Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Arnold Criel"'
Autor:
Anne Hagemeijer, A. Van Hoof, Arnold Criel, K Kargar Samani, Iwona Wlodarska, Lucienne Michaux, Michel Stul, Marie Maerevoet, S. Marichal, Hilde Demuynck, Katrina Rack, Augustin Ferrant, Peter Marynen, P. Mineur
Publikováno v:
Leukemia. 19:77-82
Although reciprocal chromosomal translocations are not typical for B-cell chronic lymphocytic leukemia (B-CLL), we identified the novel t(1;6)(p35.3;p25.2) in eight patients with this disorder. Interestingly, all cases showed lack of somatically muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4456b190bda92b66cb622deaed01c5c2
https://doi.org/10.1038/sj.leu.2403543
https://doi.org/10.1038/sj.leu.2403543
Autor:
Barbara Crescenzi, Massimo F. Martelli, Caterina Matteucci, Roberta La Starza, Herman Van den Berghe, Cristina Mecucci, Arnold Criel, Dominik Selleslag
Publikováno v:
Cancer Genetics and Cytogenetics. 105:55-59
Clonal hematopoiesis with trisomy 6 as the sole karyotypic change was revealed by cytogenetics in two cases of aplastic anemia. In both patients, dyserythropoiesis was characterized by asynchrony of maturation between nucleus and cytoplasm, binucleat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d15357631fd6e096110bddaf56299b4
https://doi.org/10.1016/s0165-4608(97)00476-7
https://doi.org/10.1016/s0165-4608(97)00476-7
Autor:
José Thomas, Andries Louwagie, Iwona Wlodarska, Arnold Criel, André Delannoy, Anne Hagemeijer, Michel Stul, Joris Vermeesch, Peter Meeus, Judith Dierlamm, Jean-Jacques Cassiman, Lucienne Michaux, Herman Van den Berghe, Cristina Mecucci, Gregor Verhoef
Publikováno v:
Genes, Chromosomes and Cancer. 20:155-166
Clinical, cytogenetic, fluorescence in situ hybridization (FISH), and Southern blot data of 18 patients with different subtypes of B-cell non-Hodgkin's lymphoma, cytogenetically characterized by partial trisomy 12, are presented. These chromosomal ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cceee9295bd4d6ec40b63a5a9281621
https://doi.org/10.1002/(sici)1098-2264(199710)20:2<155::aid-gcc6>3.0.co
https://doi.org/10.1002/(sici)1098-2264(199710)20:2<155::aid-gcc6>3.0.co
Autor:
Anna Aventin, D Falzetti, Arnold Criel, Júlia Inglés-Esteve, Jean-Jacques Cassiman, Iwona Wlodarska, Peter Marynen, Herman Van den Berghe, Cristina Mecucci
Publikováno v:
Blood. 89:1716-1722
Translocation t(5; 12)(q33; p13), resulting in an ETV6/PDGFRB gene fusion, is a recurrent chromosomal abnormality associated with chronic myelomonocytic leukemia (CMML). An analogous translocation was also found in four cell lines with features of pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dab10ca0faf754a1cfa9cf8fa90e6a1
https://doi.org/10.1182/blood.v89.5.1716
https://doi.org/10.1182/blood.v89.5.1716
Autor:
Christiane De Wolf-Peeters, Herman Van den Berghe, Michel Stul, Iwona Wlodarska, Peter Meeus, Cristina Mecucci, Arnold Criel, Jean-Jacques Cassiman, Lucienne Michaux, Angeline Van Orshoven, Jesús M. Hernández
Publikováno v:
Cancer Genetics and Cytogenetics. 93:147-151
Twelve patients with diagnosis of B-cell non-Hodgkin's lymphoma/leukemia and del[7q] were studied for their clinical, cytogenetic, and molecular characteristics. Eleven patients were classified as small cell lymphoma whereas one had a diffuse large c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11a05fd8989f9eb425b9b36b0810ffee
https://doi.org/10.1016/s0165-4608(96)00183-5
https://doi.org/10.1016/s0165-4608(96)00183-5
Autor:
J J Cassiman, J. Thomas, Pia Delaere, H. Van den Berghe, I. Wlodarska, Michel Stul, Arnold Criel, Christina Mecucci, C De Wolf-Peeters, Marc Boogaerts, W. Zeller, Judith Dierlamm, Stefania Pittaluga, Lucienne Michaux
Publikováno v:
British Journal of Haematology. 93:242-249
Trisomy 3 represents the most frequent and consistent chromosomal abnormality characterizing the recently defined entity marginal zone B-cell lymphoma (MZBCL). By cytogenetic analysis and/or fluorescence in situ hybridization (FISH) on interphase nuc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de1aa215b2c2d25173e5ed864bf78fae
https://doi.org/10.1046/j.1365-2141.1996.522522.x
https://doi.org/10.1046/j.1365-2141.1996.522522.x
Autor:
Michel Stul, Cristina Mecucci, Iwona Wlodarska, Jean-Marie Scheiff, Jesús M. Hernández, Andries Lodwagie, Marc Boogaerts, Angeline Van Orshoven, Jean-Jacques Cassiman, Henri Noël, Lucienne Michaux, Jean-Louis Michaux, Peter Meeus, Arnold Criel, Herman Van den Berghe
Publikováno v:
Genes, Chromosomes and Cancer. 15:38-47
Translocation t(14;19)(q32;q13) is a rare but recurrent abnormality in chronic lymphocytic leukemia and small cell lymphoma. It has been associated with rearrangements of the BCL3 gene, which is located at the breakpoint on chromosome 19 and is juxta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e2645f972f39dd36dc8f70b02eaaef9
https://doi.org/10.1002/(sici)1098-2264(199601)15:1<38::aid-gcc6>3.0.co
https://doi.org/10.1002/(sici)1098-2264(199601)15:1<38::aid-gcc6>3.0.co
Autor:
Andries Louwagie, W. Zeller, Judith Dierlamm, Arnold Criel, Lucienne Michaux, Iwona Wlodarska, Jean-Louis Michaux, Herman Van den Berghe, Cristina Mecucci
Publikováno v:
British Journal of Haematology. 91:885-891
Idic(X)(q13) represents a rare but recurrent chromosomal abnormality in haematological malignancies. We present five new cases characterized by this particular aberration and review the literature on this subject. The patients were elderly females wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfcf677413af28298c1df3e1d7bfc2dd
https://doi.org/10.1111/j.1365-2141.1995.tb05405.x
https://doi.org/10.1111/j.1365-2141.1995.tb05405.x
Autor:
Barbara Cauwelier, Andries Louwagie, Achiel Van Hoof, Dominik Selleslag, Johan Billiet, Arnold Criel, Friedel Nollet
Publikováno v:
Blood. 100:1097-1099
With interest we read the report of Tobin et al[1][1] describing a new subset of B-cell chronic lymphocytic leukemia (B-CLL). After mutation analysis of rearranged immunoglobulin variable heavy chain (IgVH) genes, they observed that B-CLL patients wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92aa6a97703e4b7b688398b781e02f19
https://doi.org/10.1182/blood-2002-03-0867
https://doi.org/10.1182/blood-2002-03-0867
Autor:
Herman Van den Berghe, Iwona Wlodarska, Michel Stul, Elisabeth Vandenberghe, C. De Wolf Peeters, Andries Louwagie, José Thomas, Christina Mecucci, Gregor Verhoef, Arnold Criel, Jj. Cassiman
Publikováno v:
British Journal of Haematology. 81:212-217
The clinical features, morphology and immunophenotype of 20 cases of B non Hodgkin's lymphoma (B-NHL) with chromosome abnormalities involving 11q13-14 were studied, to determine if this abnormality was closely associated with a specific sub-type of B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d8c8484f39a237bff29f61bc819eea5
https://doi.org/10.1111/j.1365-2141.1992.tb08209.x
https://doi.org/10.1111/j.1365-2141.1992.tb08209.x