Evidence map›Paper›PMID 36813966›Full record

ArticleNature2023

Chemically defined cytokine-free expansion of human haematopoietic stem cells.

Masatoshi Sakurai, Kantaro Ishitsuka, Ryoji Ito, Adam C Wilkinson, Takaharu Kimura, Eiji Mizutani, Hidekazu Nishikii, Kazuhiro Sudo, Hans Jiro Becker, Hiroshi Takemoto and 10 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
41.3field-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

96 citing papers in PubMed, 143 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 9 institutions in 5 countries.

Masatoshi Sakurai *Division of Stem Cell Biology, Center for Stem Cell Biology and Regenerative Medicine, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0002-6687-4136
Kantaro Ishitsuka *Laboratory of Stem Cell Therapy, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Ryoji ItoHuman Disease Model Laboratory, Central Institute for Experimental Animals, Kawasaki, Japan.ORCID http://orcid.org/0000-0003-2903-2332
Adam C WilkinsonDivision of Stem Cell Biology, Center for Stem Cell Biology and Regenerative Medicine, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0001-7406-0151
Takaharu KimuraLaboratory of Stem Cell Therapy, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Eiji MizutaniLaboratory of Stem Cell Therapy, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.ORCID http://orcid.org/0000-0003-0301-6780
Hidekazu NishikiiDepartment of Hematology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.ORCID http://orcid.org/0000-0002-6277-4082
Kazuhiro SudoCell Engineering Division, RIKEN BioResource Research Center, Tsukuba, Japan.
Hans Jiro BeckerDivision of Stem Cell Biology, Center for Stem Cell Biology and Regenerative Medicine, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0003-3058-9859
Hiroshi TakemotoDepartment of Neuroscience, Drug Discovery and Disease Research Laboratory, Shionogi; Business-Academia Collaborative Laboratory (Shionogi), Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0001-9893-0609
Tsubasa SanoPharma Solutions, Nutrition and Health, BASF Japan, Tokyo, Japan.ORCID http://orcid.org/0000-0002-7979-4143
Keisuke KataokaDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Satoshi TakahashiDivision of Clinical Precision Research Platform, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0002-1076-2338
Yukio NakamuraCell Engineering Division, RIKEN BioResource Research Center, Tsukuba, Japan.ORCID http://orcid.org/0000-0001-6834-4123
David G KentDepartment of Biology, York Biomedical Research Institute, University of York, York, UK.ORCID http://orcid.org/0000-0001-7871-8811
Atsushi IwamaDivision of Stem Cell and Molecular Medicine, Center for Stem Cell Biology and Regenerative Medicine, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0001-9410-8992
Shigeru ChibaDepartment of Hematology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Shinichiro OkamotoDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Hiromitsu NakauchiInstitute for Stem Cell Biology and Regenerative Medicine, Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA. nakauchi@stanford.edu.ORCID http://orcid.org/0000-0002-9841-6973
Satoshi YamazakiDivision of Stem Cell Biology, Center for Stem Cell Biology and Regenerative Medicine, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan. y-sato4@md.tsukuba.ac.jp.ORCID http://orcid.org/0000-0003-4249-3854
University of Tsukuba · JPKeio University · JPRIKEN BioResource Research Center · JPThe University of Tokyo · JPCentral Institute for Experimental Animals · JPInstitute for Stem Cell Biology and Regenerative Medicine · INShionogi (Japan) · JPUniversity of Oxford · GBWellcome/MRC Cambridge Stem Cell Institute · GB

Funding

Modulating HSC-niche interactions to understand aging and improve transplantationR01HL147124 · NHLBI · STANFORD UNIVERSITY · PI NAKAUCHI, HIROMITSU · 2018 to 2021
$1.6M
Origin of latent hematopoietic stem cells in the aged bone marrowR21AG061487 · NIA · STANFORD UNIVERSITY · PI NAKAUCHI, HIROMITSU · 2019 to 2020
$448k
Medical Research Council MC_PC_19056Medical Research Council MR/V005502/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/V001922/1NHLBI NIH HHS R01 HL147124NIA NIH HHS R21 AG061487
6 · The paper itself

Abstract

Haematopoietic stem cells (HSCs) are a rare cell type that reconstitute the entire blood and immune systems after transplantation and can be used as a curative cell therapy for a variety of haematological diseases

Indexed as

Cell Culture TechniquesCell ProliferationCytokinesHematopoietic Stem CellsAlbuminsCaprolactamClone CellsFetal BloodHematopoietic Stem Cell TransplantationHumansIndolesPhosphatidylinositol 3-KinasesPolymersPyrimidinesReceptors, ThrombopoietinSingle-Cell Gene Expression AnalysisAlbuminsCaprolactamCytokinesIndolesPhosphatidylinositol 3-KinasesPolymersPyrimidinesReceptors, ThrombopoietinUM171 compound

Identifiers

PMID36813966
OpenAlexW4321480282

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.