Mitochondrial defects and neuromuscular degeneration caused by altered expression of Drosophila Gdap1: Implications for the Charcot-Marie-Tooth neuropathy

Human Molecular Genetics

Volumn 24, Issue 1, 2015, Pages 21-36

  Del Amo, Víctor López ^a,b   Seco Cervera, Marta ^b,c   García Giménez, José Luís ^b,c   Whitworth, Alexander J ^d   Pallardó, Federico V ^b,c   Galindo, Máximo Ibo ^a,b  

^a CENTRO DE INVESTIGACIÓN PRÍNCIPE FELIPE   (Spain)

^b CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED DE ENFERMEDADES RARAS CIBERER   (Spain)

^c UNIVERSITY OF VALENCIA   (Spain)

^d UNIVERSITY OF SHEFFIELD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; GLUTATHIONE; DFSN PROTEIN, DROSOPHILA; DROSOPHILA PROTEIN; F BOX PROTEIN; GDAP PROTEIN; NERVE PROTEIN;

ADULT; ANIMAL CELL; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DROSOPHILA; GDAP1 GENE; GENE; GENE EXPRESSION; GLUTATHIONE METABOLISM; HEREDITARY MOTOR SENSORY NEUROPATHY; MITOCHONDRIAL DYNAMICS; MITOCHONDRIAL VOLUME; MITOCHONDRION; MUSCLE ATROPHY; NERVE DEGENERATION; NONHUMAN; ORTHOLOGY; OXIDATIVE STRESS; PHOTORECEPTOR; PRIORITY JOURNAL; RETINA; ANIMAL; DISEASE MODEL; DROSOPHILA MELANOGASTER; GENE EXPRESSION REGULATION; GENETICS; HUMAN; METABOLISM; NEUROMUSCULAR DISEASES; PATHOLOGY; PHYLOGENY; PHYSIOLOGY;

ANIMALS; CHARCOT-MARIE-TOOTH DISEASE; DISEASE MODELS, ANIMAL; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; F-BOX PROTEINS; GENE EXPRESSION REGULATION; HUMANS; MITOCHONDRIA; MITOCHONDRIAL SIZE; NERVE TISSUE PROTEINS; NEUROMUSCULAR DISEASES; PHYLOGENY; RETINA;

EID: 84922544988     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddu416     Document Type: Article

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