Human mitochondrial disease-like symptoms caused by a reduced tRNA aminoacylation activity in flies. - Wikidata - wikimedia - TriplyDB

Human mitochondrial disease-like symptoms caused by a reduced tRNA aminoacylation activity in flies.

Human mitochondrial disease-like symptoms caused by a reduced tRNA aminoacylation activity in flies.

http://www.wikidata.org/entity/Q37013006

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The aminoacyl-tRNA synthetases of Drosophila melanogaster Plant-Specific Preprotein and Amino Acid Transporter Proteins Are Required for tRNA Import into Mitochondria.

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Human mitochondrial disease-like symptoms caused by a reduced tRNA aminoacylation activity in flies.

http://www.wikidata.org/entity/Q37013006

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 15 May 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Human mitochondrial disease-li ...... noacylation activity in flies.

@en

Human mitochondrial disease-li ...... noacylation activity in flies.

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type

label

Human mitochondrial disease-li ...... noacylation activity in flies.

@en

Human mitochondrial disease-li ...... noacylation activity in flies.

@nl

prefLabel

Human mitochondrial disease-li ...... noacylation activity in flies.

@en

Human mitochondrial disease-li ...... noacylation activity in flies.

@nl

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Nucleic Acids Research

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Human mitochondrial disease-li ...... inoacylation activity in flies

@en

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Daria Picchioni

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

David Piñeyro

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Lluís Ribas de Pouplana

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P2860

Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels

Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome

Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation

Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy

Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndrome

Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.

An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy

Targeted gene expression as a means of altering cell fates and generating dominant phenotypes

A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila

Translation matters: protein synthesis defects in inherited disease

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6595-6608

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scholarly article

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10.1093/NAR/GKT402

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13

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2013-05-15T00:00:00Z

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