BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 16019491)

  • 21. Secondary near-tetraploidy with double der(15)t(15;17) in acute promyelocytic leukemia in relapse.
    Morita Y; Takahashi A; Yamamoto K; Miki T; Murakami N; Miura O
    Cancer Genet Cytogenet; 2004 Mar; 149(2):131-6. PubMed ID: 15036889
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Trisomy/tetrasomy 13 in seven cases of acute leukemia.
    Sreekantaiah C; Baer MR; Morgan S; Isaacs JD; Miller KB; Sandberg AA
    Leukemia; 1990 Nov; 4(11):781-5. PubMed ID: 2232892
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Two new 3' PML breakpoints in t(15;17)(q22;q21)-positive acute promyelocytic leukemia.
    Chillón MC; González M; García-Sanz R; Balanzategui A; González D; López-Pérez R; Mateos MV; Alaejos I; Rayón C; Arbeteta J; Hernández JM; Orfao A; San Miguel J
    Genes Chromosomes Cancer; 2000 Jan; 27(1):35-43. PubMed ID: 10564584
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Morphologic characterization of acute myeloid leukemia with cytogenetic or molecular evidence of t(8;21), t(15;17), inv(16) and 11q23 abnormalities.
    Rozman M; Navarro JT; Domingo A; Ayats R; Vallespí T; Gallart M; Florensa L;
    Haematologica; 2002 Aug; 87(8):886-7. PubMed ID: 12161368
    [No Abstract]   [Full Text] [Related]  

  • 25. Acute promyelocytic leukemia with insertion of PML exon 7a and partial deletion of exon 3 of RARA: a novel variant transcript related to aggressive course and not detected with real-time polymerase chain reaction analysis.
    Park TS; Kim JS; Song J; Lee KA; Yoon S; Suh B; Lee JH; Lee HJ; Kim JK; Choi JR
    Cancer Genet Cytogenet; 2009 Jan; 188(2):103-7. PubMed ID: 19100514
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Minimal residual disease. Methodologies and clinical implications].
    Ortega M; Coll MD; Solé F; Caballín MR
    Sangre (Barc); 1999 Aug; 44(4):283-90. PubMed ID: 10589280
    [No Abstract]   [Full Text] [Related]  

  • 27. Biphenotypic acute leukemia: a case report.
    Zucchini A; Fattori PP; Lanza F; Ferrari L; Bagli L; Imola M; Ravaioli A; Papa S
    J Biol Regul Homeost Agents; 2004; 18(3-4):387-91. PubMed ID: 15786709
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Cytogenetic and molecular genetic studies on a variant of t(15;17), ins(17;15)(q21;q14q22), in an acute promyelocytic leukemia patient].
    Chen SN; Xue YQ; Wu YF; Pan JL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):77-9. PubMed ID: 14767917
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Multiprobe fluorescence in situ hybridization panel in detection of the common cytogenetic abnormalities of acute myeloid leukemia].
    Xu LL; Liu XL; Du QF; Song LL; Cao R; Wei YQ; Xu N; Zhang JF
    Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi; 2011 Mar; 27(3):324-6. PubMed ID: 21638933
    [TBL] [Abstract][Full Text] [Related]  

  • 30. PML/RARA rearrangement associated with a t(15;19;17) in a case of acute myeloid leukemia with abundant myelocytes with salmon-pink cytoplasm.
    Kim IS; Kim HJ; Choung HS; Jung CW; Kim JW; Kim SH
    Cancer Genet Cytogenet; 2006 Aug; 169(1):81-2. PubMed ID: 16875944
    [No Abstract]   [Full Text] [Related]  

  • 31. Myeloid and lymphoid neoplasm with abnormalities of FGFR1 presenting with trilineage blasts and RUNX1 rearrangement: a case report and review of literature.
    Kumar KR; Chen W; Koduru PR; Luu HS
    Am J Clin Pathol; 2015 May; 143(5):738-48. PubMed ID: 25873510
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification of classic and complex t(15;17) and/or RAR alpha/PML gene fusion in APL by cytogenetic and dual color-FISH techniques.
    Acar H; Dündar M; Stewart J
    Proc Natl Sci Counc Repub China B; 1997 Apr; 21(2):54-60. PubMed ID: 9276968
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prognostic value of minimal residual disease (MRD) in acute myeloid leukemia (AML) with favorable cytogenetics [t(8;21) and inv(16)].
    Perea G; Lasa A; Aventín A; Domingo A; Villamor N; Queipo de Llano MP; Llorente A; Juncà J; Palacios C; Fernández C; Gallart M; Font L; Tormo M; Florensa L; Bargay J; Martí JM; Vivancos P; Torres P; Berlanga JJ; Badell I; Brunet S; Sierra J; Nomdedéu JF;
    Leukemia; 2006 Jan; 20(1):87-94. PubMed ID: 16281071
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cytogenetic profile of de novo acute myeloid leukemia: a study based on 1432 patients in a single institution of China.
    Cheng Y; Wang Y; Wang H; Chen Z; Lou J; Xu H; Wang H; Qian W; Meng H; Lin M; Jin J
    Leukemia; 2009 Oct; 23(10):1801-6. PubMed ID: 19474801
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Rapid diagnosis of acute promyelocytic leukemia with the PML-RARA fusion gene using a combination of droplet-reverse transcription-polymerase chain reaction and instant-quality fluorescence in situ hybridization.
    Shigeto S; Matsuda K; Yamaguchi A; Sueki A; Uehara M; Sugano M; Uehara T; Honda T
    Clin Chim Acta; 2016 Jan; 453():38-41. PubMed ID: 26656442
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Cytogenetics, molecular and ultrastructural characteristics of biphenotypic acute leukemia identified by the EGIL scoring system.
    Owaidah TM; Al Beihany A; Iqbal MA; Elkum N; Roberts GT
    Leukemia; 2006 Apr; 20(4):620-6. PubMed ID: 16437134
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Detection of aberrant chromosomes in acute lymphoblastic leukemia by fluorescence in situ hybridization].
    Yang K; Huang L
    Zhonghua Xue Ye Xue Za Zhi; 1999 Dec; 20(12):640-2. PubMed ID: 11721367
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Molecular cytogenetic aberrations in patients with multiple myeloma studied by interphase fluorescence in situ hybridization.
    Chen L; Li J; Xu W; Qiu H; Zhu Y; Zhang Y; Duan L; Qian S; Lu H
    Exp Oncol; 2007 Jun; 29(2):116-20. PubMed ID: 17704743
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.