Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Juan E. Arango Ossa"'
Autor:
Teng Gao, Ryan Ptashkin, Kelly L. Bolton, Maria Sirenko, Christopher Fong, Barbara Spitzer, Kamal Menghrajani, Juan E. Arango Ossa, Yangyu Zhou, Elsa Bernard, Max Levine, Juan S. Medina Martinez, Yanming Zhang, Sebastià Franch-Expósito, Minal Patel, Lior Z. Braunstein, Daniel Kelly, Mariko Yabe, Ryma Benayed, Nicole M. Caltabellotta, John Philip, Ederlinda Paraiso, Simon Mantha, David B. Solit, Luis A. Diaz, Michael F. Berger, Virginia Klimek, Ross L. Levine, Ahmet Zehir, Sean M. Devlin, Elli Papaemmanuil
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-11 (2021)
Patients with solid cancers have high rates of clonal haematopoiesis associated with increased risk of secondary leukemias. Here, by using peripheral blood sequencing data from patients with solid non-hematologic cancer, the authors profile the lands
Externí odkaz:
https://doaj.org/article/86f1527efcbe4a8c928f5380279e4756
Autor:
Yanis Tazi, Juan E. Arango-Ossa, Yangyu Zhou, Elsa Bernard, Ian Thomas, Amanda Gilkes, Sylvie Freeman, Yoann Pradat, Sean J. Johnson, Robert Hills, Richard Dillon, Max F. Levine, Daniel Leongamornlert, Adam Butler, Arnold Ganser, Lars Bullinger, Konstanze Döhner, Oliver Ottmann, Richard Adams, Hartmut Döhner, Peter J. Campbell, Alan K. Burnett, Michael Dennis, Nigel H. Russell, Sean M. Devlin, Brian J. P. Huntly, Elli Papaemmanuil
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-16 (2022)
Classification and risk-stratification for Acute Myeloid Leukemia (AML) at diagnosis are primarily based on cytogenetics and only a few gene mutations. Here, the authors study the genomic landscape of 3653 AML patients and characterize 16 non-overlap
Externí odkaz:
https://doaj.org/article/f0c1b3c2c89c4431b1bfec535238074b
Autor:
Jesús Gutiérrez-Abril, Daniel Leongamornlert, Neerav N Shukla, Maria Luisa Sulis, Yangyu Zhou, Max F. Levine, Emilio Barretta, SooWah Lee, Juan E. Arango-Ossa, Gunes Gundem, Juan S. Medina-Martínez, Bela Patel Wrench, Anthony V. Moorman, Adele K. Fielding, Andrew L. Kung, Elli Papaemmanuil
Publikováno v:
Blood. 140:1197-1199
Autor:
Kurt S. Bantilan, Kayleigh Rutherford, Joseph McCarter, Noushin Farnoud, Juan E. Arango-Ossa, Elli Papaemmanuil, Andrew D. Zelenetz
Publikováno v:
Blood. 140:3635-3637
Autor:
Elli Papaemmanuil, Nai Kong V. Cheung, Scott A. Armstrong, Ross L. Levine, Ahmet Zehir, Andrew L. Kung, Shakeel Modak, Brian H. Kushner, Maria E. Arcilla, Kety H. Huberman, Neeman Mohibullah, Cassidy C. Cobbs, Georgios Asimomitis, Minal A. Patel, Yangyu Zhou, Noushin Farnoud, Kelly L. Bolton, Ryan N. Ptashkin, Yi Feng, Juan S. Medina-Martínez, Yanming Zhang, Max F. Levine, Teng Gao, Irene Y. Cheung, Juan E. Arango Ossa, Nathan E. Millard, Erin M. McGovern, Gunes Gundem, Kayleigh D. Rutherford, Barbara Spitzer
Supplementary Data from Bone Marrow Surveillance of Pediatric Cancer Survivors Identifies Clones that Predict Therapy-Related Leukemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f498730950610964fb8c950585b0bbe
https://doi.org/10.1158/1078-0432.22481987.v1
https://doi.org/10.1158/1078-0432.22481987.v1
Autor:
Elli Papaemmanuil, Nai Kong V. Cheung, Scott A. Armstrong, Ross L. Levine, Ahmet Zehir, Andrew L. Kung, Shakeel Modak, Brian H. Kushner, Maria E. Arcilla, Kety H. Huberman, Neeman Mohibullah, Cassidy C. Cobbs, Georgios Asimomitis, Minal A. Patel, Yangyu Zhou, Noushin Farnoud, Kelly L. Bolton, Ryan N. Ptashkin, Yi Feng, Juan S. Medina-Martínez, Yanming Zhang, Max F. Levine, Teng Gao, Irene Y. Cheung, Juan E. Arango Ossa, Nathan E. Millard, Erin M. McGovern, Gunes Gundem, Kayleigh D. Rutherford, Barbara Spitzer
Supplementary Figure from Bone Marrow Surveillance of Pediatric Cancer Survivors Identifies Clones that Predict Therapy-Related Leukemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04c2fbac70b9b018d7b324fcd0b7264d
https://doi.org/10.1158/1078-0432.22481963
https://doi.org/10.1158/1078-0432.22481963
Autor:
Michael D. Kinnaman, Simone Zaccaria, Alvin Makohon-Moore, Brian Arnold, Max Levine, Gunes Gundem, Juan E. Arango Ossa, Dominik Glodzik, M. Irene Rodríguez-Sánchez, Nancy Bouvier, Shanita Li, Emily Stockfisch, Marisa Dunigan, Cassidy Cobbs, Umesh Bhanot, Daoqi You, Katelyn Mullen, Jerry Melchor, Michael V. Ortiz, Tara O’Donohue, Emily Slotkin, Leonard H. Wexler, Filemon S. Dela Cruz, Meera Hameed, Julia L. Glade Bender, William D. Tap, Paul A. Meyers, Elli Papaemmanuil, Andrew L. Kung, Christine A Iacobuzio-Donahue
Publikováno v:
bioRxiv
Multiple large-scale tumor genomic profiling efforts have been undertaken in osteosarcoma, however, little is known about the spatial and temporal intratumor heterogeneity and how it may drive treatment resistance. We performed whole-genome sequencin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::842580c63e2a605b39383fb19c2db973
https://doi.org/10.1101/2023.01.05.522765
https://doi.org/10.1101/2023.01.05.522765
Autor:
Gunes Gundem, Max F. Levine, Stephen S. Roberts, Irene Y. Cheung, Juan S. Medina-Martínez, Yi Feng, Juan E. Arango-Ossa, Loic Chadoutaud, Mathieu Rita, Georgios Asimomitis, Joe Zhou, Daoqi You, Nancy Bouvier, Barbara Spitzer, David B. Solit, Filemon Dela Cruz, Michael P. LaQuaglia, Brian H. Kushner, Shakeel Modak, Neerav Shukla, Christine A. Iacobuzio-Donahue, Andrew L. Kung, Nai-Kong V. Cheung, Elli Papaemmanuil
High-risk neuroblastoma is generally metastatic and often lethal. Using genomic profiling of 470 sequential and spatially separated samples from 283 patients, we characterize subtype-specific genetic evolutionary trajectories from diagnosis, through
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c93721c40b8e6e26b4ff6a26d4233ef
https://doi.org/10.1101/2022.08.15.503973
https://doi.org/10.1101/2022.08.15.503973
Autor:
Michael David Kinnaman, Simone Zaccaria, Alvin Makohon-Moore, Gunes Gundem, Juan E. Arango Ossa, Filemon S. Dela Cruz, Paul A. Meyers, Meera Hameed, William D. Tap, Julia Lynne Glade Bender, Elli Papaemmanuil, Andrew Kung, Christine Iacobuzio Donahue
Publikováno v:
Cancer Research. 83:3556-3556
Objective: The osteosarcoma genome is characterized by high levels of genomic instability, however whether there is pervasive ongoing genomic instability, or instability introduced by an early catastrophic event, is still unsettled. Methods: We perfo
Autor:
Elsa Bernard, Juan E. Arango Ossa, Heinz Tuechler, Peter L. Greenberg, Robert P. Hasserjian, Yasuhito Nannya, Sean M. Devlin, Maria Creignou, Philippe Pinel, Lily Monier, Juan S. Medina-Martinez, Dylan Domenico, Martin Jädersten, Ulrich Germing, Guillermo Sanz, Arjan A. van de Loosdrecht, Olivier Kosmider, Matilde Y. Follo, Felicitas Thol, Lurdes Zamora, Ronald F. Pinheiro, Andrea Pellagatti, Detlef Haase, Pierre Fenaux, Monika Belickova, Michael R. Savona, Virginia M. Klimek, Fabio P. Santos, Jacqueline Boultwood, Ioannis Kotsianidis, Valeria Santini, Francesc Solé, Uwe Platzbecker, Michael Heuser, Peter Valent, Kazuma Ohyashiki, Carlo Finelli, Maria Teresa Voso, Lee-Yung Shih, Michaela Fontenay, Joop H. Jansen, José Cervera, Norbert Gattermann, Benjamin L. Ebert, Rafael Bejar, Luca Malcovati, Mario Cazzola, Seishi Ogawa, Eva Hellström-Lindberg, Elli Papaemmanuil
Publikováno v:
Cancer Research. 83:6168-6168
Despite a detailed understanding of the genes mutated in myelodysplastic syndromes (MDS), diagnostic and treatment decisions for patients with MDS rely primarily on clinical and cytogenetic variables as considered by the Revised International Prognos