BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 19036120)

  • 21. Cryptic t(15;17) in a patient with AML M3 and a complex karyotype.
    Göhring G; Lange K; Atta J; Krauter J; Hölzer D; Schlegelberger B
    Cancer Genet Cytogenet; 2007 May; 175(1):77-80. PubMed ID: 17498564
    [No Abstract]   [Full Text] [Related]  

  • 22. Therapy-related acute myeloid leukemia after successful therapy for acute promyelocytic leukemia with t(15;17): A case report and literature review.
    Bao L; Lu X; Lai Y; Zhang X; Zhu H; Liu Y; Qin Y; Huang XJ
    Leuk Res; 2009 Jul; 33(7):e64-8. PubMed ID: 19297021
    [No Abstract]   [Full Text] [Related]  

  • 23. Significance of persistent Auer rods and cytogenetic abnormality after first cycle of therapy for acute promyelocytic leukaemia.
    Dalal BI; Bruyere H; Barnett MJ
    Br J Haematol; 2007 Jun; 137(5):385. PubMed ID: 17374141
    [No Abstract]   [Full Text] [Related]  

  • 24. Cryptic insertion (15;17) in a case of acute promyelocytic leukemia detected by fluorescence in situ hybridization.
    Gutiérrez NC; García JL; Chillón C; Muntión S; González M; Hernández JM
    Haematologica; 1999 Jan; 84(1):88-90. PubMed ID: 10091399
    [No Abstract]   [Full Text] [Related]  

  • 25. [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]  

  • 26. Characterization of a cryptic
    Schultz MJ; Blackburn PR; Cogbill CH; Pitel BA; Smadbeck JB; Johnson SH; Vasmatzis G; Rech KL; Sukov WR; Greipp PT; Hoppman NL; Baughn LB; Ketterling RP; Peterson JF
    Leuk Lymphoma; 2020 Apr; 61(4):975-978. PubMed ID: 31809670
    [No Abstract]   [Full Text] [Related]  

  • 27. A new complex translocation t(5;17;15)(q11;q21;q22) in acute promyelocytic leukemia.
    Abe S; Ishikawa I; Harigae H; Sugawara T
    Cancer Genet Cytogenet; 2008 Jul; 184(1):44-7. PubMed ID: 18558288
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A Paediatric Acute Promyelocytic Leukaemia Patient Harbouring a Cryptic PML-RARA Insertion due to a Complex Structural Chromosome 17 Rearrangement.
    El-Hajj Ghaoui R; St Heaps L; Hung D; Nagabushan S; Harris C; Mirochnik O; Sharma P; Kellie SJ; Wright DC
    Cytogenet Genome Res; 2017; 153(4):181-189. PubMed ID: 29550828
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Acute promyelocytic leukemia harboring a STAT5B-RARA fusion gene and a G596V missense mutation in the STAT5B SH2 domain of the STAT5B-RARA.
    Iwanaga E; Nakamura M; Nanri T; Kawakita T; Horikawa K; Mitsuya H; Asou N
    Eur J Haematol; 2009 Nov; 83(5):499-501. PubMed ID: 19624718
    [No Abstract]   [Full Text] [Related]  

  • 30. Cytogenetically cryptic and fish negative PML/RARA rearrangement in acute promyelocytic leukemia detected by RT-PCR.
    Avgerinou G; Katsibardi Κ; Filippidou M; Tzanoudaki M; Papadhimitriou SI; Kattamis A
    Leuk Lymphoma; 2020 Dec; 61(14):3526-3528. PubMed ID: 32909480
    [No Abstract]   [Full Text] [Related]  

  • 31. FISH detection of PML-RARA fusion in ins(15;17) acute promyelocytic leukaemia depends on probe size.
    Campbell LJ; Oei P; Brookwell R; Shortt J; Eaddy N; Ng A; Chew E; Browett P
    Biomed Res Int; 2013; 2013():164501. PubMed ID: 23607089
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The APL-associated fusion proteins.
    Minucci S; Cioce M; Maccarana M; Pelicci PG
    Haematologica; 1999 Jun; 84 Suppl EHA-4():70-1. PubMed ID: 10907473
    [No Abstract]   [Full Text] [Related]  

  • 33. Two new molecular PML-RARalpha variants: implications for the molecular diagnosis of APL.
    Vizmanos JL; Larrráyoz MJ; Odero MD; Lasa R; González M; Novo FJ; Calasanz MJ
    Haematologica; 2002 Aug; 87(8):ELT37. PubMed ID: 12161382
    [No Abstract]   [Full Text] [Related]  

  • 34. Polyploidy in acute promyelocytic leukemia without the 15:17 translocation.
    Matsouka P; Sambani C; Giannakoulas N; Symeonidis A; Zoumbos N
    Haematologica; 2001 Dec; 86(12):1312-3. PubMed ID: 11726325
    [No Abstract]   [Full Text] [Related]  

  • 35. Cytogenetic and molecular characterization of complex three-way translocations in acute promyelocytic leukemia.
    Freeman CE; Mercer DD; Ye Y; Van Brunt J; Li MM
    Beijing Da Xue Xue Bao Yi Xue Ban; 2009 Aug; 41(4):477-9. PubMed ID: 19727242
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Association between acute promyelocytic leukemia and ring chromosome 6.
    Park TS; Kim J; Song J; Song S; Suh B; Choi JR; Kim SJ; Lee HW; Min YH
    Cancer Genet Cytogenet; 2009 Jul; 192(1):48-50. PubMed ID: 19480938
    [No Abstract]   [Full Text] [Related]  

  • 37. Molecular and cytogenetic characterization of a new case of t(5;17)(q35;q21) variant acute promyelocytic leukemia.
    Nicci C; Ottaviani E; Luatti S; Grafone T; Tonelli M; Motta MR; Malagola M; Marzocchi G; Martinelli G; Baccarani M; Testoni N
    Leukemia; 2005 Mar; 19(3):470-2. PubMed ID: 15674421
    [No Abstract]   [Full Text] [Related]  

  • 38. Translocation (15;17)(q22;q21) not associated with acute promyelocytic leukemia and negative for PML/RARa rearrangement.
    Kwan Ma ES; Au Wy ; Kong Wan TS; Lam Kwong Y; Chan LC
    Haematologica; 2000 Jul; 85(7):768-9. PubMed ID: 10897134
    [No Abstract]   [Full Text] [Related]  

  • 39. Cryptic insertion of PML-RARA into the 3p25 locus in an acute promyelocytic leukemia with t(3;17)(p25;q21).
    Chattopadhyay A; Redner RL
    Cancer Genet Cytogenet; 2010 Aug; 201(1):28-31. PubMed ID: 20633765
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A new cytogenetic abnormality, t(2;7)(q33;q36), in acute promyelocytic leukemia.
    Owatari S; Uozumi K; Haraguchi K; Ohno N; Tokunaga M; Tokunaga M; Suzuki S; Hanada S; Arima N
    Cancer Genet Cytogenet; 2007 Feb; 173(1):71-4. PubMed ID: 17284374
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.