194 related articles for article (PubMed ID: 19279687)
21. A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene.
Murga Penas EM; Cools J; Algenstaedt P; Hinz K; Seeger D; Schafhausen P; Schilling G; Marynen P; Hossfeld DK; Dierlamm J
Genes Chromosomes Cancer; 2003 May; 37(1):79-83. PubMed ID: 12661008
[TBL] [Abstract][Full Text] [Related]
22. Intergenic splicing of MDS1 and EVI1 occurs in normal tissues as well as in myeloid leukemia and produces a new member of the PR domain family.
Fears S; Mathieu C; Zeleznik-Le N; Huang S; Rowley JD; Nucifora G
Proc Natl Acad Sci U S A; 1996 Feb; 93(4):1642-7. PubMed ID: 8643684
[TBL] [Abstract][Full Text] [Related]
23. Cryptic splice site activation during RNA processing of MLL/AF4 chimeric transcripts in infants with t(4;11) positive ALL.
Divoky V; Trka JM; Watzinger F; Lion T
Gene; 2000 Apr; 247(1-2):111-8. PubMed ID: 10773450
[TBL] [Abstract][Full Text] [Related]
24. Characterisation of genomic translocation breakpoints and identification of an alternative TCF3/PBX1 fusion transcript in t(1;19)(q23;p13)-positive acute lymphoblastic leukaemias.
Paulsson K; Jonson T; Ora I; Olofsson T; Panagopoulos I; Johansson B
Br J Haematol; 2007 Jul; 138(2):196-201. PubMed ID: 17593026
[TBL] [Abstract][Full Text] [Related]
25. FusionGDB: fusion gene annotation DataBase.
Kim P; Zhou X
Nucleic Acids Res; 2019 Jan; 47(D1):D994-D1004. PubMed ID: 30407583
[TBL] [Abstract][Full Text] [Related]
26. Molecular characterization of genomic AML1-ETO fusions in childhood leukemia.
Xiao Z; Greaves MF; Buffler P; Smith MT; Segal MR; Dicks BM; Wiencke JK; Wiemels JL
Leukemia; 2001 Dec; 15(12):1906-13. PubMed ID: 11753612
[TBL] [Abstract][Full Text] [Related]
27. Variable breakpoints target PAX5 in patients with dicentric chromosomes: a model for the basis of unbalanced translocations in cancer.
An Q; Wright SL; Konn ZJ; Matheson E; Minto L; Moorman AV; Parker H; Griffiths M; Ross FM; Davies T; Hall AG; Harrison CJ; Irving JA; Strefford JC
Proc Natl Acad Sci U S A; 2008 Nov; 105(44):17050-4. PubMed ID: 18957548
[TBL] [Abstract][Full Text] [Related]
28. Identification of chromosomal breakpoints of cancer-specific translocations by rolling circle amplification and long-distance inverse PCR.
Thorsen J; Micci F; Heim S
Cancer Genet; 2011 Aug; 204(8):458-61. PubMed ID: 21962896
[TBL] [Abstract][Full Text] [Related]
29. Multiple chromosomal mechanisms generate an EWS/FLI1 or an EWS/ERG fusion gene in Ewing tumors.
Desmaze C; Brizard F; Turc-Carel C; Melot T; Delattre O; Thomas G; Aurias A
Cancer Genet Cytogenet; 1997 Aug; 97(1):12-9. PubMed ID: 9242212
[TBL] [Abstract][Full Text] [Related]
30. Sequential combination of karyotyping and RNA-sequencing in the search for cancer-specific fusion genes.
Panagopoulos I; Thorsen J; Gorunova L; Micci F; Heim S
Int J Biochem Cell Biol; 2014 Aug; 53():462-5. PubMed ID: 24863361
[TBL] [Abstract][Full Text] [Related]
31. Reciprocal products of chromosomal translocations in human cancer pathogenesis: key players or innocent bystanders?
Rego EM; Pandolfi PP
Trends Mol Med; 2002 Aug; 8(8):396-405. PubMed ID: 12127726
[TBL] [Abstract][Full Text] [Related]
32. Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL.
Fioretos T; Panagopoulos I; Lassen C; Swedin A; Billström R; Isaksson M; Strömbeck B; Olofsson T; Mitelman F; Johansson B
Genes Chromosomes Cancer; 2001 Dec; 32(4):302-10. PubMed ID: 11746971
[TBL] [Abstract][Full Text] [Related]
33. Translocation Breakpoints Preferentially Occur in Euchromatin and Acrocentric Chromosomes.
Lin CY; Shukla A; Grady JP; Fink JL; Dray E; Duijf PHG
Cancers (Basel); 2018 Jan; 10(1):. PubMed ID: 29316705
[TBL] [Abstract][Full Text] [Related]
34. Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinoma.
Fang JM; Arlt MF; Burgess AC; Dagenais SL; Beer DG; Glover TW
Genes Chromosomes Cancer; 2001 Mar; 30(3):292-8. PubMed ID: 11170287
[TBL] [Abstract][Full Text] [Related]
35. Panhandle PCR for cDNA: a rapid method for isolation of MLL fusion transcripts involving unknown partner genes.
Megonigal MD; Rappaport EF; Wilson RB; Jones DH; Whitlock JA; Ortega JA; Slater DJ; Nowell PC; Felix CA
Proc Natl Acad Sci U S A; 2000 Aug; 97(17):9597-602. PubMed ID: 10920186
[TBL] [Abstract][Full Text] [Related]
36. ETV6-AML1 translocation breakpoints cluster near a purine/pyrimidine repeat region in the ETV6 gene.
Thandla SP; Ploski JE; Raza-Egilmez SZ; Chhalliyil PP; Block AW; de Jong PJ; Aplan PD
Blood; 1999 Jan; 93(1):293-9. PubMed ID: 9864173
[TBL] [Abstract][Full Text] [Related]
37. Chromosomal translocations in human cancer.
Rabbitts TH
Nature; 1994 Nov; 372(6502):143-9. PubMed ID: 7969446
[TBL] [Abstract][Full Text] [Related]
38. Translocation and deletion breakpoints in cancer genomes are associated with potential non-B DNA-forming sequences.
Bacolla A; Tainer JA; Vasquez KM; Cooper DN
Nucleic Acids Res; 2016 Jul; 44(12):5673-88. PubMed ID: 27084947
[TBL] [Abstract][Full Text] [Related]
39. Characteristic sequence motifs located at the genomic breakpoints of the translocation t(12;16) and t(12;22) in myxoid liposarcoma.
Xiang H; Wang J; Hisaoka M; Zhu X
Pathology; 2008 Oct; 40(6):547-52. PubMed ID: 18752119
[TBL] [Abstract][Full Text] [Related]
40. Next generation sequencing approach for detecting 491 fusion genes from human cancer.
Urakami K; Shimoda Y; Ohshima K; Nagashima T; Serizawa M; Tanabe T; Saito J; Usui T; Watanabe Y; Naruoka A; Ohnami S; Ohnami S; Mochizuki T; Kusuhara M; Yamaguchi K
Biomed Res; 2016; 37(1):51-62. PubMed ID: 26912140
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]