IDH1 and IDH2 mutation analysis in chronic- and blast-phase myeloproliferative neoplasms von Pardanani, A, Lasho, T L, Finke, C M, Mai, M, McClure, R F, Tefferi, A

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IDH mutations in primary myelofibrosis predict leukemic transformation and shortened survival: clinical evidence for leukemogenic collaboration with JAK2V617F von Tefferi, A, Jimma, T, Sulai, N H, Lasho, T L, Finke, C M, Knudson, R A, McClure, R F, Pardanani, A

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IDH1 and IDH2 mutation studies in 1473 patients with chronic-, fibrotic- or blast-phase essential thrombocythemia, polycythemia vera or myelofibrosis von Tefferi, A, Lasho, T L, Abdel-Wahab, O, Guglielmelli, P, Patel, J, Caramazza, D, Pieri, L, Finke, C M, Kilpivaara, O, Wadleigh, M, Mai, M, McClure, R F, Gilliland, D G, Levine, R L, Pardanani, A, Vannucchi, A M

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A phase-2 trial of low-dose pomalidomide in myelofibrosis von Begna, K H, Mesa, R A, Pardanani, A, Hogan, W J, Litzow, M R, McClure, R F, Tefferi, A

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Risk stratification for survival and leukemic transformation in essential thrombocythemia: a single institutional study of 605 patients von GANGAT, N, WOLANSKYJ, A. P, MCCLURE, R. F, LI, C.-Y, SCHWAGER, S, WU, W, TEFFERI, A

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JAK2 V617F is a rare finding in de novo acute myeloid leukemia, but STAT3 activation is common and remains unexplained von STEENSMA, D. P, MCCLURE, R. F, KARP, J. E, TEFFERI, A, LASHO, T. L, POWELL, H. L, DEWALD, G. W, KAUFMANN, S. H

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Recurrent IDH mutations in high-risk myelodysplastic syndrome or acute myeloid leukemia with isolated del(5q) von Pardanani, A, Patnaik, M M, Lasho, T L, Mai, M, Knudson, R A, Finke, C, Ketterling, R P, McClure, R F, Tefferi, A

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Novel FISH probes designed to detect IGK-MYC and IGL-MYC rearrangements in b-cell lineage malignancy identify a new breakpoint cluster region designated BVR2 von EINERSON, R. R, LAW, M. E, BLAIR, H. E, KURTIN, P. J, MCCLURE, R. F, KETTERLING, R. P, FLYNN, H. C, DOGAN, A, REMSTEIN, E. D

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Janus kinase 2 (V617F) mutation status, signal transducer and activator of transcription-3 phosphorylation and impaired neutrophil apoptosis in myelofibrosis with myeloid metaplasi... von MESA, R. A, TEFFERI, A, LASHO, T. S, LOEGERING, D, MCCLURE, R. F, POWELL, H. L, DAI, N. T, STEENSMA, D. P, KAUIMANN, S. H

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Clonal mast cell disease not meeting WHO criteria for diagnosis of mastocytosis: clinicopathologic features and comparison with indolent mastocytosis von Pardanani, A, Chen, D, Abdelrahman, R A, Reichard, K K, Zblewski, D, Wood, A J, McClure, R F, Butterfield, J H, Hanson, C A, Tefferi, A

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Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course von McClure, R. F., Dewald, G. W., Hoyer, J. D., Hanson, C. A.

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Use of multiple displacement amplification to amplify genomic DNA before sequencing of the α and β haemoglobin genes von Mai, M, Hoyer, J D, McClure, R F

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Serous borderline tumor of the paratestis: A report of seven cases von MCCLURE, Rebecca F, KEENEY, Gary L, SEBO, Thomas J, CHEVILLE, John C

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Validation of immunoglobulin gene rearrangement detection by PCR using commercially available BIOMED-2 primers von McClure, R F, Kaur, P, Pagel, E, Ouillette, P D, Holtegaard, C E, Treptow, C L, Kurtin, P J

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Constitutive Fas Ligand Gene Transcription in Sertoli Cells Is Regulated By Sp1 von McClure, R F, Heppelmann, C J, Paya, C V

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Multiple myeloma presenting initially as a solitary pleural effusion later complicated by malignant plasmacytic ascites von Inoue, Yoshio, Chua, Kathrina, McClure, Rebecca F., Jimenez, Manuel C., Gocke, Christopher D., Badros, Ashraf Z., Takebe, Naoko

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Essential Thrombocythemia Beyond the First Decade: Life Expectancy, Long-term Complication Rates, and Prognostic Factors von Wolanskyj, Alexandra P., Schwager, Susan M., McClure, Rebecca F., Larson, Dirk R., Tefferi, Ayalew

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The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both “atypical” myeloproliferative disorders and myelodysplastic syndromes von Steensma, David P., Dewald, Gordon W., Lasho, Terra L., Powell, Heather L., McClure, Rebecca F., Levine, Ross L., Gilliland, D. Gary, Tefferi, Ayalew

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JAK2 mutation in essential thrombocythaemia: clinical associations and long-term prognostic relevance von Wolanskyj, Alexandra P, Lasho, Terra L, Schwager, Susan M, McClure, Rebecca F, Wadleigh, Martha, Lee, Stephanie J, Gilliland, D Gary, Tefferi, Ayalew

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Do Students Studying Therapy Have More Problems? von McClure, Robert F.

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