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Publications by Mercy Davidson
Fine Mapping of Mitochondrial RNAs Derived From the mtDNA Region Containing a Point Mutation Associated With MELAS
Nucleic Acids Research
Genetics
A Pathogenic 15-Base Pair Deletion in Mitochondrial DNA-encoded CytochromecOxidase Subunit III Results in the Absence of Functional CytochromecOxidase
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Related publications
Cytochrome C Oxidase Deficiency Associated With the First Stop-Codon Point Mutation in Human mtDNA
American Journal of Human Genetics
Genetics
Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation
Annals of Otology, Rhinology and Laryngology
Medicine
Otorhinolaryngology
Natural History of MELAS Associated With Mitochondrial DNA M.3243A>G Genotype
Neurology
Neurology
MERRF/MELAS Overlap Syndrome: A Double Pathogenic Mutation in Mitochondrial tRNA Genes
Journal of Medical Genetics
Genetics
Mutation Patterns of mtDNA: Empirical Inferences for the Coding Region
BMC Evolutionary Biology
Evolution
Ecology
Systematics
Behavior
mtDNA T8993G Mutation-Induced F1f0-Atp Synthase Defect Augments Mitochondrial Dysfunction Associated With Hypoxia/Reoxygenation: The Protective Role of Melatonin
PLoS ONE
Multidisciplinary
Evidence That a 1.6 Kilobase Region of Neurospora mtDNA Was Derived by Insertion of Part of the LaBelle Mitochondrial Plasmid
Nucleic Acids Research
Genetics
Cytoplasmic Transfer of the mtDNA Nt 8993 T-->g (ATP6) Point Mutation Associated With Leigh Syndrome Into mtDNA-less Cells Demonstrates Cosegregation With a Decrease in State III Respiration and ADP/O Ratio.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation
AUDIOLOGY JAPAN
