Karin Danzer

2008-2011 Neurology Massachusetts General Hospital, Boston, MA 
"Karin Danzer"
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Brenner D, Müller K, Wieland T, et al. (2016) NEK1 mutations in familial amyotrophic lateral sclerosis. Brain : a Journal of Neurology. 139: e28
Stuendl A, Kunadt M, Kruse N, et al. (2015) Induction of α-synuclein aggregate formation by CSF exosomes from patients with Parkinson's disease and dementia with Lewy bodies. Brain : a Journal of Neurology
Helferich AM, Ruf WP, Grozdanov V, et al. (2015) α-synuclein interacts with SOD1 and promotes its oligomerization. Molecular Neurodegeneration. 10: 66
Feiler MS, Strobel B, Freischmidt A, et al. (2015) TDP-43 is intercellularly transmitted across axon terminals. The Journal of Cell Biology. 211: 897-911
Bliederhaeuser C, Grozdanov V, Speidel A, et al. (2015) Age-dependent defects of alpha-synuclein oligomer uptake in microglia and monocytes. Acta Neuropathologica
Marroquin N, Stranz S, Müller K, et al. (2015) Screening for CHCHD10 mutations in a large cohort of sporadic ALS patients: no evidence for pathogenicity of the p.P34S variant. Brain : a Journal of Neurology
Freischmidt A, Müller K, Zondler L, et al. (2015) Serum microRNAs in sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. 36: 2660.e15-20
von Einem B, Wahler A, Schips T, et al. (2015) The Golgi-Localized γ-Ear-Containing ARF-Binding (GGA) Proteins Alter Amyloid-β Precursor Protein (APP) Processing through Interaction of Their GAE Domain with the Beta-Site APP Cleaving Enzyme 1 (BACE1). Plos One. 10: e0129047
Freischmidt A, Wieland T, Richter B, et al. (2015) Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia. Nature Neuroscience. 18: 631-6
Kunadt M, Eckermann K, Stuendl A, et al. (2015) Extracellular vesicle sorting of α-Synuclein is regulated by sumoylation. Acta Neuropathologica. 129: 695-713
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