Evidence map›Paper›PMID 41804597›Full record

ArticleThe FEBS journal2026

Pml loss worsens NEK1-linked ALS and Pml induction drives NEK1 degradation, precluding disease onset.

Panagiota Georgiadou, Bahriye Erkaya, Michiko Niwa-Kawakita, Merve Oltan, Yigit Kemal Keskin, Egemen Sahin, Harun Öztürk, Fatmanur Tiryaki, Kutay Yildiz, Idil Özgenç and 9 more

Abstract read
In one paragraph

Article in The FEBS journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

19 authors.

Panagiota GeorgiadouFaculty of Engineering and Natural Sciences, Sabanci University, Istanbul, Turkey.
Bahriye ErkayaDepartment of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey.
Michiko Niwa-KawakitaCommon Laboratory, BrainEver & Center for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Paris, France.
Merve OltanFaculty of Engineering and Natural Sciences, Sabanci University, Istanbul, Turkey.
Yigit Kemal KeskinFaculty of Engineering and Natural Sciences, Sabanci University, Istanbul, Turkey.
Egemen SahinDepartment of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey.
Harun ÖztürkDepartment of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey.
Fatmanur TiryakiKoç University, School of Medicine and Department of Molecular Biology and Genetics, Istanbul, Turkey.ORCID https://orcid.org/0000-0003-0855-3817
Kutay YildizDepartment of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey.
Idil ÖzgençDepartment of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey.
Ezgi OdabasiKoç University, School of Medicine and Department of Molecular Biology and Genetics, Istanbul, Turkey.
Emre PekbilirDepartment of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey.
Sukru Anil DoganDepartment of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey.ORCID https://orcid.org/0000-0002-1800-2923
Valérie Lallemand-BreitenbachCommon Laboratory, BrainEver & Center for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Paris, France.
Stephanie VargasCommon Laboratory, BrainEver & Center for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Paris, France.
Alain ProchiantzCommon Laboratory, BrainEver & Center for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Paris, France.
Elif Nur Firat-KaralarKoç University, School of Medicine and Department of Molecular Biology and Genetics, Istanbul, Turkey.ORCID https://orcid.org/0000-0001-7589-473X
Hugues de ThéCommon Laboratory, BrainEver & Center for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Paris, France.
Umut SahinFaculty of Engineering and Natural Sciences, Sabanci University, Istanbul, Turkey.ORCID https://orcid.org/0000-0002-4100-5751

Funding

European Molecular Biology Organization Installation Grant IG3336H2020 European Research Council 679140Türkiye Bilimsel ve Teknolojik Araştırma Kurumu 119N095
6 · The paper itself

Abstract

Germinal mono-allelic loss-of-function mutations of NEK1 drive amyotrophic lateral sclerosis (ALS) at variable penetrance, presumably through haploinsufficiency. Modeling the ALS-associated Arg812Ter mutation in mice revealed that the resulting truncated Nek1 (Nek1

Indexed as

Amyotrophic Lateral SclerosisNIMA-Related Kinase 1Promyelocytic Leukemia ProteinAnimalsDisease Models, AnimalHumansMiceMutationProteolysisSumoylationNek1 protein, mouseNIMA-Related Kinase 1Pml protein, mousePromyelocytic Leukemia ProteinALSNEK1PMLSUMOubiquitin

Identifiers

PMID41804597
PMCPMC13534964

What OpenQuestion holds

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Registered trials

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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.