-
1
-
-
0025141664
-
Genetic thrombocytopenia with autosomal dominant transmission: A review of 54 cases
-
Najean Y, Lecompte T: Genetic thrombocytopenia with autosomal dominant transmission: A review of 54 cases. Br J Haematol 74:203, 1990
-
(1990)
Br J Haematol
, vol.74
, pp. 203
-
-
Najean, Y.1
Lecompte, T.2
-
2
-
-
0014382463
-
The May-Hegglin anomaly: Platelet function, ultrastructure and chromosome studies
-
Lusher JM, Schreider J, Mizukami I, Evans RK: The May-Hegglin anomaly: Platelet function, ultrastructure and chromosome studies. Blood 32:950, 1968
-
(1968)
Blood
, vol.32
, pp. 950
-
-
Lusher, J.M.1
Schreider, J.2
Mizukami, I.3
Evans, R.K.4
-
3
-
-
0019127648
-
Platelet function, ultrastructure and survival in the May-Hegglin anomaly
-
Hamilton RW, Shaikh BS, Ottie JN, Storch AE, Saleem A, White JG: Platelet function, ultrastructure and survival in the May-Hegglin anomaly. Am J Clin Pathol 74:663, 1980
-
(1980)
Am J Clin Pathol
, vol.74
, pp. 663
-
-
Hamilton, R.W.1
Shaikh, B.S.2
Ottie, J.N.3
Storch, A.E.4
Saleem, A.5
White, J.G.6
-
4
-
-
0015978724
-
May-Hegglin anomaly: A defect in megakaryocyte fragmentation
-
Goodwin HA, Ginsberg AD: May-Hegglin anomaly: A defect in megakaryocyte fragmentation. Br J Haematol 26:117, 1974
-
(1974)
Br J Haematol
, vol.26
, pp. 117
-
-
Goodwin, H.A.1
Ginsberg, A.D.2
-
5
-
-
0015304377
-
Hereditary macrothrombocytopathia, nephritis and deafness
-
Epstein CJ, Sahud MA, Piel CF, Goodman JR, Bernfield MR, Kusher JH, Ablin AR: Hereditary macrothrombocytopathia, nephritis and deafness. Am J Med 52:299, 1972
-
(1972)
Am J Med
, vol.52
, pp. 299
-
-
Epstein, C.J.1
Sahud, M.A.2
Piel, C.F.3
Goodman, J.R.4
Bernfield, M.R.5
Kusher, J.H.6
Ablin, A.R.7
-
6
-
-
0016506243
-
Hereditary thrombocytopenia, deafness and renal disease
-
Eckstein JD, Filip DJ, Watts JC: Hereditary thrombocytopenia, deafness and renal disease. Ann Intern Med 82:639, 1975
-
(1975)
Ann Intern Med
, vol.82
, pp. 639
-
-
Eckstein, J.D.1
Filip, D.J.2
Watts, J.C.3
-
7
-
-
0017169272
-
Hereditary nephritis, deafness and abnormal thrombopoiesis. Study in a new kindred
-
Parsa KP, Lee DBN, Zamboni L, Glassock RJ: Hereditary nephritis, deafness and abnormal thrombopoiesis. Study in a new kindred. Am J Med 60:665, 1976
-
(1976)
Am J Med
, vol.60
, pp. 665
-
-
Parsa, K.P.1
Lee, D.B.N.2
Zamboni, L.3
Glassock, R.J.4
-
8
-
-
84886611159
-
Thrombocytopenia, macrothrombocytopathia, nephritis and deafness
-
Berheim J, Dechavanne M, Bryon PA, Lagarde M, Colon S, Pozet N, Traeger J: Thrombocytopenia, macrothrombocytopathia, nephritis and deafness. Am J Med 61:145, 1976
-
(1976)
Am J Med
, vol.61
, pp. 145
-
-
Berheim, J.1
Dechavanne, M.2
Bryon, P.A.3
Lagarde, M.4
Colon, S.5
Pozet, N.6
Traeger, J.7
-
9
-
-
0021956321
-
Fechtner syndrome. A variant of Alport's syndrome with leucocyte inclusions and macrothrombocytopenia
-
Peterson LC, Rao KV, Crosson JT, White JG: Fechtner syndrome. A variant of Alport's syndrome with leucocyte inclusions and macrothrombocytopenia. Blood 65:397, 1985
-
(1985)
Blood
, vol.65
, pp. 397
-
-
Peterson, L.C.1
Rao, K.V.2
Crosson, J.T.3
White, J.G.4
-
10
-
-
0024232175
-
Congenital macrothrombocytopenia, leukocyte inclusions, deafness and proteinuria: Functional and electron microscopic observations on platelets and megakaryocytes
-
Heynen MJ, Blockmans D, Verwilghen RL, Vermylen J: Congenital macrothrombocytopenia, leukocyte inclusions, deafness and proteinuria: Functional and electron microscopic observations on platelets and megakaryocytes. Br J Haematol 78:441, 1988
-
(1988)
Br J Haematol
, vol.78
, pp. 441
-
-
Heynen, M.J.1
Blockmans, D.2
Verwilghen, R.L.3
Vermylen, J.4
-
11
-
-
0025606519
-
Sebastian platelet syndrome: A new variant of hereditary macrothrombocytopenia with leukocyte inclusions
-
Greinacher A, Nieuwenhuis HK, White JG: Sebastian platelet syndrome: A new variant of hereditary macrothrombocytopenia with leukocyte inclusions. Blut 61:282, 1990
-
(1990)
Blut
, vol.61
, pp. 282
-
-
Greinacher, A.1
Nieuwenhuis, H.K.2
White, J.G.3
-
12
-
-
0027440581
-
Fechtner syndrome: Report of a third family and literature review
-
Rocca B, Laghi F, Zini G, Maggiano N, Landolfi R: Fechtner syndrome: Report of a third family and literature review. Br J Haematol 85:423, 1993
-
(1993)
Br J Haematol
, vol.85
, pp. 423
-
-
Rocca, B.1
Laghi, F.2
Zini, G.3
Maggiano, N.4
Landolfi, R.5
-
13
-
-
0019444883
-
Analysis of the glycoprotein and protein composition of Bernard-Soulier platelets by single and two-dimensional sodium dodecylsulfate-polyacrylamide gel electrophoresis
-
Nurden AT, Dupuis D, Kunicki TJ, Caen JP: Analysis of the glycoprotein and protein composition of Bernard-Soulier platelets by single and two-dimensional sodium dodecylsulfate-polyacrylamide gel electrophoresis. J Clin Invest 67:14, 1981
-
(1981)
J Clin Invest
, vol.67
, pp. 14
-
-
Nurden, A.T.1
Dupuis, D.2
Kunicki, T.J.3
Caen, J.P.4
-
14
-
-
0015176866
-
Gray platelet syndrome: A variety of qualitative platelet disorder
-
Raccuglia G: Gray platelet syndrome: A variety of qualitative platelet disorder. Am J Med 51:818, 1971
-
(1971)
Am J Med
, vol.51
, pp. 818
-
-
Raccuglia, G.1
-
15
-
-
0018333833
-
Ultrastructural study of the gray platelet syndrome
-
White JG: Ultrastructural study of the gray platelet syndrome. Am J Pathol 95:445, 1979
-
(1979)
Am J Pathol
, vol.95
, pp. 445
-
-
White, J.G.1
-
16
-
-
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 102:10, 1981
-
(1981)
Am J Pathol
, vol.102
, pp. 10
-
-
Breton-Gorius, J.1
Vainchenker, W.2
Nurden, A.3
Levy-Toledano, S.4
Caen, J.5
-
17
-
-
0022377796
-
Gray platelet syndrome: Immunoelectron microscopic 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 microscopic localization of fibrinogen and von Willebrand factor in platelets and megakaryocytes. Blood 66:1309, 1985
-
(1985)
Blood
, vol.66
, pp. 1309
-
-
Cramer, E.M.1
Vainchenker, W.2
Vinci, G.3
Guichard, J.4
Breton-Gorius, J.5
-
18
-
-
24544444342
-
Thrombocytopenia due to diminished or defective platelet production
-
Williams WJ, Beutler E, Erslev AJ, Lichtman MA (eds) New York, NY, McGraw-Hill
-
George JN, Aster RH: Thrombocytopenia due to diminished or defective platelet production, in Williams WJ, Beutler E, Erslev AJ, Lichtman MA (eds): Hematology (ed 4). New York, NY, McGraw-Hill, 1990, p 1343
-
(1990)
Hematology (Ed 4)
, pp. 1343
-
-
George, J.N.1
Aster, R.H.2
-
19
-
-
0027433157
-
A novel genetic thrombocytopenia (Paris-Trousseau) associated with platelet inclusions, dysmegakaryopoiesis and chromosome deletion at 11q23
-
Favier R, Douay L, Esteva B, Portnoi MF, Gaulard P, Lecompte T, Perot C, Adam M, Lecrubier C, Van den Akker J, Lasfargues G, Najean Y, Breton-Gorius J: A novel genetic thrombocytopenia (Paris-Trousseau) associated with platelet inclusions, dysmegakaryopoiesis and chromosome deletion at 11q23. CR Acad Sci Paris 316:698, 1993
-
(1993)
CR Acad Sci Paris
, vol.316
, pp. 698
-
-
Favier, R.1
Douay, L.2
Esteva, B.3
Portnoi, M.F.4
Gaulard, P.5
Lecompte, T.6
Perot, C.7
Adam, M.8
Lecrubier, C.9
Van Den Akker, J.10
Lasfargues, G.11
Najean, Y.12
Breton-Gorius, J.13
-
20
-
-
0021125743
-
Simultaneous detection of membrane markers with monoclonal antibodies and peroxidatic activities in leukaemia: Ultrastructural analysis using a new method of fixation preserving the platelet peroxidase
-
Breton-Gorius J, Van Haeke D, Pryzwansky KB, Guichard J, Tabilio A, Vainchenker W, Carmel R: Simultaneous detection of membrane markers with monoclonal antibodies and peroxidatic activities in leukaemia: Ultrastructural analysis using a new method of fixation preserving the platelet peroxidase. Br J Haematol 58:447, 1984
-
(1984)
Br J Haematol
, vol.58
, pp. 447
-
-
Breton-Gorius, J.1
Van Haeke, D.2
Pryzwansky, K.B.3
Guichard, J.4
Tabilio, A.5
Vainchenker, W.6
Carmel, R.7
-
21
-
-
0021981476
-
Ultrastructural localization of lactoferrin and myeloperoxidase in human neutrophils by immunogold
-
Cramer EM, Pryzwansky KB, Villeval J-L, Testa U, Breton-Gorius J: Ultrastructural localization of lactoferrin and myeloperoxidase in human neutrophils by immunogold. Blood 65:423, 1985
-
(1985)
Blood
, vol.65
, pp. 423
-
-
Cramer, E.M.1
Pryzwansky, K.B.2
Villeval, J.-L.3
Testa, U.4
Breton-Gorius, J.5
-
22
-
-
0345079464
-
Ultrastructure of normal and leucocytes in human peripheral blood
-
Anderson DR: Ultrastructure of normal and leucocytes in human peripheral blood. J Ultrastruct Res 9:5, 1966
-
(1966)
J Ultrastruct Res
, vol.9
, pp. 5
-
-
Anderson, D.R.1
-
23
-
-
0025099404
-
Demonstration of a secondary lysosomes in bovine megakaryocytes and platelets using acid phosphatase cytochemistry with cerium as a trapping agent
-
Ménard M, Meyers KM, Prieur DJ: Demonstration of a secondary lysosomes in bovine megakaryocytes and platelets using acid phosphatase cytochemistry with cerium as a trapping agent. Thromb Haemost 63:127, 1990
-
(1990)
Thromb Haemost
, vol.63
, pp. 127
-
-
Ménard, M.1
Meyers, K.M.2
Prieur, D.J.3
-
24
-
-
0026515322
-
Localization of platelet osteonectin at the internal face of the α-granule membrane in platelets and megakaryocytes
-
Breton-Gorius J, Clezardin P, Guichard J, Debili N, Malaval L, Vainchenker W, Cramer EM, Delmas PD: Localization of platelet osteonectin at the internal face of the α-granule membrane in platelets and megakaryocytes. Blood 79:936, 1992
-
(1992)
Blood
, vol.79
, pp. 936
-
-
Breton-Gorius, J.1
Clezardin, P.2
Guichard, J.3
Debili, N.4
Malaval, L.5
Vainchenker, W.6
Cramer, E.M.7
Delmas, P.D.8
-
25
-
-
0027404316
-
Chromosome painting in acute monocytic leukemia
-
Cherif D, Romana S, Der-Sarkissian H, Jones C, Berger R: Chromosome painting in acute monocytic leukemia. Genes Chromosom Cancer 6:107, 1993
-
(1993)
Genes Chromosom Cancer
, vol.6
, pp. 107
-
-
Cherif, D.1
Romana, S.2
Der-Sarkissian, H.3
Jones, C.4
Berger, R.5
-
26
-
-
0028295479
-
Hunting 11q23 deletion with fluorescence in situ hybridization (FISH)
-
Cherif D, Bernard O, Paulien S, James M, Le Paslier D, Berger R: Hunting 11q23 deletion with fluorescence in situ hybridization (FISH). Leukemia 8:578, 1994
-
(1994)
Leukemia
, vol.8
, pp. 578
-
-
Cherif, D.1
Bernard, O.2
Paulien, S.3
James, M.4
Le Paslier, D.5
Berger, R.6
-
27
-
-
0025041497
-
A detailed genetic map of the long arm of chromosome 11
-
Julier C, Nakamura Y, Lathrop M, O Connell P, Leppert M, Litt M, Mohandas T, Lalouel J-M, White R: A detailed genetic map of the long arm of chromosome 11. Genomics 7:335, 1990
-
(1990)
Genomics
, vol.7
, pp. 335
-
-
Julier, C.1
Nakamura, Y.2
Lathrop, M.3
O Connell, P.4
Leppert, M.5
Litt, M.6
Mohandas, T.7
Lalouel, J.-M.8
White, R.9
-
28
-
-
0025133281
-
Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: Application to regional mapping of human chromosome 11
-
Cherif D, Julier C, Delattre O, Derré J, Lathrop GM, Berger R: Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: Application to regional mapping of human chromosome 11. Proc Natl Acad Sci USA 87:6639, 1990
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 6639
-
-
Cherif, D.1
Julier, C.2
Delattre, O.3
Derré, J.4
Lathrop, G.M.5
Berger, R.6
-
30
-
-
0027225872
-
Oligo-deoxynucleotides antisense to the proto-oncogene c-mpl specifically inhibit in vitro megakaryocytopoiesis
-
Methia N, Louache F, Vainchenker W, Wendung F: Oligo-deoxynucleotides antisense to the proto-oncogene c-mpl specifically inhibit in vitro megakaryocytopoiesis. Blood 82:1395, 1993
-
(1993)
Blood
, vol.82
, pp. 1395
-
-
Methia, N.1
Louache, F.2
Vainchenker, W.3
Wendung, F.4
-
31
-
-
0021962882
-
Eccentric localization of von Willebrand factor within a tubular structure of platelet α-granule resembling that of Weibel-Palade bodies
-
Cramer EM, Meyer D, Le Menn R, Breton-Gorius J: Eccentric localization of von Willebrand factor within a tubular structure of platelet α-granule resembling that of Weibel-Palade bodies. Blood 66:710, 1985
-
(1985)
Blood
, vol.66
, pp. 710
-
-
Cramer, E.M.1
Meyer, D.2
Le Menn, R.3
Breton-Gorius, J.4
-
32
-
-
0027751918
-
Effect of thrombin on maturing human megakaryocytes
-
Martin-Cramer E, Massé JM, Caen JP, Garcia I, Breton-Gorius J, Debili N, Vainchenker W: Effect of thrombin on maturing human megakaryocytes. Am J Pathol 143:1498, 1993
-
(1993)
Am J Pathol
, vol.143
, pp. 1498
-
-
Martin-Cramer, E.1
Massé, J.M.2
Caen, J.P.3
Garcia, I.4
Breton-Gorius, J.5
Debili, N.6
Vainchenker, W.7
-
33
-
-
0022653268
-
An ultrastructural morphometric analysis of platelet giant and fusion granules
-
Payne CM, Glasser L: An ultrastructural morphometric analysis of platelet giant and fusion granules. Blood 67:299, 1986
-
(1986)
Blood
, vol.67
, pp. 299
-
-
Payne, C.M.1
Glasser, L.2
-
34
-
-
0017155896
-
Platelet granulopathy. A new morphologic feature in preleukemia and myelomonocytic leukemia: Light microscopy and ultrastructural morphology and cytochemistry
-
Maldonado JE: Platelet granulopathy. A new morphologic feature in preleukemia and myelomonocytic leukemia: Light microscopy and ultrastructural morphology and cytochemistry. Mayo Clin Proc 51:452, 1976
-
(1976)
Mayo Clin Proc
, vol.51
, pp. 452
-
-
Maldonado, J.E.1
-
35
-
-
0017958814
-
Platelet microtubules and giant granules in the Chédiak-Higashi syndrome
-
White JG: Platelet microtubules and giant granules in the Chédiak-Higashi syndrome. Am J Med Tech 44:273, 1978
-
(1978)
Am J Med Tech
, vol.44
, pp. 273
-
-
White, J.G.1
-
36
-
-
0018747262
-
Giant granules in a child with the Chédiak-Higashi syndrome
-
Parmley RT, Poon MC, Christ WN, Malluh A: Giant granules in a child with the Chédiak-Higashi syndrome. Am J Hematol 6:51, 1979
-
(1979)
Am J Hematol
, vol.6
, pp. 51
-
-
Parmley, R.T.1
Poon, M.C.2
Christ, W.N.3
Malluh, A.4
-
37
-
-
0019131339
-
Development of giant granules in platelets during prolonged storage
-
White JG, Clawson CC: Development of giant granules in platelets during prolonged storage. Am J Pathol 101:635, 1980
-
(1980)
Am J Pathol
, vol.101
, pp. 635
-
-
White, J.G.1
Clawson, C.C.2
-
38
-
-
0025229045
-
α-Granule pool of glycoprotein IIb-IIIa in normal and pathologic platelets and megakaryocytes
-
Cramer EM, Savidge GF, Vainchenker W, Berndt MC, Pidard D, Caen JP, Massé JM, Breton-Gorius J: α-Granule pool of glycoprotein IIb-IIIa in normal and pathologic platelets and megakaryocytes. Blood 75:1220, 1990
-
(1990)
Blood
, vol.75
, pp. 1220
-
-
Cramer, E.M.1
Savidge, G.F.2
Vainchenker, W.3
Berndt, M.C.4
Pidard, D.5
Caen, J.P.6
Massé, J.M.7
Breton-Gorius, J.8
-
39
-
-
0022221113
-
An alpha granule membrane protein (GMP-140) is expressed on the plasma membrane after activation
-
Stenberg PE, Mc Ever RP, Shuman MA, Jacques YV, Bainton DF: An alpha granule membrane protein (GMP-140) is expressed on the plasma membrane after activation. J Cell Biol 101:880, 1985
-
(1985)
J Cell Biol
, vol.101
, pp. 880
-
-
Stenberg, P.E.1
Mc Ever, R.P.2
Shuman, M.A.3
Jacques, Y.V.4
Bainton, D.F.5
-
40
-
-
0026681436
-
Platelet dense granule membranes contain both granulophysin and P-selectin (GMP-140)
-
Israels SJ, Gerrard JM, Jacques YV, McNicol A, Cham B, Nishibori M, Bainton DF: Platelet dense granule membranes contain both granulophysin and P-selectin (GMP-140). Blood 80:143, 1992
-
(1992)
Blood
, vol.80
, pp. 143
-
-
Israels, S.J.1
Gerrard, J.M.2
Jacques, Y.V.3
McNicol, A.4
Cham, B.5
Nishibori, M.6
Bainton, D.F.7
-
41
-
-
0025220954
-
Synthesis of transforming growth factor-β1 by megakaryocytes and its localization to megakaryocyte and platelet α-granules
-
Fava RA, Casey TT, Wilcox J, Pelton RW, Moses HL, Nanney LB: Synthesis of transforming growth factor-β1 by megakaryocytes and its localization to megakaryocyte and platelet α-granules. Blood 76:1946, 1990
-
(1990)
Blood
, vol.76
, pp. 1946
-
-
Fava, R.A.1
Casey, T.T.2
Wilcox, J.3
Pelton, R.W.4
Moses, H.L.5
Nanney, L.B.6
-
42
-
-
0020049330
-
Myelofibrosis and acute megakaryoblastic leukemia in a child: Topographic relationship between fibroblasts and megakaryocytes with an α-granule defect
-
Breton-Gorius J, Bizet M, Reyes F, Dupuy E, Mear C, Vannier JP, Tron P: Myelofibrosis and acute megakaryoblastic leukemia in a child: Topographic relationship between fibroblasts and megakaryocytes with an α-granule defect. Leuk Res 6:97, 1982
-
(1982)
Leuk Res
, vol.6
, pp. 97
-
-
Breton-Gorius, J.1
Bizet, M.2
Reyes, F.3
Dupuy, E.4
Mear, C.5
Vannier, J.P.6
Tron, P.7
-
43
-
-
0025232370
-
The production of transforming growth factor-β in acute megakaryoblastic leukemia and its possible implications in myelofibrosis
-
Tervi T, Niitsu Y, Mahara K, Fujisaki Y, Urushizaki Y, Mogi Y, Kohgo Y, Watanabe N, Ogura M, Saito H: The production of transforming growth factor-β in acute megakaryoblastic leukemia and its possible implications in myelofibrosis. Blood 75:1540, 1990
-
(1990)
Blood
, vol.75
, pp. 1540
-
-
Tervi, T.1
Niitsu, Y.2
Mahara, K.3
Fujisaki, Y.4
Urushizaki, Y.5
Mogi, Y.6
Kohgo, Y.7
Watanabe, N.8
Ogura, M.9
Saito, H.10
-
44
-
-
0027525858
-
Characterization of an acute micromegakaryocytic leukaemia: Evidence for the pathogenesis of myelofibrosis
-
Reilly JT, Barnett D, Dolan G, Forrest P, Eastham J, Smith A: Characterization of an acute micromegakaryocytic leukaemia: Evidence for the pathogenesis of myelofibrosis. Br J Haematol 83:58, 1993
-
(1993)
Br J Haematol
, vol.83
, pp. 58
-
-
Reilly, J.T.1
Barnett, D.2
Dolan, G.3
Forrest, P.4
Eastham, J.5
Smith, A.6
-
45
-
-
0019139080
-
Light and electron microscopic observations of hepatic hematopoiesis of human fetuses II. Megakaryopoiesis
-
Enzan H, Takahashi H, Kawakami M, Yamashita S, Ohkita T, Yamamoto M: Light and electron microscopic observations of hepatic hematopoiesis of human fetuses II. Megakaryopoiesis. Acta Pathol Jpn 30:397, 1980
-
(1980)
Acta Pathol Jpn
, vol.30
, pp. 397
-
-
Enzan, H.1
Takahashi, H.2
Kawakami, M.3
Yamashita, S.4
Ohkita, T.5
Yamamoto, M.6
-
46
-
-
0026083238
-
Developmental changes in human megakaryocyte ploidy
-
Hegyi E, Nakazawa M, Debili N, Navarro S, Katz A, Breton-Gorius J, Vainchenker W: Developmental changes in human megakaryocyte ploidy. Exp Hematol 19:87, 1991
-
(1991)
Exp Hematol
, vol.19
, pp. 87
-
-
Hegyi, E.1
Nakazawa, M.2
Debili, N.3
Navarro, S.4
Katz, A.5
Breton-Gorius, J.6
Vainchenker, W.7
-
47
-
-
1842412412
-
Megakaryocyte maturation and platelet release in normal and pathologic conditions
-
Harris JR (eds) New York, NY, Plenum
-
Breton-Gorius J: Megakaryocyte maturation and platelet release in normal and pathologic conditions, in Harris JR (eds): Blood Cell Biochemistry. Megakaryocytes, Platelets, Macrophages and Eosinophils. New York, NY, Plenum, 1991, p 1
-
(1991)
Blood Cell Biochemistry. Megakaryocytes, Platelets, Macrophages and Eosinophils
, pp. 1
-
-
Breton-Gorius, J.1
-
49
-
-
0027259159
-
A radiation hybrid map of human chromosome 11q22-q23 containing the ataxia-telangiectasia disease locus
-
Richard CW III, Cox DR, Kaap L, Murnanane J, Cornelis F, Julier C, Lathrop M, James M: A radiation hybrid map of human chromosome 11q22-q23 containing the ataxia-telangiectasia disease locus. Genomics 17:1, 1993
-
(1993)
Genomics
, vol.17
, pp. 1
-
-
Richard III, C.W.1
Cox, D.R.2
Kaap, L.3
Murnanane, J.4
Cornelis, F.5
Julier, C.6
Lathrop, M.7
James, M.8
-
50
-
-
0025174969
-
Partial deletion of the long arm of chromosome 11 [del(11)(q23.3 → qter)] with abnormal white matter
-
Wardinsky TD, Weinberger E, Pagon ED, Clarrren SK, Thuline HC: Partial deletion of the long arm of chromosome 11 [del(11)(q23.3 → qter)] with abnormal white matter. Am J Med Genet 35:60, 1990
-
(1990)
Am J Med Genet
, vol.35
, pp. 60
-
-
Wardinsky, T.D.1
Weinberger, E.2
Pagon, E.D.3
Clarrren, S.K.4
Thuline, H.C.5
-
51
-
-
0026863494
-
The Ets gene family
-
Seth A, Ascione R, Fisher RJ, Mavrothalassitis GJ, Bhat NK, Papas TS: The Ets gene family. Cell Growth Differ 3:327, 1992
-
(1992)
Cell Growth Differ
, vol.3
, pp. 327
-
-
Seth, A.1
Ascione, R.2
Fisher, R.J.3
Mavrothalassitis, G.J.4
Bhat, N.K.5
Papas, T.S.6
-
52
-
-
0026215673
-
The human homolog of the mouse common viral integration region, Fli 1 maps to 11q23-q24
-
Baud V, Lipinski M, Rassart E, Poliquin L, Bergeron D: The human homolog of the mouse common viral integration region, Fli 1 maps to 11q23-q24. Genomics 11:223, 1991
-
(1991)
Genomics
, vol.11
, pp. 223
-
-
Baud, V.1
Lipinski, M.2
Rassart, E.3
Poliquin, L.4
Bergeron, D.5
-
53
-
-
0027472732
-
GATA and Ets cis-acting sequences mediate megakaryocytespecific expression
-
Lemarchandel V, Ghysdael J, Mignotte V, Rahuel C, Roméo P-H: GATA and Ets cis-acting sequences mediate megakaryocytespecific expression. Mol Cell Biol 13:668, 1993
-
(1993)
Mol Cell Biol
, vol.13
, pp. 668
-
-
Lemarchandel, V.1
Ghysdael, J.2
Mignotte, V.3
Rahuel, C.4
Roméo, P.-H.5
-
54
-
-
0027300255
-
The Fli-1 proto-oncogene involved in erythroleukemia and Ewing s sarcoma, encodes a transcriptional activator with DNA-binding specificities distinct from other Ets family members
-
Zhang L, Lemarchandel V, Roméo P-H, Ben David Y, Greer P, Bernstein A: The Fli-1 proto-oncogene involved in erythroleukemia and Ewing s sarcoma, encodes a transcriptional activator with DNA-binding specificities distinct from other Ets family members. Oncogene 8:1621, 1993
-
(1993)
Oncogene
, vol.8
, pp. 1621
-
-
Zhang, L.1
Lemarchandel, V.2
Roméo, P.-H.3
Ben David, Y.4
Greer, P.5
Bernstein, A.6
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