Ausgabe 2/2012
Inhalt (12 Artikel)
Protein degradation pathways in Parkinson’s disease: curse or blessing
Darius Ebrahimi-Fakhari, Lara Wahlster, Pamela J. McLean
Autophagic adapter protein NBR1 is localized in Lewy bodies and glial cytoplasmic inclusions and is involved in aggregate formation in α-synucleinopathy
Saori Odagiri, Kunikazu Tanji, Fumiaki Mori, Akiyoshi Kakita, Hitoshi Takahashi, Koichi Wakabayashi
Long-term proteasomal inhibition in transgenic mice by UBB+1 expression results in dysfunction of central respiration control reminiscent of brainstem neuropathology in Alzheimer patients
Martin Irmler, Romina J. G. Gentier, Frank J. A. Dennissen, Holger Schulz, Ines Bolle, Sabine M. Hölter, Magdalena Kallnik, Jing Jun Cheng, Martin Klingenspor, Jan Rozman, Nicole Ehrhardt, Denise J. H. P. Hermes, Valérie Gailus-Durner, Helmut Fuchs, Martin Hrabě de Angelis, Helmut E. Meyer, David A. Hopkins, Fred W. Van Leeuwen, Johannes Beckers
Mitochondrial DNA polymorphisms specifically modify cerebral β-amyloid proteostasis
Katja Scheffler, Markus Krohn, Tina Dunkelmann, Jan Stenzel, Bruno Miroux, Saleh Ibrahim, Oliver von Bohlen und Halbach, Hans-Jochen Heinze, Lary C. Walker, Jörg A. Gsponer, Jens Pahnke
Clonally expanded mitochondrial DNA deletions within the choroid plexus in multiple sclerosis
Graham R. Campbell, Yevgenya Kraytsberg, Kim J. Krishnan, Nobuhiko Ohno, Iryna Ziabreva, Amy Reeve, Bruce D. Trapp, Jia Newcombe, Richard Reynolds, Hans Lassmann, Konstantin Khrapko, Doug M. Turnbull, Don J. Mahad
Distinct TDP-43 pathology in ALS patients with ataxin 2 intermediate-length polyQ expansions
Michael P. Hart, Johannes Brettschneider, Virginia M. Y. Lee, John Q. Trojanowski, Aaron D. Gitler
TDP-43 regulates the mammalian spinogenesis through translational repression of Rac1
Pritha Majumder, Yi-Ting Chen, Jayarama Krishnan Bose, Cheng-Chun Wu, Wei-Cheng Cheng, Sin-Jhong Cheng, Yen-Hsin Fang, Ying-Ling Chen, Kuen-Jer Tsai, Cheng-Chang Lien, Che-Kun James Shen
Distinct disease-risk groups in pediatric supratentorial and posterior fossa ependymomas
Catherine Godfraind, Joanna M. Kaczmarska, Mehmet Kocak, James Dalton, Karen D. Wright, Robert A. Sanford, Fredrick A. Boop, Amar Gajjar, Thomas E. Merchant, David W. Ellison
Identification of novel pathways involved in the pathogenesis of human adamantinomatous craniopharyngioma
Cynthia L. Andoniadou, Carles Gaston-Massuet, Rukmini Reddy, Ralph P. Schneider, Maria A. Blasco, Paul Le Tissier, Thomas S. Jacques, Larysa H. Pevny, Mehul T. Dattani, Juan Pedro Martinez-Barbera
Next generation sequencing for molecular diagnosis of neuromuscular diseases
Nasim Vasli, Johann Böhm, Stéphanie Le Gras, Jean Muller, Cécile Pizot, Bernard Jost, Andoni Echaniz-Laguna, Vincent Laugel, Christine Tranchant, Rafaelle Bernard, Frédéric Plewniak, Serge Vicaire, Nicolas Levy, Jamel Chelly, Jean-Louis Mandel, Valérie Biancalana, Jocelyn Laporte
TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation
Maria Martinez-Lage, Laura Molina-Porcel, Dana Falcone, Leo McCluskey, Virginia M.-Y. Lee, Vivianna M. Van Deerlin, John Q. Trojanowski
Periventricular white matter immunoglobulin lambda light chain deposition disease diagnosed by proteomic analysis
Joshua R. Menke, Mark E. Jentoft, Ahmet Dogan, James M. Avent, Dylan V. Miller, Caterina Giannini