-
1
-
-
0027184229
-
Molecular cloning and characterization of PEBP2 beta, the heterodimeric partner of a novel Drosophila runt-related DNA binding protein PEBP2 alpha
-
Ogawa E, Inuzuka M, Maruyama M, et al. Molecular cloning and characterization of PEBP2 beta, the heterodimeric partner of a novel Drosophila runt-related DNA binding protein PEBP2 alpha. Virology. 1993;194:314-331.
-
(1993)
Virology
, vol.194
, pp. 314-331
-
-
Ogawa, E.1
Inuzuka, M.2
Maruyama, M.3
-
2
-
-
0037321711
-
The role of a Runt domain transcription factor AML1/RUNX1 in leukemogenesis and its clinical implications
-
Asou N. The role of a Runt domain transcription factor AML1/RUNX1 in leukemogenesis and its clinical implications. Crit Rev Oncol Hematol. 2003;45:129-150.
-
(2003)
Crit Rev Oncol Hematol
, vol.45
, pp. 129-150
-
-
Asou, N.1
-
3
-
-
2942667930
-
Point mutations in the RUNX1/AML1 gene: Another actor in RUNX leukemia
-
Osato M. Point mutations in the RUNX1/AML1 gene: another actor in RUNX leukemia. Oncogene. 2004;23:4284-4296.
-
(2004)
Oncogene
, vol.23
, pp. 4284-4296
-
-
Osato, M.1
-
4
-
-
0036636857
-
Core-binding factors in haematopoiesis and leukaemia
-
Speck NA, Gilliland DG. Core-binding factors in haematopoiesis and leukaemia. Nat Rev Cancer. 2002;2:502-513.
-
(2002)
Nat Rev Cancer
, vol.2
, pp. 502-513
-
-
Speck, N.A.1
Gilliland, D.G.2
-
5
-
-
0025746321
-
t(8;21) breakpoints on chromosome 21 in acute myeloid leukemia are clustered within a limited region of a single gene, AML1
-
Miyoshi H, Shimizu K, Kozu T, Maseki N, Kaneko Y, Ohki M. t(8;21) breakpoints on chromosome 21 in acute myeloid leukemia are clustered within a limited region of a single gene, AML1. Proc Natl Acad Sci U S A. 1991;88:10431-10434.
-
(1991)
Proc Natl Acad Sci U S A
, vol.88
, pp. 10431-10434
-
-
Miyoshi, H.1
Shimizu, K.2
Kozu, T.3
Maseki, N.4
Kaneko, Y.5
Ohki, M.6
-
6
-
-
33645964017
-
Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: A collaborative retrospective study of the Group Francais de Cytogenetique Hematologique
-
Jeandidier E, Dastugue N, Mugneret F, et al. Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Group Francais de Cytogenetique Hematologique. Cancer Genet Cytogenet. 2006;166:1-11.
-
(2006)
Cancer Genet Cytogenet
, vol.166
, pp. 1-11
-
-
Jeandidier, E.1
Dastugue, N.2
Mugneret, F.3
-
8
-
-
29144468876
-
A randomized, postremission comparison of four courses of standard-dose consolidation therapy without maintenance therapy versus three courses of standard-dose consolidation with maintenance therapy in adults with acute myeloid leukemia
-
Miyawaki S, Sakamaki H, Ohtake S, et al. A randomized, postremission comparison of four courses of standard-dose consolidation therapy without maintenance therapy versus three courses of standard-dose consolidation with maintenance therapy in adults with acute myeloid leukemia. Cancer. 2005;104:2726-2734.
-
(2005)
Cancer
, vol.104
, pp. 2726-2734
-
-
Miyawaki, S.1
Sakamaki, H.2
Ohtake, S.3
-
9
-
-
8244257352
-
Myelomonoblastic leukaemia cells carrying the PEBP2β/MYH11 fusion gene are CD34+, c-KIT + immature cells
-
Osato M, Asou N, Okubo T, et al. Myelomonoblastic leukaemia cells carrying the PEBP2β/MYH11 fusion gene are CD34+, c-KIT + immature cells. Br J Haematol. 1997;97:656-658.
-
(1997)
Br J Haematol
, vol.97
, pp. 656-658
-
-
Osato, M.1
Asou, N.2
Okubo, T.3
-
10
-
-
0033559746
-
Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2alphaB gene associated with myeloblastic leukemias
-
Osato M, Asou N, Abdalla E, et al. Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2alphaB gene associated with myeloblastic leukemias. Blood. 1999;93:1817-1824.
-
(1999)
Blood
, vol.93
, pp. 1817-1824
-
-
Osato, M.1
Asou, N.2
Abdalla, E.3
-
11
-
-
33644807219
-
Haploinsufficiency of Runx1/AML1 promotes myeloid features and leukaemogenesis in BXH2 mice
-
Yamashita N, Osato M, Huang L, et al. Haploinsufficiency of Runx1/AML1 promotes myeloid features and leukaemogenesis in BXH2 mice. Br J Haematol. 2005;131:495-507.
-
(2005)
Br J Haematol
, vol.131
, pp. 495-507
-
-
Yamashita, N.1
Osato, M.2
Huang, L.3
-
12
-
-
12644307234
-
Functional dissection of the alpha and beta subunits of transcription factor PEBP2 and the redox susceptibility of its DNA binding activity
-
Kagoshima H, Akamatsu Y, Ito Y, Shigesada K. Functional dissection of the alpha and beta subunits of transcription factor PEBP2 and the redox susceptibility of its DNA binding activity. J Biol Chem. 1996;271:33074-33082.
-
(1996)
J Biol Chem
, vol.271
, pp. 33074-33082
-
-
Kagoshima, H.1
Akamatsu, Y.2
Ito, Y.3
Shigesada, K.4
-
13
-
-
0035794663
-
Transcriptional repression and developmental functions of the atypical vertebrate GATA protein TRPS1
-
Malik TH, Shoichet SA, Latham P, Kroll TG, Peters LL, Shivdasani RA. Transcriptional repression and developmental functions of the atypical vertebrate GATA protein TRPS1. EMBO J. 2001;20:1715-1725.
-
(2001)
EMBO J
, vol.20
, pp. 1715-1725
-
-
Malik, T.H.1
Shoichet, S.A.2
Latham, P.3
Kroll, T.G.4
Peters, L.L.5
Shivdasani, R.A.6
-
14
-
-
0028118492
-
Regulation of transcription by dimerization of erythroid factor NF-E2 p45 with small Maf proteins
-
Igarashi K, Kataoka K, Itoh K, Hayashi N, Nishizawa M, Yamamoto M. Regulation of transcription by dimerization of erythroid factor NF-E2 p45 with small Maf proteins. Nature. 1994;367:568-572.
-
(1994)
Nature
, vol.367
, pp. 568-572
-
-
Igarashi, K.1
Kataoka, K.2
Itoh, K.3
Hayashi, N.4
Nishizawa, M.5
Yamamoto, M.6
-
15
-
-
0029100157
-
Alternative splicing and genomic structure of the AML1 gene involved in acute myeloid leukemia
-
Miyoshi H, Ohira M, Shimizu K, et al. Alternative splicing and genomic structure of the AML1 gene involved in acute myeloid leukemia. Nucleic Acids Res. 1995;23:2762-2769.
-
(1995)
Nucleic Acids Res
, vol.23
, pp. 2762-2769
-
-
Miyoshi, H.1
Ohira, M.2
Shimizu, K.3
-
16
-
-
0342316531
-
Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I
-
Momeni P, Glockner G, Schmidt O, et al. Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I. Nat Genet. 2000;24:71-74.
-
(2000)
Nat Genet
, vol.24
, pp. 71-74
-
-
Momeni, P.1
Glockner, G.2
Schmidt, O.3
-
17
-
-
0034612768
-
Characterization of a zinc-finger protein and its association with apoptosis in prostate cancer cells
-
Chang GT, Steenbeek M, Schippers E, et al. Characterization of a zinc-finger protein and its association with apoptosis in prostate cancer cells. J Natl Cancer Inst. 2000;92:1414-1421.
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 1414-1421
-
-
Chang, G.T.1
Steenbeek, M.2
Schippers, E.3
-
19
-
-
0037082499
-
In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: Implications for mechanisms of pathogenesis
-
Michaud J, Wu F, Osato M, et al. In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis. Blood. 2002;99:1364-1372.
-
(2002)
Blood
, vol.99
, pp. 1364-1372
-
-
Michaud, J.1
Wu, F.2
Osato, M.3
-
20
-
-
0038819114
-
RUNX1 and GATA-1 coexpression and cooperation in megakaryocytic differentiation
-
Elagib KE, Racke FK, Mogass M, Khetawat R, Delehanty LL, Goldfarb AN. RUNX1 and GATA-1 coexpression and cooperation in megakaryocytic differentiation. Blood. 2003;101:4333-4341.
-
(2003)
Blood
, vol.101
, pp. 4333-4341
-
-
Elagib, K.E.1
Racke, F.K.2
Mogass, M.3
Khetawat, R.4
Delehanty, L.L.5
Goldfarb, A.N.6
-
21
-
-
33744458176
-
Physical association of the patient-specific GATA1 mutants with RUNX1 in acute megakaryoblastic leukemia accompanying Down syndrome
-
Xu G, Kanezaki R, Toki T, et al. Physical association of the patient-specific GATA1 mutants with RUNX1 in acute megakaryoblastic leukemia accompanying Down syndrome. Leukemia. 2006;20;1002-1008.
-
(2006)
Leukemia
, vol.20
, pp. 1002-1008
-
-
Xu, G.1
Kanezaki, R.2
Toki, T.3
-
22
-
-
33644916915
-
Increased dosage of the RUNX1/AML1 gene: A third mode of RUNX leukemia?
-
Osato M, Ito Y. Increased dosage of the RUNX1/AML1 gene: a third mode of RUNX leukemia? Crit Rev Eukaryot Gene Expr. 2005;15:217-228.
-
(2005)
Crit Rev Eukaryot Gene Expr
, vol.15
, pp. 217-228
-
-
Osato, M.1
Ito, Y.2
-
23
-
-
3843124232
-
Dimerization: A versatile switch for oncogenesis
-
So CW, Clearly ML. Dimerization: a versatile switch for oncogenesis. Blood. 2004;104:919-922.
-
(2004)
Blood
, vol.104
, pp. 919-922
-
-
CW, S.1
Clearly, M.L.2
-
24
-
-
21144437550
-
AML1-FOG2 fusion protein in myelodysplasia
-
Chan EM, Comer EM, Brown FC, et al. AML1-FOG2 fusion protein in myelodysplasia. Blood. 2005;105:4523-4526.
-
(2005)
Blood
, vol.105
, pp. 4523-4526
-
-
Chan, E.M.1
Comer, E.M.2
Brown, F.C.3
-
25
-
-
33645524703
-
Erythroid inhibition by the leukemic fusion AML1-ETO is associated with impaired acetylation of the major erythroid transcription factor GATA-1
-
Choi Y, Elagib KE, Delehanty LL, Goldfarb AN. Erythroid inhibition by the leukemic fusion AML1-ETO is associated with impaired acetylation of the major erythroid transcription factor GATA-1. Cancer Res. 2006;66:2990-2996.
-
(2006)
Cancer Res
, vol.66
, pp. 2990-2996
-
-
Choi, Y.1
Elagib, K.E.2
Delehanty, L.L.3
Goldfarb, A.N.4
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