Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Adrianna Vlachos"'
Autor:
Akiko Shimamura, Alexey Maschan, Carolyn Bennett, Jason E Farrar, Sujith Samarasinghe, Brigitte Strahm, Winfred C. Wang, Adrianna Vlachos, Charlotte M. Niemeyer, Timothy S. Olson, Denise D'Alessio, Elise Burmeister Getz, Tomasz Lawniczek, Yunnan Xu, David A. Williams
Publikováno v:
Blood. 140:705-707
Autor:
Ravi Sharaf, Blanche P. Alter, Philip S. Rosenberg, Kenan Onel, Adrianna Vlachos, Eva Atsidaftos, Jeffrey M. Lipton, Jessica Kang
Publikováno v:
Blood. 132:2205-2208
TO THE EDITOR: Inherited bone marrow failure syndromes (IBMFSs), characterized by bone marrow failure and developmental anomalies, are among a group of rare cancer predisposition syndromes. As illustrated by Fanconi anemia (FA),[1][1] the unique biol
Autor:
Stanley R Clarke, Jens Lichtenberg, Adam M. Phillippy, Jaya Jagadeesh, Nancy E. Seidel, Irma Dianzani, Nisc Comparative SequencingProgram, Steven R. Ellis, Jason E. Farrar, Adrianna Vlachos, Jeffrey M. Lipton, David M. Bodine
Publikováno v:
Blood. 138:863-863
Diamond Blackfan anemia syndrome (DBAS) is a rare, heritable bone marrow failure syndrome characterized by severe macrocytic anemia, congenital anomalies and predisposition to cancer, most often diagnosed during infancy. More than 98% of DBAS patient
Autor:
Taizo A. Nakano, Adrianna Vlachos, Maggie Malsch, Alyssa L. Kennedy, Shanshan Liu, David C. Dale, James A. Connelly, Nicholas D. Camarda, James Bowman, Nobuko Hijiya, Akiko Shimamura, R. Coleman Lindsley, Edie Weller, Scott L. Carter, Jeffrey H. Lipton, Kelly Walkovich, Inga Hofmann, Chad E. Harris, Robert Klein, Sioban Keel, Steffen Boettcher, John M. Gansner, Christian Brendel, James N. Huang, Kasiani C. Myers, Wendy Stock, Chris Bahl, Adam J. Lamble, Elissa M. Furutani, Maxim Norkin, Alison A. Bertuch, Ashley Galvin, Bonnie W. Lau, Christopher J. Gibson, Gwen M. Muscato, Richard H. Ho, Mark D. Fleming, Kaitlyn Ballotti, John R. Edwards, Stella M. Davies, Elliot Stieglitz, Paul Castillo
Publikováno v:
Blood. 136:35-36
Background: Shwachman-Diamond Syndrome (SDS) is a bone marrow failure disorder caused by impaired removal of EIF6 from the nascent 60S ribosome subunit, resulting in defective ribosome assembly. SDS patients have a high risk of myeloid neoplasms (MN)
Publikováno v:
Blood. 136:25-26
Background: Diamond Blackfan anemia (DBA) is a rare inherited bone marrow failure syndrome characterized by anemia, congenital anomalies and a predisposition to cancer. Patients usually present during infancy or early childhood, but can also be diagn
Autor:
Adrianna Vlachos, G. Jayashree Jagadeesh, John G. Conboy, Nancy E. Seidel, David M. Bodine, Lionel Blanc, Jeffrey M. Lipton, Jessica Kang, Jason E. Farrar, Nisc Comparative SequencingProgram, Steven R. Ellis, Evangelia Atsidaftos, Jens Lichtenberg
Publikováno v:
Blood. 134:2502-2502
Diamond Blackfan Anemia Syndrome (DBA) is a rare, congenital bone marrow failure syndrome characterized by severe macrocytic anemia, most often diagnosed during infancy. Congenital anomalies and predisposition to cancer are also important features of
Autor:
Julien Papoin, Meagan E. Olive, Naomi Taylor, Ryan Ashley, Hongxia Yan, Brian M. Dulmovits, Christopher D. Hillyer, Nan Wang, Lydie Da Costa, Steven A. Carr, Namrata D. Udeshi, Jeffrey M. Lipton, Anupama Narla, Adrianna Vlachos, Lionel Blanc, Sandrina Kinet, Mohandas Narla, John Hale
Publikováno v:
Blood. 134:943-943
Glucocorticoids are widely used to increase red cell production in a number of hematological disorders including Diamond Blackfan anemia (DBA). Despite their clinical effectiveness we do not fully understand the mechanistic basis for the regulation o
Autor:
Audrey Anna Bolyard, David C. Dale, Matthew Rm Jotte, Laurence A. Boxer, Jun Xia, Robert S. Fulton, Amrita Ramesh, Adrianna Vlachos, Kasiani C. Myers, Megan A. Cooper, Vahagn Makaryan, Alison A. Bertuch, Jack Baty, Kelly Walkovich, Robert J. Rothbaum, Daniel C. Link, Akiko Shimamura, Christopher A. Miller, Mary C. Dinauer, Tiphanie P. Vogel, David B. Wilson
Publikováno v:
Blood. 131(4)
Severe congenital neutropenia (SCN) and Shwachman-Diamond syndrome (SDS) are congenital neutropenia syndromes with a high rate of leukemic transformation. Hematopoietic stressors may contribute to leukemic transformation by increasing the mutation ra
Autor:
Kelly A. O'Brien, Crystiana A. Tsujiura, David M. Bodine, Adrianna Vlachos, Abdel G. Elkahloun, Xiuli An, Lionel Blanc, Eva Atsidaftos, Steven R. Ellis, Jens Lichtenberg, Jason E. Farrar, Jeffrey M. Lipton, Stacie M. Anderson
Publikováno v:
Blood. 129(23)
Diamond-Blackfan anemia (DBA) is a congenital bone marrow failure syndrome characterized by erythroid hypoplasia, usually without perturbation of other hematopoietic lineages. Approximately 65% of DBA patients with autosomal dominant inheritance have
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