BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 27353332)

  • 1. Frequent occurrence of large duplications at reciprocal genomic rearrangement breakpoints in multiple myeloma and other tumors.
    Demchenko Y; Roschke A; Chen WD; Asmann Y; Bergsagel PL; Kuehl WM
    Nucleic Acids Res; 2016 Sep; 44(17):8189-98. PubMed ID: 27353332
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher disease.
    Lee JA; Inoue K; Cheung SW; Shaw CA; Stankiewicz P; Lupski JR
    Hum Mol Genet; 2006 Jul; 15(14):2250-65. PubMed ID: 16774974
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Distinguishing primary and secondary translocations in multiple myeloma.
    Gabrea A; Leif Bergsagel P; Michael Kuehl W
    DNA Repair (Amst); 2006 Sep; 5(9-10):1225-33. PubMed ID: 16829212
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements.
    D'Angelo CS; Gajecka M; Kim CA; Gentles AJ; Glotzbach CD; Shaffer LG; Koiffmann CP
    Hum Genet; 2009 Jun; 125(5-6):551-63. PubMed ID: 19271239
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Heterogeneous pattern of chromosomal breakpoints involving the MYC locus in multiple myeloma.
    Fabris S; Storlazzi CT; Baldini L; Nobili L; Lombardi L; Maiolo AT; Rocchi M; Neri A
    Genes Chromosomes Cancer; 2003 Jul; 37(3):261-9. PubMed ID: 12759924
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations.
    Gajecka M; Pavlicek A; Glotzbach CD; Ballif BC; Jarmuz M; Jurka J; Shaffer LG
    Hum Genet; 2006 Nov; 120(4):519-26. PubMed ID: 16847692
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.
    Sharp AJ; Hansen S; Selzer RR; Cheng Z; Regan R; Hurst JA; Stewart H; Price SM; Blair E; Hennekam RC; Fitzpatrick CA; Segraves R; Richmond TA; Guiver C; Albertson DG; Pinkel D; Eis PS; Schwartz S; Knight SJ; Eichler EE
    Nat Genet; 2006 Sep; 38(9):1038-42. PubMed ID: 16906162
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Segmental duplication, microinversion, and gene loss associated with a complex inversion breakpoint region in Drosophila.
    Calvete O; González J; Betrán E; Ruiz A
    Mol Biol Evol; 2012 Jul; 29(7):1875-89. PubMed ID: 22328714
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of MYC translocations in multiple myeloma cell lines.
    Dib A; Gabrea A; Glebov OK; Bergsagel PL; Kuehl WM
    J Natl Cancer Inst Monogr; 2008; (39):25-31. PubMed ID: 18647998
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Large duplications at reciprocal translocation breakpoints that might be the counterpart of large deletions and could arise from stalled replication bubbles.
    Howarth KD; Pole JC; Beavis JC; Batty EM; Newman S; Bignell GR; Edwards PA
    Genome Res; 2011 Apr; 21(4):525-34. PubMed ID: 21252201
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genomic characterization of the chromosomal breakpoints of t(4;14) of multiple myeloma suggests more than one possible aetiological mechanism.
    Fenton JA; Pratt G; Rawstron AC; Sibley K; Rothwell D; Yates Z; Dring A; Richards SJ; Ashcroft AJ; Davies FE; Owen RG; Child JA; Morgan GJ
    Oncogene; 2003 Feb; 22(7):1103-13. PubMed ID: 12592397
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Repeat mediated gene duplication in the Drosophila pseudoobscura genome.
    Meisel RP
    Gene; 2009 Jun; 438(1-2):1-7. PubMed ID: 19272434
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints.
    Newman S; Hermetz KE; Weckselblatt B; Rudd MK
    Am J Hum Genet; 2015 Feb; 96(2):208-20. PubMed ID: 25640679
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Frequent PVT1 rearrangement and novel chimeric genes PVT1-NBEA and PVT1-WWOX occur in multiple myeloma with 8q24 abnormality.
    Nagoshi H; Taki T; Hanamura I; Nitta M; Otsuki T; Nishida K; Okuda K; Sakamoto N; Kobayashi S; Yamamoto-Sugitani M; Tsutsumi Y; Kobayashi T; Matsumoto Y; Horiike S; Kuroda J; Taniwaki M
    Cancer Res; 2012 Oct; 72(19):4954-62. PubMed ID: 22869583
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Promiscuous MYC locus rearrangements hijack enhancers but mostly super-enhancers to dysregulate MYC expression in multiple myeloma.
    Affer M; Chesi M; Chen WG; Keats JJ; Demchenko YN; Roschke AV; Van Wier S; Fonseca R; Bergsagel PL; Kuehl WM
    Leukemia; 2014 Aug; 28(8):1725-1735. PubMed ID: 24518206
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
    Sinclair P; Harrison CJ; Jarosová M; Foroni L
    Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Refinement of a chimpanzee pericentric inversion breakpoint to a segmental duplication cluster.
    Locke DP; Archidiacono N; Misceo D; Cardone MF; Deschamps S; Roe B; Rocchi M; Eichler EE
    Genome Biol; 2003; 4(8):R50. PubMed ID: 12914658
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole Exome Sequencing in Multiple Myeloma to Identify Somatic Single Nucleotide Variants and Key Translocations Involving Immunoglobulin Loci and MYC.
    Walker BA
    Methods Mol Biol; 2018; 1792():71-95. PubMed ID: 29797253
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosome rearrangements in Neurospora and other filamentous fungi.
    Perkins DD
    Adv Genet; 1997; 36():239-398. PubMed ID: 9348657
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.
    Vissers LE; Bhatt SS; Janssen IM; Xia Z; Lalani SR; Pfundt R; Derwinska K; de Vries BB; Gilissen C; Hoischen A; Nesteruk M; Wisniowiecka-Kowalnik B; Smyk M; Brunner HG; Cheung SW; van Kessel AG; Veltman JA; Stankiewicz P
    Hum Mol Genet; 2009 Oct; 18(19):3579-93. PubMed ID: 19578123
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.