Evidence map›Paper›PMID 40307632›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Using Human iPSC-Derived Astrocytes to Investigate Transcription Factor-Driven Astrocyte to Neuron Transdifferentiation.

Ruven Wilkens, Jürgen Korffmann, Nathalie Nicolaisen, Tjasa Lepko Modic, Julian Roewe, Carina Habich, Lamiaa Bahnassawy, Miroslav Cik, Peter Reinhardt

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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.

Ruven WilkensAbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany. Ruven.Wilkens@abbvie.com.
Jürgen KorffmannAbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany.
Nathalie NicolaisenAbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany.
Tjasa Lepko ModicAbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany.
Julian RoeweAbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany.
Carina HabichAbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany.
Lamiaa BahnassawyAbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany.
Miroslav CikAbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany.
Peter ReinhardtAbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany. Peter.Reinhardt@abbvie.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurodegenerative diseases such as Alzheimer's or Parkinson's are marked by progressive loss of affected neurons. Even with novel disease-modifying therapies, this loss cannot be reversed. In situ astrocyte-to-neuron (AtN) transdifferentiation may provide an opportunity to convert resident astrocytes into new neurons to revert the loss of neurons incurred. Currently, most studies investigating AtN transdifferentiation in vitro rely on the use of primary mouse astrocyte cultures which require sacrificing animals and come with uncertainty regarding species differences. Conversely, human induced pluripotent stem cell (hiPSC)-derived astrocytes offer the advantage of working in a human cell culture system which improves translatability and provides the opportunity to generate large, cryopreservable batches of cells to identify and study conversion factors. This protocol details a workflow for assessing the suitability of potential conversion factors for transdifferentiating hiPSC-derived astrocytes into neurons.

Indexed as

AstrocytesCell TransdifferentiationInduced Pluripotent Stem CellsNeuronsTranscription FactorsAnimalsCell Culture TechniquesCell DifferentiationCells, CulturedHumansMiceTranscription FactorsAstrocytesDirect conversionhiPSCLineage conversionNeuronsRegenerationTransdifferentiation

Identifiers

What Socratic 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 Socratic graph.