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When a common biological role does not imply common disease outcomes: Disparate pathology linked to human mitochondrial aminoacyl-tRNA synthetases
Mitochondria: An organelle for life
Thermodynamic properties distinguish human mitochondrial aspartyl-tRNA synthetase from bacterial homolog with same 3D architecture.
Neurodegenerative disease-associated mutants of a human mitochondrial aminoacyl-tRNA synthetase present individual molecular signatures.
Released selective pressure on a structural domain gives new insights on the functional relaxation of mitochondrial aspartyl-tRNA synthetase.
Translation in mammalian mitochondria: Order and disorder linked to tRNAs and aminoacyl-tRNA synthetases.
Idiosyncrasies in decoding mitochondrial genomes.

Islandora displays