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1 (DK/DK) mice suffered from rapid-onset acute lymphoblastic lymphoma.
2 ic background, display a high rate of thymic lymphoblastic lymphoma.
3 transformation to acute myeloid leukemia and lymphoblastic lymphoma.
4 ansformation to acute myeloid leukemia and T-lymphoblastic lymphoma.
5 lopment of human multiple myeloma and T-cell lymphoblastic lymphoma.
6 -cell acute lymphoblastic leukemia or T-cell lymphoblastic lymphoma.
7 e, were observed due to an aggressive T-cell lymphoblastic lymphoma.
8 ent treatment protocols for both T-ALL and T-lymphoblastic lymphoma.
9 ession, and a biopsy showed precursor B cell lymphoblastic lymphoma.
10 eas T/T(F) causes a long-latency, pre-B-cell lymphoblastic lymphoma.
11 therapy was effective only in patients with lymphoblastic lymphoma.
12 cute lymphoblastic leukemia (ALL) and T-cell lymphoblastic lymphoma.
13 ke cell line established from a patient with lymphoblastic lymphoma.
14 The patient's diagnosis was T-lymphoblastic lymphoma.
15 t only MASH but also liver infiltration of T-lymphoblastic lymphoma.
16 g adults (younger than 25 years) with ALL or lymphoblastic lymphoma.
17 c mechanism for extranodal infiltration of T-lymphoblastic lymphoma.
18 similar to most human and mouse T-cell acute lymphoblastic lymphomas.
19 tical in the inception of human T cell acute lymphoblastic lymphomas.
20 s not detected in either case of precursor B-lymphoblastic lymphomas.
21 two Burkitt's lymphomas, and two precursor B-lymphoblastic lymphomas.
22 39 eligible patients enrolled (230 ALL, nine lymphoblastic lymphoma); 120 were assigned to pegasparga
23 mall subset of XCGD GT mice developed T cell lymphoblastic lymphoma (2.94%) and myeloid leukemia (5.8
25 ts afflicted with this syndrome present with lymphoblastic lymphoma and a myeloproliferative disorder
27 rom small non-cleaved-cell lymphoma, 16 from lymphoblastic lymphoma, and five from large-cell lymphom
28 %, and 1% of small noncleaved cell lymphoma, lymphoblastic lymphoma, and large-cell cases, respective
29 pe of NHL that includes large-cell lymphoma, lymphoblastic lymphoma, and small noncleaved-cell lympho
31 oblastic leukaemia (pre-B cell or T cell) or lymphoblastic lymphoma (B cell or T cell immunophenotype
35 -cyclin-transgenic mice developed high-grade lymphoblastic lymphoma between 3 and 12 months of age.
36 -C3 mice develop aggressive malignant thymic lymphoblastic lymphomas between 4 and 8 months of age.
37 death (septic shock and natural killer-cell lymphoblastic lymphoma); both were related to treatment.
42 he oncogenic potential of Stat5, with thymic lymphoblastic lymphomas developing in a significant prop
43 pstein-Barr virus-negative, precursor B cell lymphoblastic lymphoma diagnosed 6 months after transpla
44 omas, mantle cell lymphomas, and precursor B-lymphoblastic lymphomas) expressed significant levels of
46 manner across B-cell lymphoma, T-cell acute lymphoblastic lymphoma, hepatocellular carcinoma, renal
47 study, the genetic basis of GD/T-cell acute lymphoblastic lymphoma in 2 affected siblings was deciph
48 nt growth to Ba/F3 cells and caused a T-cell lymphoblastic lymphoma in a murine bone marrow transplan
53 now report the development of thymic T cell lymphoblastic lymphomas in transgenic mice in which Stat
54 ent-free survival (pEFS) in pediatric T-cell lymphoblastic lymphoma is about 80%, whereas survival in
56 about the outcome of pediatric patients with lymphoblastic lymphoma (LBL) who suffer from progressive
57 lymphoblastic leukemia [ALL], 13 of 21 T-ALL/lymphoblastic lymphomas [LBL], 9 of 10 B-non-Hodgkin's l
59 en during embryonic development and in acute lymphoblastic lymphoma-like biphenotypic acute leukemias
61 actory acute lymphoblastic leukemia (ALL) or lymphoblastic lymphoma (LL) have poor outcomes compared
63 rose after therapy for one case of T-lineage lymphoblastic lymphoma (LyL) and two cases of acute lymp
64 e lymphoblastic leukaemia and two had B-cell lymphoblastic lymphoma; median age 41 years [IQR 32-50])
65 h relapsed or refractory B-ALL (n = 72) or B-lymphoblastic lymphoma (n = 2), treated in two cohorts:
69 are neoplasms derived from immature T cells (lymphoblastic lymphomas), or more commonly, from mature
70 was not seen in small-cell T-cell lymphomas, lymphoblastic lymphomas, or other tumor types, including
72 ce demonstrate complete penetrance of thymic lymphoblastic lymphomas, strongly suggesting that Prkdc
73 ctivation in adult mice induces T-cell acute lymphoblastic lymphoma (T-ALL), a tumor type known to ca
74 ntribute to the pathogenesis of T cell acute lymphoblastic lymphoma (T-ALL), but how activated Notch1
76 eviously, precursor T lymphoblastic leukemia/lymphoblastic lymphoma (T-ALL/LyL) was found to express
78 phoblastic leukemia (T-ALL) and T-cell acute lymphoblastic lymphoma (T-LBL) are aggressive hematologi
81 tients with newly diagnosed pediatric T-cell lymphoblastic lymphoma (T-LL) and gained preliminary dat
85 e lymphoblastic leukemia (T-ALL) or advanced lymphoblastic lymphoma (T-NHL) were randomized at diagno
88 reases of lymphoblasts to overt monoclonal T-lymphoblastic lymphomas that involved multiple organs.
90 ng adults with relapsed/refractory CD19+ ALL/lymphoblastic lymphoma treated on 5 CD19-directed CAR T-
91 We identified patients with r/r CD19+ ALL/lymphoblastic lymphoma treated on CD19-directed CAR T-ce
92 cases of large cell lymphoma, five cases of lymphoblastic lymphoma, two cases of small, noncleaved-c
93 survival among the patients with early-stage lymphoblastic lymphoma was inferior to that among the pa
94 Tp53-deficient mouse model for T-cell acute lymphoblastic lymphoma, we reported that loss of heteroz
97 ge 1 to 21 years with newly diagnosed ALL or lymphoblastic lymphoma were randomly assigned to intrave
98 adult patients with newly diagnosed ALL and lymphoblastic lymphoma were treated with a dose-intense
99 n patients with acute lymphoblastic leukemia/lymphoblastic lymphoma who developed hypersensitivity/si
100 n with acute lymphoblastic leukemia (ALL) or lymphoblastic lymphoma who received one of three CNS-dir
101 tive B-cell acute lymphoblastic leukaemia or lymphoblastic lymphoma with CD20 expression of at least