Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Syndrome and CSF3R[original query] |
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Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G6PC3 in patients with severe congenital neutropenia. British journal of haematology 2009 Nov 147 (4): 535-42. Xia Jun, Bolyard Audrey A, Rodger Elin, Stein Steve, Aprikyan Andrew A, Dale David C, Link Daniel |
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 |
Short telomere length and its correlation with gene mutations in myelodysplastic syndrome. Journal of hematology & oncology 2016 9 (1): 62. Hwang Sang Mee, Kim Seon Young, Kim Jung Ah, Park Hee-Sue, Park Si Nae, Im Kyongok, Kim Kwantae, Kim Sung-Min, Lee Dong So |
Role of CSF3R mutations in the pathomechanism of congenital neutropenia and secondary acute myeloid leukemia. Annals of the New York Academy of Sciences 2016 Apr 1370 (1): 119-25. Klimiankou Maksim, Mellor-Heineke Sabine, Zeidler Cornelia, Welte Karl, Skokowa Jul |
Somatic mutations and clonal hematopoiesis in congenital neutropenia. Blood 2017 11 131 (4): 408-416. Xia Jun, Miller Christopher A, Baty Jack, Ramesh Amrita, Jotte Matthew R M, Fulton Robert S, Vogel Tiphanie P, Cooper Megan A, Walkovich Kelly J, Makaryan Vahagn, Bolyard Audrey A, Dinauer Mary C, Wilson David B, Vlachos Adrianna, Myers Kasiani C, Rothbaum Robert J, Bertuch Alison A, Dale David C, Shimamura Akiko, Boxer Laurence A, Link Daniel |
Idiopathic hypereosinophilia is clonal disorder? Clonality identified by targeted sequencing. PloS one 2017 12 (10): e0185602. Lee Jee-Soo, Seo Heewon, Im Kyongok, Park Si Nae, Kim Sung-Min, Lee Eun Kyoung, Kim Jung-Ah, Lee Joon-Hee, Kwon Sunghoon, Kim Miyoung, Koh Insong, Hwang Seungwoo, Park Heung-Woo, Kang Hye-Ryun, Park Kyoung Soo, Kim Ju Han, Lee Dong So |
Germ line variants in patients with acute myeloid leukemia without a suspicion of hereditary hematologic malignancy syndrome. Blood advances 2023 7 . Francesca Guijarro, Mònica López-Guerra, Jordi Morata, Alex Bataller, Sara Paz, Josep Maria Cornet-Masana, Antònia Banús-Mulet, Laia Cuesta-Casanovas, Josep Maria Carbó, Sandra Castaño-Díez, Carlos Jiménez-Vicente, Albert Cortés-Bullich, Ana Triguero, Alexandra Martínez-Roca, Daniel Esteban, Marta Gómez-Hernando, José Ramón Álamo Moreno, Irene López-Oreja, Marta Garrote, Ruth Muñoz Risueño, Raul Tonda, Ivo G Gut, Dolors Colomer, Marina Díaz-Beya, Jordi Este |
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- Page last updated:Apr 22, 2024
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