Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Toni M. Förster"'
Autor:
Toni M. Förster, Markus Magerl, Marcus Maurer, Selen Zülbahar, Susanne Zielke, Neil Inhaber, Donatello Crocetta, Arndt Rolfs, Volha Skrahina
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Hereditary Angioedema (HAE) is a genetic disorder that leads to frequent angioedema attacks in various parts of the body. In most cases it is caused by pathogenic variants in the SERPING1 gene, coding for C1-Inhibitor (C1-INH). Th
Externí odkaz:
https://doaj.org/article/42ac95988cc34c619d90eabd06f998a1
Autor:
Volha Skrahina, Ulrike Grittner, Christian Beetz, Thomas Skripuletz, Martin Juenemann, Heidrun H. Krämer, Katrin Hahn, Andreas Rieth, Volker Schaechinger, Monica Patten, Christian Tanislav, Stephan Achenbach, Birgit Assmus, Fabian Knebel, Stefan Gingele, Aliaksandr Skrahin, Jörg Hartkamp, Toni M. Förster, Sabine Roesner, Catarina Pereira, Arndt Rolfs
Publikováno v:
Annals of Medicine, Vol 53, Iss 1, Pp 1787-1796 (2021)
AbstractBackground Hereditary Transthyretin-Related Amyloidosis, a clinically heterogeneous autosomal dominant disease caused by pathogenic variants in the TTR gene, is characterized by the deposition of insoluble misfolded protein fibrils. The diagn
Externí odkaz:
https://doaj.org/article/2d66dec7cd4946c196e7e02150c90ad0
Autor:
Tatiana Usnich, Eva-Juliane Vollstedt, Nathalie Schell, Volha Skrahina, Xenia Bogdanovic, Hanaa Gaber, Toni M. Förster, Andreas Heuer, Natalia Koleva-Alazeh, Ilona Csoti, Ayse Nazli Basak, Sibel Ertan, Gencer Genc, Peter Bauer, Katja Lohmann, Anne Grünewald, Emma L. Schymanski, Joanne Trinh, Susen Schaake, Daniela Berg, Doreen Gruber, Stuart H. Isaacson, Andrea A. Kühn, Brit Mollenhauer, David J. Pedrosa, Kathrin Reetz, Esther M. Sammler, Enza Maria Valente, Franco Valzania, Jens Volkmann, Simone Zittel, Norbert Brüggemann, Meike Kasten, Arndt Rolfs, Christine Klein, The LIPAD Study Group
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: Pathogenic variants in the Leucine-rich repeat kinase 2 (LRRK2) gene are the most common known monogenic cause of Parkinson's disease (PD). LRRK2-linked PD is clinically indistinguishable from idiopathic PD and inherited in an autosomal d
Externí odkaz:
https://doaj.org/article/e0c5b9e3b35c439999b16638a0551593
Autor:
Christian Beetz, Volha Skrahina, Toni M. Förster, Hanaa Gaber, Jefri J. Paul, Filipa Curado, Arndt Rolfs, Peter Bauer, Stephan Schäfer, Volkmar Weckesser, Vivi Lieu, Mandy Radefeldt, Claudia Pöppel, Susann Krake, Krishna K. Kandaswamy, Katja Bruesehafer, Florian Vogel
Publikováno v:
Diagnostics, Vol 10, Iss 7, p 464 (2020)
The Coronavirus disease 2019 (COVID-19) pandemic caused by the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) has resulted in economic and social lockdowns in most countries all over the globe. Early identification of infected individua
Externí odkaz:
https://doaj.org/article/fe5f923659d9431fa832605881659b52
Autor:
Stefanie Allert, Toni M. Förster, Carl-Magnus Svensson, Jonathan P. Richardson, Tony Pawlik, Betty Hebecker, Sven Rudolphi, Marc Juraschitz, Martin Schaller, Mariana Blagojevic, Joachim Morschhäuser, Marc Thilo Figge, Ilse D. Jacobsen, Julian R. Naglik, Lydia Kasper, Selene Mogavero, Bernhard Hube
Publikováno v:
mBio, Vol 9, Iss 3 (2018)
ABSTRACT Life-threatening systemic infections often occur due to the translocation of pathogens across the gut barrier and into the bloodstream. While the microbial and host mechanisms permitting bacterial gut translocation are well characterized, th
Externí odkaz:
https://doaj.org/article/8caa6f60252d4a35989645f46583594a
Autor:
Neil Inhaber, Selen Zülbahar, Susanne Zielke, Arndt Rolfs, Volha Skrahina, Toni M Förster, Markus Magerl, Marcus Maurer, Donatello Crocetta
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Hereditary Angioedema (HAE) is a genetic disorder that leads to frequent angioedema attacks in various parts of the body. In most cases it is caused by pathogenic variants in the SERPING1 gene, coding for C1-Inhibitor (C1-INH). The pathoge
Autor:
Meike Kasten, Hanaa Gaber, Ana Westenberger, Xenia Bogdanovic, Norbert Brüggemann, Jefri J Paul, Maria Olmedillas, Volha Skrahina, Peter Bauer, Eva-Juliane Vollstedt, Christian Beetz, Toni M Förster, Filipa Curado, Christine Klein, Najim Ameziane, Snezana Skobalj, Selen Zülbahar, Ulrike Grittner, Arndt Rolfs, Natalia Koleva-Alazeh, Ilona Csoti, Tatiana Usnich
Publikováno v:
Movement Disorders
Background: genetic stratification of Parkinson's disease (PD) patients facilitates gene-tailored research studies and clinical trials. The objective of this study was to describe the design of and the initial data from the Rostock International Park
Autor:
Ilse D. Jacobsen, Toni M. Förster, Bernhard Hube, Selene Mogavero, Antonia Dräger, Melanie Polke, Katja Graf
Publikováno v:
Cellular Microbiology. 18:1709-1715
Candida albicans is an important human opportunistic fungal pathogen which is frequently found as part of the normal human microbiota. It is well accepted that the fungus interacts with other components of the resident microbiota and that this impact
Autor:
Simona Ioana Iancu, Shirley X. Tang, Manohursingh Runglall, Antje Häder, Julian R. Naglik, Betty Hebecker, Toni M. Förster, Duncan Wilson, Robert T. Wheeler, Remi L. Gratacap, Jon Robbins, Oliver Bader, Sarah Höfs, Ernesto Cota, Gema Vizcay, Jonathan P. Richardson, Nessim Kichik, Mariana Blagojevic, Ting Luo, Olaf Kniemeyer, Julia Wernecke, Bernhard Hube, Thomas Krüger, David L. Moyes, Selene Mogavero, Celia Murciano, Lydia Kasper, Oliver Kurzai, Thomas Gutsmann, Selvam Thavaraj
Publikováno v:
Nature 532(7597), 64-68 (2016). doi:10.1038/nature17625
Nature
Moyes, D L, Wilson, D, Richardson, J P, Mogavero, S, Tang, S X, Wernecke, J, Hofs, S, Gratacap, R L, Robbins, J, Runglall, M, Murciano, C, Blagojevic, M, Thavaraj, S, Forster, T M, Hebecker, B, Kasper, L, Vizcay-Barrena, G, Iancu, S I, Kichik, N, Hader, A, Kurzai, O, Luo, T, Kruger, T, Kniemeyer, O, Cota, E, Bader, O, Bader, O, Wheeler, R T, Gutsmann, T, Hube, B & Naglik, J R 2016, ' Candidalysin is a fungal peptide toxin critical for mucosal infection ', NATURE, vol. 532, no. 7597, pp. 64-68 . https://doi.org/10.1038/nature17625
Nature
Moyes, D L, Wilson, D, Richardson, J P, Mogavero, S, Tang, S X, Wernecke, J, Hofs, S, Gratacap, R L, Robbins, J, Runglall, M, Murciano, C, Blagojevic, M, Thavaraj, S, Forster, T M, Hebecker, B, Kasper, L, Vizcay-Barrena, G, Iancu, S I, Kichik, N, Hader, A, Kurzai, O, Luo, T, Kruger, T, Kniemeyer, O, Cota, E, Bader, O, Bader, O, Wheeler, R T, Gutsmann, T, Hube, B & Naglik, J R 2016, ' Candidalysin is a fungal peptide toxin critical for mucosal infection ', NATURE, vol. 532, no. 7597, pp. 64-68 . https://doi.org/10.1038/nature17625
Cytolytic proteins and peptide toxins are classical virulence factors of several bacterial pathogens which disrupt epithelial barrier function, damage cells and activate or modulate host immune responses. Such toxins have not been identified previous
Autor:
Stephan Schäfer, Katja Bruesehafer, Claudia Pöppel, Christian Beetz, Hanaa Gaber, Toni M Förster, Peter Bauer, Florian Vogel, Susann Krake, Volkmar Weckesser, Jefri J Paul, Vivi Lieu, Volha Skrahina, Krishna Kumar Kandaswamy, Filipa Curado, Arndt Rolfs, Mandy Radefeldt
Publikováno v:
Diagnostics
Volume 10
Issue 7
Diagnostics, Vol 10, Iss 464, p 464 (2020)
Volume 10
Issue 7
Diagnostics, Vol 10, Iss 464, p 464 (2020)
The Coronavirus disease 2019 (COVID-19) pandemic caused by the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) has resulted in economic and social lockdowns in most countries all over the globe. Early identification of infected individua