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Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis type 1 patients.
Van Roy N, Vandesompele J, Berx G, Staes K, Van Gele M, De Smet E, De Paepe A, Laureys G, van der Drift P, Versteeg R, Van Roy F, Speleman F. Van Roy N, et al. Among authors: vandesompele j. Genes Chromosomes Cancer. 2002 Oct;35(2):113-20. doi: 10.1002/gcc.10034. Genes Chromosomes Cancer. 2002. PMID: 12203774
RTPrimerDB: the real-time PCR primer and probe database.
Pattyn F, Speleman F, De Paepe A, Vandesompele J. Pattyn F, et al. Among authors: vandesompele j. Nucleic Acids Res. 2003 Jan 1;31(1):122-3. doi: 10.1093/nar/gkg011. Nucleic Acids Res. 2003. PMID: 12519963 Free PMC article.
Expression analyses identify MLL as a prominent target of 11q23 amplification and support an etiologic role for MLL gain of function in myeloid malignancies.
Poppe B, Vandesompele J, Schoch C, Lindvall C, Mrozek K, Bloomfield CD, Beverloo HB, Michaux L, Dastugue N, Herens C, Yigit N, De Paepe A, Hagemeijer A, Speleman F. Poppe B, et al. Among authors: vandesompele j. Blood. 2004 Jan 1;103(1):229-35. doi: 10.1182/blood-2003-06-2163. Epub 2003 Aug 28. Blood. 2004. PMID: 12946992 Free article.
337 results