Luke E Formosa

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 9

Top Venues

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

Human mutation

Nature communications

FASEB journal : official publication of the Federation of American Societies for Experimental Biology

Monash University

La Trobe University (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Monash University

Australia

Postdoctoral Researcher :: Department of Biochemistry and Molecular Biology

Monash University

Australia

Tutorial Coordinator for BMS3021 :: Biochemistry and Molecular Biology

Monash University

Australia

Teaching Associate for BCH3021 and BMS3021 :: Biochemistry and Molecular Biology

La Trobe University

Australia

Undergraduate demonstrator for 2nd and 3rd year Biochemistry and Molecular Biology :: Department of Biochemistry

Education History

La Trobe University

Australia

PHD :: Department of Biochemistry and Genetics

La Trobe University

Australia

BSC

Publications

Cara A Timpani, Didier Debrincat, Stephanie Kourakis, Rebecca Boyer, Luke E Formosa, Joel Ricky Steele, Haijian Zhang, Ralf Bernd Schittenhelm, Aaron P Russell, Emma Rybalka, Angus Lindsay
Loss of endogenous estrogen alters mitochondrial metabolism and muscle clock-related protein Rbm20 in female mdx mice. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 38 (11) (2024)
Rocio Rius, Neal K Bennett, Kaustuv Bhattacharya, Lisa G Riley, Zafer Yüksel, Luke E Formosa, Alison G Compton, Russell C Dale, Mark J Cowley, Velimir Gayevskiy, Saeed M Al Tala, Abdulrahman A Almehery, Michael T Ryan, David R Thorburn, Ken Nakamura, John Chrisodoulou
Biallelic pathogenic variants in COX11 are associated with an infantile-onset mitochondrial encephalopathy. Human mutation (2022)
Thomas D Jackson, Jordan James Crameri, Linden S Muellner-Wong, Ann E Frazier, Catherine S Palmer, Luke E Formosa, Daniella H Hock, Kenji M Fujihara, Tegan Stait, Alice J Sharpe, David R Thorburn, Michael T Ryan, David Arthur Stroud, Diana Stojanovski
Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module. Proceedings of the National Academy of Sciences of the United States of America 119 (13) (2022)
Luke E Formosa, Shadi Maghool, Alice J Sharpe, Boris Reljić, Linden S Muellner-Wong, David Arthur Stroud, Michael T Ryan, Megan J Maher
Mitochondrial COA7 is a heme-binding protein with disulfide reductase activity, which acts in the early stages of complex IV assembly. Proceedings of the National Academy of Sciences of the United States of America 119 (9) (2022)
Luke E Formosa, Boris Reljić, Alice J Sharpe, Daniella Helena Hock, Linden S Muellner-Wong, David Arthur Stroud, Michael T Ryan
Optic atrophy-associated TMEM126A is an assembly factor for the ND4-module of mitochondrial complex I. Proceedings of the National Academy of Sciences of the United States of America 118 (17) (2021)
Kylie M Quinn, Tabinda Hussain, Felix Kraus, Luke E Formosa, Wai Kit Lam, Michael J Dagley, Eleanor C Saunders, Lisa M Assmus, Erica Wynne-Jones, Liyen Loh, Carolien E van de Sandt, Lucy Cooper, Kim L Good-Jacobson, Katherine Kedzierska, Laura K Mackay, Malcolm J McConville, Georg Ramm, Michael T Ryan, Nicole L La Gruta
Publisher Correction: Metabolic characteristics of CD8+ T cell subsets in young and aged individuals are not predictive of functionality. Nature communications 11 (1) (2020)
Yukiko Yatsuka, Yoshihito Kishita, Luke E Formosa, Masaru Shimura, Fumihito Nozaki, Tatsuya Fujii, Kazuhiro R Nitta, Akira Ohtake, Kei Murayama, Michael T Ryan, Yasushi Okazaki
A homozygous variant in NDUFA8 is associated with developmental delay, microcephaly, and epilepsy due to mitochondrial complex I deficiency. Clinical genetics 98 (2) (2020)
Kylie M Quinn, Tabinda Hussain, Felix Kraus, Luke E Formosa, Wai Kit Lam, Michael J Dagley, Eleanor C Saunders, Lisa M Assmus, Erica Wynne-Jones, Liyen Loh, Carolien E van de Sandt, Lucy Cooper, Kim L Good-Jacobson, Katherine Kedzierska, Laura K Mackay, Malcolm J McConville, Georg Ramm, Michael T Ryan, Nicole L La Gruta
Metabolic characteristics of CD8+ T cell subsets in young and aged individuals are not predictive of functionality. Nature communications 11 (1) (2020)
Nicole J Lake, Luke E Formosa, David Arthur Stroud, Michael T Ryan, Sarah E Calvo, Vamsi K Mootha, Bharti Morar, Peter G Procopis, John Chrisodoulou, Alison G Compton, David R Thorburn
A patient with homozygous nonsense variants in two Leigh syndrome disease genes: Distinguishing a dual diagnosis from a hypomorphic protein-truncating variant. Human mutation 40 (7) (2019)

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Publication Activity (10 Years)

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Luke E Formosa