ライフサイエンスコーパス: mouse-derived

1 ed exogenic and undefined components such as mouse-derived 3T3 feeder cells and fetal bovine serum.

2 17 suppresses adipocyte differentiation from mouse-derived 3T3-L1 preadipocytes in vitro, and inhibit

3 oach to study gastric development is primary mouse-derived antral epithelium cultured as three-dimens

4 eptor, KIR3DL1, in a nonobese diabetic (NOD) mouse-derived autoantigen-specific Treg (2D2), which pro

5 C57BL/6 mouse-derived bone marrow cells were cultured with mouse

6 rt of this hypothesis, we found that C57BL/6 mouse-derived bone marrow macrophages treated with exoso

7 Task1(-/-)-mouse-derived brown adipocytes, compared with wild-type

8 ed brown adipocytes, compared with wild-type mouse-derived brown adipocytes, displayed an impaired be

9 have tested the effects of TNF-alpha on the mouse-derived C2C12 muscle cell line and on primary cult

10 Using adult rat ventricular myocytes and mouse-derived cardiac HL-1 cardiomyocytes, we demonstrat

11 c42 in beta HC-9 cells, an insulin-secreting mouse-derived cell line, resulted in a 2-fold increase i

12 a molecular clone of the HEMV provirus into mouse-derived cell lines revealed that it is replication

13 ndid 1 can infect and propagate in different mouse-derived cell lines through a low-pH-dependent, tra

14 other known PKI isoforms and that in several mouse-derived cell lines, PKIgamma is the predominant PK

15 In all mouse-derived cells tested, the pore-forming cytolysin l

16 played selective inhibitory activity against mouse-derived ceramide-specific glucosyltransferase and

17 idase 3 (DPP3), activated the ARE in primary mouse-derived cortical neurons.

18 fering RNA inhibition of LC3, or Beclin(+/-) mouse-derived DC, studies established a relationship bet

19 or functions were abrogated with CXCL10(-/-) mouse-derived DC1s.

20 he clinically relevant, melanoma Ag gp100 to mouse-derived DCs by molecular adjuvant and chaperone Gr

21 ical banding patterns for EL4.IL-2 cells and mouse-derived DNA, both of which were dissimilar to DNA

22 a in human lung endothelial cells but not in mouse-derived endothelial cells.

23 ESCs isolated so far corresponds to that of mouse-derived epiblast stem cells (EpiSCs).

24 oach to study gastric development is primary mouse-derived epithelium cultured as three-dimensional s

25 he Gfap genes bears an R236H mutation, and a mouse derived from the mating of these two lines (GFAP(T

26 nt of a large panel of eight-way RILs in the mouse, derived from eight genetically diverse parental s

27 The J4/5 loop of the group I intron in the mouse-derived fungal pathogen Pneumocystis carinii is th

28 HIV-1 infection was effectively inhibited in mouse-derived human splenocytes ex vivo.

29 Inclusion of human and mouse-derived inducible HSP70 in the vaccination protoco

30 cluding antibiotic stress and killing by the mouse-derived macrophage cell line J774.

31 with apoptosis in human neutrophils and the mouse-derived macrophage-type cell line J774.2.

32 Mouse-derived macrophages have the unique ability to res

33 nd exponential replication in permissive A/J mouse-derived macrophages, and apoptosis is delayed unti

34 ivation of caspase-1 in nonpermissive BALB/c mouse-derived macrophages, caspase-3 is not activated at

35 On the other hand, wild-type mouse-derived mast cells use both PKC-dependent and PKC-

36 bcutaneous implants of Tri-Modality Reporter Mouse derived MSCs in nude mice showed linear correlatio

37 d flow cytometry and qRT-PCR to screen fetal mouse-derived neurosphere cultures for ethanol-sensitive

38 e, we present the structural basis for how a mouse-derived neutralizing antibody (nAb), OD01, disrupt

39 ia colonized germ-free bystander mice before mouse-derived organisms.

40 Immunization with mouse-derived P. carinii produced a strong immune respon

41 antibody (MAb) termed 4F11 generated against mouse-derived P. carinii was shown by indirect immunoflu

42 differed substantially in human-, rat-, and mouse-derived P. carinii.

43 This occurred despite the detection of mouse derived peptides, suggesting that trans-splicing o

44 Herein, we conducted a mouse-derived photoreceptor (661W cell)-based high throu

45 Postmortem human eyes and mouse-derived photoreceptor cells (661W) were examined f

46 conserved ribosomal RNA group I intron from mouse-derived Pneumocystis carinii binds to a ribozyme t

47 tron from the large ribosomal subunit RNA of mouse-derived Pneumocystis carinii has been isolated and

48 s, binding to a group I intron ribozyme from mouse-derived Pneumocystis carinii was measured for the

49 Mouse-derived Polbeta null fibroblasts had severely affe

50 collection of mutants was tested in congenic mouse-derived primary macrophages, a major Nramp1-expres

51 In TRAMP mouse-derived prostate cancer cell lines, our optimal an

52 In murine peritoneal and mouse-derived RAW 264.7 macrophages, IFN-gamma-mediated

53 blood-derived CD133+ cells and FKRP L276IKI mouse derived satellite cells by a lentiviral vector exp

54 cs are blunted in insulin receptor knock-out mouse-derived skeletal myoblasts.

55 on polymerase chain reactions of B6Min x 129 mouse-derived tumors.

56 on was combined with i.v. transfer of Pmel-I mouse-derived type-1 CTLs (Tc1), glioma-bearing mice exh

57 etrotransposon insertions into two different mouse-derived yeast artificial chromosomes (YACs).