-
1
-
-
0034669997
-
Hypersensitivity of circulating progenitor cells to megakaryocyte growth and development factor (PEG-rHu MGDF) in essential thrombocythemia
-
Axelrad, A.A., Eskinazi, D., Correa, P.N. & Amato, D. (2000) Hypersensitivity of circulating progenitor cells to megakaryocyte growth and development factor (PEG-rHu MGDF) in essential thrombocythemia. Blood, 96, 3310-3321.
-
(2000)
Blood
, vol.96
, pp. 3310-3321
-
-
Axelrad, A.A.1
Eskinazi, D.2
Correa, P.N.3
Amato, D.4
-
2
-
-
0034210637
-
Translational pathophysiology: A novel molecular mechanism of human disease
-
Cazzola, M. & Skoda, R.C. (2000) Translational pathophysiology: a novel molecular mechanism of human disease. Blood, 95, 3280-3288.
-
(2000)
Blood
, vol.95
, pp. 3280-3288
-
-
Cazzola, M.1
Skoda, R.C.2
-
3
-
-
0029743453
-
Familial thrombocytosis in infancy presenting with a leukaemoid reaction
-
van Dijken, P.J., Woldendorp, K.H. & van Wouwe, J.P. (1996) Familial thrombocytosis in infancy presenting with a leukaemoid reaction. Acta Paediatrica, 85, 1132-1134.
-
(1996)
Acta Paediatrica
, vol.85
, pp. 1132-1134
-
-
Van Dijken, P.J.1
Woldendorp, K.H.2
Van Wouwe, J.P.3
-
4
-
-
2542502506
-
Familial essential thrombocythemia associated with a dominant-positive activating mutation of the c-MPL gene, which encodes for the receptor for thrombopoietin
-
Ding, J., Komatsu, H., Wakita, A., Kato-Uranishi, M., Ito, M., Satoh, A., Tsuboi, K., Nitta, M., Miyazaki, H., Iida, S. & Ueda, R. (2004) Familial essential thrombocythemia associated with a dominant-positive activating mutation of the c-MPL gene, which encodes for the receptor for thrombopoietin. Blood, 103, 4198-4200.
-
(2004)
Blood
, vol.103
, pp. 4198-4200
-
-
Ding, J.1
Komatsu, H.2
Wakita, A.3
Kato-Uranishi, M.4
Ito, M.5
Satoh, A.6
Tsuboi, K.7
Nitta, M.8
Miyazaki, H.9
Iida, S.10
Ueda, R.11
-
5
-
-
0022585336
-
Familial essential thrombocythemia
-
Eyster, M.E., Saletan, S.L., Rabellino, E.M., Karanas, A., McDonald, T.P., Locke, L.A. & Luderer, J.R. (1986) Familial essential thrombocythemia. American Journal of Medicine, 80, 497-502.
-
(1986)
American Journal of Medicine
, vol.80
, pp. 497-502
-
-
Eyster, M.E.1
Saletan, S.L.2
Rabellino, E.M.3
Karanas, A.4
McDonald, T.P.5
Locke, L.A.6
Luderer, J.R.7
-
6
-
-
0025184132
-
Familial essential thrombocythemia
-
Fernandez-Robles, E., Vermylen, C., Martiat, P., Ninane, J. & Cornu, G. (1990) Familial essential thrombocythemia. Pediatric Hematology and Oncology, 7, 373-376.
-
(1990)
Pediatric Hematology and Oncology
, vol.7
, pp. 373-376
-
-
Fernandez-Robles, E.1
Vermylen, C.2
Martiat, P.3
Ninane, J.4
Cornu, G.5
-
7
-
-
0016212656
-
Thrombocythaemia. Familial occurrence and transition into blastic crisis
-
Fickers, M. & Speck, B. (1974) Thrombocythaemia. Familial occurrence and transition into blastic crisis. Acta Haematologica, 51, 257-265.
-
(1974)
Acta Haematologica
, vol.51
, pp. 257-265
-
-
Fickers, M.1
Speck, B.2
-
8
-
-
3342967557
-
A case of familial thrombocytosis: Possible role of altered thrombopoietin production
-
Fujiwara, T., Harigae, H., Kameoka, J., Yokoyama, H., Takahashi, S., Tomiya, Y., Yamada, M., Ishizawa, K., Imaizumi, M. & Sasaki, T. (2004) A case of familial thrombocytosis: possible role of altered thrombopoietin production. American Journal of Hematology, 76, 395-397.
-
(2004)
American Journal of Hematology
, vol.76
, pp. 395-397
-
-
Fujiwara, T.1
Harigae, H.2
Kameoka, J.3
Yokoyama, H.4
Takahashi, S.5
Tomiya, Y.6
Yamada, M.7
Ishizawa, K.8
Imaizumi, M.9
Sasaki, T.10
-
9
-
-
0032757997
-
Hereditary thrombocythaemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene
-
Ghilardi, N., Wiestner, A., Kikuchi, M., Ohsaka, A. & Skoda, R.C. (1999) Hereditary thrombocythaemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene. British Journal of Haematology, 107, 310-316.
-
(1999)
British Journal of Haematology
, vol.107
, pp. 310-316
-
-
Ghilardi, N.1
Wiestner, A.2
Kikuchi, M.3
Ohsaka, A.4
Skoda, R.C.5
-
10
-
-
0030732423
-
Markedly reduced expression of platelet c-mpl receptor in essential thrombocythemia
-
Horikawa, Y., Matsumura, I., Hashimoto, K., Shiraga, M., Kosugi, S., Tadokoro, S., Kato, T., Miyazaki, H., Tomiyama, Y., Kurata, Y., Matsuzawa, Y. & Kanakura, Y. (1997) Markedly reduced expression of platelet c-mpl receptor in essential thrombocythemia. Blood, 90, 4031-4038.
-
(1997)
Blood
, vol.90
, pp. 4031-4038
-
-
Horikawa, Y.1
Matsumura, I.2
Hashimoto, K.3
Shiraga, M.4
Kosugi, S.5
Tadokoro, S.6
Kato, T.7
Miyazaki, H.8
Tomiyama, Y.9
Kurata, Y.10
Matsuzawa, Y.11
Kanakura, Y.12
-
11
-
-
0025194138
-
Esential thrombocythemia in two sisters originating from different stem cell levels
-
Janssen, J.W., Anger, B.R., Drexler, H.G., Bartram, C.R. & Heimpel, H. (1990). Esential thrombocythemia in two sisters originating from different stem cell levels. Blood, 75, 1633-1636.
-
(1990)
Blood
, vol.75
, pp. 1633-1636
-
-
Janssen, J.W.1
Anger, B.R.2
Drexler, H.G.3
Bartram, C.R.4
Heimpel, H.5
-
12
-
-
0001651349
-
Familial thrombocytosis associated with overproduction of thrombopoietin due to a novel splice donor site mutation
-
(Abstract)
-
Jorgensen, M.J., Raskind, W.H., Wolff, J.F., Bachrach, H.R. & Kaushansky, K. (1998) Familial thrombocytosis associated with overproduction of thrombopoietin due to a novel splice donor site mutation. (Abstract). Blood, 92(Suppl. 1), 205a.
-
(1998)
Blood
, vol.92
, Issue.1 SUPPL.
-
-
Jorgensen, M.J.1
Raskind, W.H.2
Wolff, J.F.3
Bachrach, H.R.4
Kaushansky, K.5
-
13
-
-
0028940028
-
Familial thrombocytosis
-
Kikuchi, M., Tayama, T., Hayakawa, H., Takahashi, I., Hoshino, H. & Ohsaka, A. (1995) Familial thrombocytosis. British Journal of Haematology, 89, 900-902.
-
(1995)
British Journal of Haematology
, vol.89
, pp. 900-902
-
-
Kikuchi, M.1
Tayama, T.2
Hayakawa, H.3
Takahashi, I.4
Hoshino, H.5
Ohsaka, A.6
-
14
-
-
0032529663
-
Familial essential thrombocythemia associated with one-base deletion in the 5′-untranslated region of the thrombopoietin gene
-
Kondo, T., Okabe, M., Sanada, M., Kurosawa, M., Suzuki, S., Kobayashi, M., Hosokawa, M. & Asaka, M. (1998) Familial essential thrombocythemia associated with one-base deletion in the 5′-untranslated region of the thrombopoietin gene. Blood, 92, 1091-1096.
-
(1998)
Blood
, vol.92
, pp. 1091-1096
-
-
Kondo, T.1
Okabe, M.2
Sanada, M.3
Kurosawa, M.4
Suzuki, S.5
Kobayashi, M.6
Hosokawa, M.7
Asaka, M.8
-
15
-
-
0031888876
-
Genes for thrombopoietin and c-mpl are not responsible for familial thrombocythaemia: A case study
-
Kunishima, S., Mizuno, S., Naoe, T., Saito, H. & Kamiya, T. (1998) Genes for thrombopoietin and c-mpl are not responsible for familial thrombocythaemia: a case study. British Journal of Haematology, 100, 383-386.
-
(1998)
British Journal of Haematology
, vol.100
, pp. 383-386
-
-
Kunishima, S.1
Mizuno, S.2
Naoe, T.3
Saito, H.4
Kamiya, T.5
-
16
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller, S.A., Dykes, D.D. & Polesky, H.F. (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Research, 16, 1215.
-
(1988)
Nucleic Acids Research
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
17
-
-
3843052277
-
Mpl Baltimore: A thrombopoietin receptor polymorphism associated with thrombocytosis
-
Moliterno, A.R., Williams, D.M., Gutierrez-Alamillo, L.I., Salvatori, R., Ingersoll, R.G. & Spivak, J.L. (2004) Mpl Baltimore: a thrombopoietin receptor polymorphism associated with thrombocytosis. Proceedings National Academy of Science of the United States of America, 101, 11444-11447.
-
(2004)
Proceedings National Academy of Science of the United States of America
, vol.101
, pp. 11444-11447
-
-
Moliterno, A.R.1
Williams, D.M.2
Gutierrez-Alamillo, L.I.3
Salvatori, R.4
Ingersoll, R.G.5
Spivak, J.L.6
-
18
-
-
0028210396
-
Familial essential thrombocythemia: Clinical characteristics of 11 cases in one family
-
Schlemper, R.J., van der Maas, A.P. & Eikenboom, J.C. (1994) Familial essential thrombocythemia: clinical characteristics of 11 cases in one family. Annals of Hematology, 68, 153-158.
-
(1994)
Annals of Hematology
, vol.68
, pp. 153-158
-
-
Schlemper, R.J.1
Van Der Maas, A.P.2
Eikenboom, J.C.3
-
19
-
-
0019406018
-
Familial myeloproliferative disease. Hematological and cytogenetic studies
-
Slee, P.H., van Everdingen, J.J., Geraedts, J.P., te Velde, J. & den Ottolander, G.J. (1981) Familial myeloproliferative disease. Hematological and cytogenetic studies. Acta Medica Scandinavica, 210, 321-327.
-
(1981)
Acta Medica Scandinavica
, vol.210
, pp. 321-327
-
-
Slee, P.H.1
Van Everdingen, J.J.2
Geraedts, J.P.3
Te Velde, J.4
Den Ottolander, G.J.5
-
20
-
-
0036376905
-
Cytogenetic and molecular genetic aspects of essential thrombocythemia
-
Steensma, D.P. & Tefferi, A. (2002) Cytogenetic and molecular genetic aspects of essential thrombocythemia. Acta Haematologica, 108, 55-65.
-
(2002)
Acta Haematologica
, vol.108
, pp. 55-65
-
-
Steensma, D.P.1
Tefferi, A.2
-
21
-
-
8944258119
-
A sensitive sandwich ELISA for measuring thrombopoietin in human serum: Serum thrombopoietin levels in healthy volunteers and in patients with haemopoietic disorders
-
Tahara, T., Usuki, K., Sato, H., Ohashi, H., Morita, H., Tsumura, H., Matsumoto, A., Miyazaki, H., Urabe, A. & Kato, T. (1996). A sensitive sandwich ELISA for measuring thrombopoietin in human serum: serum thrombopoietin levels in healthy volunteers and in patients with haemopoietic disorders. British Journal of Haematology, 93, 783-788.
-
(1996)
British Journal of Haematology
, vol.93
, pp. 783-788
-
-
Tahara, T.1
Usuki, K.2
Sato, H.3
Ohashi, H.4
Morita, H.5
Tsumura, H.6
Matsumoto, A.7
Miyazaki, H.8
Urabe, A.9
Kato, T.10
-
22
-
-
0037100542
-
The expression pattern of c-mpl in megakaryocytes correlates with thrombotic risk in essential thrombocythemia
-
Teofili, L., Pierconti, F., Di Febo, A., Maggiano, N., Vianelli, N., Ascani, S., Rossi, E., Pileri, S., Leone, G., Larocca, L.M. & De Stefano, V. (2002) The expression pattern of c-mpl in megakaryocytes correlates with thrombotic risk in essential thrombocythemia. Blood, 100, 714-717.
-
(2002)
Blood
, vol.100
, pp. 714-717
-
-
Teofili, L.1
Pierconti, F.2
Di Febo, A.3
Maggiano, N.4
Vianelli, N.5
Ascani, S.6
Rossi, E.7
Pileri, S.8
Leone, G.9
Larocca, L.M.10
De Stefano, V.11
-
23
-
-
0031554532
-
Familial essential thrombocythemia associated with von Willebrand disease
-
Ulibarrena, C., Vecino, A.M., Odriozola, J. & Cesar, J.M. (1997) [Familial essential thrombocythemia associated with von Willebrand disease]. Medicina Clinica (Barcelona), 109, 237.
-
(1997)
Medicina Clinica (Barcelona)
, vol.109
, pp. 237
-
-
Ulibarrena, C.1
Vecino, A.M.2
Odriozola, J.3
Cesar, J.M.4
-
24
-
-
0031975482
-
An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia
-
Wiestner, A., Schlemper, R.J., van der Maas, A.P. & Skoda, R.C. (1998) An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia. Nature Genetics, 18, 49-52.
-
(1998)
Nature Genetics
, vol.18
, pp. 49-52
-
-
Wiestner, A.1
Schlemper, R.J.2
Van Der Maas, A.P.3
Skoda, R.C.4
-
25
-
-
0033897370
-
Hereditary thrombocythaemia is a genetically heterogeneous disorder: Exclusion of TPO and MPL in two families with hereditary thrombocythaemia
-
Wiestner, A., Padosch, S.A., Ghilardi, N., Cesar, J.M., Odriozola, J., Shapiro, A. & Skoda, R.C. (2000) Hereditary thrombocythaemia is a genetically heterogeneous disorder: exclusion of TPO and MPL in two families with hereditary thrombocythaemia. British Journal of Haematology, 110, 104-109.
-
(2000)
British Journal of Haematology
, vol.110
, pp. 104-109
-
-
Wiestner, A.1
Padosch, S.A.2
Ghilardi, N.3
Cesar, J.M.4
Odriozola, J.5
Shapiro, A.6
Skoda, R.C.7
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