These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

265 related articles for article (PubMed ID: 11408074)

  • 1. Gain of an isochromosome 5p: a new recurrent chromosome abnormality in acute monoblastic leukemia.
    Schoch C; Bursch S; Kern W; Schnittger S; Hiddemann W; Haferlach T
    Cancer Genet Cytogenet; 2001 May; 127(1):85-8. PubMed ID: 11408074
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Gain of an isochromosome 5p: a rare recurrent abnormality in acute myeloid leukemia.
    Panani AD
    In Vivo; 2006; 20(3):359-60. PubMed ID: 16724670
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Trisomy/ tetrasomy of chromosome 8 and +i(8q) as the sole chromosome abnormality in three adult patients with myelomonocytic leukemia.
    Ferro MT; Vázquez-Mazariego Y; Ramiro S; Santiago MF; García-Sagredo JM; Nuñez R; Hernández JM; San Roman C
    Cancer Genet Cytogenet; 2000 Jul; 120(2):163-5. PubMed ID: 10942810
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Isochromosome 5p and related anomalies: a novel recurrent chromosome abnormality in myeloid disorders.
    Herry A; Douet-Guilbert N; Morel F; Le Bris MJ; Guéganic N; Berthou C; De Braekeleer M
    Cancer Genet Cytogenet; 2010 Jul; 200(2):134-9. PubMed ID: 20620596
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A new case of "complete" trisomy 5p with isochromosome 5p associated with a de novo translocation t(5;8)(q11;p23).
    Fujita M; Flori E; Lemaire F; Casanova R; Astruc D
    Clin Genet; 1994 Jun; 45(6):305-7. PubMed ID: 7923861
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of an acquired jumping translocation involving 3q13.31-qter in a patient with de novo acute monocytic leukemia.
    Kjeldsen E
    Exp Mol Pathol; 2017 Aug; 103(1):14-25. PubMed ID: 28625614
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents.
    Andersen MK; Christiansen DH; Kirchhoff M; Pedersen-Bjergaard J
    Genes Chromosomes Cancer; 2001 May; 31(1):33-41. PubMed ID: 11284033
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Microdissection and FISH investigations in acute myeloid leukemia: a step forward to full identification of complex karyotypic changes.
    Falzetti D; Vermeesch JR; Matteucci C; Ciolli S; Martelli MF; Marynen P; Mecucci C
    Cancer Genet Cytogenet; 2000 Apr; 118(1):28-34. PubMed ID: 10731587
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Tetrasomy 8 in a patient with acute monoblastic leukemia.
    Kim J; Park TS; Song J; Lee KA; Lee SG; Cheong JW; Choi JR
    Korean J Lab Med; 2008 Aug; 28(4):262-6. PubMed ID: 18728374
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Cytogenetic manifestation of chromosome 11 duplication/amplification in acute myeloid leukemia.
    Sárová I; Brezinová J; Zemanová Z; Izáková S; Lizcová L; Malinová E; Berková A; Cermák J; Maaloufová J; Nováková L; Michalová K
    Cancer Genet Cytogenet; 2010 Jun; 199(2):121-7. PubMed ID: 20471515
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cytogenetic and molecular analysis of the acute monocytic leukemia cell line THP-1 with an MLL-AF9 translocation.
    Odero MD; Zeleznik-Le NJ; Chinwalla V; Rowley JD
    Genes Chromosomes Cancer; 2000 Dec; 29(4):333-8. PubMed ID: 11066077
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isochromosome (17)(q10) and translocation (4;12)(q12;p13) in a child with acute myeloid leukemia.
    Nathan PC; Chun K; Abdelhaleem M; Malkin D
    Cancer Genet Cytogenet; 2001 Nov; 131(1):82-5. PubMed ID: 11734325
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Spontaneous remission of bone marrow aplasia associated with chromosome 8 trisomy, with subsequent evolution to acute monoblastic leukemia and recurrence of the clonal abnormality].
    Upegui RI; Betes VM; Solé F; López R
    Med Clin (Barc); 2013 Jul; 141(1):42-3. PubMed ID: 23276618
    [No Abstract]   [Full Text] [Related]  

  • 16. Cytogenetics of the chronic myeloid leukemia-derived cell line K562: karyotype clarification by multicolor fluorescence in situ hybridization, comparative genomic hybridization, and locus-specific fluorescence in situ hybridization.
    Gribble SM; Roberts I; Grace C; Andrews KM; Green AR; Nacheva EP
    Cancer Genet Cytogenet; 2000 Apr; 118(1):1-8. PubMed ID: 10731582
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cytogenetic analysis of de novo acute myeloid leukemia with trilineage myelodysplasia in comparison with myelodysplastic syndrome evolving to acute myeloid leukemia.
    Tamura S; Takemoto Y; Hashimoto-Tamaoki T; Mimura K; Sugahara Y; Senoh J; Furuyama JI; Kakishita E
    Int J Oncol; 1998 Jun; 12(6):1259-62. PubMed ID: 9592183
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new patient with pure trisomy 4p resulting from isochromosome formation and whole arm translocation.
    Zahed L; Oreibi G; El-Amine H; Obeid M; Bitar FF
    Am J Med Genet A; 2004 Jul; 128A(1):60-2. PubMed ID: 15211659
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A case of acute myeloid leukemia (AML) with an unreported combination of chromosomal abnormalities: gain of isochromosome 5p, tetrasomy 8 and unbalanced translocation der(19)t(17;19)(q23;p13).
    Paar C; Herber G; Voskova D; Fridrik M; Stekel H; Berg J
    Mol Cytogenet; 2013 Sep; 6(1):40. PubMed ID: 24079663
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.