ライフサイエンスコーパス: we injected

1 We injected 11C-Pittsburgh compound B (PIB) intravenously in

2 ay had been eliminated unilaterally with 6-hydroxydopamine, we injected a Cre-dependent virus coding for channelrhodopsin

3 Specifically, we injected a dopamine type 1 antagonist (D1A; SCH23390) or a

4 We injected adeno-associated viral vectors coding for Cre-dep

5 fy genes repressed by miRNAs in mature hepatocytes in vivo, we injected adult mice carrying floxed Dicer1 alleles with an

6 We injected alpha (alpha)-lactose into mice-infected with Pla

7 We injected an AAV8-F9 vector into neonatal and adult mice an

8 To focally inhibit p11 expression in the dorsal striatum, we injected an adeno-associated virus (AAV) vector producing

9 On days 1, 4, 7 and 10 after virus exposure, we injected animals subcutaneously with NmAbs and quantified

10 o the cytochrome oxidase (CytOx) modules in visual area V2, we injected anterograde and retrograde cholera toxin subunit

11 To investigate this question, we injected anterograde tracer into the mPFC of rats and rabb

12 whether protection could be induced by self-antigens alone, we injected apoptotic cells that carry the same oxidation-spe

13 whether the transfer of mtDNA involves whole mitochondria, we injected B16rho(0) mouse melanoma cells into syngeneic C57

14 Here, we injected cardiotoxin into gastrocnemius muscle of Hmox1(+/

15 For this purpose, we injected cerebellar neural stem cells into the cerebellum

16 tify distinct subpopulations of vagal afferents within NTS, we injected cholera toxin B subunit (CTb) and isolectin B4 (I

17 e mesolimbic dopamine neurons and their presynaptic inputs, we injected Cre-conditional GFP virus into the NAc of (anti-G

18 In vivo, we injected CSp-EMV-primed or -unprimed dermal fibroblasts (o

19 In order to increase sediment P retention, we injected dissolved aluminum into the anoxic sediment of a

20 We injected elastase intratracheally and the RAGE antagonist

21 RK-expressing neurons are supraspinally-projecting neurons, we injected Fluorogold (FG) into the ventrobasal thalamic com

22 We injected "Gene Silencing Oligonucleotides" against miR-494

23 In our experiments, we injected helium/CO2 to displace water in eight water-satur

24 induced epigenetic underpinnings of these neuroadaptations, we injected increasing METH doses to rats for 2 weeks and mea

25 As a model of the innate immune response, we injected lipopolysaccharide into the scala tympani of mous

26 Here, we injected low and high levels of kainic acid (KA) in the de

27 odel this potential contribution of LPA in the spinal cord, we injected LPA into the normal spinal cord, revealing that L

28 Subsequently, we injected MSCs or saline into the infarcted myocardium of m

29 Secondly, to analyze the AFS cell microenvironment, we injected murine YFP(+) embryonic stem cells (ESC) into the

30 Here, we injected native serum from heavy stable isotope labeled (S

31 To interfere with PDGF-B signaling, we injected nephritic rats with PDGF-B neutralizing aptamers

32 sess senescent changes in systemic immune response efficacy we injected one and four-week old flies with the entomopathog

33 To test this hypothesis, we injected plasmids with sequence variations flanking an I-S

34 To this end, we injected rats aged P0-P28 with anterograde tracers into RS

35 We injected rats with a moderate non-toxic dose of MDMA (9 mg

36 We injected RE with adeno-associated virus to transduce cells

37 We injected recombinant adeno-associated virus containing the

38 ry involved in the two types of orienting behavior in mice, we injected retrograde tracer into the intermediate and deep

39 Here, we injected retrograde tracers into four different face patch

40 s related to visual capacity and frontal placement of eyes, we injected retrograde tracers into the medial rectus muscle

41 In this study, we injected the mouse footpad with recombinant WEEV (McMillan

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 al connections potentially contribute to this reactivation, we injected tracers into electrophysiologically identified lo

46 In this study, we injected VEEV or WEEV, engineered to express bioluminescen

47 We injected vesicular stomatitis virus (VSV), a transsynaptic

48 We injected wild-type and IL-31Tg mice with combinations of G

49 We injected ZIKV intracranially into wild type C57BL/6 mice a

50 Initially, we injected zinc finger nuclease (ZFN)-encoding mRNA or DNA i