Ausgabe 1/2015
Inhalt (11 Artikel)
Analyzing dendritic spine pathology in Alzheimer’s disease: problems and opportunities
Mario M. Dorostkar, Chengyu Zou, Lidia Blazquez-Llorca, Jochen Herms
Beta-amyloid deposition in chronic traumatic encephalopathy
Thor D. Stein, Philip H. Montenigro, Victor E. Alvarez, Weiming Xia, John F. Crary, Yorghos Tripodis, Daniel H. Daneshvar, Jesse Mez, Todd Solomon, Gaoyuan Meng, Caroline A. Kubilus, Kerry A. Cormier, Steven Meng, Katharine Babcock, Patrick Kiernan, Lauren Murphy, Christopher J. Nowinski, Brett Martin, Diane Dixon, Robert A. Stern, Robert C. Cantu, Neil W. Kowall, Ann C. McKee
Aβ43 is neurotoxic and primes aggregation of Aβ40 in vivo
Sylvie Burnouf, Marianna Karina Gorsky, Jacqueline Dols, Sebastian Grönke, Linda Partridge
Low molecular weight species of TDP-43 generated by abnormal splicing form inclusions in amyotrophic lateral sclerosis and result in motor neuron death
Shangxi Xiao, Teresa Sanelli, Helen Chiang, Yulong Sun, Avijit Chakrabartty, Julia Keith, Ekaterina Rogaeva, Lorne Zinman, Janice Robertson
Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy
Johnathan Cooper-Knock, Adrian Higginbottom, Matthew J. Stopford, J. Robin Highley, Paul G. Ince, Stephen B. Wharton, Stuart Pickering-Brown, Janine Kirby, Guillaume M. Hautbergue, Pamela J. Shaw
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease
Cyril Pottier, Kevin F. Bieniek, NiCole Finch, Maartje van de Vorst, Matt Baker, Ralph Perkersen, Patricia Brown, Thomas Ravenscroft, Marka van Blitterswijk, Alexandra M. Nicholson, Michael DeTure, David S. Knopman, Keith A. Josephs, Joseph E. Parisi, Ronald C. Petersen, Kevin B. Boylan, Bradley F. Boeve, Neill R. Graff-Radford, Joris A. Veltman, Christian Gilissen, Melissa E. Murray, Dennis W. Dickson, Rosa Rademakers
Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein
Naoya Aoki, Philip J. Boyer, Cheryl Lund, Wen-Lang Lin, Shunsuke Koga, Owen A. Ross, Myron Weiner, Anne Lipton, James M. Powers, Charles L. White III, Dennis W. Dickson
Induction of endogenous Type I interferon within the central nervous system plays a protective role in experimental autoimmune encephalomyelitis
Reza Khorooshi, Marlene Thorsen Mørch, Thomas Hellesøe Holm, Carsten Tue Berg, Ruthe Truong Dieu, Dina Dræby, Shohreh Issazadeh-Navikas, Siegfried Weiss, Stefan Lienenklaus, Trevor Owens
Alterations of mGluR5 and its endogenous regulators Norbin, Tamalin and Preso1 in schizophrenia: towards a model of mGluR5 dysregulation
Natalie Matosin, Francesca Fernandez-Enright, Samantha Jane Fung, Jeremy Stephen Lum, Martin Engel, Jessica Lee Andrews, Xu-Feng Huang, Cynthia Shannon Weickert, Kelly Anne Newell
Identification of a novel MET mutation in high-grade glioma resulting in an auto-active intracellular protein
Anna C. Navis, Sanne A. M. van Lith, Sander M. J. van Duijnhoven, Maaike de Pooter, Bahar Yetkin-Arik, Pieter Wesseling, Wiljan J. A. J. Hendriks, Hanka Venselaar, Marco Timmer, Patricia van Cleef, Paul van Bergen en Henegouwen, Myron G. Best, Thomas D. Wurdinger, Bastiaan B. J. Tops, William P. J. Leenders
A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degeneration
Masataka Nakamura, Kevin F. Bieniek, Wen-Lang Lin, Neill R. Graff-Radford, Melissa E. Murray, Monica Castanedes-Casey, Pamela Desaro, Matthew C. Baker, Nicola J. Rutherford, Janice Robertson, Rosa Rademakers, Dennis W. Dickson, Kevin B. Boylan