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1 gic nerves) via intradermal microdialysis or intradermal injection.
2 1 was administered by topical application or intradermal injection.
3 ce systemic biological effects in vivo after intradermal injection.
4 ndium-111 oxyquinoline after i.v., s.c., and intradermal injection.
5 ler flowmetry in each of the digits prior to intradermal injection.
6  and edema if administered to CBA/Ca mice by intradermal injection.
7 tly facilitated tumorigenicity and growth by intradermal injection.
8 able with that previously demonstrated using intradermal injection.
9 trast to the overt skin irritation caused by intradermal injections.
10                                Notably, both intradermal injection and epicutaneous application of la
11 -HEV), whereas cynos administered vaccine by intradermal injections and cynos administered a mock DNA
12 tions separated by 10 weeks, or (3) a single intradermal injection at 10 weeks.
13 lens were randomized to receive (1) 6 repeat intradermal injections at 2-week intervals of grass poll
14 ctions of (99m)Tc-sulfur colloid followed by intradermal injections at the areolar cutaneous junction
15 ptake of fluorescently labeled albumin after intradermal injection by LECs was similar to that of der
16 case of hyperhidrosis means multiple painful intradermal injections by a skilled clinician at 6-month
17 a marker gene localized to lymph nodes after intradermal injection, constituting 1.5% of lymph node D
18 umors were constantly obtained, whereas most intradermal injections did not give rise to tumor and im
19 d with anti-interleukin-10 antibody prior to intradermal injection failed to promote tolerance.
20 s (NPs), which rapidly drain to the LN after intradermal injection, greatly enhances adjuvant efficac
21                          The group receiving intradermal injections had the greatest number of advers
22                                         Upon intradermal injection in the hindleg, a fraction of both
23                                        After intradermal injection into athymic mice, only fibroblast
24 e reporter gene luciferase, to mouse skin by intradermal injection into footpads using in vivo biolum
25 one mice induces skin inflammation following intradermal injection into normal mice.
26 sing carcinomas grew progressively following intradermal injection into syngeneic FVB mice, further d
27 peptide-based vaccine trial given monthly by intradermal injection, led to the development of a T-cel
28 skin architecture and, unlike a conventional intradermal injection, MicronJet administration of a 50m
29 rophils, lymphocytes, and monocytes in a rat intradermal injection model.
30                                              Intradermal injection of (18)F-FDG clearly revealed lymp
31                                              Intradermal injection of 10(6) wild-type but not 10(8) m
32            CIA was elicited in Lewis rats by intradermal injection of 100 microl of an emulsion of bo
33 (peripheral vascular permeability induced by intradermal injection of 9L glioma cell-conditioned medi
34 ted peptide-induced tolerance was blocked by intradermal injection of a calcitonin gene-related pepti
35 injection of full-dose influenza vaccine, an intradermal injection of a reduced dose resulted in simi
36                                              Intradermal injection of acid generates pain in both rod
37                                 Furthermore, intradermal injection of ADSCs along with BA-DEG-BA into
38 rom discrete sites within the skin following intradermal injection of allergen.
39 et al. demonstrate the feasibility of direct intradermal injection of allogeneic fibroblasts to the l
40 phocyte transfer (NLT) reaction involves the intradermal injection of allogeneic lymphocytes from one
41  a single dose of recombinant murine IL-6 or intradermal injection of an expression plasmid containin
42 ibited by neutralizing IL-23 in vitro and by intradermal injection of anti-TGFbeta neutralizing antib
43                                              Intradermal injection of anti-TSLP blocked the developme
44                                              Intradermal injection of Aspergillus fumigatus into wild
45  Angiogenesis induced by tumors arising from intradermal injection of B16 F1 melanoma cells was also
46 ation, we developed a novel system involving intradermal injection of BALB/c mouse ears.
47 rin (BCG) and subsequent activation using an intradermal injection of BCG in complete Freund adjuvant
48          Superficially applied capsaicin and intradermal injection of beta-alanine, an MrgprD agonist
49                                              Intradermal injection of bile acids and a TGR5-selective
50 ity of the skin swelling induced by means of intradermal injection of C3a or C5a required that mast c
51                                     In vivo, intradermal injection of C5aRAM inhibited C5a-induced de
52 In contrast, the area of erythema induced by intradermal injection of calcitonin gene-related peptide
53                                       Before intradermal injection of capsaicin (10 microg/10 microl)
54 e to mechanical stimuli but responded to the intradermal injection of capsaicin (69 +/- 7 APs in 10 m
55 NMDA) receptors in dorsal horn neurons after intradermal injection of capsaicin (CAP).
56 uman subjects during intense pain induced by intradermal injection of capsaicin and during post-capsa
57                                              Intradermal injection of capsaicin and NGF produce heat
58  (STT) neurons in anesthetized monkeys after intradermal injection of capsaicin depends in part on di
59 mice, as was plasma extravasation induced by intradermal injection of capsaicin into the paw.
60 pinothalamic tract (STT) neurons produced by intradermal injection of capsaicin on the descending inh
61                          We examined whether intradermal injection of capsaicin produced morphologica
62 the attenuation of PAG inhibition induced by intradermal injection of capsaicin were prevented by pre
63   Localized noxious stimuli (55 degrees C or intradermal injection of capsaicin) caused flare extendi
64 light brushing of the forearm; (iii) forearm intradermal injection of capsaicin, (iv) and (v) the wan
65 al horn neurons after noxious stimulation by intradermal injection of capsaicin.
66 T cells to mechanical stimuli was induced by intradermal injection of capsaicin.
67                                              Intradermal injection of carbamoyl PAF (CPAF; 1-hexadecy
68 and reconstituted with autologous PBMCs, the intradermal injection of CCL18 led to the cutaneous recr
69 ous thermal stimuli in either genotype after intradermal injection of CPAF.
70 elivery was comparable with that produced by intradermal injection of DNA.
71  lymphoid tumors could be induced in cats by intradermal injection of ecotropic feline leukemia virus
72  and C3H/HeN (H-2(k)) mice were immunized by intradermal injection of either single plasmids or cockt
73                                              Intradermal injection of either the inflammogen carragee
74                                              Intradermal injection of either the NOS substrate L-argi
75                                        Local intradermal injection of EPI inhibited the induction of
76 ne expression in RDEB skin in vivo by direct intradermal injection of fibroblasts.
77 ctin-1-enhanced DC migration by showing that intradermal injection of galectin-1 in MRL-fas mice, whi
78 EB include (i) ex vivo gene therapy and (ii) intradermal injection of gene-corrected DEB fibroblasts,
79             The intradermal arm tested daily intradermal injection of gentamicin solution (8 mg) or p
80                                              Intradermal injection of GsMTx-4 in the rat hindpaw reve
81 nt of adjuvant arthritis in Lewis rats after intradermal injection of heat-killed Mycobacterium tuber
82 r topical application of cowhage spicules or intradermal injection of histamine and capsaicin.
83                                Following the intradermal injection of histamine, a transient, time-de
84       Lymphoscintigraphy was performed after intradermal injection of HSA in 85 patients and SC in 21
85                                              Intradermal injection of human IL-11 (500 ng/day) delays
86 ection, we examined the responses induced by intradermal injection of human subjects with synthetic l
87 ays expressed in psoriatic lesions, a single intradermal injection of IFN-gamma was administered to a
88  local abrogation of IkappaBzeta function by intradermal injection of IkappaBzeta siRNA abolished pso
89                     We demonstrate here that intradermal injection of IL-12 cDNA induces systemic bio
90                                              Intradermal injection of IL-12 cDNA resulted in local ex
91                                     Finally, intradermal injection of IL-17A in standard diet-fed mic
92            This stage could be reproduced by intradermal injection of IL-1alpha or IL-1beta and was p
93                                              Intradermal injection of IL-23 bypassed the requirement
94 skin lesions were induced in C57BL/6 mice by intradermal injection of IL-23 in the ear or dorsum.
95                Vascular tumors arising after intradermal injection of immortalized murine endothelial
96 ersed the mechanical hyperalgesia induced by intradermal injection of inflammatory mediators.
97      We demonstrate that, in response to the intradermal injection of interleukin-8, neutrophils are
98 onstrated that high pressure, resulting from intradermal injection of large liquid volumes, facilitat
99                     A group of mice received intradermal injection of lipopolysaccharide (LPS) and PE
100 a vascular leak that exceeds the response to intradermal injection of LTC(4) or LTD(4), and that this
101 a comparable dose-dependent vascular leak to intradermal injection of LTC4 or LTD4 and an augmented r
102                       We now report that the intradermal injection of LTE(4) into the ear of mice def
103                                              Intradermal injection of mEotaxin and mMIP-1alpha, but n
104                                              Intradermal injection of N-formyl-met-leu-phe (FMLP), a
105 2 expression could be partially inhibited by intradermal injection of neutralizing Ab against IL-1bet
106   The hyperalgesia was acutely attenuated by intradermal injection of nonselective protein kinase C (
107                                     Further, intradermal injection of normal human or gene-corrected
108  subjected to the identical CHMI protocol by intradermal injection of P. falciparum sporozoites.
109    Wheal and flare responses were induced by intradermal injection of PAF, codeine and histamine in 1
110          IgG1 responses were also induced by intradermal injection of pAra h2, and by i.m. injection
111                                              Intradermal injection of PEDF substantially inhibited LP
112 ule expression could be further increased by intradermal injection of pig interferon-gamma (IFN-gamma
113 nse to beta-galactosidase induced by i.m. or intradermal injection of placZ, a plasmid DNA vector enc
114                                              Intradermal injection of plasmid DNA encoding a transcri
115        Five to seven days postapplication of intradermal injection of plasmid TGF-beta1 followed by e
116 e distribution of skin size induration after intradermal injection of PPD among 364 pulmonary TB pati
117          However, lack of skin induration to intradermal injection of PPD or PPD anergy is observed i
118  effects of ultraviolet-B irradiation versus intradermal injection of pTpT on tumor necrosis factor a
119 ayed-type hypersensitivity (DTH) reaction to intradermal injection of purified protein derivative (PP
120                                              Intradermal injection of RDEB fibroblasts overexpressing
121                                          The intradermal injection of recombinant human TNFalpha indu
122 gh doses of sensitizing antigen, or by local intradermal injection of recombinant IL-1beta immediatel
123  the skin and surrounding hair follicles via intradermal injection of recombinant R-spondin2 protein.
124 elayed-type hypersensitivity (DTH) following intradermal injection of recombinant soluble HIV-1(MN) g
125                     In separate experiments, intradermal injection of S1509a RNA into naive mice thre
126 h to address this question, and we find that intradermal injection of S1P induced significant licking
127 d not mount an inflammatory skin response to intradermal injection of SEB.
128 pe hypersensitivity (DTH), in response to an intradermal injection of specific antigen are used as a
129                                           An intradermal injection of stromelysin-1 immediately befor
130                                              Intradermal injection of submicrogram quantities of goat
131 beta T cells was not observed after a single intradermal injection of such minute amounts of SEB.
132 is when administered 2 days after orthotopic intradermal injection of the cells, or when treatment st
133  TRPM3-expressing somatosensory neurons, and intradermal injection of the compound induced a TRPM3-de
134              Subcutaneous, intramuscular and intradermal injection of the LNP-encapsulated mRNA trans
135 re documented in the serum within 24 h after intradermal injection of the pIL-12o- plasmid, which als
136                                     Repeated intradermal injection of the selective mu-opioid recepto
137                 Both topical application and intradermal injection of this oligonucleotide to albino
138         Nocifensive behaviors induced by the intradermal injection of three different P2X receptor ag
139 randomly assigned 119 subjects to receive an intradermal injection of trivalent inactivated influenza
140 ous inflammation was induced in the thigh by intradermal injection of tuberculin.
141               All patients had a single-site intradermal injection of unfiltered (99m)Tc-sulfur collo
142                   Patients had a single-site intradermal injection of unfiltered TSC in 0.05 mL norma
143 protection from lethal disease is induced by intradermal injection of vaccinia virus, whereas a prote
144 AP injection or either side of animals after intradermal injection of vehicle.
145                     Furthermore, concomitant intradermal injection of WBM EA extract in mice effectiv
146 sh) mice by intravenous, intraperitoneal, or intradermal injection of wild-type bone marrow-derived c
147                                     However, intradermal injection of Y. pestis, commonly used to mim
148              Previously, we showed that nine intradermal injections of a plasmid in which the HSVtk s
149   This is the first study demonstrating that intradermal injections of allogeneic fibroblasts have th
150  clinical benefits in humans, we gave single intradermal injections of allogeneic fibroblasts to five
151 J), and mast-cell deficient (Sl/Sld) mice by intradermal injections of anti-dinitrophenyl immunoglobu
152 d lymphadenectomy were treated with multiple intradermal injections of autologous, DNP-modified vacci
153                              Mice received 2 intradermal injections of bovine type II collagen (CII),
154 ured the magnitude of cutaneous responses to intradermal injections of C3a or C5a and the extent of I
155  influences (1) the cells' responsiveness to intradermal injections of C3a or C5a or (2) the extent o
156                  Inflammation was induced by intradermal injections of complete Freund's adjuvant (CF
157 y randomly generated sequence to receive two intradermal injections of either MVA85A or placebo.
158                                 Furthermore, intradermal injections of HP-NAP-encoding adenovirus in
159                             DTH responses to intradermal injections of HPV E7 antigen and KLH were de
160                                              Intradermal injections of LTA and the PAF-R agonist 1-he
161         Recent mouse studies have shown that intradermal injections of normal human fibroblasts can g
162 association with inflammatory skin diseases, intradermal injections of PAF induce inflammation, and k
163      Mice were immunized by intramuscular or intradermal injections of plasmid DNA derived from a nea
164 f rats immunized against adenovirus by prior intradermal injections of RAds.
165                         Furthermore, similar intradermal injections of small interfering RNA (siRNA;
166 onists or antagonists systemically, by local intradermal injection or by iontophoresis.
167 grass allergen Phl p 5 per injection), (2) 2 intradermal injections separated by 10 weeks, or (3) a s
168 ates of hTERT-specific T cells were noted at intradermal injection sites after repeated vaccination.
169 nificantly more frequent among recipients of intradermal injections than among recipients of intramus
170 , and a cynomolgus monkey by subcutaneous or intradermal injection to assess cytotoxicity or host res
171  mug keyhole limpet haemocyanin) via monthly intradermal injection until progression or intolerance,
172                           Mice vaccinated by intradermal injection using the jet injector or subcutan
173 s a rapid wheal and flare response following intradermal injection, whereas endothelin-1 (ET-1) produ
174 ferred highly significant protection against intradermal injection with 6 x 10(4) in vitro-cultivated
175 ntitumor immunity, animals were immunized by intradermal injection with expression plasmids encoding
176                           We used a model of intradermal injection with fluorescent-labeled, nonviabl
177 e responses were measured after double-blind intradermal injection with grass and birch pollen.
178                     Subjects who received an intradermal injection with one fifth the standard dose o
179 t were nasally administered with H471 before intradermal injection with the peptide.
180 ddress this, we challenged human subjects by intradermal injection with up to 1000 pmol of MIP-1 alph

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