메뉴 건너뛰기




Volumn 44, Issue 1, 2005, Pages 47-50

Normal thrombopoietin and its receptor (c-mpl) genes in children with essential thrombocythemia

Author keywords

c mpl; Essential thrombocythemia; Thrombopoietin

Indexed keywords

THROMBOPOIETIN; THROMBOPOIETIN RECEPTOR;

EID: 10044265584     PISSN: 15455009     EISSN: None     Source Type: Journal    
DOI: 10.1002/pbc.20185     Document Type: Article
Times cited : (10)

References (29)
  • 1
    • 0020709775 scopus 로고
    • Thrombocytosis and thrombocythemia
    • Murphy S. Thrombocytosis and thrombocythemia. Clin Haematol 1983;12:89-106.
    • (1983) Clin Haematol , vol.12 , pp. 89-106
    • Murphy, S.1
  • 3
    • 0034025273 scopus 로고    scopus 로고
    • Leukemia and myelodysplasia: Effect of multiple cytotoxic therapy in essential thrombocythemia
    • Randi ML, Fabris F, Girolami A. Leukemia and myelodysplasia: Effect of multiple cytotoxic therapy in essential thrombocythemia. Leuk Lymph 1997;37:379-385.
    • (1997) Leuk Lymph , vol.37 , pp. 379-385
    • Randi, M.L.1    Fabris, F.2    Girolami, A.3
  • 4
    • 0028810123 scopus 로고    scopus 로고
    • Thrombocytosis in childhood
    • Sutor AH. Thrombocytosis in childhood. Semin Thromb Hemostas 1997;21:330-339.
    • (1997) Semin Thromb Hemostas , vol.21 , pp. 330-339
    • Sutor, A.H.1
  • 5
    • 0026352986 scopus 로고
    • Thrombosis and hemorrhage in thrombocytosis: Evaluation of a large cohort of patients (357 cases)
    • Randi ML, Stocco F, Rossi C, et al. Thrombosis and hemorrhage in thrombocytosis: Evaluation of a large cohort of patients (357 cases). J Med 1991;22:213-223.
    • (1991) J Med , vol.22 , pp. 213-223
    • Randi, M.L.1    Stocco, F.2    Rossi, C.3
  • 6
    • 0019818299 scopus 로고
    • Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell
    • Fialkow PS, Fogue GB, Jacobson RJ, et al. Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell. Blood 1981;58:916-919.
    • (1981) Blood , vol.58 , pp. 916-919
    • Fialkow, P.S.1    Fogue, G.B.2    Jacobson, R.J.3
  • 7
    • 0033555392 scopus 로고    scopus 로고
    • A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications
    • Harrison CN, Gale RE, Machin SJ, et al. A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications. Blood 1999;93:417-424.
    • (1999) Blood , vol.93 , pp. 417-424
    • Harrison, C.N.1    Gale, R.E.2    Machin, S.J.3
  • 8
    • 0033982423 scopus 로고    scopus 로고
    • Features of essential thrombocythemia in childhood: A study of five children
    • Randi ML, Putti MC, Fabris F, et al. Features of essential thrombocythemia in childhood: A study of five children. Br J Haematol 2000;108:86-89.
    • (2000) Br J Haematol , vol.108 , pp. 86-89
    • Randi, M.L.1    Putti, M.C.2    Fabris, F.3
  • 9
    • 0041940289 scopus 로고    scopus 로고
    • Comparison of molecular markers in a cohort of patients with chronic myeloproliferative disorders
    • Kralowics R, Buser AS, Teo SS, et al. Comparison of molecular markers in a cohort of patients with chronic myeloproliferative disorders. Blood 2003;102:1869-1871.
    • (2003) Blood , vol.102 , pp. 1869-1871
    • Kralowics, R.1    Buser, A.S.2    Teo, S.S.3
  • 10
    • 0032757997 scopus 로고    scopus 로고
    • Hereditary thrombocythemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene
    • Ghilardi N, Wiestner A, Kikuchi M, et al. Hereditary thrombocythemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene. Br J Haematol 1999;107:310-316.
    • (1999) Br J Haematol , vol.107 , pp. 310-316
    • Ghilardi, N.1    Wiestner, A.2    Kikuchi, M.3
  • 11
    • 10044234223 scopus 로고    scopus 로고
    • Familial essential thrombocythemia associated with one-base deletion in the 5′-untranslated region of the thrombopoietin gene
    • Kondo TG, Okabe M, Sanada M, et al. Familial essential thrombocythemia associated with one-base deletion in the 5′-untranslated region of the thrombopoietin gene. Blood 1998;100:383-386.
    • (1998) Blood , vol.100 , pp. 383-386
    • Kondo, T.G.1    Okabe, M.2    Sanada, M.3
  • 12
    • 0032913316 scopus 로고    scopus 로고
    • Autonomous megacaryocytes growth in essential thrombocythemia and idiopathic myelofibrosis is not related to a c-mpl mutation or to an autocrine stimulation by mpl-L
    • Taksin AL, Couedic JPL, Dusanter-Fourt I, et al. Autonomous megacaryocytes growth in essential thrombocythemia and idiopathic myelofibrosis is not related to a c-mpl mutation or to an autocrine stimulation by mpl-L. Blood 1999;93:125-139.
    • (1999) Blood , vol.93 , pp. 125-139
    • Taksin, A.L.1    Couedic, J.P.L.2    Dusanter-Fourt, I.3
  • 13
    • 0022743745 scopus 로고
    • Essential thrombocythemia: An interim report from the polycythemia vera study group
    • Murphy S, Iland H, Rosenthal D, et al. Essential thrombocythemia: An interim report from the polycythemia vera study group. Semin Hematol 1986;23:177-182.
    • (1986) Semin Hematol , vol.23 , pp. 177-182
    • Murphy, S.1    Iland, H.2    Rosenthal, D.3
  • 14
    • 0033656596 scopus 로고    scopus 로고
    • Relevance of bone marrow features in the differential diagnosis between essential thrombocythemia and early stage idiopathic myelofibrosis
    • Thiele J, Kvasnicka HM, Zankovich R, et al. Relevance of bone marrow features in the differential diagnosis between essential thrombocythemia and early stage idiopathic myelofibrosis. Haematologica 2000;85:1126-1134.
    • (2000) Haematologica , vol.85 , pp. 1126-1134
    • Thiele, J.1    Kvasnicka, H.M.2    Zankovich, R.3
  • 16
    • 10044234222 scopus 로고    scopus 로고
    • Cytogenetics of chronic myeloproliferative disorders and related myelodysplastic syndromes
    • Adeyinka A, Dewald GW. Cytogenetics of chronic myeloproliferative disorders and related myelodysplastic syndromes. Hematol Oncol North Am 2003;110:104-109.
    • (2003) Hematol Oncol North Am , vol.110 , pp. 104-109
    • Adeyinka, A.1    Dewald, G.W.2
  • 17
    • 0033897370 scopus 로고    scopus 로고
    • Hereditary thrombocythemia is a genetically heterogeneous disorder: Exclusion of TPO and mpl in two families with hereditary thrombocythemia
    • Wiestner A, Padosch SA, Ghilardi N, et al. Hereditary thrombocythemia is a genetically heterogeneous disorder: Exclusion of TPO and mpl in two families with hereditary thrombocythemia. Br J Haematol 2000;110:104-109.
    • (2000) Br J Haematol , vol.110 , pp. 104-109
    • Wiestner, A.1    Padosch, S.A.2    Ghilardi, N.3
  • 18
    • 0028557354 scopus 로고
    • Human thrombopoietin: Gene structure, cDNA sequence, expression, and chromosomal localization
    • Foster DC, Sprecher CA, Grant FJ, et al. Human thrombopoietin: Gene structure, cDNA sequence, expression, and chromosomal localization. Proc Natl Acad Sci USA 1994;91:13023-13027.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 13023-13027
    • Foster, D.C.1    Sprecher, C.A.2    Grant, F.J.3
  • 19
    • 0029035985 scopus 로고
    • Thrombopoietin: The primary regulator of platelet production
    • Kaushanski K. Thrombopoietin: The primary regulator of platelet production. Blood 1995;86:419-431.
    • (1995) Blood , vol.86 , pp. 419-431
    • Kaushanski, K.1
  • 20
    • 7144229346 scopus 로고    scopus 로고
    • Serum thrombopoietin level is mainly regulated by megakaryocyte mass rather then platelet mass in human subjects
    • Nagasawa T, Hasegawa Y, Shimizu S, et al. Serum thrombopoietin level is mainly regulated by megakaryocyte mass rather then platelet mass in human subjects. Br J Haematol 1998;101:242-244.
    • (1998) Br J Haematol , vol.101 , pp. 242-244
    • Nagasawa, T.1    Hasegawa, Y.2    Shimizu, S.3
  • 21
    • 0029817844 scopus 로고    scopus 로고
    • Regulation of serum thrombopoietin levels by platelets and megakaryocytes in patients with aplastic anemia and idiopathic thrombocytopenic purpura
    • Ichikara N, Ishida F, Shimodaira S, et al. Regulation of serum thrombopoietin levels by platelets and megakaryocytes in patients with aplastic anemia and idiopathic thrombocytopenic purpura. Thromb Haemostas 1996;76:156-160.
    • (1996) Thromb Haemostas , vol.76 , pp. 156-160
    • Ichikara, N.1    Ishida, F.2    Shimodaira, S.3
  • 22
    • 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, et al. A sensitive sandwich ELISA for measuring thrombopoietin in human serum: Serum thrombopoietin levels in healthy volunteers and in patients with haemopoietic disorders. Br J Haematol 1996;93:783-788.
    • (1996) Br J Haematol , vol.93 , pp. 783-788
    • Tahara, T.1    Usuki, K.2    Sato, H.3
  • 23
    • 0031975482 scopus 로고    scopus 로고
    • An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia
    • Wiestner A, Schlemper RJ, van der Maas APC, et al. An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia. Nat Genet 1998;18:49-52.
    • (1998) Nat Genet , vol.18 , pp. 49-52
    • Wiestner, A.1    Schlemper, R.J.2    Van Der Maas, A.P.C.3
  • 24
    • 0031668547 scopus 로고    scopus 로고
    • The activating splice mutation in intron 3 of thrombopoietin gene is not found in patients with non-familial essential thrombocythemia
    • Harrison CN, Gale RE, Wiestner AC, et al. The activating splice mutation in intron 3 of thrombopoietin gene is not found in patients with non-familial essential thrombocythemia. Br J Haematol 1998;102:1341-1343.
    • (1998) Br J Haematol , vol.102 , pp. 1341-1343
    • Harrison, C.N.1    Gale, R.E.2    Wiestner, A.C.3
  • 25
    • 2642609475 scopus 로고    scopus 로고
    • Impaired expression of the thrombopoietin receptor by platelets from patients with polycythemia vera
    • Moliterno AR, Hankins WD, Spivak JL. Impaired expression of the thrombopoietin receptor by platelets from patients with polycythemia vera. New Engl J Med 1998;338:572-580.
    • (1998) New Engl J Med , vol.338 , pp. 572-580
    • Moliterno, A.R.1    Hankins, W.D.2    Spivak, J.L.3
  • 26
    • 0032736325 scopus 로고    scopus 로고
    • Platelet c-mpl expression is dysregulated in patients with essential thrombocythemia but this is not of diagnostic value
    • Harrison CN, Gale RE, Pezella F, et al. Platelet c-mpl expression is dysregulated in patients with essential thrombocythemia but this is not of diagnostic value. Br J Haematol 1999;107:139-147.
    • (1999) Br J Haematol , vol.107 , pp. 139-147
    • Harrison, C.N.1    Gale, R.E.2    Pezella, F.3
  • 27
    • 10044295158 scopus 로고    scopus 로고
    • Thrombopoietin receptor polymorphism associated with thrombocytosis
    • Moliterno AR, Williams DM, Gutierrez LI, et al. Thrombopoietin receptor polymorphism associated with thrombocytosis. Blood 2000;100:586a.
    • (2000) Blood , vol.100
    • Moliterno, A.R.1    Williams, D.M.2    Gutierrez, L.I.3
  • 28
    • 0031863446 scopus 로고    scopus 로고
    • Analysis of thrombopoietin and c-mpl expression in a child with essential thrombocythemia
    • Yoshida N, Ishii E, Koga N, et al. Analysis of thrombopoietin and c-mpl expression in a child with essential thrombocythemia. Ped Hematol Oncol 1998;15:359-363.
    • (1998) Ped Hematol Oncol , vol.15 , pp. 359-363
    • Yoshida, N.1    Ishii, E.2    Koga, N.3
  • 29
    • 0037441601 scopus 로고    scopus 로고
    • Mutations in the VHL gene in sporadic apparently congenital polycythemia
    • Pastore YD, Jelinek J, Ang S, et al. Mutations in the VHL gene in sporadic apparently congenital polycythemia. Blood 2003;101:1591-1595.
    • (2003) Blood , vol.101 , pp. 1591-1595
    • Pastore, Y.D.1    Jelinek, J.2    Ang, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.