Evidence map›Paper›PMID 42818272›Full record

ArticlebioRxiv : the preprint server for biology2026

Depletion of the isocitrate dehydrogenase 3 subunit IDHA-1 licenses germ cell-to-neuron direct reprogramming.

Nida Ul Fatima, Anna Reid, Amin Shadfar, Alexander Blume, Tobias Opialla, Stefan Kempa, Baris Tursun

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Nida Ul FatimaDepartment of Biology, Institute of Cell and Systems Biology, Universität Hamburg, 20146 Hamburg, Germany.
Anna ReidMax-Delbrück Center for Molecular Medicine, Berlin Institute for Medical Systems Biology, 10115 Berlin, Germany.
Amin ShadfarDepartment of Biology, Institute of Cell and Systems Biology, Universität Hamburg, 20146 Hamburg, Germany.
Alexander BlumeDepartment of Biology, Institute of Cell and Systems Biology, Universität Hamburg, 20146 Hamburg, Germany.
Tobias OpiallaMax-Delbrück Center for Molecular Medicine, Berlin Institute for Medical Systems Biology, 10115 Berlin, Germany.
Stefan KempaMax-Delbrück Center for Molecular Medicine, Berlin Institute for Medical Systems Biology, 10115 Berlin, Germany.
Baris TursunDepartment of Biology, Institute of Cell and Systems Biology, Universität Hamburg, 20146 Hamburg, Germany.ORCID 0000-0001-7293-8629

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

Direct reprogramming (DR) converts one differentiated cell identity into another and is a promising strategy for regenerative approaches when cells are lost because of injury or disease. Transcription factors (TFs) that specify a given cell type can drive DR, but inhibitory mechanisms restrict this conversion in most cell types. To identify such barriers

Indexed as

anaplerosisC. eleganscell fatedirect reprogramminggerm lineHIF-1isocitrate dehydrogenasemetabolic reprogramming barrierTCA cycleα-Ketoglutarate

Identifiers

PMID42818272
PMCPMC13622187

What OpenQuestion 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 OpenQuestion graph.