Evidence map›Paper›PMID 42738829›Full record

ArticleCells2026

Modeling Cohen Syndrome in Phoenix Cells: VPS13B Loss Causes Organelle Stress, G1/S Delay, and Fibrillary Inclusion Bodies Formation.

Ksenia N Morozova, Ekaterina R Wolf, Elena V Kiseleva, Alexander V Smirnov, Elena G Pershina, Inna E Pristyazhnyuk

Abstract read
In one paragraph

Article in Cells, 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

6 authors.

Ksenia N MorozovaInstitute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia.ORCID 0000-0003-3307-8819
Ekaterina R WolfDepartment of Genetics and Genetic Technologies, Sirius University of Science and Technology, Sirius 354340, Russia.
Elena V KiselevaInstitute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia.ORCID 0000-0002-8786-499X
Alexander V SmirnovInstitute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia.ORCID 0000-0001-5152-9914
Elena G PershinaInstitute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia.ORCID 0000-0003-2658-7906
Inna E PristyazhnyukInstitute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia.ORCID 0000-0003-0226-4213

Funding

Sirius University of Science and Technology grant of the state program of the «Sirius» Federal Territory «Scientific and technological development of the «Sirius» Federal Territory» (Agreement №26-03, 27/09/2024)
6 · The paper itself

Abstract

Cohen syndrome, caused by pathogenic variants in

Indexed as

Inclusion BodiesIntellectual DisabilityMicrocephalyModels, BiologicalMuscle HypotoniaRetinal DegenerationVesicular Transport ProteinsAutophagyCell ProliferationDevelopmental DisabilitiesEndoplasmic ReticulumFingersGolgi ApparatusHEK293 CellsHumansMitochondriaVesicular Transport ProteinsVPS13B protein, humancell-cycle arrestCOH1Cohen syndromeCRISPR-Cas9ER stressfibrillary inclusionsGolgi fragmentationproteostasisultrastructureVPS13B

Identifiers

PMID42738829
PMCPMC13564750

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.