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Mitochondrial DNA polymorphism in substantia nigra
Robert M.I. Kapsa
, M. J.Bernadette Jean-Francois
, Patcharee Lertrit
, Shan Weng
, Nurjati Siregar
, Joseline Ojaimi
, Geoffrey Donnan
, Colin Masters
, Edward Byrne
Department of Pathological Anatomy
Research output
:
Contribution to journal
›
Article
›
peer-review
22
Citations (Scopus)
Overview
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Keyphrases
Mitochondrial DNA
100%
Mitochondrial DNA Variation
100%
Substantia Nigra
100%
Transfer RNA (tRNA)
66%
Polymorphism
50%
Genotype
33%
Acquired mutations
33%
Neurodegenerative Diseases
16%
Increasing Age
16%
Elderly People
16%
Multiple Deletions
16%
Respiratory Efficiency
16%
Protein Subunit
16%
Missense
16%
Nonsense
16%
Mitochondrial tRNA
16%
Idiopathic Parkinson's Disease
16%
Bioenergetics
16%
Etiological Factors
16%
ND4 Gene
16%
Missense Polymorphism
16%
ND5 Gene
16%
Evolutionary Constraint
16%
Coding Region
16%
Age-related Neurodegeneration
16%
Nonconservative
16%
Aging Brain
16%
Mitochondrial Respiration
16%
Biological Aging
16%
Respiratory Proteins
16%
Polymorphic Site
16%
Parkinsonian
16%
Amino Acid Substitution
16%
Biochemistry, Genetics and Molecular Biology
Gene Polymorphism
100%
Mitochondrial DNA
100%
Transfer RNA
83%
Missense
33%
Acquired Mutation
33%
Genotyping
16%
Mitochondrial Genome
16%
Mitochondrial Respiration
16%
Amino Acid Substitution
16%
Coding Region
16%
Respiratory Protein
16%
Protein Subunit
16%
Arginine
16%
Bioenergetics
16%