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Journal Abstract Search

182 related items for PubMed ID: 16995886

  • 1. A family with hereditary thrombocythaemia and normal genes for thrombopoietin and c-Mpl.
    Tecuceanu N, Dardik R, Rabizadeh E, Raanani P, Inbal A.
    Br J Haematol; 2006 Nov; 135(3):348-51. PubMed ID: 16995886
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  • 3. Normal thrombopoietin and its receptor (c-mpl) genes in children with essential thrombocythemia.
    Randi ML, Putti MC, Pacquola E, Luzzatto G, Zanesco L, Fabris F.
    Pediatr Blood Cancer; 2005 Jan; 44(1):47-50. PubMed ID: 15390356
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  • 5. A de novo splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia in a Polish family.
    Liu K, Kralovics R, Rudzki Z, Grabowska B, Buser AS, Olcaydu D, Gisslinger H, Tiedt R, Frank P, Okoñ K, van der Maas AP, Skoda RC.
    Haematologica; 2008 May; 93(5):706-14. PubMed ID: 18367486
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  • 6. Hereditary thrombocythaemia is a genetically heterogeneous disorder: exclusion of TPO and MPL in two families with hereditary thrombocythaemia.
    Wiestner A, Padosch SA, Ghilardi N, Cesar JM, Odriozola J, Shapiro A, Skoda RC.
    Br J Haematol; 2000 Jul; 110(1):104-9. PubMed ID: 10930985
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  • 7. An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia.
    Wiestner A, Schlemper RJ, van der Maas AP, Skoda RC.
    Nat Genet; 1998 Jan; 18(1):49-52. PubMed ID: 9425899
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  • 8. 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.
    Br J Haematol; 1998 Feb; 100(2):383-6. PubMed ID: 9488631
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  • 12. 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.
    Am J Hematol; 2004 Aug; 76(4):395-7. PubMed ID: 15282677
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  • 13. 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 RC.
    Br J Haematol; 1999 Nov; 107(2):310-6. PubMed ID: 10583217
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  • 14. The Mpl receptor expressed on endothelial cells does not contribute significantly to the regulation of circulating thrombopoietin levels.
    Geddis AE, Fox NE, Kaushansky K.
    Exp Hematol; 2006 Jan; 34(1):82-6. PubMed ID: 16413394
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  • 15. Hereditary thrombocythemia caused by a thrombopoietin (THPO) gain-of-function mutation associated with multiple myeloma and congenital limb defects.
    Stockklausner C, Echner N, Klotter AC, Hegenbart U, Dreger P, Kulozik AE.
    Ann Hematol; 2012 Jul; 91(7):1129-33. PubMed ID: 22453305
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  • 16. Hereditary erythrocytosis, thrombocytosis and neutrophilia.
    Hong WJ, Gotlib J.
    Best Pract Res Clin Haematol; 2014 Jun; 27(2):95-106. PubMed ID: 25189721
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  • 17. Familial essential thrombocythemia with spontaneous megakaryocyte colony formation and acquired JAK2 mutations.
    Higgs JR, Sadek I, Neumann PE, Ing VW, Renault NK, Berman JN, Greer WL.
    Leukemia; 2008 Aug; 22(8):1551-6. PubMed ID: 18496561
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  • 19. Haematological abnormalities in early abstinent alcoholics are closely associated with alterations in thrombopoietin and erythropoietin serum profiles.
    Schmitt M, Gleiter CH, Nichol JL, Pralle L, Hasselblatt M, Poser W, Ehrenreich H.
    Thromb Haemost; 1999 Nov; 82(5):1422-7. PubMed ID: 10595631
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