Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation-Reference-Cited by-同舟云学术

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Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation

Published:2018-03 Issue:9 Volume:293 Page:3321-3334
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Meng Feilong,He Zheyun,Tang Xiaowen,Zheng Jing,Jin Xiaofen,Zhu Yi,Ren Xiaoyan,Zhou Mi,Wang Meng,Gong Shasha,Mo Jun Qin,Shu Qiang,Guan Min-Xin

Funder

Ministry of Science and Technology of the People's Republic of China (MOST)

National Natural Science Foundation of China (NSFC)

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference69 articles.

1. Mitochondrial deafness mutations reviewed;Fischel-Ghodsian;Hum. Mutat,1999

2. Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity;Guan;Mitochondrion,2011

3. Mitochondrial tRNA mutations associated with deafness;Zheng;Mitochondrion,2012

4. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA;Andrews;Nat. Genet,1999

5. The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression;Guan;Mol. Cell. Biol,1998

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