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Volumn 361, Issue 11, 2009, Pages 1058-1066

Recurring mutations found by sequencing an acute myeloid leukemia genome

(58)  Mardis, Elaine R a,b   Ding, Li a,b   Dooling, David J b   Larson, David E b   McLellan, Michael D b   Chen, Ken b   Koboldt, Daniel C b   Fulton, Robert S b   Delehaunty, Kim D b   McGrath, Sean D b   Fulton, Lucinda A b   Locke, Devin P b   Magrini, Vincent J a,b   Abbott, Rachel M b   Vickery, Tammi L b   Reed, Jerry S b   Robinson, Jody S b   Wylie, Todd b   Smith, Scott M b   Carmichael, Lynn b   more..


Author keywords

[No Author keywords available]

Indexed keywords

CYTARABINE; DAUNORUBICIN; ISOCITRATE DEHYDROGENASE 1; OXIDOREDUCTASE; UNCLASSIFIED DRUG;

EID: 70149093912     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMoa0903840     Document Type: Article
Times cited : (1915)

References (30)
  • 1
    • 0032830638 scopus 로고    scopus 로고
    • Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia
    • Song WJ, Sullivan MG, Legare RD, et al. Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia. Nat Genet 1999;23:166-175
    • (1999) Nat Genet , vol.23 , pp. 166-175
    • Song, W.J.1    Sullivan, M.G.2    Legare, R.D.3
  • 2
    • 37249015529 scopus 로고    scopus 로고
    • Familial myelodysplasia and acute myeloid leukaemia - A review
    • DOI 10.1111/j.1365-2141.2007.06909.x
    • Owen C, Barnett M, Fitzgibbon J. Familial myelodysplasia and acute myeloid leukaemia - a review. Br J Haematol 2008;140:123-132 (Pubitemid 350265048)
    • (2008) British Journal of Haematology , vol.140 , Issue.2 , pp. 123-132
    • Owen, C.1    Barnett, M.2    Fitzgibbon, J.3
  • 5
    • 0035469883 scopus 로고    scopus 로고
    • The predictive value of hierarchical cytogenetic classification in older adults with acute myeloid leukemia (AML): Analysis of 1065 patients entered into the United Kingdom Medical Research Council AML11 trial
    • Grimwade D, Walker H, Harrison G, et al. The predictive value of hierarchical cytogenetic classification in older adults with acute myeloid leukemia (AML): analysis of 1065 patients entered into the United Kingdom Medical Research Council AML11 trial. Blood 2001;98:1312-1320
    • (2001) Blood , vol.98 , pp. 1312-1320
    • Grimwade, D.1    Walker, H.2    Harrison, G.3
  • 8
    • 33847195418 scopus 로고    scopus 로고
    • Oligonucleotide array-CGH reveals cryptic gene copy number alterations in karyotypically normal acute myeloid leukemia [9]
    • DOI 10.1038/sj.leu.2404543, PII 2404543
    • Tyybäkinoja A, Elonen E, Piippo K, Porkka K, Knuutila S. Oligonucleotide array-CGH reveals cryptic gene copy number alterations in karyotypically normal acute myeloid leukemia. Leukemia 2007;21:571-574 (Pubitemid 46306576)
    • (2007) Leukemia , vol.21 , Issue.3 , pp. 571-574
    • Tyybakinoja, A.1    Elonen, E.2    Piippo, K.3    Porkka, K.4    Knuutila, S.5
  • 9
    • 85031338728 scopus 로고    scopus 로고
    • Acquired copy number alterations in adult acute myeloid leukemia genomes
    • (in press)
    • Walter MJ, Payton JE, Ries RE, et al. Acquired copy number alterations in adult acute myeloid leukemia genomes. Proc Natl Acad Sci U S A (in press).
    • Proc Natl Acad Sci U S A
    • Walter, M.J.1    Payton, J.E.2    Ries, R.E.3
  • 12
    • 34247858967 scopus 로고    scopus 로고
    • Clinical outcome of de novo acute myeloid leukaemia patients with normal cytogenetics is affected by molecular genetic alterations: A concise review
    • DOI 10.1111/j.1365-2141.2007.06566.x
    • Baldus CD, Mrózek K, Marcucci G, Bloomfield CD. Clinical outcome of de novo acute myeloid leukaemia patients with normal cytogenetics is affected by molecular genetic alterations: a concise review. Br J Haematol 2007;137:387-400. (Pubitemid 46698282)
    • (2007) British Journal of Haematology , vol.137 , Issue.5 , pp. 387-400
    • Baldus, C.D.1    Mrozek, K.2    Marcucci, G.3    Bloomfield, C.D.4
  • 13
    • 33845263501 scopus 로고    scopus 로고
    • High meningioma 1 (MN1) expression as a predictor for poor outcome in acute myeloid leukemia with normal cytogenetics
    • DOI 10.1182/blood-2006-04-014845
    • Heuser M, Beutel G, Krauter J, et al. High meningioma 1 (MN1) expression as a predictor for poor outcome in acute myeloid leukemia with normal cytogenetics. Blood 2006;108:3898-3905 (Pubitemid 44864574)
    • (2006) Blood , vol.108 , Issue.12 , pp. 3898-3905
    • Heuser, M.1    Beutel, G.2    Krauter, J.3    Dohner, K.4    Von Neuhoff, N.5    Schlegelberger, B.6    Ganser, A.7
  • 14
    • 45949110015 scopus 로고    scopus 로고
    • High BAALC expression associates with other molecular prognostic markers, poor outcome, and a distinct gene-expression signature in cytogenetically normal patients younger than 60 years with acute myeloid leukemia: A Cancer and Leukemia Group B (CALGB) study
    • Langer C, Radmacher MD, Ruppert AS, et al. High BAALC expression associates with other molecular prognostic markers, poor outcome, and a distinct gene-expression signature in cytogenetically normal patients younger than 60 years with acute myeloid leukemia: a Cancer and Leukemia Group B (CALGB) study. Blood 2008;111:5371-5379
    • (2008) Blood , vol.111 , pp. 5371-5379
    • Langer, C.1    Radmacher, M.D.2    Ruppert, A.S.3
  • 15
    • 42949122111 scopus 로고    scopus 로고
    • High EVI1 levels predict adverse outcome in acute myeloid leukemia: Prevalence of EVI1 overexpression and chromosome 3q26 abnormalities underestimated
    • Lugthart S, van Drunen E, van Norden Y, et al. High EVI1 levels predict adverse outcome in acute myeloid leukemia: prevalence of EVI1 overexpression and chromosome 3q26 abnormalities underestimated. Blood 2008;111:4329-4337
    • (2008) Blood , vol.111 , pp. 4329-4337
    • Lugthart, S.1    Van Drunen, E.2    Van Norden, Y.3
  • 17
    • 46749097929 scopus 로고    scopus 로고
    • Incorporating FLT3 inhibitors into acute myeloid leukemia treatment regimens
    • DOI 10.1080/10428190801895352, PII 790630277
    • Pratz K, Levis M. Incorporating FLT3 inhibitors into acute myeloid leukemia treatment regimens. Leuk Lymphoma 2008;49:852-863 (Pubitemid 351942737)
    • (2008) Leukemia and Lymphoma , vol.49 , Issue.5 , pp. 852-863
    • Pratz, K.1    Levis, M.2
  • 18
    • 55549101623 scopus 로고    scopus 로고
    • DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome
    • Ley TJ, Mardis ER, Ding L, et al. DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature 2008;456:66-72.
    • (2008) Nature , vol.456 , pp. 66-72
    • Ley, T.J.1    Mardis, E.R.2    Ding, L.3
  • 19
    • 55549089660 scopus 로고    scopus 로고
    • Accurate whole human genome sequencing using reversible terminator chemistry
    • Bentley DR, Balasubramanian S, Swerdlow HP, et al. Accurate whole human genome sequencing using reversible terminator chemistry. Nature 2008;456:53-59
    • (2008) Nature , vol.456 , pp. 53-59
    • Bentley, D.R.1    Balasubramanian, S.2    Swerdlow, H.P.3
  • 20
    • 55549097836 scopus 로고    scopus 로고
    • Mapping short DNA sequencing reads and calling variants using mapping quality scores
    • Li H, Ruan J, Durbin R. Mapping short DNA sequencing reads and calling variants using mapping quality scores. Genome Res 2008;18:1851-1858
    • (2008) Genome Res , vol.18 , pp. 1851-1858
    • Li, H.1    Ruan, J.2    Durbin, R.3
  • 21
    • 19944427850 scopus 로고    scopus 로고
    • Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype
    • [Erratum, N Engl J Med 2005;352:740.]
    • Falini B, Mecucci C, Tiacci E, et al. Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype. N Engl J Med 2005;352:254-266 [Erratum, N Engl J Med 2005;352:740.]
    • (2005) N Engl J Med , vol.352 , pp. 254-266
    • Falini, B.1    Mecucci, C.2    Tiacci, E.3
  • 22
    • 58349111311 scopus 로고    scopus 로고
    • IDH1 mutations at residue p.R132 (IDH1(R132)) occur frequently in high-grade gliomas but not in other solid tumors
    • Bleeker FE, Lamba S, Leenstra S, et al. IDH1 mutations at residue p.R132 (IDH1(R132)) occur frequently in high-grade gliomas but not in other solid tumors. Hum Mutat 2009;30:7-11.
    • (2009) Hum Mutat , vol.30 , pp. 7-11
    • Bleeker, F.E.1    Lamba, S.2    Leenstra, S.3
  • 23
    • 60849115270 scopus 로고    scopus 로고
    • IDH1 and IDH2 mutations in gliomas
    • Yan H, Parsons DW, Jin G, et al. IDH1 and IDH2 mutations in gliomas. N Engl J Med 2009;360:765-773
    • (2009) N Engl J Med , vol.360 , pp. 765-773
    • Yan, H.1    Parsons, D.W.2    Jin, G.3
  • 24
    • 67449099808 scopus 로고    scopus 로고
    • Mutational analysis of IDH1 codon 132 in glioblastomas and other common cancers
    • Kang MR, Kim MS, Oh JE, et al. Mutational analysis of IDH1 codon 132 in glioblastomas and other common cancers. Int J Cancer 2009;125:353-355
    • (2009) Int J Cancer , vol.125 , pp. 353-355
    • Kang, M.R.1    Kim, M.S.2    Oh, J.E.3
  • 25
    • 0036119504 scopus 로고    scopus 로고
    • Accounting for human polymorphisms predicted to affect protein function
    • DOI 10.1101/gr.212802
    • Ng PC, Henikoff S. Accounting for human polymorphisms predicted to affect protein function. Genome Res 2002;12:436-446 (Pubitemid 34233019)
    • (2002) Genome Research , vol.12 , Issue.3 , pp. 436-446
    • Ng, P.C.1    Henikoff, S.2
  • 28
    • 64849098267 scopus 로고    scopus 로고
    • Glioma-derived mutations in IDH1 dominantly inhibit IDH1 catalytic activity and induce HIF-1alpha
    • Zhao S, Lin Y, Xu W, et al. Glioma-derived mutations in IDH1 dominantly inhibit IDH1 catalytic activity and induce HIF-1alpha. Science 2009;324:261-265
    • (2009) Science , vol.324 , pp. 261-265
    • Zhao, S.1    Lin, Y.2    Xu, W.3
  • 29
    • 0023043847 scopus 로고
    • A turning point in cancer research: Sequencing the human genome
    • Dulbecco R. A turning point in cancer research: sequencing the human genome. Science 1986;231:1055-1056
    • (1986) Science , vol.231 , pp. 1055-1056
    • Dulbecco, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.