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1                                                             We injected 7-week-old C57/BL6 mice with LLC1 tumor cells or
2                                                       Here, we injected a labeled pH-responsive peptide to mark acidic re
3 e causal role of PVT in behavioral control during conflict, we injected AAV expressing the inhibitory hM4Di DREADD and de
4                                                             We injected adeno-associated viral vectors coding for Cre-dep
5                                              In protocol A, we injected adenoviral vectors expressing TBX18 (or the repor
6                                                             We injected alpha (alpha)-lactose into mice-infected with Pla
7 efine the relationship between alpha-syn and Abeta plaques, we injected alpha-syn preformed fibrils (alpha-syn mpffs) int
8                                                 To do this, we injected an AAV into the PB region to deliver a Cre-depend
9                      To assess PVT involvement in conflict, we injected an adeno-associated virus (AAV) expressing the ge
10   To focally inhibit p11 expression in the dorsal striatum, we injected an adeno-associated virus (AAV) vector producing
11 ter the monkey became proficient with performing the tasks, we injected an inhibitor of protein synthesis, anisomycin, in
12  whether the transfer of mtDNA involves whole mitochondria, we injected B16rho(0) mouse melanoma cells into syngeneic C57
13                                                       Here, we injected cardiotoxin into gastrocnemius muscle of Hmox1(+/
14 sive connectivity between the auditory cortex and amygdala, we injected cholera toxin subunit b (CTB), a bidirectional tr
15 e projections are modified during recoveries after the DCL, we injected cholera toxin subunit B into the hand representat
16 e mesolimbic dopamine neurons and their presynaptic inputs, we injected Cre-conditional GFP virus into the NAc of (anti-G
17                                                             We injected Cre-dependent adeno-associated virus in an Rbp4-C
18                                          To determine this, we injected Cre-dependent designer receptors exclusively acti
19           To evaluate the therapeutic potential of CRISPRa, we injected CRISPRa-recombinant adeno-associated virus into t
20                  In order to increase sediment P retention, we injected dissolved aluminum into the anoxic sediment of a
21                                           Toward this goal, we injected double-stranded RNA of ferritin2 and ferritin1 in
22                                                             We injected elastase intratracheally and the RAGE antagonist
23                                                             We injected into NAc variants of a new designer adeno-associa
24  To further evaluate the different tumor microenvironments, we injected mice with prostate tumor cells either subcutaneou
25                                               Subsequently, we injected MSCs or saline into the infarcted myocardium of m
26         Secondly, to analyze the AFS cell microenvironment, we injected murine YFP(+) embryonic stem cells (ESC) into the
27                                                             We injected neuroanatomical tracers into specified locations
28 sess senescent changes in systemic immune response efficacy we injected one and four-week old flies with the entomopathog
29                                    To test this hypothesis, we injected plasmids with sequence variations flanking an I-S
30 l fluid, the non-spermatozoa-containing component of semen, we injected queens with semen or seminal fluid alone.
31                                                To this end, we injected rats aged P0-P28 with anterograde tracers into RS
32                                                             We injected rats with a moderate non-toxic dose of MDMA (9 mg
33                                                             We injected recombinant adeno-associated virus containing the
34                                        To investigate this, we injected retrograde neuronal tracers occupying the whole v
35 ry involved in the two types of orienting behavior in mice, we injected retrograde tracer into the intermediate and deep
36 s related to visual capacity and frontal placement of eyes, we injected retrograde tracers into the medial rectus muscle
37 he prospect of using ferrets to study Zika virus infection, we injected seven pregnant jills with the PR strain subcutane
38                                                             We injected streptozotocin in male Sprague Dawley rats and tr
39                        To perform a dual-contrast protocol, we injected the agents at different times so that the first c
40                                                             We injected the local anesthetic procaine [15, 17, 18] into t
41                                                             We injected the tibialis anterior muscle of 8-week-old mdx an
42 s of dural vessels might be altered in pathological states, we injected the vasodilator calcitonin gene-related peptide (
43                                                             We injected these vectors into the cerebellar cortex of rhesu
44 ers are supplied by anatomically discrete motoneuron pools, we injected tracer into the orbital layer of the cat lateral
45                                                             We injected transient flashes resulting in very brief, spatia
46                                                             We injected two groups with shPKCdelta or shCtrl(PKCdelta) in
47                                                             We injected two other groups with shSOM or shCtrl(SOM) into C
48                                                             We injected vesicular stomatitis virus (VSV), a transsynaptic
49                                                             We injected wild-type and IL-31Tg mice with combinations of G
50                                                             We injected ZIKV intracranially into wild type C57BL/6 mice a