Evidence map›Paper›PMID 27869129›Full record

ArticleNature communications2016

Reprogramming mouse fibroblasts into engraftable myeloerythroid and lymphoid progenitors.

Hui Cheng, Heather Yin-Kuan Ang, Chadi A El Farran, Pin Li, Hai Tong Fang, Tong Ming Liu, Say Li Kong, Michael Lingzi Chin, Wei Yin Ling, Edwin Kok Hao Lim and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  7. Direct cell reprogramming: approaches, mechanisms and progress.Nature reviews. Molecular cell biology · 2021
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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

15 authors at 5 institutions in 3 countries.

Hui ChengStem Cell and Regenerative Biology Group, Genome Institute of Singapore, Singapore 138672, Singapore.
Heather Yin-Kuan AngStem Cell and Regenerative Biology Group, Genome Institute of Singapore, Singapore 138672, Singapore.
Chadi A El FarranEpigenetics and Cell Fates Laboratory, Institute of Molecular and Cell Biology, Singapore 138673, Singapore.
Pin LiStem Cell and Regenerative Biology Group, Genome Institute of Singapore, Singapore 138672, Singapore.
Hai Tong FangEpigenetics and Cell Fates Laboratory, Institute of Molecular and Cell Biology, Singapore 138673, Singapore.
Tong Ming LiuStem Cell and Regenerative Biology Group, Genome Institute of Singapore, Singapore 138672, Singapore.
Say Li KongStem Cell and Regenerative Biology Group, Genome Institute of Singapore, Singapore 138672, Singapore.
Michael Lingzi ChinStem Cell and Regenerative Biology Group, Genome Institute of Singapore, Singapore 138672, Singapore.
Wei Yin LingStem Cell and Regenerative Biology Group, Genome Institute of Singapore, Singapore 138672, Singapore.
Edwin Kok Hao LimStem Cell and Regenerative Biology Group, Genome Institute of Singapore, Singapore 138672, Singapore.
Hu LiDepartment of Molecular Pharmacology &Experimental Therapeutics, Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota 55905, USA.
Tara HuberStem Cell and Regenerative Biology Group, Genome Institute of Singapore, Singapore 138672, Singapore.
Kyle M LohDepartment of Developmental Biology, Stanford Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California 94305, USA.
Yuin-Han LohEpigenetics and Cell Fates Laboratory, Institute of Molecular and Cell Biology, Singapore 138673, Singapore.
Bing LimStem Cell and Regenerative Biology Group, Genome Institute of Singapore, Singapore 138672, Singapore.
Genome Institute of Singapore · SGNational University of Singapore · SGInstitute of Molecular and Cell Biology · SGMayo Clinic · USStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent efforts have attempted to convert non-blood cells into hematopoietic stem cells (HSCs) with the goal of generating blood lineages de novo. Here we show that hematopoietic transcription factors Scl, Lmo2, Runx1 and Bmi1 can convert a developmentally distant lineage (fibroblasts) into 'induced hematopoietic progenitors' (iHPs). Functionally, iHPs generate acetylcholinesterase

Indexed as

Cellular ReprogrammingAcetylcholinesteraseAnimalsBone Morphogenetic ProteinsCell DifferentiationExtracellular Signal-Regulated MAP KinasesFibroblastsGene Expression RegulationGenomicsHematopoietic Stem CellsHumansMegakaryocytesMiceMitogen-Activated Protein Kinase KinasesMyeloid CellsPhagocytesAcetylcholinesteraseBone Morphogenetic ProteinsExtracellular Signal-Regulated MAP KinasesMitogen-Activated Protein Kinase KinasesTranscription Factors

Identifiers

PMID27869129
PMCPMC5121332
OpenAlexW2554195059

What OpenQuestion 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 OpenQuestion graph.