186 related articles for article (PubMed ID: 19727243)
1. t(10; 12) (q24; p13) as the sole abnormality in a case with refractory acute myeloid leukemia: The first case report and literature review.
Lu G; Gurevich I; Vo BT; Chen SS
Beijing Da Xue Xue Bao Yi Xue Ban; 2009 Aug; 41(4):480-3. PubMed ID: 19727243
[TBL] [Abstract][Full Text] [Related]
2. Biallelic ETV6 rearrangements by recurrent translocations t(7;12)(p15;p13) and t(3;12)(q26.2;p13) in acute myeloid leukemia.
Yamamoto K; Yakushijin K; Funakoshi Y; Inui Y; Okamura A; Matsuoka H; Minami H
Leuk Res; 2011 Nov; 35(11):e212-4. PubMed ID: 21803420
[No Abstract] [Full Text] [Related]
3. ETV6/GOT1 fusion in a case of t(10;12)(q24;p13)-positive myelodysplastic syndrome.
Struski S; Mauvieux L; Gervais C; Hélias C; Liu KL; Lessard M
Haematologica; 2008 Mar; 93(3):467-8. PubMed ID: 18310541
[TBL] [Abstract][Full Text] [Related]
4. Next-generation sequencing and molecular cytogenetic characterization of ETV6-LYN fusion due to chromosomes 1, 8 and 12 rearrangement in acute myeloid leukemia.
Ma ESK; Wan TSK; Au CH; Ho DN; Ma SY; Ng MHL; Chan TL
Cancer Genet; 2017 Dec; 218-219():15-19. PubMed ID: 29153093
[TBL] [Abstract][Full Text] [Related]
5. Utilizing next-generation sequencing to characterize a case of acute myeloid leukemia with t(4;12)(q12;p13) in the absence of ETV6/CHIC2 and ETV6/PDGFRA gene fusions.
Koleilat A; McGarrah PW; Olteanu H; Van Dyke DL; Smadbeck JB; Johnson SH; Vasmatzis G; Hoppman NL; Xu X; Ketterling RP; Greipp PT; Baughn LB; Patnaik MS; Peterson JF
Cancer Genet; 2022 Jan; 260-261():1-5. PubMed ID: 34781094
[TBL] [Abstract][Full Text] [Related]
6. A novel t(10;12)(q21;p13) involving ETV6 in a patient with acute myeloid leukemia.
Sowa AS; Meloni-Ehrig AM; Tos A; Jahn J; Dogra S; Nava VE; Kelly JC; Mowrey PN
Cancer Genet Cytogenet; 2010 Dec; 203(2):352-4. PubMed ID: 21156259
[No Abstract] [Full Text] [Related]
7. Different clones of t(1;12)/t(12;12) involving the ETV6 gene in a case of acute myeloid leukemia.
Saitoh T; Nakamura T; Inoue M; Hatta Y; Yamazaki T; Takeuchi J; Sawada U; Horie T
Cancer Genet Cytogenet; 2002 Sep; 137(2):138-41. PubMed ID: 12393285
[TBL] [Abstract][Full Text] [Related]
8. A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene.
Murga Penas EM; Cools J; Algenstaedt P; Hinz K; Seeger D; Schafhausen P; Schilling G; Marynen P; Hossfeld DK; Dierlamm J
Genes Chromosomes Cancer; 2003 May; 37(1):79-83. PubMed ID: 12661008
[TBL] [Abstract][Full Text] [Related]
9. Fusion of TEL/ETV6 to a novel ACS2 in myelodysplastic syndrome and acute myelogenous leukemia with t(5;12)(q31;p13).
Yagasaki F; Jinnai I; Yoshida S; Yokoyama Y; Matsuda A; Kusumoto S; Kobayashi H; Terasaki H; Ohyashiki K; Asou N; Murohashi I; Bessho M; Hirashima K
Genes Chromosomes Cancer; 1999 Nov; 26(3):192-202. PubMed ID: 10502316
[TBL] [Abstract][Full Text] [Related]
10. ETV6 rearrangements are recurrent in myeloid malignancies and are frequently associated with other genetic events.
Haferlach C; Bacher U; Schnittger S; Alpermann T; Zenger M; Kern W; Haferlach T
Genes Chromosomes Cancer; 2012 Apr; 51(4):328-37. PubMed ID: 22162288
[TBL] [Abstract][Full Text] [Related]
11. Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia.
Tosi S; Hughes J; Scherer SW; Nakabayashi K; Harbott J; Haas OA; Cazzaniga G; Biondi A; Kempski H; Kearney L
Genes Chromosomes Cancer; 2003 Oct; 38(2):191-200. PubMed ID: 12939747
[TBL] [Abstract][Full Text] [Related]
12. Disruption of the ETV6 gene as a consequence of a rare translocation (12;12)(p13;q13) in treatment-induced acute myeloid leukemia after breast cancer.
Manola KN; Georgakakos VN; Margaritis D; Stavropoulou C; Panos C; Kotsianidis I; Pantelias GE; Sambani C
Cancer Genet Cytogenet; 2008 Jan; 180(1):37-42. PubMed ID: 18068531
[TBL] [Abstract][Full Text] [Related]
13. Characterization of a t(10;12)(q24;p13) in a case of CML in transformation.
Aguiar RC; Chase A; Oscier DG; Carapeti M; Goldman JM; Cross NC
Genes Chromosomes Cancer; 1997 Dec; 20(4):408-11. PubMed ID: 9408758
[TBL] [Abstract][Full Text] [Related]
14. t(7;12)(q36;p13) and t(7;12)(q32;p13)--translocations involving ETV6 in children 18 months of age or younger with myeloid disorders.
Slater RM; von Drunen E; Kroes WG; Weghuis DO; van den Berg E; Smit EM; van der Does-van den Berg A; van Wering E; Hählen K; Carroll AJ; Raimondi SC; Beverloo HB
Leukemia; 2001 Jun; 15(6):915-20. PubMed ID: 11417477
[TBL] [Abstract][Full Text] [Related]
15. Fusion of ETV6 to GOT1 in a case with myelodysplastic syndrome and t(10;12)(q24;p13).
Janssen H; Wlodarska I; Mecucci C; Hagemeijer A; Vandenberghe P; Marynen P; Cools J
Haematologica; 2006 Jul; 91(7):949-51. PubMed ID: 16757412
[TBL] [Abstract][Full Text] [Related]
16. Translocation t(5;18)(q35;q21) as a rare nonrandom abnormality in acute myeloid leukemia.
Daraki A; Bourantas LK; Manola KN
Cytogenet Genome Res; 2013; 139(4):289-94. PubMed ID: 23548668
[TBL] [Abstract][Full Text] [Related]
17. TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13).
Wlodarska I; Mecucci C; Marynen P; Guo C; Franckx D; La Starza R; Aventin A; Bosly A; Martelli MF; Cassiman JJ
Blood; 1995 May; 85(10):2848-52. PubMed ID: 7742547
[TBL] [Abstract][Full Text] [Related]
18. Clonal eosinophils are a morphologic hallmark of ETV6/ABL1 positive acute myeloid leukemia.
La Starza R; Trubia M; Testoni N; Ottaviani E; Belloni E; Crescenzi B; Martelli M; Flandrin G; Pelicci PG; Mecucci C
Haematologica; 2002 Aug; 87(8):789-94. PubMed ID: 12161353
[TBL] [Abstract][Full Text] [Related]
19. Detection of Novel t(12;17)(p12;p13) in Relapsed Refractory Acute Myeloid Leukemia by Anchored Multiplex PCR(AMP)-based Next-Generation Sequencing.
Badar T; Johnson L; Trifilo K; Wang H; Kudlow BA; Padron E; Pappenhausen PR; Hussaini MO
Appl Immunohistochem Mol Morphol; 2019 Mar; 27(3):e28-e31. PubMed ID: 28187034
[TBL] [Abstract][Full Text] [Related]
20. High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.
von Bergh AR; van Drunen E; van Wering ER; van Zutven LJ; Hainmann I; Lönnerholm G; Meijerink JP; Pieters R; Beverloo HB
Genes Chromosomes Cancer; 2006 Aug; 45(8):731-9. PubMed ID: 16646086
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
