A human mitochondrial GTP binding protein related to tRNA modification may modulate phenotypic expression of the deafness-associated mitochondrial 12S rRNA mutation

Molecular and Cellular Biology

Volumn 22, Issue 21, 2002, Pages 7701-7711

  Li, Xiaoming ^a   Guan, Min Xin ^a  

^a CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GUANINE NUCLEOTIDE BINDING PROTEIN; RIBOSOME RNA; TRANSFER RNA;

ALLELISM; ANIMAL CELL; ARTICLE; CHEMICAL MODIFICATION; CONTROLLED STUDY; CORRELATION ANALYSIS; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; MOLECULAR CLONING; MOLECULAR EVOLUTION; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; RIBONUCLEIC ACID MODIFICATION; SEQUENCE HOMOLOGY; YEAST CELL;

ALLELES; AMINO ACID SEQUENCE; BASE SEQUENCE; CLONING, MOLECULAR; DEAFNESS; DNA, COMPLEMENTARY; ESCHERICHIA COLI; GENETIC COMPLEMENTATION TEST; GLUCOSE; GLYCEROL; GTP PHOSPHOHYDROLASES; GTP-BINDING PROTEINS; HUMANS; MICROSCOPY, FLUORESCENCE; MITOCHONDRIA; MODELS, GENETIC; MOLECULAR SEQUENCE DATA; MUTATION; NUCLEAR PROTEINS; NUCLEIC ACID CONFORMATION; PHENOTYPE; PROTEIN BINDING; RNA, MESSENGER; RNA, RIBOSOMAL; RNA, TRANSFER; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID; TISSUE DISTRIBUTION;

ANIMALIA; MAMMALIA; VERTEBRATA;

EID: 0036837683     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.22.21.7701-7711.2002     Document Type: Article

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