-
1
-
-
0017662372
-
X-linked syndrome of platelet dysfunction, thrombocytopenia and imbalanced globin chain synthesis with hemolysis
-
Thompson AR, Wood WG. Stamatoyannopoulous G. X-linked syndrome of platelet dysfunction, thrombocytopenia and imbalanced globin chain synthesis with hemolysis. Blood 1977;50:303-316.
-
(1977)
Blood
, vol.50
, pp. 303-316
-
-
Thompson, A.R.1
Wood, W.G.2
Stamatoyannopoulous, G.3
-
2
-
-
0025977563
-
Erythroid differentiation in chimaeric mice blocked by a targeted mutation in the gene for transcription factor GATA-1
-
Pevny L, Simon MC, Robertson E, Klein WH, Tsai SF, D'Agati V, Orkin SH, Costantini F. Erythroid differentiation in chimaeric mice blocked by a targeted mutation in the gene for transcription factor GATA-1. Nature 1931;349:257-260.
-
(1931)
Nature
, vol.349
, pp. 257-260
-
-
Pevny, L.1
Simon, M.C.2
Robertson, E.3
Klein, W.H.4
Tsai, S.F.5
D'Agati, V.6
Orkin, S.H.7
Costantini, F.8
-
3
-
-
0028233760
-
Novel insights into erythroid development revealed through in vitro differentiation of GATA-1 embroyonic stem cells
-
Weiss MJ, Keller G, Orkin SH. Novel insights into erythroid development revealed through in vitro differentiation of GATA-1 embroyonic stem cells. Genes Dev 1994;8:1184-1197.
-
(1994)
Genes Dev
, vol.8
, pp. 1184-1197
-
-
Weiss, M.J.1
Keller, G.2
Orkin, S.H.3
-
4
-
-
0034052854
-
Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1
-
Nichols KE, Crispino JD, Poncz M, White JG, Orkin SH, Maris JM, Weiss MJ. Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1. Nat Genet 2000;24:266-270.
-
(2000)
Nat Genet
, vol.24
, 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
-
5
-
-
0035412362
-
Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA-1 mutation
-
Freson K, Devriendt K, Matthijs G, Van Hoof A, De Vos R, Thys C, Minner K, Hoylaerts M, Vermylen J, Van Geet C. Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA-1 mutation. Blood 2001;98:85-92.
-
(2001)
Blood
, vol.98
, pp. 85-92
-
-
Freson, K.1
Devriendt, K.2
Matthijs, G.3
Van Hoof, A.4
De Vos, R.5
Thys, C.6
Minner, K.7
Hoylaerts, M.8
Vermylen, J.9
Van Geet, C.10
-
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, Marien P, Hoylaerts M, Vermylen J, Van Geet C. 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;11:147-152.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 147-152
-
-
Freson, K.1
Matthijs, G.2
Thys, C.3
Marien, P.4
Hoylaerts, M.5
Vermylen, J.6
Van Geet, C.7
-
7
-
-
0030926006
-
A lineage-selective knockout establishes the critical role of transcription factor of 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 of GATA-1 in megakaryocyte growth and platelet development. Embo J 1997;16:3965-3973.
-
(1997)
Embo J
, vol.16
, pp. 3965-3973
-
-
Shivdasani, R.A.1
Fujiwara, Y.2
McDevitt, M.A.3
Orkin, S.H.4
-
8
-
-
0035525746
-
-
Mehaffey MG, Newton EL, Ghandi MJ. Crossley M. Drachman JG: X-linked thrombocytopenia caused by a novel mutation of GATA-1. Blood 2001;98:2681-2688.
-
Mehaffey MG, Newton EL, Ghandi MJ. Crossley M. Drachman JG: X-linked thrombocytopenia caused by a novel mutation of GATA-1. Blood 2001;98:2681-2688.
-
-
-
-
9
-
-
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;93:2867-2875.
-
(1999)
Blood
, vol.93
, pp. 2867-2875
-
-
Vyas, P.1
Ault, K.2
Jackson, C.W.3
Orkin, S.H.4
Shivdasani, R.A.5
-
10
-
-
33746862841
-
Congenital erythropoietic porphyria, Bthalassemia intermedia and thrombocytopenia due to a GATA-1 mutation
-
Phillips JD, Steensma DP, Spangrude GJ, Kushner JP. Congenital erythropoietic porphyria, Bthalassemia intermedia and thrombocytopenia due to a GATA-1 mutation. Blood 2005;106:15a.
-
(2005)
Blood
, vol.106
-
-
Phillips, J.D.1
Steensma, D.P.2
Spangrude, G.J.3
Kushner, J.P.4
-
11
-
-
1642434012
-
Effects of the R216 Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesis
-
Balduini CL, Pecci A, Loffredo G, Iyyo P, Noris P, Grosso M, Bergamaschi G, Rosti V, Magrini U, Ceresa IF, et al. Effects of the R216 Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesis. Blood 2004;91:129-140.
-
(2004)
Blood
, vol.91
, pp. 129-140
-
-
Balduini, C.L.1
Pecci, A.2
Loffredo, G.3
Iyyo, P.4
Noris, P.5
Grosso, M.6
Bergamaschi, G.7
Rosti, V.8
Magrini, U.9
Ceresa, I.F.10
-
12
-
-
34548305998
-
Platelet pathology in sex-linked GATA-1 dyserythropoietic macrothrombocytopenia
-
In press
-
White JG, Nichols WL, Steensma DP. Platelet pathology in sex-linked GATA-1 dyserythropoietic macrothrombocytopenia. Platelets (In press).
-
Platelets
-
-
White, J.G.1
Nichols, W.L.2
Steensma, D.P.3
-
13
-
-
33751507221
-
X-linked Gray Platelet Syndrome due to a GATA-1 Arg 216 G In mutation
-
Tubman VN, Levine JE, Camoagna DR, Fleming MD, Neufeld EJ. X-linked Gray Platelet Syndrome due to a GATA-1 Arg 216 G In mutation. Blood 2005;106:6a.
-
(2005)
Blood
, vol.106
-
-
Tubman, V.N.1
Levine, J.E.2
Camoagna, D.R.3
Fleming, M.D.4
Neufeld, E.J.5
-
14
-
-
0015176866
-
Gray platelet syndrome: A variety of qualitative platelet disorders
-
Raccuglia G. Gray platelet syndrome: A variety of qualitative platelet disorders. Am J Med 1971;51:818-828.
-
(1971)
Am J Med
, vol.51
, pp. 818-828
-
-
Raccuglia, G.1
-
15
-
-
0018333833
-
Ultrastructural studies of the gray platelet syndrome
-
White JG. Ultrastructural studies of the gray platelet syndrome. Am J Pathol 1979;95:445-462.
-
(1979)
Am J Pathol
, vol.95
, pp. 445-462
-
-
White, J.G.1
-
16
-
-
4444381049
-
-
White JG. Medich Giant Platelet Disorder: A Unique α-granule deficiency. 1. Structural abnormalities. Platelets 2004;15:345-353.
-
White JG. Medich Giant Platelet Disorder: A Unique α-granule deficiency. 1. Structural abnormalities. Platelets 2004;15:345-353.
-
-
-
-
17
-
-
0001944905
-
-
LA Harker, TS Zimmerman, editors. New York: Churchill-Livingstone;
-
White JG. The morphology of platelet function. In: LA Harker, TS Zimmerman, editors. New York: Churchill-Livingstone; 1983. pp 1-25.
-
(1983)
The morphology of platelet function
, pp. 1-25
-
-
White, J.G.1
-
18
-
-
0025067450
-
Receptor-ligand complexes are cleared to the open canalicular system of surface-activated platelets
-
Leistikow EA, Barnhart MI, Escolar G, White JG. Receptor-ligand complexes are cleared to the open canalicular system of surface-activated platelets. Br J Haematol 1990;74:93-100.
-
(1990)
Br J Haematol
, vol.74
, pp. 93-100
-
-
Leistikow, E.A.1
Barnhart, M.I.2
Escolar, G.3
White, J.G.4
-
19
-
-
0025185370
-
Induction of patching and its reversal on surface-activated human platelets
-
White JG. Induction of patching and its reversal on surface-activated human platelets. Br J Haematol 1990;76:108-115.
-
(1990)
Br J Haematol
, vol.76
, pp. 108-115
-
-
White, J.G.1
-
20
-
-
0025187153
-
Separate and combined interactions of fibrinogen-gold and latex with surface-activated platelets
-
Oct;
-
White JG. Separate and combined interactions of fibrinogen-gold and latex with surface-activated platelets. Am J Pathol 1990 Oct;137:989-998.
-
(1990)
Am J Pathol
, vol.137
, pp. 989-998
-
-
White, J.G.1
-
22
-
-
0029077581
-
Redistribution of GPIb/IX and GPIIb/IIIa during spreading of discoid platelets
-
White JG, Krumwiede MD, Johnson DK, Escolar G. Redistribution of GPIb/IX and GPIIb/IIIa during spreading of discoid platelets. Br J Haematol 1995;90:633-644.
-
(1995)
Br J Haematol
, vol.90
, pp. 633-644
-
-
White, J.G.1
Krumwiede, M.D.2
Johnson, D.K.3
Escolar, G.4
-
24
-
-
0023142807
-
The secretory pathway of bovine platelets
-
White JG. The secretory pathway of bovine platelets. Blood 1987;69:878-885.
-
(1987)
Blood
, vol.69
, pp. 878-885
-
-
White, J.G.1
-
25
-
-
0023185079
-
Further studies of the secretory pathway in thrombin-stimulated human platelets
-
White JG. Krumwiede M. Further studies of the secretory pathway in thrombin-stimulated human platelets. Blood 1987;69:1196-1203.
-
(1987)
Blood
, vol.69
, pp. 1196-1203
-
-
White, J.G.1
Krumwiede, M.2
-
26
-
-
0028807012
-
Dynamic redistribution of glycoprotein Ib/IX on surface-activated platelets: A second look
-
White JG, Krumwiede MD, Cockingjohnson D, Rao GHR, Escolar G. Dynamic redistribution of glycoprotein Ib/IX on surface-activated platelets: A second look. Am J Pathol 1995;147:1057-1067.
-
(1995)
Am J Pathol
, vol.147
, pp. 1057-1067
-
-
White, J.G.1
Krumwiede, M.D.2
Cockingjohnson, D.3
Rao, G.H.R.4
Escolar, G.5
-
27
-
-
0028826371
-
Retention of glycoprotein Ib/IX receptors on external surfaces of thrombin-activated platelets in suspension
-
White JG, Krumwiede MD, Cockingjohnson D, Rao GHR, Escolar G. Retention of glycoprotein Ib/IX receptors on external surfaces of thrombin-activated platelets in suspension. Blood 1995;86:3468-3478.
-
(1995)
Blood
, vol.86
, pp. 3468-3478
-
-
White, J.G.1
Krumwiede, M.D.2
Cockingjohnson, D.3
Rao, G.H.R.4
Escolar, G.5
-
28
-
-
0018418813
-
Bridging structures spanning the junctional gap at the triad of skeletal muscle
-
Somlyo AV. Bridging structures spanning the junctional gap at the triad of skeletal muscle. J Cell Biol 1979;80:743-748.
-
(1979)
J Cell Biol
, vol.80
, pp. 743-748
-
-
Somlyo, A.V.1
-
29
-
-
0013788124
-
The cytocfhemical demonstration of lysosomal aryl sulfatase activity by light and electron microscopy
-
Goldfischer S. The cytocfhemical demonstration of lysosomal aryl sulfatase activity by light and electron microscopy. J Histochem Cytochem 1965;13:520-523.
-
(1965)
J Histochem Cytochem
, vol.13
, pp. 520-523
-
-
Goldfischer, S.1
-
30
-
-
0016707740
-
Cytochemical localization of lysosomal enzymes in rat megakaryocytes and platelets
-
Bentfield ME, Bainton DF. Cytochemical localization of lysosomal enzymes in rat megakaryocytes and platelets. J Clin Invest 1975;56:1635-1649.
-
(1975)
J Clin Invest
, vol.56
, pp. 1635-1649
-
-
Bentfield, M.E.1
Bainton, D.F.2
-
31
-
-
33745165233
-
Localization of a lysosomal enzyme in platelets from patients with the White Platelet Syndrome
-
White JG. Localization of a lysosomal enzyme in platelets from patients with the White Platelet Syndrome. Platelets 2006;17:231-249.
-
(2006)
Platelets
, vol.17
, pp. 231-249
-
-
White, J.G.1
-
32
-
-
0032055178
-
-
Hiejnen HF, Debili N, Vainchencker W, Breton-Gorius J, Geuze HJ, Sixma JJ. Multivesicular bodies are an intermediate stage in the formation of platelet alpha granules. Blood 1998;9:2313-2325.
-
Hiejnen HF, Debili N, Vainchencker W, Breton-Gorius J, Geuze HJ, Sixma JJ. Multivesicular bodies are an intermediate stage in the formation of platelet alpha granules. Blood 1998;9:2313-2325.
-
-
-
-
33
-
-
0017151562
-
Ultrastructure of human bone marrow cell maturation
-
Breton-Gorius J, Reyes F. Ultrastructure of human bone marrow cell maturation. Int Rev Cytol 1976;46:251-321.
-
(1976)
Int Rev Cytol
, vol.46
, pp. 251-321
-
-
Breton-Gorius, J.1
Reyes, F.2
-
34
-
-
6344294584
-
Intracellular compartments and protein sorting
-
Albers B, Johnson A, Lewis J, Roff M, Roberts K, Walter P, editors, 4th ed. New York: Garland Scientific Taylor and Francis Group;
-
Albert B, Johnson A, Lewis J, Raff M, Roberts K, Walter P. Intracellular compartments and protein sorting. In: Albers B, Johnson A, Lewis J, Roff M, Roberts K, Walter P, editors. Molecular biology of the cell. 4th ed. New York: Garland Scientific Taylor and Francis Group; 2002; pp 659-766.
-
(2002)
Molecular biology of the cell
, pp. 659-766
-
-
Albert, B.1
Johnson, A.2
Lewis, J.3
Raff, M.4
Roberts, K.5
Walter, P.6
-
35
-
-
0022377796
-
Gray platelet syndrome: Immunoelectron microscope localization of fibrinogen and von Willebrand factor in platelets and megakaryocytes
-
Cramer EM, Vainchenker W, Vinci G, Guichard J, Breton-Gorius J. Gray platelet syndrome: Immunoelectron microscope localization of fibrinogen and von Willebrand factor in platelets and megakaryocytes. Blood 1985; 66:1309-1316.
-
(1985)
Blood
, vol.66
, pp. 1309-1316
-
-
Cramer, E.M.1
Vainchenker, W.2
Vinci, G.3
Guichard, J.4
Breton-Gorius, J.5
-
36
-
-
0023574858
-
Gray platelet syndrome: Demonstration of α-granule membranes that can fuse with the cell surface
-
Risa JP, George JN, Bainton DF, Nurden AT, Caen JP, McEver RP. Gray platelet syndrome: demonstration of α-granule membranes that can fuse with the cell surface. J Clin Invest 1987;80:1138-1146.
-
(1987)
J Clin Invest
, vol.80
, pp. 1138-1146
-
-
Risa, J.P.1
George, J.N.2
Bainton, D.F.3
Nurden, A.T.4
Caen, J.P.5
McEver, R.P.6
-
37
-
-
0023678534
-
Megakaryocyte and platelet ultrastructure in the Wistar Furth rat
-
Leven RM, Toblin F. Megakaryocyte and platelet ultrastructure in the Wistar Furth rat. Am J Pathol 1988;132:417-426.
-
(1988)
Am J Pathol
, vol.132
, pp. 417-426
-
-
Leven, R.M.1
Toblin, F.2
-
38
-
-
0014238228
-
Effects of ethylenediamine tetracetic acid (EDTA) on platelet fine structure
-
White JG. Effects of ethylenediamine tetracetic acid (EDTA) on platelet fine structure. Scand J Haematol 1968;5:241-254.
-
(1968)
Scand J Haematol
, vol.5
, pp. 241-254
-
-
White, J.G.1
-
39
-
-
0033404131
-
Platelet membrane interactions
-
White JG. Platelet membrane interactions. Platelets 1999;10:368-381.
-
(1999)
Platelets
, vol.10
, pp. 368-381
-
-
White, J.G.1
-
40
-
-
0021275867
-
Micropipette aspiration of human blood platelets: A defect in the Bernard-Soulier's syndrome
-
White JG, Burris SM, Hasegawa D, Johnson M. Micropipette aspiration of human blood platelets: A defect in the Bernard-Soulier's syndrome. Blood 1984;63:1249-1252.
-
(1984)
Blood
, vol.63
, pp. 1249-1252
-
-
White, J.G.1
Burris, S.M.2
Hasegawa, D.3
Johnson, M.4
-
41
-
-
2442591445
-
The white platelet syndrome: A new autosomal dominant platelet disorder.1.Structural abnormalities
-
White JG, Key NS, King RA, Vercellotti GM. The white platelet syndrome: A new autosomal dominant platelet disorder.1.Structural abnormalities. Platelets 2004;15: 173-184.
-
(2004)
Platelets
, vol.15
, pp. 173-184
-
-
White, J.G.1
Key, N.S.2
King, R.A.3
Vercellotti, G.M.4
-
42
-
-
0019434958
-
Defective α-granule production in megakaryocytes from gray platelet syndrome
-
Breton-Gorius J, Vainchenker W, Nurden A, Levy-Toledano S, Caen J. Defective α-granule production in megakaryocytes from gray platelet syndrome. Am J Pathol 1981;102:10-19.
-
(1981)
Am J Pathol
, vol.102
, pp. 10-19
-
-
Breton-Gorius, J.1
Vainchenker, W.2
Nurden, A.3
Levy-Toledano, S.4
Caen, J.5
|