Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Urszula Brykczynska"'
Autor:
Margarita C. Dinamarca, Laura Colombo, Urszula Brykczynska, Amandine Grimm, Isabelle Fruh, Imtiaz Hossain, Daniela Gabriel, Anne Eckert, Matthias Müller, Eline Pecho-Vrieseling
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2024)
Neuron-to-neuron transmission of aggregation-prone, misfolded proteins may potentially explain the spatiotemporal accumulation of pathological lesions in the brains of patients with neurodegenerative protein-misfolding diseases (PMDs). However, littl
Externí odkaz:
https://doaj.org/article/b1326b00b5cd413e9fed3e157375bf07
Autor:
Urszula Brykczynska, Marco Geigges, Sophia J. Wiedemann, Erez Dror, Marianne Böni-Schnetzler, Christoph Hess, Marc Y. Donath, Renato Paro
Publikováno v:
Cell Reports, Vol 30, Iss 5, Pp 1627-1643.e7 (2020)
Summary: The innate immune system safeguards the organism from both pathogenic and environmental stressors. Also, physiologic levels of nutrients affect organismal and intra-cellular metabolism and challenge the immune system. In the long term, over-
Externí odkaz:
https://doaj.org/article/54b0b70065bb4546aa8d688de4a57702
Autor:
Efthalia Natalia Tousiaki, Laura Colombo, Matthias Mueller, Isabelle Fruh, Margarita Dinamarca Ceballos, Daniela Gabriel, Anne Eckert, Amandine Grimm, Imtiaz Hossain, Eline Pecho-Vrieseling, Urszula Brykczynska
A potential explanation for the spatiotemporal accumulation of pathological lesions in the brain of patients with neurodegenerative protein misfolding diseases (PMDs) is cell-to-cell transmission of aggregation-prone, misfolded proteins. Little is kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c64908fc49bde7f5c6dc9567447c85cf
https://doi.org/10.21203/rs.3.rs-1114693/v1
https://doi.org/10.21203/rs.3.rs-1114693/v1
Akademický článek
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Autor:
Barna D. Fodor, Jessica Klein, Pietro Chiurazzi, Marc Bühler, Tewis Bouwmeester, Guglielmo Roma, Thierry Doll, Eline Pecho-Vrieseling, Ulrike Naumann, Isabelle Fruh, Giovanni Neri, Edward J. Oakeley, Francesco Paolo Di Giorgio, Anke Thiemeyer, Matthias Mueller, Elisabetta Tabolacci, Carole Manneville, Urszula Brykczynska, Nicholas Kelley, Baltazar Gomez-Mancilla, Sascha Fuchs, Mariavittoria Iazeolla, Martin Beibel
Publikováno v:
Stem Cell Reports
Summary In fragile X syndrome (FXS), CGG repeat expansion greater than 200 triplets is believed to trigger FMR1 gene silencing and disease etiology. However, FXS siblings have been identified with more than 200 CGGs, termed unmethylated full mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::703429636f6ea1b4c2336a1f336ebc6d
https://doi.org/10.1016/j.stemcr.2016.10.004
https://doi.org/10.1016/j.stemcr.2016.10.004
Autor:
Lütge, Almut, Zyprych-Walczak, Joanna, Kunzmann, Urszula Brykczynska, Crowell, Helena L., Calini, Daniela, Malhotra, Dheeraj, Soneson, Charlotte, Robinson, Mark D.
Publikováno v:
Life Science Alliance; Jun2021, Vol. 4 Issue 6, p1-17, 17p
Publikováno v:
Genome biology and evolution
Genome Biology and Evolution
Genome Biology and Evolution
The vomeronasal organ (VNO) is an olfactory structure that detects pheromones and environmental cues. It consists of sensory neurons that express evolutionary unrelated groups of transmembrane chemoreceptors. The predominant V1R and V2R receptor repe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4fae5db3ba1ed8da240522aaac53796
https://doi.org/10.1093/gbe/evt013
https://doi.org/10.1093/gbe/evt013
Autor:
Mizue Hisano, Urszula Brykczynska, Dirk Schübeler, Antoine H.F.M. Peters, Michael B. Stadler, Christian Beisel, Edward J Oakeley, Tim Roloff, Liliana Ramos, Serap Erkek
Publikováno v:
Nature Structural & Molecular Biology, 17, 679-87
Nature Structural & Molecular Biology, 17, 6, pp. 679-87
Nature structural & molecular biology
Nature Structural & Molecular Biology, 17, 6, pp. 679-87
Nature structural & molecular biology
Contains fulltext : 89401.pdf (Publisher’s version ) (Closed access) In higher eukaryotes, histone methylation is involved in maintaining cellular identity during somatic development. As most nucleosomes are replaced by protamines during spermatoge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b4ee83f6aba0ed1fab454eb51495475
https://hdl.handle.net/2066/89401
https://hdl.handle.net/2066/89401
Autor:
Paolo Sassone-Corsi, Hans Reimer Rodewald, Hartmut Döhner, Odile Weber, Carmen Blum, Kevin Hogeveen, Antoine H.F.M. Peters, Vikas Madan, Frederic Zilbermann, Hans Jörg Fehling, Urszula Brykczynska, Konstanze Döhner, Babita Madan
Publikováno v:
Blood. 113:1444-1454
The human Mixed-Lineage-Leukemia-5 (MLL5) gene is located in a genomic region frequently deleted in patients with myeloid malignancies and encodes a widely expressed nuclear protein most closely related to MLL1, a Trithorax transcriptional regulator
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3c9a351386ad82cba7937964938f4fb
https://doi.org/10.1182/blood-2008-02-142638
https://doi.org/10.1182/blood-2008-02-142638
Autor:
Antoine H.F.M. Peters, Raphael Thierry, Cheryl H. Arrowsmith, Rico Kunzmann, Mathieu Tardat, Mareike Albert, Shili Duan, Urszula Brykczynska, Lilia Kaustov, Zichuan Liu
Publikováno v:
Molecular cell
Molecular Cell
Molecular Cell, Elsevier, 2015, 58 (1), pp.157-171. ⟨10.1016/j.molcel.2015.02.013⟩
Molecular Cell
Molecular Cell, Elsevier, 2015, 58 (1), pp.157-171. ⟨10.1016/j.molcel.2015.02.013⟩
Polycomb repressive complexes PRC1 and PRC2 regulate expression of genes involved in proliferation and development. In mouse early embryos, however, canonical PRC1 localizes to paternal pericentric heterochromatin (pat-PCH), where it represses transc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44511f78d4f937ee67f13eb8a10a4583
https://edoc.unibas.ch/40114/
https://edoc.unibas.ch/40114/