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Fabio Moda

Showing results (41-50 of 101) with videos related to

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Scientific Reports|March 24, 2017
The Endoplasmic Reticulum Chaperone GRP78/BiP Modulates Prion Propagation in vitro and in vivoKyung-Won Park, Gyoung Eun Kim, Rodrigo Morales, et al.
Emerging Infectious Diseases|February 21, 2025
Prions in Muscles of Cervids with Chronic Wasting Disease, NorwayTram T Vuong, Federico A Cazzaniga, Linh Tran, et al.
Plos Pathogens|January 1, 2016
Synthetic prions with novel strain-specified propertiesFabio Moda, Thanh-Nhat T Le, Suzana Aulić, et al.
Human Molecular Genetics|September 18, 2012
Pantothenate kinase-associated neurodegeneration: altered mitochondria membrane potential and defective respiration in Pank2 knock-out mouse modelDario Brunetti, Sabrina Dusi, Michela Morbin, et al.
Chemistryopen|February 29, 2020
Halogenation of the <i>N</i>-Terminus Tyrosine 10 Promotes Supramolecular Stabilization of the Amyloid-β Sequence 7-12Daniele Maiolo, Andrea Pizzi, Alessandro Gori, et al.
Prion|April 21, 2018
Effects of peptidyl-prolyl isomerase 1 depletion in animal models of prion diseasesGiuseppe Legname, Tommaso Virgilio, Edoardo Bistaffa, et al.
International Journal of Molecular Sciences|September 28, 2024
Unfolding Mechanism and Fibril Formation Propensity of Human Prion Protein in the Presence of Molecular Crowding AgentsManoj Madheswaran, Nataliia Ventserova, Gianluca D'Abrosca, et al.
Scientific Reports|February 16, 2016
Strain-dependent profile of misfolded prion protein aggregatesRodrigo Morales, Ping Ping Hu, Claudia Duran-Aniotz, et al.
Chemical Science|October 24, 2022
Structural and dynamical determinants of a β-sheet-enriched intermediate involved in amyloid fibrillar assembly of human prion proteinLuigi Russo, Giulia Salzano, Andrea Corvino, et al.
Plos Pathogens|October 16, 2025
Substitution of histidine 95 by tyrosine in the prion protein causes spontaneous neurodegeneration in transgenic miceJuan-María Torres, Alba Marín-Moreno, Juan-Carlos Espinosa, et al.
Pageof 11

Showing results (41-50 of 101) with videos related to

Sort By:
Pageof 11
Scientific Reports|March 24, 2017
The Endoplasmic Reticulum Chaperone GRP78/BiP Modulates Prion Propagation in vitro and in vivoKyung-Won Park, Gyoung Eun Kim, Rodrigo Morales, et al.
Emerging Infectious Diseases|February 21, 2025
Prions in Muscles of Cervids with Chronic Wasting Disease, NorwayTram T Vuong, Federico A Cazzaniga, Linh Tran, et al.
Plos Pathogens|January 1, 2016
Synthetic prions with novel strain-specified propertiesFabio Moda, Thanh-Nhat T Le, Suzana Aulić, et al.
Human Molecular Genetics|September 18, 2012
Pantothenate kinase-associated neurodegeneration: altered mitochondria membrane potential and defective respiration in Pank2 knock-out mouse modelDario Brunetti, Sabrina Dusi, Michela Morbin, et al.
Chemistryopen|February 29, 2020
Halogenation of the <i>N</i>-Terminus Tyrosine 10 Promotes Supramolecular Stabilization of the Amyloid-β Sequence 7-12Daniele Maiolo, Andrea Pizzi, Alessandro Gori, et al.
Prion|April 21, 2018
Effects of peptidyl-prolyl isomerase 1 depletion in animal models of prion diseasesGiuseppe Legname, Tommaso Virgilio, Edoardo Bistaffa, et al.
International Journal of Molecular Sciences|September 28, 2024
Unfolding Mechanism and Fibril Formation Propensity of Human Prion Protein in the Presence of Molecular Crowding AgentsManoj Madheswaran, Nataliia Ventserova, Gianluca D'Abrosca, et al.
Scientific Reports|February 16, 2016
Strain-dependent profile of misfolded prion protein aggregatesRodrigo Morales, Ping Ping Hu, Claudia Duran-Aniotz, et al.
Chemical Science|October 24, 2022
Structural and dynamical determinants of a β-sheet-enriched intermediate involved in amyloid fibrillar assembly of human prion proteinLuigi Russo, Giulia Salzano, Andrea Corvino, et al.
Plos Pathogens|October 16, 2025
Substitution of histidine 95 by tyrosine in the prion protein causes spontaneous neurodegeneration in transgenic miceJuan-María Torres, Alba Marín-Moreno, Juan-Carlos Espinosa, et al.
Pageof 11