BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 29574397)

  • 1. High frequency of dicentric chromosomes detected by multi-centromeric FISH in patients with acute myeloid leukemia and complex karyotype.
    Sarova I; Brezinova J; Zemanova Z; Ransdorfova S; Svobodova K; Izakova S; Pavlistova L; Lizcova L; Berkova A; Skipalova K; Hodanova L; Salek C; Jonasova A; Michalova K
    Leuk Res; 2018 May; 68():85-89. PubMed ID: 29574397
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular cytogenetic analysis of dicentric chromosomes in acute myeloid leukemia.
    Sarova I; Brezinova J; Zemanova Z; Ransdorfova S; Izakova S; Svobodova K; Pavlistova L; Berkova A; Cermak J; Jonasova A; Siskova M; Michalova K
    Leuk Res; 2016 Apr; 43():51-7. PubMed ID: 26821593
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Dicentric chromosomes and 20q11.2 amplification in MDS/AML with apparent monosomy 20.
    Mackinnon RN; Campbell LJ
    Cytogenet Genome Res; 2007; 119(3-4):211-20. PubMed ID: 18253031
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Increased frequency of dicentric chromosomes in therapy-related MDS and AML compared to de novo disease is significantly related to previous treatment with alkylating agents and suggests a specific susceptibility to chromosome breakage at the centromere.
    Andersen MK; Pedersen-Bjergaard J
    Leukemia; 2000 Jan; 14(1):105-11. PubMed ID: 10637484
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia.
    Xu W; Li JY; Liu Q; Zhu Y; Pan JL; Qiu HR; Xue YQ
    Int J Lab Hematol; 2010 Feb; 32(1 Pt 1):e86-95. PubMed ID: 20089000
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Abnormalities of chromosome 17 in myeloid malignancies with complex chromosomal abnormalities].
    Zhu Y; Xu W; Liu Q; Pan J; Qiu H; Wang R; Qiao C; Jiang Y; Zhang S; Fan L; Zhang J; Shen Y; Xue Y; Li J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):579-82. PubMed ID: 18841577
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2.
    Hilgenfeld E; Padilla-Nash H; McNeil N; Knutsen T; Montagna C; Tchinda J; Horst J; Ludwig WD; Serve H; Büchner T; Berdel WE; Schröck E; Ried T
    Br J Haematol; 2001 May; 113(2):305-17. PubMed ID: 11380393
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diagnostic value of fluorescence in situ hybridization for the detection of genomic aberrations in older patients with acute myeloid leukemia.
    Fröhling S; Kayser S; Mayer C; Miller S; Wieland C; Skelin S; Schlenk RF; Döhner H; Döhner K;
    Haematologica; 2005 Feb; 90(2):194-9. PubMed ID: 15710571
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Comparison of I-FISH and G-banding for the detection of chromosomal abnormalities during the evolution of myelodysplastic syndrome.
    Pinheiro RF; Chauffaille ML
    Braz J Med Biol Res; 2009 Nov; 42(11):1110-2. PubMed ID: 19855907
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Different prognosis of acute myeloid leukemia harboring monosomal karyotype with total or partial monosomies determined by FISH: retrospective PALG study.
    Wawrzyniak E; Wierzbowska A; Kotkowska A; Siemieniuk-Rys M; Robak T; Knopinska-Posluszny W; Klonowska A; Iliszko M; Woroniecka R; Pienkowska-Grela B; Ejduk A; Wach M; Duszenko E; Jaskowiec A; Jakobczyk M; Mucha B; Kosny J; Pluta A; Grosicki S; Holowiecki J; Haus O
    Leuk Res; 2013 Mar; 37(3):293-9. PubMed ID: 23254155
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hidden monosomy 7 in acute myeloid leukemia and myelodysplastic syndrome detected by interphase fluorescence in situ hybridization.
    Arif M; Tanaka K; Damodaran C; Asou H; Kyo T; Dohy H; Kamada N
    Leuk Res; 1996 Sep; 20(9):709-16. PubMed ID: 8947579
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of two marker chromosomes in a patient with acute nonlymphocytic leukemia by two-color fluorescence in situ hybridization.
    Taniwaki M; Speicher MR; Lengauer C; Jauch A; Popp S; Cremer T
    Cancer Genet Cytogenet; 1993 Oct; 70(2):99-102. PubMed ID: 8242604
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Centromeric breakage and highly rearranged chromosome derivatives associated with mutations of TP53 are common in therapy-related MDS and AML after therapy with alkylating agents: an M-FISH study.
    Andersen MK; Christiansen DH; Pedersen-Bjergaard J
    Genes Chromosomes Cancer; 2005 Apr; 42(4):358-71. PubMed ID: 15645489
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of the type of 5q loss with complex karyotype, clonal evolution, TP53 mutation status, and prognosis in acute myeloid leukemia and myelodysplastic syndrome.
    Volkert S; Kohlmann A; Schnittger S; Kern W; Haferlach T; Haferlach C
    Genes Chromosomes Cancer; 2014 May; 53(5):402-10. PubMed ID: 24493299
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Independent Prognostic Significance of Monosomy 17 and Impact of Karyotype Complexity in Monosomal Karyotype/Complex Karyotype Acute Myeloid Leukemia: Results from Four ECOG-ACRIN Prospective Therapeutic Trials.
    Strickland SA; Sun Z; Ketterling RP; Cherry AM; Cripe LD; Dewald G; Fernandez HF; Hicks GA; Higgins RR; Lazarus HM; Litzow MR; Luger SM; Paietta EM; Rowe JM; Vance GH; Wiernik P; Wiktor AE; Zhang Y; Tallman MS;
    Leuk Res; 2017 Aug; 59():55-64. PubMed ID: 28551161
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromosomal aberrations in 17p predict in vitro drug resistance and short overall survival in acute myeloid leukemia.
    Nahi H; Lehmann S; Bengtzen S; Jansson M; Möllgård L; Paul C; Merup M
    Leuk Lymphoma; 2008 Mar; 49(3):508-16. PubMed ID: 18297528
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dual color FISH on CBF primary acute myeloid leukemia.
    Sorour A; Nafea D
    Egypt J Immunol; 2008; 15(2):25-31. PubMed ID: 20306685
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A case with dicentric translocation between chromosome 9 and 18: confirmation by fluorescent in situ hybridization on metaphase spread.
    Isoyama K; Imai M; Ishikawa A; Fujita K; Suto Y; Shinohara T
    Acta Paediatr Jpn; 1995 Feb; 37(1):101-4. PubMed ID: 7754751
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.