Luke E. Formosa

23 Innovation Walk
Melbourne, VIC 3800, Australia

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 33 publications

Structure of the lysosomal KICSTOR-GATOR1-SAMTOR nutrient-sensing supercomplex.

Structure of the lysosomal KICSTOR-GATOR1-SAMTOR nutrient-sensing supercomplex.

Journal: Cell

Published: April 15, 2025

Untargeted proteomics enables ultra-rapid variant prioritisation in mitochondrial and other rare diseases.

Untargeted proteomics enables ultra-rapid variant prioritisation in mitochondrial and other rare diseases.

Journal: Genome medicine

Published: September 18, 2024

Haptoglobin and Glutamine Synthetase May Biomark Cachexia Induced by Antiacute Myeloid Leukaemia Chemotherapy.

Haptoglobin and Glutamine Synthetase May Biomark Cachexia Induced by Antiacute Myeloid Leukaemia Chemotherapy.

Journal: Journal of cachexia, sarcopenia and muscle

Published: July 29, 2024

Mitochondrial damage in muscle specific PolG mutant mice activates the integrated stress response and disrupts the mitochondrial folate cycle.

Mitochondrial damage in muscle specific PolG mutant mice activates the integrated stress response and disrupts the mitochondrial folate cycle.

Journal: Nature communications

Published: June 23, 2024

Phosphoproteomics-directed manipulation reveals SEC22B as a hepatocellular signaling node governing metabolic actions of glucagon.

Phosphoproteomics-directed manipulation reveals SEC22B as a hepatocellular signaling node governing metabolic actions of glucagon.

Journal: Nature communications

Published: January 17, 2024

Human Tim8a, Tim8b and Tim13 are auxiliary assembly factors of mature Complex IV.

Human Tim8a, Tim8b and Tim13 are auxiliary assembly factors of mature Complex IV.

Journal: EMBO reports

Published: November 04, 2022

Biallelic pathogenic variants in COX11 are associated with an infantile-onset mitochondrial encephalopathy.

Biallelic pathogenic variants in COX11 are associated with an infantile-onset mitochondrial encephalopathy.

Journal: Human mutation

Published: April 20, 2022

Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module.

Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: March 25, 2022

Mitochondrial COA7 is a heme-binding protein with disulfide reductase activity, which acts in the early stages of complex IV assembly.

Mitochondrial COA7 is a heme-binding protein with disulfide reductase activity, which acts in the early stages of complex IV assembly.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: January 11, 2022

Inwardly rectifying potassium channels mediate polymyxin-induced nephrotoxicity.

Inwardly rectifying potassium channels mediate polymyxin-induced nephrotoxicity.

Journal: Cellular and molecular life sciences : CMLS

Published: November 11, 2021

Optic atrophy-associated TMEM126A is an assembly factor for the ND4-module of mitochondrial complex I.

Optic atrophy-associated TMEM126A is an assembly factor for the ND4-module of mitochondrial complex I.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: April 21, 2021

Two independent respiratory chains adapt OXPHOS performance to glycolytic switch.

Two independent respiratory chains adapt OXPHOS performance to glycolytic switch.

Journal: Cell metabolism

Published: February 22, 2021

Showing 1-12 of 33

Last Updated: 09/26/2026