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Volumn 135, Issue 3, 2006, Pages 348-351

A family with hereditary thrombocythaemia and normal genes for thrombopoietin and c-Mpl

Author keywords

c Mpl; Hereditary thrombocythaemia; Thrombopoietin

Indexed keywords

ERYTHROPOIETIN; THROMBOPOIETIN;

EID: 33749249387     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2006.06316.x     Document Type: Article
Times cited : (9)

References (25)
  • 1
    • 0034669997 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 7
    • 0016212656 scopus 로고
    • 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
  • 9
    • 0032757997 scopus 로고    scopus 로고
    • 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
  • 11
    • 0025194138 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 14
    • 0032529663 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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
  • 18
    • 0028210396 scopus 로고
    • 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
  • 20
    • 0036376905 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 24
    • 0031975482 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.