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Mitochondria: Impaired mitochondrial translation in human disease
British Library Online Contents | 2014| -
Annexin A9 is a periplakin interacting partner in membrane-targeted cytoskeletal linker protein complexes
British Library Online Contents | 2012| -
P30 Does a physiological COX isoform switch contribute to the clinical presentation of infantile reversible cytochrome c oxidase deficiency?
British Library Online Contents | 2014| -
The role of tRNA synthetases in neurological and neuromuscular disorders
British Library Online Contents | 2018| -
Cytolinker cross-talk: Periplakin N-terminus interacts with plectin to regulate keratin organisation and epithelial migration
British Library Online Contents | 2007| -
Defective thiolation impairs mitochondrial translation offering a therapy approach in reversible infantile respiratory chain deficiency
British Library Online Contents | 2013| -
03-P015 Rho kinase is required for cohesive behaviour of neural crest cells during outflow tract morphogenesis
British Library Online Contents | 2009| -
03-P012 Cell traction force microscopy in cardiac morphogenesis
British Library Online Contents | 2009| -
Periplakin-dependent re-organisation of keratin cytoskeleton and loss of collective migration in keratin-8-downregulated epithelial sheets
British Library Online Contents | 2006| -
Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency
British Library Online Contents | 2013| -
Mutations in glycyl-tRNA synthetase impair mitochondrial metabolism in neurons
British Library Online Contents | 2018| -
Studying the molecular basis of the reversibility in infantile reversible cytochrome c oxidase deficiency
British Library Online Contents | 2012| -
Non-Loss-of-Function Frameshift Variants in the FAD Synthase Gene Cause Combined Respiratory Chain Deficiency
British Library Online Contents | 2016| -
P29 Behrs syndrome is a mitochondrial disease due to autosomal recessive mutations in the C12orf65 gene
British Library Online Contents | 2014| -
A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies
British Library Online Contents | 2018| -
Mitochondrial dysfunction in liver failure requiring transplantation
British Library Online Contents | 2016| -
Scrib:Rac1 interactions are required for the morphogenesis of the ventricular myocardium
British Library Online Contents | 2014| -
Clinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMT
British Library Online Contents | 2013| -
Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency
Free accessBASE | 2021|
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