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135 related items for PubMed ID: 15981564
1. [Chromosomal rearrangements breakpoints clusterization: is the clonal selection involved]. Umanskaia ON, Bystritskiĭ AA, Razin SV. Mol Biol (Mosk); 2005; 39(3):355-63. PubMed ID: 15981564 [Abstract] [Full Text] [Related]
2. Chromatin structural elements and chromosomal translocations in leukemia. Zhang Y, Rowley JD. DNA Repair (Amst); 2006 Sep 08; 5(9-10):1282-97. PubMed ID: 16893685 [Abstract] [Full Text] [Related]
3. Characteristics of genomic breakpoints in TLS-CHOP translocations in liposarcomas suggest the involvement of Translin and topoisomerase II in the process of translocation. Kanoe H, Nakayama T, Hosaka T, Murakami H, Yamamoto H, Nakashima Y, Tsuboyama T, Nakamura T, Ron D, Sasaki MS, Toguchida J. Oncogene; 1999 Jan 21; 18(3):721-9. PubMed ID: 9989822 [Abstract] [Full Text] [Related]
4. Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends. Chuzhanova N, Abeysinghe SS, Krawczak M, Cooper DN. Hum Mutat; 2003 Sep 21; 22(3):245-51. PubMed ID: 12938089 [Abstract] [Full Text] [Related]
5. 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 21; 22(3):229-44. PubMed ID: 12938088 [Abstract] [Full Text] [Related]
7. Fusion transcripts involving HMGA2 are not a common molecular mechanism in uterine leiomyomata with rearrangements in 12q15. Quade BJ, Weremowicz S, Neskey DM, Vanni R, Ladd C, Dal Cin P, Morton CC. Cancer Res; 2003 Mar 15; 63(6):1351-8. PubMed ID: 12649198 [Abstract] [Full Text] [Related]
12. The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors. Kolomietz E, Meyn MS, Pandita A, Squire JA. Genes Chromosomes Cancer; 2002 Oct 15; 35(2):97-112. PubMed ID: 12203773 [Abstract] [Full Text] [Related]
14. Chemotherapy-related secondary leukemias: A role for DNA repair by error-prone non-homologous end joining in topoisomerase II - Induced chromosomal rearrangements. Kantidze OL, Razin SV. Gene; 2007 Apr 15; 391(1-2):76-9. PubMed ID: 17234368 [Abstract] [Full Text] [Related]
15. Identification of a potential "hotspot" DNA region in the RUNX1 gene targeted by mitoxantrone in therapy-related acute myeloid leukemia with t(16;21) translocation. Ottone T, Hasan SK, Montefusco E, Curzi P, Mays AN, Chessa L, Ferrari A, Conte E, Noguera NI, Lavorgna S, Ammatuna E, Divona M, Bovetti K, Amadori S, Grimwade D, Lo-Coco F. Genes Chromosomes Cancer; 2009 Mar 15; 48(3):213-21. PubMed ID: 19023877 [Abstract] [Full Text] [Related]
16. Array painting using microdissected chromosomes to map chromosomal breakpoints. Backx L, Van Esch H, Melotte C, Kosyakova N, Starke H, Frijns JP, Liehr T, Vermeesch JR. Cytogenet Genome Res; 2007 Mar 15; 116(3):158-66. PubMed ID: 17317954 [Abstract] [Full Text] [Related]
17. Genome organization influences partner selection for chromosomal rearrangements. Wijchers PJ, de Laat W. Trends Genet; 2011 Feb 15; 27(2):63-71. PubMed ID: 21144612 [Abstract] [Full Text] [Related]
18. Molecular characterization of the MLL-SEPT6 fusion gene in acute myeloid leukemia: identification of novel fusion transcripts and cloning of genomic breakpoint junctions. Cerveira N, Micci F, Santos J, Pinheiro M, Correia C, Lisboa S, Bizarro S, Norton L, Glomstein A, Asberg AE, Heim S, Teixeira MR. Haematologica; 2008 Jul 15; 93(7):1076-80. PubMed ID: 18492691 [Abstract] [Full Text] [Related]
19. Chromatin loops, illegitimate recombination, and genome evolution. Kantidze OL, Razin SV. Bioessays; 2009 Mar 15; 31(3):278-86. PubMed ID: 19260023 [Abstract] [Full Text] [Related]
20. Cloning of immunoglobulin chromosomal translocations by long-distance inverse polymerase chain reaction. Karran EL, Sonoki T, Dyer MJ. Methods Mol Med; 2005 Mar 15; 115():217-30. PubMed ID: 15998970 [Abstract] [Full Text] [Related] Page: [Next] [New Search]