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Items: 1 to 20 of 239

1.

Detection of chromosome 11q13 breakpoints by interphase fluorescence in situ hybridization. A useful ancillary method for the diagnosis of mantle cell lymphoma.

Katz RL, Caraway NP, Gu J, Jiang F, Pasco-Miller LA, Glassman AB, Luthra R, Hayes KJ, Romaguera JE, Cabanillas FF, Medeiros LJ.

Am J Clin Pathol. 2000 Aug;114(2):248-57.

PMID:
10941340
3.
4.

Detection of 11q13 rearrangements in hematologic neoplasias by double-color fluorescence in situ hybridization.

Coignet LJ, Schuuring E, Kibbelaar RE, Raap TK, Kleiverda KK, Bertheas MF, Wiegant J, Beverstock G, Kluin PM.

Blood. 1996 Feb 15;87(4):1512-9.

5.

Mantle cell lymphoma: improved diagnostics using a combined approach of immunohistochemistry and identification of t(11;14)(q13;q32) by polymerase chain reaction and fluorescence in situ hybridization.

Kodet R, Mrhalová M, Krsková L, Soukup J, Campr V, Neskudla T, Szépe P, Plank L.

Virchows Arch. 2003 Jun;442(6):538-47. Epub 2003 May 1.

PMID:
12728315
6.

Diagnostic utility of fluorescence in situ hybridization in mantle-cell lymphoma.

Remstein ED, Kurtin PJ, Buño I, Bailey RJ, Proffitt J, Wyatt WA, Hanson CA, Dewald GW.

Br J Haematol. 2000 Sep;110(4):856-62.

PMID:
11054068
7.

A comparative analysis of FISH, RT-PCR, PCR, and immunohistochemistry for the diagnosis of mantle cell lymphomas.

Belaud-Rotureau MA, Parrens M, Dubus P, Garroste JC, de Mascarel A, Merlio JP.

Mod Pathol. 2002 May;15(5):517-25.

8.

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;47(12):1086-97. doi: 10.1002/gcc.20609.

PMID:
18709664
9.

Direct visualization of dispersed 11q13 chromosomal translocations in mantle cell lymphoma by multicolor DNA fiber fluorescence in situ hybridization.

Vaandrager JW, Schuuring E, Zwikstra E, de Boer CJ, Kleiverda KK, van Krieken JH, Kluin-Nelemans HC, van Ommen GJ, Raap AK, Kluin PM.

Blood. 1996 Aug 15;88(4):1177-82.

10.

Molecular diagnosis of t(11;14) in mantle cell lymphoma using two-colour interphase fluorescence in situ hybridization.

Monteil M, Callanan M, Dascalescu C, Sotto JJ, Leroux D.

Br J Haematol. 1996 Jun;93(3):656-60.

PMID:
8652388
11.

Detection of a subset of CD30+ anaplastic large cell lymphoma by interphase fluorescence in situ hybridization.

Shin HJ, Thorson P, Gu J, Katz RL.

Diagn Cytopathol. 2003 Aug;29(2):61-6.

PMID:
12889041
12.

Detection of t(11;14) using interphase molecular cytogenetics in mantle cell lymphoma and atypical chronic lymphocytic leukemia.

Avet-Loiseau H, Garand R, Gaillard F, Daviet A, Mellerin MP, Robillard N, Bouyge I, Arcot S, Batzer M, Talmant P, Harousseau JL, Milpied N, Bataille R.

Genes Chromosomes Cancer. 1998 Oct;23(2):175-82.

PMID:
9739021
13.

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.

PMID:
10679918
14.

Blastoid and common variants of mantle cell lymphoma exhibit distinct immunophenotypic and interphase FISH features.

Parrens M, Belaud-Rotureau MA, Fitoussi O, Carerre N, Bouabdallah K, Marit G, Dubus P, de Mascarel A, Merlio JP.

Histopathology. 2006 Mar;48(4):353-62.

PMID:
16487357
15.

Banded chromosomes versus fluorescence in situ hybridization in the diagnosis of mantle cell lymphoma: a lesson from three cases.

Mohamed AN, Ali W, Kopptich F, al Katib A.

Cancer Genet Cytogenet. 2002 Jul 15;136(2):108-12.

PMID:
12237233
16.

Cytogenetic and interphase cytogenetic characterization of atypical chronic lymphocytic leukemia carrying BCL1 translocation.

Cuneo A, Bigoni R, Negrini M, Bullrich F, Veronese ML, Roberti MG, Bardi A, Rigolin GM, Cavazzini P, Croce CM, Castoldi G.

Cancer Res. 1997 Mar 15;57(6):1144-50.

18.

Molecular cytogenetic study of a mantle cell lymphoma with a complex translocation involving the CCND1 (11q13) region.

Maravelaki S, Burford A, Wotherspoon A, Joshi R, Matutes E, Catovsky D, Brito-Babapulle V.

Cancer Genet Cytogenet. 2004 Oct 1;154(1):67-71.

PMID:
15381376
19.

Mantle cell lymphoma with 8q24 chromosomal abnormalities: a report of 5 cases with blastoid features.

Hao S, Sanger W, Onciu M, Lai R, Schlette EJ, Medeiros LJ.

Mod Pathol. 2002 Dec;15(12):1266-72. Review.

20.

Variant t(2;11)(p11;q13) associated with the IgK-CCND1 rearrangement is a recurrent translocation in leukemic small-cell B-non-Hodgkin lymphoma.

Wlodarska I, Meeus P, Stul M, Thienpont L, Wouters E, Marcelis L, Demuynck H, Rummens JL, Madoe V, Hagemeijer A.

Leukemia. 2004 Oct;18(10):1705-10.

PMID:
15306823

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