Zobrazeno 1 - 10
of 13
pro vyhledávání: '"L. J. A. Coignet"'
Publikováno v:
Leukemia. 14:427-430
Deletions of the long arm of chromosomes 11 and 13 are the most frequent structural chromosome aberrations in various types of lymphoproliferative disorders. However, these regions have not been studied so far in B cell prolymphocytic leukemia (B-PLL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a30f04a15222af7ac390a57001973d3f
https://doi.org/10.1038/sj.leu.2401644
https://doi.org/10.1038/sj.leu.2401644
Myeloid- and lymphoid-specific breakpoint cluster regions in chromosome band 13q14 in acute leukemia
Autor:
Martin J. S. Dyer, Toon Min, Nick Telford, Christa Fonatsch, L. J. A. Coignet, Carmen S Lima, Angela L Bowen, John Swansbury, Soheila Swanton, Masami Nagai, Berthold Streubel, Daniel Catovsky
Publikováno v:
Genes, Chromosomes and Cancer. 25:222-229
Abnormalities of chromosome band 13q14 occur in hematologic malignancies of all lineages and at all stages of differentiation. Unlike other chromosomal translocations, which are usually specific for a given lineage, the chromosomal translocation t(12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be3b3ac473120ddb40fe39ccdf4f17a7
https://doi.org/10.1002/(sici)1098-2264(199907)25:3<222::aid-gcc4>3.0.co
https://doi.org/10.1002/(sici)1098-2264(199907)25:3<222::aid-gcc4>3.0.co
Autor:
Andrew Wotherspoon, L. J. A. Coignet, Estella Matutes, Daniel Catovsky, Alicja M. Gruszka-Westwood
Publikováno v:
British Journal of Haematology. 104:600-604
Splenic lymphoma with villous lymphocytes (SLVL) is a low-grade B-cell lymphoproliferative disorder characterized by splenomegaly and circulating villous lymphocytes. The relationship between SLVL and splenic marginal zone lymphoma (SMZL), a disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::809fbb4ca728be24eec8fe460461fac7
https://doi.org/10.1046/j.1365-2141.1999.01209.x
https://doi.org/10.1046/j.1365-2141.1999.01209.x
Autor:
Dalal M. Jadayel, L. J. A. Coignet, V. J. Zani, Martin J. S. Dyer, Stephen W. Scherer, Lap-Chee Tsui, Lucy R. Osborne
Publikováno v:
Gene. 224:35-44
The BCL7A gene, which maps to human chromosome 12q24.13, was cloned through its direct involvement with MYC and IGH in a three-way translocation in a Burkitt lymphoma cell line. Here, we describe the identification of two related human genes, BCL7B a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ee678cc8b7364b785000d2c4828bf22
https://doi.org/10.1016/s0378-1119(98)00514-9
https://doi.org/10.1016/s0378-1119(98)00514-9
Autor:
Martin J. S. Dyer, L. J. A. Coignet, Dalal M. Jadayel, Christian Bastard, M. L. M. Silva, I R Zalcberg, D. Catovsky, Michel Stul, Tony G. Willis, Jennifer Treleaven, Iwona Wlodarska
Publikováno v:
Scopus-Elsevier
Abnormalities of chromosome 1q21 are common in B-cell malignancies and have been associated with a poor response to therapy. The nature of the involved gene(s) on chromosome 1q21 remains unknown. A cell line (CEMO-1) has recently been established fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cdad3f8f58af6adf2808e38767ab5c0
https://doi.org/10.1182/blood.v91.6.1873
https://doi.org/10.1182/blood.v91.6.1873
Autor:
L. J. A. Coignet, T. G. Willis, D. Jadayel, Martin J. S. Dyer, Daniel Catovsky, Jennifer Treleaven, M. Abdul-Rauf
Publikováno v:
Blood. 90:2456-2464
Clonal rearrangements of the Ig heavy chain (IGH ) locus consisting of either intrachromosomal (VDJ ) rearrangements or interchromosomal translocations are a consistent feature of all B-cell malignancies and may be used both diagnostically and to mon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37e6822b98ca0c75096eb32c59ba7b6f
https://doi.org/10.1182/blood.v90.6.2456.2456_2456_2464
https://doi.org/10.1182/blood.v90.6.2456.2456_2456_2464
Autor:
Nazan Çetingül, Ken Toba, Sandra Cecília Botelho Costa, Yasuo Saito, Valder R. Arruda, Aliza Zeidman, Hwei-Fang Tien, Senay Öztop, Liberto Pechet, L. J. A. Coignet, Vasantha Brito-Babapulle, Ichiro Fuse, Yesim Aydinok, Giingör Nisli, Amos Cohen, Yuji Mizukami, Michael J. Misialek, Moshe Mittelman, U. H. Lewinski, Fernando Ferreira Costa, Nazli Basakh, Titus H.J. Huisman, Hans L. Willems, Dorine W. Swinkels, Tadashi Koike, Tze-Wah Kao, Joyce M. Annicchino-Bizzacchi, Chien-Ching Hung, Kaan Kavakli, D. Catovsky, Yumiko Uesugi, Akira Shibata, Shigeki Ohtake, M. Conchon, J. Garcia-Marco, Cláudio Lúcio Rossi, Shinobu Nakamura, Zinaida Fradin, L. Hiorns, Kunihiko Yokoyama, Wim van der Meer, S.H. Maljaie, Avraham Magazanik, Yee-Chun Chen, Tamotsu Matsuda, Eliana Nogueira
Publikováno v:
Acta Haematologica. 98:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30bc058836db502ecd001caf2642f330
https://doi.org/10.1159/000203620
https://doi.org/10.1159/000203620
Autor:
L. J. A. Coignet, J. Garcia-Marco, Vasantha Brito-Babapulle, D. Catovsky, S.H. Maljaie, L. Hiorns, M. Conchon
Publikováno v:
Acta Haematologica. 98:175-186
Chronic lymphoid leukaemias are clonal expansions of B and T cells with mature membrane phenotype. Cytogenetic study of these cases usually requires mitogenic stimulation and can often be hindered by a lack of response of the tumour cells to mitogen,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccfc7ad816b2f0846cbfcba87b005a08
https://doi.org/10.1159/000203621
https://doi.org/10.1159/000203621
Autor:
Daniel Catovsky, Estela Matutes, A C Wotherspoon, Vasantha Brito-Babapulle, P Carrara, N Villamor, L. J. A. Coignet
Publikováno v:
Leukemia. 13(11)
We have investigated the diagnostic value of fluorescence in situ hybridisation (FISH) to detect t(11;14) and trisomy 12 in 53 cases with a B cell leukaemia difficult to classify on clinical and laboratory grounds. These cases were initially diagnose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::555843b6f1a2dc3493acda9ed8b5a0a2
https://pubmed.ncbi.nlm.nih.gov/10557044
https://pubmed.ncbi.nlm.nih.gov/10557044
Autor:
L. J. A. Coignet, M. A. R. Yuille
Publikováno v:
Recent Results in Cancer Research ISBN: 9783642468728
The ataxia telangiectasia (A-T) gene, ATM, predisposes affected homozygotes to a wide range of malignancies. It has been suggested that this is a consequence of the genomic instability associated with the syndrome. The elevated risk of malignancy is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62c3febac228a98e7b1b2fee90082c8d
https://doi.org/10.1007/978-3-642-46870-4_9
https://doi.org/10.1007/978-3-642-46870-4_9
