Metabolic assessment of iPSC-derived neurons under ketone-enriched condition: Ketone sensor development and BHB-driven metabolic adaptation.
Overview
- Division of Nanobiotechnology, Department of Protein Science, Science for Life Laboratory, KTH Royal Institute of Technology, Solna, Sweden
- AIMES, Center for the Advancement of Integrated Medical and Engineering Sciences, Department of Neuroscience, Karolinska Institute, Solna, Sweden
- Department of Physiology and Pharmacology, Karolinska Institutet, 171 77 Stockholm, Sweden
- Center for Molecular Medicine, Karolinska Institutet, 171 76 Stockholm, Sweden
- Department of Ophthalmology, Medical Faculty, University of Bonn, Bonn, Germany
- Science for Life Laboratory, Karolinska Institutet, Department of Medical Biochemistry and Biophysics, Division of Genome Biology, 17165 Stockholm, Sweden
- Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology (IKP), Stuttgart, Germany
- University of Tübingen, Tübingen, Germany
Abstract
The abstract is not reproduced here: the paper's license (CC BY-NC-ND) does not allow it. Read it in the paper, at the publisher or on Europe PMC.
Code
The paper says that its authors' code is available on request: it was not published with the paper, so there is nothing to verify.
The paper's code and data availability statement is in the Data section.
Tracing map
A tracing map links a paper to the code its authors published: this paper has none (its code is available on request), so it has no map.
Data
No dataset and no data link were found in the paper.
Code and data availability statement
The paper has a code and data availability statement. Its license (CC BY-NC-ND) does not allow reproducing it here; in short, from what the harvester recognized in it:
- it says that the data are available on request
- it says that the code is available on request
Read it in the paper: doi.org/10.1016/j.isci.2026.115702.
Versions
The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.
Version 1, 29 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 11 authors, 3 keywords, 5 funders, 36 references, 2 RRIDs.
Cite
This paper
Nasiri, R., Fayazbakhsh, F., Sanei, R., Wu, T., Taebnia, N., Habibey, R., Fotouhi, O., Cognetti, J., Lauschke, V. M., Russom, A., & Herland, A. (2026). Metabolic assessment of iPSC-derived neurons under ketone-enriched condition: Ketone sensor development and BHB-driven metabolic adaptation. iScience, 29(5), 115702. https://
BibTeX
@article{nasiri2026metab
author = {Nasiri, Rohollah and Fayazbakhsh, Farzaneh and Sanei, Reyhaneh and Wu, Tingting and Taebnia, Nayere and Habibey, Rouhollah and Fotouhi, Omid and Cognetti, John and Lauschke, Volker M and Russom, Aman and Herland, Anna},
title = {{Metabolic assessment of iPSC-derived neurons under ketone-enriched condition: Ketone sensor development and BHB-driven metabolic adaptation}},
journal = {iScience},
year = {2026},
month = apr,
volume = {29},
number = {5},
pages = {115702},
publisher = {Elsevier},
issn = {2589-0042},
doi = {10.1016/
url = {https://
pmid = {42088362},
pmcid = {PMC13138072}
}
RIS
TY - JOUR
AU - Nasiri, Rohollah
AU - Fayazbakhsh, Farzaneh
AU - Sanei, Reyhaneh
AU - Wu, Tingting
AU - Taebnia, Nayere
AU - Habibey, Rouhollah
AU - Fotouhi, Omid
AU - Cognetti, John
AU - Lauschke, Volker M
AU - Russom, Aman
AU - Herland, Anna
TI - Metabolic assessment of iPSC-derived neurons under ketone-enriched condition: Ketone sensor development and BHB-driven metabolic adaptation
T2 - iScience
J2 - iScience
PY - 2026
DA - 2026/
VL - 29
IS - 5
SP - 115702
SN - 2589-0042
PB - Elsevier
DO - 10.1016/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1016/
"type": "article-journal",
"title": "Metabolic assessment of iPSC-derived neurons under ketone-enriched condition: Ketone sensor development and BHB-driven metabolic adaptation",
"container-title": "iScience",
"author": [
{
"family": "Nasiri",
"given": "Rohollah"
},
{
"family": "Fayazbakhsh",
"given": "Farzaneh"
},
{
"family": "Sanei",
"given": "Reyhaneh"
},
{
"family": "Wu",
"given": "Tingting"
},
{
"family": "Taebnia",
"given": "Nayere"
},
{
"family": "Habibey",
"given": "Rouhollah"
},
{
"family": "Fotouhi",
"given": "Omid"
},
{
"family": "Cognetti",
"given": "John"
},
{
"family": "Lauschke",
"given": "Volker M"
},
{
"family": "Russom",
"given": "Aman"
},
{
"family": "Herland",
"given": "Anna"
}
],
"container-title-short":
"volume": "29",
"issue": "5",
"page": "115702",
"DOI": "10.1016/
"PMID": "42088362",
"PMCID": "PMC13138072",
"ISSN": "2589-0042",
"publisher": "Elsevier",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
4,
13
]
]
}
}
Similar papers
The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.
- [1] doi:10.1038/s41467-026-76837-1 [code]
- Drug screen and machine learning predict neuroprotective agents in a preclinical human model of childhood dementia.Journal: Nature communicationsIn common: 2 references
- [2] doi:10.3390/ijms27135902
- Functional Expression of Nicotinic Receptors on iPSC-Derived Astrocytes and Signalling Disturbances by a Panel of Neonicotinoid Pesticides and Their Metabolites.Journal: International journal of molecular sciencesIn common: cellular / molecular, 1 reference
- [3] doi:10.1038/s44321-026-00491-9
- β-hydroxybutyrate restores social deficits by suppressing HDAC9 in the ACC of Shank3B-deficient mice.Journal: EMBO molecular medicineIn common: cellular / molecular, 1 reference
- [4] doi:10.1002/trc2.70278 [code]
- A combination of ketones and NAD&
lt;sup& gt;+& lt;/ sup& gt; precursor preserves white matter integrity in mild cognitive impairment. Journal: Alzheimer's & dementia (New York, N. Y.)In common: cellular / molecular, 1 reference - [5] doi:10.1038/s41467-026-76812-w [code]
- Assessing molecular, cellular and transcriptomic bases of laminar perfusion and cytoarchitecture coupling in the human cortex.Journal: Nature communicationsIn common: cellular / molecular, 1 reference
- [6] doi:10.3390/cells15121101
- Compensatory Intercellular Mitochondrial Transfer Improves Bioenergetics in P301L Tau-Affected Neuronal Cells.Journal: CellsIn common: cellular / molecular, 1 reference
- [7] doi:10.1002/ana.78203 [code]
- AI-Driven Mapping of Seizure Spread Patterns.Journal: Annals of neurologyIn common: 1 reference
- [8] doi:10.1002/mrm.70451 [code]
- Atlas of Brain Glucose Metabolism Using Deuterium Metabolic Imaging at 3 T.Journal: Magnetic resonance in medicineIn common: 1 reference
- [9] doi:10.1073/pnas.2531706123 [code]
- Metabolism-weighted brain connectome reveals synaptic integration and vulnerability to neurodegeneration.Journal: Proceedings of the National Academy of Sciences of the United States of AmericaIn common: cellular / molecular, 1 reference
- [10] doi:10.1126/sciadv.adt2527
- NPAS3-regulated astrocyte mitochondrial bioenergetics is required for cognition.Journal: Science advancesIn common: cellular / molecular, 1 reference
Contribute
The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.
Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.
Claim this paper
Correct its record
Say what each link of this record is, remove the ones that are not the paper's, add the ones that are missing. The correction becomes a new version of the record, in its Versions section.
Request its removal
To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).
Discussion, reproductions, activity
Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.
Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.
Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.
