Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove

Autophagy

Volumn 8, Issue 9, 2012, Pages 1389-1391

  Dehay, Benjamin ^a   Martinez Vicente, Marta ^b   Ramirez, Alfredo ^c,d   Perier, Celine ^b   Klein, Christine ^c   Vila, Miquel ^b,e,f   Bezard, Erwan ^a  

^a UNIVERSITÉ DE BORDEAUX   (France)

^b CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED SOBRE ENFERMEDADES NEURODEGENERATIVAS CIBERNED   (Spain)

^c UNIVERSITY OF LÜBECK   (Germany)

^d UNIVERSITY OF BONN   (Germany)

^e UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^f INSTITUCIÓ CATALANA DE RECERCA I ESTUDIS AVANÇATS ICREA   (Spain)

Author keywords

ATP13A2; Autophagy; Lysosome; Neurodegeneration; Parkinson disease

Indexed keywords

ADENOSINE TRIPHOSPHATASE; CHAPERONE; GLUCOSYLCERAMIDASE; LYSOSOME ENZYME;

ANIMAL EXPERIMENT; ANIMAL MODEL; ATP13A2 GENE; AUTOSOMAL RECESSIVE DISORDER; BRAIN; CELL VIABILITY; DEGENERATIVE DISEASE; DEMENTIA; DOPAMINERGIC NERVE CELL; ENZYME DEFICIENCY; ENZYME SUBSTRATE; GAUCHER DISEASE; GENE; GENE MUTATION; HUMAN; KUFOR RAKEB SYNDROME; LEWY BODY; LYSOSOME; LYSOSOME STORAGE DISEASE; MISSENSE MUTATION; MOUSE; NEUROLOGIC DISEASE; NEUROTOXICITY; NONHUMAN; ONSET AGE; PARKINSON DISEASE; PARKINSONISM; PROTEIN DEGRADATION; SHORT SURVEY; SUBSTANTIA NIGRA; SYNDROME;

MAMMALIA;

EID: 84866529985     PISSN: 15548627     EISSN: 15548635     Source Type: Journal    
DOI: 10.4161/auto.21011     Document Type: Short Survey

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