Stephen P. Burr
Cambridge, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 22 publications
Ubiquitin-mediated mitophagy regulates the inheritance of mitochondrial DNA mutations.
Journal: Science (New York, N.Y.)
Published: October 09, 2025
MitoPerturb-Seq identifies gene-specific single-cell responses to mitochondrial DNA depletion and heteroplasmy.
Journal: Nature structural & molecular biology
Published: June 20, 2025
Origins of tissue and cell-type specificity in mitochondrial DNA (mtDNA) disease.
Journal: Human molecular genetics
Published: December 21, 2023
LRPPRC and SLIRP synergize to maintain sufficient and orderly mammalian mitochondrial translation.
Journal: Nucleic acids research
Published: November 13, 2023
High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout life.
Journal: Science advances
Published: October 25, 2023
Measuring Single-Cell Mitochondrial DNA Copy Number and Heteroplasmy using Digital Droplet Polymerase Chain Reaction.
Journal: Journal of visualized experiments : JoVE
Published: August 01, 2022
Cell lineage-specific mitochondrial resilience during mammalian organogenesis.
Journal: Cell
Published: April 19, 2022
Mitochondrial DNA heteroplasmy is modulated during oocyte development propagating mutation transmission.
Journal: Science advances
Published: December 08, 2021
Oxygen tension modulates the mitochondrial genetic bottleneck and influences the segregation of a heteroplasmic mtDNA variant in vitro.
Journal: Communications biology
Published: October 06, 2020
ABHD11 maintains 2-oxoglutarate metabolism by preserving functional lipoylation of the 2-oxoglutarate dehydrogenase complex.
Journal: Nature communications
Published: January 09, 2020
Last Updated: 09/26/2026