HuGE Literature Finder
Records 1-9
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Impact of somatic mutations in myelodysplastic patients with isolated partial or total loss of chromosome 7.
Leukemia 2020 Feb . Crisà Elena, Kulasekararaj Austin G, Adema Vera, Such Esperanza, Schanz Julie, Haase Detlef, Shirneshan Katayoon, Best Steven, Mian Syed A, Kizilors Aytug, Cervera José, Lea Nicholas, Ferrero Dario, Germing Ulrich, Hildebrandt Barbara, Martínez Ana Belén Valencia, Santini Valeria, Sanz Guillermo F, Solé Francesc, Mufti Ghulam |
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Homogeneously staining region (hsr) on chromosome 11 is highly specific for KMT2A amplification in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS).
Cancer genetics 2019 Jul 238 18-22. Sakhdari Ali, Tang Zhenya, Ok Chi Young, Bueso-Ramos Carlos E, Medeiros L Jeffrey, Huh Yang |
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TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups.
Leukemia 2019 Jan . Haase Detlef, Stevenson Kristen E, Neuberg Donna, Maciejewski Jaroslaw P, Nazha Aziz, Sekeres Mikkael A, Ebert Benjamin L, Garcia-Manero Guillermo, Haferlach Claudia, Haferlach Torsten, Kern Wolfgang, Ogawa Seishi, Nagata Yasunobu, Yoshida Kenichi, Graubert Timothy A, Walter Matthew J, List Alan F, Komrokji Rami S, Padron Eric, Sallman David, Papaemmanuil Elli, Campbell Peter J, Savona Michael R, Seegmiller Adam, Adès Lionel, Fenaux Pierre, Shih Lee-Yung, Bowen David, Groves Michael J, Tauro Sudhir, Fontenay Michaela, Kosmider Olivier, Bar-Natan Michal, Steensma David, Stone Richard, Heuser Michael, Thol Felicitas, Cazzola Mario, Malcovati Luca, Karsan Aly, Ganster Christina, Hellström-Lindberg Eva, Boultwood Jacqueline, Pellagatti Andrea, Santini Valeria, Quek Lynn, Vyas Paresh, Tüchler Heinz, Greenberg Peter L, Bejar Rafael, |
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Granular cell astrocytoma: an aggressive IDH-wildtype diffuse gliomarwith molecular genetic features of primary glioblastoma.
Brain pathology (Zurich, Switzerland) 2018 Sep . Vizcaino M Adelita, Palsgrove Doreen N, Yuan Ming, Giannini Caterina, Cabrera-Aldana Eibar Ernesto, Pallavajjala Aparna, Burger Peter C, Rodriguez Fausto |
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Chromothripsis 18 in multiple myeloma patient with rapid extramedullary relapse.
Molecular cytogenetics 2018 11 7. Smetana Jan, Oppelt Jan, Štork Martin, Pour Lud?k, Kuglík Pe |
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"Double-hit" chronic lymphocytic leukemia: An aggressive subgroup with 17p deletion and 8q24 gain.
American journal of hematology 2017 Dec . Chapiro Elise, Lesty Claude, Gabillaud Clémentine, Durot Eric, Bouzy Simon, Armand Marine, Le Garff-Tavernier Magali, Bougacha Nadia, Struski Stéphanie, Bidet Audrey, Laharanne Elodie, Barin Carole, Veronese Lauren, Prié Nolwen, Eclache Virginie, Gaillard Baptiste, Michaux Lucienne, Lefebvre Christine, Gaillard Jean-Baptiste, Terré Christine, Penther Dominique, Bastard Christian, Nadal Nathalie, Fert-Ferrer Sandra, Auger Nathalie, Godon Catherine, Sutton Laurent, Tournilhac Olivier, Susin Santos A, Nguyen-Khac Florence, |
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Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93%.
Genes, chromosomes & cancer 2014 Jun 53 (6): 524-36. Mühlbacher Verena, Zenger Melanie, Schnittger Susanne, Weissmann Sandra, Kunze Franziska, Kohlmann Alexander, Bellos Frauke, Kern Wolfgang, Haferlach Torsten, Haferlach Claud |
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Association of the type of 5q loss with complex karyotype, clonal evolution, TP53 mutation status, and prognosis in acute myeloid leukemia and myelodysplastic syndrome.
Genes, chromosomes & cancer 2014 May 53 (5): 402-10. Volkert Sarah, Kohlmann Alexander, Schnittger Susanne, Kern Wolfgang, Haferlach Torsten, Haferlach Claud |
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Somatic changes in primary liver cancer in Russia: a pilot study.
Mutation research 2013 Aug 755 (2): 90-9. Kalinina Olga, Marchio Agnès, Urbanskii Aleksandr I, Tarkova Aleksandra B, Rebbani Khadija, Granov Dmitri A, Dejean Anne, Generalov Mikhail I, Pineau Pasc |
- Page last reviewed:Mar 16, 2019
- Page last updated:Apr 10, 2020
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