Matthew McKenzie

Centre for Genetic Diseases, Hudson institute of Medical Research

Affiliated withHudson institute of Medical Research Monash University

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 29	2017

Other Publications

Article	Year
Comparison of log P values obtained from CAChe and other sources. Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering\| PubMed ID: 12680579	2003
Functional respiratory chain analyses in murid xenomitochondrial cybrids expose coevolutionary constraints of cytochrome b and nuclear subunits of complex III. Molecular biology and evolution\| PubMed ID: 12777531	2003
Production of homoplasmic xenomitochondrial mice. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 14745024	2004
Mitochondrial disease: mutations and mechanisms. Neurochemical research\| PubMed ID: 15038606	2004
Unravelling the peculiar nucleation mechanisms for non-ideal binary mixtures with atomistic simulations. The journal of physical chemistry. B\| PubMed ID: 16494406	2006
Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients. Journal of molecular biology\| PubMed ID: 16857210	2006
Probing the nucleation mechanism for the binary n-nonane/1-alcohol series with atomistic simulations. The journal of physical chemistry. B\| PubMed ID: 16970491	2006
Analysis of mitochondrial subunit assembly into respiratory chain complexes using Blue Native polyacrylamide gel electrophoresis. Analytical biochemistry\| PubMed ID: 17391635	2007
Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I. Molecular and cellular biology\| PubMed ID: 17438127	2007
Mitochondrial ND5 gene variation associated with encephalomyopathy and mitochondrial ATP consumption. The Journal of biological chemistry\| PubMed ID: 17940288	2007
Assembly of mitochondrial complex I and defects in disease. Biochimica et biophysica acta\| PubMed ID: 18501715	2009
Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease. American journal of human genetics\| PubMed ID: 18940309	2008
Chapter 18 Analysis of respiratory chain complex assembly with radiolabeled nuclear- and mitochondrial-encoded subunits. Methods in enzymology\| PubMed ID: 19348897	2009
Assembly of nuclear DNA-encoded subunits into mitochondrial complex IV, and their preferential integration into supercomplex forms in patient mitochondria. The FEBS journal\| PubMed ID: 19843159	2009
Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome. Current biology : CB\| PubMed ID: 19962311	2009
Assembly factors of human mitochondrial complex I and their defects in disease. IUBMB life\| PubMed ID: 20552642	2010
Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndrome. American journal of human genetics\| PubMed ID: 20598274	2010
Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation. Cell metabolism\| PubMed ID: 21907147	2011
Understanding mitochondrial complex I assembly in health and disease. Biochimica et biophysica acta\| PubMed ID: 21924235	2012
The effects of nuclear reprogramming on mitochondrial DNA replication. Stem cell reviews\| PubMed ID: 21994000	2013
Mutations in the gene encoding C8orf38 block complex I assembly by inhibiting production of the mitochondria-encoded subunit ND1. Journal of molecular biology\| PubMed ID: 22019594	2011
Next-generation sequencing in molecular diagnosis: NUBPL mutations highlight the challenges of variant detection and interpretation. Human mutation\| PubMed ID: 22072591	2012
Timely attention to staffing. Nursing\| PubMed ID: 22195306	2011
Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (u... The Journal of biological chemistry\| PubMed ID: 22535952	2012
Mitochondrial DNA copy number is regulated in a tissue specific manner by DNA methylation of the nuclear-encoded DNA polymerase gamma A. Nucleic acids research\| PubMed ID: 22941637	2012
Mitochondrial dysfunction in a novel form of autosomal recessive ataxia. Mitochondrion\| PubMed ID: 23178371	2013
Mitochondrial DNA haplotypes define gene expression patterns in pluripotent and differentiating embryonic stem cells. Stem cells (Dayton, Ohio)\| PubMed ID: 23307500	2013
Modulation of ceramide-induced cell death and superoxide production by mitochondrial DNA-encoded respiratory chain defects in Rattus xenocybrid mouse cells. Biochimica et biophysica acta\| PubMed ID: 23567871	2013
Clostridium difficile infection: a multicenter study of epidemiology and outcomes in mechanically ventilated patients. Critical care medicine\| PubMed ID: 23863229	2013
Fluid balance and cardiac function in septic shock as predictors of hospital mortality. Critical care (London, England)\| PubMed ID: 24138869	2013
The identification of mitochondrial DNA variants in glioblastoma multiforme. Acta neuropathologica communications\| PubMed ID: 24383468	2014
A founder mutation in PET100 causes isolated complex IV deficiency in Lebanese individuals with Leigh syndrome. American journal of human genetics\| PubMed ID: 24462369	2014
Mitochondrial research in Australia: a major player in worldwide trends. Biochimica et biophysica acta\| PubMed ID: 24468066	2014
Effects of empiric antifungal therapy for septic shock on time to appropriate therapy for Candida infection: a pilot study. Clinical therapeutics\| PubMed ID: 25064625	2014
Critical review of bronchial thermoplasty: where should it fit into asthma therapy? Current allergy and asthma reports\| PubMed ID: 25189294	2014
Capture of somatic mtDNA point mutations with severe effects on oxidative phosphorylation in synaptosome cybrid clones from human brain. Human mutation\| PubMed ID: 25219341	2014
Characterization of mitochondrial FOXRED1 in the assembly of respiratory chain complex I. Human molecular genetics\| PubMed ID: 25678554	2015
Anti-cancer analogues ME-143 and ME-344 exert toxicity by directly inhibiting mitochondrial NADH: ubiquinone oxidoreductase (Complex I). American journal of cancer research\| PubMed ID: 25973307	2015
Conservation implications of omitting historical data sources: response to Baisre. Conservation biology : the journal of the Society for Conservation Biology\| PubMed ID: 26524216	2016
Generation of Xenomitochondrial Embryonic Stem Cells for the Production of Live Xenomitochondrial Mice. Methods in molecular biology (Clifton, N.J.)\| PubMed ID: 26530681	2016
Dietary interventions designed to protect the perinatal brain from hypoxic-ischemic encephalopathy--Creatine prophylaxis and the need for multi-organ protection. Neurochemistry international\| PubMed ID: 26576837	2016
Hydrogel-Based Drug Delivery Systems for Poorly Water-Soluble Drugs. Molecules (Basel, Switzerland)\| PubMed ID: 26580588	2015
Deletion of the Complex I Subunit NDUFS4 Adversely Modulates Cellular Differentiation. Stem cells and development\| PubMed ID: 26608563	2016
Analysis of Mitochondrial DNA in Induced Pluripotent and Embryonic Stem Cells. Methods in molecular biology (Clifton, N.J.)\| PubMed ID: 26621601	2015
Combined defects in oxidative phosphorylation and fatty acid β-oxidation in mitochondrial disease. Bioscience reports\| PubMed ID: 26839416	2016
AarF Domain Containing Kinase 3 (ADCK3) Mutant Cells Display Signs of Oxidative Stress, Defects in Mitochondrial Homeostasis and Lysosomal Accumulation. PloS one\| PubMed ID: 26866375	2016
Loss of mitochondrial DNA-encoded protein ND1 results in disruption of complex I biogenesis during early stages of assembly. FASEB journal : official publication of the Federation of American Societies for Experimental Biology\| PubMed ID: 26929434	2016
Vitamin D3 therapy in patients with asthma complicated by sinonasal disease: Secondary analysis of the Vitamin D Add-on Therapy Enhances Corticosteroid Responsiveness in Asthma trial. The Journal of allergy and clinical immunology\| PubMed ID: 26971692	2016
Restoration of normal embryogenesis by mitochondrial supplementation in pig oocytes exhibiting mitochondrial DNA deficiency. Scientific reports\| PubMed ID: 26987907	2016
Impaired Cellular Bioenergetics Causes Mitochondrial Calcium Handling Defects in MT-ND5 Mutant Cybrids. PloS one\| PubMed ID: 27110715	2016
Proof-of-Concept of Polymeric Sol-Gels in Multi-Drug Delivery and Intraoperative Image-Guided Surgery for Peritoneal Ovarian Cancer. Pharmaceutical research\| PubMed ID: 27283829	2016
Correction: AarF Domain Containing Kinase 3 (ADCK3) Mutant Cells Display Signs of Oxidative Stress, Defects in Mitochondrial Homeostasis and Lysosomal Accumulation. PloS one\| PubMed ID: 27442024	2016
Tim29 is a novel subunit of the human TIM22 translocase and is involved in complex assembly and stability. eLife\| PubMed ID: 27554484	2016
Monocytes and dendritic cells are the primary sources of interleukin 37 in human immune cells. Journal of leukocyte biology\| PubMed ID: 27881605	2016