Elucidation of separate, but collaborative functions of the rRNA methyltransferase-related human mitochondrial transcription factors B1 and B2 in mitochondrial biogenesis reveals new insight into maternally inherited deafness

Human Molecular Genetics

Volumn 18, Issue 14, 2009, Pages 2670-2682

  Cotney, Justin ^a,b   McKay, Sharen E ^a   Shadel, Gerald S ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b EMORY UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; MITOCHONDRIAL TRANSCRIPTION FACTOR B1; MITOCHONDRIAL TRANSCRIPTION FACTOR B2; RIBOSOME RNA; RNA 12S; RNA METHYLTRANSFERASE; SORBITOL; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ARTICLE; BIOGENESIS; CELL DEATH; CELL GROWTH; CELL METABOLISM; CONTROLLED STUDY; DNA TRANSCRIPTION; ENZYME ACTIVITY; GENE FUNCTION; GENE MUTATION; GENE OVEREXPRESSION; GENETIC DISORDER; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; MITOCHONDRIAL BIOGENESIS; MITOCHONDRION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; RNA METHYLATION; RNA TRANSLATION;

CELL LINE; DEAFNESS; DNA-BINDING PROTEINS; GENOMIC IMPRINTING; HUMANS; METHYLATION; METHYLTRANSFERASES; MITOCHONDRIA; MITOCHONDRIAL PROTEINS; RNA, RIBOSOMAL; TRANSCRIPTION FACTORS; TRNA METHYLTRANSFERASES;

EID: 67649876629     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddp208     Document Type: Article

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