Assembly and misassembly of mitochondrial respiratory chain Complex I

  • Ryan, Mike (Primary Chief Investigator (PCI))
  • Stroud, David, (Chief Investigator (CI))
  • Thorburn, David Ross (Chief Investigator (CI))

Project: Research

StatusActive
Effective start/end date1/01/17 → 31/12/19

Funding

  • National Health & Medical Research Council (NHMRC): AUD520,520.00
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Research Output

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

Research output: Contribution to journal › Article › Research › peer-review

Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency

Research output: Contribution to journal › Article › Research › peer-review

Sengers Syndrome-Associated Mitochondrial Acylglycerol Kinase Is a Subunit of the Human TIM22 Protein Import Complex

Research output: Contribution to journal › Article › Research › peer-review

OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect

Research output: Contribution to journal › Article › Research › peer-review

Building a complex complex: Assembly of mitochondrial respiratory chain complex I

Research output: Contribution to journal › Article › Other › peer-review

Equipment

Micro Imaging

Facility/equipment: Facility

FlowCore

Facility/equipment: Facility

Biomedical Proteomics Facility

Facility/equipment: Facility

Micromon

Facility/equipment: Facility