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1  cases were associated with a characteristic myeloproliferative syndrome.
2 ir deficiency results in a fatal lympho- and myeloproliferative syndrome.
3 th-old boy with NF1 who developed an unusual myeloproliferative syndrome.
4 impairs HSC quiescence and leads to a lethal myeloproliferative syndrome.
5 bosis, and atherogenesis, as occurs in human myeloproliferative syndromes.
6 r in murine marrow cells results in a lethal myeloproliferative syndrome and preliminary studies sugg
7 esulted in a systemic autoimmune lympho- and myeloproliferative syndrome and tissue inflammation comp
8 echanisms underlying the development of this myeloproliferative syndrome are currently unknown.
9 CR-ABL-infected SKP2(-/-) marrow developed a myeloproliferative syndrome but survival was significant
10 thepsin G regulatory sequences all develop a myeloproliferative syndrome, but only 15% to 20% develop
11 ruption of the murine SHIP gene results in a myeloproliferative syndrome characterized by a dramatic
12        Mice developed a completely penetrant myeloproliferative syndrome characterized by leukocytosi
13                                     The 8p11 myeloproliferative syndrome (EMS) is associated with tra
14 romoter in transgenic mice causes a nonfatal myeloproliferative syndrome in all mice; about 15% go on
15  primary murine hematopoietic cells caused a myeloproliferative syndrome in mice that recapitulated t
16  necessary and sufficient to cause a chronic myeloproliferative syndrome in murine bone marrow transp
17 t growth to hematopoietic cells and induce a myeloproliferative syndrome in murine bone marrow transp
18 ion of a chronic myeloid leukemia (CML)-like myeloproliferative syndrome in recipient mice when 5-flu
19 cells in culture and in the development of a myeloproliferative syndrome in transplanted mice.
20 ed in a significantly delayed and attenuated myeloproliferative syndrome induced by TEL-FGFR3 as comp
21                                     The 8p11 myeloproliferative syndrome is a rare, aggressive condit
22                                     The 8p11 myeloproliferative syndrome is an aggressive disorder ca
23 n mice leads to a phenotype similar to human myeloproliferative syndrome (MPS) and myelodysplastic sy
24          Myelodysplastic syndromes (MDS) and myeloproliferative syndromes (MPS) of childhood are a he
25  features of a Philadelphia-negative chronic myeloproliferative syndrome or chronic myelomonocytic le
26 Bcr-Abl has been associated with an indolent myeloproliferative syndrome referred to as chronic neutr
27 6 infants with Down syndrome had a transient myeloproliferative syndrome (TMS).
28 acute leukemia, myelodysplastic syndrome, or myeloproliferative syndrome were included.
29    Here, we show that loss of Foxo3 causes a myeloproliferative syndrome with splenomegaly and increa
30  has been transplantable, inducing a similar myeloproliferative syndrome within 1 month of transfer t