Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Barna D, Fodor"'
Autor:
Ewa Surdziel, Ieuan Clay, Florian Nigsch, Anke Thiemeyer, Cyril Allard, Gregory Hoffman, John S Reece-Hoyes, Tanushree Phadke, Romain Gambert, Caroline Gubser Keller, Marie-Gabrielle Ludwig, Birgit Baumgarten, Mathias Frederiksen, Dirk Schübeler, Klaus Seuwen, Tewis Bouwmeester, Barna D Fodor
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0183679 (2017)
Macrophages are key cell types of the innate immune system regulating host defense, inflammation, tissue homeostasis and cancer. Within this functional spectrum diverse and often opposing phenotypes are displayed which are dictated by environmental c
Externí odkaz:
https://doaj.org/article/ee373e8c093841f49ffecddc87bb7dda
Autor:
Michael B. Stadler, Gerhard Christofori, Fabian Wu, Chun Cao, Stefan Dirnhofer, Stephen L. Nutt, Fengyuan Tang, Mathias Frederiksen, Patrick Matthias, Hubertus Kohler, Barna D. Fodor, Simon N. Willis, Mohamed-Amin Choukrallah, Shuang Song, Jacob T. Jackson
Publikováno v:
Blood. 137(21)
OBF1 is a specific coactivator of the POU family transcription factors OCT1 and OCT2. OBF1 and OCT2 are B cell–specific and indispensable for germinal center (GC) formation, but their mechanism of action is unclear. Here, we show by chromatin immun
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
Autor:
J. Õsz, Miklos Kalman, Gábor Rákhely, K. Gyõrfi, J. Tusz, Róbert Csáki, Kornél L. Kovács, Mária Takács, Katalin Perei, Barna D. Fodor, Cs. Bagyinka, B. Polyák, Levente Bodrossy, Anna Tóth, T. Hanczár
Publikováno v:
Pflugers Archiv : European journal of physiology. 439(Suppl 1)
A fundamental and principal difficulty of the future energy supply is that the formation of fossil fuels is much slower than the rate of their exploitation. Therefore the reserves which can be recovered in an energetically feasible manner are shrinki
Autor:
Tanushree Phadke, Marie-Gabrielle Ludwig, Barna D. Fodor, Florian Nigsch, John S. Reece-Hoyes, Anke Thiemeyer, Ieuan Clay, Caroline Gubser Keller, Birgit Baumgarten, Dirk Schübeler, Cyril Allard, Gregory R. Hoffman, Tewis Bouwmeester, Mathias Frederiksen, Romain Gambert, Ewa Surdziel, Klaus Seuwen
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0183679 (2017)
PLoS ONE
PLoS ONE
Macrophages are key cell types of the innate immune system regulating host defense, inflammation, tissue homeostasis and cancer. Within this functional spectrum diverse and often opposing phenotypes are displayed which are dictated by environmental c
Autor:
Karsten Rippe, Mario Richter, Malte Wachsmuth, Caroline Marth, Fabian Erdel, Joël Beaudouin, Barna D. Fodor, Katharina P. Müller, Maïwen Caudron-Herger, Manuela Scaranaro
Publikováno v:
Biophysical Journal. 97:2876-2885
Heterochromatin protein 1 (HP1) is a central factor in establishing and maintaining the repressive heterochromatin state. To elucidate its mobility and interactions, we conducted a comprehensive analysis on different time and length scales by fluores
Autor:
Na Yin, Robert Schneider, Thomas Jenuwein, Judith M. Müller, Thomas Günther, Melanie Wissmann, Barna D. Fodor, Holger Greschik, Reinhard Buettner, Eric Metzger, Roland Schüle, Christine Vogler
Publikováno v:
Nature Cell Biology
Posttranslational modifications of histones, such as methylation, regulate chromatin structure and gene expression. Recently, lysine-specific demethylase 1 (LSD1)2, the first histone demethylase, was identified. LSD1 interacts with the androgen recep
Autor:
Barna D. Fodor, Amanda Cobos-Correa, Jessica Klein, Matthias Mueller, Tewis Bouwmeester, Isabelle Fruh, Anke Thiemeyer, Ulrich Schopfer, Pierre Rigo, Valerie Heidinger-Millot, Ansgar Schuffenhauer, Baltazar Gomez-Mancilla, Markus Kaufmann
Publikováno v:
Journal of biomolecular screening. 20(9)
Fragile X syndrome (FXS) is the most common form of inherited mental retardation, and it is caused in most of cases by epigenetic silencing of the Fmr1 gene. Today, no specific therapy exists for FXS, and current treatments are only directed to impro
Autor:
Masato Yonezawa, Roopsha Sengupta, Thomas Jenuwein, Stefan Kubicek, Susanne Opravil, Barna D. Fodor, Gunnar Schotta, Roderick J. O'Sullivan, Laura Perez-Burgos, Karl Mechtler
Publikováno v:
Genes & Development. 20:1557-1562
Histone lysine trimethyl states represent some of the most robust epigenetic modifications in eukaryotic chromatin. Using a candidate approach, we identified the subgroup of murine Jmjd2 proteins to antagonize H3K9me3 at pericentric heterochromatin.
Autor:
Kornél L. Kovács, Gábor Rákhely, Dóra Latinovics, Barna D. Fodor, Gergely Maróti, Gyula Csanádi, Ákos T. Kovács
Publikováno v:
Applied and Environmental Microbiology. 70:722-728
Structural genes coding for two membrane-associated NiFe hydrogenases in the phototrophic purple sulfur bacterium Thiocapsa roseopersicina ( hupSL and hynSL ) have recently been isolated and characterized. Deletion of both hydrogenase structural gene