BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 10616538)

  • 1. Cytogenetic triclonality in T-cell acute lymphoblastic leukemia: a conventional and molecular cytogenetic study.
    Wong KF; So CC; Siu LP
    Cancer Genet Cytogenet; 2000 Jan; 116(1):77-80. PubMed ID: 10616538
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Complex chromosome 9, 20, and 22 rearrangements in acute lymphoblastic leukemia with duplication of BCR and ABL sequences.
    Stevens-Kroef MJ; Dirckx R; Meers LE; Albrechts JC; Schouten HC; Hamers AJ
    Cancer Genet Cytogenet; 2000 Jan; 116(2):119-23. PubMed ID: 10640143
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Translocation (1;14)(p34;q11) and trisomy 8 in a T-cell acute lymphoblastic leukemia patient.
    Martín-Henao GA; Sureda A
    Cancer Genet Cytogenet; 1995 Feb; 79(2):177-81. PubMed ID: 7889516
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comparative analysis of interphase FISH and RT-PCR to detect bcr-abl translocation in chronic myelogenous leukemia and related disorders.
    Tbakhi A; Pettay J; Sreenan JJ; Abdel-Razeq H; Kalaycio M; Hoeltge G; Miller ML; Tubbs RR
    Am J Clin Pathol; 1998 Jan; 109(1):16-23. PubMed ID: 9426513
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Aberrations of chromosomes 9 and 22 in acute lymphoblastic leukemia cases detected by ES-fluorescence in situ hybridization.
    Cetin Z; Yakut S; Karadogan I; Kupesiz A; Timuragaoglu A; Salim O; Tezcan G; Alanoglu G; Ozbalci D; Hazar V; Yesilipek MA; Undar L; Luleci G; Berker S
    Genet Test Mol Biomarkers; 2012 May; 16(5):318-23. PubMed ID: 22360868
    [TBL] [Abstract][Full Text] [Related]  

  • 6. BCR rearrangement without juxtaposition of ABL in pre-T acute lymphoblastic leukaemia.
    Fosså A; Siebert R; Kasper C; Becher R; Opalka B; Thiel E; Seeber S; Nowrousian MR
    Br J Haematol; 1996 May; 93(2):403-5. PubMed ID: 8639438
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults.
    Gorello P; La Starza R; Varasano E; Chiaretti S; Elia L; Pierini V; Barba G; Brandimarte L; Crescenzi B; Vitale A; Messina M; Grammatico S; Mancini M; Matteucci C; Bardi A; Guarini A; Martelli MF; Foà R; Mecucci C
    Haematologica; 2010 Jan; 95(1):79-86. PubMed ID: 20065082
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Trisomy 4 as the sole cytogenetic abnormality in a patient with T-cell acute lymphoblastic leukemia.
    Gupta V; Chun K
    Cancer Genet Cytogenet; 2004 Jul; 152(2):158-62. PubMed ID: 15262438
    [TBL] [Abstract][Full Text] [Related]  

  • 9. ABL oncogene amplification with p16(INK4a) gene deletion in precursor T-cell acute lymphoblastic leukemia/lymphoma: report of the first case.
    Kim HJ; Woo HY; Koo HH; Tak EY; Kim SH
    Am J Hematol; 2004 Aug; 76(4):360-3. PubMed ID: 15282669
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytogenetic, fluorescent in situ hybridization & reverse transcriptase-polymerase chain reaction analysis in acute promyelocytic leukaemia patients.
    Shivakumar S; Poonkhuzhali B; Gunasekaran S; Srivastava A; Chandy M
    Indian J Med Res; 2002 Feb; 115():59-67. PubMed ID: 12138666
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Classical and molecular cytogenetic abnormalities in 124 pediatric patients with acute lymphoblastic leukemia].
    Chai YH; Lü H; Li JQ; Lu J; Xiao PF; He YX; Shao XJ
    Zhonghua Er Ke Za Zhi; 2007 Sep; 45(9):684-6. PubMed ID: 18021563
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A combination of cytomorphology, cytogenetic analysis, fluorescence in situ hybridization and reverse transcriptase polymerase chain reaction for establishing clonality in cases of persisting hypereosinophilia.
    Bacher U; Reiter A; Haferlach T; Mueller L; Schnittger S; Kern W; Schoch C
    Haematologica; 2006 Jun; 91(6):817-20. PubMed ID: 16769584
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular cytogenetics of chronic myeloid leukemia with atypical t(6;9) (p23;q34) translocation.
    Jadayel D; Calabrese G; Min T; van Rhee F; Swansbury GJ; Dyer MJ; Maitland J; Palka G; Catovsky D
    Leukemia; 1995 Jun; 9(6):981-7. PubMed ID: 7596189
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Variant intra philadelphia translocation with rearrangement of BCR-ABL and ABL-BCR within the same chromosome in a patient with cALL.
    Edelhäuser M; Raber W; Mitterbauer G; Mannhalter C; Lechner K; Fonatsch C
    Cancer Genet Cytogenet; 2000 Oct; 122(2):83-6. PubMed ID: 11106816
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Patterns of BCR/ABL gene rearrangements by interphase fluorescence in situ hybridization (FISH) in BCR/ABL+ leukemias: incidence and underlying genetic abnormalities.
    Primo D; Tabernero MD; Rasillo A; Sayagués JM; Espinosa AB; Chillón MC; Garcia-Sanz R; Gutierrez N; Giralt M; Hagemeijer A; San Miguel JF; Orfao A
    Leukemia; 2003 Jun; 17(6):1124-9. PubMed ID: 12764379
    [TBL] [Abstract][Full Text] [Related]  

  • 16. t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Français de Cytogénétique Hématologique (GFCH).
    Berger R; Dastugue N; Busson M; Van Den Akker J; Pérot C; Ballerini P; Hagemeijer A; Michaux L; Charrin C; Pages MP; Mugneret F; Andrieux J; Talmant P; Hélias C; Mauvieux L; Lafage-Pochitaloff M; Mozziconacci MJ; Cornillet-Lefebvre P; Radford I; Asnafi V; Bilhou-Nabera C; Nguyen Khac F; Léonard C; Speleman F; Poppe B; Bastard C; Taviaux S; Quilichini B; Herens C; Grégoire MJ; Cavé H; Bernard OA;
    Leukemia; 2003 Sep; 17(9):1851-7. PubMed ID: 12970786
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. The t(14;18) in a patient with de novo acute lymphoblastic leukemia is associated with t(8;9).
    Lillington DM; Monard S; Johnson PW; Evans ML; Kearney LU; Lister TA; Young BD; Gibbons B
    Leukemia; 1994 Apr; 8(4):560-3. PubMed ID: 8152251
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interphase fluorescence in situ hybridization and spectral karyotyping reveals hidden genetic aberrations in children with acute lymphoblastic leukaemia and a normal banded karyotype.
    Nordgren A; Schoumans J; Söderhäll S; Nordenskjöld M; Blennow E
    Br J Haematol; 2001 Sep; 114(4):786-93. PubMed ID: 11564064
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 9q34 rearrangements in BCR/ABL fusion-negative acute lymphoblastic leukemia.
    Dave BJ; Wiggins M; Higgins CM; Pickering DL; Perry D; Aoun P; Abromowich M; DeVetten M; Sanger WG
    Cancer Genet Cytogenet; 2005 Oct; 162(1):30-7. PubMed ID: 16157197
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.