These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 21252201)

  • 1. 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]  

  • 2. Array painting reveals a high frequency of balanced translocations in breast cancer cell lines that break in cancer-relevant genes.
    Howarth KD; Blood KA; Ng BL; Beavis JC; Chua Y; Cooke SL; Raby S; Ichimura K; Collins VP; Carter NP; Edwards PA
    Oncogene; 2008 May; 27(23):3345-59. PubMed ID: 18084325
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGH.
    Lindstrand A; Schoumans J; Gustavsson P; Hanemaaijer N; Malmgren H; Blennow E
    Clin Genet; 2010 Jun; 77(6):552-62. PubMed ID: 20236111
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes.
    Spiteri E; Babcock M; Kashork CD; Wakui K; Gogineni S; Lewis DA; Williams KM; Minoshima S; Sasaki T; Shimizu N; Potocki L; Pulijaal V; Shanske A; Shaffer LG; Morrow BE
    Hum Mol Genet; 2003 Aug; 12(15):1823-37. PubMed ID: 12874103
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH.
    Mantripragada KK; Thuresson AC; Piotrowski A; Díaz de Ståhl T; Menzel U; Grigelionis G; Ferner RE; Griffiths S; Bolund L; Mautner V; Nordling M; Legius E; Vetrie D; Dahl N; Messiaen L; Upadhyaya M; Bruder CE; Dumanski JP
    J Med Genet; 2006 Jan; 43(1):28-38. PubMed ID: 15944227
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Large inverted duplications in the human genome form via a fold-back mechanism.
    Hermetz KE; Newman S; Conneely KN; Martin CL; Ballif BC; Shaffer LG; Cody JD; Rudd MK
    PLoS Genet; 2014 Jan; 10(1):e1004139. PubMed ID: 24497845
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ultra-high resolution array painting facilitates breakpoint sequencing.
    Gribble SM; Kalaitzopoulos D; Burford DC; Prigmore E; Selzer RR; Ng BL; Matthews NS; Porter KM; Curley R; Lindsay SJ; Baptista J; Richmond TA; Carter NP
    J Med Genet; 2007 Jan; 44(1):51-8. PubMed ID: 16971479
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13).
    Gajecka M; Gentles AJ; Tsai A; Chitayat D; Mackay KL; Glotzbach CD; Lieber MR; Shaffer LG
    Genome Res; 2008 Nov; 18(11):1733-42. PubMed ID: 18765821
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Constructing defined chromosome segmental duplications in maize.
    Yu C; Danilova T; Zhang J; Birchler J; Peterson T
    Cytogenet Genome Res; 2010 Jul; 129(1-3):72-81. PubMed ID: 20551616
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis.
    Weckselblatt B; Hermetz KE; Rudd MK
    Genome Res; 2015 Jul; 25(7):937-47. PubMed ID: 26070663
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromes.
    Johnston JJ; Walker RL; Davis S; Facio F; Turner JT; Bick DP; Daentl DL; Ellison JW; Meltzer PS; Biesecker LG
    J Med Genet; 2007 Jan; 44(1):e59. PubMed ID: 17098889
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH.
    Neill NJ; Ballif BC; Lamb AN; Parikh S; Ravnan JB; Schultz RA; Torchia BS; Rosenfeld JA; Shaffer LG
    Genome Res; 2011 Apr; 21(4):535-44. PubMed ID: 21383316
    [TBL] [Abstract][Full Text] [Related]  

  • 16. De novo reciprocal translocation t(5;6)(q13;q34) in cattle: cytogenetic and molecular characterization.
    De Lorenzi L; Rossi E; Gimelli S; Parma P
    Cytogenet Genome Res; 2014; 142(2):95-100. PubMed ID: 24280638
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions.
    Ballif BC; Yu W; Shaw CA; Kashork CD; Shaffer LG
    Hum Mol Genet; 2003 Sep; 12(17):2153-65. PubMed ID: 12915474
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosome translocations in breast cancer with breakpoints at 8p12.
    Courtay-Cahen C; Morris JS; Edwards PA
    Genomics; 2000 May; 66(1):15-25. PubMed ID: 10843800
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4).
    Thomas NS; Maloney V; Bryant V; Huang S; Brewer C; Lachlan K; Jacobs PA
    Hum Genet; 2009 Mar; 125(2):181-8. PubMed ID: 19104840
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.