Evidence map›Paper›PMID 33770499›Full record

ArticleStem cell reports2021

One-step Reprogramming of Human Fibroblasts into Oligodendrocyte-like Cells by SOX10, OLIG2, and NKX6.2.

Konstantina Chanoumidou, Benjamín Hernández-Rodríguez, Farina Windener, Christian Thomas, Martin Stehling, Sabah Mozafari, Stefanie Albrecht, Linda Ottoboni, Jack Antel, Kee-Pyo Kim and 11 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.1field-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

25 citing papers in PubMed, 36 citations in OpenAlex.

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  10. Current Development of iPSC-Based Modeling in Neurodegenerative Diseases.International journal of molecular sciences · 2025
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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

21 authors at 11 institutions in 6 countries.

Konstantina ChanoumidouInstitute of Neuropathology, University Hospital Münster, Pottkamp 2, 48149 Münster, Germany.
Benjamín Hernández-RodríguezMax Planck Institute for Molecular Biomedicine, 48149 Münster, Germany.
Farina WindenerInstitute of Neuropathology, University Hospital Münster, Pottkamp 2, 48149 Münster, Germany.
Christian ThomasInstitute of Neuropathology, University Hospital Münster, Pottkamp 2, 48149 Münster, Germany.
Martin StehlingMax Planck Institute for Molecular Biomedicine, 48149 Münster, Germany.
Sabah MozafariINSERM, U1127, 75013 Paris, France; CNRS, UMR 7225, 75013 Paris, France; Sorbonne Universités UPMC Paris 06, UM-75, 75005 Paris, France; ICM-GH Pitié-Salpêtrière, 75013 Paris, France.
Stefanie AlbrechtInstitute of Neuropathology, University Hospital Münster, Pottkamp 2, 48149 Münster, Germany.
Linda OttoboniNeuroimmunology Unit, IRCCS San Raffaele Hospital and Vita Salute San Raffaele University, Milan, Italy.
Jack AntelMontreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
Kee-Pyo KimMax Planck Institute for Molecular Biomedicine, 48149 Münster, Germany.
Sergiy VelychkoMax Planck Institute for Molecular Biomedicine, 48149 Münster, Germany.
Qiao Ling CuiMontreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
Yu Kang T XuThe Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Gianvito MartinoNeuroimmunology Unit, IRCCS San Raffaele Hospital and Vita Salute San Raffaele University, Milan, Italy.
Jürgen WinklerDepartment of Molecular Neurology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen- Nürnberg, Schwabachanlage 6, 91054 Erlangen, Germany.
Hans R SchölerMax Planck Institute for Molecular Biomedicine, 48149 Münster, Germany; University of Münster, Medical Faculty, Domagkstrasse 3, Münster 48149, Germany.
Anne Baron-Van EvercoorenINSERM, U1127, 75013 Paris, France; CNRS, UMR 7225, 75013 Paris, France; Sorbonne Universités UPMC Paris 06, UM-75, 75005 Paris, France; ICM-GH Pitié-Salpêtrière, 75013 Paris, France.
Odile Boespflug-TanguyService de Neuropédiatrie et des Maladies Métaboliques, LEUKOFRANCE, AP-HP, Hôpital Robert Debré, 75019 Paris, France; Université de Paris, UMR1141 NeuroDiderot, INSERM, 75019 Paris, France.
Juan M VaquerizasMax Planck Institute for Molecular Biomedicine, 48149 Münster, Germany; Medical Research Council London Institute of Medical Sciences, Institute of Clinical Sciences, Faculty of Medicine, Imperial College London, London, UK.
Marc EhrlichInstitute of Neuropathology, University Hospital Münster, Pottkamp 2, 48149 Münster, Germany.
Tanja KuhlmannInstitute of Neuropathology, University Hospital Münster, Pottkamp 2, 48149 Münster, Germany. Electronic address: tanja.kuhlmann@ukmuenster.de.
University Hospital Münster · DEMax Planck Institute for Molecular Biomedicine · DEMontreal Neurological Institute and Hospital · CACentre National de la Recherche Scientifique · FRFriedrich-Alexander-Universität Erlangen-Nürnberg · DEImperial College London · GBInserm · FRIstituti di Ricovero e Cura a Carattere Scientifico · ITJohns Hopkins University · USNeuroDiderotVita-Salute San Raffaele University · IT

Funding

Medical Research Council MC_UP_1605/10
6 · The paper itself

Abstract

Limited access to human oligodendrocytes impairs better understanding of oligodendrocyte pathology in myelin diseases. Here, we describe a method to robustly convert human fibroblasts directly into oligodendrocyte-like cells (dc-hiOLs), which allows evaluation of remyelination-promoting compounds and disease modeling. Ectopic expression of SOX10, OLIG2, and NKX6.2 in human fibroblasts results in rapid generation of O4

Indexed as

Cellular ReprogrammingAge FactorsCell LineCell MovementChromatinChromatin Assembly and DisassemblyEpigenesis, GeneticFibroblastsGene SilencingHomeodomain ProteinsHumansMyelin SheathOligodendrocyte Transcription Factor 2OligodendrogliaPelizaeus-Merzbacher DiseaseSOXE Transcription FactorsChromatinHomeodomain ProteinsNKX6-2 protein, humanOLIG2 protein, humanOligodendrocyte Transcription Factor 2SOX10 protein, humanSOXE Transcription FactorsATAC-seqcompound screenindirect conversionepigenetic agehuman fibroblastsoligodendrocytesPMD

Identifiers

PMID33770499
PMCPMC8072064
OpenAlexW3138750498

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.