A/Prof David Stroud
Associate Professor, Biochemistry & Pharmacology
Department of Biochemistry and Pharmacology
153 Scholarly works
18 Projects
HIGHLIGHTS
2026
Journal article
Sprint interval exercise disrupts mitochondrial ultrastructure driving a unique mitochondrial stress response and remodelling in men
DOI: 10.1038/s41467-025-66625-82026
Journal article
Functional Characterization of a Novel GPC3 Missense Variant in Simpson–Golabi–Behmel Syndrome
DOI: 10.1002/ajmg.a.642872026
Journal article
Clinical proteomics in variant classification: are we there yet?
DOI: 10.1016/j.pathol.2026.01.2272022
Research grants (ARC, NHMRC, MRFF)
RDMassSpec: Mass-Spectrometry Based Functional Genomics Platform for Solving Rare Genetic Disorders
2022
Research grants (ARC, NHMRC, MRFF)
Developing a Multi-Omics Platform for the Diagnosis of Mitochondrial Disease
2021
Journal article
Intact TP-53 function is essential for sustaining durable responses to BH3-mimetic drugs in leukemias
DOI: 10.1182/blood.20200101672019
Research Grant
Understanding the Assembly of the Commander Complex
RECENT SCHOLARLY WORKS
2026
Journal article
Inhibition of heme biosynthesis triggers cuproptosis in acute myeloid leukemia
DOI: 10.1016/j.cell.2025.10.0282026
Journal article
A Nonketotic Hyperglycinemia Mouse Shows Wide-Ranging Biochemical Consequences of Elevated Glycine, Reduced Folate One-Carbon Charging, and Serine Deficiency
DOI: 10.1002/jimd.701372026
Journal article
Bi-allelic variants in NDUFA5 cause a mitochondriopathy with complex I deficiency
DOI: 10.1016/j.ajhg.2026.03.0032025
Journal article
Untargeted proteomics enables ultra-rapid variant prioritisation in mitochondrial and other rare diseases
DOI: 10.1186/s13073-025-01467-z2025
Journal article
HSD17β11 regulates PLIN5-ATGL mediated lipolysis, but not hepatic lipid metabolism in mice
DOI: 10.1016/j.jlr.2025.1009432025
Journal article
Proximity proteomics reveals a mechanism of fatty acid transfer at lipid droplet-mitochondria- endoplasmic reticulum contact sites
DOI: 10.1038/s41467-025-57405-52025
Journal article
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders
DOI: 10.1038/s44321-025-00290-8
RECENT PROJECTS
2026
Research grants (ARC, NHMRC, MRFF)
Unravelling Mitochondrial ATAD3 as an Underappreciated Cause of Rare Disease