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Holger Wille

Showing results (21-30 of 95) with videos related to

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Advances in Protein Chemistry and Structural Biology|January 14, 2020
Combining molecular dynamics simulations and experimental analyses in protein misfoldingHolger Wille, Lyudmyla Dorosh, Sara Amidian, et al.
Biophysical Journal|December 17, 2009
Molecular modeling of the misfolded insulin subunit and amyloid fibrilJay H Choi, Barnaby C H May, Holger Wille, et al.
Plos One|September 29, 2009
Evolutionary descent of prion genes from the ZIP family of metal ion transportersGerold Schmitt-Ulms, Sepehr Ehsani, Joel C Watts, et al.
Plos Pathogens|May 27, 2016
A Neuronal Culture System to Detect Prion SynaptotoxicityCheng Fang, Thibaut Imberdis, Maria Carmen Garza, 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.
Neurobiology of Aging|March 14, 2013
Plasma membrane invaginations containing clusters of full-length PrPSc are an early form of prion-associated neuropathology in vivoSusan F Godsave, Holger Wille, Jason Pierson, et al.
Arxiv|January 29, 2025
A unified model for the origins of spongiform degeneration and other neuropathological features in prion diseasesGerold Schmitt-Ulms, Xinzhu Wang, Joel Watts, et al.
Disease Models & Mechanisms|September 15, 2021
Implications of exosomes derived from cholesterol-accumulated astrocytes in Alzheimer's disease pathologyQi Wu, Leonardo Cortez, Razieh Kamali-Jamil, et al.
Protein Expression and Purification|April 8, 2017
An easy method for bacterial expression and purification of wild-type and mutant superoxide dismutase 1 (SOD1)Babila J Tachu, Katharina A Wüsten, Maria C Garza, et al.
Plos One|May 29, 2019
The human brain somatostatin interactome: SST binds selectively to P-type family ATPasesMichael Solarski, Declan Williams, Mohadeseh Mehrabian, et al.
Pageof 10

Showing results (21-30 of 95) with videos related to

Sort By:
Pageof 10
Advances in Protein Chemistry and Structural Biology|January 14, 2020
Combining molecular dynamics simulations and experimental analyses in protein misfoldingHolger Wille, Lyudmyla Dorosh, Sara Amidian, et al.
Biophysical Journal|December 17, 2009
Molecular modeling of the misfolded insulin subunit and amyloid fibrilJay H Choi, Barnaby C H May, Holger Wille, et al.
Plos One|September 29, 2009
Evolutionary descent of prion genes from the ZIP family of metal ion transportersGerold Schmitt-Ulms, Sepehr Ehsani, Joel C Watts, et al.
Plos Pathogens|May 27, 2016
A Neuronal Culture System to Detect Prion SynaptotoxicityCheng Fang, Thibaut Imberdis, Maria Carmen Garza, 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.
Neurobiology of Aging|March 14, 2013
Plasma membrane invaginations containing clusters of full-length PrPSc are an early form of prion-associated neuropathology in vivoSusan F Godsave, Holger Wille, Jason Pierson, et al.
Arxiv|January 29, 2025
A unified model for the origins of spongiform degeneration and other neuropathological features in prion diseasesGerold Schmitt-Ulms, Xinzhu Wang, Joel Watts, et al.
Disease Models & Mechanisms|September 15, 2021
Implications of exosomes derived from cholesterol-accumulated astrocytes in Alzheimer's disease pathologyQi Wu, Leonardo Cortez, Razieh Kamali-Jamil, et al.
Protein Expression and Purification|April 8, 2017
An easy method for bacterial expression and purification of wild-type and mutant superoxide dismutase 1 (SOD1)Babila J Tachu, Katharina A Wüsten, Maria C Garza, et al.
Plos One|May 29, 2019
The human brain somatostatin interactome: SST binds selectively to P-type family ATPasesMichael Solarski, Declan Williams, Mohadeseh Mehrabian, et al.
Pageof 10