Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Lisa Voges"'
Autor:
Aleksandar Rakovic, Anne Grünewald, Lisa Voges, Sarah Hofmann, Slobodanka Orolicki, Katja Lohmann, Christine Klein
Publikováno v:
Parkinson's Disease, Vol 2011 (2011)
Recent publications suggest that the Parkinson's disease- (PD-) related PINK1/Parkin pathway promotes elimination of dysfunctional mitochondria by autophagy. We used tandem affinity purification (TAP), SDS-PAGE, and mass spectrometry as a first step
Externí odkaz:
https://doaj.org/article/36a0a68540cb41d990deb9d7704cc1de
Autor:
Anne Grünewald, Lisa Voges, Aleksandar Rakovic, Meike Kasten, Himesha Vandebona, Claudia Hemmelmann, Katja Lohmann, Slobodanka Orolicki, Alfredo Ramirez, Anthony H V Schapira, Peter P Pramstaller, Carolyn M Sue, Christine Klein
Publikováno v:
PLoS ONE, Vol 5, Iss 9, p e12962 (2010)
Mutations in Parkin are the most common cause of autosomal recessive Parkinson disease (PD). The mitochondrially localized E3 ubiquitin-protein ligase Parkin has been reported to be involved in respiratory chain function and mitochondrial dynamics. M
Externí odkaz:
https://doaj.org/article/0cdf43fbc1dd4d02a28dc1e66683c592
Autor:
Aleksandar Rakovic, Slobodanka Orolicki, Anne Grünewald, Sarah Hofmann, Christine Klein, Lisa Voges, Katja Lohmann
Publikováno v:
Parkinson's Disease
Parkinson's Disease, Vol 2011 (2011)
BASE-Bielefeld Academic Search Engine
Parkinson's Disease, Vol 2011 (2011)
BASE-Bielefeld Academic Search Engine
Recent publications suggest that the Parkinson's disease- (PD-) related PINK1/Parkin pathway promotes elimination of dysfunctional mitochondria by autophagy. We used tandem affinity purification (TAP), SDS-PAGE, and mass spectrometry as a first step
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95c6924f310e8dd7b53fcb9b8ec9e44f
https://pubmed.ncbi.nlm.nih.gov/21437181
https://pubmed.ncbi.nlm.nih.gov/21437181
Autor:
Slobodanka Orolicki, Katja Lohmann, Peter P. Pramstaller, Aleksandar Rakovic, Meike Kasten, Alfredo Ramirez, Anne Grünewald, Carolyn M. Sue, Anthony H.V. Schapira, Christine Klein, Lisa Voges, Himesha Vandebona, Claudia Hemmelmann
Publikováno v:
PLoS ONE
PLoS ONE, Vol 5, Iss 9, p e12962 (2010)
PLoS ONE, Vol 5, Iss 9, p e12962 (2010)
Background: Mutations in Parkin are the most common cause of autosomal recessive Parkinson disease (PD). The mitochondrially localized E3 ubiquitin-protein ligase Parkin has been reported to be involved in respiratory chain function and mitochondrial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6937a6768cb76d6b3e0cf274a94b1b41
https://doi.org/10.1371/journal.pone.0012962
https://doi.org/10.1371/journal.pone.0012962