Frequent occurrence of mitochondrial DNA mutations in barrett's metaplasia without the presence of Dysplasia

PLoS ONE

Volumn 7, Issue 5, 2012, Pages

  Lee, Soong ^a   Han, Moon Jong ^a   Lee, Ki Sang ^a   Back, Seung Chul ^a   Hwang, David ^a   Kim, Hwan Young ^b   Shin, Jong Hee ^b   Suh, Soon Pal ^b   Ryang, Dong Wook ^b   Kim, Hye Ran ^b,c   Shin, Myung Geun ^b  

^a Seonam University   (South Korea)

^b Chonnam National University Medical School   (South Korea)

^c Chonnam National University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROGEN PEROXIDE; MITOCHONDRIAL DNA; REACTIVE OXYGEN METABOLITE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); SUCCINATE DEHYDROGENASE (UBIQUINONE); UBIQUINOL CYTOCHROME C REDUCTASE;

ARTICLE; BARRETT METAPLASIA; CLINICAL ARTICLE; CONTROLLED STUDY; COPY NUMBER VARIATION; DYSPLASIA; ESOPHAGUS DISEASE; GENE MUTATION; HETEROPLASMY; HUMAN; HUMAN TISSUE; METAPLASIA; MITOCHONDRIAL GENOME; NUCLEIC ACID BASE SUBSTITUTION;

ADENOCARCINOMA; BARRETT ESOPHAGUS; CELL TRANSFORMATION, NEOPLASTIC; DISEASE PROGRESSION; DNA, MITOCHONDRIAL; ESOPHAGEAL NEOPLASMS; ESOPHAGUS; HUMANS; HYDROGEN PEROXIDE; METAPLASIA; MUTATION; REACTIVE OXYGEN SPECIES;

EID: 84861324017     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0037571     Document Type: Article

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