Tegan L Stait

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

D. Stojanovski, Ann E. Frazier, D. Hock, 2022, Proceedings of the National Academy of Sciences of the United States of America.

Function of hTim8a in complex IV assembly in neuronal cells provides insight into pathomechanism underlying Mohr-Tranebjærg syndrome

M. McConville, D. D. De Souza, N. Clemons, 2019, eLife.

Abnormalities of mitochondrial dynamics and bioenergetics in neuronal cells from CDKL5 deficiency disorder

J. Christodoulou, L. E. Formosa, D. Stroud, 2021, Neurobiology of Disease.

Accessory subunits are integral for assembly and function of human mitochondrial complex I

Ann E. Frazier, L. E. Formosa, M. Ryan, 2016, Nature.

Characterization of mitochondrial FOXRED1 in the assembly of respiratory chain complex I.

Ann E. Frazier, L. E. Formosa, M. Ryan, 2015, Human molecular genetics.

High-intensity training induces non-stoichiometric changes in the mitochondrial proteome of human skeletal muscle without reorganisation of respiratory chain content

P. Meikle, N. Jamnick, J. Botella, 2021, Nature Communications.

Multi-omics reveal intricate network of mitochondrial adaptations to training in human skeletal muscle

P. Meikle, N. Jamnick, J. Botella, 2021 .

Neuronal-specific function of hTim8a in Complex IV assembly provides insight into the molecular mechanism underlying Mohr-Tranebjærg syndrome

M. McConville, D. Tull, D. D. De Souza, 2019, bioRxiv.

Training-induced bioenergetic improvement in human skeletal muscle is associated with non-stoichiometric changes in the mitochondrial proteome without reorganization of respiratory chain content

D. Bishop, P. Meikle, N. Jamnick, 2021, bioRxiv.

Biallelic Variants in PYROXD2 Cause a Severe Infantile Metabolic Disorder Affecting Mitochondrial Function

N. Brown, J. Christodoulou, Z. Stark, 2022, International journal of molecular sciences.