-
1
-
-
79955974326
-
Prdm16 is a physiologic regulator of hematopoietic stem cells
-
Agulio F, Avagyan S, Labar A, Sevilla A, Lee DF, Kumar P, Lemischka IR, Zhou BY, Snoeck HW. 2011. Prdm16 is a physiologic regulator of hematopoietic stem cells. Blood 117:5057-5066.
-
(2011)
Blood
, vol.117
, pp. 5057-5066
-
-
Agulio, F.1
Avagyan, S.2
Labar, A.3
Sevilla, A.4
Lee, D.F.5
Kumar, P.6
Lemischka, I.R.7
Zhou, B.Y.8
Snoeck, H.W.9
-
2
-
-
0030916736
-
The inv(11)(p15q22) chromosome translocation of de novo and therapy-related myeloid malignancies results in fusion of the nucleoporin gene, NUP98, with the putative RNA helicase case, DDX10
-
Arai Y, Hosoda F, Kobayashi H, Kawakami K, Takahara J. 1997. The inv(11)(p15q22) chromosome translocation of de novo and therapy-related myeloid malignancies results in fusion of the nucleoporin gene, NUP98, with the putative RNA helicase case, DDX10. Blood 89:3936-3944.
-
(1997)
Blood
, vol.89
, pp. 3936-3944
-
-
Arai, Y.1
Hosoda, F.2
Kobayashi, H.3
Kawakami, K.4
Takahara, J.5
-
3
-
-
0036530203
-
A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemaia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay
-
Brown J, Jawad M, Twigg SR, Saracoglu K, Sauerbrey A, Thomas AE, Eils R, Harbott J, Kearney L. 2002. A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemaia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay. Blood 99:2526-2531.
-
(2002)
Blood
, vol.99
, pp. 2526-2531
-
-
Brown, J.1
Jawad, M.2
Twigg, S.R.3
Saracoglu, K.4
Sauerbrey, A.5
Thomas, A.E.6
Eils, R.7
Harbott, J.8
Kearney, L.9
-
4
-
-
0041662187
-
Cryptic t(5;11)(q35;p15.5) in adult de novo acute myelocytic leukemia with normal karyotype
-
Casas S, Aventín A, Nomdedéu J, Sierra J. 2003. Cryptic t(5;11)(q35;p15.5) in adult de novo acute myelocytic leukemia with normal karyotype. Cancer Genet Cytogenet 145:183.
-
(2003)
Cancer Genet Cytogenet
, vol.145
, pp. 183
-
-
Casas, S.1
Aventín, A.2
Nomdedéu, J.3
Sierra, J.4
-
5
-
-
10744231835
-
Frequency of NUP98-NSD1 fusion transcript in childhood acute myeloid leukaemia
-
Cerveira N, Correia C, Dória S, Bizarro S, Rocha P, Gomes P, Torres L, Norton L, Borges BS, Castedo S, Teixeira MR. 2003. Frequency of NUP98-NSD1 fusion transcript in childhood acute myeloid leukaemia. Leukemia 17:2244-2247.
-
(2003)
Leukemia
, vol.17
, pp. 2244-2247
-
-
Cerveira, N.1
Correia, C.2
Dória, S.3
Bizarro, S.4
Rocha, P.5
Gomes, P.6
Torres, L.7
Norton, L.8
Borges, B.S.9
Castedo, S.10
Teixeira, M.R.11
-
6
-
-
67650886013
-
Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: comparative analysis of 493 adult patients
-
Chou WC, Chen CY, Hou HA, Lin LI, Tang JL, Yao M, Tsay W, Ko BS, Wu SJ, Huang SY, Hsu SC, Chen YC, Huang YN, Tseng MH, Huang CF, Tien HF. 2009. Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: comparative analysis of 493 adult patients. Leukemia 23:1303-1310.
-
(2009)
Leukemia
, vol.23
, pp. 1303-1310
-
-
Chou, W.C.1
Chen, C.Y.2
Hou, H.A.3
Lin, L.I.4
Tang, J.L.5
Yao, M.6
Tsay, W.7
Ko, B.S.8
Wu, S.J.9
Huang, S.Y.10
Hsu, S.C.11
Chen, Y.C.12
Huang, Y.N.13
Tseng, M.H.14
Huang, C.F.15
Tien, H.F.16
-
7
-
-
58749097408
-
A subtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: a genome-wide classification study
-
Den Boer ML, van Slegtenhorst M, De Menezes RX, Cheok MH, Buijs-Gladdines JG, Peters ST, Van Zutven LJ, Beverloo HB, Van der Spek PJ, Escherich G, Horstmann MA, Janka-Schaub GE, Kamps WA, Evans WE, Pieters R. 2009. A subtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: a genome-wide classification study. Lancet Oncol 10:125-134.
-
(2009)
Lancet Oncol
, vol.10
, pp. 125-134
-
-
Den Boer, M.L.1
Van Slegtenhorst, M.2
De Menezes, R.X.3
Cheok, M.H.4
Buijs-Gladdines, J.G.5
Peters, S.T.6
Van Zutven, L.J.7
Beverloo, H.B.8
Van Der Spek, P.J.9
Escherich, G.10
Horstmann, M.A.11
Janka-Schaub, G.E.12
Kamps, W.A.13
Evans, W.E.14
Pieters, R.15
-
8
-
-
28444473100
-
Mutant nucleophosmin (NPM1) predicts favorable prognosis in younger adults with acute myeloid leukemia and normal cytogenetics: interaction with other gene mutations
-
Döhner K, Schlenk RF, Habdank M, Scholl C, Rücker FG, Corbacioglu A, Bullinger L, Fröhling S, Döhner H. 2005. Mutant nucleophosmin (NPM1) predicts favorable prognosis in younger adults with acute myeloid leukemia and normal cytogenetics: interaction with other gene mutations. Blood 106:3740-3746.
-
(2005)
Blood
, vol.106
, pp. 3740-3746
-
-
Döhner, K.1
Schlenk, R.F.2
Habdank, M.3
Scholl, C.4
Rücker, F.G.5
Corbacioglu, A.6
Bullinger, L.7
Fröhling, S.8
Döhner, H.9
-
10
-
-
27244452986
-
Genetics of myeloid malignancies: Pathogenetic and clinical implications
-
Frohling S, Scholl C, Gilliland DG, Levine RL. 2005. Genetics of myeloid malignancies: Pathogenetic and clinical implications. J Clin Oncol 23:6285-6295.
-
(2005)
J Clin Oncol
, vol.23
, pp. 6285-6295
-
-
Frohling, S.1
Scholl, C.2
Gilliland, D.G.3
Levine, R.L.4
-
11
-
-
83455220210
-
NUP98 gene fusions and hematopoietic malignancies: Common themes and new biological insights
-
Gough SM, Slape CI, Aplan PD. 2011. NUP98 gene fusions and hematopoietic malignancies: Common themes and new biological insights. Blood 118:6247-6257.
-
(2011)
Blood
, vol.118
, pp. 6247-6257
-
-
Gough, S.M.1
Slape, C.I.2
Aplan, P.D.3
-
12
-
-
13644265950
-
The pathophysiology of HOX genes and their role in cancer
-
Grier DG, Thompson A, Kwasniewska A, McGonigle GJ, Halliday HL, Lappin TR. 2005. The pathophysiology of HOX genes and their role in cancer. J Pathol 205:154-171.
-
(2005)
J Pathol
, vol.205
, pp. 154-171
-
-
Grier, D.G.1
Thompson, A.2
Kwasniewska, A.3
McGonigle, G.J.4
Halliday, H.L.5
Lappin, T.R.6
-
13
-
-
80053354797
-
NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern
-
Hollink IH, van den Heuvel-Eibrink MM, Arentsen-Peters ST, Pratcorona M, Abbas S, Kuipers JE, van Galen JF, Beverloo HB, Sonneveld E, Kaspers GJ, Trka J, Baruchel A, Zimmermann M, Creutzig U, Reinhardt D, Pieters R, Valk PJ, Zwaan CM. 2011. NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern. Blood 118:3645-3656.
-
(2011)
Blood
, vol.118
, pp. 3645-3656
-
-
Hollink, I.H.1
Van Den Heuvel-Eibrink, M.M.2
Arentsen-Peters, S.T.3
Pratcorona, M.4
Abbas, S.5
Kuipers, J.E.6
Van Galen, J.F.7
Beverloo, H.B.8
Sonneveld, E.9
Kaspers, G.J.10
Trka, J.11
Baruchel, A.12
Zimmermann, M.13
Creutzig, U.14
Reinhardt, D.15
Pieters, R.16
Valk, P.J.17
Zwaan, C.M.18
-
14
-
-
33749237123
-
Common gene expression signatures in t(8;21)- and inv(16)-acute myeloid leukemia
-
Ichikawa H, Tanabe K, Mizushima H, Hayashi Y, Mizutani S, Ishii E, Hongo T, Kikuchi A, Satake M. 2006. Common gene expression signatures in t(8;21)- and inv(16)-acute myeloid leukemia. Br J Haematol 135:336-347.
-
(2006)
Br J Haematol
, vol.135
, pp. 336-347
-
-
Ichikawa, H.1
Tanabe, K.2
Mizushima, H.3
Hayashi, Y.4
Mizutani, S.5
Ishii, E.6
Hongo, T.7
Kikuchi, A.8
Satake, M.9
-
15
-
-
78650006148
-
Prospective study of a therapeutic regimen with all-trans retinoic acid and anthracyclines in combination of cytarabine in children with acute promyelocytic leukaemia: the Japanese childhood acute myeloid leukaemia cooperative study
-
Imaizumi M, Tawa A, Hanada R, Tsuchida M, Tabuchi K, Kigasawa H, Kobayashi R, Morimoto A, Nakayama H, Hamamoto K, Kudo K, Yabe H, Horibe K, Tsuchiya S, Tsukimoto I. 2011. Prospective study of a therapeutic regimen with all-trans retinoic acid and anthracyclines in combination of cytarabine in children with acute promyelocytic leukaemia: the Japanese childhood acute myeloid leukaemia cooperative study. Br J Haematol 152:89-98.
-
(2011)
Br J Haematol
, vol.152
, pp. 89-98
-
-
Imaizumi, M.1
Tawa, A.2
Hanada, R.3
Tsuchida, M.4
Tabuchi, K.5
Kigasawa, H.6
Kobayashi, R.7
Morimoto, A.8
Nakayama, H.9
Hamamoto, K.10
Kudo, K.11
Yabe, H.12
Horibe, K.13
Tsuchiya, S.14
Tsukimoto, I.15
-
16
-
-
0035883090
-
A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia
-
Jaju RJ, Fidler C, Haas OA, Strickson AJ, Watkins F, Clark K, Cross NC, Cheng JF, Aplan PD, Kearney L, Boultwood J, Wainscoat JS. 2001. A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia. Blood 98:1264-1267.
-
(2001)
Blood
, vol.98
, pp. 1264-1267
-
-
Jaju, R.J.1
Fidler, C.2
Haas, O.A.3
Strickson, A.J.4
Watkins, F.5
Clark, K.6
Cross, N.C.7
Cheng, J.F.8
Aplan, P.D.9
Kearney, L.10
Boultwood, J.11
Wainscoat, J.S.12
-
17
-
-
60649104272
-
Age-associated difference in gene expression of paediatric acute myelomonocytic lineage leukaemia (FAB M4 and M5 subtypes) and its correlation with prognosis
-
Jo A, Tsukimoto I, Ishii E, Asou N, Mitani S, Shimada A, Igarashi T, Hayashi Y, Ichikawa H. 2009. Age-associated difference in gene expression of paediatric acute myelomonocytic lineage leukaemia (FAB M4 and M5 subtypes) and its correlation with prognosis. Br J Haematol 144:917-929.
-
(2009)
Br J Haematol
, vol.144
, pp. 917-929
-
-
Jo, A.1
Tsukimoto, I.2
Ishii, E.3
Asou, N.4
Mitani, S.5
Shimada, A.6
Igarashi, T.7
Hayashi, Y.8
Ichikawa, H.9
-
18
-
-
36849053313
-
Prospective study of a pirarubicin, intermediate-dose cytarabine, and etoposide regimen in children with Down syndrome and acute myeloid leukemia: The Japanese Childhood AML Cooperative Study Group
-
Kudo K, Kojima S, Tabuchi K, Yabe H, Tawa A, Imaizumi M, Hanada R, Hamamoto K, Kobayashi R, Morimoto A, Nakayama H, Tsuchida M, Horibe K, Kigasawa H, Tsukimoto I. 2007. Prospective study of a pirarubicin, intermediate-dose cytarabine, and etoposide regimen in children with Down syndrome and acute myeloid leukemia: The Japanese Childhood AML Cooperative Study Group. J Clin Oncol 25:5442-5447.
-
(2007)
J Clin Oncol
, vol.25
, pp. 5442-5447
-
-
Kudo, K.1
Kojima, S.2
Tabuchi, K.3
Yabe, H.4
Tawa, A.5
Imaizumi, M.6
Hanada, R.7
Hamamoto, K.8
Kobayashi, R.9
Morimoto, A.10
Nakayama, H.11
Tsuchida, M.12
Horibe, K.13
Kigasawa, H.14
Tsukimoto, I.15
-
19
-
-
8444242978
-
Cryptic insertion producing two NUP98/NSD1 chimeric transcripts in adult refractory anemia with an excess of blasts
-
La Starza R, Gorello P, Rosati R, Riezzo A, Veronese A, Ferrazzi E, Martelli MF, Negrini M, Mecucci C. 2004. Cryptic insertion producing two NUP98/NSD1 chimeric transcripts in adult refractory anemia with an excess of blasts. Genes Chromosomes Cancer 41:395-399.
-
(2004)
Genes Chromosomes Cancer
, vol.41
, pp. 395-399
-
-
La Starza, R.1
Gorello, P.2
Rosati, R.3
Riezzo, A.4
Veronese, A.5
Ferrazzi, E.6
Martelli, M.F.7
Negrini, M.8
Mecucci, C.9
-
20
-
-
79952092487
-
Molecular genetics of adult acute myeloid leukemia: Prognostic and therapeutic implications
-
Marcucci G, Haferlach T, Döhner H. 2011. Molecular genetics of adult acute myeloid leukemia: Prognostic and therapeutic implications. J Clin Oncol 29:475-486.
-
(2011)
J Clin Oncol
, vol.29
, pp. 475-486
-
-
Marcucci, G.1
Haferlach, T.2
Döhner, H.3
-
21
-
-
0034332196
-
A novel gene, MEL1, mapped to 1p36.3 is highly homologous to the MDS1/EVI1 gene and is transcriptionally activated in t(1;3)(p36;q21)-positive leukemia cells
-
Mochizuki N, Shimizu S, Nagasawa T, Tanaka H, Taniwaki M, Yokota J, Morishita K. 2000. A novel gene, MEL1, mapped to 1p36.3 is highly homologous to the MDS1/EVI1 gene and is transcriptionally activated in t(1;3)(p36;q21)-positive leukemia cells. Blood 96:3209-3214.
-
(2000)
Blood
, vol.96
, pp. 3209-3214
-
-
Mochizuki, N.1
Shimizu, S.2
Nagasawa, T.3
Tanaka, H.4
Taniwaki, M.5
Yokota, J.6
Morishita, K.7
-
22
-
-
58749109707
-
Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia
-
Mullighan CG, Su X, Zhang J, Radtke I, Phillips LA, Miller CB, Ma J, Liu W, Cheng C, Schulman BA, Harvey RC, Chen IM, Clifford RJ, Carroll WL, Reaman G, Bowman WP, Devidas M, Gerhard DS, Yang W, Relling MV, Shurtleff SA, Campana D, Borowitz MJ, Pui CH, Smith M, Hunger SP, Willman CL, Downing JR. 2009. Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia. N Engl J Med 360:470-480.
-
(2009)
N Engl J Med
, vol.360
, pp. 470-480
-
-
Mullighan, C.G.1
Su, X.2
Zhang, J.3
Radtke, I.4
Phillips, L.A.5
Miller, C.B.6
Ma, J.7
Liu, W.8
Cheng, C.9
Schulman, B.A.10
Harvey, R.C.11
Chen, I.M.12
Clifford, R.J.13
Carroll, W.L.14
Reaman, G.15
Bowman, W.P.16
Devidas, M.17
Gerhard, D.S.18
Yang, W.19
Relling, M.V.20
Shurtleff, S.A.21
Campana, D.22
Borowitz, M.J.23
Pui, C.H.24
Smith, M.25
Hunger, S.P.26
Willman, C.L.27
Downing, J.R.28
more..
-
23
-
-
0141482125
-
The cardiac homeobox gene NKX2-5 is deregulated by juxtaposition with BCL11B in pediatric T-ALL cell lines via a novel t(5;14)(q35.1;q32.2)
-
Nagel S, Kaufmann M, Drexler HG, MacLeod RA. 2003. The cardiac homeobox gene NKX2-5 is deregulated by juxtaposition with BCL11B in pediatric T-ALL cell lines via a novel t(5;14)(q35.1;q32.2). Cancer Res 63:5329-5334.
-
(2003)
Cancer Res
, vol.63
, pp. 5329-5334
-
-
Nagel, S.1
Kaufmann, M.2
Drexler, H.G.3
MacLeod, R.A.4
-
24
-
-
27244452418
-
NUP98 fusion in human leukemia: Dysregulation of the nuclear pore and homeodomain proteins
-
Nakamura T. 2005. NUP98 fusion in human leukemia: Dysregulation of the nuclear pore and homeodomain proteins. Int J Hematol 82:21-27.
-
(2005)
Int J Hematol
, vol.82
, pp. 21-27
-
-
Nakamura, T.1
-
25
-
-
9044241254
-
Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia
-
Nakamura T, Largaespada DA, Lee MP, Johnson LA, Ohyashiki K, Toyama K, Chen SJ, Willman CL, Chen IM, Feinberg AP, Jenkins NA, Copeland NG, Shaughnessy JD Jr. 1996. Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia. Nature Genet 12:154-158.
-
(1996)
Nature Genet
, vol.12
, pp. 154-158
-
-
Nakamura, T.1
Largaespada, D.A.2
Lee, M.P.3
Johnson, L.A.4
Ohyashiki, K.5
Toyama, K.6
Chen, S.J.7
Willman, C.L.8
Chen, I.M.9
Feinberg, A.P.10
Jenkins, N.A.11
Copeland, N.G.12
Shaughnessy Jr, J.D.13
-
26
-
-
21244447565
-
Screening for NUP98 rearrangements in hematopoietic malignancies by fluorescence in situ hybridization
-
Nebral K, König M, Schmidt HH, Lutz D, Sperr WR, Kalwak K, Brugger S, Dworzak MN, Haas OA, Strehl S. 2005. Screening for NUP98 rearrangements in hematopoietic malignancies by fluorescence in situ hybridization. Haematologica 90:746-752.
-
(2005)
Haematologica
, vol.90
, pp. 746-752
-
-
Nebral, K.1
König, M.2
Schmidt, H.H.3
Lutz, D.4
Sperr, W.R.5
Kalwak, K.6
Brugger, S.7
Dworzak, M.N.8
Haas, O.A.9
Strehl, S.10
-
27
-
-
0032974961
-
Targeted disruption of the homeobox transcription factor Nkx2-3 in mice results in postnatal lethality and abnormal development of small intestine and spleen
-
Pabst O, Zweigerdt R, Arnold HH. 1999. Targeted disruption of the homeobox transcription factor Nkx2-3 in mice results in postnatal lethality and abnormal development of small intestine and spleen. Development 126:2215-2225.
-
(1999)
Development
, vol.126
, pp. 2215-2225
-
-
Pabst, O.1
Zweigerdt, R.2
Arnold, H.H.3
-
28
-
-
0036836507
-
Cryptic translocation t(5;11)(q35;p15.5) with involvement of the NSD1 and NUP98 genes without 5q deletion in childhood acute myeloid leukemia
-
Panarello C, Rosanda C, Morerio C. 2002. Cryptic translocation t(5;11)(q35;p15.5) with involvement of the NSD1 and NUP98 genes without 5q deletion in childhood acute myeloid leukemia. Genes Chromosomes Cancer 35:277-281.
-
(2002)
Genes Chromosomes Cancer
, vol.35
, pp. 277-281
-
-
Panarello, C.1
Rosanda, C.2
Morerio, C.3
-
29
-
-
33645383283
-
The effect of a novel recombination between the homeobox gene NKX2-5 and the TRD locus in T-cell acute lymphoblastic leukemia on activation of the NKX2-5 gene
-
Przybylski GK, Dik WA, Grabarczyk P, Wanzeck J, Chudobska P, Jankowski K, von Bergh A, van Dongen JJ, Schmidt CA, Langerak AW. 2006. The effect of a novel recombination between the homeobox gene NKX2-5 and the TRD locus in T-cell acute lymphoblastic leukemia on activation of the NKX2-5 gene. Haematologica 91:317-321.
-
(2006)
Haematologica
, vol.91
, pp. 317-321
-
-
Przybylski, G.K.1
Dik, W.A.2
Grabarczyk, P.3
Wanzeck, J.4
Chudobska, P.5
Jankowski, K.6
von Bergh, A.7
van Dongen, J.J.8
Schmidt, C.A.9
Langerak, A.W.10
-
30
-
-
79952078495
-
Biology, risk stratification, and therapy of pediatric acute leukemias: An update
-
Pui CH, Carroll WL, Meshinchi S, Arceci RJ. 2011. Biology, risk stratification, and therapy of pediatric acute leukemias: An update. J Clin Oncol 29:551-565.
-
(2011)
J Clin Oncol
, vol.29
, pp. 551-565
-
-
Pui, C.H.1
Carroll, W.L.2
Meshinchi, S.3
Arceci, R.J.4
-
31
-
-
84865118132
-
Genetic alterations activating kinase and cytokine receptor signaling in high-risk acute lymphoblastic leukemia
-
Roberts KG, Morin RD, Zhang J, Hirst M, Zhao Y, Su X, Chen SC, Payne-Turner D, Churchman ML, Harvey RC, Chen X, Kasap C, Yan C, Becksfort J, Finney RP, Teachey DT, Maude SL, Tse K, Moore R, Jones S, Mungall K, Birol I, Edmonson MN, Hu Y, Buetow KE, Chen IM, Carroll WL, Wei L, Ma J, Kleppe M, Levine RL, Garcia-Manero G, Larsen E, Shah NP, Devidas M, Reaman G, Smith M, Paugh SW, Evans WE, Grupp SA, Jeha S, Pui CH, Gerhard DS, Downing JR, Willman CL, Loh M, Hunger SP, Marra MA, Mullighan CG. 2012. Genetic alterations activating kinase and cytokine receptor signaling in high-risk acute lymphoblastic leukemia. Cancer Cell 22:153-166.
-
(2012)
Cancer Cell
, vol.22
, pp. 153-166
-
-
Roberts, K.G.1
Morin, R.D.2
Zhang, J.3
Hirst, M.4
Zhao, Y.5
Su, X.6
Chen, S.C.7
Payne-Turner, D.8
Churchman, M.L.9
Harvey, R.C.10
Chen, X.11
Kasap, C.12
Yan, C.13
Becksfort, J.14
Finney, R.P.15
Teachey, D.T.16
Maude, S.L.17
Tse, K.18
Moore, R.19
Jones, S.20
Mungall, K.21
Birol, I.22
Edmonson, M.N.23
Hu, Y.24
Buetow, K.E.25
Chen, I.M.26
Carroll, W.L.27
Wei, L.28
Ma, J.29
Kleppe, M.30
Levine, R.L.31
Garcia-Manero, G.32
Larsen, E.33
Shah, N.P.34
Devidas, M.35
Reaman, G.36
Smith, M.37
Paugh, S.W.38
Evans, W.E.39
Grupp, S.A.40
Jeha, S.41
Pui, C.H.42
Gerhard, D.S.43
Downing, J.R.44
Willman, C.L.45
Loh, M.46
Hunger, S.P.47
Marra, M.A.48
Mullighan, C.G.49
more..
-
32
-
-
33646484524
-
NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique
-
Romana SP, Radford-Weiss I, Ben Abdelali R, Schluth C, Petit A, Dastugue N, Talmant P, Bilhou-Nabera C, Mugneret F, Lafage-Pochitaloff M, Mozziconacci MJ, Andrieu J, Lai JL, Terre C, Rack K, Cornillet-Lefebvre P, Luquet I, Nadal N, Nguyen-Khac F, Perot C, Van den Akker J, Fert-Ferrer S, Cabrol C, Charrin C, Tigaud I, Poirel H, Vekemans M, Bernard OA, Berger R. 2006. NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique. Leukemia 20:696-706.
-
(2006)
Leukemia
, vol.20
, pp. 696-706
-
-
Romana, S.P.1
Radford-Weiss, I.2
Ben Abdelali, R.3
Schluth, C.4
Petit, A.5
Dastugue, N.6
Talmant, P.7
Bilhou-Nabera, C.8
Mugneret, F.9
Lafage-Pochitaloff, M.10
Mozziconacci, M.J.11
Andrieu, J.12
Lai, J.L.13
Terre, C.14
Rack, K.15
Cornillet-Lefebvre, P.16
Luquet, I.17
Nadal, N.18
Nguyen-Khac, F.19
Perot, C.20
Van Den Akker, J.21
Fert-Ferrer, S.22
Cabrol, C.23
Charrin, C.24
Tigaud, I.25
Poirel, H.26
Vekemans, M.27
Bernard, O.A.28
Berger, R.29
more..
-
33
-
-
84862864582
-
RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: A study of the Japanese Childhood AML Cooperative Study Group
-
Sano H, Shimada A, Taki T, Murata C, Park MJ, Sotomatsu M, Tabuchi K, Tawa A, Kobayashi R, Horibe K, Tsuchida M, Hanada R, Tsukimoto I, Hayashi Y. 2012. RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: A study of the Japanese Childhood AML Cooperative Study Group. Int J Hematol 95:509-515.
-
(2012)
Int J Hematol
, vol.95
, pp. 509-515
-
-
Sano, H.1
Shimada, A.2
Taki, T.3
Murata, C.4
Park, M.J.5
Sotomatsu, M.6
Tabuchi, K.7
Tawa, A.8
Kobayashi, R.9
Horibe, K.10
Tsuchida, M.11
Hanada, R.12
Tsukimoto, I.13
Hayashi, Y.14
-
34
-
-
84855801664
-
DNMT3A mutations are rare in childhood acute myeloid leukaemia, myelodysplastic syndromes and juvenile myelomonocytic leukaemia
-
Shiba N, Taki T, Park MJ, Shimada A, Sotomatsu M, Adachi S, Tawa A, Horibe K, Tsuchida M, Hanada R, Tsukimoto I, Arakawa H, Hayashi Y. 2012. DNMT3A mutations are rare in childhood acute myeloid leukaemia, myelodysplastic syndromes and juvenile myelomonocytic leukaemia. Br J Haematol 156:413-414.
-
(2012)
Br J Haematol
, vol.156
, pp. 413-414
-
-
Shiba, N.1
Taki, T.2
Park, M.J.3
Shimada, A.4
Sotomatsu, M.5
Adachi, S.6
Tawa, A.7
Horibe, K.8
Tsuchida, M.9
Hanada, R.10
Tsukimoto, I.11
Arakawa, H.12
Hayashi, Y.13
-
35
-
-
33344471932
-
KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t(8;21): a study of the Japanese Childhood AML Cooperative Study Group
-
Shimada A, Taki T, Tabuchi K, Tawa A, Horibe K, Tsuchida M, Hanada R, Tsukimoto I, Hayashi Y. 2006. KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t(8;21): a study of the Japanese Childhood AML Cooperative Study Group. Blood 107:1806-1809.
-
(2006)
Blood
, vol.107
, pp. 1806-1809
-
-
Shimada, A.1
Taki, T.2
Tabuchi, K.3
Tawa, A.4
Horibe, K.5
Tsuchida, M.6
Hanada, R.7
Tsukimoto, I.8
Hayashi, Y.9
-
36
-
-
37549071079
-
Tandem duplications of MLL and FLT3 are correlated with poor prognoses in pediatric acute myeloid leukemia: a study of the Japanese childhood AML Cooperative Study Group
-
Shimada A, Taki T, Tabuchi K, Taketani T, Hanada R, Tawa A, Tsuchida M, Horibe K, Tsukimoto I, Hayashi Y. 2008. Tandem duplications of MLL and FLT3 are correlated with poor prognoses in pediatric acute myeloid leukemia: a study of the Japanese childhood AML Cooperative Study Group. Pediatr Blood Cancer 50:264-269.
-
(2008)
Pediatr Blood Cancer
, vol.50
, pp. 264-269
-
-
Shimada, A.1
Taki, T.2
Tabuchi, K.3
Taketani, T.4
Hanada, R.5
Tawa, A.6
Tsuchida, M.7
Horibe, K.8
Tsukimoto, I.9
Hayashi, Y.10
-
37
-
-
0036143026
-
The HOXD11 gene is fused to the NUP98 gene in acute myeloid leukemia with t(2;11)(q31;p15)
-
Taketani T, Taki T, Shibuya N, Ito E, Kitazawa J, Terui K, Hayashi Y. 2002a The HOXD11 gene is fused to the NUP98 gene in acute myeloid leukemia with t(2;11)(q31;p15). Cancer Res 62:33-37.
-
(2002)
Cancer Res
, vol.62
, pp. 33-37
-
-
Taketani, T.1
Taki, T.2
Shibuya, N.3
Ito, E.4
Kitazawa, J.5
Terui, K.6
Hayashi, Y.7
-
38
-
-
0036077515
-
The chromosome translocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of the NUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9
-
Taketani T, Taki T, Ono R, Kobayashi Y, Ida K, Hayashi Y. 2002b. The chromosome translocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of the NUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9. Genes Chromosomes Cancer 34:437-443.
-
(2002)
Genes Chromosomes Cancer
, vol.34
, pp. 437-443
-
-
Taketani, T.1
Taki, T.2
Ono, R.3
Kobayashi, Y.4
Ida, K.5
Hayashi, Y.6
-
39
-
-
0037102313
-
Novel NUP98-HOXC11 fusion gene resulted from a chromosomal break within exon 1 of HOXC11 in acute myeloid leukemia with t(11;12)(p15;q13)
-
Taketani T, Taki T, Shibuya N, Kikuchi A, Hanada R, Hayashi Y. 2002c Novel NUP98-HOXC11 fusion gene resulted from a chromosomal break within exon 1 of HOXC11 in acute myeloid leukemia with t(11;12)(p15;q13). Cancer Res 62:4571-4574.
-
(2002)
Cancer Res
, vol.62
, pp. 4571-4574
-
-
Taketani, T.1
Taki, T.2
Shibuya, N.3
Kikuchi, A.4
Hanada, R.5
Hayashi, Y.6
-
40
-
-
78149467263
-
High frequencies of simultaneous FLT3-ITD, WT1 and KIT mutations in hematological malignancies with NUP98-fusion genes
-
Taketani T, Taki T, Nakamura T, Kobayashi Y, Ito E, Fukuda S, Yamaguchi S, Hayashi Y. 2010. High frequencies of simultaneous FLT3-ITD, WT1 and KIT mutations in hematological malignancies with NUP98-fusion genes. Leukemia 24:1975-1977.
-
(2010)
Leukemia
, vol.24
, pp. 1975-1977
-
-
Taketani, T.1
Taki, T.2
Nakamura, T.3
Kobayashi, Y.4
Ito, E.5
Fukuda, S.6
Yamaguchi, S.7
Hayashi, Y.8
-
41
-
-
69849101233
-
Risk-stratified therapy and the intensive use of cytarabine improves the outcome in childhood acute myeloid leukemia: The AML99 trial from the Japanese Childhood AML Cooperative Study Group
-
Tsukimoto I, Tawa A, Horibe K, Tabuchi K, Kigasawa H, Tsuchida M, Yabe H, Nakayama H, Kudo K, Kobayashi R, Hamamoto K, Imaizumi M, Morimoto A, Tsuchiya S, Hanada R. 2009. Risk-stratified therapy and the intensive use of cytarabine improves the outcome in childhood acute myeloid leukemia: The AML99 trial from the Japanese Childhood AML Cooperative Study Group. J Clin Oncol 27:4007-4013.
-
(2009)
J Clin Oncol
, vol.27
, pp. 4007-4013
-
-
Tsukimoto, I.1
Tawa, A.2
Horibe, K.3
Tabuchi, K.4
Kigasawa, H.5
Tsuchida, M.6
Yabe, H.7
Nakayama, H.8
Kudo, K.9
Kobayashi, R.10
Hamamoto, K.11
Imaizumi, M.12
Morimoto, A.13
Tsuchiya, S.14
Hanada, R.15
-
42
-
-
69149100639
-
Acquired copy number alterations in adult acute myeloid leukemia genomes
-
Walter MJ, Payton JE, Ries RE, Shannon WD, Deshmukh H, Zhao Y, Baty J, Heath S, Westervelt P, Watson MA, Tomasson MH, Nagarajan R, O'Gara BP, Bloomfield CD, Mrózek K, Selzer RR, Richmond TA, Kitzman J, Geoghegan J, Eis PS, Maupin R, Fulton RS, McLellan M, Wilson RK, Mardis ER, Link DC, Graubert TA, DiPersio JF, Ley TJ. 2009. Acquired copy number alterations in adult acute myeloid leukemia genomes. Proc Natl Acad Sci USA 106:12950-12955.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 12950-12955
-
-
Walter, M.J.1
Payton, J.E.2
Ries, R.E.3
Shannon, W.D.4
Deshmukh, H.5
Zhao, Y.6
Baty, J.7
Heath, S.8
Westervelt, P.9
Watson, M.A.10
Tomasson, M.H.11
Nagarajan, R.12
O'Gara, B.P.13
Bloomfield, C.D.14
Mrózek, K.15
Selzer, R.R.16
Richmond, T.A.17
Kitzman, J.18
Geoghegan, J.19
Eis, P.S.20
Maupin, R.21
Fulton, R.S.22
McLellan, M.23
Wilson, R.K.24
Mardis, E.R.25
Link, D.C.26
Graubert, T.A.27
DiPersio, J.F.28
Ley, T.J.29
more..
|