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Dual contribution of embryonic ventral blood island and dorsal lateral plate mesoderm during ontogeny of hemopoietic cells in Xenopus laevis
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Para-aortic splanchnopleura from early mouse embryos contains B1a cell progenitors
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Godin I, Dieterlen-Lievre F, Cumano A. Emergence of multipotent hemopoietic cells in the yolk sac and paraaortic splanchnopleura in mouse embryos, beginning at 8.5 days postcoitus. Proc Natl Acad Sci USA. 92:1995;773-777.
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Godin, I.1
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An early pre-liver intraembryonic source of CFU-S in the developing mouse
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0030039864
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Circulation of hematopoietic progenitors in the mouse embryo
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of special interest. An in vitro culture assay is used to assay successive waves of hematopoietic progenitors in the mouse embryo. This work, which is one of the first to examine carefully circulating progenitors in the embryos, complements that of [4].
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Delassus S, Cumano A. Circulation of hematopoietic progenitors in the mouse embryo. of special interest Immunity. 4:1996;97-106 An in vitro culture assay is used to assay successive waves of hematopoietic progenitors in the mouse embryo. This work, which is one of the first to examine carefully circulating progenitors in the embryos, complements that of [4].
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Immunity
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Delassus, S.1
Cumano, A.2
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7
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0028881910
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Intra-embryonic hematopoietic cell migration during vertebrate development
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Detrich HW, Kieran MW, Chan FW, Barone LM, Yee K, Rundstadler JA, Pratt S, Ransom D, Zon LI. Intra-embryonic hematopoietic cell migration during vertebrate development. Proc Natl Acad Sci USA. 92:1995;10713-10717.
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Detrich, H.W.1
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Yee, K.5
Rundstadler, J.A.6
Pratt, S.7
Ransom, D.8
Zon, L.I.9
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8
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0030061554
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AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis
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of outstanding interest. See annotation [9].
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Okuda T, Deursen JV, Hiebert SW, Grosveld G, Downing JR. AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis. of outstanding interest Cell. 84:1996;321-330 See annotation [9].
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Okuda, T.1
Deursen, J.V.2
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Grosveld, G.4
Downing, J.R.5
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9
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0029918597
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Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis
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of outstanding interest. These knockout experiments [8,9] demonstrate a cell-autonomous block to definitive, but not primitive, hematopoiesis in the absence of AML1/Cbfa2. Though this study cannot address the origin of the HSC per se, it clearly illustrates different genetic requirements between primitive and adult hematopoietic progenitors.
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Wang Q, Stacy T, Binder M, Marin-Padilla M, Sharpe AH, Speck NA. Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis. of outstanding interest Proc Natl Acad Sci USA. 93:1996;3444-3449 These knockout experiments [8,9] demonstrate a cell-autonomous block to definitive, but not primitive, hematopoiesis in the absence of AML1/Cbfa2. Though this study cannot address the origin of the HSC per se, it clearly illustrates different genetic requirements between primitive and adult hematopoietic progenitors.
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Proc Natl Acad Sci USA
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Wang, Q.1
Stacy, T.2
Binder, M.3
Marin-Padilla, M.4
Sharpe, A.H.5
Speck, N.A.6
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10
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The gene SCL is expressed during early hematopoiesis and encodes a differentiation-related DNA-binding motif
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Begley CG, Aplan PD, Denning SM, Haynes BF, Waldmann TA, Kirsch IR. The gene SCL is expressed during early hematopoiesis and encodes a differentiation-related DNA-binding motif. Proc Natl Acad Sci USA. 86:1989;10128-10132.
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Begley, C.G.1
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Waldmann, T.A.5
Kirsch, I.R.6
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11
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Tal-1 induces a T cell acute lymphoblastic leukemia-like syndrome that is accelerated by casein kinase lla
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in press
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Kelliher MA, Seldin DC, Leder P. Tal-1 induces a T cell acute lymphoblastic leukemia-like syndrome that is accelerated by casein kinase lla. EMBO J. 1996;. in press.
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EMBO J
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Kelliher, M.A.1
Seldin, D.C.2
Leder, P.3
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12
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0028858855
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Absence of blood formation in mice lacking the T-cell leukemia oncoprotein tal-1/SCL
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Shivdasani R, Mayer E, Orkin SH. Absence of blood formation in mice lacking the T-cell leukemia oncoprotein tal-1/SCL. Nature. 373:1995;432-434.
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Shivdasani, R.1
Mayer, E.2
Orkin, S.H.3
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0029121271
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Absence of yolk sac hematopoiesis from mice with a targeted disruption of the scl gene
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Robb L, Lyons I, Li R, Hartley L, Kontgen F, Harvey RP, Metcalf D, Begley CG. Absence of yolk sac hematopoiesis from mice with a targeted disruption of the scl gene. Proc Natl Acad Sci USA. 92:1995;7075-7079.
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Robb, L.1
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Li, R.3
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Harvey, R.P.6
Metcalf, D.7
Begley, C.G.8
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14
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0030581174
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The T-cell leukemia oncoprotein SCL/tal-1 is essential for development of all hematopoietic lineages
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of outstanding interest. This paper extends previous analysis of the SCL/tal-1 knockout phenotype [12, 13] and establishes a global, cell-autonomous hematopoietic defect. SCL/tal-1 is the first gene shown to be required at the earliest, definable stage of hematopoietic development, yet is dispensable for vascular formation. Rescue of SCL/tal-1 null ES cells by retroviral gene transfer is used to demonstrate that the phenotype relates specifically to SCL/tal-1 loss, rather than an unrelated consequence of gene targeting.
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Porcher C, Swat W, Rockwell K, Fujiwara Y, Alt FW, Orkin SH. The T-cell leukemia oncoprotein SCL/tal-1 is essential for development of all hematopoietic lineages. of outstanding interest Cell. 86:1996;47-57 This paper extends previous analysis of the SCL/tal-1 knockout phenotype [12, 13] and establishes a global, cell-autonomous hematopoietic defect. SCL/tal-1 is the first gene shown to be required at the earliest, definable stage of hematopoietic development, yet is dispensable for vascular formation. Rescue of SCL/tal-1 null ES cells by retroviral gene transfer is used to demonstrate that the phenotype relates specifically to SCL/tal-1 loss, rather than an unrelated consequence of gene targeting.
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Cell
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Porcher, C.1
Swat, W.2
Rockwell, K.3
Fujiwara, Y.4
Alt, F.W.5
Orkin, S.H.6
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Hox genes in vertebrate development
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Krumlauf R. Hox genes in vertebrate development. Cell. 78:1994;191-201.
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Cell
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Krumlauf, R.1
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Lawrence HJ, Largman C. Homeobox genes in normal hematopoiesis and leukemias. Blood. 80:1992;2445-2453.
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Lawrence, H.J.1
Largman, C.2
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0029091845
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Overexpression of HOXB4 in hematopoietic cells causes the selective expansion of more primitive populations in vitro and in vivo
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In this elegant study, the very impressive expansion of progenitors in demonstrated, surprisingly without ostensible effects on more differentiated lineages. These data are the most persuasive in pointing to a role for Hox genes in hematopoiesis.
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Sauvageau G, Thorsteinsdottir U, Eaves CJ, Lawrence HJ, Largman C, Landsorp PM, Humphries RK. Overexpression of HOXB4 in hematopoietic cells causes the selective expansion of more primitive populations in vitro and in vivo. Genes Dev. 9:1995;1753-1765 In this elegant study, the very impressive expansion of progenitors in demonstrated, surprisingly without ostensible effects on more differentiated lineages. These data are the most persuasive in pointing to a role for Hox genes in hematopoiesis.
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Genes Dev
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Sauvageau, G.1
Thorsteinsdottir, U.2
Eaves, C.J.3
Lawrence, H.J.4
Largman, C.5
Landsorp, P.M.6
Humphries, R.K.7
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18
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0029947439
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Overexpression of HOXB4 enhances the hematopoietic potential of embryonic stern cells differentiated in vitro
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Helgason CD, Sauvageau G, Lawrence HJ, Largman C, Humphries RK. Overexpression of HOXB4 enhances the hematopoietic potential of embryonic stern cells differentiated in vitro. Blood. 87:1996;2740-2748.
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Helgason, C.D.1
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Lawrence, H.J.3
Largman, C.4
Humphries, R.K.5
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0027180437
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Conditional immortalization of mouse myelomonocytic, megakaryocytic and mast cell progenitors by the Hox-2.4 homeobox gene
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Perkins AC, Cory S. Conditional immortalization of mouse myelomonocytic, megakaryocytic and mast cell progenitors by the Hox-2.4 homeobox gene. EMBO J. 12:1993;3835-3846.
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Perkins, A.C.1
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Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukemia
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Nakamura T, Largaespada DA, Lee MP, Johnson LA, Ohyashiki K, Toyama K, Chen SJ, Willman CL, Chen I-M, Feinberg AP, et al. Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukemia. Nat Genet. 12:1996;154-158.
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The t(7;11)(p15;p15) translocation in acute myeloid leukemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9
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Borrow J, Shearman AM, Stanton JVP, Becher R, Collins T, Williams AJ, Dube I, Katz F, Kwong YL, Morris C, et al. The t(7;11)(p15;p15) translocation in acute myeloid leukemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9. Nat Genet. 12:1996;159-167.
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Borrow, J.1
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0028869112
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Altered Hox expression and segmental identity in MII-mutant mice
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This paper reveals a role for MII in controlling Hox gene expression and segmental identity, but provides (regrettably) only limited information about hematopoiesis. Blood counts in heterozygous animals are presented but no data are given on effects in null-embryos.
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Yu BD, Hess JL, Horning SE, Brown GAJ, Korsmeyer SJ. Altered Hox expression and segmental identity in MII-mutant mice. Nature. 378:1995;505-508 This paper reveals a role for MII in controlling Hox gene expression and segmental identity, but provides (regrettably) only limited information about hematopoiesis. Blood counts in heterozygous animals are presented but no data are given on effects in null-embryos.
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Nature
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Yu, B.D.1
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23
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Involvement of bone morphogenetic protein-4 (BMP-4) and Vgr-1 in morphogenesis and neurogenesis in the mouse
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Jones CM, Lyons KM, Hogan BLM. Involvement of bone morphogenetic protein-4 (BMP-4) and Vgr-1 in morphogenesis and neurogenesis in the mouse. Development. 111:1991;531-542.
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Jones, C.M.1
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Dale L, Howes G, Price BMJ, Smith JC. Bone morphogenetic protein 4: ventralizing factor in early Xenopus development. Development. 115:1992;573-585.
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Dale, L.1
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0029013039
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Localized BMP-4 mediates dorsal/ventral patterning in the early Xenopus embryo
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0028970392
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Evidence for involvement of activin A and bone morphogenetic protein 4 in mammalian mesoderm and hematopoietic development
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Johnasson BM, Wiles MV. Evidence for involvement of activin A and bone morphogenetic protein 4 in mammalian mesoderm and hematopoietic development. Mol Cell Biol. 15:1995;141-151.
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Johnasson, B.M.1
Wiles, M.V.2
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27
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0029149656
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Bone morphogenetic protein-4 (BMP-4) is required for mesoderm formation and patterning in the mouse
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Winnier G, Blesing M, Labosky PA, Hogan BLM. Bone morphogenetic protein-4 (BMP-4) is required for mesoderm formation and patterning in the mouse. Genes Dev. 9:1995;2105-2116.
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0029740603
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BMP-4-responsive regulation of dorsoventral patterning by the homeobox protein Mix.1
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of outstanding interest. This study illustrates once again the value of expression screens for the identification of genes regulating pattern formation in Xenopus embryos. By tailoring such screens, if should be possible to isolate an array of genes whose products influence pattern information or hematopoiesis.
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Mead PE, Brivanlou IH, Kelley CM, Zon LI. BMP-4-responsive regulation of dorsoventral patterning by the homeobox protein Mix.1. of outstanding interest Nature. 382:1996;357-360 This study illustrates once again the value of expression screens for the identification of genes regulating pattern formation in Xenopus embryos. By tailoring such screens, if should be possible to isolate an array of genes whose products influence pattern information or hematopoiesis.
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Nature
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Mead, P.E.1
Brivanlou, I.H.2
Kelley, C.M.3
Zon, L.I.4
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29
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0029066359
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GATA-1 reprograms avian myelomonocytic cells into eosinophils, thromboblasts and erythroblasts
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of outstanding interest. This is the most definitive study showing the competence of GATA-1 to alter the lineage phenotype of hematopoietic cells. The dose-dependence of lineage on GATA-1 expression is provocative but unexplained.
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Kulessa H, Frampton J, Graf T. GATA-1 reprograms avian myelomonocytic cells into eosinophils, thromboblasts and erythroblasts. of outstanding interest Genes Dev. 9:1995;1250-1262 This is the most definitive study showing the competence of GATA-1 to alter the lineage phenotype of hematopoietic cells. The dose-dependence of lineage on GATA-1 expression is provocative but unexplained.
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Genes Dev
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Kulessa, H.1
Frampton, J.2
Graf, T.3
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GATA-1 but not SCL induces megakaryocytic differentiation in an early myeloid line
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Visvader JE, Elefanty AG, Strasser A, Adams JM. GATA-1 but not SCL induces megakaryocytic differentiation in an early myeloid line. EMBO J. 11:1992;4557-4564.
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Visvader, J.E.1
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Strasser, A.3
Adams, J.M.4
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0028963735
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Functional synergy and physical interactions of the erythroid transcription factor GATA-1 and Krüppel family proteins, Sp1 and EKLF
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Merika M, Orkin SH. Functional synergy and physical interactions of the erythroid transcription factor GATA-1 and Krüppel family proteins, Sp1 and EKLF. Mol Cell Biol. 15:1995;2437-2447.
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Association of erythroid transcription factors: Complexes involving the LIM protein RBTN2 and the zinc-finger protein GATA1
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Osada H, Grutz G, Axelson H, Forster A, Rabbitts TH. Association of erythroid transcription factors: complexes involving the LIM protein RBTN2 and the zinc-finger protein GATA1. Proc Natl Acad Sci USA. 92:1995;9585-9589.
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Osada, H.1
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Self-association of the erythroid transcription factor GATA-1 mediated by its zinc-finger domains
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Orkin, S.H.3
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NF-M (chicken C/EBPβ) induces eosinophilic differentiation and apoptosis in a hematopoietic progenitor cell line
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Muller C, Kowenz-Leutz E, Grieser-Ade S, Graf T, Leutz A. NF-M (chicken C/EBPβ) induces eosinophilic differentiation and apoptosis in a hematopoietic progenitor cell line. EMBO J. 14:1995;6127-6135.
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Muller, C.1
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Graf, T.4
Leutz, A.5
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0029010475
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V-Myb DNA binding is required to block thrombocytic differentiation of Myb-Ets-transformed multipotent haematopoietic progenitors
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Frampton J, McNagny K, Sieweke M, Philip A, Smith G, Graf T. v-Myb DNA binding is required to block thrombocytic differentiation of Myb-Ets-transformed multipotent haematopoietic progenitors. EMBO J. 14:1995;2866-2875.
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Graf, T.6
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36
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0029870839
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MafB is an interaction partner and repressor of Ets-1 that inhibits erythroid differentiation
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of outstanding interest. In this study, a one-hybrid screening of cDNA in yeast with the ets-1 DNA- binding domain yielded mafB, an AP-1 superfamily members, that appears rather restricted (within the hematopoietic system) to myeloid cells. The data illustrate how protein interactions might function to turn off differentiation along a given pathway (e.g. erythroid).
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Sieweke MH, Tekotte H, Frampton J, Graf T. MafB is an interaction partner and repressor of Ets-1 that inhibits erythroid differentiation. of outstanding interest Cell. 84:1996;49-60 In this study, a one-hybrid screening of cDNA in yeast with the ets-1 DNA- binding domain yielded mafB, an AP-1 superfamily members, that appears rather restricted (within the hematopoietic system) to myeloid cells. The data illustrate how protein interactions might function to turn off differentiation along a given pathway (e.g. erythroid).
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Cell
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Sieweke, M.H.1
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Frampton, J.3
Graf, T.4
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Suppression of apoptosis allows differentiation and development of a multipotent hemopoietic cell line in the absence of added growth factors
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Wu H, Liu X, Jaenisch R, Lodish HF. Generation of committed erythroid BFU-E and CFU-E progenitors does not require erythropoietin or the erythropoietin receptor. Cell. 83:1995;59-67.
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