BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 19215795)

  • 1. A tandem triplication, trp(1)(q21q32), in a patient with follicular lymphoma: a case study and review of the literature.
    Park TS; Lee ST; Song J; Lee KA; Kim J; Kim SJ; Lee JH; Song S; Choi JR
    Cancer Genet Cytogenet; 2009 Mar; 189(2):127-31. PubMed ID: 19215795
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A marginal zone phenotype in follicular lymphoma with t(14;18) is associated with secondary cytogenetic aberrations typical of marginal zone lymphoma.
    Torlakovic EE; Aamot HV; Heim S
    J Pathol; 2006 Jun; 209(2):258-64. PubMed ID: 16583359
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Serial cytogenetic alterations resulting in transformation of a low-grade follicular lymphoma to Burkitt lymphoma.
    Li L; Gupta S; Bashir T; Koduru PR; Brody J; Allen SL
    Cancer Genet Cytogenet; 2006 Oct; 170(2):140-6. PubMed ID: 17011985
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Jumping translocation of chromosome 1q associated with good clinical outcome in a case of Burkitt leukemia.
    Bessenyei B; Ujfalusi A; Balogh E; Olah E; Szegedi I; Kiss C
    Cancer Genet; 2011 Apr; 204(4):207-10. PubMed ID: 21536239
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Early transformation from follicular lymphoma to Burkitt lymphoma].
    Takahashi T; Hara T; Yoshikawa T; Shimomura Y; Tsurumi H; Yamada T; Tomita E; Moriwaki H
    Rinsho Ketsueki; 2005 Sep; 46(9):1055-9. PubMed ID: 16440764
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Triplication of 1q in Fanconi anemia.
    Ferro MT; Vazquez-Mazariego Y; Ramiro S; Sanchez-Hombre MC; Villalon C; Garcia-Sagredo JM; Ulibarrena C; Sastre JL; Roman CS
    Cancer Genet Cytogenet; 2001 May; 127(1):38-41. PubMed ID: 11408063
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Trisomy 1q in a patient with severe aplastic anemia.
    Angelidis P; Kojouri K; Lee J; Kern W; Mulvihill JJ; Li S
    Cancer Genet Cytogenet; 2006 Aug; 169(1):73-5. PubMed ID: 16875941
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Distal partial trisomy 1q: report of two cases and a review of the literature.
    Utine GE; Aktas D; Alanay Y; Gücer S; Tuncbilek E; Mrasek K; Liehr T
    Prenat Diagn; 2007 Sep; 27(9):865-71. PubMed ID: 17605151
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A case with mosaic partial duplication of 1q: prenatal and postmortem clinical and cytogenetic evaluations.
    Karaoguz MY; Biri A; Pala E; Kan D; Poyraz A; Kurdoglu M; Percin EF
    Genet Couns; 2006; 17(2):197-204. PubMed ID: 16970038
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cytogenetic abnormalities in hepatoblastoma: report of two new cases and review of the literature suggesting imbalance of chromosomal regions on chromosomes 1, 4, and 12.
    Nagata T; Nakamura M; Shichino H; Chin M; Sugito K; Ikeda T; Koshinaga T; Fukuzawa M; Inoue M; Mugishima H
    Cancer Genet Cytogenet; 2005 Jan; 156(1):8-13. PubMed ID: 15588850
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Inverted duplication dup(1)(q32q21) as sole aberration in lymphoid and myeloid malignancies.
    Bacher U; Schnittger S; Grüneisen A; Haferlach T; Kern W; Haferlach C
    Cancer Genet Cytogenet; 2009 Jan; 188(2):108-11. PubMed ID: 19100515
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Role of chromosome 1 pericentric heterochromatin (1q) in pathogenesis of myelodysplastic syndromes: report of 2 new cases.
    Millington K; Hudnall SD; Northup J; Panova N; Velagaleti G
    Exp Mol Pathol; 2008 Apr; 84(2):189-93. PubMed ID: 18339374
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Derivative (1)t(1;16)(p11;p11.1) in myelodysplastic syndrome: a case report and review of the literature.
    Lunghi M; Casorzo L; De Paoli L; Riccomagno P; Rossi D; Gaidano G
    Cancer Genet Cytogenet; 2010 Jan; 196(1):89-92. PubMed ID: 19963141
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prognostic significance of secondary cytogenetic alterations in follicular lymphomas.
    Johnson NA; Al-Tourah A; Brown CJ; Connors JM; Gascoyne RD; Horsman DE
    Genes Chromosomes Cancer; 2008 Dec; 47(12):1038-48. PubMed ID: 18720523
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pattern of trisomy 1q in hematological malignancies: a single institution experience.
    Djordjević V; Dencić-Fekete M; Jovanović J; Drakulić D; Stevanović M; Janković G; Gotić M
    Cancer Genet Cytogenet; 2008 Oct; 186(1):12-8. PubMed ID: 18786437
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chronic myelomonocytic leukemia with der(9)t(1;9)(q11;q34) as a sole abnormality.
    Suh B; Park TS; Kim JS; Song J; Kim J; Yoo JH; Choi JR
    Ann Clin Lab Sci; 2009; 39(3):307-12. PubMed ID: 19667417
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY.
    Scrideli CA; Baruffi MR; Squire JA; Ramos ES; Karaskova J; Heck B; Tone LG
    Leuk Res; 2005 Dec; 29(12):1465-7. PubMed ID: 15964069
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clonal evolution in t(14;18)-positive follicular lymphoma, evidence for multiple common pathways, and frequent parallel clonal evolution.
    d'Amore F; Chan E; Iqbal J; Geng H; Young K; Xiao L; Hess MM; Sanger WG; Smith L; Wiuf C; Hagberg O; Fu K; Chan WC; Dave BJ
    Clin Cancer Res; 2008 Nov; 14(22):7180-7. PubMed ID: 19010834
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Detailed analysis of 26 cases of 1q partial duplication/triplication syndrome.
    Watanabe S; Shimizu K; Ohashi H; Kosaki R; Okamoto N; Shimojima K; Yamamoto T; Chinen Y; Mizuno S; Dowa Y; Shiomi N; Toda Y; Tashiro K; Shichijo K; Minatozaki K; Aso S; Minagawa K; Hiraki Y; Shimokawa O; Matsumoto T; Fukuda M; Moriuchi H; Yoshiura K; Kondoh T
    Am J Med Genet A; 2016 Apr; 170A(4):908-17. PubMed ID: 26782913
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.