Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mareike E Fett"'
Autor:
Mareike E Fett, Anna Pilsl, Dominik Paquet, Frauke van Bebber, Christian Haass, Jörg Tatzelt, Bettina Schmid, Konstanze F Winklhofer
Publikováno v:
PLoS ONE, Vol 5, Iss 7, p e11783 (2010)
Mutations in the gene encoding the E3 ubiquitin ligase parkin (PARK2) are responsible for the majority of autosomal recessive parkinsonism. Similarly to other knockout mouse models of PD-associated genes, parkin knockout mice do not show a substantia
Externí odkaz:
https://doaj.org/article/88d7d03040ee4968a2ef81a834585572
Autor:
Karina Kloos, Christian Haass, Frank Vogel, Kerstin Lämmermann, Andreas S. Reichert, Lena Bouman, Julia S. Schlehe, Bettina Brunner, Wolfgang Wurst, Annerose Kurz-Drexler, A. Kathrin Lutz, Daniela Vogt-Weisenhorn, Mareike E. Fett, Nicole Exner, Konstanze F. Winklhofer, Jörg Tatzelt
Publikováno v:
J. Biol. Chem. 284, 2108-2111 (2009)
The journal of biological chemistry 284(34), 22938-22951 (2009). doi:10.1074/jbc.M109.035774
The journal of biological chemistry 284(34), 22938-22951 (2009). doi:10.1074/jbc.M109.035774
Loss-of-function mutations in the parkin gene (PARK2) and PINK1 gene (PARK6) are associated with autosomal recessive parkinsonism. PINK1 deficiency was recently linked to mitochondrial pathology in human cells and Drosophila melanogaster, which can b
Autor:
Frauke van Bebber, Dominik Paquet, Konstanze F. Winklhofer, Mareike E. Fett, Bettina Schmid, Anna Pilsl, Jörg Tatzelt, Christian Haass
Publikováno v:
PLoS ONE
PLoS ONE, Vol 5, Iss 7, p e11783 (2010)
PLOS ONE 5(7), e11783 (2010). doi:10.1371/journal.pone.0011783
PLoS ONE, Vol 5, Iss 7, p e11783 (2010)
PLOS ONE 5(7), e11783 (2010). doi:10.1371/journal.pone.0011783
Background: Mutations in the gene encoding the E3 ubiquitin ligase parkin (PARK2) are responsible for the majority of autosomal recessive parkinsonism. Similarly to other knockout mouse models of PD-associated genes, parkin knockout mice do not show