Author

Y. Xiu

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

Biology Disciplines

Click to filter author papers

Biochemistry· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Assay:DNA methylation· 2 Approach:experimental assay· 2 Assay:metabolomics· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:differential expression· 1 Research Focus:metabolism & bioenergetics· 1

Frequent Co-Authors

J. L. Fiddler· 2 shared M. S. Field· 2 shared W. N. Phinney· 2 shared A. E. Thalacker-Mercer· 1 shared C. Metallo· 1 shared J. E. Blum· 1 shared J. T. Brosnan· 1 shared K. E. Heyden· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersBiochemistry

J. L. Fiddler

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Reduced methionine synthase (Mtr) expression creates a functional vitamin B12 deficiency that leads to uracil accumulation in mouse mitochondrial DNA

K. E. Heyden, J. L. Fiddler, Y. Xiu, O. V. Malysheva, M. K. Handzlik, W. N. Phinney, L. Stiles, S. S. Stabler, C. Metallo, M. A. Caudill, M. S. Field

This study shows that reduced Mtr expression causes B12 deficiency, leading to uracil accumulation in mtDNA and impaired mitochondrial function in mice.

bioRxiv · Aug 29, 2022 · PreprintBiochemistry

Reduced Shmt2 expression impairs mitochondrial folate accumulation and respiration, and leads to uracil accumulation in mouse mitochondrial DNA

J. L. Fiddler, Y. Xiu, J. E. Blum, S. G. Lamarre, W. N. Phinney, S. P. Stabler, M. E. Brosnan, J. T. Brosnan, A. E. Thalacker-Mercer, M. S. Field

This study shows that reduced Shmt2 expression and folate deficiency impair mitochondrial dTMP synthesis, increase uracil in mtDNA, and reduce mitochondrial function in mice.

bioRxiv · Apr 12, 2021Biochemistry