Zobrazeno 1 - 10
of 2 414
pro vyhledávání: '"Lebrecht, A."'
Autor:
Deitke, Matt, Clark, Christopher, Lee, Sangho, Tripathi, Rohun, Yang, Yue, Park, Jae Sung, Salehi, Mohammadreza, Muennighoff, Niklas, Lo, Kyle, Soldaini, Luca, Lu, Jiasen, Anderson, Taira, Bransom, Erin, Ehsani, Kiana, Ngo, Huong, Chen, YenSung, Patel, Ajay, Yatskar, Mark, Callison-Burch, Chris, Head, Andrew, Hendrix, Rose, Bastani, Favyen, VanderBilt, Eli, Lambert, Nathan, Chou, Yvonne, Chheda, Arnavi, Sparks, Jenna, Skjonsberg, Sam, Schmitz, Michael, Sarnat, Aaron, Bischoff, Byron, Walsh, Pete, Newell, Chris, Wolters, Piper, Gupta, Tanmay, Zeng, Kuo-Hao, Borchardt, Jon, Groeneveld, Dirk, Dumas, Jen, Nam, Crystal, Lebrecht, Sophie, Wittlif, Caitlin, Schoenick, Carissa, Michel, Oscar, Krishna, Ranjay, Weihs, Luca, Smith, Noah A., Hajishirzi, Hannaneh, Girshick, Ross, Farhadi, Ali, Kembhavi, Aniruddha
Today's most advanced multimodal models remain proprietary. The strongest open-weight models rely heavily on synthetic data from proprietary VLMs to achieve good performance, effectively distilling these closed models into open ones. As a result, the
Externí odkaz:
http://arxiv.org/abs/2409.17146
Autor:
Ina Shehaj, Slavomir Krajnak, Katrin Almstedt, Yaman Degirmenci, Sophia Herzog, Antje Lebrecht, Valerie Catherine Linz, Roxana Schwab, Kathrin Stewen, Walburgis Brenner, Annette Hasenburg, Marcus Schmidt, Anne-Sophie Heimes
Publikováno v:
Biomedicines, Vol 12, Iss 6, p 1361 (2024)
Breast cancer (BC) poses a challenge in establishing new treatment strategies and identifying new prognostic and predictive markers due to the extensive genetic heterogeneity of BC. Very few studies have investigated the impact of mRNA expression of
Externí odkaz:
https://doaj.org/article/436bd216dafe4472bd66a3ed096dbda2
Publikováno v:
Phys. Rev. E 104, 014101 (2021)
Numerical simulations and finite-size scaling analysis have been carried out to study standard and inverse percolation of straight rigid rods on triangular lattices. In the case of standard (inverse) percolation, the lattice is initially empty(occupi
Externí odkaz:
http://arxiv.org/abs/2009.10234
Autor:
Mark Hartmann, Maximilian Schönung, Jovana Rajak, Joschka Hey, Valentin Maurer, Ling Hai, Sina Staeble, Jens Langstein, Katharina Bauer, Mariam Hakobyan, Laura Jardine, Sheila Bohler, Dominik Vonficht, Abdul-Habib Maag, Dirk Lebrecht, Katrin M. Bernt, Roland Roelz, Tobias Boch, Eleonora Khabirova, Pavlo Lutsik, Simon Haas, Muzlifah Haniffa, Sam Behjati, Jan-Philipp Mallm, Christian Buske, Michael D. Milsom, Stefan Fröhling, Marc-Jan Bonder, Charlotte Niemeyer, Christian Flotho, Christoph Plass, Miriam Erlacher, Matthias Schlesner, Daniel B. Lipka
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100065- (2023)
Externí odkaz:
https://doaj.org/article/68216411f6d742b0ab953c26f0a2b99c
Autor:
Foued Ghanjati, Miriam Erlacher, Dirk Lebrecht, Peter Nöllke, Franco Locatelli, European Working Group Of Myelodysplastic Syndromes In Childhood, Charlotte Niemeyer, Christian Flotho
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100064- (2023)
Externí odkaz:
https://doaj.org/article/26bd82afd33a45d39c5b1819b7ebb80f
Autor:
Foued Ghanjati, Annika Heck, Dirk Lebrecht, Peter Nöllke, Zoé Wehbe, Felicia Andresen, Natalia Rotari, Maximilian Schönung, Daniel Lipka, Miriam Erlacher, European Working Group Of Myelodysplastic Syndromes In Childhood, Charlotte Niemeyer, Christian Flotho
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100072- (2023)
Externí odkaz:
https://doaj.org/article/29526c501c7c433f866d581c05230605
Akademický článek
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Akademický článek
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Autor:
Miriam Erlacher, Felicia Andresen, Martina Sukova, Jan Stary, Barbara de Moerloose, Jutte van der Werff Ten Bosch, Michael Dworzak, Markus G. Seidel, Sophia Polychronopoulou, Rita Beier, Christian P. Kratz, Michaela Nathrath, Michael C. Frühwald, Gudrun Göhring, Anke K. Bergmann, Christina Mayerhofer, Dirk Lebrecht, Senthilkumar Ramamoorthy, Ayami Yoshimi, Brigitte Strahm, Marcin W. Wlodarski, Charlotte M. Niemeyer
Publikováno v:
Haematologica, Vol 109, Iss 2 (2023)
Monosomy 7 is the most common cytogenetic abnormality in pediatric myelodysplastic syndrome (MDS) and associated with a high risk of disease progression. However, in young children, spontaneous loss of monosomy 7 with concomitant hematologic recovery
Externí odkaz:
https://doaj.org/article/6e53529cf46a4b9fadc250cce7c36618
Autor:
Mark Hartmann, Maximilian Schönung, Jovana Rajak, Joschka Hey, Valentin Maurer, Ling Hai, Sina Staeble, Jens Langstein, Katharina Bauer, Mariam Hakobyan, Laura Jardine, Sheila Bohler, Dominik Vonficht, Abdul-Habib Maag, Dirk Lebrecht, Kathrin Bernt, Roland Rölz, Tobias Boch, Eleonora Khabirova, Pavlo Lutsik, Simon Haas, Muzlifah Haniffa, Sam Behjati, Jan-Philipp Mallm, Christian Buske, Michael Milsom, Stefan Fröhling, Marc-Jan Bonder, Christoph Plass, Charlotte Niemeyer, Christian Flotho, Miriam Erlacher, Matthias Schlesner, Daniel B. Lipka
Publikováno v:
HemaSphere, Vol 7, p e3927398 (2023)
Externí odkaz:
https://doaj.org/article/afeb359dd3394d38959eabffc025db6c