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1 ipopolysaccharide and later provided IL-4 by intracerebroventricular infusion.
2 xical increase in bone mass following leptin intracerebroventricular infusion.
3  and body weight (P < 0.0001) after a single intracerebroventricular infusion.
4 aged 11beta-HSD1(-/-) mice before and during intracerebroventricular infusion (10 d) of spironolacton
5 smalemmal disruption, rats (n = 21) received intracerebroventricular infusion 2 h before DTBI of a no
6                                              Intracerebroventricular infusion (3-4 d) of G(z) antisen
7  rats, we examined if PACAP (.25-1.0 microg, intracerebroventricular infusion) affects motivation as
8 able response to leptin under intravenous or intracerebroventricular infusion and the loss of respons
9 lateral ventricle of Sprague-Dawley rats for intracerebroventricular infusions, and arterial and veno
10 in treatment by intraperitoneal injection or intracerebroventricular infusion could normalize myocard
11 ing radio telemetry of arterial pressure and intracerebroventricular infusions, experiments were perf
12      Administration of recombinant leptin by intracerebroventricular infusion failed to cause complet
13 ist, leptin (0.62 microg/h) was added to the intracerebroventricular infusion for 10 days.
14                     Leptin by intravenous or intracerebroventricular infusion for 5 h was associated
15 rotein-CIP (AAV9-GFP-CIP) to brain cells via intracerebroventricular infusion in amyloid precursor pr
16 bitor, delivered directly to the brain using intracerebroventricular infusion in an aged transgenic m
17 for in vivo imaging of myelination following intracerebroventricular infusion in the rat brain.
18  IgG brain distribution after intrathecal or intracerebroventricular infusion into the cerebrospinal
19 body weight were retained at least 1 d after intracerebroventricular infusion into the left ventricle
20  (increased acoustic startle amplitude after intracerebroventricular infusion of 1 mug of CRF).
21                                          The intracerebroventricular infusion of 300 ng of alpha-MSH
22                                     Finally, intracerebroventricular infusion of 5-HT stimulated base
23              In Experiment 1, pups receiving intracerebroventricular infusion of 50 ng of the anti-in
24         Reproductive behavior is restored by intracerebroventricular infusion of 8-bromo-cGMP, the se
25                                       Direct intracerebroventricular infusion of a dominant-negative
26                                      Chronic intracerebroventricular infusion of a newly synthesized
27                           In OVX rats, 5-min intracerebroventricular infusion of a PAK inhibitor pept
28 ormance deficit could be reversed with acute intracerebroventricular infusion of a second AT4 recepto
29 nt with the in vitro findings, we found that intracerebroventricular infusion of a specific PPARdelta
30                 Direct activation of TLR3 by intracerebroventricular infusion of a TLR3 ligand impair
31 d memory impairment in mice that received an intracerebroventricular infusion of AbetaOs.
32                                 As expected, intracerebroventricular infusion of AG in mice increased
33                                      Chronic intracerebroventricular infusion of AG or dAG increased
34  fimbria-fornix-lesioned rats was blocked by intracerebroventricular infusion of alpha-bungarotoxin,
35                                              Intracerebroventricular infusion of an adenosine A1 rece
36                                      Chronic intracerebroventricular infusion of Ang II completely ab
37 food intake without causing malaise, whereas intracerebroventricular infusion of apoE antiserum stimu
38                Results showed that long-term intracerebroventricular infusion of BDNF accelerated the
39  oxygen on hippocampal neurogenesis; whereas intracerebroventricular infusion of brain-derived neurot
40  acute carbon monoxide poisoning followed by intracerebroventricular infusion of brain-derived neurot
41              Rats were rendered dependent by intracerebroventricular infusion of butorphanol (26 nmol
42 A1 and mPFC spine density observed 2 h after intracerebroventricular infusion of E2 was blocked by DH
43  lowering effects of insulin are reversed by intracerebroventricular infusion of either of two PI3K i
44              In parallel, mice were given an intracerebroventricular infusion of farnesoid X receptor
45 monoxide + hyperbaric oxygen with additional intracerebroventricular infusion of Fc fragment of tyros
46 , aged (24-month-old) rats were treated with intracerebroventricular infusion of FGF-2 or vehicle for
47            Compared with vehicle, continuous intracerebroventricular infusion of FGF21 increased both
48                                              Intracerebroventricular infusion of GDNF improved behavi
49                                              Intracerebroventricular infusion of GLP-1 in mice direct
50 WH therapy begun 3 weeks after initiation of intracerebroventricular infusion of human Abeta decrease
51                              Intracarotid or intracerebroventricular infusion of hypertonic NaCl evok
52  responses were obtained from peripheral and intracerebroventricular infusion of IL-1.
53                                              Intracerebroventricular infusion of IL-1beta also caused
54           Antagonizing the NPY1 receptors by intracerebroventricular infusion of its antagonist large
55  day (P) 7] rats received a single bilateral intracerebroventricular infusion of KA (50 nmol in 1.0 m
56 re is no leptin signaling in osteoblasts but intracerebroventricular infusion of leptin causes bone l
57 We recently showed that a 5-h intravenous or intracerebroventricular infusion of leptin elevated basa
58                                 Furthermore, intracerebroventricular infusion of leptin has shown tha
59 cts were observed after both intravenous and intracerebroventricular infusion of leptin, suggesting t
60                                     However, intracerebroventricular infusion of N(omega)-nitro-L-arg
61 ious studies, we found that a 2-week in vivo intracerebroventricular infusion of nerve growth factor
62  the BF of adult male rats following chronic intracerebroventricular infusion of NGF or cytochrome c.
63 -administration paradigm to demonstrate that intracerebroventricular infusion of NPS reinstates extin
64                                Similarly, an intracerebroventricular infusion of OLZ resulted in a tr
65                                 Furthermore, intracerebroventricular infusion of PF4800567 increased
66 n-derived neurotrophic factor signaling with intracerebroventricular infusion of recombinant human Tr
67 nd then blocked central EC signaling with an intracerebroventricular infusion of rimonabant while ass
68 e, haloperidol, or clozapine, followed by an intracerebroventricular infusion of saline or corticotro
69 allenged with a brief high-fat diet or acute intracerebroventricular infusion of saturated fatty acid
70                                              Intracerebroventricular infusion of the BACE1 inhibitor
71                                              Intracerebroventricular infusion of the CRF-sub-2 recept
72                                 By contrast, intracerebroventricular infusion of the glucose antimeta
73                   To accomplish these goals, intracerebroventricular infusion of the KOR antagonist n
74                                              Intracerebroventricular infusion of the peptide both 30
75       Previous experiments demonstrated that intracerebroventricular infusion of the protein kinase G
76                                          The intracerebroventricular infusion of trkB receptor body (
77  and memory impairment in mice that received intracerebroventricular infusions of AbetaOs.
78 ies, LC electrophysiological responsivity to intracerebroventricular infusions of CRF was assessed in
79 id fluxes in male Sprague-Dawley rats during intracerebroventricular infusions of either WIN55,212-2
80                                              Intracerebroventricular infusions of JB-1, a selective I
81 ularly concentrated in the hypothalamus, and intracerebroventricular infusions of nanomolar amounts o
82 ergic sprouting in animals receiving chronic intracerebroventricular infusions of neutralizing antibo
83                                   Similarly, intracerebroventricular infusions of oligomeric Abeta pr
84 riectomized, estradiol-treated rats received intracerebroventricular infusions of oxytocin (1 or 10 n
85                      After UVN and one-month intracerebroventricular infusions of saline, GABA(A)R ag
86 y the eIF4E-transgenic mice are corrected by intracerebroventricular infusions of the cap-dependent t
87  The effects of recombinant sAPP, applied by intracerebroventricular infusion, on hippocampal and cor
88 -sODN-Ran; we then delivered these probes by intracerebroventricular infusion or intraperitoneal inje
89            In this study, we discovered that intracerebroventricular infusion or local OVLT injection
90 ministration of nerve growth factor (NGF) by intracerebroventricular infusion or transplantation of N
91  (1 microg Fe in 2 microl) was delivered via intracerebroventricular infusion to the left cerebral ve
92 tudy, we examined the effect of BDNF chronic intracerebroventricular infusion versus K252a (a Trk rec

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