TY  - GEN
AU  - Rio-Machín, Ana
AU  - Menezes, Juliane
AU  - Maiques-Diaz, Alba
AU  - Agirre, Xabier
AU  - Ferreira, Bibiana I
AU  - Acquadro, Francesco
AU  - Rodriguez Perales, Sandra
AU  - Juaristi, Karmele A
AU  - Alvarez, Sara
AU  - Cigudosa, Juan C
PY  - 2012
UR  - https://hdl.handle.net/20.500.12105/26159
AB  - The disruption of RUNX1 function is one of the main mechanisms of disease observed in hematopoietic malignancies and the description of novel genetic events that lead to a RUNX1 loss of function has been accelerated with the development of genomic...
LA  - eng
PB  - FERRATA STORTI FOUNDATION
KW  - AML1
KW  - t(4;21)(q21;q22
KW  - RUNX1 haploinsufficiency
KW  - megakariocytic lineage maturation
TI  - Abrogation of RUNX1 gene expression in de novo myelodysplastic syndrome with t(4;21)(q21;q22).
TY  - research article
ER  -