ALKBH1 is an RNA dioxygenase responsible for cytoplasmic and mitochondrial tRNA modifications - Wikidata - wikimedia - TriplyDB

ALKBH1 is an RNA dioxygenase responsible for cytoplasmic and mitochondrial tRNA modifications

ALKBH1 is an RNA dioxygenase responsible for cytoplasmic and mitochondrial tRNA modifications

http://www.wikidata.org/entity/Q40951861

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RNA cytosine methyltransferase Nsun3 regulates embryonic stem cell differentiation by promoting mitochondrial activity.Biogenesis and iron-dependency of ribosomal RNA hydroxylation.Characterization of human AlkB homolog 1 produced in mammalian cells and demonstration of mitochondrial dysfunction in ALKBH1-deficient cells.Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease.Hydroxylation of a conserved tRNA modification establishes non-universal genetic code in echinoderm mitochondria.The mitochondrial epitranscriptome: the roles of RNA modifications in mitochondrial translation and human disease.Synthesis and Multiple Incorporations of 2'-O-Methyl-5-hydroxymethylcytidine, 5-Hydroxymethylcytidine and 5-Formylcytidine Monomers into RNA Oligonucleotides.Modifications and functional genomics of human transfer RNA.RNA modification landscape of the human mitochondrial tRNA regulates protein synthesis N6-Methyladenosine in RNA and DNA: An Epitranscriptomic and Epigenetic Player Implicated in Determination of Stem Cell Fate

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ALKBH1 is an RNA dioxygenase responsible for cytoplasmic and mitochondrial tRNA modifications

http://www.wikidata.org/entity/Q40951861

description

2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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2017年论文

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name

ALKBH1 is an RNA dioxygenase r ...... tochondrial tRNA modifications

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type

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ALKBH1 is an RNA dioxygenase r ...... tochondrial tRNA modifications

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prefLabel

ALKBH1 is an RNA dioxygenase r ...... tochondrial tRNA modifications

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Nucleic Acids Research

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ALKBH1 is an RNA dioxygenase r ...... tochondrial tRNA modifications

@en

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Kenjyo Miyauchi

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

Layla Kawarada

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

Shoji Hirata

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

Takayuki Ohira

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

Takeo Suzuki

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

Tsutomu Suzuki

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

P2860

Genome engineering using the CRISPR-Cas9 system

N6-methyladenosine in nuclear RNA is a major substrate of the obesity-associated FTO

Mammalian ALKBH8 possesses tRNA methyltransferase activity required for the biogenesis of multiple wobble uridine modifications implicated in translational decoding

The obesity-associated FTO gene encodes a 2-oxoglutarate-dependent nucleic acid demethylase

Trmt61B is a methyltransferase responsible for 1-methyladenosine at position 58 of human mitochondrial tRNAs

ALKBH5 is a mammalian RNA demethylase that impacts RNA metabolism and mouse fertility

Human AlkB homolog 1 is a mitochondrial protein that demethylates 3-methylcytosine in DNA and RNA

Identification of human tRNA:m5C methyltransferase catalysing intron-dependent m5C formation in the first position of the anticodon of the pre-tRNA Leu (CAA)

Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1

Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation.

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7401-7415

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scholarly article

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10.1093/NAR/GKX354

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12

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45

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2017-05-02T00:00:00Z

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28472312

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5499545

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