Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity.

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Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity.

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Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity.

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Item

label

Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity.

@en

Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity.

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Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity.

@en

Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity.

@nl

P1476

Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity

@en

P2093

Min-Xin Guan

http://www.w3.org/2001/XMLSchema#string

Zewen Gao

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P2860

Measuring the burden of neglected tropical diseases: the global burden of disease framework

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

Mutations in MTO2 related to tRNA modification impair mitochondrial gene expression and protein synthesis in the presence of a paromomycin resistance mutation in mitochondrial 15 S rRNA

A small particulate component of the cytoplasm

Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss

Functional hair cell mechanotransducer channels are required for aminoglycoside ototoxicity

Structure of the 30S ribosomal subunit

Structure of the 70S ribosome complexed with mRNA and tRNA

A peep into mitochondrial disorder: multifaceted from mitochondrial DNA mutations to nuclear gene modulation

Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation

P304

1-8

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P31

scholarly article

P356

10.1016/J.JOTO.2017.02.001

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Ye Chen

P577

2017-02-11T00:00:00Z

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P698

29937831

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P921

mitochondrial DNA

P932

6011804

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