Protein degradation pathways in Parkinson’s disease: curse or blessing Darius Ebrahimi-FakhariLara WahlsterPamela J. McLean Review 29 June 2012 Pages: 153 - 172
Autophagic adapter protein NBR1 is localized in Lewy bodies and glial cytoplasmic inclusions and is involved in aggregate formation in α-synucleinopathy Saori OdagiriKunikazu TanjiKoichi Wakabayashi Original Paper 07 April 2012 Pages: 173 - 186
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 IrmlerRomina J. G. GentierJohannes Beckers Original Paper Open access 23 June 2012 Pages: 187 - 197
Mitochondrial DNA polymorphisms specifically modify cerebral β-amyloid proteostasis Katja SchefflerMarkus KrohnJens Pahnke Original Paper 18 April 2012 Pages: 199 - 208
Clonally expanded mitochondrial DNA deletions within the choroid plexus in multiple sclerosis Graham R. CampbellYevgenya KraytsbergDon J. Mahad Original Paper 12 June 2012 Pages: 209 - 220
Distinct TDP-43 pathology in ALS patients with ataxin 2 intermediate-length polyQ expansions Michael P. HartJohannes BrettschneiderAaron D. Gitler Original Paper 21 April 2012 Pages: 221 - 230
TDP-43 regulates the mammalian spinogenesis through translational repression of Rac1 Pritha MajumderYi-Ting ChenChe-Kun James Shen Original Paper 04 July 2012 Pages: 231 - 245
Distinct disease-risk groups in pediatric supratentorial and posterior fossa ependymomas Catherine GodfraindJoanna M. KaczmarskaDavid W. Ellison Original Paper 21 April 2012 Pages: 247 - 257
Identification of novel pathways involved in the pathogenesis of human adamantinomatous craniopharyngioma Cynthia L. AndoniadouCarles Gaston-MassuetJuan Pedro Martinez-Barbera Original Paper Open access 18 February 2012 Pages: 259 - 271
Next generation sequencing for molecular diagnosis of neuromuscular diseases Nasim VasliJohann BöhmJocelyn Laporte Original Paper Open access 18 April 2012 Pages: 273 - 283
TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation Maria Martinez-LageLaura Molina-PorcelJohn Q. Trojanowski Case Reports 03 February 2012 Pages: 285 - 291
Periventricular white matter immunoglobulin lambda light chain deposition disease diagnosed by proteomic analysis Joshua R. MenkeMark E. JentoftCaterina Giannini Correspondence 04 July 2012 Pages: 293 - 295