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1)Mardis ER, Ding L, Dooling DJ, et al. Recurring mutations found by sequencing an acute myeloid leukemia genome. N Engl J Med. 2009; 361: 1058-66
PubMed CrossRef
医中誌リンクサービス
2)Patel JP, Gönen M, Figueroa ME, et al. Prognostic relevance of integrated genetic profiling in acute myeloid leukemia. N Engl J Med. 2012; 366: 1079-89
PubMed CrossRef
医中誌リンクサービス
3)Cancer Genome Atlas Research Network. Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. N Engl J Med. 2013; 368: 2059-74
PubMed CrossRef
医中誌リンクサービス
4)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: 683-97
PubMed CrossRef
医中誌リンクサービス
5)de Rooij JD, Hollink IH, Arentsen-Peters ST, et al. NUP98/JARID1A is a novel recurrent abnormality in pediatric acute megakaryoblastic leukemia with a distinct HOX gene expression pattern. Leukemia. (in press)
医中誌リンクサービス
6)Masetti R, Pigazzi M, Togni M, et al. CBFA2T3-GLIS2 fusion transcript is a novel common feature in pediatric, cytogenetically normal AML, not restricted to FAB M7 subtype. Blood. 2013; 121: 3469-72
PubMed CrossRef
医中誌リンクサービス
7)Yoshida K, Toki T, Okuno Y, et al. Landscape of gene mutations in Down syndrome-related myeloid disorders. Nat Genet. 2013; 45: 1293-9
PubMed CrossRef
医中誌リンクサービス
8)Nikolaev SI, Santoni F, Vannier A, et al. Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome. Blood. 2013; 122: 554-61
PubMed CrossRef
医中誌リンクサービス
9)Pui CH, Carroll WL, Meshinchi S, et al. Biology, risk stratification, and therapy of pediatric acute leukemias: an update. J Clin Oncol. 2011; 29: 551-65
PubMed CrossRef
医中誌リンクサービス
10)Hayashi Y. The molecular genetics of recurring chromosome abnormalities in acute myeloid leukemia. Semin Hematol. 2000; 37: 368-80
PubMed CrossRef
医中誌リンクサービス
11)Nagao T, Lampkin BC, Hug G. A neonate with Downʼs syndrome and transient abnormal myelopoiesis: serial blood and bone marrow studies. Blood. 1970; 36: 443-7
PubMed
医中誌リンクサービス
12)新保敏和,長尾 大,木村清次,他.白血病様血液像を呈したDown症候群(6症例)の臨床経過ならびに病理解剖所見の検討−特にTransient Abnormal Myelopoiesis (TAM)の概念について−.臨床血液.1977; 18: 99-109
PubMed J-Stage
医中誌リンクサービス
13)Hayashi Y, Eguchi M, Sugita K, et al. Cytogenetic findings and clinical features in acute leukemia and transient myeloproliferative disorder in Downʼs syndrome. Blood. 1998; 72: 15-23
PubMed
医中誌リンクサービス
14)Zipursky A. Transient leukaemia−a benign form of leukaemia in newborn infants with trisomy 21. Br J Haematol. 2003; 120: 930-8
PubMed CrossRef
医中誌リンクサービス
15)Hitzler JK, Zipursky A. Origins of leukaemia in children with Down syndrome. Nat Rev Cancer. 2005; 5: 11-20
PubMed
医中誌リンクサービス
16)Miyauchi J, Ito Y, Kawano T, et al. Unusual diffuse liver fibrosis accompanying transient myeloproliferative disorder in Downʼs syndrome: a report of four autopsy cases and proposal of a hypothesis. Blood. 1992; 80: 1521-7
PubMed
医中誌リンクサービス
17)Al-Kasim F, Doyle JJ, Massey GV, et al. Incidence and treatment of potentially lethal diseases in transient leukemia of Down syndrome: Pediatric Oncology Group Study. J Pediatr Hematol Oncol. 2002; 24: 9-13
PubMed CrossRef
医中誌リンクサービス
18)Massey GV, Zipursky A, Chang MN, et al. Childrenʼs Oncology Group (COG). A prospective study of the natural history of transient leukemia (TL) in neonates with Down syndrome (DS): Childrenʼs Oncology Group (COG) study POG-9481. Blood. 2006; 107: 4606-13
PubMed CrossRef
医中誌リンクサービス
19)Brodeur GM, Dahl GV, Williams DL, et al. Transient leukemoid reaction and trisomy 21 mosaicism in a phenotypically normal newborn. Blood. 1980; 55: 691-3
PubMed
医中誌リンクサービス
20)Klusmann JH, Creutzig U, Zimmermann M, et al. Treatment and prognostic impact of transient leukemia in neonates with Down syndrome. Blood. 2008; 111: 2991-8
PubMed CrossRef
医中誌リンクサービス
21)Gamis AS, Woods WG, Alonzo TA, et al. Increased age at diagnosis has a significantly negative effect on outcome in children with Down syndrome and acute myeloid leukemia: a report from the Childrenʼs Cancer Group Study 2891. J Clin Oncol. 2003; 21: 3415-22
PubMed CrossRef
医中誌リンクサービス
22)Creutzig U, Reinhardt D, Diekamp S, et al. AML patients with Down syndrome have a high cure rate with AML-BFM therapy with reduced dose intensity. Leukemia. 2005; 19: 1355-60
PubMed CrossRef
医中誌リンクサービス
23)Muramatsu H, Kato K, Watanabe N, et al. Risk factors for early death in neonates with Down syndrome and transient leukaemia. Br J Haematol. 2008; 142: 610-5
PubMed CrossRef
医中誌リンクサービス
24)林 泰秀.ダウン症候群に発症したtransient abnormal myelopoiesis(TAM)への対応.周産期医学.2010; 40: 937-41
医学中央雑誌刊行会
医中誌リンクサービス
25)Kitoh T, Taki T, Hayashi Y, et al. Transient abnormal myelopoiesis in a Down syndrome newborn followed by acute myeloid leukemia: identification of the same chromosomal abnormality in both stages. Cancer Genet Cytogenet. 2009; 188: 99-102
PubMed CrossRef
医中誌リンクサービス
26)Forestier E, Izraeli S, Beverloo B, et al. Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study. Blood. 2008; 111; 1575-83
PubMed
医中誌リンクサービス
27)Dastugue N, Lafage-Pochitaloff M, Pagès MP, et al. Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): a study of the Groupe Français de Cytogénétique Hématolo-gique(GFCH). Blood. 2002; 100: 618-26
PubMed CrossRef
医中誌リンクサービス
28)Hama A, Yagasaki H, Takahashi Y, et al. Acute megakaryoblastic leukaemia (AMKL) in children: a comparison of AMKL with and without Down syndrome. Br J Haematol. 2008; 140: 552-61
PubMed CrossRef
医中誌リンクサービス
29)Ma Z, Morris SW, Valentine V, et al. Fusion of two novel genes, RBM15 and MKL1, in the t(1; 22)(p13;q13) of acute megakaryoblastic leukemia. Nat Genet. 2001; 28: 220-1
PubMed CrossRef
医中誌リンクサービス
30)Mercher T, Coniat MB, Monni R, et al. Involvement of a human gene related to the Drosophila spen gene in the recurrent t(1;22) translocation of acute megakaryocytic leukemia. Proc Natl Acad Sci U S A. 2001; 98: 5776-9
PubMed CrossRef
医中誌リンクサービス
31)Bernstein J, Dastugue N, Haas OA, et al. Nineteen cases of the t(1;22)(p13;q13) acute megaka-ryoblastic leukaemia of infants/children and a review of 39 cases: report from a t(1;22) study group. Leukemia. 2000; 14: 216-8
PubMed CrossRef
医中誌リンクサービス
32)Carroll A, Civin C, Schneider N, et al. The t(1; 22)(p13;q13) is nonrandom and restricted to infants with acute megakaryoblastic leukemia: a Pediatric Oncology Group Study. Blood. 1991; 78: 748-52
PubMed
医中誌リンクサービス
33)Hara Y, Shiba N, Ohki K, et al. Comprehensive fusion gene analysis of pediatric non-Down syndrome acute megakaryoblasitc leukemia. ASH#2646. 2013
医中誌リンクサービス
34)Tallman MS, Neuberg D, Bennett JM, et al. Acute megakaryocytic leukemia: the Eastern Cooperative Oncology Group experience. Blood. 2000; 96: 2405-11
PubMed
医中誌リンクサービス
35)Reinhardt D, Diekamp S, Langebrake C, et al. Acute megakaryoblastic leukemia in children and adolescents, excluding Downʼs syndrome: improved outcome with intensified induction treatment. Leukemia. 2005; 19: 1495-6
PubMed CrossRef
医中誌リンクサービス
36)Athale UH, Razzouk BI, Raimondi SC, et al. Biology and outcome of childhood acute megakaryoblastic leukemia: a single institutionʼs experience. Blood. 2001; 97: 3727-32
PubMed CrossRef
医中誌リンクサービス
37)Balgobind BV, Raimondi SC, Harbott J, et al. Novel prognostic subgroups in childhood 11q23/MLL-rearranged acute myeloid leukemia: results of an international retrospective study. Blood. 2009; 114: 2489-96
PubMed CrossRef
医中誌リンクサービス
38)Kong XT, Ida K, Ichikawa H, et al. Consistent detection of TLS/FUS-ERG chimeric transcripts in acute myeloid leukemia with t(16;21)(p11;q22) and identification of a novel transcript. Blood. 1997; 90: 1192-9
PubMed
医中誌リンクサービス
39)Gilliland DG, Griffin JD. The roles of FLT3 in hematopoiesis and leukemia. Blood. 2002; 100: 1532-42
PubMed CrossRef
医中誌リンクサービス
40)Tefferi A. Novel mutations and their functional and clinical relevance in myeloproliferative neoplasms: JAK2, MPL, TET2, ASXL1, CBL, IDH and IKZF1. Leukemia 2010; 24: 1128-38
PubMed CrossRef
医中誌リンクサービス
41)Ernst T, Chase AJ, Score J, et al. Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders. Nat Genet. 2010; 42: 722-6
PubMed CrossRef
医中誌リンクサービス
42)Abe K, Kajii T, Niikawa N, et al. Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome. Hum Gent. 1989; 82: 561-6
医中誌リンクサービス
43)Wechsler J, Greene M, McDevitt MA, et al. Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome. Nat Genet. 2002; 32: 148-52
PubMed CrossRef
医中誌リンクサービス
44)Xu G, Nagano M, Kanezaki R, et al. Frequent mutations in the GATA-1 gene in the transient myeloproliferative disorder of Down syndrome. Blood. 2003; 102: 2960-8
PubMed CrossRef
医中誌リンクサービス
45)Shimada A, Xu G, Toki T, et al. Fetal origin of the GATA1 mutation in identical twins with transient myeloproliferative disorder and acute megakaryoblastic leukemia accompanying Down syndrome. Blood. 2004; 103: 366
PubMed CrossRef
医中誌リンクサービス
46)Kanezaki R, Toki T, Terui K, et al. Down syndrome and GATA1 mutations in transient abnormal myeloproliferative disorder: mutation classes correlate with progression to myeloid leukemia. Blood. 2010; 116: 4631-8
PubMed CrossRef
医中誌リンクサービス
47)Toki T, Kanezaki R, Kobayashi E, et al. Naturally occurring oncogenic GATA1 mutants with internal deletions in transient abnormal myelopoiesis in Down syndrome. Blood. 2013; 121: 3181-4
PubMed CrossRef
医中誌リンクサービス
48)Nasmyth K, Haering CH. Cohesin: its roles and mechanisms. Annu Rev Genet. 2009; 43: 525-58
PubMed CrossRef
医中誌リンクサービス
49)Park MJ, Shimada A, Asada H, et al. JAK2 mutation in a boy with polycythemia vera, but not in other pediatric hematologic disorders. Leukemia. 2006; 20: 1453-4
PubMed CrossRef
医中誌リンクサービス
50)Malinge S, Ragu C, Della-Valle V, et al. Activating mutations in human acute megakaryoblastic leukemia. Blood. 2008; 112: 4220-6
PubMed CrossRef
医中誌リンクサービス
51)Walters DK, Mercher T, Gu TL, et al. Activating alleles of JAK3 in acute megakaryoblastic leukemia. Cancer Cell. 2006; 10: 65-75
PubMed CrossRef
医中誌リンクサービス
52)De Vita S, Mulligan C, McElwaine S, et al. Loss-of-function JAK3 mutations in TMD and AMKL of Down syndrome. Br J Haematol. 2007; 137: 337-41
PubMed CrossRef
医中誌リンクサービス
53)Norton A, Fisher C, Liu H, et al. Analysis of JAK3, JAK2, and C-MPL mutations in transient myeloproliferative disorder and myeloid leukemia of Down syndrome blasts in children with Down syndrome. Blood. 2007; 110: 1077-9
PubMed CrossRef
医中誌リンクサービス
54)Blink M, Buitenkamp TD, van den Heuvel-Eibrink MM, et al. Frequency and prognostic implications of JAK 1-3 aberrations in Down syndrome acute lymphoblastic and myeloid leukemia. Leukemia. 2011; 25: 1365-8
PubMed CrossRef
医中誌リンクサービス
55)Kiyoi H, Yamaji S, Kojima S, et al. JAK3 mutations occur in acute megakaryoblastic leukemia both in Down syndrome children and non-Down syndrome adults. Leukemia. 2007; 21: 574-6
PubMed CrossRef
医中誌リンクサービス
56)Hama A, Yagasaki H, Takahashi Y, et al. JAK mutations in Down syndrome-associated transient myeloproliferative disorder and acute megakaryocytic leukemia. Blood. 2008; 111: 2493-4
医中誌リンクサービス
57)Hama A, Muramatsu H, Makishima H, et al. Molecular lesions in childhood and adult acute megakaryoblastic leukaemia. Br J Haematol. 2012; 156: 316-25
PubMed CrossRef
医中誌リンクサービス
58)Malkin D, Brown EJ, Zipursky A. The role of p53 in megakaryocyte differentiation and the megakaryocytic leukemias of Down syndrome. Cancer Genet Cytogenet. 2000; 116: 1-5
PubMed CrossRef
医中誌リンクサービス
59)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: 2017-31
PubMed CrossRef
医中誌リンクサービス
60)Klusmann JH, Reinhardt D, Hasle H, et al. Janus kinase mutations in the development of acute megakaryoblastic leukemia in children with and without Downʼs syndrome. Leukemia. 2007; 21: 1584-7
PubMed CrossRef
医中誌リンクサービス
61)Welch JS, Ley TJ, Link DC, et al. The origin and evolution of mutations in acute myeloid leukemia. Cell. 2012; 150: 264-78
PubMed CrossRef
医中誌リンクサービス
62)Wen Q, Goldenson B, Silver SJ, et al. Identification of regulators of polyploidization presents therapeutic targets for treatment of AMKL. Cell. 2012; 150: 575-89
PubMed CrossRef
医中誌リンクサービス
63)Sano H, Shimada A, Tabuchi K, et al. WT1 mutation in pediatric patients with acute myeloid leukemia: a report from the Japanese Childhood AML Cooperative Study Group. Int J Hematol. 2013; 98: 437-45
医学中央雑誌刊行会  CrossRef
医中誌リンクサービス
64)Hussein K, Bock O, Theophile K, et al. MPLW515L mutation in acute megakaryoblastic leukaemia. Leukemia. 2009; 23: 852-5
PubMed CrossRef
医中誌リンクサービス
65)Oki K, Takita J, Hiwatari M, et al. IDH1 and IDH2 mutations are rare in pediatric myeloid malignancies. Leukemia. 2011; 25: 382-4
PubMed CrossRef
医中誌リンクサービス
66)Taketani T, Taki T, Takita J, et al. Mutation of the AML1/RUNX1 gene in a transient myeloproliferative disorder patient with Down syndrome. Leukemia. 2002; 16: 1866-7
PubMed CrossRef
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