BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 16769584)

  • 1. 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]  

  • 2. Molecular characterization of the idiopathic hypereosinophilic syndrome (HES) in 35 French patients with normal conventional cytogenetics.
    Roche-Lestienne C; Lepers S; Soenen-Cornu V; Kahn JE; Laï JL; Hachulla E; Drupt F; Demarty AL; Roumier AS; Gardembas M; Dib M; Philippe N; Cambier N; Barete S; Libersa C; Bletry O; Hatron PY; Quesnel B; Rose C; Maloum K; Blanchet O; Fenaux P; Prin L; Preudhomme C
    Leukemia; 2005 May; 19(5):792-8. PubMed ID: 15772698
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two novel imatinib-responsive PDGFRA fusion genes in chronic eosinophilic leukaemia.
    Curtis CE; Grand FH; Musto P; Clark A; Murphy J; Perla G; Minervini MM; Stewart J; Reiter A; Cross NC
    Br J Haematol; 2007 Jul; 138(1):77-81. PubMed ID: 17555450
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Characteristics of cytogenetics and molecular biology in patients with eosinophilia].
    Qu SQ; Ai XF; Li CW; Li QH; Xu ZF; Qin TJ; Zhang Y; Xiao ZJ
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2012 Oct; 20(5):1216-20. PubMed ID: 23114151
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Transient response to imatinib in a chronic eosinophilic leukemia associated with ins(9;4)(q33;q12q25) and a CDK5RAP2-PDGFRA fusion gene.
    Walz C; Curtis C; Schnittger S; Schultheis B; Metzgeroth G; Schoch C; Lengfelder E; Erben P; Müller MC; Haferlach T; Hochhaus A; Hehlmann R; Cross NC; Reiter A
    Genes Chromosomes Cancer; 2006 Oct; 45(10):950-6. PubMed ID: 16845659
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [The application of fluorescence in situ hybridization to diagnosis of acute promyelocytic leukemia].
    Li CW; Liu SH; Bo LJ; Qin S; Liu XP; Dai Y; Wang JX
    Zhonghua Xue Ye Xue Za Zhi; 2004 Jun; 25(6):346-50. PubMed ID: 15308013
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular and cytogenetic characterization of a novel rearrangement involving chromosomes 9, 12, and 17 resulting in ETV6 (TEL) and ABL fusion.
    Tirado CA; Sebastian S; Moore JO; Gong JZ; Goodman BK
    Cancer Genet Cytogenet; 2005 Feb; 157(1):74-7. PubMed ID: 15676152
    [TBL] [Abstract][Full Text] [Related]  

  • 8. t(5;9)(q11;q34): a novel familial translocation involving Abelson oncogene and association with hypereosinophilia.
    Bakhshi S; Hamre M; Mohamed AN; Feldman G; Ravindranath Y
    J Pediatr Hematol Oncol; 2003 Jan; 25(1):82-4. PubMed ID: 12544780
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of PML-RARA rearrangement by RT-PCR and sequencing in an acute promyelocytic leukemia without t(15;17) on G-banding and FISH.
    Han JY; Kim KE; Kim KH; Park JI; Kim JS
    Leuk Res; 2007 Feb; 31(2):239-43. PubMed ID: 16797070
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mammalian mastermind like 2 11q21 gene rearrangement in bronchopulmonary mucoepidermoid carcinoma.
    Achcar Rde O; Nikiforova MN; Dacic S; Nicholson AG; Yousem SA
    Hum Pathol; 2009 Jun; 40(6):854-60. PubMed ID: 19269006
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Establishment and characterization of a new human acute myelocytic leukemia cell line SH-2 with a loss of Y chromosome, a derivative chromosome 16 resulting from an unbalanced translocation between chromosomes 16 and 17, monosomy 17, trisomy 19, and p53 alteration.
    Qiu H; Xue Y; Zhang J; Pan J; Dai H; Wu Y; Wang Y; Chen S; Wu D
    Exp Hematol; 2008 Nov; 36(11):1487-95. PubMed ID: 18715689
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Derivative (7)t(7;8): The sole karyotype abnormality in acute promyelocytic leukemia with PML/RARA rearrangement identified by RT-PCR and sequence analysis.
    Wang Y; Fang M; Jing Y; Li J; Jiang F; Wang Y
    Leuk Res; 2009 Jul; 33(7):e55-8. PubMed ID: 19162322
    [No Abstract]   [Full Text] [Related]  

  • 13. Dermatofibrosarcoma protuberans COL1A1-PDGFB fusion is identified in virtually all dermatofibrosarcoma protuberans cases when investigated by newly developed multiplex reverse transcription polymerase chain reaction and fluorescence in situ hybridization assays.
    Patel KU; Szabo SS; Hernandez VS; Prieto VG; Abruzzo LV; Lazar AJ; López-Terrada D
    Hum Pathol; 2008 Feb; 39(2):184-93. PubMed ID: 17950782
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mucosa-associated lymphoid tissue lymphoma: novel translocations including rearrangements of ODZ2, JMJD2C, and CNN3.
    Vinatzer U; Gollinger M; Müllauer L; Raderer M; Chott A; Streubel B
    Clin Cancer Res; 2008 Oct; 14(20):6426-31. PubMed ID: 18927281
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel acquired cryptic three-way translocation t(2;11;5)(p21.3;q13.5;q23.2) with a submicroscopic deletion at 11p14.3 in an adult with hypereosinophilic syndrome.
    Kjeldsen E
    Exp Mol Pathol; 2015 Aug; 99(1):50-5. PubMed ID: 25962659
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular cytogenetic findings in a four-way t(1;12;5;12)(p36;p13;q33;q24) underlying the ETV6-PDGFRB fusion gene in chronic myelomonocytic leukemia.
    Crescenzi B; La Starza R; Nozzoli C; Ciolli S; Matteucci C; Romoli S; Rigacci L; Gorello P; Bosi A; Martelli MF; Marynen P; Mecucci C
    Cancer Genet Cytogenet; 2007 Jul; 176(1):67-71. PubMed ID: 17574967
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Interphase fluorescence in situ hybridization is more sensitive than BIOMED-2 polymerase chain reaction protocol in detecting IGH-BCL2 rearrangement in both fixed and frozen lymph node with follicular lymphoma.
    Belaud-Rotureau MA; Parrens M; Carrere N; Turmo M; Ferrer J; de Mascarel A; Dubus P; Merlio JP
    Hum Pathol; 2007 Feb; 38(2):365-72. PubMed ID: 17134735
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Acute myeloid leukemia with t(16;21)(q24;q22) and eosinophilia: case report and review of the literature.
    Park IJ; Park JE; Kim HJ; Jung HJ; Lee WG; Cho SR
    Cancer Genet Cytogenet; 2010 Jan; 196(1):105-8. PubMed ID: 19963144
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Fluorescence in situ hybridization studies on a myeloid leukemia patient with ins(8;21)(q22;q22.1q22.3)].
    Wu YF; Xue YQ; Bai SX; Zhang J; Yao L; Wang Y; Qiu HY; Shen J; Pan JL; Ma QF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):203-6. PubMed ID: 19350517
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.