Author

Xiaomeng Xing

University of Nottingham

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cancer Biology· 1 Cell Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Approach:experimental assay· 3 Organism:human· 3 Assay:imaging· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell-cell communication· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Alison J. BeckettiD· 2 shared Daniel G. BoothiD· 2 shared Eva L. SimpsoniD· 2 shared Ian A. PrioriD· 2 shared Ahmed BayyoomiiD· 1 shared Aleksandra Byrska· 1 shared Alexandra Sarginson· 1 shared Alice WorkeriD· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersCancer Biology

Alison J. BeckettORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Nucleophosmin mutations lead to abnormal, but reversible, nucleoli architecture and aggregate formation - implications for NPM1-targeting therapies in AML

Martin A. Grundy, Kellie Lucken, Xiaomeng Xing, Eva L. Simpson, Alice Worker, Ahmed Bayyoomi, Alison J. Beckett, Ian A. Prior, Daniel G. Booth, Claire Seedhouse

This study shows that NPM1 mutations cause abnormal nucleoli structure and reversible aggregates in AML, suggesting new therapeutic targets.

Journal of Cell Science · Apr 22, 2025Peer-reviewedCancer Biology

The Chromosome Periphery is an Essential Compartment of Oocyte Chromosomes

Eva L. Simpson, Benjamin Wetherall, Aleksandra Byrska, Liam P. Cheeseman, Tania Mendonca, Xiaomeng Xing, Alison J. Beckett, Hélder Maiato, Alexandra Sarginson, Ian A. Prior, Geraldine M. Hartshorne, Andrew D. McAinsh, Suzanne Madgwick, Daniel G. Booth

This study investigates the role of the chromosome periphery in oocyte meiosis, showing its impact on chromosome structure and meiotic progression in human and mouse oocytes.

bioRxiv · Dec 20, 2024 · PreprintCell Biology

Regulation of Toxic RNA Foci and Repeat Expansion DMPK Transcripts: Role of MBNL Proteins and RNA Decay Pathways

Xiaomeng Xing, Róbert Márkus, Tushar Ghosh, Sarah Buxton, Daniel J. Nieves, Marzena Wojciechowska, J. David Brook

This study investigates how MBNL proteins and RNA decay pathways regulate mutant DMPK mRNA in DM1, showing that their absence reduces RNA foci and promotes mRNA degradation.

bioRxiv · Sep 28, 2023 · PreprintGenetics