Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Bärbel Felder"'
Autor:
Fatemeh Behjati Ardakani, Kathrin Kattler, Karl Nordström, Nina Gasparoni, Gilles Gasparoni, Sarah Fuchs, Anupam Sinha, Matthias Barann, Peter Ebert, Jonas Fischer, Barbara Hutter, Gideon Zipprich, Charles D. Imbusch, Bärbel Felder, Jürgen Eils, Benedikt Brors, Thomas Lengauer, Thomas Manke, Philip Rosenstiel, Jörn Walter, Marcel H. Schulz
Publikováno v:
Epigenetics & Chromatin, Vol 11, Iss 1, Pp 1-14 (2018)
Abstract Background Bidirectional promoters (BPs) are prevalent in eukaryotic genomes. However, it is poorly understood how the cell integrates different epigenomic information, such as transcription factor (TF) binding and chromatin marks, to drive
Externí odkaz:
https://doaj.org/article/aeda19e919924fcba37b9cf5784814fb
Autor:
Sibylle Loibl, Jan Hauke, Karen Gelmon, Frederik Marmé, Corinna Ernst, Miguel Martin, Michael Untch, Hervé Bonnefoi, Erik Knudsen, Seock-Ah Im, Angela DeMichele, Laura Van’t Veer, Sung-Bae Kim, Harry Bear, Nicole McCarthy, Nicholas Turner, Agnieszka Witkiewicz, Federico Rojo, Peter A Fasching, José A García-Sáenz, Catherine M Kelly, Toralf Reimer, Masakazu Toi, Hope S Rugo, Carsten Denkert, Michael Gnant, Andreas Makris, Yuan Liu, Olga Valota, Bärbel Felder, Karsten Weber, Valentina Nekljudova, Eric Hahnen
Publikováno v:
Cancer Research. 82:P5-13
Background: In high-risk hormone-receptor (HR)+/HER2- BC patients germline (g) mutations can be found in approximately 14% in BRCA1/2 and in BRCA1/2 and other BC predisposition genes in 20% (Pohl-Rescigno E, et al. JAMA Oncol 2020). In metastatic BC
Autor:
Carsten Denkert, Frederik Marmé, Miguel Martin, Michael Untch, Hervé Bonnefoi, Sung-Bae Kim, Harry Bear, Agnieszka Witkiewicz, Seock-Ah Im, Angela DeMichele, Laura Van’t Veer, Nicole McCarthy, Thorsten Stiewe, Karen A. Gelmon, José A. García-Sáenz, Catherine M. Kelly, Toralf Reimer, Erik Knudsen, Nicholas Turner, Federico Rojo, Peter A. Fasching, Julia Teply-Szymanski, Yuan Liu, Masakazu Toi, Hope S. Rugo, Michael Gnant, Andreas Makris, Bärbel Felder, Karsten Weber, Sibylle Loibl
Publikováno v:
Cancer Research. 82:PD2-04
Background: Molecular plasticity of breast cancer is crucial for the development of therapy-resistant disease. In this investigation, we studied changes in molecular signatures between pretherapeutic (pre-Tx) and post-therapeutic (post-NACT) tumor sa
The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery
Autor:
Sergio Abrignani, David Adams, Melanie de Almeida, ALTUCCI, Lucia, Viren Amin, Ido Amit, Stylianos E, Antonarakis, Samuel Aparicio, Takahiro Arima, Laura Arrigoni, Rob Arts, Vahid Asnafi, Manel Esteller, Jae Bum Bae, Kevin Bassler, Stephan Beck, Benjamin Berkman, Bradley E, Bernstein, Mikhail Bilenky, Adrian Bird, Christoph Bock, Bernhard Boehm, Guillaume Bourque, Charles E, Breeze, Benedikt Brors, David Bujold, Oliver Burren, Marion J, Bussemakers, Adam Butterworth, Elias Campo, Enrique Carrillo de Santa Pau, Lisa Chadwick, Kui Ming Chan, Wei Chen, Tom H, Cheung, Luca Chiapperino, Nak Hyen Choi, Ho Ryun Chung, Laura Clarke, Joseph M, Connors, Philippe Cronet, John Danesh, Manolis Dermitzakis, Gerard Drewes, Pawel Durek, Stephanie Dyke, Tomasz Dylag, Connie J, Eaves, Peter Ebert, Roland Eils, Jürgen Eils, Catherine A, Ennis, Tariq Enver, Elise A, Feingold, Bärbel Felder, Anne Ferguson Smith, Jude Fitzgibbon, Paul Flicek, Roger S, Y, Foo, Peter Fraser, Mattia Frontini, Eileen Furlong, Sitanshu Gakkhar, Nina Gasparoni, Gilles Gasparoni, Daniel H, Geschwind, Petar Glažar, Thomas Graf, Frank Grosveld, Xin Yuan Guan, Roderic Guigo, Ivo G, Gut, Alf Hamann, Bok Ghee Han, R, Alan Harris, Simon Heath, Kristian Helin, Jan G, Hengstler, Alireza Heravi Moussavi, Karl Herrup, Steven Hill, Jason A, Hilton, Benjamin C, Hitz, Bernhard Horsthemke, Ming Hu, Joo Yeon Hwang, Nancy Y, Takashi Ito, Biola Maria Javierre, Sasa Jenko, Thomas Jenuwein, Yann Joly, Steven J, M, Jones, Yae Kanai, Hee Gyung Kang, Aly Karsan, Alexandra K, Kiemer, Song Cheol Kim, Bong Jo Kim, Hyeon Hoe Kim, Hiroshi Kimura, Sarah Kinkley, Filippos Klironomos, In Uk Koh, Myrto Kostadima, Christopher Kressler, Roman Kreuzhuber, Anshul Kundaje, Ralf Küppers, Carolyn Larabell, Paul Lasko, Mark Lathrop, S, Lee, Suman Lee, Hans Lehrach, Elsa Leitão, Thomas Lengauer, Åke Lernmark, David Leslie, Gilberto K, K, Leung, Danny Leung, Markus Loeffler, Yussanne Ma, Antonello Mai, Thomas Manke, Eric R, Marcotte, Marco A, Marra, Joost H, A, Martens, Jose Ignacio Martin Subero, Karen Maschke, Christoph Merten, Aleksandar Milosavljevic, Saverio Minucci, Totai Mitsuyama, Richard A, Moore, Fabian Müller, Andrew J, Mungall, Mihai G, Netea, Karl Nordström, Irene Norstedt, Hiroaki Okae, Vitor Onuchic, Francis Ouellette, Willem Ouwehand, Massimiliano Pagani, Vera Pancaldi, Thomas Pap, Tomi Pastinen, Ronak Patel, Dirk S, Paul, Michael J, Pazin, Pier Giuseppe Pelicci, Anthony G, Phillips, Julia Polansky, Bo Porse, J, Andrew Pospisilik, Shyam Prabhakar, Dena C, Procaccini, Andreas Radbruch, Nikolaus Rajewsky, Vardham Rakyan, Wolf Reik, Bing Ren, David Richardson, Andreas Richter, Daniel Rico, David J, Roberts, Philip Rosenstiel, Mark Rothstein, Abdulrahman Salhab, Hiroyuki Sasaki, John S, Satterlee, Sascha Sauer, Claudia Schacht, Florian Schmidt, Gerd Schmitz, Stefan Schreiber, Christopher Schröder, Dirk Schübeler, Joachim L, Schultze, Ronald P, Schulyer, Marcel Schulz, Martin Seifert, Katsuhiko Shirahige, Reiner Siebert, Thomas Sierocinski, Laura Siminoff, Anupam Sinha, Nicole Soranzo, Salvatore Spicuglia, Mikhail Spivakov, Christian Steidl, Seth Strattan, Michael Stratton, Peter Südbeck, Hao Sun, Narumi Suzuki, Yutaka Suzuki, Amos Tanay, David Torrents, Frederick L, Tyson, Thomas Ulas, Sebastian Ullrich, Toshikazu Ushijima, Alfonso Valencia, Edo Vellenga, Martin Vingron, Chris Wallace, Stefan Wallner, Jörn Walter, Huating Wang, Stephanie Weber, Nina Weiler, Andreas Weller, Andrew Weng, Steven Wilder, Sam M, Wiseman, Angela R, Zhenguo Wu, Jieyi Xiong, Yasuhiro Yamashita, Xinyi Yang, Desmond Y, Yap, Kevin Y, Yip, Stephen Yip, Jae Il Yoo, Daniel Zerbino, Gideon Zipprich
Publikováno v:
Cell, Vol. 167, No 5 (2016) pp. 1145-1149
Cell, 167, 1145-1149
Cell
Cell, 2016, 167 (5), pp.1145--1149. ⟨10.1016/j.cell.2016.11.007⟩
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Cell, 167, 5, pp. 1145-1149
Cell, 167, 1145-1149
Cell
Cell, 2016, 167 (5), pp.1145--1149. ⟨10.1016/j.cell.2016.11.007⟩
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Cell, 167, 5, pp. 1145-1149
Item does not contain fulltext The International Human Epigenome Consortium (IHEC) coordinates the generation of a catalog of high-resolution reference epigenomes of major primary human cell types. The studies now presented (see the Cell Press IHEC w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::845e48803a7d1e4ee8470ca376fb77af
https://archive-ouverte.unige.ch/unige:90729
https://archive-ouverte.unige.ch/unige:90729
Autor:
Karl Nordström, Gilles Gasparoni, Sebastian Fröhler, Gideon Zipprich, Elsa Leitão, Thomas Manke, Ludger Klein-Hitpass, Wei Chen, Daniela Beißer, Christopher Schröder, Gerd Schmitz, Bernhard Horsthemke, Tea Berulava, Jörn Walter, Matthias Barann, Thomas Lengauer, Philip Rosenstiel, Ulrike Bönisch, Stefan Wallner, Claudia Haak, Corinna Attenberger, Filippos Klironomos, Bärbel Felder, Sven Rahmann, Peter Ebert, Laura Arrigoni, Andreas S. Richter, Fabian Müller, Benedikt Brors, Nikolaus Rajewsky
Publikováno v:
Epigenetics & Chromatin
Background Monocyte-to-macrophage differentiation involves major biochemical and structural changes. In order to elucidate the role of gene regulatory changes during this process, we used high-throughput sequencing to analyze the complete transcripto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90b0d643fe419e417dd56d39097064a7
https://hdl.handle.net/11858/00-001M-0000-002B-1693-211858/00-001M-0000-002B-1691-6
https://hdl.handle.net/11858/00-001M-0000-002B-1693-211858/00-001M-0000-002B-1691-6
Autor:
Pawel, Durek, Karl, Nordström, Gilles, Gasparoni, Abdulrahman, Salhab, Christopher, Kressler, Melanie, de Almeida, Kevin, Bassler, Thomas, Ulas, Florian, Schmidt, Jieyi, Xiong, Petar, Glažar, Filippos, Klironomos, Anupam, Sinha, Sarah, Kinkley, Xinyi, Yang, Laura, Arrigoni, Azim Dehghani, Amirabad, Fatemeh Behjati, Ardakani, Lars, Feuerbach, Oliver, Gorka, Peter, Ebert, Fabian, Müller, Na, Li, Stefan, Frischbutter, Stephan, Schlickeiser, Carla, Cendon, Sebastian, Fröhler, Bärbel, Felder, Nina, Gasparoni, Charles D, Imbusch, Barbara, Hutter, Gideon, Zipprich, Yvonne, Tauchmann, Simon, Reinke, Georgi, Wassilew, Ute, Hoffmann, Andreas S, Richter, Lina, Sieverling, Hyun-Dong, Chang, Uta, Syrbe, Ulrich, Kalus, Jürgen, Eils, Benedikt, Brors, Thomas, Manke, Jürgen, Ruland, Thomas, Lengauer, Nikolaus, Rajewsky, Wei, Chen, Jun, Dong, Birgit, Sawitzki, Ho-Ryun, Chung, Philip, Rosenstiel, Marcel H, Schulz, Joachim L, Schultze, Andreas, Radbruch, Jörn, Walter, Alf, Hamann, Julia K, Polansky
Publikováno v:
Immunity. 45(5)
The impact of epigenetics on the differentiation of memory T (Tmem) cells is poorly defined. We generated deep epigenomes comprising genome-wide profiles of DNA methylation, histone modifications, DNA accessibility, and coding and non-coding RNA expr
Autor:
Almut Schultealbert, Manuela C. Koch, Frank Geller, Bärbel Felder, Elisabeth Strehl, August Ermert, Karolin Stegmann
Publikováno v:
European Journal of Human Genetics. 10:753-756
Neural tube defects (NTD) are among the most common congenital malformations in humans. The current view is that there are no major genes causing NTDs, but combinations of sequence variants in different genes have additive effects on determining the
Autor:
Gabriele Schmötzer, Bernhard Radlwimmer, Annemarie Poustka, Claudia Schuster, Grischa Tödt, Axel Benner, Kim S. Beyer, Sven Bölte, Sabine M. Klauck, Peter Lichter, Fritz Poustka, Bärbel Felder, Antoaneta Mincheva
Publikováno v:
American journal of medical genetics. Part A. (5)
We describe a patient with autism and brachymetaphalangy, meeting criteria for 2q37 deletion syndrome (also called Albright Hereditary Osteodystrophy-like syndrome or Brachydactyly-Mental Retardation syndrome, OMIM 600430). Our molecular cytogenetic
Autor:
Peter, Szatmari, Andrew D, Paterson, Lonnie, Zwaigenbaum, Wendy, Roberts, Jessica, Brian, Xiao-Qing, Liu, John B, Vincent, Jennifer L, Skaug, Ann P, Thompson, Lili, Senman, Lars, Feuk, Cheng, Qian, Susan E, Bryson, Marshall B, Jones, Christian R, Marshall, Stephen W, Scherer, Veronica J, Vieland, Christopher, Bartlett, La Vonne, Mangin, Rhinda, Goedken, Alberto, Segre, Margaret A, Pericak-Vance, Michael L, Cuccaro, John R, Gilbert, Harry H, Wright, Ruth K, Abramson, Catalina, Betancur, Thomas, Bourgeron, Christopher, Gillberg, Marion, Leboyer, Joseph D, Buxbaum, Kenneth L, Davis, Eric, Hollander, Jeremy M, Silverman, Joachim, Hallmayer, Linda, Lotspeich, James S, Sutcliffe, Jonathan L, Haines, Susan E, Folstein, Joseph, Piven, Thomas H, Wassink, Val, Sheffield, Daniel H, Geschwind, Maja, Bucan, W Ted, Brown, Rita M, Cantor, John N, Constantino, T Conrad, Gilliam, Martha, Herbert, Clara, Lajonchere, David H, Ledbetter, Christa, Lese-Martin, Janet, Miller, Stan, Nelson, Carol A, Samango-Sprouse, Sarah, Spence, Matthew, State, Rudolph E, Tanzi, Hilary, Coon, Geraldine, Dawson, Bernie, Devlin, Annette, Estes, Pamela, Flodman, Lambertus, Klei, William M, McMahon, Nancy, Minshew, Jeff, Munson, Elena, Korvatska, Patricia M, Rodier, Gerard D, Schellenberg, Moyra, Smith, M Anne, Spence, Chris, Stodgell, Ping Guo, Tepper, Ellen M, Wijsman, Chang-En, Yu, Bernadette, Rogé, Carine, Mantoulan, Kerstin, Wittemeyer, Annemarie, Poustka, Bärbel, Felder, Sabine M, Klauck, Claudia, Schuster, Fritz, Poustka, Sven, Bölte, Sabine, Feineis-Matthews, Evelyn, Herbrecht, Gabi, Schmötzer, John, Tsiantis, Katerina, Papanikolaou, Elena, Maestrini, Elena, Bacchelli, Francesca, Blasi, Simona, Carone, Claudio, Toma, Herman, Van Engeland, Maretha, de Jonge, Chantal, Kemner, Frederieke, Koop, Frederike, Koop, Marjolein, Langemeijer, Marjolijn, Langemeijer, Channa, Hijmans, Channa, Hijimans, Wouter G, Staal, Gillian, Baird, Patrick F, Bolton, Michael L, Rutter, Emma, Weisblatt, Jonathan, Green, Catherine, Aldred, Julie-Anne, Wilkinson, Andrew, Pickles, Ann, Le Couteur, Tom, Berney, Helen, McConachie, Anthony J, Bailey, Kostas, Francis, Gemma, Honeyman, Aislinn, Hutchinson, Jeremy R, Parr, Simon, Wallace, Anthony P, Monaco, Gabrielle, Barnby, Kazuhiro, Kobayashi, Janine A, Lamb, Ines, Sousa, Nuala, Sykes, Edwin H, Cook, Stephen J, Guter, Bennett L, Leventhal, Jeff, Salt, Catherine, Lord, Christina, Corsello, Vanessa, Hus, Daniel E, Weeks, Fred, Volkmar, Maïté, Tauber, Eric, Fombonne, Andy, Shih, Kacie J, Meyer
Publikováno v:
Nature Genetics
Nature Genetics, Nature Publishing Group, 2007, 39 (3), pp.319-28. ⟨10.1038/ng1985⟩
Nature Genetics, 39(3), 319-28. Nature Publishing Group
Nature Genetics, 2007, 39 (3), pp.319-28. ⟨10.1038/ng1985⟩
Szatmari, P, Paterson, A D, Zwaigenbaum, L, Roberts, W, Brian, J, Liu, X-Q, Vincent, J B, Skaug, J L, Thompson, A P, Senman, L, Feuk, L, Qian, C, Bryson, S E, Jones, M B, Marshall, C R, Scherer, S W, Vieland, V J, Bartlett, C, Mangin, L V, Goedken, R, Segre, A, Pericak-Vance, M A, Cuccaro, M L, Gilbert, J R, Wright, H H, Abramson, R K, Betancur, C, Bourgeron, T, Gillberg, C, Leboyer, M, Buxbaum, J D, Davis, K L, Hollander, E, Silverman, J M, Hallmayer, J, Lotspeich, L, Sutcliffe, J S, Haines, J L, Folstein, S E, Piven, J, Wassink, T H, Sheffield, V, Geschwind, D H, Bucan, M, Brown, W T, Cantor, R M, Constantino, J N, Baird, G, Bolton, P F, Rutter, M L 2007, ' Mapping autism risk loci using genetic linkage and chromosomal rearrangements ', Nature Genetics, vol. 39, no. 3, pp. 319-328 . https://doi.org/10.1038/ng1985
Nature Genetics, Nature Publishing Group, 2007, 39 (3), pp.319-28. ⟨10.1038/ng1985⟩
Nature Genetics, 39(3), 319-28. Nature Publishing Group
Nature Genetics, 2007, 39 (3), pp.319-28. ⟨10.1038/ng1985⟩
Szatmari, P, Paterson, A D, Zwaigenbaum, L, Roberts, W, Brian, J, Liu, X-Q, Vincent, J B, Skaug, J L, Thompson, A P, Senman, L, Feuk, L, Qian, C, Bryson, S E, Jones, M B, Marshall, C R, Scherer, S W, Vieland, V J, Bartlett, C, Mangin, L V, Goedken, R, Segre, A, Pericak-Vance, M A, Cuccaro, M L, Gilbert, J R, Wright, H H, Abramson, R K, Betancur, C, Bourgeron, T, Gillberg, C, Leboyer, M, Buxbaum, J D, Davis, K L, Hollander, E, Silverman, J M, Hallmayer, J, Lotspeich, L, Sutcliffe, J S, Haines, J L, Folstein, S E, Piven, J, Wassink, T H, Sheffield, V, Geschwind, D H, Bucan, M, Brown, W T, Cantor, R M, Constantino, J N, Baird, G, Bolton, P F, Rutter, M L 2007, ' Mapping autism risk loci using genetic linkage and chromosomal rearrangements ', Nature Genetics, vol. 39, no. 3, pp. 319-328 . https://doi.org/10.1038/ng1985
International audience; Autism spectrum disorders (ASDs) are common, heritable neurodevelopmental conditions. The genetic architecture of ASDs is complex, requiring large samples to overcome heterogeneity. Here we broaden coverage and sample size rel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b4ba5a0896229e2dd78390a6ddd5723
https://www.hal.inserm.fr/inserm-00937094/file/AGP_Nat_Genet_2007.pdf
https://www.hal.inserm.fr/inserm-00937094/file/AGP_Nat_Genet_2007.pdf