Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Ellen Muir"'
Autor:
Zi Yang Kang, Ellen Muir
Publikováno v:
Proceedings of the 23rd ACM Conference on Economics and Computation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8b8663938ca6207c8aaed2d5040ccc9
https://doi.org/10.1145/3490486.3538260
https://doi.org/10.1145/3490486.3538260
Autor:
Simon Loertscher, Ellen Muir
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b23b352f6c21455a66601290aca86003
https://doi.org/10.2139/ssrn.4153370
https://doi.org/10.2139/ssrn.4153370
Autor:
Jason E. Farrar, Anupama Narla, Kelly Walkovich, Helge Hartung, Grzegorz Nalepa, Adrianna Vlachos, Evangelia Atsidaftos, Jeffrey M. Lipton, Mohammad Lutfi Lababidi, Jonathan Bernstein, Ellen Muir, Zora R. Rogers, Thomas W. Loew, Waseem Alhushki, Colin A. Sieff, Bertil Glader, Barbara Gruner, Christine M. Knoll, Arun R Panigrahi
Publikováno v:
Pediatr Blood Cancer
Background Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome characterized by anemia, short stature, congenital anomalies, and cancer predisposition. Most cases are due to mutations in genes encoding ribosomal proteins (RP) l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f35da0422ca685604b2d6c0cfaafb63
https://europepmc.org/articles/PMC8273758/
https://europepmc.org/articles/PMC8273758/
Diminutive somatic deletions in the 5q region lead to a phenotype atypical of classical 5q− syndrome
Autor:
Eva Atsidaftos, Michael Landowski, Anupama Narla, Johnson M. Liu, Robert J. Arceci, Jeffrey M. Lipton, Thomas C. Markello, Sharon A. Singh, Adrianna Vlachos, Ellen Muir, Steven R. Ellis, Hanna T. Gazda, Lionel Blanc, David M. Bodine, Jason E. Farrar, Benjamin L. Ebert
Publikováno v:
Blood. 122:2487-2490
Classical 5q- syndrome is an acquired macrocytic anemia of the elderly. Similar to Diamond Blackfan anemia (DBA), an inherited red cell aplasia, the bone marrow is characterized by a paucity of erythroid precursors. RPS14 deletions in combination wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67b44f943b6bba120bed2b47692d36b7
https://doi.org/10.1182/blood-2013-06-509935
https://doi.org/10.1182/blood-2013-06-509935
Autor:
Barbara Gruner, Kelly Walkovich, Christine M. Knoll, Mohammad Lufti Lababidi, Jason E. Farrar, Anupama Narla, Helge Hartung, Zora R. Rogers, Waseem Alhushki, Evangelia Atsidaftos, Ellen Muir, Bertil Glader, Arun R Panigrahi, Colin A. Sieff, Jeffrey M. Lipton, Adrianna Vlachos, Grzegorz Nalepa
Publikováno v:
Blood. 132:755-755
Diamond Blackfan anemia (DBA) is a rare, inherited bone marrow failure syndrome characterized by anemia, congenital anomalies and a predisposition to cancer. The patients usually present during infancy or early childhood, but can also present in adul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b29c4e5bf0f45033599eb182f40142b5
https://doi.org/10.1182/blood-2018-99-113570
https://doi.org/10.1182/blood-2018-99-113570
Autor:
Ellen Muir, Adrianna Vlachos
Diamond-Blackfan anemia (DBA) is characterized by red cell failure, the presence of congenital anomalies, and cancer predisposition. In addition to being an inherited bone marrow failure syndrome, DBA is also categorized as a ribosomopathy as, in mor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15902d9740f79f20b649ad0175d73d26
https://europepmc.org/articles/PMC2981532/
https://europepmc.org/articles/PMC2981532/
Autor:
Jeffrey M. Lipton, Hanna T. Gazda, David M. Bodine, Ellen Muir, Michael Landowski, Lionel Blanc, Benjamin L. Ebert, Thomas C. Markello, Adrianna Vlachos, Anupama Narla, Steven R. Ellis, Eva Atsidaftos, Jason E. Farrar, Sharon A. Singh, Robert J. Arceci, J.M. Liu
Publikováno v:
Leukemia Research. 37:S59
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae10b57bf4d5273fad15c72b8a1ef86e
https://doi.org/10.1016/s0145-2126(13)70132-2
https://doi.org/10.1016/s0145-2126(13)70132-2
Autor:
Sharon A. Singh, Jason E. Farrar, Robert J. Arceci, Ellen Muir, Adrianna Vlachos, Steven R. Ellis, David M. Bodine, Jeffrey M. Lipton, Johnson M. Liu, Thomas C. Markello, Eva Atsidaftos
Publikováno v:
Blood. 116:4430-4430
Abstract 4430 Background: Diamond Blackfan anemia is a rare heritable red cell aplasia which usually presents in infancy but can also be diagnosed in childhood and even adulthood. Mutations or deletions in eleven ribosomal protein (RP) genes, resulti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f690b9ee405f319070b6e3a20650f57b
https://doi.org/10.1182/blood.v116.21.4430.4430
https://doi.org/10.1182/blood.v116.21.4430.4430
Autor:
Robert J. Arceci, Adrianna Vlachos, Steven R. Ellis, Jason E. Farrar, Johnson M. Liu, Thomas C. Markello, Ellen Muir, Sharon A. Singh, Eva Atsidaftos, David M. Bodine, Jeffrey M. Lipton
Publikováno v:
Blood. 116:LBA-2
Abstract LBA-2 Background: 5q- myelodysplastic syndrome is a rare, acquired macrocytic anemia with a female predominance. The bone marrow is characterized by a paucity of erythroid precursors with relatively normal leukocyte and platelet counts and n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4bd62ab6c21e5b2a1f225a719cd1495
https://doi.org/10.1182/blood.v116.21.lba-2.lba-2
https://doi.org/10.1182/blood.v116.21.lba-2.lba-2
Autor:
Loertscher, Simon, Marx, Leslie M.
Publikováno v:
In Games and Economic Behavior January 2023 137:68-90