ライフサイエンスコーパス: T-lymphoma

1 insight into how deficiencies in E2A lead to T lymphoma.

2 ranscription when these cells are fused to a T lymphoma.

3 s essential for the efficient development of T lymphoma.

4 ible to N-methyl-N-nitrosourea (MNU)-induced T lymphomas.

5 ation and the ability of the virus to induce T lymphomas.

6 on EBV-transformed B cells, but not on B or T lymphomas.

7 ha-tTA/Tet-O-MYC(ON) mice bearing MYC-driven T-lymphomas.

8 c-myb and outside the transcription unit in T-lymphomas (Ahi-1, fit-1, and Mis-2) and monocytic and

9 CD44 to cell rolling, a CD44-negative mouse T lymphoma AKR1 was transfected with wild type (WT) or m

10 m during PDT-induced apoptosis, Jurkat human T lymphoma and Chinese hamster ovary cells were labeled

11 highly oncogenic herpesvirus that can cause T lymphomas and peripheral nerve demyelination in chicke

12 are present on the surface of a murine EL-4 T-lymphoma and a human carcinoma cell (HeLa), 2) arrive

13 c leukemia (T-ALL), T-lymphoid blast crisis, T-lymphoma, and B-cell chronic lymphocytic leukemia (B-C

14 Residual mNK cells in spleens of MYC(ON) T-lymphoma-bearing mice exhibit perturbations in the ter

15 Treating T-lymphoma-bearing mice with Type I IFN improves surviva

16 for the lineage marker CD5 selectively kill T-lymphoma but not normal T cells, although both express

17 nterfering RNA treatment of the Jurkat human T lymphoma cell line or human peripheral blood T cells d

18 emosensitivity assays, using the L5178 mouse T lymphoma cell line transfected with the human MDR1 gen

19 A mutant YAC-1 T lymphoma cell line, which was selected for resistance

20 e expression differences between two related T lymphoma cell lines, HuT78 and H9, were identified.

21 serum starvation-induced apoptosis in human T lymphoma cell lines.

22 for genes that increase the invasiveness of T lymphoma cell lines.

23 in domain of MDC-L supported adhesion of the T-lymphoma cell line, Jurkat, in a concentration- and di

24 its ability to support cell adhesion of the T-lymphoma cell line, Jurkat.

25 RNA) stability decreases rapidly when murine T lymphoma cells are treated with the synthetic glucocor

26 we show that Fas-dependent killing of Jurkat T lymphoma cells by SW620 colon cancer cells requires ca

27 DOX/DNA nanocomplexes eradicated EL4 T lymphoma cells in a time-dependent manner, eventually

28 Injection of MBL2 murine T lymphoma cells into ear skin of C57BL/6 and immunodefi

29 Tonsillar lymphocytes and SKW3 T lymphoma cells tethered and rolled on monolayers of cu

30 n human epidermoid carcinoma A431 and Jurkat T lymphoma cells that are, respectively, rich in or lack

31 rs (IL-2R) in plasma membranes of Kit 225 K6 T lymphoma cells were investigated by fluorescence reson

32 We used a single source of RNA (HuT78 T lymphoma cells) to eliminate sample variation and quan

33 se required for galectin-1 susceptibility of T lymphoma cells, indicating that similar O-glycan ligan

34 Using the SKW3 human T lymphoma cells, we show that integrin alphaLbeta2 enga

35 TCR-induced NF-kappa B activation in Jurkat T lymphoma cells.

36 ne, on maintenance DNA methylation in Jurkat T lymphoma cells.

37 em, we studied the role of Rho in murine EL4 T lymphoma cells.

38 ot induce significant cytotoxicity to feline T-lymphoma cells (3201B) or human T-lymphoma cells (CEM)

39 to feline T-lymphoma cells (3201B) or human T-lymphoma cells (CEM).

40 Treatment of S49 T-lymphoma cells (which possess lipid rafts but lack cav

41 current studies, we used wild-type (WT) S49 T-lymphoma cells and the kin(-) variant (which lacks pro

42 blocks T-cell-receptor-mediated apoptosis in T-lymphoma cells does not block anti-mu-induced apoptosi

43 c domain of TNFR2 (p75) and is detectable in T-lymphoma cells stably transfected with the TRAF2A cDNA

44 he small GTPase Rac1 on p53-deficient B- and T-lymphoma cells was investigated.

45 In wild-type (WT) S49 T-lymphoma cells, signaling by cAMP and glucocorticoids

46 In T-lymphoma cells, such crosslinking results in upregulat

47 th, identifying a new survival mechanism for T-lymphoma cells.

48 when cultured in vitro with the human Jurkat T lymphoma, CHL-1 melanoma, and SBC-3 small cell lung ca

49 mature NK cells is sufficient to delay both T-lymphoma growth and recurrence post MYC inactivation.

50 lymphocyte-specific genes in plasmacytoma x T lymphoma hybrids can be prevented by preserving Oct-2

51 on factor on the phenotype of plasmacytoma x T lymphoma hybrids established a critical role for Oct-2

52 the most oncogenic herpesviruses and induces T lymphomas in chickens within weeks after infection.

53 Here, we identify T lymphoma invasion and metastasis (Tiam) 1 as the Rac1-

54 Rac1 is mediated through the suppression of T lymphoma invasion and metastasis 1 (Tiam1) and its ups

55 potential miR-10b targets identified Tiam1 (T lymphoma invasion and metastasis 1), a guanidine excha

56 c guanine nucleotide exchange factor, Tiam1 (T lymphoma invasion and metastasis 1), in transducing a

57 observed for the amino-terminal PH domain of T lymphoma invasion and metastasis protein (Tiam-1), the

58 -specific guanine nucleotide exchange factor T-lymphoma invasion and metastasis 1 (Tiam1) to speciali

59 Tiam1 (T-lymphoma invasion and metastasis 1) is one of the know

60 al structure of the DH and PH domains of the T-lymphoma invasion and metastasis factor 1 (Tiam1) prot

61 d increase in protein and mRNA expression of T-lymphoma invasion and metastasis gene 1 (Tiam1), a gua

62 The prolactin (PRL)-dependent rat Nb2 T lymphoma is a valuable model for investigation of mole

63 at-stable growth inhibitor secreted by a rat T lymphoma line when cultured at high cell density.

64 r of c-myb was provided by one of the murine T-lymphoma lines bearing an insertion at Ahi-1 (p/m16i)

65 pment of hemopathies and is downregulated in T-lymphomas, such as anaplastic large-cell lymphoma (ALC

66 s of GNLY were evaluated using the syngeneic T lymphoma tumor C6VL.

67 mice also develop at lower frequencies B and T lymphomas with antigen receptor locus translocations.