Mutations in mitochondrial-encoded cytochrome c oxidase subunits I,II, and III genes detected in Alzheimer's disease using single-strand conformation polymorphism

Electrophoresis

Volumn 27, Issue 2, 2006, Pages 398-408

  Hamblet, Natasha S ^a   Ragland, Brian ^a   Ali, Mervat ^a   Conyers, Barbara ^a   Castora, Frank J ^a  

^a EASTERN VIRGINIA MEDICAL SCHOOL   (United States)

Author keywords

Alzheimer's disease; Mitochondrial DNA; Polymorphism; SSCP

Indexed keywords

AMINO ACIDS; C (PROGRAMMING LANGUAGE); DNA; DNA SEQUENCES; GENE ENCODING; NEURODEGENERATIVE DISEASES; POLYMORPHISM;

AGE-MATCHED CONTROLS; ALZHEIMERS DISEASE; BRAIN SAMPLE; CYTOCHROME OXIDASE; CYTOCHROME OXIDASE I; CYTOCHROME-C OXIDASE; MITOCHONDRIAL DNA; OXIDASE ACTIVITY; SSCP; STRAND CONFORMATION;

BRAIN;

AMINO ACID; CYTOCHROME C OXIDASE; LEUCINE; MITOCHONDRIAL DNA; PHENYLALANINE; PROTEIN SUBUNIT;

AGE DISTRIBUTION; ALZHEIMER DISEASE; AMINO ACID SUBSTITUTION; ARTICLE; BRAIN TISSUE; CONTROLLED STUDY; DNA SEQUENCE; ELECTROPHORESIS; ENZYME ACTIVITY; ENZYME SUBUNIT; GENE EXPRESSION; GENETIC ANALYSIS; GENETIC CODE; GENETIC CONSERVATION; GENETIC VARIABILITY; HUMAN; HUMAN TISSUE; MITOCHONDRIAL GENETICS; MUTATIONAL ANALYSIS; PHENOTYPE; POINT MUTATION; PROTEIN FUNCTION; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 32244449019     PISSN: 01730835     EISSN: 15222683     Source Type: Journal    
DOI: 10.1002/elps.200500420     Document Type: Article

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