BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

61 related articles for article (PubMed ID: 21986343)

  • 1. Fast approach for clarification of chromosomal aberrations by using LM-PCR and FT-CGH in leukaemic sample.
    Dittmann K; Przybylski GK; Grabarczyk P; Dölken G; Gesk S; Siebert R; Schmidt CA
    Acta Haematol; 2012; 127(1):16-9. PubMed ID: 21986343
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular characterization of a novel chromosomal translocation t(12;14)(q23;q11.2) in T-lymphoblastic lymphoma between the T-cell receptor delta-deleting elements (TRDREC and TRAJ61) and the hypothetical gene C12orf42.
    Przybylski GK; Dittmann K; Grabarczyk P; Dölken G; Gesk S; Harder L; Landmann E; Siebert R; Schmidt CA
    Eur J Haematol; 2010 Nov; 85(5):452-6. PubMed ID: 20659153
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Efficacy of high-resolution comparative genomic hybridization (HR-CGH) in detection of chromosomal abnormalities in children with acute leukaemia.
    Vranova V; Mentzlova D; Oltova A; Linkova V; Zezulkova D; Filkova H; Mendelova D; Sterba J; Kuglik P
    Neoplasma; 2008; 55(1):23-30. PubMed ID: 18190236
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotypic and genetic characterization of adult T-cell acute lymphoblastic leukemia with del(9)(q34);SET-NUP214 rearrangement.
    Chae H; Lim J; Kim M; Park J; Kim Y; Han K; Lee S; Min WS
    Ann Hematol; 2012 Feb; 91(2):193-201. PubMed ID: 21720744
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Structural and numerical abnormalities resolved in one-step analysis: the most common chromosomal rearrangements detected by comparative genomic hybridization in childhood acute lymphoblastic leukemia.
    Kowalczyk JR; Babicz M; Gaworczyk A; Lejman M; Winnicka D; Styka B; Jaszczuk I
    Cancer Genet Cytogenet; 2010 Jul; 200(2):161-6. PubMed ID: 20620600
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A complex pattern of recurrent chromosomal losses and gains in T-cell prolymphocytic leukemia.
    Soulier J; Pierron G; Vecchione D; Garand R; Brizard F; Sigaux F; Stern MH; Aurias A
    Genes Chromosomes Cancer; 2001 Jul; 31(3):248-54. PubMed ID: 11391795
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nonrandom chromosomal imbalances in primary mediastinal B-cell lymphoma detected by arbitrarily primed PCR fingerprinting.
    Scarpa A; Taruscio D; Scardoni M; Iosi F; Paradisi S; Ennas MG; Rigaud G; Moore PS; Menestrina F
    Genes Chromosomes Cancer; 1999 Nov; 26(3):203-9. PubMed ID: 10502317
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosomal aberrations in follicular non-Hodgkin lymphomas of Japanese patients, detected with comparative genomic hybridization and polymerase chain reaction analysis.
    D'Haese JG; Tsukasaki K; Cremer FW; Fischer C; Bartram CR; Jauch A
    Cancer Genet Cytogenet; 2005 Oct; 162(2):107-14. PubMed ID: 16213357
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosomal imbalances in diffuse large B-cell lymphoma detected by comparative genomic hybridization.
    Berglund M; Enblad G; Flordal E; Lui WO; Backlin C; Thunberg U; Sundström C; Roos G; Allander SV; Erlanson M; Rosenquist R; Larsson C; Lagercrantz S
    Mod Pathol; 2002 Aug; 15(8):807-16. PubMed ID: 12181265
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Tissue microarray-based screening for chromosomal breakpoints affecting the T-cell receptor gene loci in mature T-cell lymphomas.
    Leich E; Haralambieva E; Zettl A; Chott A; Rüdiger T; Höller S; Müller-Hermelink HK; Ott G; Rosenwald A
    J Pathol; 2007 Sep; 213(1):99-105. PubMed ID: 17582237
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
    Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
    Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities.
    Ness GO; Lybaek H; Houge G
    Am J Med Genet; 2002 Nov; 113(2):125-36. PubMed ID: 12407702
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Integration of conventional cytogenetics, comparative genomic hybridisation and interphase fluorescence in situ hybridisation for the detection of genomic rearrangements in acute leukaemia.
    McGrattan P; Campbell S; Cuthbert R; Jones FG; McMullin MF; Humphreys M
    J Clin Pathol; 2008 Aug; 61(8):903-8. PubMed ID: 18474541
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screening of genomic imbalances in glioblastoma multiforme using high-resolution comparative genomic hybridization.
    Vranová V; Necesalová E; Kuglík P; Cejpek P; Pesáková M; Budínská E; Relichová J; Veselská R
    Oncol Rep; 2007 Feb; 17(2):457-64. PubMed ID: 17203188
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Whole genome amplification for CGH analysis: Linker-adapter PCR as the method of choice for difficult and limited samples.
    Pirker C; Raidl M; Steiner E; Elbling L; Holzmann K; Spiegl-Kreinecker S; Aubele M; Grasl-Kraupp B; Marosi C; Micksche M; Berger W
    Cytometry A; 2004 Sep; 61(1):26-34. PubMed ID: 15351986
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia.
    Casas S; Aventín A; Fuentes F; Vallespí T; Granada I; Carrió A; Angel Martínez-Climent J; Solé F; Teixidó M; Bernués M; Duarte J; Maria Hernández J; Brunet S; Dolors Coll M; Sierra J
    Cancer Genet Cytogenet; 2004 Aug; 153(1):16-25. PubMed ID: 15325089
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Combined spectral karyotyping, comparative genomic hybridization, and in vitro apoptyping of a panel of Burkitt's lymphoma-derived B cell lines reveals an unexpected complexity of chromosomal aberrations and a recurrence of specific abnormalities in chemoresistant cell lines.
    Karpova MB; Schoumans J; Blennow E; Ernberg I; Henter JI; Smirnov AF; Nordenskjöld M; Fadeel B
    Int J Oncol; 2006 Mar; 28(3):605-17. PubMed ID: 16465364
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities].
    ten Kate LP
    Ned Tijdschr Geneeskd; 2006 Jul; 150(29):1608-12. PubMed ID: 16901063
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study.
    Matteucci C; Barba G; Varasano E; Vitale A; Mancini M; Testoni N; Cuneo A; Rege-Cambrin G; Elia L; La Starza R; Pierini V; Brandimarte L; Vignetti M; Foà R; Mecucci C;
    Br J Haematol; 2010 Apr; 149(1):70-8. PubMed ID: 20067559
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.