226 related articles for article (PubMed ID: 30439701)
1. A Novel and Cytogenetically Cryptic t(7;21)(q36.1;q22) Disrupting RUNX1 in Acute Myeloid Leukemia.
Zámečníkova A; Al Bahar S
Cytogenet Genome Res; 2018; 156(3):140-143. PubMed ID: 30439701
[TBL] [Abstract][Full Text] [Related]
2. A novel t(7;21)(q32;q22) translocation disrupting the RUNX1 gene in an adult patient with acute myeloid leukemia.
Angelova S; Zechev J; Stoimenov A; Spassov B; Romanova M; Shivarov V
Leuk Lymphoma; 2011 Dec; 52(12):2396-8. PubMed ID: 21749308
[No Abstract] [Full Text] [Related]
3. 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]
4. Transcriptome sequencing reveals CHD1 as a novel fusion partner of RUNX1 in acute myeloid leukemia with t(5;21)(q21;q22).
Yao H; Pan J; Wu C; Shen H; Xie J; Wang Q; Wen L; Wang Q; Ma L; Wu L; Ping N; Zhao Y; Sun A; Chen S
Mol Cancer; 2015 Apr; 14():81. PubMed ID: 25879624
[TBL] [Abstract][Full Text] [Related]
5. Microhomologies and topoisomerase II consensus sequences identified near the breakpoint junctions of the recurrent t(7;21)(p22;q22) translocation in acute myeloid leukemia.
Giguère A; Hébert J
Genes Chromosomes Cancer; 2011 Apr; 50(4):228-38. PubMed ID: 21319259
[TBL] [Abstract][Full Text] [Related]
6. A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42.
Paulsson K; Békássy AN; Olofsson T; Mitelman F; Johansson B; Panagopoulos I
Leukemia; 2006 Feb; 20(2):224-9. PubMed ID: 16357831
[TBL] [Abstract][Full Text] [Related]
7. A new complex translocation t(8;11;21)(q22;q24;q22) in acute myeloid leukemia with RUNX1/RUNX1T1.
Yamamoto K; Yakushijin K; Funakoshi Y; Sanada Y; Kawamoto S; Matsuoka H; Minami H
J Clin Exp Hematop; 2014; 54(2):167-70. PubMed ID: 25318951
[No Abstract] [Full Text] [Related]
8. Acute myeloid leukemia patients with variant or unusual translocations involving chromosomes 8 and 21 - A comprehensive cytogenetic profiling of three cases with review of literature.
Akhila Raj TV; Gopinath P; Geetha Raj JA; Narayanan G; Nair SG; Joy Philip DS; Raveendran S; Geetha P; Sreedharan H
J Cancer Res Ther; 2022; 18(3):697-703. PubMed ID: 35900542
[TBL] [Abstract][Full Text] [Related]
9. Myeloid neoplasms with t(16;21)(q24;q22)/RUNX1-RUNX1T3 mimics acute myeloid leukemia with RUNX1-RUNX1T1.
Liu H; Wang SA; Schlette EJ; Xu J; Jorgensen JL; Cameron Yin C; Li S; Jeffrey Medeiros L; Tang G
Ann Hematol; 2018 Oct; 97(10):1775-1783. PubMed ID: 29872884
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia.
De Figueiredo AF; Liehr T; Bhatt S; Binato R; De Souza MT; De Matos RR; Salles Tde J; Jordy FC; Ribeiro RC; Abdelhay E; Silva ML
Leuk Lymphoma; 2011 Aug; 52(8):1593-6. PubMed ID: 21657952
[No Abstract] [Full Text] [Related]
12. 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]
13. A novel RUNX1-C11orf41 fusion gene in a case of acute myeloid leukemia with a t(11;21)(p14;q22).
Abe A; Katsumi A; Kobayashi M; Okamoto A; Tokuda M; Kanie T; Yamamoto Y; Naoe T; Emi N
Cancer Genet; 2012 Nov; 205(11):608-11. PubMed ID: 23102734
[TBL] [Abstract][Full Text] [Related]
14. Acute myeloid leukemia with t(7;21)(q11.2;q22) expresses a novel, reversed-sequence RUNX1-DTX2 chimera.
Maki K; Sasaki K; Sugita F; Nakamura Y; Mitani K
Int J Hematol; 2012 Aug; 96(2):268-73. PubMed ID: 22661044
[TBL] [Abstract][Full Text] [Related]
15. Acute myeloid leukemia with a novel t(8;21) variant: paracentric inversion-associated ins(21;8).
Lee JH; Wan TS; Ha JS
Leuk Lymphoma; 2014 Feb; 55(2):441-3. PubMed ID: 23672346
[No Abstract] [Full Text] [Related]
16. Novel Four-Way t(8;14;15;21)(q22;q22;q15;q22.1) Translocation Variant in Acute Myeloid Leukemia with
Tsuge N; Ogasawara F; Kondo T; Yoshida S; Kojima K
Turk J Haematol; 2024 May; 41(2):128-129. PubMed ID: 38488305
[No Abstract] [Full Text] [Related]
17. RUNX1-MTG16 fusion gene in acute myeloblastic leukemia with t(16;21)(q24;q22): case report and review of the literature.
De Braekeleer E; Douet-Guilbert N; Le Bris MJ; Morel F; Férec C; De Braekeleer M
Cancer Genet Cytogenet; 2008 Aug; 185(1):47-50. PubMed ID: 18656694
[TBL] [Abstract][Full Text] [Related]
18. RUNX1 upregulation via disruption of long-range transcriptional control by a novel t(5;21)(q13;q22) translocation in acute myeloid leukemia.
Cheng CK; Wong THY; Wan TSK; Wang AZ; Chan NPH; Chan NCN; Li CK; Ng MHL
Mol Cancer; 2018 Aug; 17(1):133. PubMed ID: 30157851
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Acute myeloid leukemia with t(3;21)(q13;q22), a novel simple variant of the 21q22/RUNX1 translocation].
Tsuruoka Y; Sakai H; Uchida A; Uemura Y; Sato K; Yokoi S; Nishio Y; Matsunawa M; Suzuki Y; Isobe Y; Kato M; Tomita N; Inoue Y; Miura I
Rinsho Ketsueki; 2017; 58(1):3-8. PubMed ID: 28190862
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
