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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
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
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
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
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
34 fimbria-fornix-lesioned rats was blocked by intracerebroventricular infusion of alpha-bungarotoxin,
37 food intake without causing malaise, whereas intracerebroventricular infusion of apoE antiserum stimu
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
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
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
50 WH therapy begun 3 weeks after initiation of intracerebroventricular infusion of human Abeta decrease
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
59 cts were observed after both intravenous and intracerebroventricular infusion of leptin, suggesting t
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
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
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
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
84 riectomized, estradiol-treated rats received intracerebroventricular infusions of oxytocin (1 or 10 n
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
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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