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Nancy G Kennaway Selected Research

heme a

10/2003Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.
1/2003Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy.

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Nancy G Kennaway Research Topics

Disease

3Mitochondrial Diseases (Mitochondrial Disease)
08/2012 - 01/2003
2Cytochrome-c Oxidase Deficiency
10/2003 - 01/2003
1Deafness (Deaf Mutism)
08/2012
1Epilepsy (Aura)
08/2012
1Fatigue
08/2012
1Muscular Diseases (Myopathy)
08/2012
1Retinal Degeneration
08/2012
1Brain Diseases (Brain Disorder)
10/2005
1Mitochondrial Encephalomyopathies (Mitochondrial Encephalomyopathy)
02/2005
1Mitochondrial Myopathies (Mitochondrial Myopathy)
02/2005
1Hypertrophic Cardiomyopathy (Hypertrophic Obstructive Cardiomyopathy)
01/2003

Drug/Important Bio-Agent (IBA)

2heme aIBA
10/2003 - 01/2003
1Ser Transfer RNAIBA
08/2012
1Mitochondrial DNA (mtDNA)IBA
08/2012
1Molecular Chaperones (Chaperone, Molecular)IBA
10/2005
1Leu Transfer RNAIBA
02/2005
1AnticodonIBA
02/2005
1Trp Transfer RNA (tRNA(Trp))IBA
02/2005
1Glu Transfer RNAIBA
02/2005
1Retinaldehyde (Retinal)IBA
02/2005
1Electron Transport Complex I (NADH-CoQ Reductase)IBA
10/2003
1Proteins (Proteins, Gene)FDA Link
01/2003
1Heme (Haem)IBA
01/2003
1EnzymesIBA
01/2003
1Electron Transport Complex IV (Cytochrome c Oxidase)IBA
01/2003
1Complement System Proteins (Complement)IBA
01/2003