Lista de obras - Michael Beekes - Dominio Público Uruguay

Accumulation of pathological prion protein PrPSc in the skin of animals with experimental and natural scrapie

artículo científico publicado en 2007

Acid inactivation of prions: efficient at elevated temperature or high acid concentration

artículo científico publicado en 2006

Analytical applications of Fourier transform-infrared (FT-IR) spectroscopy in microbiology and prion research

artículo científico publicado en 2007

Antemortem identification of bovine spongiform encephalopathy from serum using infrared spectroscopy

artículo científico publicado en 2003

Aspects of risk assessment and risk management of nosocomial transmission of classical and variant Creutzfeldt-Jakob disease with special attention to German regulations

artículo científico publicado en 2004

Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases

artículo científico publicado en 2013

Autocatalytic self-propagation of misfolded prion protein

artículo científico publicado en 2004

Avoid brain contamination from surgery

artículo científico publicado en 2019

BSE-associated prion-amyloid cardiomyopathy in primates

artículo científico publicado en 2013

Cell-free formation of misfolded prion protein with authentic prion infectivity

artículo científico publicado en 2006

Changes in protein structure and distribution observed at pre-clinical stages of scrapie pathogenesis.

artículo científico publicado en 2008

Chronic wasting disease: fingerprinting the culprit in risk assessments

artículo científico publicado en 2012

Codon 129 polymorphism and the E200K mutation do not affect the cellular prion protein isoform composition in the cerebrospinal fluid from patients with Creutzfeldt-Jakob disease

artículo científico publicado en 2010

Decontamination of medical devices from pathological amyloid-β-, tau- and α-synuclein aggregates

artículo científico publicado en 2014

Decontamination of surgical instruments from prion proteins: in vitro studies on the detachment, destabilization and degradation of PrPSc bound to steel surfaces

artículo científico publicado en 2004

Decontamination of surgical instruments from prions. II. In vivo findings with a model system for testing the removal of scrapie infectivity from steel surfaces

artículo científico publicado en 2008

Deposition of disease-associated prion protein involves the peripheral nervous system in experimental scrapie

scientific article published on 01 November 1999

Detection of pathological molecular alterations in scrapie-infected hamster brain by Fourier transform infrared (FT-IR) spectroscopy

artículo científico publicado en 2000

Detection of preclinical scrapie from serum by infrared spectroscopy and chemometrics

artículo científico publicado en 2006

Detection of prion particles in samples of BSE and scrapie by fluorescence correlation spectroscopy without proteinase K digestion

artículo científico publicado en 2006

Discriminating scrapie and bovine spongiform encephalopathy isolates by infrared spectroscopy of pathological prion protein

artículo científico publicado en 2004

Early accumulation of pathological PrP in the enteric nervous system and gut-associated lymphoid tissue of hamsters orally infected with scrapie

scientific article published on 01 January 2000

Early spread of scrapie from the gastrointestinal tract to the central nervous system involves autonomic fibers of the splanchnic and vagus nerves

artículo científico publicado en 2001

Effect of repeated oral infection of hamsters with scrapie

scientific article published on 01 March 1998

Evidence for an alternative direct route of access for the scrapie agent to the brain bypassing the spinal cord

artículo científico publicado en 1997

FTIR-microspectroscopy of prion-infected nervous tissue.

artículo científico publicado en 2006

Faecal shedding, alimentary clearance and intestinal spread of prions in hamsters fed with scrapie

artículo científico publicado en 2008

Fast, broad-range disinfection of bacteria, fungi, viruses and prions

artículo científico publicado en 2009

Foodborne transmission of bovine spongiform encephalopathy to nonhuman primates

artículo científico publicado en 2013

Generation of genuine prion infectivity by serial PMCA.

artículo científico publicado en 2007

Harnessing prions as test agents for the development of broad-range disinfectants

artículo científico publicado en 2012

Identification of scrapie infection from blood serum by Fourier transform infrared spectroscopy

artículo científico publicado en 2002

In situ identification of protein structural changes in prion-infected tissue.

artículo científico publicado en 2003

Infrared microspectroscopy detects protein misfolding cyclic amplification (PMCA)-induced conformational alterations in hamster scrapie progeny seeds

scientific article published on 25 October 2013

Is there a risk of prion-like disease transmission by Alzheimer- or Parkinson-associated protein particles?

artículo científico publicado en 2014

Late increase of serum S100 beta protein levels in hamsters after oral or intraperitoneal infection with scrapie

artículo científico publicado en 1999

Pathological PrP is abundant in sympathetic and sensory ganglia of hamsters fed with scrapie

artículo científico publicado en 1999

Pathological prion protein in muscles of hamsters and mice infected with rodent-adapted BSE or vCJD.

artículo científico publicado en 2006

Photo-induced crosslinking of prion protein oligomers and prions

artículo científico publicado en 2006

PrPTSE in muscle-associated lymphatic tissue during the preclinical stage of mice infected orally with bovine spongiform encephalopathy

artículo científico publicado en 2009

Preclinical deposition of pathological prion protein PrPSc in muscles of hamsters orally exposed to scrapie

artículo científico publicado en 2004

Presence and seeding activity of pathological prion protein (PrP(TSE)) in skeletal muscles of white-tailed deer infected with chronic wasting disease

artículo científico publicado en 2011

Preserving prion strain identity upon replication of prions in vitro using recombinant prion protein

artículo científico

Prion propagation in a nerve conduit model containing segments devoid of axons

artículo científico publicado en 2007

Prion research: past, present, and future

artículo científico publicado en 2007

Prions and prion diseases

scientific article published on 01 February 2007

Propagation of scrapie in peripheral nerves after footpad infection in normal and neurotoxin exposed hamsters

artículo científico publicado en 2006

Quantitative detection and biological propagation of scrapie seeding activity in vitro facilitate use of prions as model pathogens for disinfection

artículo científico publicado en 2011

Relevance of the regional lymph node in scrapie pathogenesis after peripheral infection of hamsters

artículo científico publicado en 2007

Reversible off and on switching of prion infectivity via removing and reinstalling prion sialylation

artículo científico publicado en 2016

Scrapie Agent (Strain 263K) can transmit disease via the oral route after persistence in soil over years

artículo científico publicado en 2007

Scrapie-infected cells, isolated prions, and recombinant prion protein: a comparative study.

artículo científico publicado en 2004

Sequential appearance and accumulation of pathognomonic markers in the central nervous system of hamsters orally infected with scrapie

artículo científico publicado en 1996

Sialylation Controls Prion Fate in Vivo

artículo científico publicado en 2016

Sterilization techniques: Counter the risk of Alzheimer's transfer

artículo científico publicado en 2016

Structural differences between TSEs strains investigated by FT-IR spectroscopy

artículo científico publicado en 2006

Synthetic scrapie infectivity: interaction between recombinant PrP and scrapie brain-derived RNA.

artículo científico publicado en 2015

The nature of the scrapie agent: the virus theory

artículo científico publicado en 1994

The polysaccharide scaffold of PrP 27-30 is a common compound of natural prions and consists of alpha-linked polyglucose

artículo científico publicado en 2005

The spread of prions through the body in naturally acquired transmissible spongiform encephalopathies

artículo científico publicado en 2007

Towards further reduction and replacement of animal bioassays in prion research by cell and protein misfolding cyclic amplification assays

artículo científico publicado en 2013

Transmissible spongiform encephalopathies: virally transmitted amyloidoses.

artículo científico publicado en 1993

Western blot mapping of disease-specific amyloid in various animal species and humans with transmissible spongiform encephalopathies using a high-yield purification method

artículo científico publicado en 1995

Widespread PrPSc accumulation in muscles of hamsters orally infected with scrapie

artículo científico publicado en 2003

[BSE and Creutzfeldt-Jakob disease. Implication on health politics in Germany and Europe]

artículo científico publicado en 2002

[Clinical aspects of risk assessment and prevention of nosocomial transmission of classical and variant CJD]

artículo científico publicado en 2002

[Inactivation and removal of prions in producing medical products. A contribution to evaluation and declaration of possible methods]

artículo científico publicado en 2004

[Variant Creutzfeld-Jakob disease (vCJD) : Epidemiology and prevention from human to human secondary transmission]

scientific article published on 01 June 2010

Lista de obras de Michael Beekes

Accumulation of pathological prion protein PrPSc in the skin of animals with experimental and natural scrapie

Acid inactivation of prions: efficient at elevated temperature or high acid concentration

Analytical applications of Fourier transform-infrared (FT-IR) spectroscopy in microbiology and prion research

Antemortem identification of bovine spongiform encephalopathy from serum using infrared spectroscopy

Aspects of risk assessment and risk management of nosocomial transmission of classical and variant Creutzfeldt-Jakob disease with special attention to German regulations

Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases

Autocatalytic self-propagation of misfolded prion protein

Avoid brain contamination from surgery

BSE-associated prion-amyloid cardiomyopathy in primates

Cell-free formation of misfolded prion protein with authentic prion infectivity

Changes in protein structure and distribution observed at pre-clinical stages of scrapie pathogenesis.

Chronic wasting disease: fingerprinting the culprit in risk assessments

Codon 129 polymorphism and the E200K mutation do not affect the cellular prion protein isoform composition in the cerebrospinal fluid from patients with Creutzfeldt-Jakob disease

Decontamination of medical devices from pathological amyloid-β-, tau- and α-synuclein aggregates

Decontamination of surgical instruments from prion proteins: in vitro studies on the detachment, destabilization and degradation of PrPSc bound to steel surfaces

Decontamination of surgical instruments from prions. II. In vivo findings with a model system for testing the removal of scrapie infectivity from steel surfaces

Deposition of disease-associated prion protein involves the peripheral nervous system in experimental scrapie

Detection of pathological molecular alterations in scrapie-infected hamster brain by Fourier transform infrared (FT-IR) spectroscopy

Detection of preclinical scrapie from serum by infrared spectroscopy and chemometrics

Detection of prion particles in samples of BSE and scrapie by fluorescence correlation spectroscopy without proteinase K digestion

Discriminating scrapie and bovine spongiform encephalopathy isolates by infrared spectroscopy of pathological prion protein

Early accumulation of pathological PrP in the enteric nervous system and gut-associated lymphoid tissue of hamsters orally infected with scrapie

Early spread of scrapie from the gastrointestinal tract to the central nervous system involves autonomic fibers of the splanchnic and vagus nerves

Effect of repeated oral infection of hamsters with scrapie

Evidence for an alternative direct route of access for the scrapie agent to the brain bypassing the spinal cord

FTIR-microspectroscopy of prion-infected nervous tissue.

Faecal shedding, alimentary clearance and intestinal spread of prions in hamsters fed with scrapie

Fast, broad-range disinfection of bacteria, fungi, viruses and prions

Foodborne transmission of bovine spongiform encephalopathy to nonhuman primates

Generation of genuine prion infectivity by serial PMCA.

Harnessing prions as test agents for the development of broad-range disinfectants

Identification of scrapie infection from blood serum by Fourier transform infrared spectroscopy

In situ identification of protein structural changes in prion-infected tissue.

Infrared microspectroscopy detects protein misfolding cyclic amplification (PMCA)-induced conformational alterations in hamster scrapie progeny seeds

Is there a risk of prion-like disease transmission by Alzheimer- or Parkinson-associated protein particles?

Late increase of serum S100 beta protein levels in hamsters after oral or intraperitoneal infection with scrapie

Pathological PrP is abundant in sympathetic and sensory ganglia of hamsters fed with scrapie

Pathological prion protein in muscles of hamsters and mice infected with rodent-adapted BSE or vCJD.

Photo-induced crosslinking of prion protein oligomers and prions

PrPTSE in muscle-associated lymphatic tissue during the preclinical stage of mice infected orally with bovine spongiform encephalopathy

Preclinical deposition of pathological prion protein PrPSc in muscles of hamsters orally exposed to scrapie

Presence and seeding activity of pathological prion protein (PrP(TSE)) in skeletal muscles of white-tailed deer infected with chronic wasting disease

Preserving prion strain identity upon replication of prions in vitro using recombinant prion protein

Prion propagation in a nerve conduit model containing segments devoid of axons

Prion research: past, present, and future

Prions and prion diseases

Propagation of scrapie in peripheral nerves after footpad infection in normal and neurotoxin exposed hamsters

Quantitative detection and biological propagation of scrapie seeding activity in vitro facilitate use of prions as model pathogens for disinfection

Relevance of the regional lymph node in scrapie pathogenesis after peripheral infection of hamsters

Reversible off and on switching of prion infectivity via removing and reinstalling prion sialylation

Scrapie Agent (Strain 263K) can transmit disease via the oral route after persistence in soil over years

Scrapie-infected cells, isolated prions, and recombinant prion protein: a comparative study.

Sequential appearance and accumulation of pathognomonic markers in the central nervous system of hamsters orally infected with scrapie

Sialylation Controls Prion Fate in Vivo

Sterilization techniques: Counter the risk of Alzheimer's transfer

Structural differences between TSEs strains investigated by FT-IR spectroscopy

Synthetic scrapie infectivity: interaction between recombinant PrP and scrapie brain-derived RNA.

The nature of the scrapie agent: the virus theory

The polysaccharide scaffold of PrP 27-30 is a common compound of natural prions and consists of alpha-linked polyglucose

The spread of prions through the body in naturally acquired transmissible spongiform encephalopathies

Towards further reduction and replacement of animal bioassays in prion research by cell and protein misfolding cyclic amplification assays

Transmissible spongiform encephalopathies: virally transmitted amyloidoses.

Western blot mapping of disease-specific amyloid in various animal species and humans with transmissible spongiform encephalopathies using a high-yield purification method

Widespread PrPSc accumulation in muscles of hamsters orally infected with scrapie

[BSE and Creutzfeldt-Jakob disease. Implication on health politics in Germany and Europe]

[Clinical aspects of risk assessment and prevention of nosocomial transmission of classical and variant CJD]

[Inactivation and removal of prions in producing medical products. A contribution to evaluation and declaration of possible methods]

[Variant Creutzfeld-Jakob disease (vCJD) : Epidemiology and prevention from human to human secondary transmission]