Centre for Genetic Diseases
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Comparison of log P values obtained from CAChe and other sources.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering Mar, 2003 | Pubmed ID: 12680579
Functional respiratory chain analyses in murid xenomitochondrial cybrids expose coevolutionary constraints of cytochrome b and nuclear subunits of complex III.
Molecular biology and evolution Jul, 2003 | Pubmed ID: 12777531
Production of homoplasmic xenomitochondrial mice.
Proceedings of the National Academy of Sciences of the United States of America Feb, 2004 | Pubmed ID: 14745024
Mitochondrial disease: mutations and mechanisms.
Neurochemical research Mar, 2004 | Pubmed ID: 15038606
Unravelling the peculiar nucleation mechanisms for non-ideal binary mixtures with atomistic simulations.
The journal of physical chemistry. B Mar, 2006 | Pubmed ID: 16494406
Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients.
Journal of molecular biology Aug, 2006 | Pubmed ID: 16857210
Probing the nucleation mechanism for the binary n-nonane/1-alcohol series with atomistic simulations.
The journal of physical chemistry. B Sep, 2006 | Pubmed ID: 16970491
Analysis of mitochondrial subunit assembly into respiratory chain complexes using Blue Native polyacrylamide gel electrophoresis.
Analytical biochemistry May, 2007 | Pubmed ID: 17391635
Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I.
Molecular and cellular biology Jun, 2007 | Pubmed ID: 17438127
Mitochondrial ND5 gene variation associated with encephalomyopathy and mitochondrial ATP consumption.
The Journal of biological chemistry Dec, 2007 | Pubmed ID: 17940288
Assembly of mitochondrial complex I and defects in disease.
Biochimica et biophysica acta Jan, 2009 | Pubmed ID: 18501715
Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease.
American journal of human genetics Oct, 2008 | Pubmed ID: 18940309
Chapter 18 Analysis of respiratory chain complex assembly with radiolabeled nuclear- and mitochondrial-encoded subunits.
Methods in enzymology , 2009 | Pubmed ID: 19348897
Assembly of nuclear DNA-encoded subunits into mitochondrial complex IV, and their preferential integration into supercomplex forms in patient mitochondria.
The FEBS journal Nov, 2009 | Pubmed ID: 19843159
Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome.
Current biology : CB Dec, 2009 | Pubmed ID: 19962311
Assembly factors of human mitochondrial complex I and their defects in disease.
IUBMB life Jul, 2010 | Pubmed ID: 20552642
Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndrome.
American journal of human genetics Jul, 2010 | Pubmed ID: 20598274
Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation.
Cell metabolism Sep, 2011 | Pubmed ID: 21907147
Understanding mitochondrial complex I assembly in health and disease.
Biochimica et biophysica acta Jun, 2012 | Pubmed ID: 21924235
The effects of nuclear reprogramming on mitochondrial DNA replication.
Stem cell reviews Feb, 2013 | Pubmed ID: 21994000
Mutations in the gene encoding C8orf38 block complex I assembly by inhibiting production of the mitochondria-encoded subunit ND1.
Journal of molecular biology Dec, 2011 | Pubmed ID: 22019594
Next-generation sequencing in molecular diagnosis: NUBPL mutations highlight the challenges of variant detection and interpretation.
Human mutation Feb, 2012 | Pubmed ID: 22072591
Timely attention to staffing.
Nursing Dec, 2011 | Pubmed ID: 22195306
Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) gene.
The Journal of biological chemistry Jun, 2012 | Pubmed ID: 22535952
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 Nov, 2012 | Pubmed ID: 22941637
Mitochondrial dysfunction in a novel form of autosomal recessive ataxia.
Mitochondrion May, 2013 | Pubmed ID: 23178371
Mitochondrial DNA haplotypes define gene expression patterns in pluripotent and differentiating embryonic stem cells.
Stem cells (Dayton, Ohio) Apr, 2013 | Pubmed ID: 23307500
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 Jul, 2013 | Pubmed ID: 23567871
Clostridium difficile infection: a multicenter study of epidemiology and outcomes in mechanically ventilated patients.
Critical care medicine Aug, 2013 | Pubmed ID: 23863229
Fluid balance and cardiac function in septic shock as predictors of hospital mortality.
Critical care (London, England) Oct, 2013 | Pubmed ID: 24138869
The identification of mitochondrial DNA variants in glioblastoma multiforme.
Acta neuropathologica communications Jan, 2014 | Pubmed ID: 24383468
A founder mutation in PET100 causes isolated complex IV deficiency in Lebanese individuals with Leigh syndrome.
American journal of human genetics Feb, 2014 | Pubmed ID: 24462369
Mitochondrial research in Australia: a major player in worldwide trends.
Biochimica et biophysica acta Apr, 2014 | Pubmed ID: 24468066
Effects of empiric antifungal therapy for septic shock on time to appropriate therapy for Candida infection: a pilot study.
Clinical therapeutics Sep, 2014 | Pubmed ID: 25064625
Critical review of bronchial thermoplasty: where should it fit into asthma therapy?
Current allergy and asthma reports Nov, 2014 | Pubmed ID: 25189294
Capture of somatic mtDNA point mutations with severe effects on oxidative phosphorylation in synaptosome cybrid clones from human brain.
Human mutation Dec, 2014 | Pubmed ID: 25219341
Characterization of mitochondrial FOXRED1 in the assembly of respiratory chain complex I.
Human molecular genetics May, 2015 | Pubmed ID: 25678554
Anti-cancer analogues ME-143 and ME-344 exert toxicity by directly inhibiting mitochondrial NADH: ubiquinone oxidoreductase (Complex I).
American journal of cancer research , 2015 | Pubmed ID: 25973307
Conservation implications of omitting historical data sources: response to Baisre.
Conservation biology : the journal of the Society for Conservation Biology Feb, 2016 | Pubmed ID: 26524216
Generation of Xenomitochondrial Embryonic Stem Cells for the Production of Live Xenomitochondrial Mice.
Methods in molecular biology (Clifton, N.J.) , 2016 | Pubmed ID: 26530681
Dietary interventions designed to protect the perinatal brain from hypoxic-ischemic encephalopathy--Creatine prophylaxis and the need for multi-organ protection.
Neurochemistry international May, 2016 | Pubmed ID: 26576837
Hydrogel-Based Drug Delivery Systems for Poorly Water-Soluble Drugs.
Molecules (Basel, Switzerland) Nov, 2015 | Pubmed ID: 26580588
Deletion of the Complex I Subunit NDUFS4 Adversely Modulates Cellular Differentiation.
Stem cells and development Feb, 2016 | Pubmed ID: 26608563
Analysis of Mitochondrial DNA in Induced Pluripotent and Embryonic Stem Cells.
Methods in molecular biology (Clifton, N.J.) , 2015 | Pubmed ID: 26621601
Combined defects in oxidative phosphorylation and fatty acid β-oxidation in mitochondrial disease.
Bioscience reports Feb, 2016 | Pubmed ID: 26839416
AarF Domain Containing Kinase 3 (ADCK3) Mutant Cells Display Signs of Oxidative Stress, Defects in Mitochondrial Homeostasis and Lysosomal Accumulation.
PloS one , 2016 | Pubmed ID: 26866375
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 Jun, 2016 | Pubmed ID: 26929434
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 Aug, 2016 | Pubmed ID: 26971692
Restoration of normal embryogenesis by mitochondrial supplementation in pig oocytes exhibiting mitochondrial DNA deficiency.
Scientific reports Mar, 2016 | Pubmed ID: 26987907
Impaired Cellular Bioenergetics Causes Mitochondrial Calcium Handling Defects in MT-ND5 Mutant Cybrids.
PloS one , 2016 | Pubmed ID: 27110715
Proof-of-Concept of Polymeric Sol-Gels in Multi-Drug Delivery and Intraoperative Image-Guided Surgery for Peritoneal Ovarian Cancer.
Pharmaceutical research Sep, 2016 | Pubmed ID: 27283829
Correction: AarF Domain Containing Kinase 3 (ADCK3) Mutant Cells Display Signs of Oxidative Stress, Defects in Mitochondrial Homeostasis and Lysosomal Accumulation.
PloS one , 2016 | Pubmed ID: 27442024
Tim29 is a novel subunit of the human TIM22 translocase and is involved in complex assembly and stability.
eLife Aug, 2016 | Pubmed ID: 27554484
Monocytes and dendritic cells are the primary sources of interleukin 37 in human immune cells.
Journal of leukocyte biology Nov, 2016 | Pubmed ID: 27881605
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