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scopus: 7006326556

Horstmann, M.A.

(Martin Horstmann)


patient t-all leukemia deletion expression lymphoblastic leukemia analysis mutation set-nup identi fied lymphoblastic set-nup 214 figure tlx 3 study blood fication t-cell subtype identi abnormality number cohort fusion region erasmus mc t-all cases classi genomic notch bcr –abl precursor probe bcr –abl disease translocation precursor b-all cases b-all group sample chromosome protein coall bcr –abl cases array-cgh activation table chromosomal mll-rearranged netherland loucy inactivation cluster value mll-rearranged aml children erasmu classi fication loucy cell line nf 1 microdeletions fish analysis tlx 3 expression disease gene-expression 3 patients cancer bcr –abl subtype speci microdeletion breakpoint 6–runx nf 1 inactivation outcome sirna nf 1 gene tumor hoxa gene cluster treatment volume hybridization b-other




4 Most Recent Publications

A subtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: a genome-wide classification study (Article)
Boer, M.L. den Slegtenhorst, M. van Horstmann, M.A. Janka-Schaub, G.E. Kamps, W.A. Evans, W.E. Pieters, R. Menezes, R.X. de Cheok, M.H. Buijs-Gladdines, J.G.C.A.M. Peters, S.T. Zutven, L.J.C.M. van Beverloo, H.B. Spek, P.J. van der Escherich, G.
2009-02-01
The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia (Article)
Vlierberghe, P. van Grotel, M. van Buijs-Gladdines, J.G.C.A.M. Horstmann, M.A. Wering, E.R. van Soulier, J. Pieters, R. Meijerink, J.P.P. Tchinda, J. Lee, C. Beverloo, H.B. Spek, P.J. van der Stubbs, A. Cools, J. Nagata, K. Fornerod, M.W.J.
2008-05-01
Leukemia-associated NF1 inactivation in patients with pediatric T-ALL and AML lacking evidence for neurofibromatosis (Article)
Balgobind, B.V. Vlierberghe, P. van Zwaan, C.M. Heuvel-Eibrink, M.M. van den Meijerink, J.P.P. Ouweland, A.M.W. van den Beverloo, H.B. Terlouw-Kromosoeto, J.N.R. Wering, E.R. van Reinhardt, D. Horstmann, M.A. Kaspers, G.J. Pieters, R.
2008-04-15
Cooperative genetic defects in TLX3 rearranged pediatric T-ALL (Article)
Vlierberghe, P. van Homminga, I. Zuurbier, L. Buijs-Gladdines, J.G.C.A.M. Wering, E.R. van Horstmann, M.A. Beverloo, H.B. Pieters, R. Meijerink, J.P.P.
2008-04-01