Mitochondrial fusion: Reaching the end of mitofusin’s tether

od Formosa, Luke E., Ryan, Michael T.
izdano v J Cell Biol (2016)

Gene Knockout Using Transcription Activator-like Effector Nucleases (TALENs) Reveals That Human NDUFA9 Protein Is Essential for Stabilizing the Junction between Membrane and Matrix...

od Stroud, David A., Formosa, Luke E., Wijeyeratne, Xiaonan W., Nguyen, Thanh N., Ryan, Michael T.
Izdano 2013

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

od Formosa, Luke E., Reljic, Boris, Sharpe, Alice J., Hock, Daniella H., Muellner-Wong, Linden, Stroud, David A., Ryan, Michael T.
izdano v Proc Natl Acad Sci U S A (2021)

Preservation of skeletal muscle mitochondrial content in older adults: relationship between mitochondria, fibre type and high‐intensity exercise training

od Wyckelsma, Victoria L., Levinger, Itamar, McKenna, Michael J., Formosa, Luke E., Ryan, Michael T., Petersen, Aaron C., Anderson, Mitchell J., Murphy, Robyn M.
izdano v J Physiol (2017)

A Role for the Mitochondrial Protein Mrpl44 in Maintaining OXPHOS Capacity

od Yeo, Janet H. C., Skinner, Jarrod P. J., Bird, Matthew J., Formosa, Luke E., Zhang, Jian-Guo, Kluck, Ruth M., Belz, Gabrielle T., Chong, Mark M. W.
izdano v PLoS One (2015)

The Mitochondrial Acyl-carrier Protein Interaction Network Highlights Important Roles for LYRM Family Members in Complex I and Mitoribosome Assembly

od Dibley, Marris G., Formosa, Luke E., Lyu, Baobei, Reljic, Boris, McGann, Dylan, Muellner-Wong, Linden, Kraus, Felix, Sharpe, Alice J., Stroud, David A., Ryan, Michael T.
izdano v Mol Cell Proteomics (2020)

A patient with homozygous nonsense variants in two Leigh syndrome disease genes: distinguishing a dual diagnosis from a hypomorphic protein-truncating variant

od Lake, Nicole J., Formosa, Luke E., Stroud, David A., Ryan, Michael T., Calvo, Sarah E., Mootha, Vamsi K., Morar, Bharti, Procopis, Peter G, Christodoulou, John, Compton, Alison G., Thorburn, David R.
izdano v Hum Mutat (2019)

Metabolic characteristics of CD8(+) T cell subsets in young and aged individuals are not predictive of functionality

od Quinn, Kylie M., Hussain, Tabinda, Kraus, Felix, Formosa, Luke E., Lam, Wai K., Dagley, Michael J., Saunders, Eleanor C., Assmus, Lisa M., Wynne-Jones, Erica, Loh, Liyen, van de Sandt, Carolien E., Cooper, Lucy, Good-Jacobson, Kim L., Kedzierska, Katherine, Mackay, Laura K., McConville, Malcolm J., Ramm, Georg, Ryan, Michael T., La Gruta, Nicole L.
izdano v Nat Commun (2020)

Publisher Correction: Metabolic characteristics of CD8(+) T cell subsets in young and aged individuals are not predictive of functionality

od Quinn, Kylie M., Hussain, Tabinda, Kraus, Felix, Formosa, Luke E., Lam, Wai K., Dagley, Michael J., Saunders, Eleanor C., Assmus, Lisa M., Wynne-Jones, Erica, Loh, Liyen, van de Sandt, Carolien E., Cooper, Lucy, Good-Jacobson, Kim L., Kedzierska, Katherine, Mackay, Laura K., McConville, Malcolm J., Ramm, Georg, Ryan, Michael T., La Gruta, Nicole L.
izdano v Nat Commun (2020)

OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect

od Thompson, Kyle, Mai, Nicole, Oláhová, Monika, Scialó, Filippo, Formosa, Luke E, Stroud, David A, Garrett, Madeleine, Lax, Nichola Z, Robertson, Fiona M, Jou, Cristina, Nascimento, Andres, Ortez, Carlos, Jimenez‐Mallebrera, Cecilia, Hardy, Steven A, He, Langping, Brown, Garry K, Marttinen, Paula, McFarland, Robert, Sanz, Alberto, Battersby, Brendan J, Bonnen, Penelope E, Ryan, Michael T, Chrzanowska‐Lightowlers, Zofia MA, Lightowlers, Robert N, Taylor, Robert W
izdano v EMBO Mol Med (2018)

Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype

od Alston, Charlotte L., Compton, Alison G., Formosa, Luke E., Strecker, Valentina, Oláhová, Monika, Haack, Tobias B., Smet, Joél, Stouffs, Katrien, Diakumis, Peter, Ciara, Elżbieta, Cassiman, David, Romain, Nadine, Yarham, John W., He, Langping, De Paepe, Boel, Vanlander, Arnaud V., Seneca, Sara, Feichtinger, René G., Płoski, Rafal, Rokicki, Dariusz, Pronicka, Ewa, Haller, Ronald G., Van Hove, Johan L.K., Bahlo, Melanie, Mayr, Johannes A., Van Coster, Rudy, Prokisch, Holger, Wittig, Ilka, Ryan, Michael T., Thorburn, David R., Taylor, Robert W.
izdano v Am J Hum Genet (2016)

Fatal perinatal mitochondrial cardiac failure caused by recurrent de novo duplications in the ATAD3 locus

od Frazier, Ann E., Compton, Alison G., Kishita, Yoshihito, Hock, Daniella H., Welch, AnneMarie E., Amarasekera, Sumudu S.C., Rius, Rocio, Formosa, Luke E., Imai-Okazaki, Atsuko, Francis, David, Wang, Min, Lake, Nicole J., Tregoning, Simone, Jabbari, Jafar S., Lucattini, Alexis, Nitta, Kazuhiro R., Ohtake, Akira, Murayama, Kei, Amor, David J., McGillivray, George, Wong, Flora Y., van der Knaap, Marjo S., Jeroen Vermeulen, R., Wiltshire, Esko J., Fletcher, Janice M., Lewis, Barry, Baynam, Gareth, Ellaway, Carolyn, Balasubramaniam, Shanti, Bhattacharya, Kaustuv, Freckmann, Mary-Louise, Arbuckle, Susan, Rodriguez, Michael, Taft, Ryan J., Sadedin, Simon, Cowley, Mark J., Minoche, André E., Calvo, Sarah E., Mootha, Vamsi K., Ryan, Michael T., Okazaki, Yasushi, Stroud, David A., Simons, Cas, Christodoulou, John, Thorburn, David R.
izdano v Med (N Y) (2020)