150 related articles for article (PubMed ID: 28993357)
21. Acute myeloid leukemia with a RUNX1-RUNX1T1 t(1;21;8)(q21;q22;q22) novel variant: a case report and review of the literature.
Kim H; Moon HW; Hur M; Yun YM; Lee MH
Acta Haematol; 2011; 125(4):237-41. PubMed ID: 21325813
[TBL] [Abstract][Full Text] [Related]
22. Assessing the miRNA sponge potential of RUNX1T1 in t(8;21) acute myeloid leukemia.
Junge A; Zandi R; Havgaard JH; Gorodkin J; Cowland JB
Gene; 2017 Jun; 615():35-40. PubMed ID: 28322996
[TBL] [Abstract][Full Text] [Related]
23. A three-miRNA-based expression signature at diagnosis can predict occurrence of relapse in children with t(8;21) RUNX1-RUNX1T1 acute myeloid leukaemia.
Zampini M; Bisio V; Leszl A; Putti MC; Menna G; Rizzari C; Pession A; Locatelli F; Basso G; Tregnago C; Pigazzi M
Br J Haematol; 2018 Oct; 183(2):298-301. PubMed ID: 28961307
[No Abstract] [Full Text] [Related]
24. CSF3R Mutations are frequently associated with abnormalities of RUNX1, CBFB, CEBPA, and NPM1 genes in acute myeloid leukemia.
Zhang Y; Wang F; Chen X; Zhang Y; Wang M; Liu H; Cao P; Ma X; Wang T; Zhang J; Zhang X; Lu P; Liu H
Cancer; 2018 Aug; 124(16):3329-3338. PubMed ID: 29932212
[TBL] [Abstract][Full Text] [Related]
25. Epigenetic heterogeneity affects the risk of relapse in children with t(8;21)RUNX1-RUNX1T1-rearranged AML.
Zampini M; Tregnago C; Bisio V; Simula L; Borella G; Manara E; Zanon C; Zonta F; Serafin V; Accordi B; Campello S; Buldini B; Pession A; Locatelli F; Basso G; Pigazzi M
Leukemia; 2018 May; 32(5):1124-1134. PubMed ID: 29472719
[TBL] [Abstract][Full Text] [Related]
26. Clinical Relevance of RUNX1 and CBFB Alterations in Acute Myeloid Leukemia and Other Hematological Disorders.
Metzeler KH; Bloomfield CD
Adv Exp Med Biol; 2017; 962():175-199. PubMed ID: 28299658
[TBL] [Abstract][Full Text] [Related]
27. Minimal residual disease (MRD) monitoring and mutational landscape in AML with RUNX1-RUNX1T1: a study on 134 patients.
Höllein A; Jeromin S; Meggendorfer M; Fasan A; Nadarajah N; Kern W; Haferlach C; Haferlach T
Leukemia; 2018 Oct; 32(10):2270-2274. PubMed ID: 29568097
[No Abstract] [Full Text] [Related]
28. A novel case of intrachromosomal amplification and insertion of RUNX1 on derivative chromosome 2 in pediatric AML.
Jain H; Shetty D; Roy Moulik N; Narula G; Subramanian PG; Banavali S
Cancer Genet; 2021 Jun; 254-255():65-69. PubMed ID: 33647813
[TBL] [Abstract][Full Text] [Related]
29. Cytogenetic and Cytogenomic Microarray Characterization of Chromothripsis in Chromosome 8 Affecting MOZ/NCOA2 (TIF2), FGFR1, RUNX1T1, and RUNX1 in a Pediatric Acute Myeloid Leukemia.
Koduru PR; Wilson K; Wen J; Garcia R; Patel S; Monaghan SA
J Pediatr Hematol Oncol; 2017 May; 39(4):e227-e232. PubMed ID: 28085746
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Acute myeloid leukemia with del(X)(p21) and cryptic RUNX1/RUNX1T1 from ins(8;21)(q22;q22q22) revealed by atypical FISH signals.
Jang JH; Yoo EH; Kim HJ; Kim DH; Jung CW; Kim SH
Ann Clin Lab Sci; 2010; 40(1):80-4. PubMed ID: 20124335
[TBL] [Abstract][Full Text] [Related]
32. Transcriptional dysregulation mediated by RUNX1-RUNX1T1 in normal human progenitor cells and in acute myeloid leukaemia.
Tonks A; Pearn L; Musson M; Gilkes A; Mills KI; Burnett AK; Darley RL
Leukemia; 2007 Dec; 21(12):2495-505. PubMed ID: 17898786
[TBL] [Abstract][Full Text] [Related]
33. More than a fusion gene: the
Haferlach T; Meggendorfer M
Blood; 2019 Mar; 133(10):1006-1007. PubMed ID: 30846508
[No Abstract] [Full Text] [Related]
34. Low WT1 transcript levels at diagnosis predicted poor outcomes of acute myeloid leukemia patients with t(8;21) who received chemotherapy or allogeneic hematopoietic stem cell transplantation.
Qin YZ; Wang Y; Zhu HH; Gale RP; Zhang MJ; Jiang Q; Jiang H; Xu LP; Chen H; Zhang XH; Liu YR; Lai YY; Jiang B; Liu KY; Huang XJ
Chin J Cancer; 2016 May; 35():46. PubMed ID: 27197573
[TBL] [Abstract][Full Text] [Related]
35. CNS erythroblastic sarcoma: a potential emerging pediatric tumor type characterized by NFIA::RUNX1T1/3 fusions.
Tauziède-Espariat A; Lew-Derivry L; Abbou S; Métais A; Pierron G; Reynaud S; Masliah-Planchon J; Mariet C; Hasty L; Dangouloff-Ros V; Boddaert N; Csanyi M; Aline-Fardin A; Lamaison C; Chrétien F; Beccaria K; Puget S; Varlet P
Acta Neuropathol Commun; 2024 Jan; 12(1):12. PubMed ID: 38243303
[TBL] [Abstract][Full Text] [Related]
36. KIT D816 mutation associates with adverse outcomes in core binding factor acute myeloid leukemia, especially in the subgroup with RUNX1/RUNX1T1 rearrangement.
Kim HJ; Ahn HK; Jung CW; Moon JH; Park CH; Lee KO; Kim SH; Kim YK; Kim HJ; Sohn SK; Kim SH; Lee WS; Kim KH; Mun YC; Kim H; Park J; Min WS; Kim HJ; Kim DH;
Ann Hematol; 2013 Jan; 92(2):163-71. PubMed ID: 23053179
[TBL] [Abstract][Full Text] [Related]
37. Rare BCR-ABL1 transcript in a RUNX1-RUNX1T1-positive de novo acute myeloid leukemia: The chicken and egg tale.
Gupta R; Mittal N; Rahman K; Sharma A; Singh P; Kumar S; Nityanand S
Int J Lab Hematol; 2018 Apr; 40(2):e24-e27. PubMed ID: 29393574
[No Abstract] [Full Text] [Related]
38. RUNX1 Mutations Can Lead to Aberrant Expression of CD79a and PAX5 in Acute Myelogenous Leukemias: A Potential Diagnostic Pitfall.
Menter T; Lundberg P; Wenzel F; Dirks J; Fernandez P; Friess D; Dirnhofer S; Tzankov A
Pathobiology; 2019; 86(2-3):162-166. PubMed ID: 30396184
[TBL] [Abstract][Full Text] [Related]
39. Prognostic value of AML 1/ETO fusion transcripts in patients with acute myelogenous leukemia.
Cho EK; Bang SM; Ahn JY; Yoo SM; Park PW; Seo YH; Shin DB; Lee JH
Korean J Intern Med; 2003 Mar; 18(1):13-20. PubMed ID: 12760263
[TBL] [Abstract][Full Text] [Related]
40. Acute multilineage (B/myeloid) leukemia with RUNX1 duplication/amplification and hypereosinophilia.
Holmes A; Coviello J; Velagaleti G
Eur J Haematol; 2014 Nov; 93(5):449-52. PubMed ID: 24912843
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
