170 related articles for article (PubMed ID: 11921281)
1. Double minute chromosomes in acute myeloid leukemia and myelodysplastic syndrome: identification of new amplification regions by fluorescence in situ hybridization and spectral karyotyping.
Sait SN; Qadir MU; Conroy JM; Matsui S; Nowak NJ; Baer MR
Genes Chromosomes Cancer; 2002 May; 34(1):42-7. PubMed ID: 11921281
[TBL] [Abstract][Full Text] [Related]
2. Double minute chromosomes in acute myeloid leukemia, myelodysplastic syndromes, and chronic myelomonocytic leukemia are associated with micronuclei, MYC or MLL amplification, and complex karyotype.
Huh YO; Tang G; Talwalkar SS; Khoury JD; Ohanian M; Bueso-Ramos CE; Abruzzo LV
Cancer Genet; 2016; 209(7-8):313-20. PubMed ID: 27318442
[TBL] [Abstract][Full Text] [Related]
3. Double minute chromosomes in a patient with myelodysplastic syndrome transforming into acute myeloid leukemia.
Michalová K; Cermák J; Brezinová J; Zemanová Z
Cancer Genet Cytogenet; 1999 Feb; 109(1):76-8. PubMed ID: 9973965
[TBL] [Abstract][Full Text] [Related]
4. Amplified c-MYC sequences localized by fluorescence in-situ hybridization on double minute chromosomes in acute myeloid leukemias.
Fugazza G; Bruzzone R; Puppo L; Patrone F; Sessarego M
Leuk Res; 1997 Aug; 21(8):703-9. PubMed ID: 9379677
[TBL] [Abstract][Full Text] [Related]
5. Amplification of the MLL gene on double minutes, a homogeneously staining region, and ring chromosomes in five patients with acute myeloid leukemia or myelodysplastic syndrome.
Streubel B; Valent P; Jäger U; Edelhäuser M; Wandt H; Wagner T; Büchner T; Lechner K; Fonatsch C
Genes Chromosomes Cancer; 2000 Apr; 27(4):380-6. PubMed ID: 10719368
[TBL] [Abstract][Full Text] [Related]
6. MYC Amplification in the Form of Ring Chromosomes 8 in Acute Myeloid Leukemia with t(11;16)(q13;p11.2).
Yamamoto K; Kawamoto S; Kurata K; Kitao A; Mizutani Y; Ichikawa H; Yakushijin K; Kajimoto K; Hayashi Y; Matsuoka H; Minami H
Cytogenet Genome Res; 2017; 153(3):131-137. PubMed ID: 29393095
[TBL] [Abstract][Full Text] [Related]
7. [Prompt cytogenetic response by venetoclax plus azacitidine regimen in a patient with AML harboring double-minute chromosomes with MYC gene amplification].
Fujii F; Nojima S; Matsuoka S; Kakinoki Y
Rinsho Ketsueki; 2023; 64(7):626-632. PubMed ID: 37544722
[TBL] [Abstract][Full Text] [Related]
8. Double minutes (dmin) and homogeneously staining regions (hsr) in myeloid disorders: a new case suggesting that dmin form hsr in vivo.
Reddy KS
Cytogenet Genome Res; 2007; 119(1-2):53-9. PubMed ID: 18160782
[TBL] [Abstract][Full Text] [Related]
9. Double minute chromosomes contain amplified c-myc oncogene sequences in acute myeloid leukemia.
Mohamed AN; Mahalak S; Goldfarb SB; Palutke M
Hematopathol Mol Hematol; 1996; 10(4):193-9. PubMed ID: 9042662
[TBL] [Abstract][Full Text] [Related]
10. Gene amplification in myeloid leukemias elucidated by fluorescence in situ hybridization.
Rayeroux KC; Campbell LJ
Cancer Genet Cytogenet; 2009 Aug; 193(1):44-53. PubMed ID: 19602463
[TBL] [Abstract][Full Text] [Related]
11. Localization of amplified MYC gene sequences to double minute chromosomes in acute myelogenous leukemia.
Slovak ML; Ho JP; Pettenati MJ; Khan A; Douer D; Lal S; Traweek ST
Genes Chromosomes Cancer; 1994 Jan; 9(1):62-7. PubMed ID: 7507702
[TBL] [Abstract][Full Text] [Related]
12. Double minutes and c-MYC amplification in acute myelogenous leukemia: Are they prognostic factors?
Bruckert P; Kappler R; Scherthan H; Link H; Hagmann F; Zankl H
Cancer Genet Cytogenet; 2000 Jul; 120(1):73-9. PubMed ID: 10913679
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Double minute chromosomes in monoblastic (M5) and myeloblastic (M2) acute myeloid leukemia: two case reports and a review of literature.
Thomas L; Stamberg J; Gojo I; Ning Y; Rapoport AP
Am J Hematol; 2004 Sep; 77(1):55-61. PubMed ID: 15307107
[TBL] [Abstract][Full Text] [Related]
15. Fluorescence in situ hybridization panel for monitoring of minimal residual disease in patients with double minute chromosomes.
Jeon Y; Kim SY; Kim M; Park HK; Lee SH; See CJ; Kwon J; Lee DS
Blood Cells Mol Dis; 2014 Apr; 52(4):208-13. PubMed ID: 24211232
[TBL] [Abstract][Full Text] [Related]
16. Amplification of c-MYC oncogene and point mutation of N-RAS oncogene point mutation in acute myelocytic leukemias with double minute chromosomes.
Tanaka K; Takechi M; Nishimura S; Oguma N; Kamada N
Leukemia; 1993 Mar; 7(3):469-71. PubMed ID: 8445953
[TBL] [Abstract][Full Text] [Related]
17. [Complete remission after standard induction therapy in a patient with acute myeloid leukemia associated with double-minute chromosomes].
Goto M; Fukushima N; Iida S; Ito M; Kawamura Y; Ukai S; Sagou K; Fukuyama R; Kohno A; Ozeki K
Rinsho Ketsueki; 2021; 62(4):245-250. PubMed ID: 33967147
[TBL] [Abstract][Full Text] [Related]
18. Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.
Receveur A; Ong J; Merlin L; Azgui Z; Merle-Béral H; Berger R; Nguyen-Khac F
Ann Genet; 2004; 47(4):423-7. PubMed ID: 15581842
[TBL] [Abstract][Full Text] [Related]
19. MYC amplification in two further cases of acute myeloid leukemia with trisomy 4 and double minute chromosomes.
O'Malley F; Rayeroux K; Cole-Sinclair M; Tong M; Campbell LJ
Cancer Genet Cytogenet; 1999 Mar; 109(2):123-5. PubMed ID: 10087944
[TBL] [Abstract][Full Text] [Related]
20. MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene.
Storlazzi CT; Fioretos T; Surace C; Lonoce A; Mastrorilli A; Strömbeck B; D'Addabbo P; Iacovelli F; Minervini C; Aventin A; Dastugue N; Fonatsch C; Hagemeijer A; Jotterand M; Mühlematter D; Lafage-Pochitaloff M; Nguyen-Khac F; Schoch C; Slovak ML; Smith A; Solè F; Van Roy N; Johansson B; Rocchi M
Hum Mol Genet; 2006 Mar; 15(6):933-42. PubMed ID: 16452126
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
