Zobrazeno 1 - 10
of 105
pro vyhledávání: '"Witting, Anke"'
Autor:
Witting, Anke
Mikrogliazellen stellen die professionellen Phagozyten des zentralen Nervensystems dar und sind maßgeblich bei der Entfernung apoptotischer Neurone aus dem Gewebe beteiligt. Die Erkennungsmechanismen, die zu einer Erkennung und Phagozytose apoptotis
Externí odkaz:
http://edoc.hu-berlin.de/18452/15197
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2004 Mar 01. 101(9), 3214-3219.
Externí odkaz:
https://www.jstor.org/stable/3371181
Autor:
Pasquarelli, Noemi, Porazik, Christoph, Bayer, Hanna, Buck, Eva, Schildknecht, Stefan, Weydt, Patrick, Witting, Anke, Ferger, Boris
Publikováno v:
In Neurochemistry International November 2017 110:14-24
Autor:
Witting, Anke, Chen, Lanfen, Cudaback, Eiron, Straiker, Alex, Walter, Lisa, Rickman, Barry, Möller, Thomas, Brosnan, Celia, Stella, Nephi
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2006 Apr . 103(16), 6362-6367.
Externí odkaz:
https://www.jstor.org/stable/30051472
Autor:
Ferger Annette I, Campanelli Loretta, Reimer Valentina, Muth Katharina N, Merdian Irma, Ludolph Albert C, Witting Anke
Publikováno v:
Journal of Neuroinflammation, Vol 7, Iss 1, p 45 (2010)
Abstract Background Neurodegenerative diseases are characterized by both mitochondrial dysfunction and activation of microglia, the macrophages of the brain. Here, we investigate the effects of mitochondrial dysfunction on the activation profile of m
Externí odkaz:
https://doaj.org/article/f1e14b0ae54c43a997fcec17e6949bee
Autor:
Buck, Eva, Bayer, Hanna, Lindenberg, Katrin S., Hanselmann, Johannes, Pasquarelli, Noemi, Ludolph, Albert C., Weydt, Patrick, Witting, Anke
Publikováno v:
Frontiers in Molecular Neuroscience. 10
Neurodegenerative diseases are characterized by distinct patterns of neuronal loss. In amyotrophic lateral sclerosis (ALS) upper and lower motoneurons degenerate whereas in Huntington’s disease (HD) medium spiny neurons in the striatum are preferen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=frontiers___::cd4574f5b6e931714a5a8b48d181c8ce
Autor:
Soyal, Selma M., Felder, Thomas K., Auer, Simon, Hahne, Penelope, Oberkofler, Hannes, Witting, Anke, Paulmichl, Markus, Landwehrmeyer, G. Bernhard, Weydt, Patrick, Patsch, Wolfgang, European Huntington Disease Network, Romano, Silvia
Publikováno v:
Human Molecular Genetics. 21:3461-3473
PGC-1α has been implicated in the pathogenesis of neurodegenerative disorders. Several single-nucleotide polymorphisms (SNPs) located in two separate haplotype blocks of PPARGC1A have shown associations with Huntington's disease (HD) and Parkinson's
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db931ed16e4082def0815bf85859eda5
https://doi.org/10.1093/hmg/dds177
https://doi.org/10.1093/hmg/dds177
Autor:
Vercruysse, Pauline, Sinniger, Jérôme, Dreyhaupt, Jens, Grehl, Torsten, Hermann, Andreas, Grosskreutz, Julian, Witting, Anke, Van Den Bosch, Ludo, Spreux-Varoquaux, Odile, Group, GERP ALS Study, Ludolph, Albert C, Dupuis, Luc, El Oussini, Hajer, Borisow, Nadja, Holm, Theresa, Maier, Andre, Meyer, Thomas, Budde, Paula, Gruhn, Kai, Bewersdorff, Malte, Heneka, Michael, Storch, Alexander, Scekic-Zahirovic, Jelena, Frank, Tobias, Göricke, Bettina, Weishaupt, Jochen, Eger, Katharina, Hanisch, Frank, Zierz, Stephan, Boeck, Anna-Lena, Dengler, Reinhard, Koerner, Sonja, Kollewe, Katja, Dieterlé, Stéphane, Petri, Susanne, Prell, Tino, Ringer, Thomas, Zinke, Jan, Anneser, Johanna, Borasio, Gian Domenico, Chahli, Christine, Winkler, Andrea S, Boentert, Matthias, Stubbe-Draeger, Bianca, Young, Peter, Bogdahn, Ulrich, Franz, Steffen, Haringer, Verena, Weidner, Norbert, Benecke, Reiner, Meister, Stefanie, Prudlo, Johannes, Wittstock, Matthias, Dorst, Johannes, Hendrich, Corinna, Sperfeld, Anne-Dorte, Weiland, Ulrike, Neidhardt, Sabine, Schrank, Berthold, Beck, Marcus, Kraft, Peter, Toyka, Klaus, Ulzheimer, Jochen, Wessig, Carsten, Kassubek, Jan, Fischer, Wilhelm
Publikováno v:
Brain 139(4), 1106-1122 (2016). doi:10.1093/brain/aww004
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2016, 139 (4), pp.1106-1122. ⟨10.1093/brain/aww004⟩
Brain-A Journal of Neurology, 2016, 139 (4), pp.1106-1122. ⟨10.1093/brain/aww004⟩
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2016, 139 (4), pp.1106-1122. ⟨10.1093/brain/aww004⟩
Brain-A Journal of Neurology, 2016, 139 (4), pp.1106-1122. ⟨10.1093/brain/aww004⟩
International audience; Amyotrophic lateral sclerosis, the most common adult-onset motor neuron disease, leads to death within 3 to 5 years after onset. Beyond progressive motor impairment, patients with amyotrophic lateral sclerosis suffer from majo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2100cab1af8c6c87b161388fec439336
https://pubmed.ncbi.nlm.nih.gov/26984187
https://pubmed.ncbi.nlm.nih.gov/26984187
Autor:
Eschbach, Judith, von Einem, Bjoern, Mueller, Kathrin, Bayer, Hanna, Scheffold, Annika, Morrison, Bradley E, Rudolph, K Lenhard, Thal, Dietmar, Witting, Anke, Weydt, Patrick, Otto, Markus, Fauler, Michael, Liss, Birgit, McLean, Pamela J, La Spada, Albert R, Ludolph, Albert C, Weishaupt, Jochen H, Danzer, Karin M
OBJECTIVE: Aggregation of α-synuclein (α-syn) and α-syn cytotoxicity are hallmarks of sporadic and familial Parkinson disease (PD), with accumulating evidence that prefibrillar oligomers and protofibrils are the pathogenic species in PD and relate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1131::4cbe07c940355d3bec40f476582d5ccb
https://lirias.kuleuven.be/handle/123456789/509971
https://lirias.kuleuven.be/handle/123456789/509971