129 related articles for article (PubMed ID: 15124686)
21. Variant translocation t(2;21;8)(q36;q22;q22) with RUNX1/CBFA2T1 (AML1/ETO) transcript in a case of acute myelogenous leukemia.
Hsiao HH; Sashida G; Kodama A; Fukutake K; Ohyashiki K
Cancer Genet Cytogenet; 2005 May; 159(1):96-7. PubMed ID: 15860366
[No Abstract] [Full Text] [Related]
22. Identification of novel Runx1 (AML1) translocation partner genes SH3D19, YTHDf2, and ZNF687 in acute myeloid leukemia.
Nguyen TT; Ma LN; Slovak ML; Bangs CD; Cherry AM; Arber DA
Genes Chromosomes Cancer; 2006 Oct; 45(10):918-32. PubMed ID: 16858696
[TBL] [Abstract][Full Text] [Related]
23. Complex chromosome 8;21 translocation with associated hyperdiploidy in acute myeloid leukemia (FAB-M2).
Corral Mdel P; Villa O; Alfaro EM; Alonso CN; Baro C; Felice MS; Rossi J; Solé F; Gallego MS
Pediatr Blood Cancer; 2008 Mar; 50(3):651-4. PubMed ID: 17405156
[TBL] [Abstract][Full Text] [Related]
24. The RUNX1-ETO target gene RASSF2 suppresses t(8;21) AML development and regulates Rac GTPase signaling.
Stoner SA; Liu KTH; Andrews ET; Liu M; Arimoto KI; Yan M; Davis AG; Weng S; Dow M; Xian S; DeKelver RC; Carter H; Zhang DE
Blood Cancer J; 2020 Feb; 10(2):16. PubMed ID: 32029705
[TBL] [Abstract][Full Text] [Related]
25. Rearrangement of VPS13B, a causative gene of Cohen syndrome, in a case of RUNX1-RUNX1T1 leukemia with t(8;12;21).
Abe A; Yamamoto Y; Katsumi A; Okamoto A; Tokuda M; Inaguma Y; Yamamoto K; Yanada M; Kanie T; Tomita A; Akatsuka Y; Okamoto M; Kameyama T; Mayeda A; Emi N
Int J Hematol; 2018 Aug; 108(2):208-212. PubMed ID: 29264741
[TBL] [Abstract][Full Text] [Related]
26. Two novel translocations disrupt the RUNX1 gene in acute myeloid leukemia.
Dai H; Xue Y; Pan J; Wu Y; Wang Y; Shen J; Zhang J
Cancer Genet Cytogenet; 2007 Sep; 177(2):120-4. PubMed ID: 17854666
[TBL] [Abstract][Full Text] [Related]
27. Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21).
Choi J; Song J; Kim SJ; Choi JR; Kim SJ; Min YH; Park TS; Cho SY; Kim MJ
Cancer Genet Cytogenet; 2010 Oct; 202(2):141-3. PubMed ID: 20875878
[No Abstract] [Full Text] [Related]
28. A distinct epigenetic signature at targets of a leukemia protein.
Rossetti S; Hoogeveen AT; Liang P; Stanciu C; van der Spek P; Sacchi N
BMC Genomics; 2007 Feb; 8():38. PubMed ID: 17266773
[TBL] [Abstract][Full Text] [Related]
29. Core binding factor acute myeloid leukemia. Cancer and Leukemia Group B (CALGB) Study 8461.
Bloomfield CD; Ruppert AS; Mrózek K; Kolitz JE; Moore JO; Mayer RJ; Edwards CG; Sterling LJ; Vardiman JW; Carroll AJ; Pettenati MJ; Stamberg J; Byrd JC; Marcucci G; Larson RA;
Ann Hematol; 2004; 83 Suppl 1():S84-5. PubMed ID: 15124687
[No Abstract] [Full Text] [Related]
30. Interplay of RUNX1/MTG8 and DNA methyltransferase 1 in acute myeloid leukemia.
Liu S; Shen T; Huynh L; Klisovic MI; Rush LJ; Ford JL; Yu J; Becknell B; Li Y; Liu C; Vukosavljevic T; Whitman SP; Chang KS; Byrd JC; Perrotti D; Plass C; Marcucci G
Cancer Res; 2005 Feb; 65(4):1277-84. PubMed ID: 15735013
[TBL] [Abstract][Full Text] [Related]
31. Targeting the oligomerization domain of ETO interferes with RUNX1/ETO oncogenic activity in t(8;21)-positive leukemic cells.
Wichmann C; Chen L; Heinrich M; Baus D; Pfitzner E; Zörnig M; Ottmann OG; Grez M
Cancer Res; 2007 Mar; 67(5):2280-9. PubMed ID: 17332359
[TBL] [Abstract][Full Text] [Related]
32. Novel RUNX1-PRDM16 fusion transcripts in a patient with acute myeloid leukemia showing t(1;21)(p36;q22).
Sakai I; Tamura T; Narumi H; Uchida N; Yakushijin Y; Hato T; Fujita S; Yasukawa M
Genes Chromosomes Cancer; 2005 Nov; 44(3):265-70. PubMed ID: 16015645
[TBL] [Abstract][Full Text] [Related]
33. A patient with de novo AML M1 and t(16;21) with karyotype evolution.
Zatkova A; Fonatsch C; Sperr WR; Valent P
Leuk Res; 2007 Sep; 31(9):1319-21. PubMed ID: 17126398
[No Abstract] [Full Text] [Related]
34. Pseudo-Chediak-Higashi anomaly in acute myeloid leukemia with t (8;21).
Bozkaya IO; Yarali N; Sac RU; Tavil B; Kara A; Azik F; Tunç B
J Pediatr Hematol Oncol; 2012 Apr; 34(3):242. PubMed ID: 22441711
[No Abstract] [Full Text] [Related]
35. Acute myeloid leukemia (M2) with a cryptic RUNX1/RUNX1T1 t(1;21;8)(p36;q22;q22) variant.
Tirado CA; Chen W; Valdez FJ; Henderson S; Doolittle J; Garcia R; Patel S; Holdridge S; Chastain C; Collins RH
Cancer Genet Cytogenet; 2009 Aug; 193(1):67-9. PubMed ID: 19602466
[No Abstract] [Full Text] [Related]
36. ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1-RUNX1T1 and associated with a better prognosis.
Yamato G; Shiba N; Yoshida K; Shiraishi Y; Hara Y; Ohki K; Okubo J; Okuno H; Chiba K; Tanaka H; Kinoshita A; Moritake H; Kiyokawa N; Tomizawa D; Park MJ; Sotomatsu M; Taga T; Adachi S; Tawa A; Horibe K; Arakawa H; Miyano S; Ogawa S; Hayashi Y
Genes Chromosomes Cancer; 2017 May; 56(5):382-393. PubMed ID: 28063196
[TBL] [Abstract][Full Text] [Related]
37. Complex translocation (8;12;21): a new variant of t(8;21) in acute myeloid leukemia.
Farra C; Awwad J; Valent A; Lozach F; Bernheim A
Cancer Genet Cytogenet; 2004 Dec; 155(2):138-42. PubMed ID: 15571799
[TBL] [Abstract][Full Text] [Related]
38. Acute myeloid leukemia in a child with hereditary thrombocytopenia.
Rheingold SR
Pediatr Blood Cancer; 2007 Jan; 48(1):105-7. PubMed ID: 16276527
[TBL] [Abstract][Full Text] [Related]
39. A case of acute promyelocytic leukemia presenting with a nonleukemic granulocytic sarcoma of the ovary, with subsequent development of acute myeloid leukemia associated with t(8;21).
Wang X; Liu H; Wu Z; Xu X; Chen X; Zhai Z; Sun Z
Leuk Res; 2009 Apr; 33(4):580-2. PubMed ID: 18804280
[No Abstract] [Full Text] [Related]
40. GATA1 mutations are not a hallmark of acute myeloid leukaemia with t(8;21).
Hoeller S; Bihl MP; Arber C; Dirnhofer S; Tzankov A
J Clin Pathol; 2010 May; 63(5):471-2. PubMed ID: 20418238
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
