Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs - Wikidata - wikimedia - TriplyDB

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

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

http://www.wikidata.org/entity/Q27027853

about

Nucleoside modifications in the regulation of gene expression: focus on tRNA Taurine: the appeal of a safe amino acid for skeletal muscle disorders Modification of the wobble uridine in bacterial and mitochondrial tRNAs reading NNA/NNG triplets of 2-codon boxes Methylated nucleosides in tRNA and tRNA methyltransferases The human mitochondrial transcriptome and the RNA-binding proteins that regulate its expression tRNA biology in mitochondria Modify or die?--RNA modification defects in metazoans Mitochondrial 16S rRNA Is Methylated by tRNA Methyltransferase TRMT61B in All Vertebrates NSUN3 methylase initiates 5-formylcytidine biogenesis in human mitochondrial tRNA(Met)Chemical synthesis of the 5-taurinomethyl(-2-thio)uridine modified anticodon arm of the human mitochondrial tRNA(Leu(UUR)) and tRNA(Lys)The 2'-O-methyladenosine nucleoside modification gene OsTRM13 positively regulates salt stress tolerance in rice A-to-I editing in human miRNAs is enriched in seed sequence, influenced by sequence contexts and significantly hypoedited in glioblastoma multiforme.A complete landscape of post-transcriptional modifications in mammalian mitochondrial tRNAs.Taurine-containing uridine modifications in tRNA anticodons are required to decipher non-universal genetic codes in ascidian mitochondria.Defective Expression of the Mitochondrial-tRNA Modifying Enzyme GTPBP3 Triggers AMPK-Mediated Adaptive Responses Involving Complex I Assembly Factors, Uncoupling Protein 2, and the Mitochondrial Pyruvate Carrier.A mass spectrometry-based method for comprehensive quantitative determination of post-transcriptional RNA modifications: the complete chemical structure of Schizosaccharomyces pombe ribosomal RNAs A comprehensive collection of annotations to interpret sequence variation in human mitochondrial transfer RNAs.Nucleoside analog studies indicate mechanistic differences between RNA-editing adenosine deaminases.A homozygous splicing mutation in ELAC2 suggests phenotypic variability including intellectual disability with minimal cardiac involvement.Human mitochondrial DNA: roles of inherited and somatic mutations.tRNA Modification and Genetic Code Variations in Animal Mitochondria.Neuroprotective Mechanisms of Taurine against Ischemic Stroke.microRNA-mediated differential expression of TRMU, GTPBP3 and MTO1 in cell models of mitochondrial-DNA diseases.Acquired cisplatin resistance in human ovarian A2780 cancer cells correlates with shift in taurine homeostasis and ability to volume regulate.Capture, Unfolding, and Detection of Individual tRNA Molecules Using a Nanopore Device Multilevel functional and structural defects induced by two pathogenic mitochondrial tRNA mutations.Decoding mechanism of non-universal genetic codes in Loligo bleekeri mitochondria.The tRNA-modifying function of MnmE is controlled by post-hydrolysis steps of its GTPase cycle.Conformational preferences of modified nucleoside N(4)-acetylcytidine, ac4C occur at "wobble" 34th position in the anticodon loop of tRNA.mt-tRNA components: synthesis of (2-thio)uridines modified with blocked glycine/taurine moieties at C-5,1.Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease.The mitochondrial epitranscriptome: the roles of RNA modifications in mitochondrial translation and human disease.A natural non-Watson-Crick base pair in human mitochondrial tRNAThr causes structural and functional susceptibility to local mutations.Advances in the Treatment of MELAS Syndrome: Could Cognitive Rehabilitation Have a Role?CO2-sensitive tRNA modification associated with human mitochondrial disease.Nano LC-MS using capillary columns enables accurate quantification of modified ribonucleosides at low femtomol levels

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P2860

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

http://www.wikidata.org/entity/Q27027853

description

2011 nî lūn-bûn

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2011 թուականին հրատարակուած գիտական յօդուած

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2011 թվականին հրատարակված գիտական հոդված

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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name

Human mitochondrial diseases c ...... ication in mitochondrial tRNAs

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Human mitochondrial diseases c ...... ication in mitochondrial tRNAs

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Human mitochondrial diseases c ...... ication in mitochondrial tRNAs

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type

label

Human mitochondrial diseases c ...... ication in mitochondrial tRNAs

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Human mitochondrial diseases c ...... ication in mitochondrial tRNAs

@en

Human mitochondrial diseases c ...... ication in mitochondrial tRNAs

@nl

prefLabel

Human mitochondrial diseases c ...... ication in mitochondrial tRNAs

@ast

Human mitochondrial diseases c ...... ication in mitochondrial tRNAs

@en

Human mitochondrial diseases c ...... ication in mitochondrial tRNAs

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P2860

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P1433

Wiley interdisciplinary reviews. RNA

P1476

Human mitochondrial diseases c ...... ication in mitochondrial tRNAs

@en

P2093

Nagao Asuteka

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

Suzuki Takeo

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

Suzuki Tsutomu

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

P2860

Biogenesis of glutaminyl-mt tRNAGln in human mitochondria

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

MITOMAP: a human mitochondrial genome database--2004 update

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

Mitochondria-specific RNA-modifying enzymes responsible for the biosynthesis of the wobble base in mitochondrial tRNAs. Implications for the molecular pathogenesis of human mitochondrial diseases.

Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu)(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease

Single-molecule LATE-PCR analysis of human mitochondrial genomic sequence variations

Taurine as a constituent of mitochondrial tRNAs: new insights into the functions of taurine and human mitochondrial diseases

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376-86

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scholarly article

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2225508

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10.1002/WRNA.65

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3

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2

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2011-01-01T00:00:00Z

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21957023

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