Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sandra S Mimoso Pinhancos"'
Autor:
Ronald W. Stam, M. Emmy M. Dolman, Anke H. W. Essing, Pauline Schneider, Mark Kerstjens, Rob Pieters, P. Castro, Jan J. Molenaar, Sandra S Mimoso Pinhancos, Eddy H.J. van Roon
Publikováno v:
eJHaem. 1:527-536
Autor:
J.A.P. Spijkers-Hagelstein, Pauline Schneider, Patricia Garrido Castro, Rob Pieters, Sandra S Mimoso Pinhancos, Ronald W. Stam
Publikováno v:
European Journal of Cancer, 50(9), 1665-1674. Elsevier Ltd.
Aim of the study Resistance to glucocorticoids (GCs) remains a major problem in the treatment of infants with acute lymphoblastic leukaemia (ALL) carrying Mixed Lineage Leukaemia ( MLL ) translocations. Despite intensive research, the mechanism(s) un
Autor:
Rob Pieters, Paola De Lorenzo, Ronald W. Stam, Maria Grazia Valsecchi, Pauline Schneider, Sandra S Mimoso Pinhancos, Emma M. C. Driessen
Publikováno v:
European Journal of Cancer, 57, 87-90. Elsevier Ltd.
Acute lymphoblastic leukaemia (ALL) in infants (
Autor:
Sandra S Mimoso Pinhancos, Clara Bueno, Patricia Garrido Castro, Merel Willekes, Eddy H.J. van Roon, Ronald W. Stam, Pauline Schneider, Pablo Menendez, Rob Pieters
Publikováno v:
Blood. 124:878-878
BACKGROUND: MLL-rearranged acute lymphoblastic leukemia (MLLr-ALL) in infants ( AIMS: This study aims at defining MLLr-associated miRNA expression patterns using high-throughput miRNA profiling of a comprehensive MLLr- and non-MLL B-cell precursor-AL
Autor:
Rob Pieters, Mark Kerstjens, Merel Willekes, Pauline Schneider, Patricia Garrido Castro, Eddy H.J. van Roon, Sandra S Mimoso Pinhancos, Ronald W. Stam
Publikováno v:
Blood. 124:3709-3709
BACKGROUND: Infant acute lymphoblastic leukaemia (ALL) is a rare but aggressive malignancy, mainly presenting with chromosomal rearrangements of the MLL (Mixed Lineage Leukaemia) gene locus on 11q23. The majority of these MLL rearrangements involve t
Autor:
Sandra S Mimoso Pinhancos, Emma M. C. Driessen, Rob Pieters, Merel Willekes, Ronald W. Stam, Mark Kerstjens
Publikováno v:
Blood. 124:919-919
Background: Acute Lymphoblastic Leukemia (ALL) in infants is characterized by a high incidence (~80%) of chromosomal rearrangements of the Mixed Lineage Leukemia (MLL) gene, fusing the N-terminal portion of MLL to the C-terminal region of one of its