Search Results - "Wessels, J.W"

A novel cryptic CBFB-MYH11 gene fusion present at birth leading to acute myeloid leukemia and allowing molecular monitoring for minimal residual disease by Poddighe, P.J, Veening, M.A, Mansur, M.B, Loonen, A.H, Westers, T.M, Merle, P.A, Wessels, J.W, de Haas, V, Kors, W.A, Bhola, S.L, Wondergem, M.J, Ford, A.M, Kaspers, G.J.L

“…AbstractAcute myeloid leukemia (AML) with the inv(16)/t(16;16) karyotype is associated with a favourable prognosis, showing longer periods of complete…”
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Alpha satellite DNAs on chromosomes 10 and 12 are both members of the dimeric suprachromosomal subfamily, but display little identity at the nucleotide sequence level by Looijenga, L H, Oosterhuis, J W, Smit, V T, Wessels, J W, Mollevanger, P, Devilee, P

“…We have investigated the organization and complexity of alpha satellite DNA on chromosomes 10 and 12 by restriction endonuclease mapping, in situ hybridization…”
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Die verwydering van stofas uit die skoorstene van die SASOL kragstasie by J.W Wessels

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Detection of Monosomy 7 and Trisomy 8 in Myeloid Neoplasia: A Comparison of Banding and Fluorescence In Situ Hybridization by Kibbelaar, R.E., Mulder, J.W.R., Dreef, E.J., van Kamp, H., Fibbe, W.E., Wessels, J.W., Beverstock, G.C., Haak, H.L., Kluin, Ph.M.

“…Fluorescence in situ hybridization (FISH) is a powerful tool for detection of numerical and structural chromosomal aberrations. We have compared conventional…”
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Detection of the Philadelphia chromosome in interphase nuclei by Arnoldus, E P, Wiegant, J, Noordermeer, I A, Wessels, J W, Beverstock, G C, Grosveld, G C, van der Ploeg, M, Raap, A K

“…Double fluorescence in situ hybridization was used to detect Philadelphia (Ph) chromosomes in interphase nuclei and metaphases of patients with chronic myeloid…”
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Myeloid But Not Lymphoid Cells Carry the 5q Deletion: Polymerase Chain Reaction Analysis of Loss of Heterozygosity Using Mini-Repeat Sequences on Highly Purified Cell Fractions by Kroef, M.J.P.L., Fibbe, W.E., Mout, R., Jansen, R.P.M., Haak, H.L., Wessels, J.W., Kamp, H. Van, Willemze, R., Landegent, J.E.

“…Interstitial deletions of the long arm of chromosome 5 are among the most characteristic abnormalities observed in myeloid disorders. To assess the lineage…”
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Extensive Cross-Homology Between the Long and the Short Arm of Chromosome 16 May Explain Leukemic Inversions and Translocations by Dauwerse, J.G., Jumelet, E.A., Wessels, J.W., Saris, J.J., Hagemeijer, A., Beverstock, G.C., Ommen, G.J.B. van, Breuning, M.H.

“…Specific rearrangements of chromosome 16 are well known in acute nonlymphocytic leukemia with abnormal eosinophils. While mapping cosmids relative to…”
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Tricyclic antidepressants for major depressive disorder: a comprehensive evaluation of current practice in the Netherlands by Vos, Cornelis F, Aarnoutse, Rob E, Op de Coul, Marijke J. M, Spijker, Jan, Groothedde-Kuyvenhoven, Mascha M, Mihaescu, Raluca, Wessels-Basten, Sonja J. W, Rovers, Jordy J. E, ter Hark, Sophie E, Schene, Aart H, Hulscher, Marlies E. J. L, Janzing, Joost G. E

“…Background Traditionally tricyclic antidepressants (TCAs) have an important place in treatment of major depressive disorder (MDD). Today, often other…”
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Cloning the breakpoint cluster region of the inv(16) in acute nonlymphocytic leukemia M4 Eo by Dauwerse, J G, Wessels, J W, Giles, R H, Wiegant, J, van der Reijden, B A, Fugazza, G, Jumelet, E A, Smit, E, Baas, F, Raap, A K

“…The pericentric inversion of chromosome 16 and the t(16;16) are two recurrent aberrations in bone marrow of patients with acute nonlymphocytic leukemia subtype…”
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Localization and polymorphism of a chromosome 12-specific alpha satellite DNA sequence by Looijenga, L H, Smit, V T, Wessels, J W, Mollevanger, P, Oosterhuis, J W, Cornelisse, C J, Devilee, P

“…The isolation and localization of a chromosome 12-specific alpha satellite DNA sequence, p alpha 12H8, is described. This clone contains a complete copy of the…”
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Detection of trisomy 8 in hematological disorders by in situ hybridization by Kibbelaar, R E, van Kamp, H, Dreef, E J, Wessels, J W, Beverstock, G C, Raap, A K, Fibbe, W E, den Ottolander, G J, Kluin, P M

“…An alphoid repetitive DNA (D8Z2) probe specific for the pericentromeric region of chromosome 8 was used to detect extra copies of chromosome 8 in bone marrow…”
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Two Distinct Loci on the Short Arm of Chromosome 16 Are Involved in Myeloid Leukemia by Wessels, J.W., Mollevanger, P., Dauwerse, J.G., Cluitmans, F.H.M., Breuning, M.H., Beverstock, G.C.

“…We report a case of acute nonlymphocytic leukemia (ANLL) M5 with the characteristic t(8;16)(p11;p13). The breakpoint in the short arm was regionally localized…”
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Combined GTG-banding and nonradioactive in situ hybridization improves characterization of complex karyotypes by Smit, V T, Wessels, J W, Mollevanger, P, Schrier, P I, Raap, A K, Beverstock, G C, Cornelisse, C J

“…Nonradioactive in situ hybridization (ISH) using biotinylated centromere probes for chromosomes 1, 6, 7, 10, 16, 17, 18, and the X, respectively, was combined…”
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t(5;12)(q31;p12). A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia by Wessels, J W, Fibbe, W E, van der Keur, D, Landegent, J E, van der Plas, D C, den Ottolander, G J, Roozendaal, K J, Beverstock, G C

“…We report two patients with a myeloproliferative disorder (Philadelphia chromosome-negative chronic myeloid leukemia) and t(5;12)(q31;p12). Until now, only…”
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