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Jan Stöhr

Showing results (1-10 of 34) with videos related to

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Sub-Cellular Biochemistry|December 11, 2012
Prion protein aggregation and fibrillogenesis in vitroJan Stöhr
Cold Spring Harbor Perspectives in Medicine|December 23, 2016
Structural Biology of PrP PrionsGerald Stubbs, Jan Stöhr
Prion|September 2, 2015
Truncated forms of the prion protein PrP demonstrate the need for complexity in prion structureWilliam Wan, Jan Stöhr, Amy Kendall, et al.
Neurobiology of Disease|January 20, 2026
Astrocytic lysosome deficits reduce alpha-synuclein degradation and induce the spread of pathologyLindsay M Roth, Olga Morozova, Jan Stöhr, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2008
Structural changes of membrane-anchored native PrP(C)Kerstin Elfrink, Julian Ollesch, Jan Stöhr, et al.
Biophysical Journal|June 9, 2012
Degradation of fungal prion HET-s(218-289) induces formation of a generic amyloid foldWilliam Wan, Holger Wille, Jan Stöhr, et al.
Biological Chemistry|April 12, 2011
In vitro conversion and seeded fibrillization of posttranslationally modified prion proteinJan Stöhr, Kerstin Elfrink, Nicole Weinmann, et al.
Biological Chemistry|July 12, 2005
Assembly of natural and recombinant prion protein into fibrilsKarl-Werner Leffers, Holger Wille, Jan Stöhr, et al.
Biopolymers|January 11, 2018
A long-lived Aβ oligomer resistant to fibrillizationMimi Nick, Yibing Wu, Nathan W Schmidt, et al.
Biochemical and Biophysical Research Communications|July 1, 2008
Spontaneous and BSE-prion-seeded amyloid formation of full length recombinant bovine prion proteinGiannantonio Panza, Jan Stöhr, Christian Dumpitak, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Sub-Cellular Biochemistry|December 11, 2012
Prion protein aggregation and fibrillogenesis in vitroJan Stöhr
Cold Spring Harbor Perspectives in Medicine|December 23, 2016
Structural Biology of PrP PrionsGerald Stubbs, Jan Stöhr
Prion|September 2, 2015
Truncated forms of the prion protein PrP demonstrate the need for complexity in prion structureWilliam Wan, Jan Stöhr, Amy Kendall, et al.
Neurobiology of Disease|January 20, 2026
Astrocytic lysosome deficits reduce alpha-synuclein degradation and induce the spread of pathologyLindsay M Roth, Olga Morozova, Jan Stöhr, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2008
Structural changes of membrane-anchored native PrP(C)Kerstin Elfrink, Julian Ollesch, Jan Stöhr, et al.
Biophysical Journal|June 9, 2012
Degradation of fungal prion HET-s(218-289) induces formation of a generic amyloid foldWilliam Wan, Holger Wille, Jan Stöhr, et al.
Biological Chemistry|April 12, 2011
In vitro conversion and seeded fibrillization of posttranslationally modified prion proteinJan Stöhr, Kerstin Elfrink, Nicole Weinmann, et al.
Biological Chemistry|July 12, 2005
Assembly of natural and recombinant prion protein into fibrilsKarl-Werner Leffers, Holger Wille, Jan Stöhr, et al.
Biopolymers|January 11, 2018
A long-lived Aβ oligomer resistant to fibrillizationMimi Nick, Yibing Wu, Nathan W Schmidt, et al.
Biochemical and Biophysical Research Communications|July 1, 2008
Spontaneous and BSE-prion-seeded amyloid formation of full length recombinant bovine prion proteinGiannantonio Panza, Jan Stöhr, Christian Dumpitak, et al.
Pageof 4