| Accessory subunits are integral for assembly and function of human mitochondrial complex I DA Stroud, EE Surgenor, LE Formosa, B Reljic, AE Frazier, MG Dibley, ... Nature 538 (7623), 123-126, 2016 | 508 | 2016 |
| Building a complex complex: Assembly of mitochondrial respiratory chain complex I LE Formosa, MG Dibley, DA Stroud, MT Ryan Seminars in cell & developmental biology 76, 154-162, 2018 | 184 | 2018 |
| Gene knockout using transcription activator-like effector nucleases (TALENs) reveals that human NDUFA9 protein is essential for stabilizing the junction between membrane and … DA Stroud, LE Formosa, XW Wijeyeratne, TN Nguyen, MT Ryan Journal of Biological Chemistry 288 (3), 1685-1690, 2013 | 99 | 2013 |
| Preservation of skeletal muscle mitochondrial content in older adults: relationship between mitochondria, fibre type and high‐intensity exercise training VL Wyckelsma, I Levinger, MJ McKenna, LE Formosa, MT Ryan, ... The Journal of physiology 595 (11), 3345-3359, 2017 | 87 | 2017 |
| The ‘mitochondrial contact site and cristae organising system’(MICOS) in health and human disease MJ Eramo, V Lisnyak, LE Formosa, MT Ryan The Journal of Biochemistry 167 (3), 243-255, 2020 | 80 | 2020 |
| Characterization of mitochondrial FOXRED1 in the assembly of respiratory chain complex I LE Formosa, M Mimaki, AE Frazier, M McKenzie, TL Stait, DR Thorburn, ... Human molecular genetics 24 (10), 2952-2965, 2015 | 77 | 2015 |
| Dissecting the Roles of Mitochondrial Complex I Intermediate Assembly Complex Factors in the Biogenesis of Complex I LE Formosa, L Muellner-Wong, B Reljic, AJ Sharpe, TD Jackson, ... Cell Reports 31 (3), 107541, 2020 | 75 | 2020 |
| OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect K Thompson, N Mai, M Oláhová, F Scialó, LE Formosa, DA Stroud, ... EMBO Molecular Medicine 10 (11), e9060, 2018 | 72 | 2018 |
| Biallelic mutations in TMEM126B cause severe complex I deficiency with a variable clinical phenotype CL Alston, AG Compton, LE Formosa, V Strecker, M Oláhová, TB Haack, ... The American Journal of Human Genetics 99 (1), 217-227, 2016 | 71 | 2016 |
| Mitochondrial OXPHOS complex assembly lines LE Formosa, MT Ryan Nature cell biology 20 (5), 511-513, 2018 | 62 | 2018 |
| Fatal perinatal mitochondrial cardiac failure caused by recurrent de novo duplications in the ATAD3 locus AE Frazier, AG Compton, Y Kishita, DH Hock, AME Welch, ... Med 2 (1), 49-73. e10, 2021 | 53 | 2021 |
| The mitochondrial acyl-carrier protein interaction network highlights important roles for LYRM family members in complex I and mitoribosome assembly MG Dibley, LE Formosa, B Lyu, B Reljic, D McGann, L Muellner-Wong, ... Molecular & Cellular Proteomics 19 (1), 65-77, 2020 | 46 | 2020 |
| Metabolic characteristics of CD8+ T cell subsets in young and aged individuals are not predictive of functionality KM Quinn, T Hussain, F Kraus, LE Formosa, WK Lam, MJ Dagley, ... Nature Communications 11 (1), 2857, 2020 | 39 | 2020 |
| Two independent respiratory chains adapt OXPHOS performance to glycolytic switch E Fernandez-Vizarra, S Lopez-Calcerrada, A Sierra-Magro, ... Cell Metabolism 34 (11), 1792-1808. e6, 2022 | 31 | 2022 |
| Mitochondrial fusion: Reaching the end of mitofusin’s tether LE Formosa, MT Ryan The Journal of Cell Biology 215 (5), 597, 2016 | 29 | 2016 |
| Optic atrophy–associated TMEM126A is an assembly factor for the ND4-module of mitochondrial complex I LE Formosa, B Reljic, AJ Sharpe, DH Hock, L Muellner-Wong, DA Stroud, ... Proceedings of the National Academy of Sciences 118 (17), e2019665118, 2021 | 24 | 2021 |
| A homozygous variant in NDUFA8 is associated with developmental delay, microcephaly, and epilepsy due to mitochondrial complex I deficiency Y Yatsuka, Y Kishita, LE Formosa, M Shimura, F Nozaki, T Fujii, KR Nitta, ... Clinical Genetics 98 (2), 155-165, 2020 | 20 | 2020 |
| Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module TD Jackson, JJ Crameri, L Muellner-Wong, AE Frazier, CS Palmer, ... Proceedings of the National Academy of Sciences 119 (13), e2115566119, 2022 | 18 | 2022 |
| SILAC-based complexome profiling dissects the structural organization of the human respiratory supercomplexes in SCAFIKO cells E Fernández-Vizarra, S López-Calcerrada, LE Formosa, R Pérez-Pérez, ... Biochimica et Biophysica Acta (BBA)-Bioenergetics 1862 (7), 148414, 2021 | 17 | 2021 |
| Mitochondrial COA7 is a heme-binding protein with disulfide reductase activity, which acts in the early stages of complex IV assembly LE Formosa, S Maghool, AJ Sharpe, B Reljic, L Muellner-Wong, ... Proceedings of the National Academy of Sciences 119 (9), e2110357119, 2022 | 16* | 2022 |
Michael T RyanMonash University, Melbourne在 monash.edu 的电子邮件经过验证
