Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Anne Roethig"'
Autor:
Christian Frezza, Luca Scorrano, Joél Smet, Rudy Van Coster, Wilhelm Mandemakers, Vanessa A. Morais, Anne Roethig, Wolfgang Wurst, An Snellinx, Dominik Haddad, Bart De Strooper, Daniela Vogt-Weisenhorn, Patrik Verstreken, Mieke Vanbrabant
Publikováno v:
EMBO Molecular Medicine. 1:99-111
Mutations of the mitochondrial PTEN (phosphatase and tensin homologue)-induced kinase1 (PINK1) are important causes of recessive Parkinson disease (PD). Studies on loss of function and overexpression implicate PINK1 in apoptosis, abnormal mitochondri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f060bab73c0ba9c03c35209e27c238fe
https://doi.org/10.1002/emmm.200900006
https://doi.org/10.1002/emmm.200900006
Autor:
Ralf Kühn, Ulrich Hafen, Martin Hrabé de Angelis, Andreas Hofmann, Karina Kloos, Daniela M. Vogt Weisenhorn, Julia Zerle, Lisa Glasl, Sabine M. Hölter, Konstanze F. Winklhofer, Florian Giesert, Anne Roethig, Jingzhong Zhang, Wolfgang Wurst, Barbara Di Benedetto
Publikováno v:
Experimental neurology 235(1), 214-227 (2012). doi:10.1016/j.expneurol.2012.01.002
Parkinson's Disease (PD) is the most common neurodegenerative movement disorder. Autosomal-recessive mutations in the mitochondrial protein kinase PINK1 (PTEN-induced kinase 1) account for 1-2% of the hereditary early-onset cases. To study the mechan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98f86d1881576dcab83bb1a0a9e5d001
https://pubmed.ncbi.nlm.nih.gov/22265660
https://pubmed.ncbi.nlm.nih.gov/22265660