Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Abnormalities and BCOR[original query] |
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Human gene copy number spectra analysis in congenital heart malformations. Physiological genomics 2012 Feb . Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME |
Clonal hematopoiesis in acquired aplastic anemia. Blood 2016 Apr . Ogawa Seis |
RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features. Leukemia 2016 May . Gaidzik V I, Teleanu V, Papaemmanuil E, Weber D, Paschka P, Hahn J, Wallrabenstein T, Kolbinger B, Köhne C-H, Horst H A, Brossart P, Held G, Kündgen A, Ringhoffer M, Götze K, Rummel M, Gerstung M, Campbell P, Kraus J M, Kestler H A, Thol F, Heuser M, Schlegelberger B, Ganser A, Bullinger L, Schlenk R F, Döhner K, Döhner |
Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes. PloS one 2016 11 (10): e0164370. Abáigar María, Robledo Cristina, Benito Rocío, Ramos Fernando, Díez-Campelo María, Hermosín Lourdes, Sánchez-Del-Real Javier, Alonso Jose M, Cuello Rebeca, Megido Marta, Rodríguez Juan N, Martín-Núñez Guillermo, Aguilar Carlos, Vargas Manuel, Martín Ana A, García Juan L, Kohlmann Alexander, Del Cañizo M Consuelo, Hernández-Rivas Jesús |
Genetic characterization of B-cell prolymphocytic leukemia: a prognostic model involving MYC and TP53. Blood 2019 9 134 (21): 1821-1831. Chapiro Elise, Pramil Elodie, Diop M'boyba, Roos-Weil Damien, Dillard Clémentine, Gabillaud Clémentine, Maloum Karim, Settegrana Catherine, Baseggio Lucile, Lesesve Jean-François, Yon Mélanie, Jondreville Ludovic, Lesty Claude, Davi Frédéric, Le Garff-Tavernier Magali, Droin Nathalie, Dessen Philippe, Algrin Caroline, Leblond Véronique, Gabarre Jean, Bouzy Simon, Eclache Virginie, Gaillard Baptiste, Callet-Bauchu Evelyne, Muller Marc, Lefebvre Christine, Nadal Nathalie, Ittel Antoine, Struski Stéphanie, Collonge-Rame Marie-Agnès, Quilichini Benoit, Fert-Ferrer Sandra, Auger Nathalie, Radford-Weiss Isabelle, Wagner Lena, Scheinost Sebastian, Zenz Thorsten, Susin Santos A, Bernard Olivier A, Nguyen-Khac Florence, , |
Loss-of-function mutations in BCOR contribute to chemotherapy resistance in acute myeloid leukemia. Experimental hematology 2021 8 101-102 42-48.e11. Honda Akira, Koya Junji, Yoshimi Akihide, Miyauchi Masashi, Taoka Kazuki, Kataoka Keisuke, Arai Shunya, Kurokawa Min |
Features and impacts on the prognosis of gene mutations in patients with acute myeloid leukemia. Neoplasma 2021 5 68 (5): 1072-1078. Wu Ming, Guo Zi-Wen, Huang Gui-Nian, Ye Yong-B |
Somatic Mutations and the Risk of Undifferentiated Autoinflammatory Disease in MDS: An Under-Recognized but Prognostically Important Complication. Frontiers in immunology 2021 3 12 610019. Watad Abdulla, Kacar Mark, Bragazzi Nicola Luigi, Zhou Qiao, Jassam Miriam, Taylor Jan, Roman Eve, Smith Alexandra, Jones Richard A, Amital Howard, Cargo Catherine, McGonagle Dennis, Savic Sini |
Predictors of clonal evolution and myeloid neoplasia following immunosuppressive therapy in severe aplastic anemia. Leukemia 2022 7 36 (9): 2328-2337. Groarke Emma M, Patel Bhavisha A, Shalhoub Ruba, Gutierrez-Rodrigues Fernanda, Desai Parth, Leuva Harshraj, Zaimoku Yoshitaka, Paton Casey, Spitofsky Nina, Lotter Jennifer, Rios Olga, Childs Richard W, Young David J, Dulau-Florea Alina, Dunbar Cynthia E, Calvo Katherine R, Wu Colin O, Young Neal |
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- Page last updated:Apr 22, 2024
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