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 *

139 related articles for article (PubMed ID: 15611930)

  • 1. Analysis of myelodysplastic syndromes with complex karyotypes by high-resolution comparative genomic hybridization and subtelomeric CGH array.
    Martínez-Ramírez A; Urioste M; Melchor L; Blesa D; Valle L; de Andrés SA; Kok K; Calasanz MJ; Cigudosa JC; Benítez J
    Genes Chromosomes Cancer; 2005 Mar; 42(3):287-98. PubMed ID: 15611930
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization.
    Dierlamm J; Rosenberg C; Stul M; Pittaluga S; Wlodarska I; Michaux L; Dehaen M; Verhoef G; Thomas J; de Kelver W; Bakker-Schut T; Cassiman JJ; Raap AK; De Wolf-Peeters C; Van den Berghe H; Hagemeijer A
    Leukemia; 1997 May; 11(5):747-58. PubMed ID: 9180302
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Distinct sequences on 11q13.5 and 11q23-24 are frequently coamplified with MLL in complexly organized 11q amplicons in AML/MDS patients.
    Zatkova A; Ullmann R; Rouillard JM; Lamb BJ; Kuick R; Hanash SM; Schnittger S; Schoch C; Fonatsch C; Wimmer K
    Genes Chromosomes Cancer; 2004 Apr; 39(4):263-76. PubMed ID: 14978788
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Gains, losses and complex karyotypes in myeloid disorders: a light at the end of the tunnel.
    Alvarez S; Cigudosa JC
    Hematol Oncol; 2005 Mar; 23(1):18-25. PubMed ID: 16142824
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Oncogene amplification in transforming myelodysplasia.
    Papenhausen PR; Griffin S; Tepperberg J
    Exp Mol Pathol; 2005 Oct; 79(2):168-75. PubMed ID: 16026782
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The application of comparative genomic hybridization as an additional tool in the chromosome analysis of acute myeloid leukemia and myelodysplastic syndromes.
    Kim MH; Stewart J; Devlin C; Kim YT; Boyd E; Connor M
    Cancer Genet Cytogenet; 2001 Apr; 126(1):26-33. PubMed ID: 11343775
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comparative genomic hybridization-aided unraveling of complex karyotypes in human hematopoietic neoplasias.
    Verdorfer I; Brecevic L; Saul W; Schenker B; Kirsch M; Trautmann U; Helm G; Gramatzki M; Gebhart E
    Cancer Genet Cytogenet; 2001 Jan; 124(1):1-6. PubMed ID: 11165314
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Routine fluorescence in situ hybridization with the MLL probe does not reliably detect two separate signals on one chromosome 11 in patients with trisomy 11.
    Smith A; Robson L; Heaps LS; Sharma P; Dunlop L; Bhave A; Bradstock K
    Cancer Genet Cytogenet; 2001 Sep; 129(2):173-6. PubMed ID: 11566351
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The value of fluorescence in situ hybridization for the detection of 11q in multiple myeloma.
    González MB; Hernández JM; García JL; Lumbreras E; Castellanos M; Hernández JM; Fernández-Calvo J; Gutiérrez NC; San Miguel JF
    Haematologica; 2004 Oct; 89(10):1213-8. PubMed ID: 15477206
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Disclosure of candidate genes in acute myeloid leukemia with complex karyotypes using microarray-based molecular characterization.
    Rücker FG; Bullinger L; Schwaenen C; Lipka DB; Wessendorf S; Fröhling S; Bentz M; Miller S; Scholl C; Schlenk RF; Radlwimmer B; Kestler HA; Pollack JR; Lichter P; Döhner K; Döhner H
    J Clin Oncol; 2006 Aug; 24(24):3887-94. PubMed ID: 16864856
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia.
    Casas S; Aventín A; Fuentes F; Vallespí T; Granada I; Carrió A; Angel Martínez-Climent J; Solé F; Teixidó M; Bernués M; Duarte J; Maria Hernández J; Brunet S; Dolors Coll M; Sierra J
    Cancer Genet Cytogenet; 2004 Aug; 153(1):16-25. PubMed ID: 15325089
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Lymphocyte predominance Hodgkin disease is characterized by recurrent genomic imbalances.
    Franke S; Wlodarska I; Maes B; Vandenberghe P; Delabie J; Hagemeijer A; De Wolf-Peeters C
    Blood; 2001 Mar; 97(6):1845-53. PubMed ID: 11238128
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of hematologic diseases using conventional karyotyping, fluorescence in situ hybridization (FISH), and comparative genomic hybridization (CGH).
    Wilkens L; Tchinda J; Burkhardt D; Nolte M; Werner M; Georgii A
    Hum Pathol; 1998 Aug; 29(8):833-9. PubMed ID: 9712425
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance.
    Thiel A; Beier M; Ingenhag D; Servan K; Hein M; Moeller V; Betz B; Hildebrandt B; Evers C; Germing U; Royer-Pokora B
    Leukemia; 2011 Mar; 25(3):387-99. PubMed ID: 21274003
    [TBL] [Abstract][Full Text] [Related]  

  • 16. IS THE AMPLIFICATION OF c-MYC, MLL AND RUNX1 GENES IN AML AND MDS PATIENTS WITH TRISOMY 8, 11 AND 21 A FACTOR FOR A CLONAL EVOLUTION IN THEIR KARYOTYPE?
    Angelova S; Spassov B; Nikolova V; Christov I; Tzvetkov N; Simeonova M
    Tsitol Genet; 2015; 49(3):25-32. PubMed ID: 26214902
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cytogenetic aberrations in myelodysplastic syndrome detected by comparative genomic hybridization and fluorescence in situ hybridization.
    Wilkens L; Burkhardt D; Tchinda J; Büsche G; Werner M; Nolte M; Ganser A; Georgii A
    Diagn Mol Pathol; 1999 Mar; 8(1):47-53. PubMed ID: 10408793
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular cytogenetic analysis of non-small cell lung carcinoma by spectral karyotyping and comparative genomic hybridization.
    Luk C; Tsao MS; Bayani J; Shepherd F; Squire JA
    Cancer Genet Cytogenet; 2001 Mar; 125(2):87-99. PubMed ID: 11369051
    [TBL] [Abstract][Full Text] [Related]  

  • 19. AML/MDS with 11q/MLL amplification show characteristic gene expression signature and interplay of DNA copy number changes.
    Zatkova A; Merk S; Wendehack M; Bilban M; Muzik EM; Muradyan A; Haferlach C; Haferlach T; Wimmer K; Fonatsch C; Ullmann R
    Genes Chromosomes Cancer; 2009 Jun; 48(6):510-20. PubMed ID: 19306356
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosomal imbalances in diffuse large B-cell lymphoma detected by comparative genomic hybridization.
    Berglund M; Enblad G; Flordal E; Lui WO; Backlin C; Thunberg U; Sundström C; Roos G; Allander SV; Erlanson M; Rosenquist R; Larsson C; Lagercrantz S
    Mod Pathol; 2002 Aug; 15(8):807-16. PubMed ID: 12181265
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.