Evidence map›Paper›PMID 29456178›Full record

ArticleStem cell reports2018

HOXB4 Promotes Hemogenic Endothelium Formation without Perturbing Endothelial Cell Development.

Nadine Teichweyde, Lara Kasperidus, Sebastian Carotta, Valerie Kouskoff, Georges Lacaud, Peter A Horn, Stefan Heinrichs, Hannes Klump

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2018. 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
4.5field-weighted citation impact, top 5% 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, 29 citations in OpenAlex.

  1. HOXB4 Promotes Bladder Cancer Progression in Part Through Transcriptional Activation of Smoothened.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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

8 authors at 4 institutions in 3 countries.

Nadine TeichweydeInstitute for Transfusion Medicine, University Hospital Essen, Virchowstraße 179, 45147 Essen, Germany.
Lara KasperidusInstitute for Transfusion Medicine, University Hospital Essen, Virchowstraße 179, 45147 Essen, Germany; Department of Bone Marrow Transplantation, University Hospital Essen, Hufelandstraße 55, 45147 Essen, Germany.
Sebastian CarottaCancer Cell Signaling, Boehringer Ingelheim RCV, Dr Boehringer-Gasse, 1120 Vienna, Austria.
Valerie KouskoffCancer Research UK Stem Cell Haematopoiesis Group, Cancer Research UK Manchester Institute, The University of Manchester, Wilmslow Road, Manchester M20 4BX, UK.
Georges LacaudCancer Research UK Stem Cell Biology Group, Cancer Research UK Manchester Institute, The University of Manchester, Wilmslow Road, Manchester M20 4BX, UK.
Peter A HornInstitute for Transfusion Medicine, University Hospital Essen, Virchowstraße 179, 45147 Essen, Germany.
Stefan HeinrichsInstitute for Transfusion Medicine, University Hospital Essen, Virchowstraße 179, 45147 Essen, Germany.
Hannes KlumpInstitute for Transfusion Medicine, University Hospital Essen, Virchowstraße 179, 45147 Essen, Germany. Electronic address: hannes.klump@uk-essen.de.
Essen University Hospital · DEBoehringer Ingelheim (Austria) · ATCancer Research UK Manchester Institute · GBUniversity of Manchester · GB

Funding

Biotechnology and Biological Sciences Research Council BB/I001794/1Cancer Research UK 12487Cancer Research UK 19565Cancer Research UK C5759/A20971Medical Research Council MR/P000673/1
6 · The paper itself

Abstract

Generation of hematopoietic stem cells (HSCs) from pluripotent stem cells, in vitro, holds great promise for regenerative therapies. Primarily, this has been achieved in mouse cells by overexpression of the homeotic selector protein HOXB4. The exact cellular stage at which HOXB4 promotes hematopoietic development, in vitro, is not yet known. However, its identification is a prerequisite to unambiguously identify the molecular circuits controlling hematopoiesis, since the activity of HOX proteins is highly cell and context dependent. To identify that stage, we retrovirally expressed HOXB4 in differentiating mouse embryonic stem cells (ESCs). Through the use of Runx1

Indexed as

AnimalsCell DifferentiationCells, CulturedCore Binding Factor Alpha 2 SubunitEmbryonic Stem CellsEndothelial CellsEndotheliumGene Expression ProfilingHematopoiesisHematopoietic Stem CellsHomeodomain ProteinsMicePluripotent Stem CellsTranscription FactorsTranscription, GeneticUp-RegulationCore Binding Factor Alpha 2 SubunitHomeodomain ProteinsHoxb4 protein, mouseTranscription FactorsEHThemangioblasthematopoietic specificationhematopoietic stem cellshemogenic endotheliumHOXB4pluripotent stem cellsRUNX1

Identifiers

PMID29456178
PMCPMC5919293
OpenAlexW2785920133

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.