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Ignazio Cali

Showing results (11-20 of 45) with videos related to

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Neuropathology and Applied Neurobiology|May 5, 2026
Understanding the Phenotypic Heterogeneity Within the Sporadic Creutzfeldt-Jakob Disease MV1 SubtypeSatish K Nemani, Leonardo M Cortez, Jennifer Myskiw, et al.
Acta Neuropathologica Communications|May 31, 2019
Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragmentsLaura Cracco, Xiangzhu Xiao, Satish K Nemani, et al.
Aging|March 22, 2013
Protease-sensitive prions with 144-bp insertion mutationsXiangzhu Xiao, Ignazio Cali, Zhiqian Dong, et al.
The Journal of Biological Chemistry|September 22, 2006
Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brainsJue Yuan, Xiangzhu Xiao, John McGeehan, et al.
Scientific Reports|March 28, 2019
PMCA-replicated PrP<sup>D</sup> in urine of vCJD patients maintains infectivity and strain characteristics of brain PrP<sup>D</sup>: Transmission studyIgnazio Cali, Jody Lavrich, Fabio Moda, et al.
Acta Neuropathologica Communications|August 31, 2023
Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotypeLaura Cracco, Gianfranco Puoti, Antonio Cornacchia, et al.
Acta Neuropathologica|January 13, 2026
Genetic Creutzfeldt-Jakob disease linked to the E200K mutation: a large cohort studyBrian S Appleby, Matteo Manca, Megan S Piazza, et al.
Scientific Reports|February 1, 2020
Co-existence of PrP<sup>D</sup> types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristicsIgnazio Cali, Gianfranco Puoti, Jason Smucny, et al.
Acta Neuropathologica Communications|September 27, 2021
Generation of human chronic wasting disease in transgenic miceZerui Wang, Kefeng Qin, Manuel V Camacho, et al.
Brain : a Journal of Neurology|November 24, 2023
Efficient transmission of human prion diseases to a glycan-free prion protein-expressing hostLaura Cracco, Ignazio Cali, Mark L Cohen, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Neuropathology and Applied Neurobiology|May 5, 2026
Understanding the Phenotypic Heterogeneity Within the Sporadic Creutzfeldt-Jakob Disease MV1 SubtypeSatish K Nemani, Leonardo M Cortez, Jennifer Myskiw, et al.
Acta Neuropathologica Communications|May 31, 2019
Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragmentsLaura Cracco, Xiangzhu Xiao, Satish K Nemani, et al.
Aging|March 22, 2013
Protease-sensitive prions with 144-bp insertion mutationsXiangzhu Xiao, Ignazio Cali, Zhiqian Dong, et al.
The Journal of Biological Chemistry|September 22, 2006
Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brainsJue Yuan, Xiangzhu Xiao, John McGeehan, et al.
Scientific Reports|March 28, 2019
PMCA-replicated PrP<sup>D</sup> in urine of vCJD patients maintains infectivity and strain characteristics of brain PrP<sup>D</sup>: Transmission studyIgnazio Cali, Jody Lavrich, Fabio Moda, et al.
Acta Neuropathologica Communications|August 31, 2023
Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotypeLaura Cracco, Gianfranco Puoti, Antonio Cornacchia, et al.
Acta Neuropathologica|January 13, 2026
Genetic Creutzfeldt-Jakob disease linked to the E200K mutation: a large cohort studyBrian S Appleby, Matteo Manca, Megan S Piazza, et al.
Scientific Reports|February 1, 2020
Co-existence of PrP<sup>D</sup> types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristicsIgnazio Cali, Gianfranco Puoti, Jason Smucny, et al.
Acta Neuropathologica Communications|September 27, 2021
Generation of human chronic wasting disease in transgenic miceZerui Wang, Kefeng Qin, Manuel V Camacho, et al.
Brain : a Journal of Neurology|November 24, 2023
Efficient transmission of human prion diseases to a glycan-free prion protein-expressing hostLaura Cracco, Ignazio Cali, Mark L Cohen, et al.
Pageof 5