Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Eduard Urich"'
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 6, p 3172 (2022)
Successful therapy with anti-CD20 monoclonal antibodies (mAbs) has reinforced the key role of B cells in the immunopathology of multiple sclerosis (MS). This study aimed to determine the effects of a novel class of anti-CD20 mAbs on vascular and extr
Externí odkaz:
https://doaj.org/article/74079c47786a4d048d578dae44441df0
Publikováno v:
PLoS ONE, Vol 15, Iss 3, p e0229850 (2020)
Reducing Amyloid β (Aβ) in the brain is of fundamental importance for advancing the therapeutics for Alzheimer`s disease. The endogenous metallopeptidase neprilysin (NEP) has been identified as one of the key Aβ-degrading enzymes. Delivery of NEP
Externí odkaz:
https://doaj.org/article/aa89271f13884ee2b314a47af6c49151
Autor:
Thomas Breakell, Sabine Tacke, Verena Schropp, Henrik Zetterberg, Kaj Blennow, Eduard Urich, Stefanie Kuerten
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 18, p 6864 (2020)
B cell-depleting therapies have recently proven to be clinically highly successful in the treatment of multiple sclerosis (MS). This study aimed to determine the effects of the novel type II anti-human CD20 (huCD20) monoclonal antibody (mAb) obinutuz
Externí odkaz:
https://doaj.org/article/8a041cce063140998bfe924f1ebd8ec2
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e38149 (2012)
Brain microvascular endothelial cells (BEC) constitute the blood-brain barrier (BBB) which forms a dynamic interface between the blood and the central nervous system (CNS). This highly specialized interface restricts paracellular diffusion of fluids
Externí odkaz:
https://doaj.org/article/2a01e4953ad04c77be093beeb02a809d
Autor:
Julien Bryois, Daniela Calini, Will Macnair, Lynette Foo, Eduard Urich, Ward Ortmann, Victor Alejandro Iglesias, Suresh Selvaraj, Erik Nutma, Manuel Marzin, Sandra Amor, Anna Williams, Gonçalo Castelo-Branco, Vilas Menon, Philip De Jager, Dheeraj Malhotra
Publikováno v:
Nature Neuroscience, 25(8), 1104-1112. Nature Publishing Group
Bryois, J, Calini, D, Macnair, W, Foo, L, Urich, E, Ortmann, W, Iglesias, V A, Selvaraj, S, Nutma, E, Marzin, M, Amor, S, Williams, A, Castelo-Branco, G, Menon, V, De Jager, P & Malhotra, D 2022, ' Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders ', Nature Neuroscience, vol. 25, no. 8, pp. 1104-1112 . https://doi.org/10.1038/s41593-022-01128-z
Bryois, J, Calini, D, Macnair, W, Foo, L, Urich, E, Ortmann, W, Iglesias, V A, Selvaraj, S, Nutma, E, Marzin, M, Amor, S, Williams, A, Castelo-Branco, G, Menon, V, De Jager, P & Malhotra, D 2022, ' Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders ', Nature Neuroscience, vol. 25, no. 8, pp. 1104-1112 . https://doi.org/10.1038/s41593-022-01128-z
To date, most expression quantitative trait loci (eQTL) studies, which investigate how genetic variants contribute to gene expression, have been performed in heterogeneous brain tissues rather than specific cell types. In this study, we performed an
Autor:
Will Macnair, Daniela Calini, Eneritz Agirre, Julien Bryois, Sarah Jäkel, Petra Kukanja, Nadine Stokar-Regenscheit, Virginie Ott, Lynette C. Foo, Ludovic Collin, Sven Schippling, Eduard Urich, Erik Nutma, Manuel Marzin, Sandra Amor, Roberta Magliozzi, Elyas Heidari, Mark D. Robinson, Charles ffrench-Constant, Gonçalo Castelo-Branco, Anna Williams, Dheeraj Malhotra
The lack of understanding as to the cellular and molecular basis of clinical and genetic heterogeneity in progressive multiple sclerosis (MS) has hindered the search for new effective therapies and biomarkers. Here, to address this gap, we analysed 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82ac11ba9c2fd8f4a2ebc946257f7694
https://doi.org/10.1101/2022.04.06.487263
https://doi.org/10.1101/2022.04.06.487263
Autor:
Verena Schropp, Rittika Chunder, Arif B. Ekici, Philipp Kirchner, Sabine Tacke, Stefanie Kuerten, Eduard Urich
BackgroundSuccessful therapy with anti-CD20 monoclonal antibodies (mAbs) has reinforced the key role of B cells in the immunopathology of multiple sclerosis. While treatment with currently available anti-CD20 mAbs results in rapid and robust eliminat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::320ee76d3cda25cdc81dfa42101dafe9
https://doi.org/10.21203/rs.3.rs-776877/v1
https://doi.org/10.21203/rs.3.rs-776877/v1
Autor:
Stefanie Kuerten, Henrik Zetterberg, Verena Schropp, Eduard Urich, Sabine Tacke, Kaj Blennow, Thomas Breakell
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 6864, p 6864 (2020)
International Journal of Molecular Sciences
Volume 21
Issue 18
International Journal of Molecular Sciences
Volume 21
Issue 18
B cell-depleting therapies have recently proven to be clinically highly successful in the treatment of multiple sclerosis (MS). This study aimed to determine the effects of the novel type II anti-human CD20 (huCD20) monoclonal antibody (mAb) obinutuz
Publikováno v:
The Journal of Immunology. 206:21.06-21.06
Anti-CD20 B cell depletion therapy has provided evidence for the pathogenic roles of B cells in multiple sclerosis (MS). Terminally differentiated plasma cells (PCs) are spared by anti-CD20, and our lab has previously shown that during experimental a
Publikováno v:
Neurology® Neuroimmunology & Neuroinflammation
article-version (Version of Record) 3
article-version (Version of Record) 3
ObjectiveTherapies targeting B cells have been used in the clinic for multiple sclerosis (MS). In patients with relapsing MS, anti-CD20 therapy often suppresses relapse activity; yet, their effect on disease progression has been disappointing. Most a