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342 related items for PubMed ID: 18367489

  • 1. Genomic aberrations in mantle cell lymphoma detected by interphase fluorescence in situ hybridization. Incidence and clinicopathological correlations.
    Sander S, Bullinger L, Leupolt E, Benner A, Kienle D, Katzenberger T, Kalla J, Ott G, Müller-Hermelink HK, Barth TF, Möller P, Lichter P, Döhner H, Stilgenbauer S.
    Haematologica; 2008 May; 93(5):680-7. PubMed ID: 18367489
    [Abstract] [Full Text] [Related]

  • 2. [Cytogenetics of mantle cell lymphoma].
    Obukhova TN, Lorie IuIu, Vodinskaia LA, Alimova GA, Nikitin EA, Samoĭlova RS, Kaplanskaia IB, Domracheva EV.
    Ter Arkh; 2004 May; 76(7):70-7. PubMed ID: 15379132
    [Abstract] [Full Text] [Related]

  • 3. Cytogenetic abnormalities additional to t(11;14) correlate with clinical features in leukaemic presentation of mantle cell lymphoma, and may influence prognosis: a study of 60 cases by FISH.
    Parry-Jones N, Matutes E, Morilla R, Brito-Babapulle V, Wotherspoon A, Swansbury GJ, Catovsky D.
    Br J Haematol; 2007 Apr; 137(2):117-24. PubMed ID: 17391491
    [Abstract] [Full Text] [Related]

  • 4. t(11;14)-positive mantle cell lymphomas exhibit complex karyotypes and share similarities with B-cell chronic lymphocytic leukemia.
    Bentz M, Plesch A, Bullinger L, Stilgenbauer S, Ott G, Müller-Hermelink HK, Baudis M, Barth TF, Möller P, Lichter P, Döhner H.
    Genes Chromosomes Cancer; 2000 Mar; 27(3):285-94. PubMed ID: 10679918
    [Abstract] [Full Text] [Related]

  • 5. Delineation of distinct tumour profiles in mantle cell lymphoma by detailed cytogenetic, interphase genetic and morphological analysis.
    Katzenberger T, Kienle D, Stilgenbauer S, Höller S, Schilling C, Mäder U, Puppe B, Petzoldt C, Sander S, Bullinger L, Stöcklein H, Kalla J, Hartmann E, Adam P, Ott MM, Müller-Hermelink HK, Rosenwald A, Ott G.
    Br J Haematol; 2008 Aug; 142(4):538-50. PubMed ID: 18564361
    [Abstract] [Full Text] [Related]

  • 6. Molecular cytogenetic aberrations in patients with multiple myeloma studied by interphase fluorescence in situ hybridization.
    Chen L, Li J, Xu W, Qiu H, Zhu Y, Zhang Y, Duan L, Qian S, Lu H.
    Exp Oncol; 2007 Jun; 29(2):116-20. PubMed ID: 17704743
    [Abstract] [Full Text] [Related]

  • 7. Detection of gene copy number aberrations in mantle cell lymphoma by a single quantitative multiplex PCR assay: clinicopathological relevance and prognosis value.
    Jardin F, Picquenot JM, Parmentier F, Ruminy P, Cornic M, Penther D, Bertrand P, Lanic H, Cassuto O, Humbrecht C, Lemasle E, Wautier A, Bastard C, Tilly H.
    Br J Haematol; 2009 Sep; 146(6):607-18. PubMed ID: 19594747
    [Abstract] [Full Text] [Related]

  • 8. The utility of interphase fluorescence in situ hybridization for the detection of the translocation t(11;14)(q13;q32) in the diagnosis of mantle cell lymphoma on fine-needle aspiration specimens.
    Caraway NP, Gu J, Lin P, Romaguera JE, Glassman A, Katz R.
    Cancer; 2005 Apr 25; 105(2):110-8. PubMed ID: 15712276
    [Abstract] [Full Text] [Related]

  • 9. Incidence and prognostic impact of secondary cytogenetic aberrations in a series of 145 patients with mantle cell lymphoma.
    Espinet B, Salaverria I, Beà S, Ruiz-Xivillé N, Balagué O, Salido M, Costa D, Carreras J, Rodríguez-Vicente AE, Luís García J, Hernández-Rivas JM, Calasanz MJ, Siebert R, Ferrer A, Salar A, Carrió A, Polo N, García-Marco JA, Domingo A, González-Barca E, Romagosa V, Marugán I, López-Guillermo A, Millá F, Luís Mate J, Luño E, Sanzo C, Collado R, Oliver I, Monzó S, Palacín A, González T, Sant F, Salinas R, Ardanaz MT, Font L, Escoda L, Florensa L, Serrano S, Campo E, Solé F.
    Genes Chromosomes Cancer; 2010 May 25; 49(5):439-51. PubMed ID: 20143418
    [Abstract] [Full Text] [Related]

  • 10. Comprehensive whole genome array CGH profiling of mantle cell lymphoma model genomes.
    de Leeuw RJ, Davies JJ, Rosenwald A, Bebb G, Gascoyne RD, Dyer MJ, Staudt LM, Martinez-Climent JA, Lam WL.
    Hum Mol Genet; 2004 Sep 01; 13(17):1827-37. PubMed ID: 15229187
    [Abstract] [Full Text] [Related]

  • 11. Molecular cytogenetic characterization of marginal zone B-cell lymphoma: correlation with clinicopathologic findings in 14 cases.
    Cuneo A, Bigoni R, Roberti MG, Milani R, Agostini P, Cavazzini F, Minotto C, De Angeli C, Bardi A, Tammiso E, Negrini M, Cavazzini P, Castoldi G.
    Haematologica; 2001 Jan 01; 86(1):64-70. PubMed ID: 11146573
    [Abstract] [Full Text] [Related]

  • 12. Multiple recurrent chromosomal breakpoints in mantle cell lymphoma revealed by a combination of molecular cytogenetic techniques.
    Salaverria I, Espinet B, Carrió A, Costa D, Astier L, Slotta-Huspenina J, Quintanilla-Martinez L, Fend F, Solé F, Colomer D, Serrano S, Miró R, Beà S, Campo E.
    Genes Chromosomes Cancer; 2008 Dec 01; 47(12):1086-97. PubMed ID: 18709664
    [Abstract] [Full Text] [Related]

  • 13. Allelic genotyping reveals a hierarchy of genomic alterations in mantle cell lymphoma associated to cell proliferation.
    Hutter G, Scheubner M, Ott G, Zimmermann Y, Hübler K, Roth S, Stilgenbauer S, Kalla J, Stöcklein H, Hiddemann W, Dreyling M.
    Ann Hematol; 2009 Sep 01; 88(9):821-8. PubMed ID: 19137297
    [Abstract] [Full Text] [Related]

  • 14. Detailed assessment of copy number alterations revealing homozygous deletions in 1p and 13q in mantle cell lymphoma.
    Flordal Thelander E, Ichimura K, Collins VP, Walsh SH, Barbany G, Hagberg A, Laurell A, Rosenquist R, Larsson C, Lagercrantz S.
    Leuk Res; 2007 Sep 01; 31(9):1219-30. PubMed ID: 17161458
    [Abstract] [Full Text] [Related]

  • 15. Loss of chromosome 11q21-23.1 and 17p and gain of chromosome 6p are independent prognostic indicators in B-cell non-Hodgkin's lymphoma.
    Stokke T, DeAngelis P, Smedshammer L, Galteland E, Steen HB, Smeland EB, Delabie J, Holte H.
    Br J Cancer; 2001 Dec 14; 85(12):1900-13. PubMed ID: 11747333
    [Abstract] [Full Text] [Related]

  • 16. Comparative genome profiling across subtypes of low-grade B-cell lymphoma identifies type-specific and common aberrations that target genes with a role in B-cell neoplasia.
    Ferreira BI, García JF, Suela J, Mollejo M, Camacho FI, Carro A, Montes S, Piris MA, Cigudosa JC.
    Haematologica; 2008 May 14; 93(5):670-9. PubMed ID: 18367492
    [Abstract] [Full Text] [Related]

  • 17. High incidence and intraclonal heterogeneity of chromosome 11 aberrations in patients with newly diagnosed multiple myeloma detected by multiprobe interphase FISH.
    Cremer FW, Kartal M, Hose D, Bila J, Buck I, Bellos F, Raab MS, Brough M, Moebus A, Hager HD, Goldschmidt H, Moos M, Bartram CR, Jauch A.
    Cancer Genet Cytogenet; 2005 Sep 14; 161(2):116-24. PubMed ID: 16102581
    [Abstract] [Full Text] [Related]

  • 18. [Relationship between p53 gene and chromosome 13q14 variations and prognosis in primary intestinal lymphoma].
    Feng LJ, Zhang GP, Xie M, Cao PF, Fu CY, Hu ZL, Dai M.
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 Jul 14; 11(7):555-8. PubMed ID: 19650989
    [Abstract] [Full Text] [Related]

  • 19. High-resolution genomic screening in mantle cell lymphoma--specific changes correlate with genomic complexity, the proliferation signature and survival.
    Halldórsdóttir AM, Sander B, Göransson H, Isaksson A, Kimby E, Mansouri M, Rosenquist R, Ehrencrona H.
    Genes Chromosomes Cancer; 2011 Feb 14; 50(2):113-21. PubMed ID: 21117067
    [Abstract] [Full Text] [Related]

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