Autor: |
Kroeze, L.I., Aslanyan, M.G., Rooij, A. van, Koorenhof-Scheele, T.N., Massop, M., Carell, T., Boezeman, J.B., Marie, J.P., Halkes, C.J.M., Witte, T. de, Huls, G., Suciu, S., Wevers, R.A., Reijden, B.A. van der, Jansen, J.H., EORTC Leukemia Grp, GIMEMA |
Rok vydání: |
2014 |
Předmět: |
|
Zdroj: |
Blood, 124, 7, pp. 1110-8 Blood, 124, 1110-8 Blood, 124(7), 1110-1118 |
ISSN: |
1528-0020 0006-4971 |
DOI: |
10.1182/blood-2013-08-518514 |
Popis: |
Contains fulltext : 137617.pdf (Publisher’s version ) (Closed access) Patients with acute myeloid leukemia (AML) frequently harbor mutations in genes involved in the DNA (hydroxy)methylation pathway (DNMT3A, TET2, IDH1, and IDH2). In this study, we measured 5-hydroxymethylcytosine (5hmC) levels in 206 clinically and molecularly well-characterized younger adult AML patients ( |
Databáze: |
OpenAIRE |
Externí odkaz: |
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