The role of glyoxalases for sugar stress and aging, with relevance for dyskinesia, anxiety, dementia and Parkinson's disease

Por Auburger, Georg, Kurz, Alexander
Publicado em 2011

Methyl-Arginine Profile of Brain from Aged PINK1-KO+A53T-SNCA Mice Suggests Altered Mitochondrial Biogenesis

Por Auburger, Georg, Gispert, Suzana, Brehm, Nadine
Publicado no Parkinsons Dis (2016)

PINK1 and Ataxin-2 as modifiers of growth

Por Sen, Nesli E., Gispert, Suzana, Auburger, Georg
Publicado no Oncotarget (2017)

Striatal Dopamine Transmission Is Subtly Modified in Human A53Tα-Synuclein Overexpressing Mice

Por Platt, Nicola J., Gispert, Suzana, Auburger, Georg, Cragg, Stephanie J.
Publicado em 2012

Ataxin-2 (Atxn2)-Knock-Out Mice Show Branched Chain Amino Acids and Fatty Acids Pathway Alterations

Por Meierhofer, David, Halbach, Melanie, Şen, Nesli Ece, Gispert, Suzana, Auburger, Georg
Publicado no Mol Cell Proteomics (2016)

Dysregulated expression of lipid storage and membrane dynamics factors in Tia1 knockout mouse nervous tissue

Por Heck, Melanie Vanessa, Azizov, Mekhman, Stehning, Tanja, Walter, Michael, Kedersha, Nancy, Auburger, Georg
Publicado em 2014

Atxn2 Knockout and CAG42-Knock-in Cerebellum Shows Similarly Dysregulated Expression in Calcium Homeostasis Pathway

Por Halbach, Melanie Vanessa, Gispert, Suzana, Stehning, Tanja, Damrath, Ewa, Walter, Michael, Auburger, Georg
Publicado no Cerebellum (2016)

Alpha-synuclein deficiency leads to increased glyoxalase I expression and glycation stress

Por Kurz, Alexander, Rabbani, Naila, Walter, Michael, Bonin, Michael, Thornalley, Paul, Auburger, Georg, Gispert, Suzana
Publicado em 2010

12q24 locus association with type 1 diabetes: SH2B3 or ATXN2?

Por Auburger, Georg, Gispert, Suzana, Lahut, Suna, Ömür, Özgür, Damrath, Ewa, Heck, Melanie, Başak, Nazlı
Publicado em 2014

PINK1 and Parkin Control Localized Translation of Respiratory Chain Component mRNAs on Mitochondria Outer Membrane

Por Gehrke, Stephan, Wu, Zhihao, Klinkenberg, Michael, Sun, Yaping, Auburger, Georg, Guo, Su, Lu, Bingwei
Publicado no Cell Metab (2015)

Complexin-1 and Foxp1 Expression Changes Are Novel Brain Effects of Alpha-Synuclein Pathology

Por Gispert, Suzana, Kurz, Alexander, Brehm, Nadine, Rau, Katrin, Walter, Michael, Riess, Olaf, Auburger, Georg
Publicado no Mol Neurobiol (2014)

Regulation of mRNA Translation by MID1: A Common Mechanism of Expanded CAG Repeat RNAs

Por Griesche, Nadine, Schilling, Judith, Weber, Stephanie, Rohm, Marlena, Pesch, Verena, Matthes, Frank, Auburger, Georg, Krauss, Sybille
Publicado no Front Cell Neurosci (2016)

Both Ubiquitin Ligases FBXW8 and PARK2 Are Sequestrated into Insolubility by ATXN2 PolyQ Expansions, but Only FBXW8 Expression Is Dysregulated

Por Halbach, Melanie Vanessa, Stehning, Tanja, Damrath, Ewa, Jendrach, Marina, Şen, Nesli Ece, Başak, A. Nazlı, Auburger, Georg
Publicado no PLoS One (2015)

Potentiation of neurotoxicity in double-mutant mice with Pink1 ablation and A53T-SNCA overexpression

Por Gispert, Suzana, Brehm, Nadine, Weil, Jonas, Seidel, Kay, Rüb, Udo, Kern, Beatrice, Walter, Michael, Roeper, Jochen, Auburger, Georg
Publicado no Hum Mol Genet (2015)

A53T-alpha-synuclein-overexpression in the mouse nigrostriatal pathway leads to early increase of 14-3-3 epsilon and late increase of GFAP

Por Kurz, Alexander, May, Caroline, Schmidt, Oliver, Müller, Thorsten, Stephan, Christian, Meyer, Helmut E., Gispert, Suzana, Auburger, Georg, Marcus, Katrin
Publicado em 2011

ATXN2-CAG42 Sequesters PABPC1 into Insolubility and Induces FBXW8 in Cerebellum of Old Ataxic Knock-In Mice

Por Damrath, Ewa, Heck, Melanie V., Gispert, Suzana, Azizov, Mekhman, Nowock, Joachim, Seifried, Carola, Rüb, Udo, Walter, Michael, Auburger, Georg
Publicado em 2012

Solving a 50 year mystery of a missing <it>OPA1 </it>mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy

Por Zrenner Eberhart, Auburger Georg, Alexander Christiane, Leo-Kottler Beate, Kamenisch York, Schimpf Simone, Fuhrmann Nico, Wissinger Bernd, Alavi Marcel V
Publicado em 2010-06-01

Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy

Por Fuhrmann, Nico, Schimpf, Simone, Kamenisch, York, Leo-Kottler, Beate, Alexander, Christiane, Auburger, Georg, Zrenner, Eberhart, Wissinger, Bernd, Alavi, Marcel V
Publicado em 2010

MAMMALIAN ATAXIN-2 MODULATES TRANSLATION CONTROL AT THE PRE-INITITATION COMPLEX VIA PI3K/MTOR AND IS INDUCED BY STARVATION

Por Lastres-Becker, Isabel, Nonis, David, Eich, Florian, Klinkenberg, Michael, Gorospe, Myriam, Kötter, Peter, Klein, Fabrice A. C., Kedersha, Nancy, Auburger, Georg
Publicado no Biochim Biophys Acta (2016)

Ataxin-2 Modulates the Levels of Grb2 and Src but Not Ras Signaling

Por Drost, Jessica, Nonis, David, Eich, Florian, Leske, Oliver, Damrath, Ewa, Brunt, Ewout R., Lastres-Becker, Isabel, Heumann, Rolf, Nowock, Joachim, Auburger, Georg
Publicado em 2013