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Birgit Liss

Showing results (51-60 of 54) with videos related to

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Nature Genetics|September 12, 2006
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPaseAlfredo Ramirez, André Heimbach, Jan Gründemann, et al.
Annals of Neurology|November 4, 2014
Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerizationJudith Eschbach, Björn von Einem, Kathrin Müller, et al.
Cell Reports|November 28, 2019
In Vivo Protein Complementation Demonstrates Presynaptic α-Synuclein Oligomerization and Age-Dependent Accumulation of 8-16-mer Oligomer SpeciesMartin Kiechle, Bjoern von Einem, Lennart Höfs, et al.
Nature Communications|November 10, 2019
Cav2.3 channels contribute to dopaminergic neuron loss in a model of Parkinson's diseaseJulia Benkert, Simon Hess, Shoumik Roy, et al.
Pageof 6

Showing results (51-60 of 54) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 54 results.
Nature Genetics|September 12, 2006
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPaseAlfredo Ramirez, André Heimbach, Jan Gründemann, et al.
Annals of Neurology|November 4, 2014
Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerizationJudith Eschbach, Björn von Einem, Kathrin Müller, et al.
Cell Reports|November 28, 2019
In Vivo Protein Complementation Demonstrates Presynaptic α-Synuclein Oligomerization and Age-Dependent Accumulation of 8-16-mer Oligomer SpeciesMartin Kiechle, Bjoern von Einem, Lennart Höfs, et al.
Nature Communications|November 10, 2019
Cav2.3 channels contribute to dopaminergic neuron loss in a model of Parkinson's diseaseJulia Benkert, Simon Hess, Shoumik Roy, et al.
Pageof 6