Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease.

about

CO2-sensitive tRNA modification associated with human mitochondrial disease.Differentiating Positional Isomers of Nucleoside Modifications by Higher-Energy Collisional Dissociation Mass Spectrometry (HCD MS)

P2860

Q55332430-1C448BCE-3560-4024-8173-969267D562A8 Q57258751-9113F286-2848-4A4E-908E-D57CBB7DA7FF

P2860

Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease.

Item

http://www.wikidata.org/entity/Q47640677

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh-hant

name

Metabolic and chemical regulat ...... deficiency and human disease.

@en

Metabolic and chemical regulat ...... deficiency and human disease.

@nl

type

Item

label

Metabolic and chemical regulat ...... deficiency and human disease.

@en

Metabolic and chemical regulat ...... deficiency and human disease.

@nl

prefLabel

Metabolic and chemical regulat ...... deficiency and human disease.

@en

Metabolic and chemical regulat ...... deficiency and human disease.

@nl

P1476

Metabolic and chemical regulat ...... e deficiency and human disease

@en

P2093

Akira Ohtake

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

Ayaka Saito

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

Fan-Yan Wei

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

Kana Asano

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

Kazuhito Tomizawa

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

Kei Murayama

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

Takanobu Goto

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

Takeo Suzuki

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

Takeshi Yamamoto

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

Tomoyuki Numata

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

P2860

A mutation inactivating the mitochondrial inner membrane folate transporter creates a glycine requirement for survival of chinese hamster cells

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

Multiplex genome engineering using CRISPR/Cas systems

Nucleoside modifications in the regulation of gene expression: focus on tRNA

Control of protein synthesis in yeast mitochondria: the concept of translational activators

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

MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathy.

Modified uridines with C5-methylene substituents at the first position of the tRNA anticodon stabilize U.G wobble pairing during decoding

Conserved cysteine residues of GidA are essential for biogenesis of 5-carboxymethylaminomethyluridine at tRNA anticodon

MTO1 codes for a mitochondrial protein required for respiration in paromomycin-resistant mutants of Saccharomyces cerevisiae.

P304

1565-1583

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

P31

scholarly article

P356

10.1093/NAR/GKY068

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

P407

English

P433

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

P478

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

P50

Ryou Tanaka

Yoshihito Kishita

P577

2018-02-01T00:00:00Z

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

P698

29390138

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

P932

5829720

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

Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease.

about

P2860

P2860

Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932