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 *

88 related articles for article (PubMed ID: 18628311)

  • 21. Chromatin structural elements and chromosomal translocations in leukemia.
    Zhang Y; Rowley JD
    DNA Repair (Amst); 2006 Sep; 5(9-10):1282-97. PubMed ID: 16893685
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Activation of HOX11L2 by juxtaposition with 3'-BCL11B in an acute lymphoblastic leukemia cell line (HPB-ALL) with t(5;14)(q35;q32.2).
    MacLeod RA; Nagel S; Kaufmann M; Janssen JW; Drexler HG
    Genes Chromosomes Cancer; 2003 May; 37(1):84-91. PubMed ID: 12661009
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Evolutionarily plastic regions at human 3p21.3 coincide with tumor breakpoints identified by the "elimination test".
    Darai E; Kost-Alimova M; Kiss H; Kansoul H; Klein G; Imreh S
    Genomics; 2005 Jul; 86(1):1-12. PubMed ID: 15913951
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Breakpoint analysis of the pericentric inversion distinguishing human chromosome 4 from the homologous chromosome in the chimpanzee (Pan troglodytes).
    Kehrer-Sawatzki H; Sandig C; Chuzhanova N; Goidts V; Szamalek JM; Tänzer S; Müller S; Platzer M; Cooper DN; Hameister H
    Hum Mutat; 2005 Jan; 25(1):45-55. PubMed ID: 15580561
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Multiple recurrent chromosomal breakpoints in mantle cell lymphoma revealed by a combination of molecular cytogenetic techniques.
    Salaverria I; Espinet B; Carrió A; Costa D; Astier L; Slotta-Huspenina J; Quintanilla-Martinez L; Fend F; Solé F; Colomer D; Serrano S; Miró R; Beà S; Campo E
    Genes Chromosomes Cancer; 2008 Dec; 47(12):1086-97. PubMed ID: 18709664
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Analysis of segmental duplications, mouse genome synteny and recurrent cancer-associated amplicons in human chromosome 6p21-p12.
    Martin JW; Yoshimoto M; Ludkovski O; Thorner PS; Zielenska M; Squire JA; Nuin PA
    Cytogenet Genome Res; 2010 Jun; 128(4):199-213. PubMed ID: 20453501
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A rare case of a boy with de novo microduplication at 5q35.2q35.3 from central Brazil.
    Reis FG; Pinto IP; Minasi LB; Melo AV; Cunha DM; Ribeiro CL; da Silva CC; Silva DM; da Cruz AD
    Genet Mol Res; 2017 Jan; 16(1):. PubMed ID: 28128410
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
    Lestou VS; Ludkovski O; Connors JM; Gascoyne RD; Lam WL; Horsman DE
    Genes Chromosomes Cancer; 2003 Apr; 36(4):375-81. PubMed ID: 12619161
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs.
    Abeysinghe SS; Chuzhanova N; Krawczak M; Ball EV; Cooper DN
    Hum Mutat; 2003 Sep; 22(3):229-44. PubMed ID: 12938088
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Diverse chromosome breakage mechanisms underlie subtelomeric rearrangements, a common cause of mental retardation.
    Rooms L; Reyniers E; Kooy RF
    Hum Mutat; 2007 Feb; 28(2):177-82. PubMed ID: 16991117
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular characterization of the genomic breakpoint junction in a t(11;22) translocation in Ewing sarcoma.
    Obata K; Hiraga H; Nojima T; Yoshida MC; Abe S
    Genes Chromosomes Cancer; 1999 May; 25(1):6-15. PubMed ID: 10221334
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification of candidate genes on chromosome band 20q12 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines.
    MacGrogan D; Alvarez S; DeBlasio T; Jhanwar SC; Nimer SD
    Oncogene; 2001 Jul; 20(31):4150-60. PubMed ID: 11464281
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Characterization of a recurrent translocation t(2;3)(p15-22;q26) occurring in acute myeloid leukaemia.
    Trubia M; Albano F; Cavazzini F; Cambrin GR; Quarta G; Fabbiano F; Ciambelli F; Magro D; Hernandezo JM; Mancini M; Diverio D; Pelicci PG; Coco FL; Mecucci C; Specchia G; Rocchi M; Liso V; Castoldi G; Cuneo A
    Leukemia; 2006 Jan; 20(1):48-54. PubMed ID: 16619048
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular characterisation of the pericentric inversion that distinguishes human chromosome 5 from the homologous chimpanzee chromosome.
    Szamalek JM; Goidts V; Chuzhanova N; Hameister H; Cooper DN; Kehrer-Sawatzki H
    Hum Genet; 2005 Jul; 117(2-3):168-76. PubMed ID: 15883840
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Copy number variation at the breakpoint region of isochromosome 17q.
    Carvalho CM; Lupski JR
    Genome Res; 2008 Nov; 18(11):1724-32. PubMed ID: 18714090
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanisms.
    Shaw CJ; Lupski JR
    Hum Genet; 2005 Jan; 116(1-2):1-7. PubMed ID: 15526218
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Unbalanced der(5)t(5;20) translocation associated with megalencephaly, perisylvian polymicrogyria, polydactyly and hydrocephalus.
    Verkerk AJ; Schot R; van Waterschoot L; Douben H; Poddighe PJ; Lequin MH; de Vries LS; Terhal P; Hahnemann JM; de Coo IF; de Wit MC; Wafelman LS; Garavelli L; Dobyns WB; Van der Spek PJ; de Klein A; Mancini GM
    Am J Med Genet A; 2010 Jun; 152A(6):1488-97. PubMed ID: 20503325
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.