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Shu G Chen

Showing results (31-40 of 58) with videos related to

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The American Journal of Pathology|November 30, 2005
Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJDManuela Pastore, Steven S Chin, Karen L Bell, et al.
Human Molecular Genetics|October 31, 2014
Glutaredoxin deficiency exacerbates neurodegeneration in C. elegans models of Parkinson's diseaseWilliam M Johnson, Chen Yao, Sandra L Siedlak, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 17, 2004
Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: implications for species barrier in prion uptake from the intestineRavi Shankar Mishra, Subhabrata Basu, Yaping Gu, et al.
The Journal of Biological Chemistry|July 31, 2010
Characterization of the prion protein in human urineAyuna Dagdanova, Serguei Ilchenko, Silvio Notari, et al.
Neurobiology of Disease|April 13, 2010
LRRK2-mediated neurodegeneration and dysfunction of dopaminergic neurons in a Caenorhabditis elegans model of Parkinson's diseaseChen Yao, Rabih El Khoury, Wen Wang, et al.
Neurological Research|July 22, 2004
Is nitric oxide a key target in the pathogenesis of brain lesions during the development of Alzheimer's disease?Ali Aliyev, Dilara Seyidova, Nizami Rzayev, et al.
Free Radical Biology & Medicine|April 12, 2015
Prion protein functions as a ferrireductase partner for ZIP14 and DMT1Ajai K Tripathi, Swati Haldar, Juan Qian, et al.
Emerging Infectious Diseases|January 21, 2012
Assessing prion infectivity of human urine in sporadic Creutzfeldt-Jakob diseaseSilvio Notari, Liuting Qing, Maurizio Pocchiari, et al.
NPJ Parkinson'S Disease|November 16, 2021
Diagnostic value of skin RT-QuIC in Parkinson's disease: a two-laboratory studyAnastasia Kuzkina, Connor Bargar, Daniela Schmitt, et al.
Scientific Reports|January 17, 2017
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion typeLaura Cracco, Silvio Notari, Ignazio Cali, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
The American Journal of Pathology|November 30, 2005
Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJDManuela Pastore, Steven S Chin, Karen L Bell, et al.
Human Molecular Genetics|October 31, 2014
Glutaredoxin deficiency exacerbates neurodegeneration in C. elegans models of Parkinson's diseaseWilliam M Johnson, Chen Yao, Sandra L Siedlak, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 17, 2004
Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: implications for species barrier in prion uptake from the intestineRavi Shankar Mishra, Subhabrata Basu, Yaping Gu, et al.
The Journal of Biological Chemistry|July 31, 2010
Characterization of the prion protein in human urineAyuna Dagdanova, Serguei Ilchenko, Silvio Notari, et al.
Neurobiology of Disease|April 13, 2010
LRRK2-mediated neurodegeneration and dysfunction of dopaminergic neurons in a Caenorhabditis elegans model of Parkinson's diseaseChen Yao, Rabih El Khoury, Wen Wang, et al.
Neurological Research|July 22, 2004
Is nitric oxide a key target in the pathogenesis of brain lesions during the development of Alzheimer's disease?Ali Aliyev, Dilara Seyidova, Nizami Rzayev, et al.
Free Radical Biology & Medicine|April 12, 2015
Prion protein functions as a ferrireductase partner for ZIP14 and DMT1Ajai K Tripathi, Swati Haldar, Juan Qian, et al.
Emerging Infectious Diseases|January 21, 2012
Assessing prion infectivity of human urine in sporadic Creutzfeldt-Jakob diseaseSilvio Notari, Liuting Qing, Maurizio Pocchiari, et al.
NPJ Parkinson'S Disease|November 16, 2021
Diagnostic value of skin RT-QuIC in Parkinson's disease: a two-laboratory studyAnastasia Kuzkina, Connor Bargar, Daniela Schmitt, et al.
Scientific Reports|January 17, 2017
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion typeLaura Cracco, Silvio Notari, Ignazio Cali, et al.
Pageof 6