Zobrazeno 1 - 10
of 113
pro vyhledávání: '"M-J Le Bris"'
Autor:
M. De Braekeleer, K.G.L. Fonseka, T. Voet, M. Yerle, D. Wells, A. Kanesky, J. Navarro, L. Ramos, J. Riquet, J.L. Barbero, A. Estop, M. Regev, D.K. Griffin, Satz Mengensatzproduktion, F. Morel, N. Mary, U. Eichenlaub-Ritter, F. Vidal, A.L. Marston, O. Reish, A. Pinton, Franck Pellestor, V. Amice, M.-J. Le Bris, M. Bordedebat, C. Templado, I. Matos, A. Mantzouratou, S. Girafi, A. Basinko, F. Pacchierotti, I. Lebedev, H. Barasc, J. Selva, N. Gueganic, I. Raymond Letron, F. Vialard, J.R. Vermeesch, N. Douet-Guilbert, N. Bonnet, D. Gisselsson, E. Fragouli, A. Ducos, A. Calgaro, Druck Reinhardt Druck Basel, Joy D. A. Delhanty, J.D.A. Delhanty, K. Feve, A.M. Dudez, M. Mashevich, H. Homer, A. Obradors, D. Molina-Gomes, F. Boitrelle, G. Daina, H. Maiato, K. Massip, A. Perrin, J. Benet, D. Clift, E. Vanneste, M. Rius, D. Ioannou
Publikováno v:
Cytogenetic and Genome Research. 133:I-IV
Autor:
M. De Braekeleer, V. Amice, Frédéric Morel, P. May-Panloup, Nathalie Douet-Guilbert, A. Perrin, J. Amice, A. Guichet, M.-J. Le Bris
Publikováno v:
International Journal of Andrology. 32:231-234
Semen analysis of a 31-year-old infertile man showed a severe oligoteratozoospermia. Karyotyping of peripheral blood lymphocytes showed a 47,XY,+18[13]/46,XY[16] mosaicism. Cultured skin fibroblasts, right and left jugal smears showed 3, 50 and 65% t
Autor:
Frédéric Morel, M. De Braekeleer, Nathalie Douet-Guilbert, M.-J. Le Bris, Audrey Basinko, Angèle Herry
Publikováno v:
Pathologie Biologie. 56:362-367
Resume Les marqueurs chromosomiques surnumeraires (MCS) sont des chromosomes additionnels dont la structure est indeterminee par les techniques de cytogenetique conventionnelle. Les MCS constituent un groupe heterogene d’anomalies chromosomiques de
Autor:
Frédéric Morel, L. Pinson, Angèle Herry, M.-J. Le Bris, Nathalie Douet-Guilbert, M. De Braekeleer, H. Marical
Publikováno v:
Cytogenetic and Genome Research. 116:18-23
Marker chromosomes are defined as ‘structurally abnormal chromosomes in which no part can be identified’ (ISCN 1995). Supernumerary marker chromosomes (SMC) are ‘additional markers’ whose origin and composition cannot be determined by convent
Autor:
Izabel Bernicot, Angèle Herry, M.-J. Le Bris, Nathalie Douet-Guilbert, M. De Braekeleer, Frédéric Morel
Publikováno v:
Cytogenetic and Genome Research. 118:345-352
Rearrangements involving the IGH gene have been identified in about 50% of non-Hodgkin B-cell lymphomas (NHLs) and correlated to clinically relevant subgroups. However, the detection rate largely varied with the technique used. We analyzed the incide
Autor:
Bruno Delobel, M.-J. Le Bris, A. Moerman, M. De Braekeleer, B. Duban, C. Marchetti, V. Amice, Frédéric Morel, Nathalie Douet-Guilbert
Publikováno v:
MHR: Basic science of reproductive medicine. 10:835-838
The objective of this study was to determine the aneuploidy level in spermatozoa in two men with globozoospermia. Sperm nuclei were analysed by fluorescence in-situ hybridization (FISH) in two infertile males with globozoospermia. Dual FISH for chrom
Autor:
Minh Nguyen, S. Roche, Philippe Parent, Aurore Perrin, Nathalie Douet-Guilbert, M. De Braekeleer, Frédéric Morel, P. Pennamen, Audrey Basinko, M.-J. Le Bris
Publikováno v:
Andrologia. 47(2)
Complex chromosome rearrangements (CCRs) are structural rearrangements involving at least three chromosomes and three or more chromosome breakpoints. Generally, balanced CCR carriers have a normal phenotype but they are at a higher reproductive risk.
Autor:
Christian Berthou, Patrick Morice, Marc De Braekeleer, Pascal Bourquard, M-J Le Bris, N Guilbert-Douet, Frédéric Morel
Publikováno v:
Leukemia. 18:1140-1142
Clonal chromosomal abnormalities in the Philadelphia chromosome negative cells of chronic myeloid leukemia patients treated with imatinib
Autor:
Nadia Guéganic, Frédéric Morel, Nathalie Douet-Guilbert, Braekeleer M De, M.-J. Le Bris, Clément Bovo, Angèle Herry, Audrey Basinko
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Review on i(5)(p10) in acute myeloid leukemia, with data on clinics, and the genes involved.
Autor:
E De Braekeleer, Audrey Basinko, Christian Berthou, A Dos Santos, Angèle Herry, M. De Braekeleer, K Trillet, Jean-Richard Eveillard, Nadia Guéganic, Clément Bovo, Frédéric Morel, M.-J. Le Bris, Nathalie Douet-Guilbert
Publikováno v:
Leukemia. 26(7)
Molecular characterization of deletions of the long arm of chromosome 5 (del(5q)) in 94 MDS/AML patients