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          Institute: MPI für Psychiatrie     Collection: Publikationen MPI für Psychiatrie     Display Documents



  history
ID: 451189.0, MPI für Psychiatrie / Publikationen MPI für Psychiatrie
Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function
Authors:Morais, V. A.; Verstreken, P.; Roethig, A.; Smet, J.; Snellinx, A.; Vanbrabant, M.; Haddad, D.; Frezza, C.; Mandemakers, W.; Vogt-Weisenhorn, D.; Van Coster, R.; Wurst, W.; Scorrano, L.; De Strooper, B.
Language:English
Date of Publication (YYYY-MM-DD):2009-05
Title of Journal:EMBO Molecular Medicine
Journal Abbrev.:EMBO Mol. Med.
Volume:1
Issue / Number:2
Start Page:99
End Page:111
Review Status:Peer-review
Audience:Not Specified
Free Keywords:Complex I; mitochondrial dysfunction; Parkinson's disease; reserve pool deficit
External Publication Status:published
Document Type:Article
Version Comment:Automatic journal name synchronization
Communicated by:N. N.
Affiliations:MPI für Psychiatrie
External Affiliations:[Morais, Vanessa A.; Verstreken, Patrik; Snellinx, An; Vanbrabant, Mieke; Haddad, Dominik; Mandemakers, Wim; De Strooper, Bart] Katholieke Univ Leuven, Ctr Human Genet, Leuven, Belgium.; [Morais, Vanessa A.; Verstreken, Patrik; Snellinx, An; Vanbrabant, Mieke; Haddad, Dominik; Mandemakers, Wim; De Strooper, Bart] VIB, Dept Mol & Dev Genet, Leuven, Belgium.; [Roethig, Anne; Vogt-Weisenhorn, Daniela; Wurst, Wolfgang] Tech Univ Munich, Helmholtz Ctr Munich, Inst Dev Genet, Max Planck Inst Psychiat, Munich, Germany.; [Smet, Joel; Van Coster, Rudy] Ghent Univ Hosp, Div Neurol & Metab, Dept Pediat, Ghent, Belgium.; [Frezza, Christian] Venetian Inst Mol Med, Dulbecco Telethon Inst, Padua, Italy.; [Scorrano, Luca] Univ Geneva, Dept Cell Physiol & Metab, Geneva, Switzerland.
Identifiers:ISI:000273563000006 [ID No:1]
ISSN:1757-4676 [ID No:2]
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