Cargando…

Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease

Differentiating iatrogenic Creutzfeldt-Jakob disease (iCJD) from sporadic CJD (sCJD) would be useful for the identification and prevention of human-to-human prion transmission. Currently, the diagnosis of iCJD depends on identification of a recognized source of contamination to which patients have b...

Descripción completa

Detalles Bibliográficos
Autores principales:	Xiao, Xiangzhu, Yuan, Jue, Qing, Liuting, Cali, Ignazio, Mikol, Jacqueline, Delisle, Marie-Bernadette, Uro-Coste, Emmanuelle, Zeng, Liang, Abouelsaad, Mai, Gazgalis, Dimitris, Martinez, Manuel Camacho, Wang, Gong-Xian, Brown, Paul, Ironside, James W., Gambetti, Pierluigi, Kong, Qingzhong, Zou, Wen-Quan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2014
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240320/ https://www.ncbi.nlm.nih.gov/pubmed/25419482 http://dx.doi.org/10.4172/2155-9899.1000240

Ejemplares similares

Assessing Prion Infectivity of Human Urine in Sporadic Creutzfeldt-Jakob Disease
por: Notari, Silvio, et al.
Publicado: (2012)

The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients
por: Moore, Roger A., et al.
Publicado: (2016)

Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures
por: Cassard, Hervé, et al.
Publicado: (2020)

Correction: The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients
por: Moore, Roger A., et al.
Publicado: (2016)

Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone
por: Cali, Ignazio, et al.
Publicado: (2015)

Co-existence of PrP(D) types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics
por: Cali, Ignazio, et al.
Publicado: (2020)

Protease-sensitive prions with 144-bp insertion mutations
por: Xiao, Xiangzhu, et al.
Publicado: (2013)

Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob Disease
por: Llorens, Franc, et al.
Publicado: (2020)

Synthetic Aβ peptides acquire prion-like properties in the brain
por: Xiao, Xiangzhu, et al.
Publicado: (2014)

Multifocal hits for propagation of prion protein in sporadic Creutzfeldt-Jakob disease
por: Kasuga, Kensaku, et al.
Publicado: (2014)

Sporadic Creutzfeldt-Jakob disease prion infection of human cerebral organoids
por: Groveman, Bradley R., et al.
Publicado: (2019)

Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt–Jakob disease
por: Pascuzzo, Riccardo, et al.
Publicado: (2020)

A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease
por: Nemani, Satish K., et al.
Publicado: (2020)

Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study
por: Cali, Ignazio, et al.
Publicado: (2018)

Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease
por: Xiao, Xiangzhu, et al.
Publicado: (2013)

Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease Patients
por: Orrù, Christina D., et al.
Publicado: (2018)

Correction: Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease
por: Xiao, Xiangzhu, et al.
Publicado: (2013)

Characterization of Sporadic Creutzfeldt-Jakob Disease and History of Neurosurgery to Identify Potential Iatrogenic Cases
por: Hamaguchi, Tsuyoshi, et al.
Publicado: (2020)

High-Depth PRNP Sequencing in Brains With Sporadic Creutzfeldt-Jakob Disease
por: Murley, Alexander G., et al.
Publicado: (2023)

Biomarkers for sporadic Creutzfeldt–Jakob disease
por: Soomro, Sanam, et al.
Publicado: (2016)

Chorea in Sporadic Creutzfeldt-Jakob Disease
por: Tan, Ai Huey, et al.
Publicado: (2018)

Analysis of Prion Strains by PrP(Sc) Profiling in Sporadic Creutzfeldt–Jakob Disease
por: Schoch, Gaby, et al.
Publicado: (2006)

Differentiation of Prions from L-type BSE versus Sporadic Creutzfeldt-Jakob Disease
por: Nicot, Simon, et al.
Publicado: (2012)

Prion-Seeding Activity Is widely Distributed in Tissues of Sporadic Creutzfeldt-Jakob Disease Patients
por: Takatsuki, Hanae, et al.
Publicado: (2016)

Prion type 2 selection in sporadic Creutzfeldt–Jakob disease affecting peripheral ganglia
por: Hofmann, Anna, et al.
Publicado: (2021)

PMCA-Based Detection of Prions in the Olfactory Mucosa of Patients With Sporadic Creutzfeldt–Jakob Disease
por: Cazzaniga, Federico Angelo, et al.
Publicado: (2022)

Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype
por: Cracco, Laura, et al.
Publicado: (2023)

Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment
por: Brown, Paul, et al.
Publicado: (2012)

Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United Kingdom
por: Urwin, Patrick, et al.
Publicado: (2017)

Beyond PrP(res) Type 1/Type 2 Dichotomy in Creutzfeldt-Jakob Disease
por: Uro-Coste, Emmanuelle, et al.
Publicado: (2008)

A Case of sporadic Creutzfeldt-Jakob disease
por: Şimşek, Fatma, et al.
Publicado: (2023)

Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt-Jakob disease
por: Choi, Ed M., et al.
Publicado: (2009)

Corrigendum: PMCA-based detection of prions in the olfactory mucosa of patients with sporadic Creutzfeldt–Jakob disease
por: Cazzaniga, Federico Angelo, et al.
Publicado: (2023)

Subtype Diagnosis of Sporadic Creutzfeldt–Jakob Disease with Diffusion Magnetic Resonance Imaging
por: Bizzi, Alberto, et al.
Publicado: (2020)

UK Iatrogenic Creutzfeldt–Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approaches
por: Ritchie, Diane L., et al.
Publicado: (2016)

Phenotypic diversity of genetic Creutzfeldt–Jakob disease: a histo-molecular-based classification
por: Baiardi, Simone, et al.
Publicado: (2021)

Risk Assessment of Transmission of Sporadic Creutzfeldt-Jakob Disease in Endodontic Practice in Absence of Adequate Prion Inactivation
por: Bourvis, Nadège, et al.
Publicado: (2007)

Sporadic Creutzfeldt-Jakob Disease: Prion Pathology in Medulla Oblongata—Possible Routes of Infection and Host Susceptibility
por: Iacono, Diego, et al.
Publicado: (2015)

Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt–Jakob disease
por: Bishop, Matthew T., et al.
Publicado: (2013)

A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques
por: Bayazid, Rabeah, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_p0g66e3seujihd9rgff85i5ime