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 nd -resistant patient-derived xenografts and mouse-derived allografts, Pedretti and colleagues show i

4 breast cancer patient-derived xenografts and mouse-derived allografts.

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

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

7 Ex vivo treatment of Nlrp3 mutant mouse-derived BMDMs with Nlrp3-specific ASO demonstrated

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

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

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

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

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

13 Mouse-derived cancer organoids (MDCOs) are becoming incr

14 o persistence to that of syngeneic humanized mouse-derived CAR-T cells.

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

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

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

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

19 le S-acylation in multiple human-, rat-, and mouse-derived cell lines, catalyzed by zinc-finger Asp-H

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

21 Our investigation involving human- and mouse-derived cells revealed that vitamin D instructs th

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

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

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

25 e human brain-derived enhancer databases and mouse-derived data to provide a comprehensive computatio

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

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

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

29 IL26 enhanced mouse-derived DNA induction of inflammatory cytokines, w

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

31 cting Azami-Green (AG)-positive C57BL/6 (B6) mouse-derived embryonic stem cells (ESCs) into ICR Flk-1

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

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

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

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

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

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

38 We provide evidence that mouse-derived human open chromatin profiles can serve as

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

40 hu) FcepsilonRIalpha mAbs were produced with mouse-derived immunoglobulin variable regions and huIgG(

41 ti-human (hu) FceRIa mAbs were produced with mouse-derived immunoglobulin variable regions and huIgG(

42 Mouse-derived in situ Trex1 models of transcoding mutati

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

44 rns were observed akin to those reported for mouse-derived mAbs, but with early evidence of differing

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

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

47 Mouse-derived macrophages have the unique ability to res

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

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

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

51 We anticipate that adopting wild mouse-derived microbiota as standard for laboratory mous

52 Currently, only mouse-derived monoclonal antibodies (mAbs) are available

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

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

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

56 Rictor (mTORC2 scaffold protein) in primary mouse-derived neutrophils affects their chemotaxis by fM

57 retinal microvascular endothelial cells and mouse-derived neutrophils under high glucose conditions

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

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

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

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

62 d in mice bearing genetically engineered KPC mouse-derived pancreatic ductal adenocarcinoma tumors.

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

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

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

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

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

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

69 Mouse-derived Polbeta null fibroblasts had severely affe

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

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

72 Cross-validation of human- and mouse-derived protocols identified human-specific diseas

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

74 for improved removal of NOD scid gamma (NSG) mouse-derived reads from sequencing data.

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

76 or treatment-induced immune responses to the mouse-derived single-chain variable fragments included i

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

78 re-melanosome protein (Pmel)-Trx1 transgenic mouse-derived splenic T cells, flow cytometry, and gene

79 O.11-green fluorescent protein IL-4 reporter mouse-derived T(H)2-skewed cells in a transfer model dem

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

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

82 g evidence for laboratory contamination with mouse-derived virus and viral DNA sequences became accep

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