Evidence map›Paper›PMID 41171811›Full record

ArticleThe Journal of general virology2025

Conserved mode of nuclear lamina distortion by primate cytomegaloviruses: importance of the pSer22 motif, viral kinase and

Kishore Dhotre, Martin Schütz, Sofia von Essen, Lucio Fortelny, Christina Wangen, Friedrich Hahn, Heinrich Sticht, Manfred Marschall

Abstract read
In one paragraph

Article in The Journal of general virology, 2025. 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

8 authors.

Kishore DhotreHarald zur Hausen Institute of Virology, Friedrich-Alexander University of Erlangen-Nürnberg (FAU), Erlangen, Germany.
Martin SchützHarald zur Hausen Institute of Virology, Friedrich-Alexander University of Erlangen-Nürnberg (FAU), Erlangen, Germany.
Sofia von EssenHarald zur Hausen Institute of Virology, Friedrich-Alexander University of Erlangen-Nürnberg (FAU), Erlangen, Germany.
Lucio FortelnyHarald zur Hausen Institute of Virology, Friedrich-Alexander University of Erlangen-Nürnberg (FAU), Erlangen, Germany.
Christina WangenHarald zur Hausen Institute of Virology, Friedrich-Alexander University of Erlangen-Nürnberg (FAU), Erlangen, Germany.
Friedrich HahnHarald zur Hausen Institute of Virology, Friedrich-Alexander University of Erlangen-Nürnberg (FAU), Erlangen, Germany.
Heinrich StichtDivision of Bioinformatics, Institute of Biochemistry, Friedrich-Alexander University of Erlangen-Nürnberg (FAU), Erlangen, Germany.
Manfred MarschallHarald zur Hausen Institute of Virology, Friedrich-Alexander University of Erlangen-Nürnberg (FAU), Erlangen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) is a ubiquitous human pathogen of high clinical relevance. In terms of pathogenic determination, the regulatory factors of HCMV-host interaction play a crucial role, and recently we reported on virus-supportive functions of the cellular peptidyl-prolyl

Indexed as

CytomegalovirusNIMA-Interacting Peptidylprolyl IsomeraseNuclear LaminaViral ProteinsAmino Acid MotifsAnimalsCytomegalovirus InfectionsFibroblastsHost-Pathogen InteractionsHumansLamin Type APhosphorylationVirus ReplicationLamin Type ANIMA-Interacting Peptidylprolyl IsomerasePIN1 protein, humanViral Proteinscytomegalovirus replicationnuclear lamina distortionpeptidyl-prolyl cis/trans isomerase Pin1regulatory viral kinasessite-specific lamin phosphorylationviral nuclear egress

Identifiers

PMID41171811
PMCPMC12578131

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.