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  • 1
    Rabbitts TH. Chromosomal translocations in human cancer (Review). Nature 1994; 372: 1439.
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    Kim BK, Surti U, Pandya AG, Swerdlow SH. Primary and secondary cutaneous diffuse large B-cell lymphomas; a multiparameter analysis of 25 cases including fluorescence in situ hybridization for t(14;18) translocation. Am. J Surg Pathol 2003; 27: 35664.
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    Nomura K, Yoshino T, Nakamura S, Akano Y, Tagawa H, Nishida K, Seto M, Nakamura S, Ueda R, Yamagishi H, Taniwaki M. Detection of t(ll;18)(q21;q21) in marginal zone lymphoma of mucosa-associated lym-phocytic tissue type on paraffin-embedded tissue sections by using fluorescence in situ hybridization. Cancer Genet Cytogenet 2003; 140: 4954.
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    Neat MJ, Foot N, Jenner M, Goff L, Ashcroft K, Burford D, Dunham A, Norton A, Lister TA, Fitzgibbon J. Localisation of a novel region of recurrent amplification in follicular lymphoma to an approximately 6.8 Mb region of 13q32–33. Genes Chromosom. Cancer 2001; 32: 23643.
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    Allen JE, Hough RE, Goepel JR, Bottomley S, Wilson GA, Alcock HE, Baird M, Lorigan PC, Vandenberghe EA, Hancock BW, Hammond DW. Identification of novel regions of amplification and deletion within mantle cell lymphoma DNA by comparative genomic hybridization. Br J Haematol 2002; 116: 2918.
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    Bentz M, Werner CA, Dohner H, Joos S, Earth TF, Siebert R, Schroder M, Stilgenbauer S, Fischer K, Moller P, Lichter P. High incidence of chromosomal imbalances and gene amplifications in the classical follicular variant of follicle center lymphoma. Blood 1996; 88: 143744.
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    Monni O, Oinonen R, Eloen E, Franssia K, Terenhovi L, Joensuu H, Knuutia S. Gain of 3q and deletion of 11q22 are frequent aberrations in mantle cell lymphoma. Genes Chromosom Cancer 1998; 21: 298307.
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    Nagy M, Balazs M, Adam Z, Petko Z, Timar B, Szereday Z, Laszlo T, Warnke RA, Matolcsy A. Genetic instability is associated with histological transformation of follicle center lymphoma. Leukemia 2000; 14: 21428.
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    Rao PH, Houldsworth J, Dyomina K, Parsa NZ, Cigudosa JC, Louie DC, Popplewell L, Offit K, Jhanwar SC, Chaganti RSK. Chromosomal and gene amplification in diffuse large B-cell lymphoma. Blood 1998; 92: 23440.
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    Berglund M, Enblad G, Flordal E, Lui WO, Backlin C, Thunberg U, Sundstrom C, Roos G, Allander SV, Erlanson M, Rosenquist R, Larsson C, Lagercrantz S. Chromosomal imbalances in diffuse large B-cell lymphoma detected by comparative genomic hybridization. Mod Pathol 2002; 15: 80716.
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    Viardot A, Martin-Subero JISiebert R, Harder S, Gesk S, Bentz M, Schlegellberger B. Detection of secondary genetic aberrations in follicular center cell derived lymphoma: assessment of the reliability of comparative genomic hybridization and standard chromosome analysis. Leukemia 2001; 15: 17783.
  • 12
    Karnan S, Tagawa H, Suzuki R, Suguro M, Yamaguchi M, Okamoto M, Morishima Y, Nakamura S, Seto M. Analysis of chromosomal imbalances in de novo CD5-positive diffuse large-B-cell lymphoma detected by comparative genomic hybridization. Genes Chromosom. Cancer 2004; 39: 7781.
  • 13
    Lossos IS, Alizadeh AA, Diehn M, Warnke R, Thorstenson Y, Oefner PJ, Brown PO, Botstein D, Levy R. Transformation of follicular lymphoma to diffuse large-cell lymphoma: alternative patterns with increased or decreased expression of c-myc and its regulated genes. Proc Natl Acad Sci USA 2002; 99: 888691.
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    Martinez-Climent JA, Alizadeh AA, Segraves R, Blesa D, Rubio-Moscardo F, Albertson DG, Garcia-Conde J, Dyer MJ, Levy R, Pinkel D, Lossos IS. Transformation of follicular lymphoma to diffuse large cell lymphoma is associated with a heterogeneous set of DNA copy number and gene expression alterations. Blood 2003; 101: 310917.
  • 15
    Jaffe ES, Harris NL, Stein H, Vardiman JW World Health Organization classification of tumours: Pathology and genetics. Tumours of haematopoietic and lymphoid tissues. Lyon : IARC Press; 2001.
  • 16
    Hu J, Khanna V, Jones M, Surti U. Genomic alterations in uterine leiomyosa-rcomas: potential markers for clinical diagnosis and prognosis. Genes Chromosom. Cancer 2001; 31: 11724.
  • 17
    Franke S, Wlodarska I, Maes B, Vandenberghe P, Delabie J, Hagemeijer A, De Wolf-Peeters C. Lymphocyte predominance Hodgkin disease is characterized by recurrent genomic imbalances. Blood 2001; 97: 184553.
  • 18
    Beà S, López Guillermo A, Ribas M, Puig X, Pinyol M, Carrió A, Zamora L, Soler F, Bosch F, Stilgenbauer S, Colomer D, Miró R, Montserrat E, Campo E. Genetic imbalances in progressed B-cell chronic lymphocytic leukemia and transformed large-cell lymphoma (Richter's syndrome). Am J Pathol 2002; 161: 95768.
  • 19
    Barrans SL, Evans PA, O'Connor SJ, Kendall SJ, Owen RG, Haynes AP, Morgan GJ, Jack AS. The t(14;18) is associated with germinal center-derived diffuse large B-cell lymphoma and is a strong predictor of outcome. Clin Cancer Res 2003; 9: 21339.
  • 20
    Avet-Loiseau H, Vigier M, Moreau A, Mellerin MP, Gaillard F, Harousseau JL, Bataille R, Milpied N. Comparative genomic hybridization detects genomic abnormalities in 80% of follicular lymphomas. Br J Haematol 1997; 97: 11922.
  • 21
    Harada S, Suzuki R, Uehira K, Yatabe Y, Kagami Y, Ogura M, Suzuki H, Oyama A, Kodera Y, Ueda R, Morishima Y, Nakamura S, Seto M. Molecular and immunological dissection of diffuse large B cell lymphoma: CD5+, and CD5-with CD10+ groups may constitute clinically relevant subtypes. Leukemia 1999; 13: 14417.
  • 22
    Cigudosa JC, Parsa NZ, Louie DC, Filippa DA, Jhanwar SC, Johansson B, Mitelman F, Chaganti RSK. Cytogenetic analysis of 363 consecutively ascertained diffuse large B-cell lymphomas. Genes Chromosom Cancer 1999; 25: 12333.
  • 23
    Ree HJ, Ohsima K, Aozasa K, Takeuchi K, Kim CW, Yang WI, Huh JY, Lee SS, Ko YH, Kwon MS, Cho EY, Choi YL, Rhee JC, Kikuchi M, Mori S. Detection of germinal center B-cell lymphoma in archival specimens: critical evaluation of Bcl-6 protein expression in diffuse large B-cell lymphoma of the tonsil. Hum. Pathol 2003; 34: 6106.