Publications by authors named "David Stroud"

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HSD17β11 regulates PLIN5-ATGL mediated lipolysis, but not hepatic lipid metabolism in mice.
Stacey N Keenan, Natasha D Suriani, Gio Fidelito, Jackie Bayliss, Jieqiong Lou, David A Stroud

J Lipid Res· December 2025

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Postnatal Abrogation of VEGFR2 Blocks Terminal Cap2 Differentiation by Preventing the Developmental Progression from a Capillary Intermediate Cell State.
Daoqin Zhang, Carsten Knutsen, David J Stroud, Xibing Che, David N Cornfield

bioRxiv· November 2025

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Inhibition of heme biosynthesis triggers cuproptosis in acute myeloid leukemia.
Alexander C Lewis, Emily Gruber, Rheana Franich, Jessica Armstrong, Madison J Kelly, David A Stroud

Cell· November 2025

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Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders.
Sara M Fielder, Marisa W Friederich, Daniella H Hock, Jessie R Zhang, Liana M Valin, David A Stroud

EMBO Mol Med· October 2025

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Functional Characterization of a Novel GPC3 Missense Variant in Simpson-Golabi-Behmel Syndrome.
Teresa Zhao, Kirsten Allan, Juliet Taylor, David R Thorburn, Susan M White, David A Stroud

Am J Med Genet A· October 2025

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Complex II assembly drives metabolic adaptation to OXPHOS dysfunction.
Roopasingam Kugapreethan, Sheik Nadeem Elahee Doomun, Joanna Sacharz, Ann E Frazier, Tanavi Sharma, David A Stroud

Sci Adv· August 2025

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Generative AI and digital twins: shaping a paradigm shift from precision to truly personalized medicine.
Maria Bordukova, Alina J Arneth, Nikita Makarov, Robyn M Brown, Elena K Schneider-Futschik, David Stroud

Expert Opin Drug Discov· July 2025

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Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation.
Jiemin Nah, Sreya Mahendran, Baptiste Kerouanton, Liang Cui, Daniella H Hock, David A Stroud

Mol Cell· July 2025

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Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders.
Sara M Fielder, Marisa W Friederich, Daniella H Hock, Jessie R Zhang, Liana M Valin, David A Stroud

medRxiv· July 2025

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Variant and Rett Syndrome: Overlapping Phenotypes, Molecular Convergence, and Expanding the Genetic Spectrum.
Elaine Zhang, Teresa Zhao, Tim Sikora, Carolyn Ellaway, Wendy A Gold, David A Stroud

Hum Mutat· June 2025

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HMGCS1 variants cause rigid spine syndrome amenable to mevalonic acid treatment in an animal model.
Lein N H Dofash, Lee B Miles, Yoshihiko Saito, Eloy Rivas, Vanessa Calcinotto, David A Stroud

Brain· May 2025

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Untargeted proteomics enables ultra-rapid variant prioritisation in mitochondrial and other rare diseases.
Daniella H Hock, Nikeisha J Caruana, Liana N Semcesen, Nicole J Lake, Luke E Formosa, David A Stroud

Genome Med· May 2025

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Proximity proteomics reveals a mechanism of fatty acid transfer at lipid droplet-mitochondria- endoplasmic reticulum contact sites.
Ayenachew Bezawork-Geleta, Camille J Devereux, Stacey N Keenan, Jieqiong Lou, Ellie Cho, David A Stroud

Nat Commun· March 2025

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Review: Utility of mass spectrometry in rare disease research and diagnosis.
Teresa Zhao, Daniella H Hock, James Pitt, David R Thorburn, David A Stroud

NPJ Genom Med· March 2025

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Formation of I+III supercomplex rescues respiratory chain defects.
Chao Liang, Abhilash Padavannil, Shan Zhang, Sheryl Beh, David R L Robinson, David A Stroud

Cell Metab· February 2025

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The Australian Genomics Mitochondrial Flagship: A national program delivering mitochondrial diagnoses.
Rocio Rius, Alison G Compton, Naomi L Baker, Shanti Balasubramaniam, Stephanie Best, David A Stroud

Genet Med· January 2025

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An integrated multi-omics approach allowed ultra-rapid diagnosis of a deep intronic pathogenic variant in PDHX and precision treatment in a neonate critically ill with lactic acidosis.
Rodrigo T Starosta, Austin A Larson, Naomi J L Meeks, Sara Gracie, Marisa W Friederich, David A Stroud

Mitochondrion· November 2024

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Generating mammalian knock-out cell lines to investigate mitochondrial protein complex assembly.
Liana N Semcesen, David R L Robinson, David A Stroud

Methods Enzymol· November 2024

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A micro-costing study of mass-spectrometry based quantitative proteomics testing applied to the diagnostic pipeline of mitochondrial and other rare disorders.
Francisco Santos Gonzalez, Daniella H Hock, David R Thorburn, Dylan Mordaunt, Nicholas A Williamson, David A Stroud

Orphanet J Rare Dis· November 2024

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ACAD9 treatment with bezafibrate and nicotinamide riboside temporarily stabilizes cardiomyopathy and lactic acidosis.
Johan L K Van Hove, Marisa W Friederich, Daniella H Hock, David A Stroud, Nikeisha J Caruana

Mitochondrion· September 2024

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Fibre-specific mitochondrial protein abundance is linked to resting and post-training mitochondrial content in the muscle of men.
Elizabeth G Reisman, Javier Botella, Cheng Huang, Ralf B Schittenhelm, David A Stroud

Nat Commun· September 2024

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Dual diagnosis of -related mitochondrial complex III deficiency and recessive -related cataracts.
Elizabeth E Blue, Samuel J Huang, Alyna Khan, Katie Golden-Grant, Brenna Boyd, David A Stroud

Rare· August 2024

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Mtfp1 ablation enhances mitochondrial respiration and protects against hepatic steatosis.
Cecilia Patitucci, Juan Diego Hernández-Camacho, Elodie Vimont, Sonny Yde, Thomas Cokelaer, David A Stroud

Nat Commun· December 2023

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Loss of the large conductance calcium-activated potassium channel causes an increase in mitochondrial reactive oxygen species in glioblastoma cells.
Bogusz Kulawiak, Monika Żochowska, Piotr Bednarczyk, Andrzej Galuba, David A Stroud

Pflugers Arch· September 2023

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-encoded microprotein mitoregulin regulates fatty acid metabolism at the mitochondrial outer membrane.
Shan Zhang, Yabo Guo, Gio Fidelito, David R L Robinson, Chao Liang, David A Stroud

iScience· September 2023

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