Lineage and Development, CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, GIBH-HKU Guangdong-Hong Kong Stem Cell and Regenerative Medicine Research Centre, Guangzhou Institutes of Biomedicine and Health, University of the Chinese Academy of Sciences, Chinese Academy of Sciences, 510530, Guangzhou, China.
Zhen ZhangCenter for Cell Lineage and Development, CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, GIBH-HKU Guangdong-Hong Kong Stem Cell and Regenerative Medicine Research Centre, Guangzhou Institutes of Biomedicine and Health, University of the Chinese Academy of Sciences, Chinese Academy of Sciences, 510530, Guangzhou, China.
Minhan WangCenter for Cell Lineage and Development, CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, GIBH-HKU Guangdong-Hong Kong Stem Cell and Regenerative Medicine Research Centre, Guangzhou Institutes of Biomedicine and Health, University of the Chinese Academy of Sciences, Chinese Academy of Sciences, 510530, Guangzhou, China.
Guangming WuCenter for Cell Lineage and Atlas, Bioland Laboratory, Guangzhou, China.
Duanqing PeiLaboratory of Cell Fate Control, School of Life Sciences, Westlake University, Hangzhou, China.ORCID 0000-0002-5222-014X
Jiekai ChenCenter for Cell Lineage and Atlas, Bioland Laboratory, Guangzhou, China.ORCID 0000-0001-5168-7074
Guizhong CuiCenter for Cell Lineage and Atlas, Bioland Laboratory, Guangzhou, China. cui_guizhong@gzlab.ac.cn.ORCID 0000-0001-6394-2773
Shengbao SuoGuangzhou Laboratory, 510005, Guangzhou, Guangdong, China. suo_shengbao@gzlab.ac.cn.ORCID 0009-0008-8943-2956
Guangdun PengCenter for Cell Lineage and Atlas, Bioland Laboratory, Guangzhou, China. peng_guangdun@gibh.ac.cn.ORCID 0000-0002-8586-0637

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mammalian embryos exhibit sophisticated cellular patterning that is intricately orchestrated at both molecular and cellular level. It has recently become apparent that cells within the animal body display significant heterogeneity, both in terms of their cellular properties and spatial distributions. However, current spatial transcriptomic profiling either lacks three-dimensional representation or is limited in its ability to capture the complexity of embryonic tissues and organs. Here, we present a spatial transcriptomic atlas of all major organs at embryonic day 13.5 in the mouse embryo, and provide a three-dimensional rendering of molecular regulation for embryonic patterning with stacked sections. By integrating the spatial atlas with corresponding single-cell transcriptomic data, we offer a detailed molecular annotation of the dynamic nature of organ development, spatial cellular interactions, embryonic axes, and divergence of cell fates that underlie mammalian development, which would pave the way for precise organ engineering and stem cell-based regenerative medicine.

Indexed as

OrganogenesisTranscriptomeAnimalsEmbryo, MammalianGene Expression ProfilingMammalsMiceStem Cells

Identifiers

PMID37524711
PMCPMC10390492

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.