Mitochondrial morphology and cellular distribution are altered in SPG31 patients and are linked to DRP1 hyperphosphorylation

Human Molecular Genetics

Volumn 26, Issue 4, 2017, Pages 674-685

  Lavie, Julie ^a,b   Serrat, Román ^b,c   Bellance, Nadège ^a,b   Courtand, Gilles ^b   Dupuy, Jean William ^b,d   Tesson, Christelle ^e,f   Coupry, Isabelle ^a,b   Brice, Alexis ^e   Lacombe, Didier ^a,b   Durr, Alexandra ^e   Stevanin, Giovanni ^e,f   Darios, Frèderic ^e   Rossignol, Rodrigue ^a,b   Goizet, Cyril ^a,b   Bènard, Giovanni ^a,b  

^a HÔPITAL PELLEGRIN   (France)

^b UNIVERSITÉ DE BORDEAUX   (France)

^c INSTITUT FRANÇOIS MAGENDIE   (France)

^d Bordeaux Functional Genomic Center   (France)

^e INSTITUT DU CERVEAU ET DE LA MOELLE ÉPINIÈRE   (France)

^f PSL RESEARCH UNIVERSITY   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DRP1 PROTEIN; MICROTUBULE PROTEIN; MITOCHONDRIAL PROTEIN; RECEPTOR EXPRESSION ENHANCING PROTEIN 1; SERINE; SPG31 PROTEIN; UNCLASSIFIED DRUG; CARRIER PROTEIN; DNM1L PROTEIN, HUMAN; GUANOSINE TRIPHOSPHATASE; MICROTUBULE ASSOCIATED PROTEIN; PGAM5 PROTEIN, HUMAN; PHOSPHOPROTEIN PHOSPHATASE; REEP1 PROTEIN, HUMAN;

ANIMAL CELL; ARTICLE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; ECTOPIC EXPRESSION; FEMALE; FIBROBLAST; MALE; MITOCHONDRIAL DYNAMICS; MOUSE; NERVE CELL CULTURE; NONHUMAN; PRIORITY JOURNAL; PROTEIN INTERACTION; PROTEIN PHOSPHORYLATION; ANIMAL; CELL CULTURE; CELL NUCLEUS; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; METABOLISM; MITOCHONDRION; NERVE CELL; PATHOLOGY; PHOSPHORYLATION;

ANIMALS; CELL NUCLEUS; CELLS, CULTURED; FEMALE; GTP PHOSPHOHYDROLASES; HUMANS; MALE; MEMBRANE TRANSPORT PROTEINS; MICE; MICROTUBULE-ASSOCIATED PROTEINS; MITOCHONDRIA; MITOCHONDRIAL PROTEINS; NEURONS; PHOSPHOPROTEIN PHOSPHATASES; PHOSPHORYLATION; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 85018445174     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddw425     Document Type: Article

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