Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Neutropenia and RUNX1[original query] |
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A variant allele of Growth Factor Independence 1 (GFI1) is associated with acute myeloid leukemia. Blood 2010 Mar 115 (12): 2462-72. Khandanpour Cyrus, Thiede Christian, Valk Peter J M, Sharif-Askari Ehssan, Nückel Holger, Lohmann Dietmar, Horsthemke Bernhard, Siffert Winfried, Neubauer Andreas, Grzeschik Karl-Heinz, Bloomfield Clara D, Marcucci Guido, Maharry Kati, Slovak Marilyn L, van der Reijden Bert A, Jansen Joop H, Schackert Hans K, Afshar Khashayar, Schnittger Susanne, Peeters Justine K, Kroschinsky Frank, Ehninger Gerhard, Lowenberg Bob, Dührsen Ulrich, Möröy Tar |
Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis. Blood 2014 Apr 123 (14): 2229-37. Skokowa Julia, Steinemann Doris, Katsman-Kuipers Jenny E, Zeidler Cornelia, Klimenkova Olga, Klimiankou Maksim, Unalan Murat, Kandabarau Siarhei, Makaryan Vahagn, Beekman Renee, Behrens Kira, Stocking Carol, Obenauer Julia, Schnittger Susanne, Kohlmann Alexander, Valkhof Marijke G, Hoogenboezem Remco, Göhring Gudrun, Reinhardt Dirk, Schlegelberger Brigitte, Stanulla Martin, Vandenberghe Peter, Donadieu Jean, Zwaan C Michel, Touw Ivo P, van den Heuvel-Eibrink Marry M, Dale David C, Welte Ka |
A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome. Aging clinical and experimental research 2020 9 33 (7): 1987-1992. Ferrari Silvia, Regazzo Daniela, Omenetto Elisabetta, Scaroni Carla, Semenzato Gianpietro, Fabris Fabrizio, Vianello Fabriz |
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- Page last updated:Apr 16, 2024
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