Evolutionary and structural annotation of disease-associated mutations in human aminoacyl-tRNA synthetases. - sprookjes - yvandenbroek - TriplyDB

Evolutionary and structural annotation of disease-associated mutations in human aminoacyl-tRNA synthetases.

Evolutionary and structural annotation of disease-associated mutations in human aminoacyl-tRNA synthetases.

http://www.wikidata.org/entity/Q35492670

about

Evolutionary Limitation and Opportunities for Developing tRNA Synthetase Inhibitors with 5-Binding-Mode Classification Backbone Brackets and Arginine Tweezers delineate Class I and Class II aminoacyl tRNA synthetases.mutations presenting with pure spastic paraplegia and lesions of the dentate nuclei

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P2860

Evolutionary and structural annotation of disease-associated mutations in human aminoacyl-tRNA synthetases.

http://www.wikidata.org/entity/Q35492670

description

2014 nî lūn-bûn

@nan

2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

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2014年論文

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2014年論文

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2014年論文

@zh-hk

2014年論文

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2014年論文

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2014年论文

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name

Evolutionary and structural an ...... an aminoacyl-tRNA synthetases.

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Evolutionary and structural an ...... an aminoacyl-tRNA synthetases.

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Evolutionary and structural an ...... an aminoacyl-tRNA synthetases.

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Evolutionary and structural an ...... an aminoacyl-tRNA synthetases.

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Evolutionary and structural an ...... an aminoacyl-tRNA synthetases.

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Evolutionary and structural an ...... an aminoacyl-tRNA synthetases.

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1471-2164-15-1063

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Evolutionary and structural an ...... an aminoacyl-tRNA synthetases.

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Amit Sharma

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P2860

The human lysyl-tRNA synthetase gene encodes both the cytoplasmic and mitochondrial enzymes by means of an unusual alternative splicing of the primary transcript

Toward the full set of human mitochondrial aminoacyl-tRNA synthetases: characterization of AspRS and TyrRS

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

The C-terminal appended domain of human cytosolic leucyl-tRNA synthetase is indispensable in its interaction with arginyl-tRNA synthetase in the multi-tRNA synthetase complex

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

TM-align: a protein structure alignment algorithm based on the TM-score

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

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

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scholarly article

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