BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 18164759)

  • 1. Isochromosome i(17q) as a sole cytogenetic abnormality in a case of leukemic transformation from myelodysplastic syndrome (MDS)/myeloproliferative diseases (MPD).
    Nishida H; Ueno H; Park JW; Yano T
    Leuk Res; 2008 Aug; 32(8):1325-7. PubMed ID: 18164759
    [No Abstract]   [Full Text] [Related]  

  • 2. Concomitant isochromosome 17q and trisomy 14 in a patient with myelodysplastic syndrome in leukemic transformation.
    Park TS; Song J; Lee JH; Kim JS; Yang WI; Choi JR
    Ann Clin Lab Sci; 2009; 39(2):176-81. PubMed ID: 19429805
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53.
    Kanagal-Shamanna R; Bueso-Ramos CE; Barkoh B; Lu G; Wang S; Garcia-Manero G; Vadhan-Raj S; Hoehn D; Medeiros LJ; Yin CC
    Cancer; 2012 Jun; 118(11):2879-88. PubMed ID: 22038701
    [TBL] [Abstract][Full Text] [Related]  

  • 4. del11(p11-13) with overexpression of Wilms' tumor gene during leukemic transformation of myelodysplastic syndrome.
    Suzuki S; Hashino S; Yoshida S; Chiba K; Izumiyama K; Kurosawa M; Musashi M; Asaka M
    Ann Hematol; 2002 Oct; 81(10):605-8. PubMed ID: 12424545
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Isochromosome of a deleted 20q: a rare but recurrent chromosome abnormality in myelodysplastic syndromes.
    Saunders K; Czepulkowski B; Sivalingam R; Hayes JP; Aldouri M; Sekhar M; Cummins M; Ho A; Mufti GJ
    Cancer Genet Cytogenet; 2005 Jan; 156(2):154-7. PubMed ID: 15642396
    [TBL] [Abstract][Full Text] [Related]  

  • 6. dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in myelodysplastic syndromes.
    Alfaro R; Pérez-Granero A; Durán MA; Besalduch J; Rosell J; Bernués M
    Leuk Res; 2008 Jan; 32(1):159-61. PubMed ID: 17509681
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Exacerbation of acute leukemia bearing isolated i(17q) along with proliferation of blasts with high BMI-1 expression].
    Mihara K; Kido M; Nakaju N; Fukumoto S; Matsumoto R; Takihara Y; Kimura A
    Rinsho Ketsueki; 2007 Aug; 48(8):659-63. PubMed ID: 17867304
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Case report of isochromosome 17q in acute myeloid leukemia with myelodysplasia-related changes after treatment with a hypomethylating agent.
    Sousa JC; Germano RT; Castro CC; Magalhaes SM; Pinheiro RF
    Genet Mol Res; 2012 Aug; 11(3):2045-50. PubMed ID: 22911588
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Isochromosome 1q in a myelodysplastic syndrome after treatment for acute promyelocytic leukemia.
    Pawarode A; Finlay E; Sait SN; Barcos M; Baer MR
    Cancer Genet Cytogenet; 2006 Jun; 167(2):155-60. PubMed ID: 16737916
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course.
    McClure RF; Dewald GW; Hoyer JD; Hanson CA
    Br J Haematol; 1999 Aug; 106(2):445-54. PubMed ID: 10460605
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Isochromosome 17q in patients with myelodysplastic syndromes: six new cases.
    Xiao Z; Liu S; Yu M; Xu Z; Hao Y
    Haematologica; 2003 Jun; 88(6):714-5. PubMed ID: 12801850
    [No Abstract]   [Full Text] [Related]  

  • 12. Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions.
    Douet-Guilbert N; Basinko A; Morel F; Le Bris MJ; Ugo V; Morice P; Berthou C; De Braekeleer M
    Ann Hematol; 2008 Jul; 87(7):537-44. PubMed ID: 18350294
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Isochromosome 17q in MDS: a marker of a distinct entity.
    Pinheiro RF; Chauffaille Mde L; Silva MR
    Cancer Genet Cytogenet; 2006 Apr; 166(2):189-90. PubMed ID: 16631479
    [No Abstract]   [Full Text] [Related]  

  • 14. Isochromosome 17q as a sole anomaly: a distinct myelodysplastic syndrome entity?
    Solé F; Torrabadella M; Granada I; Florensa L; Vallespi T; Ribera JM; Irriguible D; Milla F; Woessner S
    Leuk Res; 1993 Aug; 17(8):717-20. PubMed ID: 8355516
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bortezomib is an effective agent for MDS/MPD syndrome with 5q- anomaly and thrombocytosis.
    Terpos E; Verrou E; Banti A; Kaloutsi V; Lazaridou A; Zervas K
    Leuk Res; 2007 Apr; 31(4):559-62. PubMed ID: 16820206
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Acute nonlymphocytic leukemia (ANLL) with isochromosome i(17q) as the sole chromosomal anomaly: a distinct entity?
    Weh HJ; Kuse R; Hossfeld DK
    Eur J Haematol; 1990 May; 44(5):312-4. PubMed ID: 2369943
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Unclassified chronic myeloproliferative Ph(-); i(17q); +8 syndrome with mixed myelo-megakaryoblastic crisis--case report].
    Mariańska B; Apel D; Seferyńska I; Maj S
    Acta Haematol Pol; 1996; 27(1):85-8. PubMed ID: 8629449
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A myeloproliferative disorder associated with isochromosome 14q.
    Saghir F; Abboud E; Veres C; Feldman L
    Am J Med Sci; 2002 Sep; 324(3):166-9. PubMed ID: 12240716
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The landscape of myeloid neoplasms with isochromosome 17q discloses a specific mutation profile and is characterized by an accumulation of prognostically adverse molecular markers.
    Meggendorfer M; Haferlach C; Zenger M; Macijewski K; Kern W; Haferlach T
    Leukemia; 2016 Jul; 30(7):1624-7. PubMed ID: 26859077
    [No Abstract]   [Full Text] [Related]  

  • 20. SBDS mutations and isochromosome 7q in a patient with Shwachman-Diamond syndrome: no predisposition to malignant transformation?
    Mellink CH; Alders M; van der Lelie H; Hennekam RH; Kuijpers TW
    Cancer Genet Cytogenet; 2004 Oct; 154(2):144-9. PubMed ID: 15474150
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.