메뉴 건너뛰기




Volumn 121, Issue 17, 2013, Pages 3469-3472

CBFA2T3-GLIS2 fusion transcript is a novel common feature in pediatric, cytogenetically normal AML, not restricted to FAB M7 subtype

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTOME; CBFA2T3 GLIS2 FUSION PROTEIN, HUMAN; CBFA2T3-GLIS2 FUSION PROTEIN, HUMAN; MESSENGER RNA; ONCOPROTEIN; TUMOR MARKER;

EID: 84879397326     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2012-11-469825     Document Type: Article
Times cited : (115)

References (21)
  • 1
    • 79952078495 scopus 로고    scopus 로고
    • Biology, risk stratification, and therapy of pediatric acute leukemias: An update
    • Pui CH, Carroll WL, Meshinchi S, et al. Biology, risk stratification, and therapy of pediatric acute leukemias: an update. J Clin Oncol. 2011;29(5): 551-565.
    • (2011) J Clin Oncol , vol.29 , Issue.5 , pp. 551-565
    • Pui, C.H.1    Carroll, W.L.2    Meshinchi, S.3
  • 2
    • 69249229646 scopus 로고    scopus 로고
    • Prevalence and prognostic implications of cebpa mutations in pediatric acute myeloid leukemia (aml): A report from the children’s oncology group
    • Ho PA, Alonzo TA, Gerbing RB, et al. Prevalence and prognostic implications of CEBPA mutations in pediatric acute myeloid leukemia (AML): a report from the Children’s Oncology Group. Blood. 2009;113(26):6558-6566.
    • (2009) Blood , vol.113 , Issue.26 , pp. 6558-6566
    • Ho, P.A.1    Alonzo, T.A.2    Gerbing, R.B.3
  • 3
    • 23744479178 scopus 로고    scopus 로고
    • Nucleophosmin mutations in childhood acute myelogenous leukemia with normal karyotype
    • Cazzaniga G, Dell’Oro MG, Mecucci C, et al. Nucleophosmin mutations in childhood acute myelogenous leukemia with normal karyotype. Blood. 2005;106(4):1419-1422.
    • (2005) Blood , vol.106 , Issue.4 , pp. 1419-1422
    • Cazzaniga, G.1    Dell’Oro, M.G.2    Mecucci, C.3
  • 4
    • 0035168677 scopus 로고    scopus 로고
    • Prevalence and prognostic significance of flt3 internal tandem duplication in pediatric acute myeloid leukemia
    • Meshinchi S, Woods WG, Stirewalt DL, et al. Prevalence and prognostic significance of Flt3 internal tandem duplication in pediatric acute myeloid leukemia. Blood. 2001;97(1):89-94.
    • (2001) Blood , vol.97 , Issue.1 , pp. 89-94
    • Meshinchi, S.1    Woods, W.G.2    Stirewalt, D.L.3
  • 5
    • 82155183329 scopus 로고    scopus 로고
    • Presence of flt3-itd and high baalc expression are independent prognostic markers in childhood acute myeloid leukemia
    • Nordic Society of Pediatric Hematology and Oncology (NOPHO)
    • Staffas A, Kanduri M, Hovland R, et al; Nordic Society of Pediatric Hematology and Oncology (NOPHO). Presence of FLT3-ITD and high BAALC expression are independent prognostic markers in childhood acute myeloid leukemia. Blood. 2011;118(22):5905-5913.
    • (2011) Blood , vol.118 , Issue.22 , pp. 5905-5913
    • Staffas, A.1    Kanduri, M.2    Hovland, R.3
  • 6
    • 84867440163 scopus 로고    scopus 로고
    • Childhood acute myeloid leukaemia
    • Rubnitz JE, Inaba H. Childhood acute myeloid leukaemia. Br J Haematol. 2012;159(3):259-276.
    • (2012) Br J Haematol , vol.159 , Issue.3 , pp. 259-276
    • Rubnitz, J.E.1    Inaba, H.2
  • 7
    • 70149093912 scopus 로고    scopus 로고
    • Recurring mutations found by sequencing an acute myeloid leukemia genome
    • Mardis ER, Ding L, Dooling DJ, et al. Recurring mutations found by sequencing an acute myeloid leukemia genome. N Engl J Med. 2009;361(11): 1058-1066.
    • (2009) N Engl J Med. , vol.361 , Issue.11 , pp. 1058-1066
    • Mardis, E.R.1    Ding, L.2    Dooling, D.J.3
  • 8
    • 78649906060 scopus 로고    scopus 로고
    • Dnmt3a mutations in acute myeloid leukemia
    • Ley TJ, Ding L, Walter MJ, et al. DNMT3A mutations in acute myeloid leukemia. N Engl J Med. 2010;363(25):2424-2433.
    • (2010) N Engl J Med. , vol.363 , Issue.25 , pp. 2424-2433
    • Ley, T.J.1    Ding, L.2    Walter, M.J.3
  • 9
    • 80054035931 scopus 로고    scopus 로고
    • Idh1 and idh2 mutations in pediatric acute leukemia
    • Andersson AK, Miller DW, Lynch JA, et al. IDH1 and IDH2 mutations in pediatric acute leukemia. Leukemia. 2011;25(10):1570-1577.
    • (2011) Leukemia , vol.25 , Issue.10 , pp. 1570-1577
    • Andersson, A.K.1    Miller, D.W.2    Lynch, J.A.3
  • 10
    • 78651323053 scopus 로고    scopus 로고
    • Low prevalence of idh1 gene mutation in childhood aml in italy
    • Pigazzi M, Ferrari G, Masetti R, et al. Low prevalence of IDH1 gene mutation in childhood AML in Italy. Leukemia. 2011;25(1):173-174.
    • (2011) Leukemia , vol.25 , Issue.1 , pp. 173-174
    • Pigazzi, M.1    Ferrari, G.2    Masetti, R.3
  • 11
    • 82855172180 scopus 로고    scopus 로고
    • Dna methyltransferase 3a hot-spot locus is not mutated in pediatric patients affected by acute myeloid or t-cell acute lymphoblastic leukemia: An italian study
    • Paganin M, Pigazzi M, Bresolin S, et al. DNA methyltransferase 3a hot-spot locus is not mutated in pediatric patients affected by acute myeloid or T-cell acute lymphoblastic leukemia: an Italian study. Haematologica. 2011;96(12): 1886-1887.
    • (2011) Haematologica , vol.96 , Issue.12 , pp. 1886-1887
    • Paganin, M.1    Pigazzi, M.2    Bresolin, S.3
  • 12
    • 84869009858 scopus 로고    scopus 로고
    • An inv(16)(p13.3q24.3)-encoded cbfa2t3-glis2 fusion protein defines an aggressive subtype of pediatric acute megakaryoblastic leukemia
    • Gruber TA, Larson Gedman A, Zhang J, et al. An Inv(16)(p13.3q24.3)-encoded CBFA2T3-GLIS2 fusion protein defines an aggressive subtype of pediatric acute megakaryoblastic leukemia. Cancer Cell. 2012;22(5):683-697.
    • (2012) Cancer Cell , vol.22 , Issue.5 , pp. 683-697
    • Gruber, T.A.1    Larson Gedman, A.2    Zhang, J.3
  • 13
    • 84870256595 scopus 로고    scopus 로고
    • Characterization of novel genomic alterations and therapeutic approaches using acute megakaryoblastic leukemia xenograft models
    • Thiollier C, Lopez CK, Gerby B, et al. Characterization of novel genomic alterations and therapeutic approaches using acute megakaryoblastic leukemia xenograft models. J Exp Med. 2012;209(11):2017-2031.
    • (2012) J Exp Med , vol.209 , Issue.11 , pp. 2017-2031
    • Thiollier, C.1    Lopez, C.K.2    Gerby, B.3
  • 14
    • 77957020934 scopus 로고    scopus 로고
    • Results of the Aieop aml 2002/01 study for treatment of children with acute myeloid leukemia
    • abstract [ASH Annual Meeting Abstracts]
    • Pession A, Rizzari C, Putti MC, et al. Results of the AIEOP AML 2002/01 study for treatment of children with acute myeloid leukemia [abstract]. Blood. 2009;114.Abstract 17. [ASH Annual Meeting Abstracts]
    • (2009) Blood , vol.114
    • Pession, A.1    Rizzari, C.2    Putti, M.C.3
  • 16
    • 65449136284 scopus 로고    scopus 로고
    • Tophat: Discovering splice junctions with rna-seq
    • Trapnell C, Pachter L, Salzberg SL. TopHat: discovering splice junctions with RNA-Seq. Bioinformatics. 2009;25(9):1105-1111.
    • (2009) Bioinformatics , vol.25 , Issue.9 , pp. 1105-1111
    • Trapnell, C.1    Pachter, L.2    Salzberg, S.L.3
  • 17
    • 79957829805 scopus 로고    scopus 로고
    • Defuse: An algorithm for gene fusion discovery in tumor rna-seq data
    • McPherson A, Hormozdiari F, Zayed A, et al. deFuse: an algorithm for gene fusion discovery in tumor RNA-Seq data. PLOS Comput Biol. 2011; 7(5):e1001138.
    • (2011) PLOS Comput Biol , vol.7 , Issue.5
    • McPherson, A.1    Hormozdiari, F.2    Zayed, A.3
  • 18
    • 80054003528 scopus 로고    scopus 로고
    • Chimerascan: A tool for identifying chimeric transcription in sequencing data
    • Iyer MK, Chinnaiyan AM, Maher CA. ChimeraScan: a tool for identifying chimeric transcription in sequencing data. Bioinformatics. 2011;27(20):2903-2904.
    • (2011) Bioinformatics , vol.27 , Issue.20 , pp. 2903-2904
    • Iyer, M.K.1    Chinnaiyan, A.M.2    Maher, C.A.3
  • 19
    • 0030048518 scopus 로고    scopus 로고
    • Secondary acute myeloblastic leukemia with t(16;21) (q24;q22). Involving the aml1 gene
    • Berger R, Le Coniat M, Romana SP, et al. Secondary acute myeloblastic leukemia with t(16;21) (q24;q22). involving the AML1 gene. Hematol Cell Ther. 1996;38(2): 183-186.
    • (1996) Hematol Cell Ther , vol.38 , Issue.2 , pp. 183-186
    • Berger, R.1    Le Coniat, M.2    Romana, S.P.3
  • 20
    • 0032101547 scopus 로고    scopus 로고
    • The partner gene of aml1 in t(16;21) myeloid malignancies is a novel member of the mtg8(eto) family
    • Gamou T, Kitamura E, Hosoda F, et al. The partner gene of AML1 in t(16;21) myeloid malignancies is a novel member of the MTG8(ETO) family. Blood. 1998;91(11): 4028-4037.
    • (1998) Blood , vol.91 , Issue.11 , pp. 4028-4037
    • Gamou, T.1    Kitamura, E.2    Hosoda, F.3
  • 21
    • 80053948530 scopus 로고    scopus 로고
    • Increased hedgehog signaling in postnatal kidney results in aberrant activation of nephron developmental programs
    • Li B, Rauhauser AA, Dai J, et al. Increased hedgehog signaling in postnatal kidney results in aberrant activation of nephron developmental programs. Hum Mol Genet. 2011;20(21): 4155-4166.
    • (2011) Hum Mol Genet , vol.20 , Issue.21 , pp. 4155-4166
    • Li, B.1    Rauhauser, A.A.2    Dai, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.