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1                                          The chimeric mouse (Agtr1a -/- <--> +/+) is made up of wild-
2 olk sac hematopoietic progenitor assays, and chimeric mouse analysis, we found that Hex is required f
3       The clinical application of rituximab (chimeric mouse anti-human CD20 mAb, Rituxan, IDEC-C2B8),
4                           Development of the chimeric mouse antihuman CD20 antibody, Rituximab, prese
5                                 Furthermore, chimeric mouse bone marrow studies showed that resident
6 ith studies using novel Tg mice expressing a chimeric mouse-BoPrP gene.
7 ts has led to the development of human glial chimeric mouse brains, which provides new opportunities
8     When wild-type veins were grafted into a chimeric mouse carrying TIE2-LacZ genes in bone marrow c
9 on and its mode of action, we have generated chimeric mouse embryos and performed tissue layer recomb
10 ax6 in eye and nasal development we produced chimeric mouse embryos composed of wild-type and Sey mut
11                           Analysis of staged chimeric mouse embryos with a high contribution from emb
12 CVRI in establishing left-right asymmetry in chimeric mouse embryos.
13 nd Sey/+ cells with continued development in chimeric mouse eyes.
14 e structural analysis of PrP(Sc), a redacted chimeric mouse-hamster PrP of 106 amino acids (MHM2 PrP1
15     When transplanted into naive recipients, chimeric mouse hearts had significantly prolonged surviv
16                  These data demonstrate that chimeric mouse-human antibodies are a viable alternative
17  occurred after introduction of cetuximab, a chimeric mouse-human antibody, for cancer treatment.
18           Consistent with this, an aglycosyl chimeric mouse-human DII-FL MAb (E28) variant that lacks
19 IgG1kappa constant domains and the resulting chimeric mouse-human genes were cloned into plant expres
20                                 Cetuximab, a chimeric mouse-human IgG1 monoclonal antibody against th
21 ride (LPS) were used to generate a series of chimeric mouse-human monoclonal antibodies with identica
22     Transgenic (Tg) mouse lines that express chimeric mouse-human prion protein (PrP), designated MHu
23 understand TERT protein function by creating chimeric mouse-human TERT proteins.
24 ablish a plant-based production system for a chimeric mouse-human version of mAb 62-71-3, to characte
25 r immunotherapy of B-cell malignancies using chimeric (mouse/human) or radiolabeled murine monoclonal
26                                       Native chimeric (mouse/human) snRNP particles were used to immu
27                          Studies using nAChR chimeric mouse/human alpha6 subunits indicated that resi
28 epsilon primary transcript were expressed as chimeric mouse/human anti 5-dimethylamino-1-naphthalenes
29             Therefore, we have constructed a chimeric mouse/human antibody based on the structure of
30 egrin alphaIIbbeta3 inhibitor abciximab is a chimeric mouse/human antibody that induces thrombocytope
31 a FAD-linked human PS1 variant (A246E) and a chimeric mouse/human APP harboring mutations linked to S
32     Studies involving WT or gain-of-function chimeric mouse/human beta3 subunits narrowed the search
33  from structural insights on the topology of chimeric mouse/human CD3epsilondelta dimers.
34  of regulatory interactions between CFTR and chimeric mouse/human ENaCs suggest that the 20 C-termina
35 oped a new knock-in mouse model of HD with a chimeric mouse/human exon 1 containing 140 CAG repeats i
36                                        Using chimeric mouse/human hybrid TfR1 constructs, we determin
37                              Mice expressing chimeric mouse/human PrP transgenes were produced.
38 o address this issue, we developed a prestin chimeric mouse in which both ROSA26 wild-type (WT) and p
39              In contrast, rat hepatocytes in chimeric mouse livers displayed rat kinetics despite the
40 ection of woodchuck hepatocytes in uPA/RAG-2 chimeric mouse livers.
41 in radiolabeled cross-linked fibrin in TM-/- chimeric mouse lung as compared with wild-type mice.
42 the progression of prion disease in a unique chimeric mouse model (see the related article beginning
43 man fluorescent endometriotic cell lines and chimeric mouse model as preclinical testing platform, ou
44                            In this report, a chimeric mouse model based on CD40 knockout and wild-typ
45                                      Using a chimeric mouse model for renal ischemia-reperfusion inju
46 n in vitro liver-stage growth assay and in a chimeric mouse model harboring human hepatocytes.
47                                 We created a chimeric mouse model in which A(2A)Rs on bone marrow-der
48 -relevant molecular pathways, we generated a chimeric mouse model in which sarcoma-associated genetic
49 sis, we enhanced beta-catenin signaling in a chimeric mouse model in which the stem cell selection co
50                    The establishment of this chimeric mouse model is a significant advance toward und
51                      Using a newly developed chimeric mouse model of AAA, we now demonstrate that mac
52 g in endothelial repair in apoE(-/-) mice, a chimeric mouse model was created by bone marrow transpla
53                             This human liver chimeric mouse model will expand the experimental possib
54                                         In a chimeric mouse model, B2G1 and polyclonal Ig preparation
55                          Using a human liver-chimeric mouse model, we show that a monoclonal antibody
56  patient-derived envelopes and a human-liver chimeric mouse model.
57  HCV quasispecies challenge in a human liver-chimeric mouse model.
58  Using in vitro cell culture and human liver-chimeric mouse models, we show that a human mAb targetin
59 the cochlear partition, similar to all other chimeric mouse models.
60 ive or noninvasive Salmonella organisms, and chimeric mouse studies revealed the key role of MyD88-de
61 l grafting approach to surgically assemble a chimeric mouse that was part wild-type (WT) and part cir
62 een fluorescence protein (GFP) hematopoietic chimeric mouse, we determined that 90% of the dividing c

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