-
1
-
-
84867280730
-
Combinatorial regulation of tissue specification by GATA and FOG factors
-
Chlon TM, Crispino JD. Combinatorial regulation of tissue specification by GATA and FOG factors. Development. 2012;139(21):3905-3916.
-
(2012)
Development
, vol.139
, Issue.21
, pp. 3905-3916
-
-
Chlon, T.M.1
Crispino, J.D.2
-
2
-
-
84863649033
-
Master regulatory GATA transcription factors: Mechanistic principles and emerging links to hematologic malignancies
-
Bresnick EH, Katsumura KR, Lee HY, Johnson KD, Perkins AS. Master regulatory GATA transcription factors: Mechanistic principles and emerging links to hematologic malignancies. Nucleic Acids Res. 2012;40(13):5819-5831.
-
(2012)
Nucleic Acids Res
, vol.40
, Issue.13
, pp. 5819-5831
-
-
Bresnick, E.H.1
Katsumura, K.R.2
Lee, H.Y.3
Johnson, K.D.4
Perkins, A.S.5
-
3
-
-
84903175117
-
Erythro-megakaryocytic transcription factors associated with hereditary anemia
-
Crispino JD, Weiss MJ. Erythro-megakaryocytic transcription factors associated with hereditary anemia. Blood. 2014;123(20):3080-3088.
-
(2014)
Blood
, vol.123
, Issue.20
, pp. 3080-3088
-
-
Crispino, J.D.1
Weiss, M.J.2
-
4
-
-
0036727413
-
Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome
-
Wechsler J, Greene M, McDevitt MA, et al. Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome. Nat Genet. 2002;32(1):148-152.
-
(2002)
Nat Genet
, vol.32
, Issue.1
, pp. 148-152
-
-
Wechsler, J.1
Greene, M.2
McDevitt, M.A.3
-
5
-
-
0038142390
-
Mutagenesis of GATA1 is an initiating event in Down syndrome leukemogenesis
-
Mundschau G, Gurbuxani S, Gamis AS, Greene ME, Arceci RJ, Crispino JD. Mutagenesis of GATA1 is an initiating event in Down syndrome leukemogenesis. Blood. 2003;101(11): 4298-4300.
-
(2003)
Blood
, vol.101
, Issue.11
, pp. 4298-4300
-
-
Mundschau, G.1
Gurbuxani, S.2
Gamis, A.S.3
Greene, M.E.4
Arceci, R.J.5
Crispino, J.D.6
-
6
-
-
84926408535
-
Haematopoietic and immune defects associated with GATA2 mutation
-
Collin M, Dickinson R, Bigley V. Haematopoietic and immune defects associated with GATA2 mutation. Br J Haematol. 2015;169(2):173-187.
-
(2015)
Br J Haematol
, vol.169
, Issue.2
, pp. 173-187
-
-
Collin, M.1
Dickinson, R.2
Bigley, V.3
-
7
-
-
79961074298
-
Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome
-
Hsu AP, Sampaio EP, Khan J, et al. Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome. Blood. 2011;118(10):2653-2655.
-
(2011)
Blood
, vol.118
, Issue.10
, pp. 2653-2655
-
-
Hsu, A.P.1
Sampaio, E.P.2
Khan, J.3
-
8
-
-
84888219405
-
Clinical and biological implications of driver mutations in myelodysplastic syndromes
-
Chronic Myeloid Disorders Working Group of the International Cancer Genome Consortium.
-
Papaemmanuil E, Gerstung M, Malcovati L, et al; Chronic Myeloid Disorders Working Group of the International Cancer Genome Consortium. Clinical and biological implications of driver mutations in myelodysplastic syndromes. Blood. 2013; 122(22):3616-3627.
-
(2013)
Blood
, vol.122
, Issue.22
, pp. 3616-3627
-
-
Papaemmanuil, E.1
Gerstung, M.2
Malcovati, L.3
-
9
-
-
79953176952
-
Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia
-
Yan XJ, Xu J, Gu ZH, et al. Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia. Nat Genet. 2011;43(4): 309-315
-
(2011)
Nat Genet
, vol.43
, Issue.4
, pp. 309-315
-
-
Yan, X.J.1
Xu, J.2
Gu, Z.H.3
-
10
-
-
84889588564
-
Mutations of the GATA2 and CEBPA genes in paediatric acute myeloid leukaemia
-
Shiba N, Funato M, Ohki K, et al. Mutations of the GATA2 and CEBPA genes in paediatric acute myeloid leukaemia. Br J Haematol. 2014; 164(1):142-145.
-
(2014)
Br J Haematol
, vol.164
, Issue.1
, pp. 142-145
-
-
Shiba, N.1
Funato, M.2
Ohki, K.3
-
11
-
-
41149169150
-
Gain-offunction mutation of GATA-2 in acute myeloid transformation of chronic myeloid leukemia
-
Zhang SJ, Ma LY, Huang QH, et al. Gain-offunction mutation of GATA-2 in acute myeloid transformation of chronic myeloid leukemia. Proc Natl Acad Sci USA. 2008;105(6):2076-2081.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, Issue.6
, pp. 2076-2081
-
-
Zhang, S.J.1
Ma, L.Y.2
Huang, Q.H.3
-
12
-
-
84879414890
-
GATA-3 controls the maintenance and proliferation of T cells downstream of TCR and cytokine signaling
-
Wang Y, Misumi I, Gu AD, et al. GATA-3 controls the maintenance and proliferation of T cells downstream of TCR and cytokine signaling. Nat Immunol. 2013;14(7):714-722.
-
(2013)
Nat Immunol
, vol.14
, Issue.7
, pp. 714-722
-
-
Wang, Y.1
Misumi, I.2
Gu, A.D.3
-
13
-
-
0034721115
-
GATA3 haplo-insufficiency causes human HDR syndrome
-
Van Esch H, Groenen P, Nesbit MA, et al. GATA3 haplo-insufficiency causes human HDR syndrome. Nature. 2000;406(6794):419-422.
-
(2000)
Nature
, vol.406
, Issue.6794
, pp. 419-422
-
-
Van Esch, H.1
Groenen, P.2
Nesbit, M.A.3
-
14
-
-
84974633247
-
A microscopic landscape of the invasive breast cancer genome
-
Ping Z, Xia Y, Shen T, et al. A microscopic landscape of the invasive breast cancer genome. Sci Rep. 2016;6:27545.
-
(2016)
Sci Rep
, vol.6
, pp. 27545
-
-
Ping, Z.1
Xia, Y.2
Shen, T.3
-
15
-
-
84888311432
-
Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse
-
Perez-Andreu V, Roberts KG, Harvey RC, et al. Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse. Nat Genet. 2013;45(12): 1494-1498.
-
(2013)
Nat Genet
, vol.45
, Issue.12
, pp. 1494-1498
-
-
Perez-Andreu, V.1
Roberts, K.G.2
Harvey, R.C.3
-
16
-
-
12344287006
-
The roles of GATA-4, -5 and -6 in vertebrate heart development
-
Peterkin T, Gibson A, Loose M, Patient R. The roles of GATA-4, -5 and -6 in vertebrate heart development. Semin Cell Dev Biol. 2005;16(1): 83-94.
-
(2005)
Semin Cell Dev Biol
, vol.16
, Issue.1
, pp. 83-94
-
-
Peterkin, T.1
Gibson, A.2
Loose, M.3
Patient, R.4
-
17
-
-
84867274607
-
An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects
-
Ackerman C, Locke AE, Feingold E, et al. An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects. Am J Hum Genet. 2012;91(4):646-659.
-
(2012)
Am J Hum Genet
, vol.91
, Issue.4
, pp. 646-659
-
-
Ackerman, C.1
Locke, A.E.2
Feingold, E.3
-
18
-
-
0345184762
-
An erythrocyte-specific DNA-binding factor recognizes a regulatory sequence common to all chicken globin genes
-
Evans T, Reitman M, Felsenfeld G. An erythrocyte-specific DNA-binding factor recognizes a regulatory sequence common to all chicken globin genes. Proc Natl Acad Sci USA. 1988;85(16):5976-5980.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, Issue.16
, pp. 5976-5980
-
-
Evans, T.1
Reitman, M.2
Felsenfeld, G.3
-
19
-
-
0024560650
-
Increased gammaglobin expression in a nondeletion HPFH mediated by an erythroid-specific DNA-binding factor
-
Martin DI, Tsai SF, Orkin SH. Increased gammaglobin expression in a nondeletion HPFH mediated by an erythroid-specific DNA-binding factor. Nature. 1989;338(6214):435-438.
-
(1989)
Nature
, vol.338
, Issue.6214
, pp. 435-438
-
-
Martin, D.I.1
Tsai, S.F.2
Orkin, S.H.3
-
20
-
-
0024080427
-
The human betaglobin gene 39 enhancer contains multiple binding sites for an erythroid-specific protein
-
Wall L, deBoer E, Grosveld F. The human betaglobin gene 39 enhancer contains multiple binding sites for an erythroid-specific protein. Genes Dev. 1988;2(9):1089-1100.
-
(1988)
Genes Dev
, vol.2
, Issue.9
, pp. 1089-1100
-
-
Wall, L.1
DeBoer, E.2
Grosveld, F.3
-
21
-
-
0029863093
-
A palindromic regulatory site within vertebrate GATA-1 promoters requires both zinc fingers of the GATA-1 DNA-binding domain for high-affinity interaction
-
Trainor CD, Omichinski JG, Vandergon TL, Gronenborn AM, Clore GM, Felsenfeld G. A palindromic regulatory site within vertebrate GATA-1 promoters requires both zinc fingers of the GATA-1 DNA-binding domain for high-affinity interaction. Mol Cell Biol. 1996;16(5):2238-2247.
-
(1996)
Mol Cell Biol
, vol.16
, Issue.5
, pp. 2238-2247
-
-
Trainor, C.D.1
Omichinski, J.G.2
Vandergon, T.L.3
Gronenborn, A.M.4
Clore, G.M.5
Felsenfeld, G.6
-
22
-
-
0031472234
-
FOG, a multitype zinc finger protein, acts as a cofactor for transcription factor GATA-1 in erythroid and megakaryocytic differentiation
-
Tsang AP, Visvader JE, Turner CA, et al. FOG, a multitype zinc finger protein, acts as a cofactor for transcription factor GATA-1 in erythroid and megakaryocytic differentiation. Cell. 1997;90(1): 109-119.
-
(1997)
Cell
, vol.90
, Issue.1
, pp. 109-119
-
-
Tsang, A.P.1
Visvader, J.E.2
Turner, C.A.3
-
23
-
-
0025203886
-
Transcriptional activation and DNA binding by the erythroid factor GF-1/NF-E1/Eryf 1
-
Martin DI, Orkin SH. Transcriptional activation and DNA binding by the erythroid factor GF-1/NF-E1/Eryf 1. Genes Dev. 1990;4(11): 1886-1898.
-
(1990)
Genes Dev
, vol.4
, Issue.11
, pp. 1886-1898
-
-
Martin, D.I.1
Orkin, S.H.2
-
24
-
-
0029926485
-
Arrested development of embryonic red cell precursors in mouse embryos lacking transcription factor GATA-1
-
Fujiwara Y, Browne CP, Cunniff K, Goff SC, Orkin SH. Arrested development of embryonic red cell precursors in mouse embryos lacking transcription factor GATA-1. Proc Natl Acad Sci USA. 1996;93(22):12355-12358.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, Issue.22
, pp. 12355-12358
-
-
Fujiwara, Y.1
Browne, C.P.2
Cunniff, K.3
Goff, S.C.4
Orkin, S.H.5
-
25
-
-
0028800317
-
Transcription factor GATA- 1 permits survival and maturation of erythroid precursors by preventing apoptosis
-
Weiss MJ, Orkin SH. Transcription factor GATA- 1 permits survival and maturation of erythroid precursors by preventing apoptosis. Proc Natl Acad Sci USA. 1995;92(21):9623-9627.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, Issue.21
, pp. 9623-9627
-
-
Weiss, M.J.1
Orkin, S.H.2
-
26
-
-
0033168769
-
GATA-1 and erythropoietin cooperate to promote erythroid cell survival by regulating bcl-xL expression
-
Gregory T, Yu C, Ma A, Orkin SH, Blobel GA, Weiss MJ. GATA-1 and erythropoietin cooperate to promote erythroid cell survival by regulating bcl-xL expression. Blood. 1999;94(1):87-96.
-
(1999)
Blood
, vol.94
, Issue.1
, pp. 87-96
-
-
Gregory, T.1
Yu, C.2
Ma, A.3
Orkin, S.H.4
Blobel, G.A.5
Weiss, M.J.6
-
27
-
-
43249086780
-
Ablation of Gata1 in adult mice results in aplastic crisis, revealing its essential role in steady-state and stress erythropoiesis
-
Gutiérrez L, Tsukamoto S, Suzuki M, et al. Ablation of Gata1 in adult mice results in aplastic crisis, revealing its essential role in steady-state and stress erythropoiesis. Blood. 2008;111(8): 4375-4385.
-
(2008)
Blood
, vol.111
, Issue.8
, pp. 4375-4385
-
-
Gutiérrez, L.1
Tsukamoto, S.2
Suzuki, M.3
-
28
-
-
0030963918
-
A "knockdown" mutation created by cis-element gene targeting reveals the dependence of erythroid cell maturation on the level of transcription factor GATA-1
-
McDevitt MA, Shivdasani RA, Fujiwara Y, Yang H, Orkin SHA. A "knockdown" mutation created by cis-element gene targeting reveals the dependence of erythroid cell maturation on the level of transcription factor GATA-1. Proc Natl Acad Sci USA. 1997;94(13):6781-6785.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, Issue.13
, pp. 6781-6785
-
-
McDevitt, M.A.1
Shivdasani, R.A.2
Fujiwara, Y.3
Yang, H.4
Orkin, S.H.A.5
-
29
-
-
0030926006
-
A lineage-selective knockout establishes the critical role of transcription factor GATA-1 in megakaryocyte growth and platelet development
-
Shivdasani RA, Fujiwara Y, McDevitt MA, Orkin SH. A lineage-selective knockout establishes the critical role of transcription factor GATA-1 in megakaryocyte growth and platelet development. EMBO J. 1997;16(13):3965-3973.
-
(1997)
EMBO J
, vol.16
, Issue.13
, pp. 3965-3973
-
-
Shivdasani, R.A.1
Fujiwara, Y.2
McDevitt, M.A.3
Orkin, S.H.4
-
30
-
-
0033134831
-
Consequences of GATA-1 deficiency in megakaryocytes and platelets
-
Vyas P, Ault K, Jackson CW, Orkin SH, Shivdasani RA. Consequences of GATA-1 deficiency in megakaryocytes and platelets. Blood. 1999;93(9):2867-2875.
-
(1999)
Blood
, vol.93
, Issue.9
, pp. 2867-2875
-
-
Vyas, P.1
Ault, K.2
Jackson, C.W.3
Orkin, S.H.4
Shivdasani, R.A.5
-
31
-
-
23044499360
-
Differential requirements for the activation domain and FOG-interaction surface of GATA-1 in megakaryocyte gene expression and development
-
Muntean AG, Crispino JD. Differential requirements for the activation domain and FOG-interaction surface of GATA-1 in megakaryocyte gene expression and development. Blood. 2005;106(4):1223-1231.
-
(2005)
Blood
, vol.106
, Issue.4
, pp. 1223-1231
-
-
Muntean, A.G.1
Crispino, J.D.2
-
32
-
-
25444497962
-
GATA1-mediated megakaryocyte differentiation and growth control can be uncoupled and mapped to different domains in GATA1
-
Kuhl C, Atzberger A, Iborra F, Nieswandt B, Porcher C, Vyas P. GATA1-mediated megakaryocyte differentiation and growth control can be uncoupled and mapped to different domains in GATA1. Mol Cell Biol. 2005;25(19): 8592-8606.
-
(2005)
Mol Cell Biol
, vol.25
, Issue.19
, pp. 8592-8606
-
-
Kuhl, C.1
Atzberger, A.2
Iborra, F.3
Nieswandt, B.4
Porcher, C.5
Vyas, P.6
-
33
-
-
0037415557
-
GATA-1 as a regulator of mast cell differentiation revealed by the phenotype of the GATA-1low mouse mutant
-
Migliaccio AR, Rana RA, Sanchez M, et al. GATA-1 as a regulator of mast cell differentiation revealed by the phenotype of the GATA-1low mouse mutant. J Exp Med. 2003;197(3): 281-296.
-
(2003)
J Exp Med
, vol.197
, Issue.3
, pp. 281-296
-
-
Migliaccio, A.R.1
Rana, R.A.2
Sanchez, M.3
-
34
-
-
0037013924
-
Targeted deletion of a high-affinity GATA-binding site in the GATA-1 promoter leads to selective loss of the eosinophil lineage in vivo
-
Yu C, Cantor AB, Yang H, et al. Targeted deletion of a high-affinity GATA-binding site in the GATA-1 promoter leads to selective loss of the eosinophil lineage in vivo. J Exp Med. 2002; 195(11):1387-1395.
-
(2002)
J Exp Med
, vol.195
, Issue.11
, pp. 1387-1395
-
-
Yu, C.1
Cantor, A.B.2
Yang, H.3
-
35
-
-
0037013877
-
Essential and instructive roles of GATA factors in eosinophil development
-
Hirasawa R, Shimizu R, Takahashi S, et al. Essential and instructive roles of GATA factors in eosinophil development. J Exp Med. 2002; 195(11):1379-1386.
-
(2002)
J Exp Med
, vol.195
, Issue.11
, pp. 1379-1386
-
-
Hirasawa, R.1
Shimizu, R.2
Takahashi, S.3
-
36
-
-
84887436574
-
GATA-1 regulates the generation and function of basophils
-
Nei Y, Obata-Ninomiya K, Tsutsui H, et al. GATA-1 regulates the generation and function of basophils. Proc Natl Acad Sci USA. 2013; 110(46):18620-18625.
-
(2013)
Proc Natl Acad Sci USA
, vol.110
, Issue.46
, pp. 18620-18625
-
-
Nei, Y.1
Obata-Ninomiya, K.2
Tsutsui, H.3
-
37
-
-
77952906744
-
Dynamic regulation of Gata1 expression during the maturation of conventional dendritic cells
-
Kozma GT, Martelli F, Verrucci M, et al. Dynamic regulation of Gata1 expression during the maturation of conventional dendritic cells. Exp Hematol. 2010;38(6):489-503.e1.
-
(2010)
Exp Hematol
, vol.38
, Issue.6
, pp. 489e1
-
-
Kozma, G.T.1
Martelli, F.2
Verrucci, M.3
-
38
-
-
0032522474
-
Failure of megakaryopoiesis and arrested erythropoiesis in mice lacking the GATA-1 transcriptional cofactor FOG
-
Tsang AP, Fujiwara Y, Hom DB, Orkin SH. Failure of megakaryopoiesis and arrested erythropoiesis in mice lacking the GATA-1 transcriptional cofactor FOG. Genes Dev. 1998; 12(8):1176-1188.
-
(1998)
Genes Dev
, vol.12
, Issue.8
, pp. 1176-1188
-
-
Tsang, A.P.1
Fujiwara, Y.2
Hom, D.B.3
Orkin, S.H.4
-
39
-
-
0037047059
-
GATAfactor dependence of the multitype zinc-finger protein FOG-1 for its essential role in megakaryopoiesis
-
Chang AN, Cantor AB, Fujiwara Y, et al. GATAfactor dependence of the multitype zinc-finger protein FOG-1 for its essential role in megakaryopoiesis. Proc Natl Acad Sci USA. 2002;99(14):9237-9242.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, Issue.14
, pp. 9237-9242
-
-
Chang, A.N.1
Cantor, A.B.2
Fujiwara, Y.3
-
40
-
-
0034052854
-
Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1
-
Nichols KE, Crispino JD, Poncz M, et al. Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1. Nat Genet. 2000;24(3):266-270.
-
(2000)
Nat Genet
, vol.24
, Issue.3
, pp. 266-270
-
-
Nichols, K.E.1
Crispino, J.D.2
Poncz, M.3
-
41
-
-
0035525746
-
X-linked thrombocytopenia caused by a novel mutation of GATA-1
-
Mehaffey MG, Newton AL, Gandhi MJ, Crossley M, Drachman JG. X-linked thrombocytopenia caused by a novel mutation of GATA-1. Blood. 2001;98(9):2681-2688.
-
(2001)
Blood
, vol.98
, Issue.9
, pp. 2681-2688
-
-
Mehaffey, M.G.1
Newton, A.L.2
Gandhi, M.J.3
Crossley, M.4
Drachman, J.G.5
-
42
-
-
0035412362
-
Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation
-
Freson K, Devriendt K, Matthijs G, et al. Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation. Blood. 2001;98(1):85-92.
-
(2001)
Blood
, vol.98
, Issue.1
, pp. 85-92
-
-
Freson, K.1
Devriendt, K.2
Matthijs, G.3
-
43
-
-
0037081819
-
Different substitutions at residue D218 of the X-linked transcription factor GATA1 lead to altered clinical severity of macrothrombocytopenia and anemia and are associated with variable skewed X inactivation
-
Freson K, Matthijs G, Thys C, et al. Different substitutions at residue D218 of the X-linked transcription factor GATA1 lead to altered clinical severity of macrothrombocytopenia and anemia and are associated with variable skewed X inactivation. Hum Mol Genet. 2002;11(2):147-152.
-
(2002)
Hum Mol Genet
, vol.11
, Issue.2
, pp. 147-152
-
-
Freson, K.1
Matthijs, G.2
Thys, C.3
-
44
-
-
0037105495
-
X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction
-
Yu C, Niakan KK, Matsushita M, Stamatoyannopoulos G, Orkin SH, Raskind WH. X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction. Blood. 2002;100(6):2040-2045.
-
(2002)
Blood
, vol.100
, Issue.6
, pp. 2040-2045
-
-
Yu, C.1
Niakan, K.K.2
Matsushita, M.3
Stamatoyannopoulos, G.4
Orkin, S.H.5
Raskind, W.H.6
-
45
-
-
1642434012
-
Effects of the R216Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesis
-
Balduini CL, Pecci A, Loffredo G, et al. Effects of the R216Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesis. Thromb Haemost. 2004;91(1):129-140.
-
(2004)
Thromb Haemost
, vol.91
, Issue.1
, pp. 129-140
-
-
Balduini, C.L.1
Pecci, A.2
Loffredo, G.3
-
46
-
-
33947223723
-
Congenital erythropoietic porphyria due to a mutation in GATA1: The first trans-acting mutation causative for a human porphyria
-
Phillips JD, Steensma DP, Pulsipher MA, Spangrude GJ, Kushner JP. Congenital erythropoietic porphyria due to a mutation in GATA1: The first trans-acting mutation causative for a human porphyria. Blood. 2007;109(6): 2618-2621.
-
(2007)
Blood
, vol.109
, Issue.6
, pp. 2618-2621
-
-
Phillips, J.D.1
Steensma, D.P.2
Pulsipher, M.A.3
Spangrude, G.J.4
Kushner, J.P.5
-
47
-
-
34147165665
-
X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation
-
Tubman VN, Levine JE, Campagna DR, et al. X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation. Blood. 2007; 109(8):3297-3299.
-
(2007)
Blood
, vol.109
, Issue.8
, pp. 3297-3299
-
-
Tubman, V.N.1
Levine, J.E.2
Campagna, D.R.3
-
48
-
-
33745579586
-
An inherited mutation leading to production of only the short isoform of GATA-1 is associated with impaired erythropoiesis
-
Hollanda LM, Lima CS, Cunha AF, et al. An inherited mutation leading to production of only the short isoform of GATA-1 is associated with impaired erythropoiesis. Nat Genet. 2006;38(7): 807-812.
-
(2006)
Nat Genet
, vol.38
, Issue.7
, pp. 807-812
-
-
Hollanda, L.M.1
Lima, C.S.2
Cunha, A.F.3
-
49
-
-
0029558618
-
Alternative translation initiation site usage results in two functionally distinct forms of the GATA-1 transcription factor
-
Calligaris R, Bottardi S, Cogoi S, Apezteguia I, Santoro C. Alternative translation initiation site usage results in two functionally distinct forms of the GATA-1 transcription factor. Proc Natl Acad Sci USA. 1995;92(25):11598-11602.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, Issue.25
, pp. 11598-11602
-
-
Calligaris, R.1
Bottardi, S.2
Cogoi, S.3
Apezteguia, I.4
Santoro, C.5
-
50
-
-
0032907438
-
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia
-
Draptchinskaia N, Gustavsson P, Andersson B, et al. The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia. Nat Genet. 1999;21(2):169-175.
-
(1999)
Nat Genet
, vol.21
, Issue.2
, pp. 169-175
-
-
Draptchinskaia, N.1
Gustavsson, P.2
Andersson, B.3
-
51
-
-
77951431225
-
Ribosomopathies: Human disorders of ribosome dysfunction
-
Narla A, Ebert BL. Ribosomopathies: Human disorders of ribosome dysfunction. Blood. 2010; 115(16):3196-3205.
-
(2010)
Blood
, vol.115
, Issue.16
, pp. 3196-3205
-
-
Narla, A.1
Ebert, B.L.2
-
52
-
-
84863554398
-
Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia
-
Sankaran VG, Ghazvinian R, Do R, et al. Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia. J Clin Invest. 2012;122(7):2439-2443.
-
(2012)
J Clin Invest
, vol.122
, Issue.7
, pp. 2439-2443
-
-
Sankaran, V.G.1
Ghazvinian, R.2
Do, R.3
-
53
-
-
84904021040
-
Altered translation of GATA1 in Diamond-Blackfan anemia
-
Ludwig LS, Gazda HT, Eng JC, et al. Altered translation of GATA1 in Diamond-Blackfan anemia. Nat Med. 2014;20(7):748-753.
-
(2014)
Nat Med
, vol.20
, Issue.7
, pp. 748-753
-
-
Ludwig, L.S.1
Gazda, H.T.2
Eng, J.C.3
-
54
-
-
84899666581
-
Loss of GATA-1 full length as a cause of Diamond- Blackfan anemia phenotype
-
Parrella S, Aspesi A, Quarello P, et al. Loss of GATA-1 full length as a cause of Diamond- Blackfan anemia phenotype. Pediatr Blood Cancer. 2014;61(7):1319-1321.
-
(2014)
Pediatr Blood Cancer
, vol.61
, Issue.7
, pp. 1319-1321
-
-
Parrella, S.1
Aspesi, A.2
Quarello, P.3
-
55
-
-
0035903475
-
In vivo requirements for GATA-1 functional domains during primitive and definitive erythropoiesis
-
Shimizu R, Takahashi S, Ohneda K, Engel JD, Yamamoto M. In vivo requirements for GATA-1 functional domains during primitive and definitive erythropoiesis. EMBO J. 2001;20(18): 5250-5260.
-
(2001)
EMBO J
, vol.20
, Issue.18
, pp. 5250-5260
-
-
Shimizu, R.1
Takahashi, S.2
Ohneda, K.3
Engel, J.D.4
Yamamoto, M.5
-
57
-
-
11144242549
-
Origins of leukaemia in children with Down syndrome
-
Hitzler JK, Zipursky A. Origins of leukaemia in children with Down syndrome. Nat Rev Cancer. 2005;5(1):11-20.
-
(2005)
Nat Rev Cancer
, vol.5
, Issue.1
, pp. 11-20
-
-
Hitzler, J.K.1
Zipursky, A.2
-
58
-
-
33745076542
-
A prospective study of the natural history of transient leukemia (TL) in neonates with Down syndrome (DS): Children's Oncology Group (COG) study POG-9481
-
Children's Oncology Group (COG).
-
Massey GV, Zipursky A, Chang MN, et al; Children's Oncology Group (COG). A prospective study of the natural history of transient leukemia (TL) in neonates with Down syndrome (DS): Children's Oncology Group (COG) study POG-9481. Blood. 2006;107(12): 4606-4613.
-
(2006)
Blood
, vol.107
, Issue.12
, pp. 4606-4613
-
-
Massey, G.V.1
Zipursky, A.2
Chang, M.N.3
-
59
-
-
84255176504
-
Natural history of transient myeloproliferative disorder clinically diagnosed in Down syndrome neonates: A report from the Children's Oncology Group Study A2971
-
quiz 6996
-
Gamis AS, Alonzo TA, Gerbing RB, et al. Natural history of transient myeloproliferative disorder clinically diagnosed in Down syndrome neonates: A report from the Children's Oncology Group Study A2971. Blood. 2011;118(26): 6752-6759, quiz 6996.
-
(2011)
Blood
, vol.118
, Issue.26
, pp. 6752-6759
-
-
Gamis, A.S.1
Alonzo, T.A.2
Gerbing, R.B.3
-
60
-
-
84940024502
-
The biology of pediatric acute megakaryoblastic leukemia
-
Gruber TA, Downing JR. The biology of pediatric acute megakaryoblastic leukemia. Blood. 2015; 126(8):943-949.
-
(2015)
Blood
, vol.126
, Issue.8
, pp. 943-949
-
-
Gruber, T.A.1
Downing, J.R.2
-
61
-
-
3042636440
-
Microarray transcript profiling distinguishes the transient from the acute type of megakaryoblastic leukaemia (M7) in Down's syndrome, revealing PRAME as a specific discriminating marker
-
McElwaine S, Mulligan C, Groet J, et al. Microarray transcript profiling distinguishes the transient from the acute type of megakaryoblastic leukaemia (M7) in Down's syndrome, revealing PRAME as a specific discriminating marker. Br J Haematol. 2004; 125(6):729-742.
-
(2004)
Br J Haematol
, vol.125
, Issue.6
, pp. 729-742
-
-
McElwaine, S.1
Mulligan, C.2
Groet, J.3
-
62
-
-
0042243593
-
Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21
-
Rainis L, Bercovich D, Strehl S, et al. Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21. Blood. 2003;102(3):981-986.
-
(2003)
Blood
, vol.102
, Issue.3
, pp. 981-986
-
-
Rainis, L.1
Bercovich, D.2
Strehl, S.3
-
63
-
-
84902119138
-
GATA1s induces hyperproliferation of eosinophil precursors in Down syndrome transient leukemia
-
Maroz A, Stachorski L, Emmrich S, et al. GATA1s induces hyperproliferation of eosinophil precursors in Down syndrome transient leukemia. Leukemia. 2014;28(6):1259-1270.
-
(2014)
Leukemia
, vol.28
, Issue.6
, pp. 1259-1270
-
-
Maroz, A.1
Stachorski, L.2
Emmrich, S.3
-
64
-
-
84891061196
-
GATA1-mutant clones are frequent and often unsuspected in babies with Down syndrome: Identification of a population at risk of leukemia
-
Oxford- Imperial Down Syndrome Cohort Study Group.
-
Roberts I, Alford K, Hall G, et al; Oxford- Imperial Down Syndrome Cohort Study Group. GATA1-mutant clones are frequent and often unsuspected in babies with Down syndrome: Identification of a population at risk of leukemia. Blood. 2013;122(24):3908-3917.
-
(2013)
Blood
, vol.122
, Issue.24
, pp. 3908-3917
-
-
Roberts, I.1
Alford, K.2
Hall, G.3
-
65
-
-
84870256595
-
Characterization of novel genomic alterations and therapeutic approaches using acute megakaryoblastic leukemia xenograft models
-
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(11):2017-2031.
-
(2012)
J Exp Med
, vol.209
, Issue.11
, pp. 2017-2031
-
-
Thiollier, C.1
Lopez, C.K.2
Gerby, B.3
-
67
-
-
84942279812
-
Heterogeneous cytogenetic subgroups and outcomes in childhood acute megakaryoblastic leukemia: A retrospective international study
-
Inaba H, Zhou Y, Abla O, et al. Heterogeneous cytogenetic subgroups and outcomes in childhood acute megakaryoblastic leukemia: A retrospective international study. Blood. 2015;126(13):1575-1584.
-
(2015)
Blood
, vol.126
, Issue.13
, pp. 1575-1584
-
-
Inaba, H.1
Zhou, Y.2
Abla, O.3
-
68
-
-
0034307375
-
Acute megakaryocytic leukemia: The Eastern Cooperative Oncology Group experience
-
Tallman MS, Neuberg D, Bennett JM, et al. Acute megakaryocytic leukemia: The Eastern Cooperative Oncology Group experience. Blood. 2000;96(7):2405-2411.
-
(2000)
Blood
, vol.96
, Issue.7
, pp. 2405-2411
-
-
Tallman, M.S.1
Neuberg, D.2
Bennett, J.M.3
-
69
-
-
84915749961
-
Down syndrome preleukemia and leukemia
-
Maloney KW, Taub JW, Ravindranath Y, Roberts I, Vyas P. Down syndrome preleukemia and leukemia. Pediatr Clin North Am. 2015; 62(1):121-137.
-
(2015)
Pediatr Clin North Am
, vol.62
, Issue.1
, pp. 121-137
-
-
Maloney, K.W.1
Taub, J.W.2
Ravindranath, Y.3
Roberts, I.4
Vyas, P.5
-
70
-
-
13744252262
-
GATA1, cytidine deaminase, and the high cure rate of Down syndrome children with acute megakaryocytic leukemia
-
Ge Y, Stout ML, Tatman DA, et al. GATA1, cytidine deaminase, and the high cure rate of Down syndrome children with acute megakaryocytic leukemia. J Natl Cancer Inst. 2005;97(3):226-231.
-
(2005)
J Natl Cancer Inst
, vol.97
, Issue.3
, pp. 226-231
-
-
Ge, Y.1
Stout, M.L.2
Tatman, D.A.3
-
71
-
-
20044381309
-
Developmental stageselective effect of somatically mutated leukemogenic transcription factor GATA1
-
Li Z, Godinho FJ, Klusmann JH, Garriga-Canut M, Yu C, Orkin SH. Developmental stageselective effect of somatically mutated leukemogenic transcription factor GATA1. Nat Genet. 2005;37(6):613-619.
-
(2005)
Nat Genet
, vol.37
, Issue.6
, pp. 613-619
-
-
Li, Z.1
Godinho, F.J.2
Klusmann, J.H.3
Garriga-Canut, M.4
Yu, C.5
Orkin, S.H.6
-
72
-
-
84857814609
-
Increased dosage of the chromosome 21 ortholog Dyrk1a promotes megakaryoblastic leukemia in a murine model of Down syndrome
-
Malinge S, Bliss-Moreau M, Kirsammer G, et al. Increased dosage of the chromosome 21 ortholog Dyrk1a promotes megakaryoblastic leukemia in a murine model of Down syndrome. J Clin Invest. 2012;122(3):948-962.
-
(2012)
J Clin Invest
, vol.122
, Issue.3
, pp. 948-962
-
-
Malinge, S.1
Bliss-Moreau, M.2
Kirsammer, G.3
-
73
-
-
84887117736
-
The landscape of somatic mutations in Down syndrome-related myeloid disorders
-
Yoshida K, Toki T, Okuno Y, et al. The landscape of somatic mutations in Down syndrome-related myeloid disorders. Nat Genet. 2013;45(11):1293-1299.
-
(2013)
Nat Genet
, vol.45
, Issue.11
, pp. 1293-1299
-
-
Yoshida, K.1
Toki, T.2
Okuno, Y.3
-
74
-
-
58149380865
-
Abnormalities in the myeloid progenitor compartment in Down syndrome fetal liver precede acquisition of GATA1 mutations
-
Tunstall-Pedoe O, Roy A, Karadimitris A, et al. Abnormalities in the myeloid progenitor compartment in Down syndrome fetal liver precede acquisition of GATA1 mutations. Blood. 2008;112(12):4507-4511.
-
(2008)
Blood
, vol.112
, Issue.12
, pp. 4507-4511
-
-
Tunstall-Pedoe, O.1
Roy, A.2
Karadimitris, A.3
-
75
-
-
84867903663
-
Trisomy 21-associated defects in human primitive hematopoiesis revealed through induced pluripotent stem cells
-
Chou ST, Byrska-Bishop M, Tober JM, et al. Trisomy 21-associated defects in human primitive hematopoiesis revealed through induced pluripotent stem cells. Proc Natl Acad Sci USA. 2012;109(43):17573-17578.
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, Issue.43
, pp. 17573-17578
-
-
Chou, S.T.1
Byrska-Bishop, M.2
Tober, J.M.3
-
76
-
-
84867904859
-
Altered hematopoiesis in trisomy 21 as revealed through in vitro differentiation of isogenic human pluripotent cells
-
Maclean GA, Menne TF, Guo G, et al. Altered hematopoiesis in trisomy 21 as revealed through in vitro differentiation of isogenic human pluripotent cells. Proc Natl Acad Sci USA. 2012; 109(43):17567-17572.
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, Issue.43
, pp. 17567-17572
-
-
Maclean, G.A.1
Menne, T.F.2
Guo, G.3
-
77
-
-
84924029426
-
Pluripotent stem cells reveal erythroidspecific activities of the GATA1 N-terminus
-
Byrska-Bishop M, VanDorn D, Campbell AE, et al. Pluripotent stem cells reveal erythroidspecific activities of the GATA1 N-terminus. J Clin Invest. 2015;125(3):993-1005.
-
(2015)
J Clin Invest
, vol.125
, Issue.3
, pp. 993-1005
-
-
Byrska-Bishop, M.1
VanDorn, D.2
Campbell, A.E.3
-
78
-
-
0037103206
-
Development of myelofibrosis in mice genetically impaired for GATA-1 expression (GATA-1(low) mice)
-
Vannucchi AM, Bianchi L, Cellai C, et al. Development of myelofibrosis in mice genetically impaired for GATA-1 expression (GATA-1(low) mice). Blood. 2002;100(4):1123-1132.
-
(2002)
Blood
, vol.100
, Issue.4
, pp. 1123-1132
-
-
Vannucchi, A.M.1
Bianchi, L.2
Cellai, C.3
-
79
-
-
24044524612
-
Abnormalities of GATA-1 in megakaryocytes from patients with idiopathic myelofibrosis
-
Vannucchi AM, Pancrazzi A, Guglielmelli P, et al. Abnormalities of GATA-1 in megakaryocytes from patients with idiopathic myelofibrosis. Am J Pathol. 2005;167(3):849-858.
-
(2005)
Am J Pathol
, vol.167
, Issue.3
, pp. 849-858
-
-
Vannucchi, A.M.1
Pancrazzi, A.2
Guglielmelli, P.3
-
80
-
-
84879390119
-
Characterization of the TGF-b1 signaling abnormalities in the Gata1low mouse model of myelofibrosis
-
Zingariello M, Martelli F, Ciaffoni F, et al. Characterization of the TGF-b1 signaling abnormalities in the Gata1low mouse model of myelofibrosis. Blood. 2013;121(17):3345-3363.
-
(2013)
Blood
, vol.121
, Issue.17
, pp. 3345-3363
-
-
Zingariello, M.1
Martelli, F.2
Ciaffoni, F.3
-
81
-
-
0041806587
-
GATA-1-dependent transcriptional repression of GATA-2 via disruption of positive autoregulation and domain-wide chromatin remodeling
-
Grass JA, Boyer ME, Pal S, Wu J, Weiss MJ, Bresnick EH. GATA-1-dependent transcriptional repression of GATA-2 via disruption of positive autoregulation and domain-wide chromatin remodeling. Proc Natl Acad Sci USA. 2003; 100(15):8811-8816.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, Issue.15
, pp. 8811-8816
-
-
Grass, J.A.1
Boyer, M.E.2
Pal, S.3
Wu, J.4
Weiss, M.J.5
Bresnick, E.H.6
-
82
-
-
0028022916
-
An early haematopoietic defect in mice lacking the transcription factor GATA-2
-
Tsai FY, Keller G, Kuo FC, et al. An early haematopoietic defect in mice lacking the transcription factor GATA-2. Nature. 1994; 371(6494):221-226.
-
(1994)
Nature
, vol.371
, Issue.6494
, pp. 221-226
-
-
Tsai, F.Y.1
Keller, G.2
Kuo, F.C.3
-
83
-
-
22144476881
-
Haploinsufficiency of GATA-2 perturbs adult hematopoietic stem-cell homeostasis
-
Rodrigues NP, Janzen V, Forkert R, et al. Haploinsufficiency of GATA-2 perturbs adult hematopoietic stem-cell homeostasis. Blood. 2005;106(2):477-484.
-
(2005)
Blood
, vol.106
, Issue.2
, pp. 477-484
-
-
Rodrigues, N.P.1
Janzen, V.2
Forkert, R.3
-
84
-
-
80053383273
-
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia
-
Hahn CN, Chong CE, Carmichael CL, et al. Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia. Nat Genet. 2011;43(10): 1012-1017.
-
(2011)
Nat Genet
, vol.43
, Issue.10
, pp. 1012-1017
-
-
Hahn, C.N.1
Chong, C.E.2
Carmichael, C.L.3
-
85
-
-
80053385569
-
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
-
Ostergaard P, Simpson MA, Connell FC, et al. Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome). Nat Genet. 2011;43(10):929-931.
-
(2011)
Nat Genet
, vol.43
, Issue.10
, pp. 929-931
-
-
Ostergaard, P.1
Simpson, M.A.2
Connell, F.C.3
-
86
-
-
80052089944
-
-
Dickinson RE, Griffin H, Bigley V, et al. Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency. 2011;118(10):2656-2658.
-
(2011)
Exome Sequencing Identifies GATA-2 Mutation As the Cause of Dendritic Cell, Monocyte, B and NK Lymphoid Deficiency
, vol.118
, Issue.10
, pp. 2656-2658
-
-
Dickinson, R.E.1
Griffin, H.2
Bigley, V.3
-
87
-
-
84873530537
-
High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome
-
Pasquet M, Bellanné-Chantelot C, Tavitian S, et al. High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia. 2013;121(5):822-829.
-
(2013)
Myelodysplasia, and Acute Myeloid Leukemia
, vol.121
, Issue.5
, pp. 822-829
-
-
Pasquet, M.1
Bellanné-Chantelot, C.2
Tavitian, S.3
-
88
-
-
84920622721
-
GATA2 deficiency-associated bone marrow disorder differs from idiopathic aplastic anemia
-
Ganapathi KA, Townsley DM, Hsu AP, et al. GATA2 deficiency-associated bone marrow disorder differs from idiopathic aplastic anemia. Blood. 2015;125(1):56-70.
-
(2015)
Blood
, vol.125
, Issue.1
, pp. 56-70
-
-
Ganapathi, K.A.1
Townsley, D.M.2
Hsu, A.P.3
-
89
-
-
84971578103
-
Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome
-
Nováková M, Žaliová M, Suková M, et al. Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome. Haematologica. 2016;101(6):707-716.
-
(2016)
Haematologica
, vol.101
, Issue.6
, pp. 707-716
-
-
Nováková, M.1
Žaliová, M.2
Suková, M.3
-
90
-
-
84962621954
-
Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents
-
EWOG-MDS.
-
Wlodarski MW, Hirabayashi S, Pastor V, et al; EWOG-MDS. Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents. Blood. 2016;127(11):1387-1397.
-
(2016)
Blood
, vol.127
, Issue.11
, pp. 1387-1397
-
-
Wlodarski, M.W.1
Hirabayashi, S.2
Pastor, V.3
-
91
-
-
84896732313
-
Acquired ASXL1 mutations are common in patients with inherited GATA2 mutations and correlate with myeloid transformation
-
West RR, Hsu AP, Holland SM, Cuellar- Rodriguez J, Hickstein DD. Acquired ASXL1 mutations are common in patients with inherited GATA2 mutations and correlate with myeloid transformation. Haematologica. 2014;99(2): 276-281.
-
(2014)
Haematologica
, vol.99
, Issue.2
, pp. 276-281
-
-
West, R.R.1
Hsu, A.P.2
Holland, S.M.3
Cuellar-Rodriguez, J.4
Hickstein, D.D.5
-
92
-
-
84981170035
-
Association of GATA2 deficiency with severe primary Epstein- Barr virus (EBV) infection and EBV-associated cancers
-
Cohen JI, Dropulic L, Hsu AP, et al. Association of GATA2 deficiency with severe primary Epstein- Barr virus (EBV) infection and EBV-associated cancers. Clin Infect Dis. 2016;63(1):41-47.
-
(2016)
Clin Infect Dis
, vol.63
, Issue.1
, pp. 41-47
-
-
Cohen, J.I.1
Dropulic, L.2
Hsu, A.P.3
-
93
-
-
84983268735
-
Acute lymphoblastic leukemia in a patient with MonoMAC syndrome/GATA2 haploinsufficiency
-
Koegel AK, Hofmann I, Moffitt K, Degar B, Duncan C, Tubman VN. Acute lymphoblastic leukemia in a patient with MonoMAC syndrome/GATA2 haploinsufficiency. Pediatr Blood Cancer. 2016;63(10):1844-1847.
-
(2016)
Pediatr Blood Cancer
, vol.63
, Issue.10
, pp. 1844-1847
-
-
Koegel, A.K.1
Hofmann, I.2
Moffitt, K.3
Degar, B.4
Duncan, C.5
Tubman, V.N.6
-
94
-
-
84920172497
-
Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity
-
Zhang MY, Keel SB, Walsh T, et al. Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity. Haematologica. 2015;100(1):42-48.
-
(2015)
Haematologica
, vol.100
, Issue.1
, pp. 42-48
-
-
Zhang, M.Y.1
Keel, S.B.2
Walsh, T.3
-
95
-
-
84894095710
-
GATA2 deficiency: A protean disorder of hematopoiesis, lymphatics, and immunity
-
Spinner MA, Sanchez LA, Hsu AP, et al. GATA2 deficiency: A protean disorder of hematopoiesis, lymphatics, and immunity. Blood. 2014;123(6): 809-821.
-
(2014)
Blood
, vol.123
, Issue.6
, pp. 809-821
-
-
Spinner, M.A.1
Sanchez, L.A.2
Hsu, A.P.3
-
96
-
-
84894078016
-
The evolution of cellular deficiency in GATA2 mutation
-
Dickinson RE, Milne P, Jardine L, et al. The evolution of cellular deficiency in GATA2 mutation. Blood. 2014;123(6):863-874.
-
(2014)
Blood
, vol.123
, Issue.6
, pp. 863-874
-
-
Dickinson, R.E.1
Milne, P.2
Jardine, L.3
-
97
-
-
84863012056
-
Loss-offunction germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature
-
Kazenwadel J, Secker GA, Liu YJ, et al. Loss-offunction germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature. Blood. 2012;119(5):1283-1291.
-
(2012)
Blood
, vol.119
, Issue.5
, pp. 1283-1291
-
-
Kazenwadel, J.1
Secker, G.A.2
Liu, Y.J.3
-
98
-
-
84938966132
-
Characterisation of a compound in-cis GATA2 germline mutation in a pedigree presenting with myelodysplastic syndrome/acute myeloid leukemia with concurrent thrombocytopenia
-
Hahn CN, Brautigan PJ, Chong CE, et al. Characterisation of a compound in-cis GATA2 germline mutation in a pedigree presenting with myelodysplastic syndrome/acute myeloid leukemia with concurrent thrombocytopenia. Leukemia. 2015;29(8):1795-1797.
-
(2015)
Leukemia
, vol.29
, Issue.8
, pp. 1795-1797
-
-
Hahn, C.N.1
Brautigan, P.J.2
Chong, C.E.3
-
99
-
-
84899934011
-
Heritable GATA2 mutations associated with familial AMLMDS: A case report and review of literature
-
Gao J, Gentzler RD, Timms AE, et al. Heritable GATA2 mutations associated with familial AMLMDS: A case report and review of literature. J Hematol Oncol. 2014;7:36.
-
(2014)
J Hematol Oncol
, vol.7
, pp. 36
-
-
Gao, J.1
Gentzler, R.D.2
Timms, A.E.3
-
100
-
-
84959206499
-
Single-gene association between GATA-2 and autoimmune hepatitis: A novel genetic insight highlighting immunologic pathways to disease
-
Webb G, Chen YY, Li KK, et al. Single-gene association between GATA-2 and autoimmune hepatitis: A novel genetic insight highlighting immunologic pathways to disease. J Hepatol. 2016;64(5):1190-1193.
-
(2016)
J Hepatol
, vol.64
, Issue.5
, pp. 1190-1193
-
-
Webb, G.1
Chen, Y.Y.2
Li, K.K.3
-
101
-
-
79951693243
-
The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency
-
Bigley V, Haniffa M, Doulatov S, et al. The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency. J Exp Med. 2011;208(2):227-234.
-
(2011)
J Exp Med
, vol.208
, Issue.2
, pp. 227-234
-
-
Bigley, V.1
Haniffa, M.2
Doulatov, S.3
-
102
-
-
0029760542
-
A family inheriting different subtypes of acute myelogenous leukemia
-
Horwitz M, Sabath DE, Smithson WA, Radich J. A family inheriting different subtypes of acute myelogenous leukemia. Am J Hematol. 1996; 52(4):295-304.
-
(1996)
Am J Hematol
, vol.52
, Issue.4
, pp. 295-304
-
-
Horwitz, M.1
Sabath, D.E.2
Smithson, W.A.3
Radich, J.4
-
103
-
-
84859464786
-
MonoMAC and GATA2 deficiency: Overlapping clinical and pathological features with aplastic anemia and idiopathic CD41 lymphocytopenia
-
Reply to Haematologica. 2012;97(4):058669
-
Calvo KR, Hickstein DD, Holland SM. MonoMAC and GATA2 deficiency: Overlapping clinical and pathological features with aplastic anemia and idiopathic CD41 lymphocytopenia. Reply to Haematologica. 2012;97(4):058669. Haematologica. 2012;97(4):e12-e13.
-
(2012)
Haematologica
, vol.97
, Issue.4
, pp. e12-e13
-
-
Calvo, K.R.1
Hickstein, D.D.2
Holland, S.M.3
-
104
-
-
85019256897
-
Unexpected high frequency of GATA2 mutations in children with non-familial MDS and monosomy 7 [abstract]
-
Abstract 1699
-
Hirabayashi S, Strahm B, Urbaniak S, et al. Unexpected high frequency of GATA2 mutations in children with non-familial MDS and monosomy 7 [abstract]. Blood. 2012;120(21). Abstract 1699.
-
(2012)
Blood
, vol.120
, Issue.21
-
-
Hirabayashi, S.1
Strahm, B.2
Urbaniak, S.3
-
105
-
-
80053342603
-
Successful allogeneic hematopoietic stem cell transplantation for GATA2 deficiency
-
Cuellar-Rodriguez J, Gea-Banacloche J, Freeman AF, et al. Successful allogeneic hematopoietic stem cell transplantation for GATA2 deficiency. Blood. 2011;118(13): 3715-3720.
-
(2011)
Blood
, vol.118
, Issue.13
, pp. 3715-3720
-
-
Cuellar-Rodriguez, J.1
Gea-Banacloche, J.2
Freeman, A.F.3
-
106
-
-
84912570787
-
Nonmyeloablative allogeneic hematopoietic stem cell transplantation for GATA2 deficiency
-
Grossman J, Cuellar-Rodriguez J, Gea- Banacloche J, et al. Nonmyeloablative allogeneic hematopoietic stem cell transplantation for GATA2 deficiency. Biol Blood Marrow Transplant. 2014;20(12):1940-1948.
-
(2014)
Biol Blood Marrow Transplant
, vol.20
, Issue.12
, pp. 1940-1948
-
-
Grossman, J.1
Cuellar-Rodriguez, J.2
Gea-Banacloche, J.3
-
107
-
-
84948976984
-
Genomic analysis of germ line and somatic variants in familial myelodysplasia/acute myeloid leukemia
-
Churpek JE, Pyrtel K, Kanchi KL, et al. Genomic analysis of germ line and somatic variants in familial myelodysplasia/acute myeloid leukemia. Blood. 2015;126(22):2484-2490.
-
(2015)
Blood
, vol.126
, Issue.22
, pp. 2484-2490
-
-
Churpek, J.E.1
Pyrtel, K.2
Kanchi, K.L.3
-
108
-
-
84905594843
-
Identification of acquired mutations by whole-genome sequencing in GATA-2 deficiency evolving into myelodysplasia and acute leukemia
-
Fujiwara T, Fukuhara N, Funayama R, et al. Identification of acquired mutations by whole-genome sequencing in GATA-2 deficiency evolving into myelodysplasia and acute leukemia. Ann Hematol. 2014;93(9):1515-1522.
-
(2014)
Ann Hematol
, vol.93
, Issue.9
, pp. 1515-1522
-
-
Fujiwara, T.1
Fukuhara, N.2
Funayama, R.3
-
109
-
-
84880449489
-
GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome
-
Hsu AP, Johnson KD, Falcone EL, et al. GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome. Blood. 2013;121(19):3830-3837, S1-S7.
-
(2013)
Blood
, vol.121
, Issue.19
, pp. 3830S1-3837S7
-
-
Hsu, A.P.1
Johnson, K.D.2
Falcone, E.L.3
-
110
-
-
84867163662
-
Cis-element mutated in GATA2-dependent immunodeficiency governs hematopoiesis and vascular integrity
-
Johnson KD, Hsu AP, Ryu MJ, et al. Cis-element mutated in GATA2-dependent immunodeficiency governs hematopoiesis and vascular integrity. J Clin Invest. 2012;122(10):3692-3704.
-
(2012)
J Clin Invest
, vol.122
, Issue.10
, pp. 3692-3704
-
-
Johnson, K.D.1
Hsu, A.P.2
Ryu, M.J.3
-
111
-
-
14144252920
-
Zinc fingers as protein recognition motifs: Structural basis for the GATA-1/friend of GATA interaction
-
Liew CK, Simpson RJ, Kwan AH, et al. Zinc fingers as protein recognition motifs: Structural basis for the GATA-1/friend of GATA interaction. Proc Natl Acad Sci USA. 2005;102(3):583-588.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, Issue.3
, pp. 583-588
-
-
Liew, C.K.1
Simpson, R.J.2
Kwan, A.H.3
-
112
-
-
84957091411
-
GATA1 directly mediates interactions with closely spaced pseudopalindromic but not distantly spaced double GATA sites on DNA
-
Wilkinson-White L, Lester KL, Ripin N, Jacques DA, Mitchell Guss J, Matthews JM. GATA1 directly mediates interactions with closely spaced pseudopalindromic but not distantly spaced double GATA sites on DNA. Protein Sci. 2015;24(10):1649-1659.
-
(2015)
Protein Sci
, vol.24
, Issue.10
, pp. 1649-1659
-
-
Wilkinson-White, L.1
Lester, K.L.2
Ripin, N.3
Jacques, D.A.4
Mitchell Guss, J.5
Matthews, J.M.6
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