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 *

105 related articles for article (PubMed ID: 2187596)

  • 1. Molecular cytogenetic analysis discloses complex genetic imbalance in a t(11;21) myelodysplastic syndrome.
    Kerim S; Rege-Cambrin G; Guerrasio A; Rosso C; Van Den Berghe H
    Cancer Genet Cytogenet; 1990 Jun; 46(2):243-50. PubMed ID: 2187596
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation.
    Wlodarska I; Selleri L; La Starza R; Paternotte C; Evans GA; Boogaerts M; Van den Berghe H; Mecucci C
    Genes Chromosomes Cancer; 1999 Mar; 24(3):199-206. PubMed ID: 10451699
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Translocation t(11;21)(q24;q11.2) is a new nonrandomly occurring chromosome change in myelodysplastic syndromes.
    Rege-Cambrin G; Mecucci C; Kerim S; Scaravaglio P; Boogaerts M; Van den Berghe H
    Cancer Genet Cytogenet; 1988 Aug; 34(1):33-40. PubMed ID: 3395992
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytogenetic changes at 11q11, 11q23, and 17q11 in myelodysplastic syndrome.
    Ohyashiki K; Yoshida MA; Gibas LM; Ohyashiki JH; Katsunuma H; Ryan DH; Rowe J; Sandberg AA
    Cancer Genet Cytogenet; 1986 Apr; 21(4):287-95. PubMed ID: 3456822
    [TBL] [Abstract][Full Text] [Related]  

  • 5. ETS1 gene in myelodysplastic syndrome with chromosome change at 11q23.
    Ohyashiki K; Ohyashiki JH; Tauchi T; Iwabuchi H; Iwabuchi A; Toyama K
    Cancer Genet Cytogenet; 1990 Mar; 45(1):73-80. PubMed ID: 2302688
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Unbalanced translocation der(11)t(11;12)(q23;q13): a new recurrent cytogenetic aberration in myelodysplastic syndrome with a complex karyotype.
    Yamamoto K; Hato A; Minagawa K; Yakushijin K; Urahama N; Gomyo H; Sada A; Okamura A; Ito M; Matsui T
    Cancer Genet Cytogenet; 2004 Nov; 155(1):67-73. PubMed ID: 15527905
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Unbalanced 1q whole-arm translocation resulting in der(14)t(1;14)(q11-12;p11) in myelodysplastic syndrome.
    Fogu G; Campus PM; Cambosu F; Moro MA; Sanna R; Fozza C; Nieddu RM; Longinotti M; Montella A
    Cytogenet Genome Res; 2012; 136(4):256-63. PubMed ID: 22571950
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytogenetic profile of myelodysplastic syndromes with complex karyotypes: an analysis using spectral karyotyping.
    Martínez-Ramírez A; Urioste M; Alvarez S; Vizmanos JL; Calasanz MJ; Cigudosa JC; Benítez J
    Cancer Genet Cytogenet; 2004 Aug; 153(1):39-47. PubMed ID: 15325092
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Der(16)t(1;16)(q11;q11) in myelodysplastic syndromes: a new non-random abnormality characterized by cytogenic and fluorescence in situ hybridization studies.
    Mugneret F; Dastugue N; Favre B; Sidaner I; Salles B; Huguet-Rigal F; Solary E
    Br J Haematol; 1995 May; 90(1):119-24. PubMed ID: 7786773
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia.
    Matteucci C; La Starza R; Crescenzi B; Romoli S; Santoro A; Magrin S; Lauria F; Coco FL; Martelli MF; Mecucci C
    Cancer Genet Cytogenet; 2003 Jan; 140(1):13-7. PubMed ID: 12550752
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Down's syndrome with myelodysplastic syndrome showing t(7;11)(p13;p14).
    Ohnishi H; Taki T; Tabuchi K; Kobayashi M; Bessho F; Hayashi Y
    Am J Hematol; 2000 Sep; 65(1):62-5. PubMed ID: 10936866
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Trisomy of the long arm of chromosome 1 resulting in a dicentric derivative (6)t(1;6) chromosome in a child with myelodysplastic syndrome following treatment for a primitive neuroectodermal tumor.
    Mathew S; Head D; Rodriguez-Galindo C; Raimondi SC
    Leuk Lymphoma; 2000 Mar; 37(1-2):213-8. PubMed ID: 10721789
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Combined trisomy 1q and monosomy 17p due to translocation t(1;17) in a patient with myelodysplastic syndrome.
    Mamaev N; Mamaeva SE; Pavlova VA; Patterson D
    Cancer Genet Cytogenet; 1988 Oct; 35(1):21-5. PubMed ID: 3180004
    [TBL] [Abstract][Full Text] [Related]  

  • 15. New recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of short arm of chromosome 6.
    Tassano E; Tavella E; Valli R; Micalizzi C; Cuoco C; Maserati E; Pasquali F; Morerio C
    Leuk Lymphoma; 2012 Dec; 53(12):2434-8. PubMed ID: 22616618
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Translocation between chromosomes 8q24 and 14q11 in T-cell acute lymphoblastic leukemia.
    Inaba T; Murakami S; Oku N; Itoh K; Ura Y; Nakanishi S; Shimazaki C; Nishio A; Nakagawa M; Fujita N
    Cancer Genet Cytogenet; 1990 Oct; 49(1):69-74. PubMed ID: 2397475
    [TBL] [Abstract][Full Text] [Related]  

  • 17. der(3)t(3;5). Another recurring abnormality in myelodysplastic disorder.
    Lindgren V; Gibson L; Yang-Feng TL
    Cancer Genet Cytogenet; 1991 Jul; 54(1):129-31. PubMed ID: 2065307
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7.
    Alitalo T; Willard HF; de la Chapelle A
    Cytogenet Cell Genet; 1989; 50(1):49-53. PubMed ID: 2743817
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Two myelodysplastic syndrome cases with the inv(11)(p15q23) as a sole chromosomal abnormality.
    Mitani K; Sato Y; Hayashi Y; Miura Y; Miyagawa K; Yazaki Y; Hirai H
    Br J Haematol; 1992 Aug; 81(4):512-5. PubMed ID: 1390237
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.