Bouman, L., A. Schlierf, A. K. Lutz, J. Shan, A. Deinlein, J. Kast, Z. Galehdar, V. Palmisano, N. Patenge, D. Berg, T. Gasser, R. Augustin, D. Trümbach, I. Irrcher, D. S. Park, W. Wurst, M. S. Kilberg, J. Tatzelt and K. F. Winklhofer: Parkin is transcriptionally regulated by ATF4: evidence for an interconnection between mitochondrial stress and ER stress. In: Cell Death and Differentiation 18, 5, 769-782 (2011).
Luecking, C. B., P. Lichtner, E. R. Kramer, C. Gieger, T. Illig, M. Dichgans, D. Berg and T. Gasser: Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern Germany. In: Neurobiology of Aging 31, 1, 167-168 (2010).
Eglin, T., P. Ciais, S. L. Piao, P. Barre, V. Bellassen, P. Cadule, C. C. Chenu, T. Gasser, C. Koven, M. Reichstein and P. Smith: Historical and future perspectives of global soil carbon response to climate and land-use changes. In: Tellus Series B-Chemical and Physical Meteorology 62, 700-718 (2010).
localid: BGC1408
Golub, Y., D. Berg, D. B. Calne, R. F. Pfeiffer, R. J. Uitti, A. J. Stoessl, Z. K. Wszolek, M. J. Farrer, J. C. Mueller, T. Gasser and J. Fuchs: Genetic factors influencing age at onset in LRRK2-linked Parkinson disease. In: Parkinsonism & Related Disorders 15, 7, 539-541 (2009).
Fernandez-Santiago, R., S. Hoenig, P. Lichtner, A. D. Sperfeld, M. Sharma, D. Berg, O. Weichenrieder, T. Illig, K. Eger, T. Meyer, J. Anneser, C. Münch, S. Zierz, T. Gasser and A. Ludolph: Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis. In: J Neurol 256, 8, 1337-1342 (2009).
Ludolph, A. C., J. Kassubek, B. G. Landwehrmeyer, E. Mandelkow, E. M. Mandelkow, D. J. Burn, D. Caparros-Lefebvre, K. A. Frey, J. G. de Yebenes, T. Gasser, P. Heutink, G. Hoglinger, Z. Jamrozik, K. A. Jellinger, A. Kazantsev, H. Kretzschmar, A. E. Lang, I. Litvan, J. J. Lucas, P. L. McGeer, S. Melquist, W. Oertel, M. Otto, D. Paviour, T. Reum, A. Saint-Raymond, J. C. Steele, M. Tolnay, H. Tumani, J. C. van Swieten, M. T. Vanier, J. P. Vonsattel, S. Wagner and Z. K. Wszolek: Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options. In: European Journal of Neurology 16, 3, 297-309 (2009).
Fuchs, J., A. Tichopad, Y. Golub, M. Munz, K. J. Schweitzer, B. Wolf, D. Berg, J. C. Mueller and T. Gasser: Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brain. In: FASEB Journal 22, 5, 1327-1334 (2008).
Rosenberger, A., M. Sharma, B. Müller-Myhsok, T. Gasser and H. Bickeböller: Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease. In: BMC Genetics 8, Seq. No.: doi: 10.1186/1471-2156-8-44 (2007).
Bender, A., W. Koch, M. Elstner, Y. Schombacher, J. Bender, M. Moeschl, F. Gekeler, B. Müller-Myhsok, T. Gasser, K. Tatsch and T. Klopstock: Creatine supplementation in Parkinson disease: A placebo-controlled randomized pilot trial. In: Neurology 67, 7, 1262-1264 (2006).
Liebetanz, K. M., J. Winkelmann, C. Trenkwalder, B. Pütz, M. Dichgans, T. Gasser and B. Müller-Myhsok: RLS3: Fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity. In: Neurology 67, 2, 320-321 (2006).
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