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

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Overexpression of human mitochondrial alanyl-tRNA synthetase suppresses biochemical defects of the mt-tRNA mutation in cybrids

P2860

Q58798246-B56B4C92-B4A7-4EF8-B525-9A524D533C0B

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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.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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name

Contribution of the tRNAIle 43 ...... ial 12S rRNA 1555A>G mutation.

@en

Contribution of the tRNAIle 43 ...... ial 12S rRNA 1555A>G mutation.

@nl

type

Item

label

Contribution of the tRNAIle 43 ...... ial 12S rRNA 1555A>G mutation.

@en

Contribution of the tRNAIle 43 ...... ial 12S rRNA 1555A>G mutation.

@nl

prefLabel

Contribution of the tRNAIle 43 ...... ial 12S rRNA 1555A>G mutation.

@en

Contribution of the tRNAIle 43 ...... ial 12S rRNA 1555A>G mutation.

@nl

P1476

Contribution of the tRNAIle 43 ...... ial 12S rRNA 1555A>G mutation.

@en

P2093

Feilong Meng

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

Jing Zheng

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

Jun Qin Mo

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

Meng Wang

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

Mi Zhou

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Min-Xin Guan

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

Qiang Shu

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Shasha Gong

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

Xiaofen Jin

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

Xiaowen Tang

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P2860

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

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

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

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

Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations

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

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

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

Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3

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scholarly article

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10.1074/JBC.RA117.000530

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English

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2018-01-18T00:00:00Z

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P698

29348176

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P932

5836119

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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.

about

P2860

P2860

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

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P1433

P1476

P2093

P2860

P31

P356

P407

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P31

P356

P407

P577

P698

P932