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193 related items for PubMed ID: 17713554

  • 1. Combined single nucleotide polymorphism-based genomic mapping and global gene expression profiling identifies novel chromosomal imbalances, mechanisms and candidate genes important in the pathogenesis of T-cell prolymphocytic leukemia with inv(14)(q11q32).
    Dürig J, Bug S, Klein-Hitpass L, Boes T, Jöns T, Martin-Subero JI, Harder L, Baudis M, Dührsen U, Siebert R.
    Leukemia; 2007 Oct; 21(10):2153-63. PubMed ID: 17713554
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  • 2. Inversions and tandem translocations involving chromosome 14q11 and 14q32 in T-prolymphocytic leukemia and T-cell leukemias in patients with ataxia telangiectasia.
    Brito-Babapulle V, Catovsky D.
    Cancer Genet Cytogenet; 1991 Aug; 55(1):1-9. PubMed ID: 1913594
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  • 3. A complex pattern of recurrent chromosomal losses and gains in T-cell prolymphocytic leukemia.
    Soulier J, Pierron G, Vecchione D, Garand R, Brizard F, Sigaux F, Stern MH, Aurias A.
    Genes Chromosomes Cancer; 2001 Jul; 31(3):248-54. PubMed ID: 11391795
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  • 4. Application of cross-species color banding (RxFISH) in the study of T-prolymphocytic leukemia.
    Espinet B, Solé F, Salido M, Lloveras E, Abella E, Besses C, Serrano S, Woessner S, Florensa L.
    Haematologica; 2000 Jun; 85(6):607-12. PubMed ID: 10870117
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  • 5. Abnormalities of chromosomes 8, 11, 14, and X in T-prolymphocytic leukemia studied by fluorescence in situ hybridization.
    Maljaei SH, Brito-Babapulle V, Hiorns LR, Catovsky D.
    Cancer Genet Cytogenet; 1998 Jun; 103(2):110-6. PubMed ID: 9614908
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  • 6. High levels of chromosomal imbalances in typical and small-cell variants of T-cell prolymphocytic leukemia.
    Costa D, Queralt R, Aymerich M, Carrió A, Rozman M, Vallespí T, Colomer D, Nomdedeu B, Montserrat E, Campo E.
    Cancer Genet Cytogenet; 2003 Nov; 147(1):36-43. PubMed ID: 14580769
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  • 7. Tissue microarray-based screening for chromosomal breakpoints affecting the T-cell receptor gene loci in mature T-cell lymphomas.
    Leich E, Haralambieva E, Zettl A, Chott A, Rüdiger T, Höller S, Müller-Hermelink HK, Ott G, Rosenwald A.
    J Pathol; 2007 Sep; 213(1):99-105. PubMed ID: 17582237
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  • 10. Integrated genomic and expression profiling in mantle cell lymphoma: identification of gene-dosage regulated candidate genes.
    Schraders M, Jares P, Bea S, Schoenmakers EF, van Krieken JH, Campo E, Groenen PJ.
    Br J Haematol; 2008 Oct; 143(2):210-21. PubMed ID: 18699851
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  • 11. Trisomy 8q due to i(8q) or der(8) t(8;8) is a frequent lesion in T-prolymphocytic leukaemia: four new cases and a review of the literature.
    Mossafa H, Brizard A, Huret JL, Brizard F, Lessard M, Guilhot F, Tanzer J.
    Br J Haematol; 1994 Apr; 86(4):780-5. PubMed ID: 7918072
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  • 14. Disclosure of candidate genes in acute myeloid leukemia with complex karyotypes using microarray-based molecular characterization.
    Rücker FG, Bullinger L, Schwaenen C, Lipka DB, Wessendorf S, Fröhling S, Bentz M, Miller S, Scholl C, Schlenk RF, Radlwimmer B, Kestler HA, Pollack JR, Lichter P, Döhner K, Döhner H.
    J Clin Oncol; 2006 Aug 20; 24(24):3887-94. PubMed ID: 16864856
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  • 17. T-cell prolymphocytic leukemia: an aggressive T cell malignancy with frequent cutaneous tropism.
    Magro CM, Morrison CD, Heerema N, Porcu P, Sroa N, Deng AC.
    J Am Acad Dermatol; 2006 Sep 20; 55(3):467-77. PubMed ID: 16908353
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  • 19. T cell prolymphocytic leukemia with new chromosome rearrangements.
    Zver S, Kokalj Vokac N, Zagradisnik B, Erjavec A, Zagorac A, Zupan IP, Cernelc P.
    Acta Haematol; 2004 Sep 20; 111(3):168-70. PubMed ID: 15034240
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  • 20. A gene on chromosome Xq28 associated with T-cell prolymphocytic leukemia in two patients with ataxia telangiectasia.
    Thick J, Mak YF, Metcalfe J, Beatty D, Taylor AM.
    Leukemia; 1994 Apr 20; 8(4):564-73. PubMed ID: 8152252
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