Lista de obras - Theodoros Sklaviadis - Dominio Público Uruguay

A short purification process for quantitative isolation of PrPSc from naturally occurring and experimental transmissible spongiform encephalopathies.

artículo científico publicado en 2002

A survey of more than 11 years of neurologic diseases of ruminants with special reference to transmissible spongiform encephalopathies (TSEs) in Greece

scientific article published on 01 May 2000

Altered mechanisms of protein synthesis in frontal cortex in Alzheimer disease and a mouse model

artículo científico publicado en 2017

Analysis of Creutzfeldt-Jakob disease infectious fractions by gel permeation chromatography and sedimentation field flow fractionation.

artículo científico publicado en 1992

Antigenic profile of human recombinant PrP: generation and characterization of a versatile polyclonal antiserum.

artículo científico publicado en 2004

Assessing proteinase K resistance of fish prion proteins in a scrapie-infected mouse neuroblastoma cell line

artículo científico publicado en 2014

Astrocyte gene expression in Creutzfeldt-Jakob disease.

artículo científico publicado en 1987

Atomic force microscopy to characterize the molecular size of prion protein.

artículo científico publicado en 2008

CSF analysis in patients with sporadic CJD and other transmissible spongiform encephalopathies.

artículo científico publicado en 2007

CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.

artículo científico publicado en 2006

Caprine PrP variants harboring Asp-146, His-154 and Gln-211 alleles display reduced convertibility upon interaction with pathogenic murine prion protein in scrapie infected cells

artículo científico publicado en 2016

Cellular prion protein co-localizes with nAChR beta4 subunit in brain and gastrointestinal tract.

artículo científico publicado en 2008

Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt-Jakob disease and rapid dementias: a longitudinal multicentre study over 10 years

artículo científico publicado en 2012

Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies

artículo científico publicado en 2009

Cerebrospinal fluid neurofilament light levels in neurodegenerative dementia: Evaluation of diagnostic accuracy in the differential diagnosis of prion diseases

artículo científico publicado en 2018

Characterization of the murine BSE infectious agent

artículo científico publicado en 2000

Design and validation of a high-throughput assay to detect codon 146 polymorphisms in the caprine prion protein gene

artículo científico publicado en 2009

Disparate evolution of prion protein domains and the distinct origin of Doppel- and prion-related loci revealed by fish-to-mammal comparisons

scientific article published on 13 December 2005

EU-approved rapid tests might underestimate bovine spongiform encephalopathy infection in goats.

artículo científico publicado en 2017

Evaluation of the possible transmission of BSE and scrapie to gilthead sea bream (Sparus aurata)

artículo científico publicado en 2009

Evaluation of α-synuclein as a novel cerebrospinal fluid biomarker in different forms of prion diseases

artículo científico publicado en 2016

Evidence suggesting that PrP is not the infectious agent in Creutzfeldt-Jakob disease.

artículo científico publicado en 1987

Functional cross-talk between the cellular prion protein and the neural cell adhesion molecule is critical for neuronal differentiation of neural stem/precursor cells

artículo científico publicado en 2014

Genetic, histochemical and biochemical studies on goat TSE cases from Cyprus

artículo científico publicado en 2016

Genotyping for PrP gene polymorphisms in rare Greek breeds of sheep

artículo científico publicado en 2007

Homogenous photocatalytic decontamination of prion infected stainless steel and titanium surfaces

artículo científico publicado en 2013

Identification of proteins co-purifying with scrapie infectivity.

artículo científico publicado en 2009

Immunization with recombinant prion protein leads to partial protection in a murine model of TSEs through a novel mechanism

artículo científico publicado en 2013

Influence of timing on CSF tests value for Creutzfeldt-Jakob disease diagnosis

scientific article published on 25 March 2007

Inhibition of PrP(Sc) formation in scrapie infected N2a cells by 5,7,8-trimethyl-3,4-dihydro-2H-1,4-benzoxazine derivatives.

artículo científico publicado en 2012

Marked increase of neuronal prion protein immunoreactivity in Alzheimer's disease and human prion diseases

artículo científico publicado en 2001

Methionine sulfoxides on PrPSc: a prion-specific covalent signature

artículo científico publicado en 2008

Nuclease treatment results in high specific purification of Creutzfeldt-Jakob disease infectivity with a density characteristic of nucleic acid-protein complexes.

artículo científico publicado en 1990

Perspectives of a scrapie resistance breeding scheme targeting Q211, S146 and K222 caprine PRNP alleles in Greek goats.

artículo científico publicado en 2014

Photocatalytic degradation and drug activity reduction of Chloramphenicol.

artículo científico publicado en 2007

Photocatalytic degradation of prions using the photo-Fenton reagent.

artículo científico publicado en 2008

Prion protein gene polymorphisms in natural goat scrapie

artículo científico publicado en 2002

Proteinase K-resistant material in ARR/VRQ sheep brain affected with classical scrapie is composed mainly of VRQ prion protein.

artículo científico publicado en 2011

Purification and properties of ornithine decarboxylase from Tetrahymena pyriformis

artículo científico publicado en 1985

Regional and subtype-dependent miRNA signatures in sporadic Creutzfeldt-Jakob disease are accompanied by alterations in miRNA silencing machinery and biogenesis.

artículo científico publicado en 2018

Species and strain glycosylation patterns of PrPSc

artículo científico publicado en 2009

State-of-the-art review of goat TSE in the European Union, with special emphasis on PRNP genetics and epidemiology

artículo científico publicado en 2009

Tissue plasminogen activator in brain tissues infected with transmissible spongiform encephalopathies.

artículo científico publicado en 2005

Validation of 14-3-3 Protein as a Marker in Sporadic Creutzfeldt-Jakob Disease Diagnostic

artículo científico publicado en 2015

Viral particles are required for infection in neurodegenerative Creutzfeldt-Jakob disease.

artículo científico publicado en 1995

Western blot detection of PrP(Sc)in Cyprus sheep with natural scrapie

artículo científico publicado en 2000

YKL-40 in the brain and cerebrospinal fluid of neurodegenerative dementias.

artículo científico publicado en 2017

Lista de obras de Theodoros Sklaviadis

A short purification process for quantitative isolation of PrPSc from naturally occurring and experimental transmissible spongiform encephalopathies.

A survey of more than 11 years of neurologic diseases of ruminants with special reference to transmissible spongiform encephalopathies (TSEs) in Greece

Altered mechanisms of protein synthesis in frontal cortex in Alzheimer disease and a mouse model

Analysis of Creutzfeldt-Jakob disease infectious fractions by gel permeation chromatography and sedimentation field flow fractionation.

Antigenic profile of human recombinant PrP: generation and characterization of a versatile polyclonal antiserum.

Assessing proteinase K resistance of fish prion proteins in a scrapie-infected mouse neuroblastoma cell line

Astrocyte gene expression in Creutzfeldt-Jakob disease.

Atomic force microscopy to characterize the molecular size of prion protein.

CSF analysis in patients with sporadic CJD and other transmissible spongiform encephalopathies.

CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.

Caprine PrP variants harboring Asp-146, His-154 and Gln-211 alleles display reduced convertibility upon interaction with pathogenic murine prion protein in scrapie infected cells

Cellular prion protein co-localizes with nAChR beta4 subunit in brain and gastrointestinal tract.

Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt-Jakob disease and rapid dementias: a longitudinal multicentre study over 10 years

Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies

Cerebrospinal fluid neurofilament light levels in neurodegenerative dementia: Evaluation of diagnostic accuracy in the differential diagnosis of prion diseases

Characterization of the murine BSE infectious agent

Design and validation of a high-throughput assay to detect codon 146 polymorphisms in the caprine prion protein gene

Disparate evolution of prion protein domains and the distinct origin of Doppel- and prion-related loci revealed by fish-to-mammal comparisons

EU-approved rapid tests might underestimate bovine spongiform encephalopathy infection in goats.

Evaluation of the possible transmission of BSE and scrapie to gilthead sea bream (Sparus aurata)

Evaluation of α-synuclein as a novel cerebrospinal fluid biomarker in different forms of prion diseases

Evidence suggesting that PrP is not the infectious agent in Creutzfeldt-Jakob disease.

Functional cross-talk between the cellular prion protein and the neural cell adhesion molecule is critical for neuronal differentiation of neural stem/precursor cells

Genetic, histochemical and biochemical studies on goat TSE cases from Cyprus

Genotyping for PrP gene polymorphisms in rare Greek breeds of sheep

Homogenous photocatalytic decontamination of prion infected stainless steel and titanium surfaces

Identification of proteins co-purifying with scrapie infectivity.

Immunization with recombinant prion protein leads to partial protection in a murine model of TSEs through a novel mechanism

Influence of timing on CSF tests value for Creutzfeldt-Jakob disease diagnosis

Inhibition of PrP(Sc) formation in scrapie infected N2a cells by 5,7,8-trimethyl-3,4-dihydro-2H-1,4-benzoxazine derivatives.

Marked increase of neuronal prion protein immunoreactivity in Alzheimer's disease and human prion diseases

Methionine sulfoxides on PrPSc: a prion-specific covalent signature

Nuclease treatment results in high specific purification of Creutzfeldt-Jakob disease infectivity with a density characteristic of nucleic acid-protein complexes.

Perspectives of a scrapie resistance breeding scheme targeting Q211, S146 and K222 caprine PRNP alleles in Greek goats.

Photocatalytic degradation and drug activity reduction of Chloramphenicol.

Photocatalytic degradation of prions using the photo-Fenton reagent.

Prion protein gene polymorphisms in natural goat scrapie

Proteinase K-resistant material in ARR/VRQ sheep brain affected with classical scrapie is composed mainly of VRQ prion protein.

Purification and properties of ornithine decarboxylase from Tetrahymena pyriformis

Regional and subtype-dependent miRNA signatures in sporadic Creutzfeldt-Jakob disease are accompanied by alterations in miRNA silencing machinery and biogenesis.

Species and strain glycosylation patterns of PrPSc

State-of-the-art review of goat TSE in the European Union, with special emphasis on PRNP genetics and epidemiology

Tissue plasminogen activator in brain tissues infected with transmissible spongiform encephalopathies.

Validation of 14-3-3 Protein as a Marker in Sporadic Creutzfeldt-Jakob Disease Diagnostic

Viral particles are required for infection in neurodegenerative Creutzfeldt-Jakob disease.

Western blot detection of PrP(Sc)in Cyprus sheep with natural scrapie

YKL-40 in the brain and cerebrospinal fluid of neurodegenerative dementias.