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- Mullally, A
- Li, C-Y
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- Gilliland, D G
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In:
Leukemia vol. 23
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TG101209, a small molecule JAK2-selective kinase inhibitor potently inhibits myeloproliferative disorder-associated JAK2V617F and MPLW515L/K mutations. [electronic resource] by
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- Noronha, G
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- Mak, C C
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- Zhu, H
- Soll, R
- Gilliland, D G
- Tefferi, A
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In:
Leukemia vol. 21
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83.
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Bone marrow transplantation for therapy-related myelodysplasia: comparison with primary myelodysplasia. [electronic resource] by
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- Weinstein, H J
- Antin, J H
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Bone marrow transplantation vol. 20
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Transformation of hematopoietic cell lines to growth-factor independence and induction of a fatal myelo- and lymphoproliferative disease in mice by retrovirally transduced TEL/JAK2 fusion genes. [electronic resource] by
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In:
The EMBO journal vol. 17
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H4(D10S170), a gene frequently rearranged in papillary thyroid carcinoma, is fused to the platelet-derived growth factor receptor beta gene in atypical chronic myeloid leukemia with t(5;10)(q33;q22). [electronic resource] by
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- Anastasiadou, E
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- Crescenzi, B
- Sternberg, D W
- Andreasson, P
- Schiavo, R
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- Gilliland, D G
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Blood vol. 97
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PKC 412 FLT3 inhibitor therapy in AML: results of a phase II trial. [electronic resource] by
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- Grandin, W
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- Yap, A
- Cohen, P
- Fox, E
- Neuberg, D
- Clark, J
- Gilliland, D G
- Griffin, J D
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In:
Annals of hematology vol. 83 Suppl 1
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87.
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Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2. [electronic resource] by
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- Saxena, R
- DeHart, D B
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- Aster, J C
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- Li, F P
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Blood vol. 87
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TEL/AML-1 dimerizes and is associated with a favorable outcome in childhood acute lymphoblastic leukemia. [electronic resource] by
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- Stegmaier, K
- Tantravahi, R
- Ritz, J
- Koeffler, H P
- Takeuchi, S
- Janssen, J W
- Seriu, T
- Bartram, C R
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- Gilliland, D G
- Golub, T R
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Clinical and molecular features of FIP1L1-PDFGRA (+) chronic eosinophilic leukemias. [electronic resource] by
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- Wlodarska, I
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- Zachée, P
- Boogaerts, M
- Vanstraelen, D
- Herregods, M-C
- Van Hoof, A
- Selleslag, D
- Roufosse, F
- Maerevoet, M
- Verhoef, G
- Cools, J
- Gilliland, D G
- Hagemeijer, A
- Marynen, P
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Leukemia vol. 18
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90.
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Analysis of genomic aberrations and gene expression profiling identifies novel lesions and pathways in myeloproliferative neoplasms. [electronic resource] by
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- Wolniak, K
- Ebert, B L
- Berkofsky-Fessler, W
- Buzzai, M
- Sun, Y
- Xi, C
- Elkin, P
- Levine, R
- Golub, T
- Gilliland, D G
- Crispino, J D
- Licht, J D
- Zhang, W
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91.
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Stat5 is essential for the myelo- and lymphoproliferative disease induced by TEL/JAK2. [electronic resource] by
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- Cain, D
- Aster, J C
- Williams, I R
- Lee, C K
- Gerthner, R
- Kitamura, T
- Frantsve, J
- Anastasiadou, E
- Loh, M L
- Levy, D E
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- Gilliland, D G
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In:
Molecular cell vol. 6
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92.
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IDH1 and IDH2 mutation studies in 1473 patients with chronic-, fibrotic- or blast-phase essential thrombocythemia, polycythemia vera or myelofibrosis. [electronic resource] by
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- 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
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Leukemia vol. 24
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Accurate detection of uniparental disomy and microdeletions by SNP array analysis in myelodysplastic syndromes with normal cytogenetics. [electronic resource] by
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- Levine, R L
- Loh, M L
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- Kornblau, S M
- Issa, J-P
- Gilliland, D G
- Garcia-Manero, G
- Kantarjian, H M
- Estey, E H
- Look, A T
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In:
Leukemia vol. 23
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94.
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TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis. [electronic resource] by
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- Pardanani, A
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- Abdel-Wahab, O
- Lasho, T L
- Patel, J
- Gangat, N
- Finke, C M
- Schwager, S
- Mullally, A
- Li, C-Y
- Hanson, C A
- Mesa, R
- Bernard, O
- Delhommeau, F
- Vainchenker, W
- Gilliland, D G
- Levine, R L
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In:
Leukemia vol. 23
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95.
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Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia. [electronic resource] by
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- Cools, J
- Melotte, C
- Quentmeier, H
- Ferrando, A
- Levine, R
- Vermeesch, J R
- Stul, M
- Dutta, B
- Boeckx, N
- Bosly, A
- Heimann, P
- Uyttebroeck, A
- Mentens, N
- Somers, R
- MacLeod, R A F
- Drexler, H G
- Look, A T
- Gilliland, D G
- Michaux, L
- Vandenberghe, P
- Wlodarska, I
- Marynen, Peter
- Hagemeijer, Anne
Producer: 20041102
In:
Nature genetics vol. 36
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96.
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Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia. [electronic resource] by
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- Sullivan, M G
- Legare, R D
- Hutchings, S
- Tan, X
- Kufrin, D
- Ratajczak, J
- Resende, I C
- Haworth, C
- Hock, R
- Loh, M
- Felix, C
- Roy, D C
- Busque, L
- Kurnit, D
- Willman, C
- Gewirtz, A M
- Speck, N A
- Bushweller, J H
- Li, F P
- Gardiner, K
- Poncz, M
- Maris, J M
- Gilliland, D G
Producer: 19991019
In:
Nature genetics vol. 23
Availability: No items available.
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