共 8 条
[1]
Baxter E.J., Scott L.M., Campbell P.J., Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders, Lancet, 365, 9464, pp. 1054-1061, (2005)
[2]
Kralovics R., Passamonti F., Buser A.S., A gain-of-function mutation of JAK2 in myeloproliferative disorders, N Engl J Med, 352, 17, pp. 1779-1790, (2005)
[3]
Tefferi A., Primary myelofibrosis: 2012 update on diagnosis, risk stratification, and management, Am J Hematol, 86, 12, pp. 1017-1026, (2011)
[4]
Deisseroth A.B., Kaminskas E., Grillo J., Chen W., Saber H., Lu H., Rothmann M.D., Brar S.S., Wang J., Garnett C., Bullock J., Burke L., Rahman A., Sridhara R., Farrell A., US Food and Drug Administration Approval: Ruxolitinib for the Treatment of Patients with intermediate and high Risk Myelofibrosis, Clin Cancer Res, 15, 12, pp. 3212-3217, (2012)
[5]
Harrison C., Kiladjian J.J., Al-Ali H.K., Gisslinger H., Waltzman R., Stalbovskaya V., McQuitty M., Hunter D.S., Levy R., Knoops L., Cervantes F., Vannucchi A.M., Barbui T., Barosi G., JAK inhibition with ruxolitinib versus best available therapy for myelofibrosis, N Engl J Med, 366, 9, pp. 787-798, (2012)
[6]
Verstovsek S., Kantarjian H., Mesa R.A., Pardanani A.D., Cortes-Franco J., Thomas D.A., Safety and efficacy of INCB018424, a JAK1 and JAK2 inhibitor, in myelofibrosis, N Engl J Med, 363, 12, pp. 1117-1127, (2010)
[7]
Ostojic A., Vrhovac R., Verstovsek S., Ruxolitinib for the treatment of myelofibrosis: Its clinical potential, Ther Clin Risk Manag, 8, pp. 95-103, (2012)
[8]
Boehm U., Klamp T., Groot M., Howard J.C., Cellular responses to interferon-gamma, Annu Rev Immunol, 15, pp. 749-795, (1997)

