Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Ina Vorberg"'
Autor:
Emiel Michiels, Kenny Roose, Rodrigo Gallardo, Ladan Khodaparast, Laleh Khodaparast, Rob van der Kant, Maxime Siemons, Bert Houben, Meine Ramakers, Hannah Wilkinson, Patricia Guerreiro, Nikolaos Louros, Suzanne J. F. Kaptein, Lorena Itatí Ibañez, Anouk Smet, Pieter Baatsen, Shu Liu, Ina Vorberg, Guy Bormans, Johan Neyts, Xavier Saelens, Frederic Rousseau, Joost Schymkowitz
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/c25558682e604351be0ae8e8c8234335
Autor:
Emiel Michiels, Kenny Roose, Rodrigo Gallardo, Ladan Khodaparast, Laleh Khodaparast, Rob van der Kant, Maxime Siemons, Bert Houben, Meine Ramakers, Hannah Wilkinson, Patricia Guerreiro, Nikolaos Louros, Suzanne J. F. Kaptein, Lorena Itatí Ibañez, Anouk Smet, Pieter Baatsen, Shu Liu, Ina Vorberg, Guy Bormans, Johan Neyts, Xavier Saelens, Frederic Rousseau, Joost Schymkowitz
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-13 (2020)
Abstract Human amyloids have been shown to interact with viruses and interfere with viral replication. Based on this observation, we employed a synthetic biology approach in which we engineered virus-specific amyloids against influenza A and Zika pro
Externí odkaz:
https://doaj.org/article/ffcec336575043bba6212cbf4b6b3b72
Autor:
Emiel Michiels, Shu Liu, Rodrigo Gallardo, Nikolaos Louros, Marion Mathelié-Guinlet, Yves Dufrêne, Joost Schymkowitz, Ina Vorberg, Frederic Rousseau
Publikováno v:
Cell Reports, Vol 30, Iss 8, Pp 2834-2845.e3 (2020)
Summary: Prions of lower eukaryotes are self-templating protein aggregates with cores formed by parallel in-register beta strands. Short aggregation-prone glutamine (Q)- and asparagine (N)-rich regions embedded in longer disordered domains have been
Externí odkaz:
https://doaj.org/article/fb35d88312474e96830afa8056164722
Autor:
Theophilos Tzaridis, Daniel Bachurski, Shu Liu, Kristin Surmann, Felix Babatz, Manuela Gesell Salazar, Uwe Völker, Michael Hallek, Ulrich Herrlinger, Ina Vorberg, Christoph Coch, Katrin S. Reiners, Gunther Hartmann
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 17, p 9211 (2021)
Extracellular vesicles (EVs) are reminiscent of their cell of origin and thus represent a valuable source of biomarkers. However, for EVs to be used as biomarkers in clinical practice, simple, comparable, and reproducible analytical methods must be a
Externí odkaz:
https://doaj.org/article/1a448b98f650422a907d11fe166ed025
Publikováno v:
Viruses, Vol 5, Iss 1, Pp 374-405 (2013)
Prion diseases or transmissible spongiform encephalopathies (TSEs) are fatal neurodegenerative disorders in mammals that are caused by unconventional agents predominantly composed of aggregated misfolded prion protein (PrP). Prions self-propagate by
Externí odkaz:
https://doaj.org/article/babfd9d5bdd647eb9110b0ef6226d1a9
Autor:
Sybille Krauss, Ina Vorberg
Publikováno v:
International Journal of Cell Biology, Vol 2013 (2013)
Prions are unconventional infectious agents that are composed of misfolded aggregated prion protein. Prions replicate their conformation by template-assisted conversion of the endogenous prion protein PrP. Templated conversion of soluble proteins int
Externí odkaz:
https://doaj.org/article/e04b0a90c964416198c307f0acc3b0ca
Publikováno v:
Swiss Medical Weekly, Vol 142, Iss 0304 (2012)
Transmissible spongiform encephalopathies are fatal neurodegenerative diseases that affect mammals including humans. The proteinaceous nature of the infectious agent, the prion, and its propagation, challenge established dogmas in biology. It is now
Externí odkaz:
https://doaj.org/article/adcaf0914b364aa9917d28cf05d633c2
Autor:
Iva Hafner-Bratkovič, Lars Gaedtke, Andrej Ondracka, Peter Veranič, Ina Vorberg, Roman Jerala
Publikováno v:
PLoS ONE, Vol 6, Iss 9, p e24238 (2011)
Prion diseases are fatal neurodegenerative diseases, which can be acquired, sporadic or genetic, the latter being linked to mutations in the gene encoding prion protein. We have recently described the importance of subdomain separation in the convers
Externí odkaz:
https://doaj.org/article/6ab439aafc474a6da1b90419bb7fab32
Autor:
Pascal Leblanc, Ina Vorberg
Publikováno v:
PLoS pathogens 18(8), e1010670 (2022). doi:10.1371/journal.ppat.1010670
Neurodegenerative diseases (NDs) such as Alzheimer’s and Parkinson’s disease are fatal neurological diseases that can be of idiopathic, genetic, or even infectious origin, as in the case of transmissible spongiform encephalopathies. The etiologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2871fc9956f0e96095e7565da607f7e5
https://doi.org/10.1371/journal.ppat.1010670
https://doi.org/10.1371/journal.ppat.1010670
Autor:
Aloys Schepers, Helmut Blum, Xia Wu, Elisabeth Kremmer, Olivier Hyrien, Alexander Buschle, Stefan Krebs, Ina Vorberg, Nina Kirstein, Laurent Lacroix, Wolfgang Hammerschmidt, Benjamin Audit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::237d7dcf5f713a8d6be3f6452774d14d
https://doi.org/10.7554/elife.62161.sa2
https://doi.org/10.7554/elife.62161.sa2
