BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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]
    of 10.