Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Cody Coblentz"'
Autor:
Theodore P. Braun, Mariam Okhovat, Cody Coblentz, Sarah A. Carratt, Amy Foley, Zachary Schonrock, Brittany M. Smith, Kimberly Nevonen, Brett Davis, Brianna Garcia, Dorian LaTocha, Benjamin R. Weeder, Michal R. Grzadkowski, Joey C. Estabrook, Hannah G. Manning, Kevin Watanabe-Smith, Sophia Jeng, Jenny L. Smith, Amanda R. Leonti, Rhonda E. Ries, Shannon McWeeney, Cristina Di Genua, Roy Drissen, Claus Nerlov, Soheil Meshinchi, Lucia Carbone, Brian J. Druker, Julia E. Maxson
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
Acute Myeloid Leukemia (AML) develops following multiple mutations of differing impact. Here, the authors show that activating mutations of CSF3R co-operate with loss-of-function mutations of CEBPA to promote AML development through an enhancer-depen
Externí odkaz:
https://doaj.org/article/c4f5920cda714e2080bbc04d4c0c3d87
Autor:
Theodore P. Braun, Mariam Okhovat, Cody Coblentz, Sarah A. Carratt, Amy Foley, Zachary Schonrock, Brittany M. Curtiss, Kimberly Nevonen, Brett Davis, Brianna Garcia, Dorian LaTocha, Benjamin R. Weeder, Michal R. Grzadkowski, Joey C. Estabrook, Hannah G. Manning, Kevin Watanabe-Smith, Sophia Jeng, Jenny L. Smith, Amanda R. Leonti, Rhonda E. Ries, Shannon McWeeney, Cristina Di Genua, Roy Drissen, Claus Nerlov, Soheil Meshinchi, Lucia Carbone, Brian J. Druker, Julia E. Maxson
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/c3c2338ac9144f60aac72e27a406a213
RUNX1::ETO translocations must precede CSF3R mutations to promote acute myeloid leukemia development
Autor:
Sarah A. Carratt, Garth L. Kong, Cody Coblentz, Zachary Schonrock, Lauren Maloney, Ben Weeder, Will Yashar, Rowan Callahan, Hunter Blaylock, Colin Coleman, Dan Coleman, Theodore P. Braun, Julia E. Maxson
Publikováno v:
Leukemia. 37:1141-1146
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51ddd4b290c34c20a5564b2cc6d067bb
https://doi.org/10.1038/s41375-023-01862-8
https://doi.org/10.1038/s41375-023-01862-8
Autor:
Theodore P. Braun, Joseph Estabrook, Zachary Schonrock, Brittany M. Curtiss, Lucie Darmusey, Jommel Macaraeg, Trevor Enright, Cody Coblentz, Rowan Callahan, William Yashar, Akram Taherinasab, Hisham Mohammed, Daniel J. Coleman, Brian J. Druker, Emek Demir, Theresa A. Lusardi, Julia E. Maxson
Publikováno v:
Leukemia. 37:478-487
Mutations in the gene Additional Sex-Combs Like 1 (ASXL1) are recurrent in myeloid malignancies as well as the pre-malignant condition clonal hematopoiesis, where they are universally associated with poor prognosis. However, the role of ASXL1 in myel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9547834293d29eff46db9b2b292473ed
https://doi.org/10.1038/s41375-022-01792-x
https://doi.org/10.1038/s41375-022-01792-x
Autor:
Sarah A. Carratt, Theodore P. Braun, Cody Coblentz, Zachary Schonrock, Rowan Callahan, Brittany M. Curtiss, Lauren Maloney, Amy C. Foley, Julia E. Maxson
Publikováno v:
Leukemia.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abfadeffa4736a04bedd7606c3f80aca
https://doi.org/10.1038/s41375-022-01710-1
https://doi.org/10.1038/s41375-022-01710-1
Autor:
Daniel Bottomly, Nicola Long, Anna Reister Schultz, Stephen E. Kurtz, Cristina E. Tognon, Kara Johnson, Melissa Abel, Anupriya Agarwal, Sammantha Avaylan, Erik Benton, Aurora Blucher, Uma Borate, Theodore Braun, Jordana Brown, Jade Bryant, Russell Burke, Amy Carlos, Bill H. Chang, Hyun Jun Cho, Stephen Christy, Cody Coblentz, Aaron M. Cohen, Amanda d’Almeida, Rachel Cook, Alexey Danilov, Kim-Hien T. Dao, Michie Degnin, James Dibb, Christopher A. Eide, Isabel A. English, Stuart Hagler, Heath Harrelson, Rachel Henson, Hibery Ho, Sunil Joshi, Brian Junio, Andy Kaempf, Yoko Kosaka, Ted Laderas, Matt Lawhead, Hyunjung Lee, Jessica T. Leonard, Chenwei Lin, Evan F. Lind, Selina Qiuying Liu, Pierrette Lo, Marc M. Loriaux, Samuel Luty, Julia E. Maxson, Tara Macey, Jacqueline Martinez, Jessica Minnier, Andrea Monteblanco, Motomi Mori, Quinlan Morrow, Dylan Nelson, Justin Ramsdill, Angela Rofelty, Alexandra Rogers, Peter Ryabinin, Jennifer N. Saultz, David A. Sampson, Samantha L. Savage, Robert Schuff, Robert Searles, Rebecca L. Smith, Stephen E. Spurgeon, Tyler Sweeney, Ronan T. Swords, Aashis Thapa, Karina Thiel-Klare, Elie Traer, Jake Wagner, Beth Wilmot, Joelle Wolf, Guanming Wu, Amy Yates, Haijiao Zhang, Christopher Cogle, Robert H. Collins, Michael W. Deininger, Christopher S. Hourigan, Craig T. Jordan, Tara L. Lin, Micaela E. Martinez, Rachel R. Pallapati, Daniel Pollyea, Tony Pomicter, Justin M. Watts, Scott Weir, Brian J. Druker, Shannon K. McWeeney, Jeffrey W. Tyner
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cb02f596cf7945b6c746e259cdd2427
https://doi.org/10.2139/ssrn.4041405
https://doi.org/10.2139/ssrn.4041405
Autor:
Sarah A. Carratt, Theodore P. Braun, Cody Coblentz, Zachary Schonrock, Rowan Callahan, Brittany M. Curtiss, Lauren Maloney, Amy C. Foley, Julia E. Maxson
Publikováno v:
Leukemia. 36:2149-2149
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3af5a46329d9e0f0316a1eedd982d6c
https://doi.org/10.1038/s41375-022-01646-6
https://doi.org/10.1038/s41375-022-01646-6
Autor:
Julia E. Maxson, Sarah A. Carratt, Theodore P. Braun, Amy Foley, Rowan Callahan, Lauren Maloney, Brittany M. Smith, Zachary Schonrock, Cody Coblentz
Publikováno v:
Leukemia
Mutations in SET binding protein 1 (SETBP1) are associated with poor outcomes in myeloid leukemias. In the Ras-driven leukemia, juvenile myelomonocytic leukemia, SETBP1 mutations are enriched in relapsed disease. While some mechanisms for SETBP1-driv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45b5e09962f3e03021e66d7cc1f21dff
https://doi.org/10.1101/2021.02.01.429244
https://doi.org/10.1101/2021.02.01.429244
Autor:
Theodore P. Braun, Joseph Estabrook, Lucie Darmusey, Daniel J. Coleman, Zachary Schonrock, Brittany M. Smith, Akram Taherinasab, Trevor Enright, Cody Coblentz, William Yashar, Rowan Callahan, Hisham Mohammed, Brian J. Druker, Theresa A. Lusardi, Julia E. Maxson
Mutations in the gene Additional Sex-Combs Like 1 (ASXL1) are recurrent in myeloid malignancies as well as the pre-malignant condition clonal hematopoiesis, where they are universally associated with poor prognosis. An epigenetic regulator, ASXL1 can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::005680f5dbbfc348a2d188a4ccb6c9c5
https://doi.org/10.1101/2020.09.14.295295
https://doi.org/10.1101/2020.09.14.295295
Publikováno v:
Journal of Advances in Molecular Biology. 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1d217e44b238f6b69472dfd7c1ee30e
https://doi.org/10.22606/jamb.2020.42001
https://doi.org/10.22606/jamb.2020.42001