Lista de obras - Baskakov IV - Dominio Público Uruguay

A new mechanism for transmissible prion diseases

artículo científico publicado en 2012

Amyloid features and neuronal toxicity of mature prion fibrils are highly sensitive to high pressure

artículo científico publicado en 2011

Amyloid fibrils of mammalian prion protein induce axonal degeneration in NTERA2-derived terminally differentiated neurons

artículo científico publicado en 2007

Analysis of Covalent Modifications of Amyloidogenic Proteins Using Two-Dimensional Electrophoresis: Prion Protein and Its Sialylation

artículo científico publicado en 2018

Annealing prion protein amyloid fibrils at high temperature results in extension of a proteinase K-resistant core

artículo científico publicado en 2005

Assessment of Strain-Specific PrPSc Elongation Rates Revealed a Transformation of PrPSc Properties during Protein Misfolding Cyclic Amplification ⬇️

artículo científico publicado el 17 de julio de 2012

Atomic force fluorescence microscopy in the characterization of amyloid fibril assembly and oligomeric intermediates

artículo científico publicado en 2012

Atypical and classical forms of the disease-associated state of the prion protein exhibit distinct neuronal tropism, deposition patterns, and lesion profiles

artículo científico publicado en 2013

Changes in prion replication environment cause prion strain mutation

artículo científico publicado en 2013

Chemoenzymatic synthesis of HIV-1 V3 glycopeptides carrying two N-glycans and effects of glycosylation on the peptide domain

artículo científico publicado en 2005

Conformational stability of PrP amyloid fibrils controls their smallest possible fragment size

artículo científico publicado en 2008

Conformational switching within individual amyloid fibrils.

artículo científico publicado en 2009

Converting the prion protein: what makes the protein infectious.

artículo científico publicado en 2006

Copper(II) inhibits in vitro conversion of prion protein into amyloid fibrils

artículo científico publicado en 2005

Correction to: preserving prion strain identity upon replication of prions in vitro using recombinant prion protein

scholarly article published in Acta neuropathologica communications

Cross-seeding of prions by aggregated α-synuclein leads to transmissible spongiform encephalopathy

artículo científico publicado en 2017

Design and construction of diverse mammalian prion strains

artículo científico publicado en 2009

Dichotomous versus palm-type mechanisms of lateral assembly of amyloid fibrils

artículo científico publicado en 2006

Dissecting Structure of Prion Amyloid Fibrils by Hydrogen–Deuterium Exchange Ultraviolet Raman Spectroscopy ⬇️

artículo científico publicado el 26 de junio de 2012

Expression and purification of full-length recombinant PrP of high purity

artículo científico publicado en 2008

Fast and ultrasensitive method for quantitating prion infectivity titre ⬇️

artículo científico publicado el 13 de marzo de 2012

Genesis of mammalian prions: from non-infectious amyloid fibrils to a transmissible prion disease

artículo científico publicado en 2011

Genesis of tramsmissible protein states via deformed templating ⬇️

artículo científico publicado el 1 de julio de 2012

Hemicentin assembly in the extracellular matrix is mediated by distinct structural modules

artículo científico publicado en 2006

Highly efficient protein misfolding cyclic amplification

artículo científico publicado en 2011

Highly promiscuous nature of prion polymerization.

artículo científico publicado en 2007

In vitro conversion of full-length mammalian prion protein produces amyloid form with physical properties of PrP(Sc).

artículo científico publicado en 2004

In vitro conversion of mammalian prion protein into amyloid fibrils displays unusual features

artículo científico publicado en 2005

Inflammatory response of microglia to prions is controlled by sialylation of PrPSc.

artículo científico publicado en 2018

Light-dependent electrogenic activity of cyanobacteria

artículo científico publicado en 2010

Loss of Cellular Sialidases Does Not Affect the Sialylation Status of the Prion Protein but Increases the Amounts of Its Proteolytic Fragment C1

artículo científico publicado en 2015

Methionine oxidation interferes with conversion of the prion protein into the fibrillar proteinase K-resistant conformation

artículo científico publicado en 2005

Methods for conversion of prion protein into amyloid fibrils

artículo científico publicado en 2008

Methods of Protein Misfolding Cyclic Amplification

artículo científico publicado en 2017

Molecular structure of amyloid fibrils controls the relationship between fibrillar size and toxicity.

artículo científico publicado en 2011

Multifaceted Role of Sialylation in Prion Diseases

artículo científico publicado en 2016

Nanostructured polypyrrole-coated anode for sun-powered microbial fuel cells

artículo científico publicado en 2009

New Molecular Insight into Mechanism of Evolution of Mammalian Synthetic Prions

artículo científico publicado en 2016

Nonpolar substitution at the C-terminus of the prion protein, a mimic of the glycosylphosphatidylinositol anchor, partially impairs amyloid fibril formation

artículo científico publicado en 2007

Oligomeric-induced activity by thienyl pyrimidine compounds traps prion infectivity

artículo científico publicado en 2011

Pathway complexity of prion protein assembly into amyloid

artículo científico publicado en 2002

Photosynthetic microbial fuel cells with positive light response

scientific article published on 01 December 2009

Polymorphism and ultrastructural organization of prion protein amyloid fibrils: an insight from high resolution atomic force microscopy

artículo científico publicado en 2006

Post-conversion sialylation of prions in lymphoid tissues

artículo científico publicado en 2015

Posttranslational modifications define course of prion strain adaptation and disease phenotype

scientific article published on 02 June 2020

PrP charge structure encodes interdomain interactions

artículo científico publicado en 2015

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

artículo científico

Prion Strain-Specific Structure and Pathology: A View from the Perspective of Glycobiology

scholarly article by Ilia V Baskakov et al published 18 December 2018 in Viruses

Prion replication environment defines the fate of prion strain adaptation.

artículo científico publicado en 2018

Probing the conformation of the prion protein within a single amyloid fibril using a novel immunoconformational assay

artículo científico publicado en 2006

Protease-sensitive synthetic prions

artículo científico publicado en 2010

Purification and Fibrillation of Full-Length Recombinant PrP.

artículo científico publicado en 2017

Purification and fibrillation of full-length recombinant PrP.

scientific article published on January 2012

Recombinant prion protein induces a new transmissible prion disease in wild-type animals

artículo científico publicado en 2010

Region-Specific Response of Astrocytes to Prion Infection

scientific article published on 09 October 2019

Region-Specific Sialylation Pattern of Prion Strains Provides Novel Insight into Prion Neurotropism

scientific article published on 28 January 2020

Region-specific glial homeostatic signature in prion diseases is replaced by a uniform neuroinflammation signature, common for brain regions and prion strains with different cell tropism

artículo científico publicado en 2020

Relationship between Conformational Stability and Amplification Efficiency of Prions ⬇️

artículo científico publicado el 24 de agosto de 2011

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

artículo científico publicado en 2016

Role of the photosynthetic electron transfer chain in electrogenic activity of cyanobacteria

scientific article published on 12 April 2011

Selective Amplification of Classical and Atypical Prions Using Modified Protein Misfolding Cyclic Amplification ⬇️

artículo científico publicado el 20 de noviembre de 2012

Semiautomated cell-free conversion of prion protein: applications for high-throughput screening of potential antiprion drugs

artículo científico publicado en 2005

Sialylation Controls Prion Fate in Vivo

artículo científico publicado en 2016

Sialylation of Glycosylphosphatidylinositol (GPI) Anchors of Mammalian Prions Is Regulated in a Host-, Tissue-, and Cell-specific Manner

artículo científico publicado en 2016

Sialylation of prion protein controls the rate of prion amplification, the cross-species barrier, the ratio of PrPSc glycoform and prion infectivity

artículo científico publicado en 2014

Sialylation of the prion protein glycans controls prion replication rate and glycoform ratio

artículo científico publicado en 2015

Site-specific conformational studies of prion protein (PrP) amyloid fibrils revealed two cooperative folding domains within amyloid structure

artículo científico publicado en 2007

Stabilization of a prion strain of synthetic origin requires multiple serial passages

artículo científico publicado en 2012

Strain-dependent profile of misfolded prion protein aggregates

artículo científico publicado en 2016

Strain-specified characteristics of mouse synthetic prions

artículo científico publicado en 2005

Synthetic mammalian prions

artículo científico publicado en 2004

Synthetic prions generated in vitro are similar to a newly identified subpopulation of PrPSc from sporadic Creutzfeldt-Jakob Disease

artículo científico publicado en 2005

The cellular form of the prion protein guides the differentiation of human embryonic stem cells into neuron-, oligodendrocyte-, and astrocyte-committed lineages

artículo científico publicado en 2014

The cellular form of the prion protein is involved in controlling cell cycle dynamics, self-renewal, and the fate of human embryonic stem cell differentiation.

artículo científico publicado en 2012

The diversity and relationship of prion protein self-replicating states

artículo científico publicado en 2014

The dominant-negative effect of the Q218K variant of the prion protein does not require protein X.

artículo científico publicado en 2007

The evolution of transmissible prions: the role of deformed templating

artículo científico publicado en 2013

The peculiar nature of unfolding of the human prion protein

artículo científico publicado en 2004

The polybasic N-terminal region of the prion protein controls the physical properties of both the cellular and fibrillar forms of PrP.

artículo científico publicado en 2008

The presence of valine at residue 129 in human prion protein accelerates amyloid formation.

artículo científico publicado en 2005

The same primary structure of the prion protein yields two distinct self-propagating states

artículo científico publicado en 2008

The α-helical C-terminal domain of full-length recombinant PrP converts to an in-register parallel β-sheet structure in PrP fibrils: evidence from solid state nuclear magnetic resonance

artículo científico publicado en 2010

Treatment with normal prion protein delays differentiation and helps to maintain high proliferation activity in human embryonic stem cells

artículo científico publicado en 2010

Two alternative pathways for generating transmissible prion disease de novo

artículo científico publicado en 2015

Two amyloid States of the prion protein display significantly different folding patterns

artículo científico publicado en 2010

Lista de obras de Baskakov IV

A new mechanism for transmissible prion diseases

Amyloid features and neuronal toxicity of mature prion fibrils are highly sensitive to high pressure

Amyloid fibrils of mammalian prion protein induce axonal degeneration in NTERA2-derived terminally differentiated neurons

Analysis of Covalent Modifications of Amyloidogenic Proteins Using Two-Dimensional Electrophoresis: Prion Protein and Its Sialylation

Annealing prion protein amyloid fibrils at high temperature results in extension of a proteinase K-resistant core

Assessment of Strain-Specific PrPSc Elongation Rates Revealed a Transformation of PrPSc Properties during Protein Misfolding Cyclic Amplification ⬇️

Atomic force fluorescence microscopy in the characterization of amyloid fibril assembly and oligomeric intermediates

Atypical and classical forms of the disease-associated state of the prion protein exhibit distinct neuronal tropism, deposition patterns, and lesion profiles

Changes in prion replication environment cause prion strain mutation

Chemoenzymatic synthesis of HIV-1 V3 glycopeptides carrying two N-glycans and effects of glycosylation on the peptide domain

Conformational stability of PrP amyloid fibrils controls their smallest possible fragment size

Conformational switching within individual amyloid fibrils.

Converting the prion protein: what makes the protein infectious.

Copper(II) inhibits in vitro conversion of prion protein into amyloid fibrils

Correction to: preserving prion strain identity upon replication of prions in vitro using recombinant prion protein

Cross-seeding of prions by aggregated α-synuclein leads to transmissible spongiform encephalopathy

Design and construction of diverse mammalian prion strains

Dichotomous versus palm-type mechanisms of lateral assembly of amyloid fibrils

Dissecting Structure of Prion Amyloid Fibrils by Hydrogen–Deuterium Exchange Ultraviolet Raman Spectroscopy ⬇️

Expression and purification of full-length recombinant PrP of high purity

Fast and ultrasensitive method for quantitating prion infectivity titre ⬇️

Genesis of mammalian prions: from non-infectious amyloid fibrils to a transmissible prion disease

Genesis of tramsmissible protein states via deformed templating ⬇️

Hemicentin assembly in the extracellular matrix is mediated by distinct structural modules

Highly efficient protein misfolding cyclic amplification

Highly promiscuous nature of prion polymerization.

In vitro conversion of full-length mammalian prion protein produces amyloid form with physical properties of PrP(Sc).

In vitro conversion of mammalian prion protein into amyloid fibrils displays unusual features

Inflammatory response of microglia to prions is controlled by sialylation of PrPSc.

Light-dependent electrogenic activity of cyanobacteria

Loss of Cellular Sialidases Does Not Affect the Sialylation Status of the Prion Protein but Increases the Amounts of Its Proteolytic Fragment C1

Methionine oxidation interferes with conversion of the prion protein into the fibrillar proteinase K-resistant conformation

Methods for conversion of prion protein into amyloid fibrils

Methods of Protein Misfolding Cyclic Amplification

Molecular structure of amyloid fibrils controls the relationship between fibrillar size and toxicity.

Multifaceted Role of Sialylation in Prion Diseases

Nanostructured polypyrrole-coated anode for sun-powered microbial fuel cells

New Molecular Insight into Mechanism of Evolution of Mammalian Synthetic Prions

Nonpolar substitution at the C-terminus of the prion protein, a mimic of the glycosylphosphatidylinositol anchor, partially impairs amyloid fibril formation

Oligomeric-induced activity by thienyl pyrimidine compounds traps prion infectivity

Pathway complexity of prion protein assembly into amyloid

Photosynthetic microbial fuel cells with positive light response

Polymorphism and ultrastructural organization of prion protein amyloid fibrils: an insight from high resolution atomic force microscopy

Post-conversion sialylation of prions in lymphoid tissues

Posttranslational modifications define course of prion strain adaptation and disease phenotype

PrP charge structure encodes interdomain interactions

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

Prion Strain-Specific Structure and Pathology: A View from the Perspective of Glycobiology

Prion replication environment defines the fate of prion strain adaptation.

Probing the conformation of the prion protein within a single amyloid fibril using a novel immunoconformational assay

Protease-sensitive synthetic prions

Purification and Fibrillation of Full-Length Recombinant PrP.

Purification and fibrillation of full-length recombinant PrP.

Recombinant prion protein induces a new transmissible prion disease in wild-type animals

Region-Specific Response of Astrocytes to Prion Infection

Region-Specific Sialylation Pattern of Prion Strains Provides Novel Insight into Prion Neurotropism

Region-specific glial homeostatic signature in prion diseases is replaced by a uniform neuroinflammation signature, common for brain regions and prion strains with different cell tropism

Relationship between Conformational Stability and Amplification Efficiency of Prions ⬇️

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

Role of the photosynthetic electron transfer chain in electrogenic activity of cyanobacteria

Selective Amplification of Classical and Atypical Prions Using Modified Protein Misfolding Cyclic Amplification ⬇️

Semiautomated cell-free conversion of prion protein: applications for high-throughput screening of potential antiprion drugs

Sialylation Controls Prion Fate in Vivo

Sialylation of Glycosylphosphatidylinositol (GPI) Anchors of Mammalian Prions Is Regulated in a Host-, Tissue-, and Cell-specific Manner

Sialylation of prion protein controls the rate of prion amplification, the cross-species barrier, the ratio of PrPSc glycoform and prion infectivity

Sialylation of the prion protein glycans controls prion replication rate and glycoform ratio

Site-specific conformational studies of prion protein (PrP) amyloid fibrils revealed two cooperative folding domains within amyloid structure

Stabilization of a prion strain of synthetic origin requires multiple serial passages

Strain-dependent profile of misfolded prion protein aggregates

Strain-specified characteristics of mouse synthetic prions

Synthetic mammalian prions

Synthetic prions generated in vitro are similar to a newly identified subpopulation of PrPSc from sporadic Creutzfeldt-Jakob Disease

The cellular form of the prion protein guides the differentiation of human embryonic stem cells into neuron-, oligodendrocyte-, and astrocyte-committed lineages

The cellular form of the prion protein is involved in controlling cell cycle dynamics, self-renewal, and the fate of human embryonic stem cell differentiation.

The diversity and relationship of prion protein self-replicating states

The dominant-negative effect of the Q218K variant of the prion protein does not require protein X.

The evolution of transmissible prions: the role of deformed templating

The peculiar nature of unfolding of the human prion protein

The polybasic N-terminal region of the prion protein controls the physical properties of both the cellular and fibrillar forms of PrP.