Charcot-Marie-Tooth disease-associated mutants of GDAP1 dissociate its roles in peroxisomal and mitochondrial fission

EMBO Reports

Volumn 14, Issue 6, 2013, Pages 545-552

  Huber, Nina ^a   Guimaraes, Sofia ^b   Schrader, Michael ^b,c   Suter, Ueli ^a   Niemann, Axel ^a  

^a ETH ZURICH   (Switzerland)

^b UNIVERSITY OF AVEIRO   (Portugal)

^c UNIVERSITY OF EXETER   (United Kingdom)

Author keywords

glutathione S transferase; mitochondrial dynamics; peripheral neuropathy; tail anchored protein

Indexed keywords

GDAP1 PROTEIN; MITOCHONDRIAL PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; MISSENSE MUTATION; MITOCHONDRION; MUTANT; PERIPHERAL NEUROPATHY; PEROXISOME; PRIORITY JOURNAL; PROTEIN EXPRESSION;

ANIMALS; CELL SHAPE; CERCOPITHECUS AETHIOPS; CHARCOT-MARIE-TOOTH DISEASE; COS CELLS; GTP PHOSPHOHYDROLASES; HEK293 CELLS; HIPPOCAMPUS; HUMANS; MEMBRANE PROTEINS; MICE; MICE, INBRED C57BL; MICROTUBULE-ASSOCIATED PROTEINS; MITOCHONDRIAL DYNAMICS; MITOCHONDRIAL MEMBRANES; MITOCHONDRIAL PROTEINS; MUTATION, MISSENSE; NERVE TISSUE PROTEINS; NEURONS; PEROXISOMES; PRIMARY CELL CULTURE; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT;

EID: 84878588576     PISSN: 1469221X     EISSN: 14693178     Source Type: Journal    
DOI: 10.1038/embor.2013.56     Document Type: Article

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