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Journal Abstract Search

194 related items for PubMed ID: 15282677

  • 21. Mpl Baltimore: a thrombopoietin receptor polymorphism associated with thrombocytosis.
    Moliterno AR, Williams DM, Gutierrez-Alamillo LI, Salvatori R, Ingersoll RG, Spivak JL.
    Proc Natl Acad Sci U S A; 2004 Aug 03; 101(31):11444-7. PubMed ID: 15269348
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  • 23. Refined chromosomal localization of the human thrombopoietin gene to 3q27-q28 and exclusion as the responsible gene for thrombocytosis in patients with rearrangements of 3q21 and 3q26.
    Schnittger S, de Sauvage FJ, Le Paslier D, Fonatsch C.
    Leukemia; 1996 Dec 03; 10(12):1891-6. PubMed ID: 8946927
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  • 26. The physiology of platelet production.
    Kuter DJ.
    Stem Cells; 1996 Dec 03; 14 Suppl 1():88-101. PubMed ID: 11012207
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  • 28. The molecular and cellular biology of thrombopoietin: the primary regulator of platelet production.
    Kaushansky K, Drachman JG.
    Oncogene; 2002 May 13; 21(21):3359-67. PubMed ID: 12032774
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  • 29. Measurement of thrombopoietic levels: clinical and biological relationships.
    Verbeek W, Faulhaber M, Griesinger F, Brittinger G.
    Curr Opin Hematol; 2000 May 13; 7(3):143-9. PubMed ID: 10786650
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  • 32. 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 13; 93(5):706-14. PubMed ID: 18367486
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  • 33. Hereditary erythrocytosis, thrombocytosis and neutrophilia.
    Hong WJ, Gotlib J.
    Best Pract Res Clin Haematol; 2014 Jun 13; 27(2):95-106. PubMed ID: 25189721
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  • 35. Association of hereditary thrombocythemia and distal limb defects with a thrombopoietin gene mutation.
    Graziano C, Carone S, Panza E, Marino F, Magini P, Romeo G, Pession A, Seri M.
    Blood; 2009 Aug 20; 114(8):1655-7. PubMed ID: 19553636
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  • 36. Elevated serum thrombopoietin and interleukin-6 concentrations in thrombocytosis associated with inflammatory bowel disease.
    Heits F, Stahl M, Ludwig D, Stange EF, Jelkmann W.
    J Interferon Cytokine Res; 1999 Jul 20; 19(7):757-60. PubMed ID: 10454346
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  • 38. 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 20; 110(1):104-9. PubMed ID: 10930985
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  • 39. A case of acute promyelocytic leukemia showing transient thrombocytosis caused by increased interleukin-6 and thrombopoietin after treatment with all-trans retinoic acid and chemotherapy.
    Kondo M, Nakabayashi Y, Sugiyama A, Tominaga T, Shinohara K.
    Gan To Kagaku Ryoho; 2009 May 20; 36(5):827-30. PubMed ID: 19461187
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