270 related articles for article (PubMed ID: 21258086)
1. The FRA2C common fragile site maps to the borders of MYCN amplicons in neuroblastoma and is associated with gross chromosomal rearrangements in different cancers.
Blumrich A; Zapatka M; Brueckner LM; Zheglo D; Schwab M; Savelyeva L
Hum Mol Genet; 2011 Apr; 20(8):1488-501. PubMed ID: 21258086
[TBL] [Abstract][Full Text] [Related]
2. Characterization of a complex genomic alteration on chromosome 2p that leads to four alternatively spliced fusion transcripts in the neuroblastoma cell lines IMR-5, IMR-5/75 and IMR-32.
Oberthuer A; Skowron M; Spitz R; Kahlert Y; Westermann F; Mehler K; Berthold F; Fischer M
Gene; 2005 Dec; 363():41-50. PubMed ID: 16216448
[TBL] [Abstract][Full Text] [Related]
3. Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.
Selzer RR; Richmond TA; Pofahl NJ; Green RD; Eis PS; Nair P; Brothman AR; Stallings RL
Genes Chromosomes Cancer; 2005 Nov; 44(3):305-19. PubMed ID: 16075461
[TBL] [Abstract][Full Text] [Related]
4. Relational mapping of MYCN and DDXI in band 2p24 and analysis of amplicon arrays in double minute chromosomes and homogeneously staining regions by use of free chromatin FISH.
Pandita A; Godbout R; Zielenska M; Thorner P; Bayani J; Squire JA
Genes Chromosomes Cancer; 1997 Nov; 20(3):243-52. PubMed ID: 9365831
[TBL] [Abstract][Full Text] [Related]
5. High-resolution mapping of a 130-kb core region of the MYCN amplicon in neuroblastomas.
Reiter JL; Brodeur GM
Genomics; 1996 Feb; 32(1):97-103. PubMed ID: 8786126
[TBL] [Abstract][Full Text] [Related]
6. Characterization of FRA7B, a human common fragile site mapped at the 7p chromosome terminal region.
Bosco N; Pelliccia F; Rocchi A
Cancer Genet Cytogenet; 2010 Oct; 202(1):47-52. PubMed ID: 20804921
[TBL] [Abstract][Full Text] [Related]
7. Coamplification of multiple regions of chromosome 2, including MYCN, in a single patchwork amplicon in cancer cell lines.
Kitada K; Aida S; Aikawa S
Cytogenet Genome Res; 2012; 136(1):30-7. PubMed ID: 22123490
[TBL] [Abstract][Full Text] [Related]
8. The DDX1 gene maps within 400 kbp 5' to MYCN and is frequently coamplified in human neuroblastoma.
Amler LC; Schürmann J; Schwab M
Genes Chromosomes Cancer; 1996 Feb; 15(2):134-7. PubMed ID: 8834178
[TBL] [Abstract][Full Text] [Related]
9. Common fragile sites in colon cancer cell lines: role of mismatch repair, RAD51 and poly(ADP-ribose) polymerase-1.
Vernole P; Muzi A; Volpi A; Terrinoni A; Dorio AS; Tentori L; Shah GM; Graziani G
Mutat Res; 2011 Jul; 712(1-2):40-8. PubMed ID: 21570414
[TBL] [Abstract][Full Text] [Related]
10. Physical mapping of the DDX1 gene to 340 kb 5' of MYCN.
Kuroda H; White PS; Sulman EP; Manohar CF; Reiter JL; Cohn SL; Brodeur GM
Oncogene; 1996 Oct; 13(7):1561-5. PubMed ID: 8875996
[TBL] [Abstract][Full Text] [Related]
11. Neuroblastomas have distinct genomic DNA profiles that predict clinical phenotype and regional gene expression.
Mosse YP; Diskin SJ; Wasserman N; Rinaldi K; Attiyeh EF; Cole K; Jagannathan J; Bhambhani K; Winter C; Maris JM
Genes Chromosomes Cancer; 2007 Oct; 46(10):936-49. PubMed ID: 17647283
[TBL] [Abstract][Full Text] [Related]
12. Three chromosomal rearrangements in neuroblastoma cluster within a 300-kb region on 1p36.1.
Spieker N; Beitsma M; Van Sluis P; Chan A; Caron H; Versteeg R
Genes Chromosomes Cancer; 2001 Jun; 31(2):172-81. PubMed ID: 11319804
[TBL] [Abstract][Full Text] [Related]
13. RORA, a large common fragile site gene, is involved in cellular stress response.
Zhu Y; McAvoy S; Kuhn R; Smith DI
Oncogene; 2006 May; 25(20):2901-8. PubMed ID: 16462772
[TBL] [Abstract][Full Text] [Related]
14. Common fragile site FRA11G and rare fragile site FRA11B at 11q23.3 encompass distinct genomic regions.
Fechter A; Buettel I; Kuehnel E; Savelyeva L; Schwab M
Genes Chromosomes Cancer; 2007 Jan; 46(1):98-106. PubMed ID: 17063465
[TBL] [Abstract][Full Text] [Related]
15. Low-copy repeats on chromosome 22q11.2 show replication timing switches, DNA flexibility peaks and stress inducible asynchrony, sharing instability features with fragile sites.
Puliti A; Rizzato C; Conti V; Bedini A; Gimelli G; Barale R; Sbrana I
Mutat Res; 2010 Apr; 686(1-2):74-83. PubMed ID: 20138061
[TBL] [Abstract][Full Text] [Related]
16. Stably transfected common fragile site sequences exhibit instability at ectopic sites.
Ragland RL; Glynn MW; Arlt MF; Glover TW
Genes Chromosomes Cancer; 2008 Oct; 47(10):860-72. PubMed ID: 18615677
[TBL] [Abstract][Full Text] [Related]
17. Genomic rearrangements at the FRA2H common fragile site frequently involve non-homologous recombination events across LTR and L1(LINE) repeats.
Brueckner LM; Sagulenko E; Hess EM; Zheglo D; Blumrich A; Schwab M; Savelyeva L
Hum Genet; 2012 Aug; 131(8):1345-59. PubMed ID: 22476624
[TBL] [Abstract][Full Text] [Related]
18. Disabled-1 is a large common fragile site gene, inactivated in multiple cancers.
McAvoy S; Zhu Y; Perez DS; James CD; Smith DI
Genes Chromosomes Cancer; 2008 Feb; 47(2):165-74. PubMed ID: 18008369
[TBL] [Abstract][Full Text] [Related]
19. An integrated mBAND and submegabase resolution tiling set (SMRT) CGH array analysis of focal amplification, microdeletions, and ladder structures consistent with breakage-fusion-bridge cycle events in osteosarcoma.
Lim G; Karaskova J; Beheshti B; Vukovic B; Bayani J; Selvarajah S; Watson SK; Lam WL; Zielenska M; Squire JA
Genes Chromosomes Cancer; 2005 Apr; 42(4):392-403. PubMed ID: 15660435
[TBL] [Abstract][Full Text] [Related]
20. Non-random inactivation of large common fragile site genes in different cancers.
McAvoy S; Ganapathiraju SC; Ducharme-Smith AL; Pritchett JR; Kosari F; Perez DS; Zhu Y; James CD; Smith DI
Cytogenet Genome Res; 2007; 118(2-4):260-9. PubMed ID: 18000379
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
