Evidence map›Paper›PMID 31595840›Full record

ArticleStem cells and development2019

Enhanced Ex Vivo Generation of Erythroid Cells from Human Induced Pluripotent Stem Cells in a Simplified Cell Culture System with Low Cytokine Support.

Claudia Bernecker, Mania Ackermann, Nico Lachmann, Lisa Rohrhofer, Holm Zaehres, Marcos J Araúzo-Bravo, Emile van den Akker, Peter Schlenke, Isabel Dorn

Open access · hybridAbstract read
In one paragraph

Article in Stem cells and development, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

43 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
  2. Blood Pharming of Red Cells.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2026
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  19. Article
  20. Generation of hiPSCs withFrontiers in genetics · 2023
    Article
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

9 authors at 5 institutions in 4 countries.

Claudia BerneckerDepartment of Blood Group Serology and Transfusion Medicine, Medical University Graz, Graz, Austria.
Mania AckermannRG Translational Hematology of Congenital Diseases, Institute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Nico LachmannRG Translational Hematology of Congenital Diseases, Institute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Lisa RohrhoferDepartment of Blood Group Serology and Transfusion Medicine, Medical University Graz, Graz, Austria.
Holm ZaehresDepartment of Anatomy and Molecular Embryology, Ruhr-University Bochum, Bochum, Germany.
Marcos J Araúzo-BravoComputational Biology and Systems Biomedicine Research Group, Biodonostia Health Research Institute, San Sebastián, Spain.
Emile van den AkkerDepartment of Hematopoiesis, Sanquin Research, Amsterdam, the Netherlands.
Peter SchlenkeDepartment of Blood Group Serology and Transfusion Medicine, Medical University Graz, Graz, Austria.
Isabel DornDepartment of Blood Group Serology and Transfusion Medicine, Medical University Graz, Graz, Austria.
Medical University of Graz · ATMedizinische Hochschule Hannover · DEIkerbasque · ESRuhr University Bochum · DESanquin · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Red blood cell (RBC) differentiation from human induced pluripotent stem cells (hiPSCs) offers great potential for developmental studies and innovative therapies. However, ex vivo erythropoiesis from hiPSCs is currently limited by low efficiency and unphysiological conditions of common culture systems. Especially, the absence of a physiological niche may impair cell growth and lineage-specific differentiation. We here describe a simplified, xeno- and feeder-free culture system for prolonged RBC generation that uses low numbers of supporting cytokines [stem cell factor (SCF), erythropoietin (EPO), and interleukin 3 (IL-3)] and is based on the intermediate development of a "hematopoietic cell forming complex (HCFC)." From this HCFC, CD43

Indexed as

CD36 AntigensCell Culture TechniquesCell DifferentiationCell LineageCellular MicroenvironmentCytokinesErythrocytesErythroid CellsErythropoiesisHematopoietic Stem CellsHumansInduced Pluripotent Stem CellsLeukosialinCD36 AntigensCytokinesLeukosialinerythropoiesishematopoiesisinduced pluripotent stem cellsnichered blood cell

Identifiers

PMID31595840
PMCPMC6882453
OpenAlexW2979615590

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.