185 related articles for article (PubMed ID: 11579465)
1. 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]
2. 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]
3. 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]
4. 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]
5. Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage-fusion-bridge cycles of a 1q12 approximately 23 amplicon.
Sawyer JR; Tian E; Thomas E; Koller M; Stangeby C; Sammartino G; Goosen L; Swanson C; Binz RL; Barlogie B; Shaughnessy J
Br J Haematol; 2009 Nov; 147(4):484-94. PubMed ID: 19744130
[TBL] [Abstract][Full Text] [Related]
6. Genetics and epigenetics of 1q rearrangements in hematological malignancies.
Fournier A; Florin A; Lefebvre C; Solly F; Leroux D; Callanan MB
Cytogenet Genome Res; 2007; 118(2-4):320-7. PubMed ID: 18000386
[TBL] [Abstract][Full Text] [Related]
7. Centromeric instability of chromosome 1 resulting in multibranched chromosomes, telomeric fusions, and "jumping translocations" of 1q in a human immunodeficiency virus-related non-Hodgkin's lymphoma.
Sawyer JR; Swanson CM; Koller MA; North PE; Ross SW
Cancer; 1995 Oct; 76(7):1238-44. PubMed ID: 8630904
[TBL] [Abstract][Full Text] [Related]
8. Involvement of BCL6 in chromosomal aberrations affecting band 3q27 in B-cell non-Hodgkin lymphoma.
Chaganti SR; Chen W; Parsa N; Offit K; Louie DC; Dalla-Favera R; Chaganti RS
Genes Chromosomes Cancer; 1998 Dec; 23(4):323-7. PubMed ID: 9824205
[TBL] [Abstract][Full Text] [Related]
9. Rearrangement of the BCL6 gene in B-cell lymphoid neoplasms: comparison with lymphomas associated with BCL2 rearrangement.
Muramatsu M; Akasaka T; Kadowaki N; Ohno H; Yamabe H; Edamura S; Dor S; Mori T; Okuma M; Fukuhara S
Br J Haematol; 1996 Jun; 93(4):911-20. PubMed ID: 8703825
[TBL] [Abstract][Full Text] [Related]
10. Bcl-2 rearrangements with breakpoints in both vcr and mbr in non-Hodgkin's lymphomas and chronic lymphocytic leukaemia.
Merup M; Spasokoukotskaja T; Einhorn S; Smith CI; Gahrton G; Juliusson G
Br J Haematol; 1996 Mar; 92(3):647-52. PubMed ID: 8616030
[TBL] [Abstract][Full Text] [Related]
11. Rearrangement of the chromosome 11 bcl-1 locus in centrocytic lymphoma: analysis with multiple breakpoint probes.
Williams ME; Meeker TC; Swerdlow SH
Blood; 1991 Jul; 78(2):493-8. PubMed ID: 2070085
[TBL] [Abstract][Full Text] [Related]
12. Sequential analysis of 43 patients with non-Hodgkin's lymphoma: clinical correlations with cytogenetic, histologic, immunophenotyping, and molecular studies.
Whang-Peng J; Knutsen T; Jaffe ES; Steinberg SM; Raffeld M; Zhao WP; Duffey P; Condron K; Yano T; Longo DL
Blood; 1995 Jan; 85(1):203-16. PubMed ID: 7803794
[TBL] [Abstract][Full Text] [Related]
13. Rearrangement of the BCL6 gene in B-cell lymphoid neoplasms.
Muramatsu M; Akasaka T; Kadowaki N; Ohno H; Fukuhara S; Okuma M
Leukemia; 1997 Apr; 11 Suppl 3():318-20. PubMed ID: 9209377
[TBL] [Abstract][Full Text] [Related]
14. Role of chromosome 1 pericentric heterochromatin (1q) in pathogenesis of myelodysplastic syndromes: report of 2 new cases.
Millington K; Hudnall SD; Northup J; Panova N; Velagaleti G
Exp Mol Pathol; 2008 Apr; 84(2):189-93. PubMed ID: 18339374
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study.
Parada LA; Limon J; Iliszko M; Czauderna P; Gisselsson D; Höglund M; Kullendorff CM; Wiebe T; Mertens F; Johansson B
Med Pediatr Oncol; 2000 Mar; 34(3):165-70. PubMed ID: 10696121
[TBL] [Abstract][Full Text] [Related]
17. Rearrangement of the 5' cluster region of the BCL2 gene in lymphoid neoplasm: a summary of nine cases.
Yabumoto K; Akasaka T; Muramatsu M; Kadowaki N; Hayashi T; Ohno H; Fukuhara S; Okuma M
Leukemia; 1996 Jun; 10(6):970-7. PubMed ID: 8667654
[TBL] [Abstract][Full Text] [Related]
18. Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progression-related mechanisms.
Rudolph C; Liehr T; Steinemann D; Emura M; Daibata M; Matsuo Y; Emi N; Abe M; Lai R; Mrasek K; Claussen U; Schlegelberger B
Cytogenet Genome Res; 2006; 112(3-4):213-21. PubMed ID: 16484775
[TBL] [Abstract][Full Text] [Related]
19. Heterogeneous chromosomal aberrations generate 3' truncations of the NFKB2/lyt-10 gene in lymphoid malignancies.
Migliazza A; Lombardi L; Rocchi M; Trecca D; Chang CC; Antonacci R; Fracchiolla NS; Ciana P; Maiolo AT; Neri A
Blood; 1994 Dec; 84(11):3850-60. PubMed ID: 7949142
[TBL] [Abstract][Full Text] [Related]
20. Evidence of an epigenetic origin for high-risk 1q21 copy number aberrations in multiple myeloma.
Sawyer JR; Tian E; Heuck CJ; Johann DJ; Epstein J; Swanson CM; Lukacs JL; Binz RL; Johnson M; Sammartino G; Zangari M; Davies FE; van Rhee F; Morgan GJ; Barlogie B
Blood; 2015 Jun; 125(24):3756-9. PubMed ID: 25943786
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
