Wessels H - Search Results

1

Genome wide molecular analysis of minimally differentiated acute myeloid leukemia.

Silva FP, Almeida I, Morolli B, Brouwer-Mandema G, Wessels H, Vossen R, Vrieling H, Marijt EW, Valk PJ, Kluin-Nelemans HC, Sperr WR, Ludwig WD, Giphart-Gassler M. Silva FP, et al. Among authors: wessels h. Haematologica. 2009 Nov;94(11):1546-54. doi: 10.3324/haematol.2009.009324. Epub 2009 Sep 22. Haematologica. 2009. PMID: 19773259 Free PMC article.

2

Identification of RUNX1/AML1 as a classical tumor suppressor gene.

Silva FP, Morolli B, Storlazzi CT, Anelli L, Wessels H, Bezrookove V, Kluin-Nelemans HC, Giphart-Gassler M. Silva FP, et al. Among authors: wessels h. Oncogene. 2003 Jan 30;22(4):538-47. doi: 10.1038/sj.onc.1206141. Oncogene. 2003. PMID: 12555067

3

Characterization of a novel malignant B cell line with t(14;18) and t(4;11) established from a patient with acute monoblastic leukemia.

de Kroon JF, Kluin-Nelemans HC, Kluin PM, Schuuring E, van Bergen CA, Oving I, Wessels H, Willemze R, Falkenburg JH. de Kroon JF, et al. Among authors: wessels h. Exp Hematol. 1997 Sep;25(10):1062-8. Exp Hematol. 1997. PMID: 9293903

4

Proliferation and cytogenetic analysis of hairy cell leukemia upon stimulation via the CD40 antigen.

Kluin-Nelemans HC, Beverstock GC, Mollevanger P, Wessels HW, Hoogendoorn E, Willemze R, Falkenburg JH. Kluin-Nelemans HC, et al. Among authors: wessels hw. Blood. 1994 Nov 1;84(9):3134-41. Blood. 1994. PMID: 7524766 Free article.

5

Characterization of a New Human B Cell Line (Bonna-12) with Trisomy 9 and Trisomy 12 Chromosomal Abnormality.

Wientjens GJ, Jansen JH, Wessels HW, Kibbelaar RE, Beverstock GC, Brederoo P, Kluin-Nelemans HC. Wientjens GJ, et al. Among authors: wessels hw. Leuk Lymphoma. 1991;5(5-6):415-22. doi: 10.3109/10428199109067637. Leuk Lymphoma. 1991. PMID: 27463354

6

Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered.

van der Reijden BA, Dauwerse HG, Giles RH, Jagmohan-Changur S, Wijmenga C, Liu PP, Smit B, Wessels HW, Beverstock GC, Jotterand-Bellomo M, Martinet D, Mühlematter D, Lafage-Pochitaloff M, Gabert J, Reiffers J, Bilhou-Nabera C, van Ommen GJ, Hagemeijer A, Breuning MH. van der Reijden BA, et al. Among authors: wessels hw. Oncogene. 1999 Jan 14;18(2):543-50. doi: 10.1038/sj.onc.1202321. Oncogene. 1999. PMID: 9927211

7

A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia.

Beverstock GC, de Meijer PH, ten Bokkel Huinink D, Pruijt JF, den Ottolander GJ, Wessels HW, Mollevanger P. Beverstock GC, et al. Among authors: wessels hw. Cancer Genet Cytogenet. 1996 Jul 15;89(2):132-5. doi: 10.1016/0165-4608(95)00316-9. Cancer Genet Cytogenet. 1996. PMID: 8697419

8

Nonradioactive in situ hybridisation of the translocation t(1;7) in myeloid malignancies.

Kibbelaar RE, Mulder JW, van Kamp H, Dreef EJ, Wessels HW, Beverstock GC, Haak HL, Raap AK, Kluin PM. Kibbelaar RE, et al. Among authors: wessels hw. Genes Chromosomes Cancer. 1992 Mar;4(2):128-34. doi: 10.1002/gcc.2870040205. Genes Chromosomes Cancer. 1992. PMID: 1373312

9

Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p.

Dauwerse JG, Kievits T, Beverstock GC, van der Keur D, Smit E, Wessels HW, Hagemeijer A, Pearson PL, van Ommen GJ, Breuning MH. Dauwerse JG, et al. Among authors: wessels hw. Cytogenet Cell Genet. 1990;53(2-3):126-8. doi: 10.1159/000132911. Cytogenet Cell Genet. 1990. PMID: 2369839

10

RT-PCR diagnosis of patients with acute nonlymphocytic leukemia and inv(16)(p13q22) and identification of new alternative splicing in CBFB-MYH11 transcripts.

van der Reijden BA, Lombardo M, Dauwerse HG, Giles RH, Mühlematter D, Bellomo MJ, Wessels HW, Beverstock GC, van Ommen GJ, Hagemeijer A, et al. van der Reijden BA, et al. Among authors: wessels hw. Blood. 1995 Jul 1;86(1):277-82. Blood. 1995. PMID: 7795233 Free article.

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