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Sub-Cellular Biochemistry
|
December 11, 2012
Prion protein aggregation and fibrillogenesis in vitro
Jan Stöhr
Cold Spring Harbor Perspectives in Medicine
|
December 23, 2016
Structural Biology of PrP Prions
Gerald Stubbs, Jan Stöhr
Prion
|
September 2, 2015
Truncated forms of the prion protein PrP demonstrate the need for complexity in prion structure
William 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 pathology
Lindsay 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 fold
William Wan, Holger Wille, Jan Stöhr, et al.
Biological Chemistry
|
April 12, 2011
In vitro conversion and seeded fibrillization of posttranslationally modified prion protein
Jan Stöhr, Kerstin Elfrink, Nicole Weinmann, et al.
Biological Chemistry
|
July 12, 2005
Assembly of natural and recombinant prion protein into fibrils
Karl-Werner Leffers, Holger Wille, Jan Stöhr, et al.
Biopolymers
|
January 11, 2018
A long-lived Aβ oligomer resistant to fibrillization
Mimi 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 protein
Giannantonio Panza, Jan Stöhr, Christian Dumpitak, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 4
Sub-Cellular Biochemistry
|
December 11, 2012
Prion protein aggregation and fibrillogenesis in vitro
Jan Stöhr
Cold Spring Harbor Perspectives in Medicine
|
December 23, 2016
Structural Biology of PrP Prions
Gerald Stubbs, Jan Stöhr
Prion
|
September 2, 2015
Truncated forms of the prion protein PrP demonstrate the need for complexity in prion structure
William 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 pathology
Lindsay 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 fold
William Wan, Holger Wille, Jan Stöhr, et al.
Biological Chemistry
|
April 12, 2011
In vitro conversion and seeded fibrillization of posttranslationally modified prion protein
Jan Stöhr, Kerstin Elfrink, Nicole Weinmann, et al.
Biological Chemistry
|
July 12, 2005
Assembly of natural and recombinant prion protein into fibrils
Karl-Werner Leffers, Holger Wille, Jan Stöhr, et al.
Biopolymers
|
January 11, 2018
A long-lived Aβ oligomer resistant to fibrillization
Mimi 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 protein
Giannantonio Panza, Jan Stöhr, Christian Dumpitak, et al.
Page
of 4