List of works - Ina Vorberg

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

scientific article published on 7 May 2004

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

scientific article

Cellular Aspects of Prion Replication In Vitro ⬇️

scientific article published on January 22, 2013

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

scientific article published on 09 July 2021

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

scientific article published on February 2006

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

scientific article published on 31 January 2019

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

scientific article

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

scientific article

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

scientific article published on June 2008

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

scientific article published on 15 March 2018

Entropic Bristles Tune the Seeding Efficiency of Prion-Nucleating Fragments

scientific article published on 01 February 2020

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

scientific article published on 01 February 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.

scientific article

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

scientific article

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

scientific article published on 19 October 2021

Identification of possible animal origins of prion disease in human beings

scientific article published in June 2004

Inhibition of cholesterol recycling impairs cellular PrP(Sc) propagation

scientific article published on 13 October 2009

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

scientific article published on 29 January 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

scientific article published on 10 September 2013

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

scientific article

Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies

scientific article published on January 2004

Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies

scientific article published on 01 May 2006

Molecular basis of scrapie strain glycoform variation

scientific article published on 23 July 2002

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

scientific article

Prion infection influences murine endogenous retrovirus expression in neuronal cells

scientific article published on 15 March 2006

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

scientific article

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

scientific article

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

scientific article

Prion strains depend on different endocytic routes for productive infection.

scientific article

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

scientific article published on 11 September 2009

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

scientific article published in October 2014

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

scientific article published on 04 October 2009

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

scientific article published on 26 October 2013

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

scientific article

Reverse engineering synthetic antiviral amyloids

scientific article published on 05 June 2020

Susceptibility of common fibroblast cell lines to transmissible spongiform encephalopathy agents

scientific article published on 21 January 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

scientific article

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

scientific article published in February 2009

List of works by 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