Resultados de procura - Adrian M. Stütz
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The Th2 Cell Cytokines IL-4 and IL-13 Regulate Found in Inflammatory Zone 1/Resistin-Like Molecule α Gene Expression by a STAT6 and CCAAT/Enhancer-Binding Protein-Dependent Mechani... por Adrian M. Stütz, Louise A. Pickart, Alexandre Trifilieff, Thomas Baumruker, Eva Prieschl-Strassmayr, Maximilian Woisetschläger
Publicado 2003Artigo -
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Systematic Inference of Copy-Number Genotypes from Personal Genome Sequencing Data Reveals Extensive Olfactory Receptor Gene Content Diversity por Sebastian M. Waszak, Yehudit Hasin-Brumshtein, Thomas Zichner, Tsviya Olender, Ifat Keydar, Miriam Khen, Adrian M. Stütz, Andreas Schlattl, Doron Lancet, Jan O. Korbel
Publicado 2010Artigo -
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Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms por Alexej Abyzov, Shantao Li, Daniel Kim, Marghoob Mohiyuddin, Adrian M. Stütz, Nicholas F. Parrish, Xinmeng Jasmine Mu, Wyatt T. Clark, Ken Chen, Matthew E. Hurles, Jan O. Korbel, Hugo Y. K. Lam, Charles Lee, Mark Gerstein
Publicado 2015Artigo -
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Primate genome architecture influences structural variation mechanisms and functional consequences por Ömer Gökçümen, Verena Tischler, Jelena Tica, Qihui Zhu, Rebecca C. Iskow, Eunjung Lee, Markus Hsi-Yang Fritz, Amy Langdon, Adrian M. Stütz, Pavlos Pavlidis, Vladimı́r Beneš, Ryan E. Mills, Peter J. Park, Charles Lee, Jan O. Korbel
Publicado 2013Artigo -
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A cell‐based model system links chromothripsis with hyperploidy por Balca R. Mardin, Alexandros P. Drainas, Sebastian M. Waszak, Joachim Weischenfeldt, Mayumi Isokane, Adrian M. Stütz, Benjamin Raeder, Theocharis Efthymiopoulos, Christopher Buccitelli, Maia Segura‐Wang, Paul A. Northcott, Stefan M. Pfister, Peter Lichter, Jan Ellenberg, Jan O. Korbel
Publicado 2015Artigo -
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Comprehensive characterization of complex structural variations in cancer by directly comparing genome sequence reads por Valentí Moncunill, Santiago González, Sı́lvia Beà, Lise O. Andrieux, Itziar Salaverría, Cristina Royo, Laura Martínez Gómez, Montserrat Puiggròs, Maia Segura‐Wang, Adrian M. Stütz, Alba Navarro, Romina Royo, Josep Lluis Gelpí, Marta Gut, Carlos López‐Otín, Modesto Orozco, Jan O. Korbel, Elı́as Campo, Xosé S. Puente, David Torrents
Publicado 2014Artigo -
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A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans por Chip Stewart, Deniz Kural, Michael P. Strömberg, Jerilyn A. Walker, Miriam K. Konkel, Adrian M. Stütz, Alexander E. Urban, Fabian Grubert, Hugo Y. K. Lam, Wan-Ping Lee, Michele Busby, Amit Indap, Erik Garrison, Chad D. Huff, Jinchuan Xing, M Snyder, Lynn B. Jorde, Mark A. Batzer, Jan O. Korbel, Gábor Marth
Publicado 2011Artigo -
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Pediatric T-cell lymphoblastic leukemia evolves into relapse by clonal selection, acquisition of mutations and promoter hypomethylation por Joachim B. Kunz, Tobias Rausch, Obul Reddy Bandapalli, June Eilers, Paulina Richter‐Pechańska, S. Schuessele, Yassen Assenov, Adrian M. Stütz, Renate Kirschner‐Schwabe, Jana Hof, Cornelia Eckert, A von Stackelberg, M. Schrappe, M. Stanulla, Rolf Koehler, Smadar Avigad, Sarah Elitzur, Rupert Handgretinger, Vladimı́r Beneš, Joachim Weischenfeldt, Jan O. Korbel, Martina U. Muckenthaler, Andreas E. Kulozik
Publicado 2015Artigo -
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The activating STAT5B N642H mutation is a common abnormality in pediatric T-cell acute lymphoblastic leukemia and confers a higher risk of relapse por Obul Reddy Bandapalli, S. Schuessele, Joachim B. Kunz, Tobias Rausch, Adrian M. Stütz, Noam Tal, Ifat Geron, Nava Gershman, Shai Izraeli, June Eilers, Nina Vaezipour, Renate Kirschner‐Schwabe, Jana Hof, A von Stackelberg, Martin Schrappe, M. Stanulla, M Zimmermann, Rolf Koehler, S. Avigad, Rupert Handgretinger, Viktoras Frismantas, Jean‐Pierre Bourquin, Beat Bornhäuser, Jan O. Korbel, Martina U. Muckenthaler, A. E. Kulozik
Publicado 2014Carta -
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Assembly and diploid architecture of an individual human genome via single-molecule technologies por Matthew Pendleton, Robert Sebra, Andy Wing Chun Pang, Ajay Ummat, Oscar Franzén, Tobias Rausch, Adrian M. Stütz, William Stedman, Thomas Anantharaman, Alex Hastie, Dai Heng, Markus Hsi-Yang Fritz, Han Cao, Ariella Cohain, Gintaras Deikus, R. Durrett, Scott C. Blanchard, Russ B. Altman, Chen-Shan Chin, Yan Guo, Ellen E. Paxinos, Jan O. Korbel, Robert B. Darnell, W. Richard McCombie, Pui‐Yan Kwok, Christopher E. Mason, Eric E. Schadt, Ali Bashir
Publicado 2015Artigo -
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Pan-cancer analysis of somatic copy-number alterations implicates IRS4 and IGF2 in enhancer hijacking por Joachim Weischenfeldt, Taronish D. Dubash, Alexandros P. Drainas, Balca R. Mardin, Yuanyuan Chen, Adrian M. Stütz, Sebastian M. Waszak, Graziella Bosco, Ann Rita Halvorsen, Benjamin Raeder, Theocharis Efthymiopoulos, Serap Erkek, Christine Siegl, Hermann Brenner, Odd Terje Brustugun, Sebastian M. Dieter, Paul A. Northcott, Iver Petersen, Stefan M. Pfister, Martin Schneider, Steinar Solberg, Erik Thunissen, Wilko Weichert, Thomas Zichner, Roman K. Thomas, Martin Peifer, Åslaug Helland, Claudia R. Ball, Martin Jechlinger, Rocı́o Sotillo, Hanno Glimm, Jan O. Korbel
Publicado 2016Artigo -
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Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burden por Peter Peneder, Adrian M. Stütz, Didier Surdez, Manuela Krumbholz, S Semper, Mathieu Chicard, Nathan C. Sheffield, Gaëlle Pierron, Eve Lapouble, Marcus Tötzl, Bekir Ergüner, Daniele Barreca, André F. Rendeiro, Abbas Agaimy, Heidrun Boztug, Gernot Engstler, Michael Dworzak, Marie Bernkopf, Sabine Taschner‐Mandl, Inge M. Ambros, Ola Myklebost, Perrine Marec‐Bérard, Susan A. Burchill, Bernadette Brennan, Sandra J. Strauss, Jeremy Whelan, Gudrun Schleiermacher, Christiane Schaefer, Uta Dirksen, Caroline Hutter, Kjetil Boye, Peter F. Ambros, Olivier Delattre, Markus Metzler, Christoph Bock, Eleni M. Tomazou
Publicado 2021Artigo -
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Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations por Tobias Rausch, David Jones, Marc Zapatka, Adrian M. Stütz, Thomas Zichner, Joachim Weischenfeldt, Natalie Jäger, Marc Remke, David Shih, Paul A. Northcott, Elke Pfaff, Jelena Tica, Qi Wang, Luca Massimi, Hendrik Witt, Sebastian Bender, Sabrina Pleier, Huriye Cin, Cynthia Hawkins, Christian Beck, Andreas von Deimling, Volkmar Hans, Benedikt Brors, Roland Eils, Wolfram Scheurlen, Jonathon Blake, Vladimı́r Beneš, Andreas E. Kulozik, Olaf Witt, Dianna C. Martin, Cindy Zhang, Rinnat M. Porat, Diana M. Merino, Jonathan D. Wasserman, Nada Jabado, Adam M. Fontebasso, Lars Bullinger, Frank G. Rücker, Konstanze Döhner, Hartmut Döhner, Jan Köster, Jan J. Molenaar, Rogier Versteeg, Marcel Kool, Uri Tabori, David Malkin, Andrey Korshunov, Michael D. Taylor, Peter Lichter, Stefan M. Pfister, Jan O. Korbel
Publicado 2012Artigo -
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Integrative Genomic Analyses Reveal an Androgen-Driven Somatic Alteration Landscape in Early-Onset Prostate Cancer por Joachim Weischenfeldt, Ronald Simon, Lars Feuerbach, Karin Schlangen, Dieter Weichenhan, Sarah Minner, Daniela Wuttig, Hans-Jörg Warnatz, Henning Stehr, Tobias Rausch, Natalie Jäger, Lei Gu, Olga Bogatyrova, Adrian M. Stütz, Rainer Claus, Roland Eils, Roland Eils, Clarissa Gerhäuser, Po-Hsien Huang, Barbara Hutter, Rolf Kabbe, Christian Lawerenz, Sylwester Radomski, Cynthia C. Bartholomae, Maria Fälth, Stephan Gade, Manfred Schmidt, Nina Amschler, Thomas Haß, Rami Galal, Jovisa Gjoni, Ruprecht Kuner, Constance Baer, Sawinee Masser, Christof von Kalle, Thomas Zichner, Vladimı́r Beneš, Benjamin Raeder, Malte Mäder, Vyacheslav Amstislavskiy, Meryem Avci, Hans Lehrach, Dmitri Parkhomchuk, Marc Sultan, Lia Burkhardt, Markus Graefen, Hartwig Huland, Martina Kluth, Antje Krohn, Hüseyin Sirma, Laura Stumm, Stefan Steurer, Katharina Grupp, Holger Sültmann, Guido Sauter, Christoph Plass, Benedikt Brors, Marie-Laure Yaspo, Jan O. Korbel, Thorsten Schlomm
Publicado 2013Artigo -
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Molecular Evolution of Early-Onset Prostate Cancer Identifies Molecular Risk Markers and Clinical Trajectories por Clarissa Gerhäuser, Francesco Favero, Thomas S. Risch, Ronald Simon, Lars Feuerbach, Yassen Assenov, Doreen Heckmann, Nikos Sidiropoulos, Sebastian M. Waszak, Daniel Hübschmann, Alfonso Urbanucci, Etsehiwot G. Girma, Vladimir Kuryshev, Leszek J. Klimczak, Natalie Saini, Adrian M. Stütz, Dieter Weichenhan, Lisa-Marie Böttcher, Réka Tóth, J D Hendriksen, Christina Koop, Pavlo Lutsik, Sören Matzk, Hans-Jörg Warnatz, Vyacheslav Amstislavskiy, Clarissa Feuerstein, Benjamin Raeder, Olga Bogatyrova, Eva-Maria Schmitz, Claudia Hube‐Magg, Martina Kluth, Hartwig Huland, Markus Graefen, Chris Lawerenz, Gervaise H. Henry, Takafumi N. Yamaguchi, Alicia Malewska, Jan Meiners, Daniela Schilling, Eva Reisinger, Roland Eils, Matthias Schlesner, Douglas W. Strand, Robert G. Bristow, Paul C. Boutros, Christof von Kalle, Dmitry A. Gordenin, Holger Sültmann, Benedikt Brors, Guido Sauter, Christoph Plass, Marie-Laure Yaspo, Jan O. Korbel, Thorsten Schlomm, Joachim Weischenfeldt
Publicado 2018Artigo
Ferramentas de procura:
Materias Relacionadas
Biology
Genetics
Gene
Computational biology
Genome
Cancer research
Structural variation
Human genome
Copy-number variation
Cancer
Evolutionary biology
Genotype
DNA
DNA sequencing
Gene expression
Medicine
Medulloblastoma
Single-nucleotide polymorphism
1000 Genomes Project
Chromothripsis
DNA damage
Demography
Genome instability
Genomics
Mutation
Population
Sociology
Somatic cell
Transcription factor
Bioinformatics