CO2-sensitive tRNA modification associated with human mitochondrial disease.

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Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype

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Q58713895-8C5120B3-B537-40A1-AF5F-3809DC7A878B

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CO2-sensitive tRNA modification associated with human mitochondrial disease.

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http://www.wikidata.org/entity/Q55332430

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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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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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2018年學術文章

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name

CO2-sensitive tRNA modification associated with human mitochondrial disease.

@en

CO2-sensitive tRNA modification associated with human mitochondrial disease.

@nl

type

Item

label

CO2-sensitive tRNA modification associated with human mitochondrial disease.

@en

CO2-sensitive tRNA modification associated with human mitochondrial disease.

@nl

prefLabel

CO2-sensitive tRNA modification associated with human mitochondrial disease.

@en

CO2-sensitive tRNA modification associated with human mitochondrial disease.

@nl

P1476

CO2-sensitive tRNA modification associated with human mitochondrial disease

@en

P2093

Eri Takeshita

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

Hideki Yagasaki

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

Hirofumi Komaki

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

Kaori Yanaka

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

Kaoru Fujioka

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

Kenjyo Miyauchi

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

Ryo Okita

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

Shinichi Nakagawa

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

Tai Harada

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

Yu-Ichi Goto

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P2860

Understanding the Warburg effect: the metabolic requirements of cell proliferation

Multiplex genome engineering using CRISPR/Cas systems

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

WoLF PSORT: protein localization predictor

Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs

Reconstitution and characterization of eukaryotic N6-threonylcarbamoylation of tRNA using a minimal enzyme system

Targeting HIF-1 for cancer therapy

The highly conserved KEOPS/EKC complex is essential for a universal tRNA modification, t6A.

Functional assignment of KEOPS/EKC complex subunits in the biosynthesis of the universal t6A tRNA modification.

A cyclic form of N6-threonylcarbamoyladenosine as a widely distributed tRNA hypermodification.

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s41467-018-04250-4

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1875

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scholarly article

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10.1038/S41467-018-04250-4

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English

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

P478

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

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Tsutomu Suzuki

Huan Lin

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2018-05-14T00:00:00Z

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

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1103889242

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

P698

29760464

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

P932

5951830

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

CO2-sensitive tRNA modification associated with human mitochondrial disease.

about

P2860

P2860

CO2-sensitive tRNA modification associated with human mitochondrial disease.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P50

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P50

P577

P6179

P698

P932