Lista de obras - Ina Vorberg - Dominio Público Uruguay

Acute formation of protease-resistant prion protein does not always lead to persistent scrapie infection in vitro

artículo científico publicado en 2004

Cell line dependent RNA expression profiles of prion-infected mouse neuronal cells

artículo científico publicado en 2005

Cellular Aspects of Prion Replication In Vitro ⬇️

artículo científico publicado el 22 de enero de 2013

Co-factor-free aggregation of tau into seeding-competent RNA-sequestering amyloid fibrils

artículo científico publicado en 2021

DNA aptamers that bind to PrP(C) and not PrP(Sc) show sequence and structure specificity

artículo científico

Deregulated Splicing Is a Major Mechanism of RNA-Induced Toxicity in Huntington's Disease

artículo científico publicado en 2019

Dynamic interactions of Sup35p and PrP prion protein domains modulate aggregate nucleation and seeding

artículo científico publicado en 2008

Effect of hydrophobic mutations in the H2-H3 subdomain of prion protein on stability and conversion in vitro and in vivo.

artículo científico publicado en 2011

Endocytosis of prion protein is required for ERK1/2 signaling induced by stress-inducible protein 1.

artículo científico publicado en 2008

Endoplasmic Reticulum Stress Induces Myostatin High Molecular Weight Aggregates and Impairs Mature Myostatin Secretion

artículo científico publicado en 2018

Entropic Bristles Tune the Seeding Efficiency of Prion-Nucleating Fragments

artículo científico publicado en 2020

Experimental models to study prion disease pathogenesis and identify potential therapeutic compounds

artículo científico publicado en 2019

Fibril-induced glutamine-/asparagine-rich prions recruit stress granule proteins in mammalian cells

scientific article published on 02 July 2019

Genetic human prion disease modelled in PrP transgenic Drosophila.

artículo científico publicado en 2017

Globular domain of the prion protein needs to be unlocked by domain swapping to support prion protein conversion

artículo científico publicado en 2011

Highly efficient intercellular spreading of protein misfolding mediated by viral ligand-receptor interactions

artículo científico publicado en 2021

Identification of possible animal origins of prion disease in human beings

artículo científico publicado en 2004

Inhibition of cholesterol recycling impairs cellular PrP(Sc) propagation

artículo científico publicado en 2009

Inhibition of the MID1 protein complex: a novel approach targeting APP protein synthesis.

artículo científico publicado en 2018

Intercellular Transmission of a Synthetic Bacterial Cytotoxic Prion-Like Protein in Mammalian Cells

scientific article published on 14 April 2020

Life cycle of cytosolic prions

artículo científico publicado en 2013

Modulation of Glycosaminoglycans Affects PrPSc Metabolism but Does Not Block PrPSc Uptake.

artículo científico publicado en 2015

Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies

artículo científico publicado en 2004

Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies

artículo científico publicado en 2006

Molecular basis of scrapie strain glycoform variation

artículo científico publicado en 2002

Multiple amino acid residues within the rabbit prion protein inhibit formation of its abnormal isoform

artículo científico publicado en 2003

Prion infection influences murine endogenous retrovirus expression in neuronal cells

artículo científico publicado en 2006

Prion protein interaction with stress-inducible protein 1 enhances neuronal protein synthesis via mTOR

artículo científico publicado en 2010

Prion protein/protein interactions: fusion with yeast Sup35p-NM modulates cytosolic PrP aggregation in mammalian cells.

artículo científico publicado en 2007

Prion replication in the mammalian cytosol: Functional regions within a prion domain driving induction, propagation and inheritance.

artículo científico publicado en 2018

Prion strains depend on different endocytic routes for productive infection.

artículo científico publicado en 2017

Prion-induced activation of cholesterogenic gene expression by Srebp2 in neuronal cells

artículo científico publicado en 2009

Prion-induced and spontaneous formation of transmissible toxicity in PrP transgenic Drosophila

artículo científico publicado en 2014

Prion-like propagation of cytosolic protein aggregates: insights from cell culture models

artículo científico publicado en 2009

Prions Ex Vivo: What Cell Culture Models Tell Us about Infectious Proteins

artículo científico publicado en 2013

Proteasomal dysfunction and endoplasmic reticulum stress enhance trafficking of prion protein aggregates through the secretory pathway and increase accumulation of pathologic prion protein

artículo científico publicado en 2011

Reverse engineering synthetic antiviral amyloids

artículo científico publicado en 2020

Susceptibility of common fibroblast cell lines to transmissible spongiform encephalopathy agents

artículo científico publicado en 2004

Tetracysteine-tagged prion protein allows discrimination between the native and converted forms

scientific journal article

The novel sorting nexin SNX33 interferes with cellular PrP formation by modulation of PrP shedding

artículo científico publicado en 2008

The yeast Sup35NM domain propagates as a prion in mammalian cells

scholarly article

Therapy in prion diseases: from molecular and cellular biology to therapeutic targets

artículo científico publicado en 2009

Lista de obras de Ina Vorberg

Acute formation of protease-resistant prion protein does not always lead to persistent scrapie infection in vitro

Cell line dependent RNA expression profiles of prion-infected mouse neuronal cells

Cellular Aspects of Prion Replication In Vitro ⬇️

Co-factor-free aggregation of tau into seeding-competent RNA-sequestering amyloid fibrils

DNA aptamers that bind to PrP(C) and not PrP(Sc) show sequence and structure specificity

Deregulated Splicing Is a Major Mechanism of RNA-Induced Toxicity in Huntington's Disease

Dynamic interactions of Sup35p and PrP prion protein domains modulate aggregate nucleation and seeding

Effect of hydrophobic mutations in the H2-H3 subdomain of prion protein on stability and conversion in vitro and in vivo.

Endocytosis of prion protein is required for ERK1/2 signaling induced by stress-inducible protein 1.

Endoplasmic Reticulum Stress Induces Myostatin High Molecular Weight Aggregates and Impairs Mature Myostatin Secretion

Entropic Bristles Tune the Seeding Efficiency of Prion-Nucleating Fragments

Experimental models to study prion disease pathogenesis and identify potential therapeutic compounds

Fibril-induced glutamine-/asparagine-rich prions recruit stress granule proteins in mammalian cells

Genetic human prion disease modelled in PrP transgenic Drosophila.

Globular domain of the prion protein needs to be unlocked by domain swapping to support prion protein conversion

Highly efficient intercellular spreading of protein misfolding mediated by viral ligand-receptor interactions

Identification of possible animal origins of prion disease in human beings

Inhibition of cholesterol recycling impairs cellular PrP(Sc) propagation

Inhibition of the MID1 protein complex: a novel approach targeting APP protein synthesis.

Intercellular Transmission of a Synthetic Bacterial Cytotoxic Prion-Like Protein in Mammalian Cells

Life cycle of cytosolic prions

Modulation of Glycosaminoglycans Affects PrPSc Metabolism but Does Not Block PrPSc Uptake.

Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies

Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies

Molecular basis of scrapie strain glycoform variation

Multiple amino acid residues within the rabbit prion protein inhibit formation of its abnormal isoform

Prion infection influences murine endogenous retrovirus expression in neuronal cells

Prion protein interaction with stress-inducible protein 1 enhances neuronal protein synthesis via mTOR

Prion protein/protein interactions: fusion with yeast Sup35p-NM modulates cytosolic PrP aggregation in mammalian cells.

Prion replication in the mammalian cytosol: Functional regions within a prion domain driving induction, propagation and inheritance.

Prion strains depend on different endocytic routes for productive infection.

Prion-induced activation of cholesterogenic gene expression by Srebp2 in neuronal cells

Prion-induced and spontaneous formation of transmissible toxicity in PrP transgenic Drosophila

Prion-like propagation of cytosolic protein aggregates: insights from cell culture models

Prions Ex Vivo: What Cell Culture Models Tell Us about Infectious Proteins

Proteasomal dysfunction and endoplasmic reticulum stress enhance trafficking of prion protein aggregates through the secretory pathway and increase accumulation of pathologic prion protein

Reverse engineering synthetic antiviral amyloids

Susceptibility of common fibroblast cell lines to transmissible spongiform encephalopathy agents

Tetracysteine-tagged prion protein allows discrimination between the native and converted forms

The novel sorting nexin SNX33 interferes with cellular PrP formation by modulation of PrP shedding

The yeast Sup35NM domain propagates as a prion in mammalian cells

Therapy in prion diseases: from molecular and cellular biology to therapeutic targets