Publications 2008

Monique L. Den Boer, Marjon van Slegtenhorst, Renée X. De Menezes, Meyling H. Cheok, Jessica G.C.A.M. Buijs-Gladdines, Susan T.C.J.M. Peters, Laura J.C.M. Van Zutven, H. Berna Beverloo, Peter J. Van der Spek, Gaby Escherich, Martin Horstmann, Gritta E. Janka-Schaub , Willem A. Kamps, William E. Evans and Rob Pieters:
Genome-wide classification of childhood acute lymphoblastic leukemia identified a new BCR-ABL-like subtype with a poor treatment outcome. Im Druck, Lancet Oncology, 2009.

Van Vlierberghe P, Beverloo HB, Buijs-Gladdines J, van Wering ER, Horstmann M, Pieters R, Meijerink JP.:
Monoallelic or biallelic LMO2 expression in relation to the LMO2 rearrangement status in pediatric T-cell acute lymphoblastic leukemia. Leukemia. 2008 Jul;22(7):1434-7.

Balgobind BV, Van Vlierberghe P, van den Ouweland AM, Beverloo HB, Terlouw-Kromosoeto JN, van Wering ER, Reinhardt D, Horstmann M, Kaspers GJ, Pieters R, Zwaan CM, Van den Heuvel-Eibrink MM, Meijerink JP.:
Leukemia-associated NF1 inactivation in patients with pediatric T-ALL and AML lacking evidence for neurofibromatosis. Blood. 2008 Apr 15;111(8):4322-8. Epub 2008 Jan 2.

Van Vlierberghe P, Homminga I, Zuurbier L, Gladdines-Buijs J, van Wering ER, Horstmann M, Beverloo HB, Pieters R, Meijerink JP.:
Cooperative genetic defects in TLX3 rearranged pediatric T-ALL. Leukemia. 2008 Apr;22(4):762-70. Epub 2008 Jan 10.

Van Vlierberghe P, van Grotel M, Tchinda J, Lee C, Beverloo HB, van der Spek PJ, Stubbs A, Cools J, Nagata K, Fornerod M, Buijs-Gladdines J, Horstmann M, van Wering ER, Soulier J, Pieters R, Meijerink JP.:
The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia. Blood. 2008 May 1;111(9):4668-80. Epub 2008 Feb 25.

Bhojwani D, Kang H, Menezes RX, Yang W, Sather H, Moskowitz NP, Min DJ, Potter JW, Harvey R, Hunger SP, Seibel N, Raetz EA, Pieters R, Horstmann MA, Relling MV, den Boer ML, Willman CL, Carroll WL.:
Gene expression signatures predictive of early response and outcome in high-risk childhood acute lymphoblastic leukemia: a Children's Oncology Group Study on behalf of the Dutch Childhood Oncology Group and the German Cooperative Study Group for Childhood Acute Lymphoblastic Leukemia. J Clin Oncol. 2008 Sep 20;26(27):4376-84.

Trizzino A, zur Stadt U, Ueda I, Risma K, Janka G, Ishii E, Beutel K, Sumegi J, Cannella S, Pende D, Mian A, Henter JI, Griffiths G, Santoro A, Filipovich A, Aricò M; Histiocyte Society HLH Study group.:
Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations.J Med Genet. 2008 Jan;45(1):15-21. Epub 2007 Sep 14.

Elisabeth Scherber, Karin Beutel, Rainer Ganschow, Ansgar Schulz, Gritta Janka, Udo zur Stadt:
Molecular analysis and clinical aspects of 4 patients with Chédiak-Higashi syndrome (CHS); Clinical Genetics, in press