-
1
-
-
33746508365
-
Megakaryocyte development and platelet production
-
DOI 10.1111/j.1365-2141.2006.06215.x
-
Deutsch VR, Tomer A. Megakaryocyte development and platelet production. Br J Haematol. 2006;134(5):453-466. (Pubitemid 44141711)
-
(2006)
British Journal of Haematology
, vol.134
, Issue.5
, pp. 453-466
-
-
Deutsch, V.R.1
Tomer, A.2
-
2
-
-
13444270650
-
GATA1 function, a paradigm for transcription factors in hematopoiesis
-
DOI 10.1128/MCB.25.4.1215-1227.2005
-
Ferreira R, Ohneda K, Yamamoto M, Philipsen S. GATA1 function, a paradigm for transcription factors in hematopoiesis. Mol Cell Biol. 2005;25(4):1215- 1227. (Pubitemid 40204902)
-
(2005)
Molecular and Cellular Biology
, vol.25
, Issue.4
, pp. 1215-1227
-
-
Ferreira, R.1
Ohneda, K.2
Yamamoto, M.3
Philipsen, S.4
-
3
-
-
0034052854
-
Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA 1
-
DOI 10.1038/73480
-
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. (Pubitemid 30132195)
-
(2000)
Nature Genetics
, vol.24
, Issue.3
, pp. 266-270
-
-
Nichols, K.E.1
Crispino, J.D.2
Poncz, M.3
White, J.G.4
Orkin, S.H.5
Maris, J.M.6
Weiss, M.J.7
-
4
-
-
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
-
5
-
-
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
-
6
-
-
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(2):11:147-152.
-
(2002)
Hum Mol Genet
, Issue.2
-
-
Freson, K.1
Matthijs, G.2
Thys, C.3
-
7
-
-
0037105495
-
X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction
-
DOI 10.1182/blood-2002-02-0387
-
Yu C, Niakan KK, Matsushita M, Stamatoyannopoulos G, Orkin SH, Raskind WH. X-linked thrombocytopenia with thalassemia due to a mutation in the amino finger of GATA-1 affecting DNA-binding rather than FOG-1 interaction. Blood. 2002;100(7):2040-2045. (Pubitemid 35001235)
-
(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
-
8
-
-
33947223723
-
Congenital erythropoietic porphyria due to a mutation in GATA1: The first trans-acting mutation causative for a human porphyria
-
DOI 10.1182/blood-2006-06-022848
-
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. (Pubitemid 46425911)
-
(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
-
9
-
-
34147165665
-
X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation
-
DOI 10.1182/blood-2006-02-004101
-
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. (Pubitemid 46572516)
-
(2007)
Blood
, vol.109
, Issue.8
, pp. 3297-3299
-
-
Tubman, V.N.1
Levine, J.E.2
Campagna, D.R.3
Monahan-Earley, R.4
Dvorak, A.M.5
Neufeld, E.J.6
Fleming, M.D.7
-
10
-
-
34249788708
-
Platelet pathology in sex-linked GATA-1 dyserythropoietic macrothrombocytopenia I ultrastructure
-
DOI 10.1080/09537100601065825, PII 779138377
-
White JG, Nichols WL, Steensma DP. Platelet pathology in sex-linked GATA-1 dyserythropoietic macrothrombocytopenia I ultrastructure. Platelets. 2007;18(4):273-283. (Pubitemid 46854821)
-
(2007)
Platelets
, vol.18
, Issue.4
, pp. 273-283
-
-
White, J.G.1
Nichols, W.L.2
Steensma, D.P.3
-
11
-
-
55349086889
-
Cytoskeletons of X-linked GATA-1, G208S macrothrombocytes are deficient in talin
-
White JG, Burris SM. Cytoskeletons of X-linked GATA-1, G208S macrothrombocytes are deficient in talin. Platelets. 2008;19(7):543-550.
-
(2008)
Platelets
, vol.19
, Issue.7
, pp. 543-550
-
-
White, J.G.1
Burris, S.M.2
-
12
-
-
22744436722
-
FOG-1 recruits the NuRD repressor complex to mediate transcriptional repression by GATA-1
-
DOI 10.1038/sj.emboj.7600703
-
Hong W, Nakazawa M, Chen YY, et al. FOG-1 recruits the NuRD repressor complex to mediate transcriptional repression by GATA-1. EMBO J. 2005;24(13):2367-2378. (Pubitemid 41032588)
-
(2005)
EMBO Journal
, vol.24
, Issue.13
, pp. 2367-2378
-
-
Hong, W.1
Nakazawa, M.2
Chen, Y.-Y.3
Kori, R.4
Vakoc, C.R.5
Rakowski, C.6
Blobel, G.A.7
-
13
-
-
74949090052
-
NuRD mediates activating and repressive functions of GATA-1 and FOG-1 during blood development
-
Miccio A, Wang Y, Hong W, et al. NuRD mediates activating and repressive functions of GATA-1 and FOG-1 during blood development. EMBO J. 2010;29(2):442-456.
-
(2010)
EMBO J
, vol.29
, Issue.2
, pp. 442-456
-
-
Miccio, A.1
Wang, Y.2
Hong, W.3
-
14
-
-
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(8):2867-2875. (Pubitemid 29200777)
-
(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
-
15
-
-
79960921968
-
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet alpha-granules
-
Gunay-Aygun M, Falik-Zaccai TC, Vilboux T, et al. NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet alpha-granules. Nat. Genet. 2011;43(8):732-734.
-
(2011)
Nat Genet
, vol.43
, Issue.8
, pp. 732-734
-
-
Gunay-Aygun, M.1
Falik-Zaccai, T.C.2
Vilboux, T.3
-
16
-
-
79960903114
-
Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome
-
Kahr WHA, Hinckley J, Li L, et al. Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome. Nat. Genet. 2011;43(8):738-740.
-
(2011)
Nat Genet
, vol.43
, Issue.8
, pp. 738-740
-
-
Kahr, W.H.A.1
Hinckley, J.2
Li, L.3
-
17
-
-
79960895154
-
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome
-
Albers CA, Cvejic A, Favier R, et al. Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome. Nat. Genet. 2011;43(8):735-737.
-
(2011)
Nat Genet
, vol.43
, Issue.8
, pp. 735-737
-
-
Albers, C.A.1
Cvejic, A.2
Favier, R.3
-
18
-
-
33749331642
-
Maturation stage-specific regulation of megakaryopoiesis by pointed-domain Ets proteins
-
DOI 10.1182/blood-2006-04-019760
-
Pang L, Xue HH, Szalai G, et al. Maturation stage-specific regulation of megakaryopoiesis by pointed-domain Ets proteins. Blood. 2006;108(7):2198-2206. (Pubitemid 44497500)
-
(2006)
Blood
, vol.108
, Issue.7
, pp. 2198-2206
-
-
Pang, L.1
Xue, H.-H.2
Szalai, G.3
Wang, X.4
Wang, Y.5
Watson, D.K.6
Leonard, W.J.7
Blobel, G.A.8
Poncz, M.9
-
19
-
-
65249099633
-
Localization to mature melanosomes by virtue of cytoplasmic dileucine motifs is required for human OCA2 function
-
Sitaram A, Piccirillo R, Palmisano I, et al. Localization to mature melanosomes by virtue of cytoplasmic dileucine motifs is required for human OCA2 function. Mol Biol Cell. 2009;20(5):1464-1477.
-
(2009)
Mol Biol Cell
, vol.20
, Issue.5
, pp. 1464-1477
-
-
Sitaram, A.1
Piccirillo, R.2
Palmisano, I.3
-
20
-
-
34548823786
-
Evidence that differential packaging of the major platelet granule proteins von Willebrand factor and fibrinogen can support their differential release
-
DOI 10.1111/j.1538-7836.2007.02698.x
-
Sehgal S, Storrie B. Evidence that differential packaging of the major platelet granule proteins von Willebrand factor and fibrinogen can support their differential release. J Thromb Haemost. 2007;5(10):2009-2016. (Pubitemid 47450016)
-
(2007)
Journal of Thrombosis and Haemostasis
, vol.5
, Issue.10
, pp. 2009-2016
-
-
Sehgal, S.1
Storrie, B.2
-
21
-
-
0028820625
-
A lysosomal targeting signal in the cytoplasmic tail of the beta chain directs HLA-DM to the MHC class II compartments
-
Marks MS, Roche PA, van Donselaar E,Woodruff L, Peters PJ, Bonifacino JS. A lysosomal targeting signal in the cytoplasmic tail of the beta chain directs HLA-DM to the MHC class II compartments. J Cell Biol. 1995;131(2):351-369.
-
(1995)
J Cell Biol
, vol.131
, Issue.2
, pp. 351-369
-
-
Marks, M.S.1
Roche, P.A.2
Van Donselaar, E.3
Woodruff, L.4
Peters, P.J.5
Bonifacino, J.S.6
-
22
-
-
77956502480
-
The platelet interior revisited: Electron tomography reveals tubular alphagranule subtypes
-
Pannerden HN, Haas FD, GeertsW, Posthuma G, Dijk SV, Heijnen HFG. The platelet interior revisited: electron tomography reveals tubular alphagranule subtypes. Blood. 2010;116(7):1147-1156.
-
(2010)
Blood
, vol.116
, Issue.7
, pp. 1147-1156
-
-
Pannerden, H.N.1
Haas, F.D.2
Geerts, W.3
Posthuma, G.4
Dijk, S.V.5
Heijnen, H.F.G.6
-
23
-
-
21644440111
-
Flow-cytometric analysis of mouse platelet function
-
Nieswandt B, Schulte V, Bergmeier W. Flow-cytometric analysis of mouse platelet function. Methods Mol. Biol. 2004;272(1):255-268.
-
(2004)
Methods Mol Biol
, vol.272
, Issue.1
, pp. 255-268
-
-
Nieswandt, B.1
Schulte, V.2
Bergmeier, W.3
-
24
-
-
59649120717
-
Species differences in small molecule binding to alpha IIb beta 3 are the result of sequence differences in 2 loops of the alpha IIb beta propeller
-
Basani RB, Zhu H, Thornton MA, et al. Species differences in small molecule binding to alpha IIb beta 3 are the result of sequence differences in 2 loops of the alpha IIb beta propeller. Blood. 2009;113(4):902-910.
-
(2009)
Blood
, vol.113
, Issue.4
, pp. 902-910
-
-
Basani, R.B.1
Zhu, H.2
Thornton, M.A.3
-
25
-
-
1042301420
-
i Signaling Pathways
-
DOI 10.1074/jbc.M306162200
-
Kim S, Jin J, Kunapuli SP. Akt activation in platelets depends on Gi signaling pathways. J Biol Chem. 2004;279(6):4186-4195. (Pubitemid 38199005)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.6
, pp. 4186-4195
-
-
Kim, S.1
Jin, J.2
Kunapuli, S.P.3
-
26
-
-
10744231807
-
Factor VIII ectopically expressed in platelets: Efficacy in hemophilia A treatment
-
DOI 10.1182/blood-2003-05-1519
-
Yarovoi HV, Kufrin D, Eslin DE, et al. Factor VIII ectopically expressed in platelets: efficacy in hemophilia A treatment. Blood. 2003;102(12):4006-4013. (Pubitemid 37486982)
-
(2003)
Blood
, vol.102
, Issue.12
, pp. 4006-4013
-
-
Yarovoi, H.V.1
Kufrin, D.2
Eslin, D.E.3
Thornton, M.A.4
Haberichter, S.L.5
Shi, Q.6
Zhu, H.7
Camire, R.8
Fakharzadeh, S.S.9
Kowalska, M.A.10
Wilcox, D.A.11
Sachais, B.S.12
Montgomery, R.R.13
Poncz, M.14
-
27
-
-
33644867882
-
Differences in vascular bed disease susceptibility reflect differences in gene expression response to atherogenic stimuli
-
Deng DXF, Tsalenko A, Vailaya A, et al. Differences in vascular bed disease susceptibility reflect differences in gene expression response to atherogenic stimuli. Circ Res. 2006;98(2):200-208.
-
(2006)
Circ Res
, vol.98
, Issue.2
, pp. 200-208
-
-
Deng, D.X.F.1
Tsalenko, A.2
Vailaya, A.3
-
28
-
-
0344198634
-
Endothelial lineage-mediated loss of the GATA cofactor Friend of GATA 1 impairs cardiac development
-
DOI 10.1073/pnas.1936250100
-
Katz SG, Williams A, Yang J, et al. Endothelial lineage-mediated loss of the GATA cofactor Friend of GATA 1 impairs cardiac development. Proc Natl Acad Sci U S A. 2003;100(24):14030-14035. (Pubitemid 37499185)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.SUPPL. 2
, pp. 14030-14035
-
-
Katz, S.G.1
Williams, A.2
Yang, J.3
Fujiwara, Y.4
Tsang, A.P.5
Epstein, J.A.6
Orkin, S.H.7
-
29
-
-
0024496315
-
Structural and biosynthetic studies of the granule membrane protein, GMP-140, from human platelets and endothelial cells
-
Johnston GI, Kurosky A, McEver RP. Structural and biosynthetic studies of the granule membrane protein, GMP-140, from human platelets and endothelial cells. J Biol Chem. 1989;264(3):1816-1823. (Pubitemid 19051029)
-
(1989)
Journal of Biological Chemistry
, vol.264
, Issue.3
, pp. 1816-1823
-
-
Johnston, G.I.1
Kurosky, A.2
McEver, R.P.3
-
30
-
-
0034976384
-
AP-3 adaptor functions in targeting P-selectin to secretory granules in endothelial cells
-
DOI 10.1034/j.1600-0854.2001.002006406.x
-
Daugherty BL, Straley KS, Sanders JM, et al. AP-3 adaptor functions in targeting P-selectin to secretory granules in endothelial cells. Traffic. 2001;2(6):406-413. (Pubitemid 32574007)
-
(2001)
Traffic
, vol.2
, Issue.6
, pp. 406-413
-
-
Daugherty, B.L.1
Straley, K.S.2
Sanders, J.M.3
Phillips, J.W.4
Disdier, M.5
McEver, R.P.6
Green, S.A.7
-
31
-
-
0023906055
-
Isolation and sequencing of a cDNA clone encoding lysosomal membrane glycoprotein mouse LAMP-1: Sequence similarity to proteins bearing onco-differentiation antigens
-
Chen JW, Cha Y, Yuksel KU, Gracy RW, August JT. Isolation and sequencing of a cDNA clone encoding lysosomal membrane glycoprotein mouse LAMP-1: sequence similarity to proteins bearing onco-differentiation antigens. J Biol Chem. 1988;263(18):8754-8758.
-
(1988)
J Biol Chem
, vol.263
, Issue.18
, pp. 8754-8758
-
-
Chen, J.W.1
Cha, Y.2
Yuksel, K.U.3
Gracy, R.W.4
August, J.T.5
-
32
-
-
31544455817
-
Relative contribution of G-protein-coupled pathways to protease-activated receptor-mediated Akt phosphorylation in platelets
-
DOI 10.1182/blood-2005-07-3040
-
Kim S, Jin J, Kunapuli SP. Relative contribution of G-protein-coupled pathways to protease-activated receptor-mediated Akt phosphorylation in platelets. Blood. 2006;107(3):947-954. (Pubitemid 43156291)
-
(2006)
Blood
, vol.107
, Issue.3
, pp. 947-954
-
-
Kim, S.1
Jin, J.2
Kunapuli, S.P.3
-
33
-
-
19344365158
-
Selective impairment of platelet activation to collagen in the absence of GATA1
-
DOI 10.1182/blood-2004-10-4098
-
Hughan SC, Senis Y, Best D, et al. Selective impairment of platelet activation to collagen in the absence of GATA1. Blood. 2005;105(11):4369-4376. (Pubitemid 40720783)
-
(2005)
Blood
, vol.105
, Issue.11
, pp. 4369-4376
-
-
Hughan, S.C.1
Senis, Y.2
Best, D.3
Thomas, A.4
Frampton, J.5
Vyas, P.6
Watson, S.P.7
-
34
-
-
0024935752
-
++ mobilization in the platelet
-
Mori K, Suzuki S, Akutsu Y, Ishikawa M, Sakai H. Gray platelet syndrome: relationship between morphological abnormality of the dense tubular system (DTS) and intracellular Ca++ mobilization in the platelet. Nippon Ketsueki Gakkai Zasshi. 1989;52(8):1534-1541. (Pubitemid 20115689)
-
(1989)
Acta Haematologica Japonica
, vol.52
, Issue.8
, pp. 1534-1541
-
-
Mori, K.1
Suzuki, S.2
Akutsu, Y.3
Ishikawa, M.4
Sakai, H.5
-
35
-
-
77956519683
-
Munc13-4 is a limiting factor in the pathway required for platelet granule release and hemostasis
-
Ren Q, Wimmer C, Chicka MC, et al. Munc13-4 is a limiting factor in the pathway required for platelet granule release and hemostasis. Blood. 2010;116(6):869-877.
-
(2010)
Blood
, vol.116
, Issue.6
, pp. 869-877
-
-
Ren, Q.1
Wimmer, C.2
Chicka, M.C.3
-
36
-
-
1642275392
-
Munc13-4 Is a GTP-Rab27-binding Protein Regulating Dense Core Granule Secretion in Platelets
-
DOI 10.1074/jbc.M309426200
-
Shirakawa R, Higashi T, Tabuchi A, et al. Munc13-4 is a GTP-Rab27-binding protein regulating dense core granule secretion in platelets. J Biol Chem. 2004;279(11):10730-10737. (Pubitemid 38372686)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.11
, pp. 10730-10737
-
-
Shirakawa, R.1
Higashi, T.2
Tabuchi, A.3
Yoshioka, A.4
Nishioka, H.5
Fukuda, M.6
Kita, T.7
Horiuchi, H.8
-
37
-
-
33846201270
-
The gray platelet syndrome: Clinical spectrum of the disease
-
DOI 10.1016/j.blre.2005.12.003, PII S0268960X05000718
-
Nurden AT, Nurden P. The gray platelet syndrome: clinical spectrum of the disease. Blood Rev. 2007;21(1):21-36. (Pubitemid 46097190)
-
(2007)
Blood Reviews
, vol.21
, Issue.1
, pp. 21-36
-
-
Nurden, A.T.1
Nurden, P.2
-
38
-
-
0028304622
-
Gray platelet syndrome with splenomegaly and signs of extramedullary hematopoiesis: A case report with review of the literature
-
DOI 10.1002/ajh.2830460311
-
Jantunen E, Hänninen A, Naukkarinen A, Vornanen M, Lahtinen R. Gray platelet syndrome with splenomegaly and signs of extramedullary hematopoiesis: a case report with review of the literature. Am J Hematol. 1994;46(1):218-224. (Pubitemid 24206748)
-
(1994)
American Journal of Hematology
, vol.46
, Issue.3
, pp. 218-224
-
-
Jantunen, E.1
Hanninen, A.2
Naukkarinen, A.3
Vornanen, M.4
Lahtinen, R.5
-
39
-
-
78649751014
-
Filling a void in gray platelets
-
Flaumenhaft R. Filling a void in gray platelets. Blood. 2010;116(23):4738-4740.
-
(2010)
Blood
, vol.116
, Issue.23
, pp. 4738-4740
-
-
Flaumenhaft, R.1
-
41
-
-
0021748223
-
Electron microscopic and functional studies on platelets in gray platelet syndrome
-
Mori K, Suzuki S, Sugai K. Electron microscopic and functional studies on platelets in gray platelet syndrome. Tohoku J Exp Med. 1984;143(3):261-287. (Pubitemid 15195597)
-
(1984)
Tohoku Journal of Experimental Medicine
, vol.143
, Issue.3
, pp. 261-287
-
-
Mori, K.1
Suzuki, S.2
Sugai, K.3
-
42
-
-
3042839777
-
Severe deficiency of glycoprotein VI in a patient with gray platelet syndrome
-
DOI 10.1182/blood-2003-11-3842
-
Nurden P, Jandrot-Perrus M, Combrié R, et al. Severe deficiency of glycoprotein VI in a patient with gray platelet syndrome. Blood. 2004;104(1):107-114. (Pubitemid 38879845)
-
(2004)
Blood
, vol.104
, Issue.1
, pp. 107-114
-
-
Nurden, P.1
Jandrot-Perrus, M.2
Combrie, R.3
Winckler, J.4
Arocas, V.5
Lecut, C.6
Pasquet, J.-M.7
Kunicki, T.J.8
Nurden, A.T.9
-
43
-
-
0025347106
-
Simultaneous occurrence of grey platelet syndrome and idiopathic pulmonary fibrosis: A role for abnormal megakaryocytes in the pathogenesis of pulmonary fibrosis?
-
Facon T, Goudemand J, Caron C et al. Simultaneous occurrence of grey platelet syndrome and idiopathic pulmonary fibrosis: a role for abnormal megakaryocytes in the pathogenesis of pulmonary fibrosis? Br J Haematol. 1990;74(4):542-543. (Pubitemid 20122762)
-
(1990)
British Journal of Haematology
, vol.74
, Issue.4
, pp. 542-543
-
-
Facon, T.1
Goudemand, J.2
Caron, C.3
Zandecki, M.4
Estienne, M.-H.5
Fenaux, P.6
Cosson, A.7
-
44
-
-
0038819114
-
RUNX1 and GATA-1 coexpression and cooperation in megakaryocytic differentiation
-
DOI 10.1182/blood-2002-09-2708
-
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(11):4333-4341. (Pubitemid 36857797)
-
(2003)
Blood
, vol.101
, Issue.11
, 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
-
45
-
-
0032830638
-
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia
-
DOI 10.1038/13793
-
Song WJ, Sullivan MG, Legare RD, et al. Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia. Nat Genet. 1999;23(2):166-175. (Pubitemid 29455388)
-
(1999)
Nature Genetics
, vol.23
, Issue.2
, pp. 166-175
-
-
Song, W.-J.1
Sullivan, M.G.2
Legare, R.D.3
Hutchings, S.4
Tan, X.5
Kufrin, D.6
Ratajczak, J.7
Resende, I.C.8
Haworth, C.9
Hock, R.10
Loh, M.11
Felix, C.12
Roy, R.-C.13
Busque, L.14
Kurnit, D.15
Willman, C.16
Gewirtz, A.M.17
Speck, N.A.18
Bushweller, J.H.19
Li, F.P.20
Gardiner, K.21
Poncz, M.22
Maris, J.M.23
Gilliland, D.G.24
more..
-
46
-
-
78650665647
-
Regulation of platelet myosin light chain (MYL9) by RUNX1: Implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency
-
Jalagadugula G, Mao G, Kaur G, Goldfinger LE, Dhanasekaran DN, Rao AK. Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency. Blood. 2010;116(26):6037-6045.
-
(2010)
Blood
, vol.116
, Issue.26
, pp. 6037-6045
-
-
Jalagadugula, G.1
Mao, G.2
Kaur, G.3
Goldfinger, L.E.4
Dhanasekaran, D.N.5
Rao, A.K.6
-
47
-
-
79953738438
-
Platelet protein kinase C-theta deficiency with human RUNX1 mutation: PRKCQ is a transcriptional target of RUNX1
-
Jalagadugula G, Mao G, Kaur G, Dhanasekaran DN, Rao AK. Platelet protein kinase C-theta deficiency with human RUNX1 mutation: PRKCQ is a transcriptional target of RUNX1. Arterioscler Thromb Vasc Biol. 2011;31(4):921-927.
-
(2011)
Arterioscler Thromb Vasc Biol
, vol.31
, Issue.4
, pp. 921-927
-
-
Jalagadugula, G.1
Mao, G.2
Kaur, G.3
Dhanasekaran, D.N.4
Rao, A.K.5
-
48
-
-
79251588435
-
Mechanism of platelet factor 4 (PF4) deficiency with RUNX1 haplodeficiency: RUNX1 is a transcriptional regulator of PF4
-
Aneja K, Jalagadugula G, Mao G, Singh A, RaoAK. Mechanism of platelet factor 4 (PF4) deficiency with RUNX1 haplodeficiency: RUNX1 is a transcriptional regulator of PF4. J Thromb Haemost. 2011;9(2):383-391.
-
(2011)
J Thromb Haemost
, vol.9
, Issue.2
, pp. 383-391
-
-
Aneja, K.1
Jalagadugula, G.2
Mao, G.3
Singh, A.4
Rao, A.K.5
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