An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells

Human Mutation

Volumn 30, Issue 3, 2009, Pages 391-396

  Gasparre, Giuseppe ^a   Iommarini, Luisa ^b   Porcelli, Anna Maria ^b   Lang, Martin ^a   Ferri, Gian Gaetano ^a   Kurelac, Ivana ^a   Zuntini, Roberta ^a   Mariani, Elisa ^b   Pennisi, Lucia Fiammetta ^a   Pasquini, Ernesto ^a   Pasquinelli, Gianandrea ^a   Ghelli, Anna ^b   Bonora, Elena ^a   Ceccarelli, Claudio ^a   Rugolo, Michela ^b   Salfi, Nunzio ^a   Romeo, Giovanni ^a   Carelli, Valerio ^b  

^a UNIVERSITY OF BOLOGNA   (Italy)

^b UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

Complex I subunits; Disruptive mutations; Mitochondrial DNA; mtDNA; ND1; ND5; ND6; Oncocytic

Indexed keywords

AGED; ARTICLE; CANCER CELL; CANCER RECURRENCE; CANCER SCREENING; CONTROLLED STUDY; GENE MUTATION; HUMAN; HUMAN TISSUE; INHERITANCE; MALE; MITOCHONDRIAL DNA DISORDER; NASOPHARYNX TUMOR; PRIORITY JOURNAL; TUMOR CELL;

AGED; AMINO ACID SEQUENCE; BASE SEQUENCE; BLOTTING, WESTERN; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX I; FRAMESHIFT MUTATION; GERM-LINE MUTATION; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MICROSCOPY, ELECTRON; MOLECULAR SEQUENCE DATA; NASOPHARYNGEAL NEOPLASMS; PEDIGREE; SEQUENCE DELETION; SEQUENCE HOMOLOGY, AMINO ACID; SIBLINGS;

EID: 61649090450     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.20870     Document Type: Article

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