ライフサイエンスコーパス: we transduced

1 the alphaVbeta6 integrin is a principal receptor for FMDV, we transduced a bovine kidney cell line to stably express bot

2 expression-clone molecules capable of binding adiponectin, we transduced a C2C12 myoblast cDNA retroviral expression lib

3 ntivectors are competent for encapsidation and integration, we transduced a lentiviral packaging cell line with a SIN len

4 To test this hypothesis, we transduced a mouse epidermal-derived DC line XS106 to expr

5 er understand the autocrine role of HIFs in the epicardium, we transduced adenovirus mediated expression of constitutivel

6 To assess AgmTRIM5alpha restriction in primary cells, we transduced AgmTRIM5alpha into primary rhesus macaque CD4 T

7 To investigate the significance of this finding, we transduced an alphav-negative human SCC line with retrovir

8 To characterize the role of miR-21 in melanoma behavior, we transduced B16 cells with lentivirus encoding a miR-21 ant

9 xpression of HMGA2 and JAK2V617F mutation in hematopoiesis, we transduced bone marrow cells from Jak2(V617F) knockin mice

10 To identify miRNAs implicated in EGFR signaling, we transduced bronchial epithelial BEAS-2B cells with retrovi

11 To analyze the function of RIP2 during differentiation, we transduced C2C12 myoblasts with retroviral vectors to cons

12 We transduced cells with amphotropic retroviral constructs co

13 We transduced chronic lymphocytic leukemia (CLL) cells lackin

14 We transduced dominant negative (dn) HIV TAT-Ras protein into

15 To test this hypothesis, we transduced enriched hematopoietic progenitor cells with a

16 In this study, we transduced exogenous LIGHT into embryonic stem cells (ES c

17 We transduced healthy human CD34(+) peripheral blood-mobilize

18 e efficiency and durability of antigen presentation by DCs, we transduced hematopoietic stem-progenitor cells (HSCs) with

19 To identify the missing factors, we transduced Huh-7.5 human hepatoma cells with a pooled lent

20 tigate mechanisms of resistance to angiogenesis inhibitors, we transduced human glioblastoma cells with retroviruses enco

21 s by which AREG regulates autocrine epithelial cell growth, we transduced human keratinocytes (KCs) with lentiviral const

22 E5 alters the pHs of additional intracellular compartments, we transduced human keratinocytes with a codon-optimized E5 v

23 We transduced human NK cell lines NK-92 and NKL, and primary

24 In this study, we transduced human NOD/SCID repopulating cells (SRCs) with M

25 To evaluate aniLV performance in primary cells, we transduced lineage-depleted murine hematopoietic progenito

26 To clarify the role of LMX1B in ovarian carcinogenesis, we transduced LMX1B into a panel of mouse and human OVCA cell

27 We transduced mBMSCs with Msx1 and Msx2 genes and compared os

28 We transduced mouse primary hepatic progenitor cells, lineage

29 t to increase tumor metastasis in an organ-specific manner, we transduced murine B16 melanoma cells with CXCR4 (CXCR4-B16

30 We transduced murine marrow cells with C/EBPalpha-estradiol r

31 We transduced NAcore astrocytes with an adeno-associated viru

32 We transduced neurons postinjury to express a constitutively

33 To test the requirement for MCT4 in vitro, we transduced neurospheres with lentiviruses encoding short-h

34 To enhance tumor apoptosis, we transduced non-small cell lung cancer cells with retrovira

35 We transduced nonhuman primate CD34+ hematopoietic cells with

36 ntribution of cyclin D3 in the proliferation of B-1a cells, we transduced p16(INK4a) peptidyl mimetics (TAT-p16) into B-1

37 ifferences in signal transduction affected IL-2 production, we transduced primary human CD4 T cells with a lentiviral vec

38 ct of retroviral vector integration on transcript splicing, we transduced primary human cells or cultured cells with HIV-

39 and telomerase expression during cellular immortalization, we transduced primary human cervical epithelial cells with th

40 We transduced primary human prostate basal and luminal cells

41 To address this issue, we transduced primary neurons from Sprague-Dawley rats or APP

42 Next, we transduced rat neonatal cardiomyocytes with adenovirus-exp

43 In the present study, we transduced recombinant adenovirus-mediated HIF-1alpha in e

44 we found that HSV2-gD27 could not infect Vero cells unless we transduced the cells with a retrovirus expressing HVEM.

45 he unique ability of the OFT cardiomyocytes to execute PCD, we transduced the embryonic chicken heart in ovo with recombi

46 To test this hypothesis, we transduced tumor and normal cells with a lentivirus encodi

47 Using adenovirus-mediated delivery we transduced umbrella cells in situ with either dominant act

48 Here, we transduced wild-type and conditional Cbfb-MYH11 knockin (K

49 opmental and regional differences influence transformation, we transduced wild-type or mutationally stabilized murine N-m

50 We transduced X-CGD patient-mobilized CD34(+) peripheral bloo