Cargando…

Genomic and post-genomic analyses of human prion diseases

Prion diseases share common features of neurodegenerative disorders, infectious diseases and pathologies linked to misfolded proteins. Whether these aspects are independently and fortuitously present in prion diseases or are somewhat linked together remains unsettled, but the contribution of genomic...

Descripción completa

Detalles Bibliográficos
Autores principales:	Pocchiari, Maurizio, Poleggi, Anna, Principe, Serena, Graziano, Silvia, Cardone, Franco
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2009
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2703872/ https://www.ncbi.nlm.nih.gov/pubmed/19566915 http://dx.doi.org/10.1186/gm63

Ejemplares similares

Age at Death of Creutzfeldt-Jakob Disease in Subsequent Family Generation Carrying the E200K Mutation of the Prion Protein Gene
por: Pocchiari, Maurizio, et al.
Publicado: (2013)

Prions and related neurological diseases
por: Pocchiari, Maurizio
Publicado: (1994)

Biochemical and Neuropathological Findings in a Creutzfeldt–Jakob Disease Patient with the Rare Val180Ile-129Val Haplotype in the Prion Protein Gene
por: Zanusso, Gianluigi, et al.
Publicado: (2022)

Identification of Misfolded Proteins in Body Fluids for the Diagnosis of Prion Diseases
por: Properzi, Francesca, et al.
Publicado: (2013)

Evaluation of Human Cerebrospinal Fluid Malate Dehydrogenase 1 as a Marker in Genetic Prion Disease Patients
por: Zerr, Inga, et al.
Publicado: (2019)

The Use of Real-Time Quaking-Induced Conversion for the Diagnosis of Human Prion Diseases
por: Poleggi, Anna, et al.
Publicado: (2022)

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

Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory Findings
por: Baiardi, Simone, et al.
Publicado: (2015)

Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases
por: Schmitz, Matthias, et al.
Publicado: (2022)

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

What's next for genomics and prion diseases?
por: Booth, Stephanie A
Publicado: (2017)

Diagnostic and prognostic performance of CSF α‐synuclein in prion disease in the context of rapidly progressive dementia
por: Mastrangelo, Andrea, et al.
Publicado: (2021)

Clinicopathological features of the rare form of Creutzfeldt-Jakob disease in R208H-V129V PRNP carrier
por: Tiple, Dorina, et al.
Publicado: (2019)

An overview of human prion diseases
por: Imran, Muhammad, et al.
Publicado: (2011)

Prion Diseases of Humans and Animals
por: Esiri, Margaret
Publicado: (1994)

Human prion diseases and the prion protein – what is the current state of knowledge?
por: Nafe, Reinhold, et al.
Publicado: (2023)

Molecular Pathology of Human Prion Diseases
por: Kovacs, Gabor G., et al.
Publicado: (2009)

Molecular pathology of human prion disease
por: Wadsworth, Jonathan D. F., et al.
Publicado: (2010)

Genetic Studies in Human Prion Diseases
por: Jeong, Byung-Hoon, et al.
Publicado: (2014)

Kuru, the First Human Prion Disease †
por: Liberski, Paweł P., et al.
Publicado: (2019)

Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases
por: Pirisinu, Laura, et al.
Publicado: (2016)

Genome-wide association study of behavioural and psychiatric features in human prion disease
por: Thompson, A G B, et al.
Publicado: (2015)

Sporadic Creutzfeldt–Jakob disease subtype-specific alterations of the brain proteome: Impact on Rab3a recycling
por: Gawinecka, Joanna, et al.
Publicado: (2012)

Prions and Prion Diseases: Current Perspectives
por: Belay, Ermias D.
Publicado: (2004)

Comparative genomic analysis of prion genes
por: Premzl, Marko, et al.
Publicado: (2007)

Epidemiological characteristics of human prion diseases
por: Chen, Cao, et al.
Publicado: (2016)

Proteomics Analyses for the Global Proteins in the Brain Tissues of Different Human Prion Diseases
por: Shi, Qi, et al.
Publicado: (2015)

Establishment of a Special Platform for the Research of Prion and the Diagnosis of Human Prion Disease — China’s Studies
por: Xiao, Kang, et al.
Publicado: (2022)

Prion and Prion-like Diseases in Humans: Poster Abstracts
Publicado: (2013)

Human Prion Diseases
por: Esiri, Margaret M
Publicado: (1993)

Modulation of Neuroinflammation by the Gut Microbiota in Prion and Prion-Like Diseases
por: Trichka, Josephine, et al.
Publicado: (2021)

Neuroinflammation in Prion Disease
por: Li, Bei, et al.
Publicado: (2021)

Prion Diseases in Humans: Oral and Dental Implications
por: Jayanthi, P, et al.
Publicado: (2013)

Gene-Based Antibody Strategies for Prion Diseases
por: Cardinale, Alessio, et al.
Publicado: (2013)

Application of Bayesian genomic prediction methods to genome-wide association analyses
por: Wolc, Anna, et al.
Publicado: (2022)

Characteristic CSF Prion Seeding Efficiency in Humans with Prion Diseases
por: Cramm, Maria, et al.
Publicado: (2014)

From Prion Diseases to Prion-Like Propagation Mechanisms of Neurodegenerative Diseases
por: Acquatella-Tran Van Ba, Isabelle, et al.
Publicado: (2013)

N-Terminal Regions of Prion Protein: Functions and Roles in Prion Diseases
por: Hara, Hideyuki, et al.
Publicado: (2020)

Differential Accumulation of Misfolded Prion Strains in Natural Hosts of Prion Diseases
por: Lambert, Zoe J., et al.
Publicado: (2021)

Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene
por: Di Fede, Giuseppe, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_ltc3v2pak4np2vjl5vc2vu2h8e