BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

291 related articles for article (PubMed ID: 11721367)

  • 21. [Identification of chromosome 21 anomalies in patients with acute myeloid leukemia by fluorescence in situ hybridization].
    Zhang LJ; Wang PP; Lu XL; He J; Li Y; Zhai M
    Zhonghua Yi Xue Za Zhi; 2006 Dec; 86(48):3393-6. PubMed ID: 17313849
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Karyotype refinement by multicolor fluorescence in situ hybridization analysis in 18 patients with acute lymphoblastic leukemia.
    Calabrese G; Taraborelli T; Fantasia D; Guanciali Franchi P; Spadano A; Palka G
    Haematologica; 2002 Aug; 87(8):888-9. PubMed ID: 12161369
    [No Abstract]   [Full Text] [Related]  

  • 23. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
    Chen LJ; Li JY; Xiao B; Zhu Y; Liu Q; Pan JL; Qiu HR; Fan L; Zhang SJ; Lu RN; Xu W; Xue YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):635-9. PubMed ID: 18067073
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Molecular genetics in chronic myeloid leukemia with variant Ph translocation].
    Wu W; Li JY; Zhu Y; Qiu HR; Pan JL; Xu W; Chen LJ; Shen YF; Xue YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):470-3. PubMed ID: 17680547
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Detection of minimal residual disease using fluorescence DNA in situ hybridization: a follow-up study in leukemia and lymphoma patients.
    Nylund SJ; Ruutu T; Saarinen U; Larramendy ML; Knuutila S
    Leukemia; 1994 Apr; 8(4):587-94. PubMed ID: 8152255
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Fluorescent in situ hybridization for assessing the proportion of cells with trisomy 4 in a patient with acute non-lymphoblastic leukemia.
    Mark HF; Sikov W; Safran H; King TC; Griffith RC
    Ann Clin Lab Sci; 1995; 25(4):330-5. PubMed ID: 7668816
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Fluorescence in situ hybridization: a rapid analysis to verify chromosome aberrations.
    Tocharoentanaphol C; Parinayok R; Punthuwattana N; Kangwanpong D
    J Med Assoc Thai; 2000 Mar; 83 Suppl 1():S76-81. PubMed ID: 10865411
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Rapid detection of numerical aberrations of chromosomes in the first trimester of pregnancy by using fluorescence in situ hybridization (FISH)].
    Xiang Y; Bryndorf T; Philip J; Sun N
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Apr; 17(2):120-4. PubMed ID: 7656391
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Rapid detection of karyotype changes in interphase bone marrow cells by oligonucleotide primed in situ hybridization (PRINS).
    Wilkens L; Komminoth P; Nasarek A; von Wasielewski R; Werner M
    J Pathol; 1997 Apr; 181(4):368-73. PubMed ID: 9196432
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Clinical and laboratory characteristics of two acute lymphoblastic leukemia patients with dicentric (9; 20) (p11 - 13; q11)].
    Gong SL; Qiu HY; Li JY; Han FL; Song XM; Huang ZX; Wang JM
    Zhonghua Xue Ye Xue Za Zhi; 2006 May; 27(5):306-9. PubMed ID: 16875578
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The role of fluorescence in situ hybridization (FISH) for monitoring hematologic malignancies with BCR/ABL or ETO/AML1 rearrangement: a comparative study with FISH and G-banding on 919 consecutive specimens of hematologic malignancies.
    Lee DY; Cho HI; Kang YH; Yun SS; Park SY; Lee YS; Kim Y; Lee DS
    Cancer Genet Cytogenet; 2004 Jul; 152(1):1-7. PubMed ID: 15193435
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
    Sinclair P; Harrison CJ; Jarosová M; Foroni L
    Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Aberrations involving 13q12 approximately q14 are frequent secondary events in childhood acute lymphoblastic leukemia.
    Kovacs BZ; Niggli FK; Betts DR
    Cancer Genet Cytogenet; 2004 Jun; 151(2):157-61. PubMed ID: 15172754
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.
    Schoch C; Haferlach T; Bursch S; Gerstner D; Schnittger S; Dugas M; Kern W; Löffler H; Hiddemann W
    Genes Chromosomes Cancer; 2002 Sep; 35(1):20-9. PubMed ID: 12203786
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [FISH detected 11q23 microdeletion and translocation at the long arm of chromosome 11 in a child with normal karyotypic acute lymphoblastic leukemia].
    Matsubara K; Yura K
    Rinsho Ketsueki; 2004 Jan; 45(1):61-5. PubMed ID: 14999936
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fluorescent in situ hybridization (FISH) in bone marrow and peripheral blood of leukemia patients: implications for occupational surveillance.
    McDevitt MA; Condon M; Stamberg J; Karp JE; McDiarmid M
    Mutat Res; 2007 Apr; 629(1):24-31. PubMed ID: 17276720
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [A case of acute promyelocytic leukemia with variant t(5;17) and trisomy 22].
    Qiu HR; Li JY; Miao KR; Wang R; Zhang JF; Xu W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug; 25(4):430-3. PubMed ID: 18683144
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Double target in situ hybridization applied to the study of numerical aberrations in childhood acute lymphoblastic leukemia.
    Tosi S; Ritterbach J; Maglia O; Harbott J; Riehm H; Masera G; Biondi A; Lampert F
    Cancer Genet Cytogenet; 1994 Apr; 73(2):103-8. PubMed ID: 8174084
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Dicentric (19;21)(p13;p13), a novel chromosomal abnormality occurring in a case of Philadelphia chromosome-positive acute lymphoblastic leukemia.
    Schilling G; Dierlamm J; Murga Penas EM; Hinz K; Seeger D; Hossfeld DK
    Cancer Genet Cytogenet; 2004 Jul; 152(2):129-31. PubMed ID: 15262431
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics.
    Beyer V; Castagné C; Mühlematter D; Parlier V; Gmür J; Hess U; Kovacsovics T; Meyer-Monard S; Tichelli A; Tobler A; Jacky E; Schanz U; Bargetzi M; Hagemeijer A; de Witte T; van Melle G; Jotterand M
    Cancer Genet Cytogenet; 2004 Jul; 152(1):29-41. PubMed ID: 15193439
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.