217 related articles for article (PubMed ID: 12378526)
1. Molecular cytogenetic analysis of genomic instability at the 1q12-22 chromosomal site in B-cell non-Hodgkin lymphoma.
Itoyama T; Nanjungud G; Chen W; Dyomin VG; Teruya-Feldstein J; Jhanwar SC; Zelenetz AD; Chaganti RS
Genes Chromosomes Cancer; 2002 Dec; 35(4):318-28. PubMed ID: 12378526
[TBL] [Abstract][Full Text] [Related]
2. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
Lestou VS; Ludkovski O; Connors JM; Gascoyne RD; Lam WL; Horsman DE
Genes Chromosomes Cancer; 2003 Apr; 36(4):375-81. PubMed ID: 12619161
[TBL] [Abstract][Full Text] [Related]
3. Novel evidence of a role for chromosome 1 pericentric heterochromatin in the pathogenesis of B-cell lymphoma and multiple myeloma.
Le Baccon P; Leroux D; Dascalescu C; Duley S; Marais D; Esmenjaud E; Sotto JJ; Callanan M
Genes Chromosomes Cancer; 2001 Nov; 32(3):250-64. PubMed ID: 11579465
[TBL] [Abstract][Full Text] [Related]
4. Genomic instability in multiple myeloma: evidence for jumping segmental duplications of chromosome arm 1q.
Sawyer JR; Tricot G; Lukacs JL; Binz RL; Tian E; Barlogie B; Shaughnessy J
Genes Chromosomes Cancer; 2005 Jan; 42(1):95-106. PubMed ID: 15472896
[TBL] [Abstract][Full Text] [Related]
5. Frequent aberrations of chromosome 8 in aggressive B-cell non-Hodgkin lymphoma.
Pienkowska-Grela B; Witkowska A; Grygalewicz B; Rymkiewicz G; Rygier J; Woroniecka R; Walewski J
Cancer Genet Cytogenet; 2005 Jan; 156(2):114-21. PubMed ID: 15642390
[TBL] [Abstract][Full Text] [Related]
6. Uncovering novel inter- and intrachromosomal chromosome 1 aberrations in follicular lymphomas by using an innovative multicolor banding technique.
Lestou VS; Gascoyne RD; Salski C; Connors JM; Horsman DE
Genes Chromosomes Cancer; 2002 Jun; 34(2):201-10. PubMed ID: 11979554
[TBL] [Abstract][Full Text] [Related]
7. Delineation of the frequently deleted region on chromosome arm 13q in B-cell non-Hodgkin's lymphoma.
Wada M; Okamura T; Okada M; Teramura M; Masuda M; Motoji T; Mizoguchi H
Int J Hematol; 2000 Feb; 71(2):159-66. PubMed ID: 10745626
[TBL] [Abstract][Full Text] [Related]
8. Differences in nuclear positioning of 1q12 pericentric heterochromatin in normal and tumor B lymphocytes with 1q rearrangements.
Barki-Celli L; Lefebvre C; Le Baccon P; Nadeau G; Bonnefoix T; Usson Y; Vourc'h C; Khochbin S; Leroux D; Callanan M
Genes Chromosomes Cancer; 2005 Aug; 43(4):339-49. PubMed ID: 15846776
[TBL] [Abstract][Full Text] [Related]
9. Molecular cytogenetic delineation of the breakpoint at 18q21.1 in low-grade B-cell lymphoma of mucosa-associated lymphoid tissue.
Akagi T; Tamura A; Motegi M; Suzuki R; Hosokawa Y; Nakamura S; Morishima Y; Seto M; Taniwaki M
Genes Chromosomes Cancer; 1999 Apr; 24(4):315-21. PubMed ID: 10092129
[TBL] [Abstract][Full Text] [Related]
10. Pathogenesis of jumping translocations: a molecular cytogenetics study.
Wan TS; Ma SK; Chow EY; Li YH; Lin SY; Chan LC
Leuk Res; 2004 Oct; 28(10):1075-9. PubMed ID: 15289020
[TBL] [Abstract][Full Text] [Related]
11. FISH identifies different types of duplications with 12q13-15 as the commonly involved segment in B-cell lymphoproliferative malignancies characterized by partial trisomy 12.
Dierlamm J; Wlodarska I; Michaux L; Vermeesch JR; Meeus P; Stul M; Criel A; Verhoef G; Thomas J; Delannoy A; Louwagie A; Cassiman JJ; Mecucci C; Hagemeijer A; Van den Berghe H
Genes Chromosomes Cancer; 1997 Oct; 20(2):155-66. PubMed ID: 9331566
[TBL] [Abstract][Full Text] [Related]
12. Low level of DNA repair in human chromosome 1 heterochromatin.
Surrallés J; Darroudi F; Natarajan AT
Genes Chromosomes Cancer; 1997 Oct; 20(2):173-84. PubMed ID: 9331568
[TBL] [Abstract][Full Text] [Related]
13. A marginal zone phenotype in follicular lymphoma with t(14;18) is associated with secondary cytogenetic aberrations typical of marginal zone lymphoma.
Torlakovic EE; Aamot HV; Heim S
J Pathol; 2006 Jun; 209(2):258-64. PubMed ID: 16583359
[TBL] [Abstract][Full Text] [Related]
14. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
[TBL] [Abstract][Full Text] [Related]
15. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
[TBL] [Abstract][Full Text] [Related]
16. Deregulation of FCGR2B expression by 1q21 rearrangements in follicular lymphomas.
Chen W; Palanisamy N; Schmidt H; Teruya-Feldstein J; Jhanwar SC; Zelenetz AD; Houldsworth J; Chaganti RS
Oncogene; 2001 Nov; 20(52):7686-93. PubMed ID: 11753646
[TBL] [Abstract][Full Text] [Related]
17. Cytogenetic and molecular delineation of a region of chromosome 3q commonly gained in marginal zone B-cell lymphoma.
Gazzo S; Baseggio L; Coignet L; Poncet C; Morel D; Coiffier B; Felman P; Berger F; Salles G; Callet-Bauchu E
Haematologica; 2003 Jan; 88(1):31-8. PubMed ID: 12551824
[TBL] [Abstract][Full Text] [Related]
18. Molecular cytogenetic aberrations in 21 Chinese patients with plasma cell leukemia.
Xu W; Li JY; Fan L; Chen LJ; Qiu HR; Qiu HX; Lu H
Int J Lab Hematol; 2009 Jun; 31(3):338-43. PubMed ID: 18284415
[TBL] [Abstract][Full Text] [Related]
19. Molecular cytogenetic characterization of variant Philadelphia translocations in chronic myeloid leukemia: genesis and deletion of derivative chromosome 9.
Bennour A; Sennana H; Laatiri MA; Elloumi M; Khelif A; Saad A
Cancer Genet Cytogenet; 2009 Oct; 194(1):30-7. PubMed ID: 19737651
[TBL] [Abstract][Full Text] [Related]
20. Array comparative genomic hybridization reveals a very high frequency of deletions of the long arm of chromosome 6 in testicular lymphoma.
Bosga-Bouwer AG; Kok K; Booman M; Boven L; van der Vlies P; van den Berg A; van den Berg E; de Jong B; Poppema S; Kluin P
Genes Chromosomes Cancer; 2006 Oct; 45(10):976-81. PubMed ID: 16865685
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
